Felis catus (domestic cat): 101082082 Help Entry 101082082         CDS       T02385                                  Symbol PSMD1 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 1   KO K03032   26S proteasome regulatory subunit N2 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101082082 (PSMD1)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101082082 (PSMD1)   09164 Neurodegenerative disease    05010 Alzheimer disease     101082082 (PSMD1)    05012 Parkinson disease     101082082 (PSMD1)    05014 Amyotrophic lateral sclerosis     101082082 (PSMD1)    05016 Huntington disease     101082082 (PSMD1)    05017 Spinocerebellar ataxia     101082082 (PSMD1)    05020 Prion disease     101082082 (PSMD1)    05022 Pathways of neurodegeneration - multiple diseases     101082082 (PSMD1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101082082 (PSMD1) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101082082 (PSMD1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RPN2_C PC_rep HEAT_2 Tim54 Motif Other DBs NCBI-GeneID:  101082082 NCBI-ProteinID:  XP_011283930 Ensembl:  ENSFCAG00000010085 UniProt:  A0A337SSW7 LinkDB All DBs Position C1:214188677..214284680 Genome browser AA seq 953 aa AA seqDB search MITSAAGIISLLDEEEPQLKEFALHKLNAVVNDFWAEISESVDKIEVLYEDEGFRSRQFA ALVASKVFYHLGAFEESLNYALGAGDLFNVNDNSEYVETIIAKCIDHYTKQCVENADLPE GEKKPIDQRLEGIVNKMFQRCLDDHKYKQAIGIALETRRLDVFEKTILESNDVPGMLAYS LKLCMSLMQNKQFRNKVLRVLVKIYMNLEKPDFINVCQCLIFLDDPQAVSDILEKLVKED NLLMAYQICFDLYESASQQFLSSVIQNLRTVGTPIASVPGSTNTGTVPGSEKDSDSMETE EKPGSVLVGKTPEVSPEPKDQTLKMIKILSGEMAIELHLQFLIRNNNTDLMILKNTKDAV RNSVCHTATVIANSFMHCGTTSDQFLRDNLEWLARATNWAKFTATASLGVIHKGHEKEAL QLMATYLPKDTSPGSAYQEGGGLYALGLIHANHGGDIIDYLLNQLKNASNDIVRHGGSLG LGLAAMGTARQDVYDLLKTNLYQDDAVTGEAAGLALGLVMLGSKNAQAIEDMVGYAQETQ HEKILRGLAVGIALVMYGRMEEADALIESLCRDKDPILRRSGMYTVAMAYCGSGNNKAIR RLLHVAVSDVNDDVRRAAVESLGFILFRTPEQCPSVVSLLSESYNPHVRYGAAMALGICC AGTGNKEAINLLEPMTNDPVNYVRQGALIASALIMIQQTEITCPKVNQFRQLYSKVINDK HDDVMAKFGAILAQGILDAGGHNVTISLQSRTGHTHMPSVVGVLVFTQFWFWFPLSHFLS LAYTPTCVIGLNKDLKMPKVQYKSNCKPSTFAYPAPLEVPKEKEKEKVSTAVLSITAKAK KKEKEKEKKEEEKMEVDEAEKKEEKEKKKEPEPNFQLLDNPARVMPAQLKVLTMPETCRY QPFKPLSIGGIIILKDTSEDTEELVEPVAAHGPKIEEEEQEPEPPEPFEYIDD NT seq 2862 nt NT seq  +upstreamnt  +downstreamnt atgatcacctcagctgctggaattatttctcttctggatgaggaagaaccacagcttaag gaatttgcactacacaaattgaatgcagttgtcaatgatttctgggcagaaatttctgag tctgtagataaaatagaagttttgtatgaagatgaaggtttccggagtcggcagtttgca gccttagtggcatctaaagtattttatcaccttggggcttttgaggaatctctgaattat gcacttggagctggtgacctcttcaatgtcaatgataactctgaatacgtggagactatt atagcaaaatgcattgatcactacaccaaacaatgtgtggaaaatgcagatttgccagaa ggagaaaaaaaaccaattgaccagagattagaaggaattgtaaataaaatgttccagcga tgtctagatgatcacaagtataagcaagctattggcattgctctggagacacgaagactg gacgtctttgagaagactatactggagtcgaatgatgtcccaggaatgctagcctatagc ctcaagctctgcatgtctttaatgcagaataaacagtttcggaataaggtactaagggtt ctagtgaaaatctacatgaatttggagaaacccgatttcatcaatgtttgtcagtgctta attttcttagatgatcctcaggccgtgagtgatatcttagaaaaactggtcaaggaagac aacctcctgatggcttatcagatttgttttgatttgtatgaaagtgctagccagcagttt ttgtcatctgtaatccagaatcttcgaactgttggcacccctattgcttctgtgcctgga tccaccaatacgggtactgtcccaggatcagagaaagacagtgactcaatggaaacagaa gaaaagccaggtagtgtacttgtaggaaagacaccagaagtgagtccagagcccaaggac cagactttgaaaatgattaaaattttaagcggtgaaatggctattgagttacatctacag tttttaatacgaaataataacacagatctcatgattctaaaaaacacaaaggatgcagta cggaattctgtatgtcacacagcaaccgttatagcaaattcttttatgcactgtgggact accagtgaccagtttcttagagataacttggaatggttggccagagccactaactgggcg aaatttacagctacagccagtttgggtgtaattcataagggtcacgagaaggaggcatta cagttaatggcaacatatcttcccaaggacacttctccaggatccgcctatcaggaaggt ggaggtctctatgcattaggtcttattcatgccaatcatggtggtgatataattgactat ctgcttaaccagcttaagaatgctagcaatgatatcgttcgacatgggggcagcctgggc ctgggtttggctgccatggggactgcacgccaggatgtatatgacttgctaaaaacgaac ctttatcaggatgatgctgtgacaggggaagcagctggcctggccctaggtttggttatg ttgggctctaaaaatgcccaggctattgaggacatggtcggctatgcacaggaaactcaa catgagaagattctgcgtggtcttgcagttggcattgcattagtgatgtatgggaggatg gaggaggctgatgctctcattgaatctctctgccgtgataaggacccaattcttcgacga tctggaatgtacactgtagccatggcttattgtggctcgggtaacaacaaagctatccgg cgcctgctacatgttgctgtaagtgacgttaatgatgatgtcaggagggcagcagtagaa tcacttgggttcattcttttcaggacccctgaacagtgccccagcgttgtttcattgttg tcagagagttacaatcctcacgtgcgttatggagctgctatggccctaggcatctgctgt gctggtaccggaaacaaggaggcaattaatttgctagaaccgatgacaaatgatcctgtg aactatgtgaggcaaggagctcttatagcttcagctctcatcatgatccagcagacggaa atcacttgtccaaaggtgaatcagttcagacagctgtattccaaagttatcaatgataaa catgatgatgtcatggccaagtttggcgctattttggcccagggcatactggatgcaggt ggtcataatgtcacaatctccttgcagtccaggactgggcacacccatatgccttctgta gttggcgtccttgtctttacccagttctggttctggtttcctctttcacacttcctgtca ttggcttatacccctacctgtgtcattggccttaacaaggacttaaagatgccgaaagtt cagtataaatcaaactgtaaaccatccacatttgcatatcctgcccctctggaagtacca aaagaaaaagaaaaggaaaaggtttccactgctgtgttatctattactgccaaggctaaa aaaaaggaaaaagaaaaagaaaaaaaagaggaggagaaaatggaagtggacgaagcagaa aaaaaggaagaaaaagagaagaaaaaagaacctgagccaaacttccagttattggataac ccagcccgagttatgcctgcccagcttaaggtcctgaccatgccagagacctgtagatac cagcctttcaaaccactctccattggaggcatcataatcctgaaggataccagtgaagac actgaagagctggtagaacctgtggcagcccacggcccaaaaattgaggaagaagaacaa gagccagaacccccagagccatttgagtatatcgatgattaa

Felis catus (domestic cat): 101082405 Help Entry 101082405         CDS       T02385                                  Name (RefSeq) LOW QUALITY PROTEIN: 26S proteasome regulatory subunit 4-like   KO K03062   26S proteasome regulatory subunit T2 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05165   Human papillomavirus infection fca05169   Epstein-Barr virus infection fca05203   Viral carcinogenesis Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101082405  09160 Human Diseases   09161 Cancer: overview    05203 Viral carcinogenesis     101082405   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101082405    05165 Human papillomavirus infection     101082405   09164 Neurodegenerative disease    05010 Alzheimer disease     101082405    05012 Parkinson disease     101082405    05014 Amyotrophic lateral sclerosis     101082405    05016 Huntington disease     101082405    05017 Spinocerebellar ataxia     101082405    05020 Prion disease     101082405    05022 Pathways of neurodegeneration - multiple diseases     101082405  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101082405 Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     ATPase subunits      101082405 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  AAA AAA_lid_3 Prot_ATP_ID_OB AAA_2 AAA_22 DUF815 AAA_16 DivIC AAA_5 PhoH IstB_IS21 AAA_28 RNA_helicase RuvB_N TsaE ABC_tran AAA_7 Sigma54_activat AAA_18 IPT AAA_33 Mg_chelatase Motif Other DBs NCBI-GeneID:  101082405 NCBI-ProteinID:  XP_023110519 LinkDB All DBs Position B2:77850795..77852407 Genome browser AA seq 435 aa AA seqDB search MGQSQSSGHGPGGVKKDDKDKRKKYKPPVPNRVPTKGTDAASKLPLVTPHTRCHLKLLKX RIKDYLLMEEEFIRNQEQMKPLEEKQEEERSKVDDLRGTPMLVGTLEEIIDDNHTIVSTS VGSEHYISILSFVDKDLLEPGCSVLLNRKVHAIIGVLMDDTDPLVMMMKVEKXPQETQAD IGGLDNQIQEIKESVELPLTHPEYYEEMGIKPPTGVILYGPTGTGKTLLAKAVANQTSAT FPRVVGSELIQKYLGDRPKLVWELFRVAEEHGPFIVFIGEIDAIGTKRYDSNSSGEREIQ RTMLELLNQLDGFDSRGDQKVIMAINQIETLDLALIRPGHIDRKNESPTKPDEKTEKCIF QIHTSRMMLADDVTLDDLIMAKDDLSGADIKATCTEAGVMALREHRMKVTNEDFKKSKEN VLYKKQEGTLEDLYL NT seq 1308 nt NT seq  +upstreamnt  +downstreamnt atgggtcaaagtcagagtagtggtcatggccctggaggtgtcaagaaggatgacaaggac aagagaaagaagtacaaacctcctgtaccaaacagagtaccaaccaaagggactgatgct gccagcaagctgccactggtgacacctcacactcggtgccacttaaaattactcaagntt agaattaaagactatcttctcatggaggaagaattcattagaaatcaggaacaaatgaag cctttagaagaaaagcaagaggaggaaagatcaaaggtggatgatctgagggggacccca atgttggtaggaacgttggaagagatcattgatgacaatcataccatcgtgtccacatct gtgggctcagaacactacatcagcattctttcctttgtagacaaggacctgctggagcca ggctgttcagttctgctcaaccgcaaggtacatgccataataggggtgctcatggatgac acggatcccttggtcatgatgatgaaagtagaaaagngcccccaggaaacccaagctgat attggggggttggacaaccaaatccaggaaattaaggaatctgtggagcttcctctcact catcctgaatattatgaagagatgggtataaagcccccaacaggggtcattctctatgga ccaactggcacaggtaaaaccttattagccaaagcggtagcaaaccaaacctcagccact ttcccaagagtggttggctctgaacttattcagaagtacctaggtgataggcccaaactc gtttgggagttgtttcgagttgcagaagaacatgggccattcatcgtgtttattggtgaa attgatgccattggaaccaaaagatatgattcaaattccagtggtgaaagagaaattcaa cgaacaatgttggaactgttgaaccagttggatggatttgattcaaggggtgaccagaaa gttatcatggccataaaccaaatagaaactttggatctagcacttatcagaccaggccac attgacaggaaaaatgagtcccccaccaagcctgatgaaaagactgagaagtgcatcttt cagatccacacaagcaggatgatgctggctgatgatgtgaccctggacgacttgatcatg gctaaagatgacctctctggggccgacatcaaggcgacctgtacagaagctggtgtgatg gccttgagagaacacagaatgaaagtaacaaatgaagactttaaaaaatccaaagaaaat gttctttataaaaaacaagaaggcacccttgaagacctctacttgtag

Felis catus (domestic cat): 101085106 Help Entry 101085106         CDS       T02385                                  Symbol PSMD6 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 6   KO K03037   26S proteasome regulatory subunit N7 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101085106 (PSMD6)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101085106 (PSMD6)   09164 Neurodegenerative disease    05010 Alzheimer disease     101085106 (PSMD6)    05012 Parkinson disease     101085106 (PSMD6)    05014 Amyotrophic lateral sclerosis     101085106 (PSMD6)    05016 Huntington disease     101085106 (PSMD6)    05017 Spinocerebellar ataxia     101085106 (PSMD6)    05020 Prion disease     101085106 (PSMD6)    05022 Pathways of neurodegeneration - multiple diseases     101085106 (PSMD6)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101085106 (PSMD6) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101085106 (PSMD6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RPN7 PCI Motif Other DBs NCBI-GeneID:  101085106 NCBI-ProteinID:  XP_003982446 Ensembl:  ENSFCAG00000000573 LinkDB All DBs Position A2:complement(31526196..31541857) Genome browser AA seq 389 aa AA seqDB search MPLENLEEEGLPKNPDLRIAQLRFLLSLPEHRGDAAVRDELMAAVRDNNMAPYYEALCKS LDWQMDTDLLSKMKKANEEELKRLDEELEDAEKNLGESEIRDAMMAKAEYLCRIGDKEGA LTAFRKTYDKTVALGHRLDIVFYLLRIGLFYMDNDLITRNTEKAKSLIEEGGDWDRRNRL KVYQGLYCVAIRDFKQAAELFLDTVSTFTSYELMDYKTFVTYTVYVSMIALERPDLREKV IKGAEILEVLHSLPAVRQYLFSLYECRYSVFFQSLAVVEQEMKKDWLFAPHYRYYVREMR IHAYSQLLESYRSLTLGYMAEAFGVGVEFIDQELSRFIAAGRLHCKIDKVNEIVETNRPD SKNWQYQETIKKGDLLLNRVQKLSRVINM NT seq 1170 nt NT seq  +upstreamnt  +downstreamnt atgccgctggagaacctcgaggaggagggtctgcccaagaaccccgacctgcgcatcgcg cagctgcgtttcctgctcagcctgcccgagcaccgcggagacgcggccgtgcgcgacgag ctgatggcggccgtccgggataataacatggctccttattacgaagccctgtgcaaatcc ctcgactggcagatggatacagacctgctcagtaagatgaagaaggcgaatgaggaagag ttgaaacgtttggacgaggagctggaagatgcagagaagaatctgggagagagcgaaatc cgggatgccatgatggcgaaggccgagtacctgtgccggataggtgacaaggagggtgct ctgacagcctttcgcaagacatatgacaaaaccgtggccttgggtcaccgactggatatt gtgttttatcttcttaggattggcttattttatatggataatgatctcatcacacgaaac acagagaaggccaaaagcttaatagaggaaggaggagattgggacaggagaaaccgccta aaagtatatcaaggtctttactgtgtggctattcgtgatttcaaacaggcagctgaactc ttccttgacacagtttcaacatttacatcctatgaacttatggattataaaacctttgtg acttacactgtctatgtcagcatgattgccttagaaagacctgatctccgggaaaaggtg attaaaggagcagagatcctggaggtgttgcacagccttccggcagttcggcagtatctg ttttccctctatgaatgtcgttactcggttttcttccagtcattagctgttgtggaacag gaaatgaaaaaggactggctttttgctcctcattatcgatactatgtaagagaaatgaga attcatgcatacagccagctgctggaatcctataggtcattaactcttggctatatggca gaagcctttggtgttggtgtggaattcattgatcaggaactctccagatttattgctgca gggagactacactgcaaaatagataaagtaaatgaaatagtggaaaccaacagacctgat agcaagaactggcagtaccaagaaactatcaagaaaggagatctgctgctaaacagagtt cagaaactttccagagtaattaatatgtaa

Felis catus (domestic cat): 101086215 Help Entry 101086215         CDS       T02385                                  Symbol PSMC2 Name (RefSeq) 26S proteasome regulatory subunit 7   KO K03061   26S proteasome regulatory subunit T1 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101086215 (PSMC2)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101086215 (PSMC2)   09164 Neurodegenerative disease    05010 Alzheimer disease     101086215 (PSMC2)    05012 Parkinson disease     101086215 (PSMC2)    05014 Amyotrophic lateral sclerosis     101086215 (PSMC2)    05016 Huntington disease     101086215 (PSMC2)    05017 Spinocerebellar ataxia     101086215 (PSMC2)    05020 Prion disease     101086215 (PSMC2)    05022 Pathways of neurodegeneration - multiple diseases     101086215 (PSMC2)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101086215 (PSMC2) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     ATPase subunits      101086215 (PSMC2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  AAA AAA_lid_3 AAA_22 AAA_5 AAA_16 DUF815 AAA_2 RuvB_N AAA_33 AAA_7 AAA_28 AAA_18 Sigma54_activ_2 Mg_chelatase AAA_14 TIP49 AAA_24 RNA_helicase HMW1C_N T2SSE IstB_IS21 Motif Other DBs NCBI-GeneID:  101086215 NCBI-ProteinID:  XP_003982735 Ensembl:  ENSFCAG00000000638 UniProt:  M3VV51 LinkDB All DBs Position A2:complement(82931577..82944675) Genome browser AA seq 433 aa AA seqDB search MPDYLGADQRKTKEDEKDDKPIRALDEGDIALLKTYGQSTYSRQIKQVEDDIQQLLKKIN ELTGIKESDTGLAPPALWDLAADKQTLQSEQPLQVARCTKIINADSEDPKYIINVKQFAK FVVDLSDQVAPTDIEEGMRVGVDRNKYQIHIPLPPKIDPTVTMMQVEEKPDVTYSDVGGC KEQIEKLREVVETPLLHPERFVNLGIEPPKGVLLFGPPGTGKTLCARAVANRTDACFIRV IGSELVQKYVGEGARMVRELFEMARTKKACLIFFDEIDAIGGARFDDGAGGDNEVQRTML ELINQLDGFDPRGNIKVLMATNRPDTLDPALMRPGRLDRKIEFSLPDLEGRTHIFKIHAR SMSVERDIRFELLARLCPNSTGAEIRSVCTEAGMFAIRARRKIATEKDFLEAVNKVIKSY AKFSATPRYMTYN NT seq 1302 nt NT seq  +upstreamnt  +downstreamnt atgcctgattacctcggtgccgatcagcggaaaaccaaagaggatgagaaggacgacaag cccatccgagctctggatgagggggatattgccttgctgaaaacttacggtcagagcact tactctaggcagataaagcaggttgaagatgatattcaacaacttctcaagaagatcaat gagcttactggtatcaaagaatctgatactggcctggccccaccagcactctgggatttg gctgcagataagcaaacactgcagagtgaacagcctttgcaggttgcgaggtgtacaaag atcatcaatgctgattcagaggacccaaagtacattatcaacgtgaagcagtttgccaag tttgtggtggaccttagtgatcaggtggcacctactgacattgaagaagggatgagagtt ggtgtggacagaaataagtatcagattcacattccgctgcctcccaagattgacccaaca gttaccatgatgcaggtggaggaaaaacctgatgtcacatacagtgacgtgggtggctgt aaagaacagattgagaaacttcgagaagtagttgaaaccccattacttcatccggagagg tttgttaaccttggcattgagcctcccaagggtgtgctgctctttggcccaccgggtaca ggcaagacactctgtgctcgggcagttgctaacaggacagatgcttgcttcattcgagtt attggatctgaacttgtacagaagtacgttggtgagggggctcgaatggttcgggagctc tttgaaatggccagaacaaaaaaagcctgccttatcttctttgatgaaattgatgctatt ggaggggctcgttttgatgatggtgctggaggagacaacgaagtgcagagaacgatgctg gaactgatcaatcaactggacggttttgatcctcgaggtaacattaaagtgctgatggcc actaacagacctgacactttggatccagcactgatgaggccagggagattggacagaaag attgaatttagcttacctgatctagagggtcggactcatatttttaagatccacgctcgc tcaatgagcgtggaaagagatatcagatttgaactgttagcacgactgtgtccaaatagc actggtgctgagattagaagtgtatgcacagaagctggtatgtttgctatcagagcacgg cgaaaaattgctactgagaaagatttcctggaggctgtaaataaggtcattaagtcttat gccaaattcagtgctactccccgctatatgacatacaactga

Felis catus (domestic cat): 101086493 Help Entry 101086493         CDS       T02385                                  Name (RefSeq) LOW QUALITY PROTEIN: 26S proteasome complex subunit SEM1   KO K10881   26 proteasome complex subunit DSS1 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca03440   Homologous recombination fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101086493   09124 Replication and repair    03440 Homologous recombination     101086493  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101086493   09164 Neurodegenerative disease    05010 Alzheimer disease     101086493    05012 Parkinson disease     101086493    05014 Amyotrophic lateral sclerosis     101086493    05016 Huntington disease     101086493    05017 Spinocerebellar ataxia     101086493    05020 Prion disease     101086493    05022 Pathways of neurodegeneration - multiple diseases     101086493  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03019 Messenger RNA biogenesis [BR:fca03019]     101086493    04131 Membrane trafficking [BR:fca04131]     101086493    03051 Proteasome [BR:fca03051]     101086493    03400 DNA repair and recombination proteins [BR:fca03400]     101086493 Messenger RNA biogenesis [BR:fca03019]  Eukaryotic type   mRNA surveillance and transport factors    Transport factors     TREX-2 complex      101086493 Membrane trafficking [BR:fca04131]  Exocytosis   Tethering complex    Exocyst complex assembly proteins     101086493 Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101086493 DNA repair and recombination proteins [BR:fca03400]  Eukaryotic type   DSBR (double strand breaks repair)    HR (homologous recombination)     Other HR factors      101086493 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  DSS1_SEM1 Motif Other DBs NCBI-GeneID:  101086493 NCBI-ProteinID:  XP_019694746 LinkDB All DBs Position C1:160868367..160868589 Genome browser AA seq 70 aa AA seqDB search MSEKKQLVDLGLWEEDNEFREFPKEDWAGLDENEEADVXENNWDFDNVEGNFSNLIXGKS ETHGYKMETS NT seq 213 nt NT seq  +upstreamnt  +downstreamnt atgtcagagaaaaagcagctggtggacttaggtctctgggaggaggacaacgagttcagg gagttccccaaggaagactgggctggtttagatgaaaatgaagaagcagatgtctaggaa aataactgggattttgacaatgtagagggtaacttctccaatctgatatgaggtaaatca gagacacatggttataagatggagacctcatag

Felis catus (domestic cat): 101090224 Help Entry 101090224         CDS       T02385                                  Symbol PSMC4 Name (RefSeq) 26S proteasome regulatory subunit 6B isoform X1   KO K03063   26S proteasome regulatory subunit T3 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101090224 (PSMC4)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101090224 (PSMC4)   09164 Neurodegenerative disease    05010 Alzheimer disease     101090224 (PSMC4)    05012 Parkinson disease     101090224 (PSMC4)    05014 Amyotrophic lateral sclerosis     101090224 (PSMC4)    05016 Huntington disease     101090224 (PSMC4)    05017 Spinocerebellar ataxia     101090224 (PSMC4)    05020 Prion disease     101090224 (PSMC4)    05022 Pathways of neurodegeneration - multiple diseases     101090224 (PSMC4)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101090224 (PSMC4) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     ATPase subunits      101090224 (PSMC4) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  AAA Prot_ATP_ID_OB AAA_lid_3 AAA_2 AAA_5 AAA_16 RuvB_N DUF815 AAA_22 RNA_helicase AAA_14 Mg_chelatase AAA_28 NTPase_1 AAA_18 AAA_33 Sigma54_activat NACHT TIP49 AAA_3 CENP-F_leu_zip IstB_IS21 AAA_7 TsaE ATPase_2 Zeta_toxin AAA_24 AAA_25 AAA_17 NB-ARC Parvo_NS1 DUF3450 ABC_tran AAA_30 Motif Other DBs NCBI-GeneID:  101090224 NCBI-ProteinID:  XP_011288187 Ensembl:  ENSFCAG00000001026 UniProt:  M3VVV5 LinkDB All DBs Position E2:complement(14517601..14529831) Genome browser AA seq 418 aa AA seqDB search MEEIGILVEKAQDEIPALSVSRPQTGLSFLGPEPEDLEDLYSRYKKLQQELEFLEVQEEY IKDEQKNLKKEFLHAQEEVKRIQSIPLVIGQFLEAVDQNTAIVGSTTGSNYYVRILSTID RELLKPNASVALHKHSNALVDVLPPEADSSIMMLTSDQKPDVMYADIGGMDIQKQEVREA VELPLTHFELYKQIGIDPPRGVLMYGPPGCGKTMLAKAVAHHTTAAFIRVVGSEFVQKYL GEGPRMVRDVFRLAKENAPAIIFIDEIDAIATKRFDAQTGADREVQRILLELLNQMDGFD QNVNVKVIMATNRADTLDPALLRPGRLDRKIEFPLPDRRQKRLIFSTITSKMNLSEEVDL EDYVARPDKISGADINSICQESGMLAVRENRYIVLAKDFEKAYKTVIKKDEQEHEFYK NT seq 1257 nt NT seq  +upstreamnt  +downstreamnt atggaggagataggcatcttggtagagaaagctcaggatgagatcccagcactgtctgtg tctcggccccagactggcctttccttcctggggccggagcctgaggacctggaggacctg tacagccgctacaagaagctgcagcaagagttggagttcctggaggtgcaggaggaatac atcaaggatgagcagaagaacctgaagaaggaattcctccatgcccaggaggaggtgaag cgaatccaaagcatcccactggtcattgggcagtttctggaggctgtggatcagaataca gccattgtgggctccaccacaggctccaactactacgtgcgcatcctgagcaccattgat cgggagctgctcaagcctaacgcctcggtggccctgcacaagcacagcaatgccctggtg gacgtgctgcctcctgaggctgacagcagcatcatgatgctcacctcagaccagaagccg gatgtgatgtatgcagacatcgggggcatggacatccagaagcaggaggtgcgggaggct gtggagctcccacttacacacttcgagctgtataagcagatcggcatcgaccctccccga ggcgtcctcatgtatggcccacctggctgcgggaagaccatgctggcgaaggctgtggct catcacacgacagctgcgtttatccgggtcgtgggctccgagtttgtacagaaatacctg ggcgagggcccccgcatggtccgggacgtgttccgcctggccaaggagaacgcacctgcc atcatcttcatagatgagattgacgccattgccaccaagagatttgatgcccagacgggg gctgacagggaggttcagagaatcctgctggagctgctgaatcaaatggacggatttgac cagaacgttaacgtcaaggtgatcatggccacgaacagagcagacactctggatcctgcc ctgctgcggccaggacgccttgatcgtaaaattgaatttccactccctgaccgccgccag aagagattgattttctccactatcaccagcaagatgaatctctctgaggaggttgacttg gaagactatgtggcccgaccagataagatttcaggagccgatatcaactccatctgtcag gagagtggaatgttggctgtccgtgagaaccgctacattgttctggctaaggacttcgag aaagcatacaagacagtcatcaagaaggatgaacaggagcatgagttttataagtga

Felis catus (domestic cat): 101091665 Help Entry 101091665         CDS       T02385                                  Symbol PSMD11 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 11   KO K03036   26S proteasome regulatory subunit N6 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101091665 (PSMD11)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101091665 (PSMD11)   09164 Neurodegenerative disease    05010 Alzheimer disease     101091665 (PSMD11)    05012 Parkinson disease     101091665 (PSMD11)    05014 Amyotrophic lateral sclerosis     101091665 (PSMD11)    05016 Huntington disease     101091665 (PSMD11)    05017 Spinocerebellar ataxia     101091665 (PSMD11)    05020 Prion disease     101091665 (PSMD11)    05022 Pathways of neurodegeneration - multiple diseases     101091665 (PSMD11)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101091665 (PSMD11) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101091665 (PSMD11) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RPN6_N PCI RPN6_C_helix TPR_12 DDRGK DUF2153 AAA_16 Motif Other DBs NCBI-GeneID:  101091665 NCBI-ProteinID:  XP_023099204 Ensembl:  ENSFCAG00000002060 LinkDB All DBs Position E1:20497196..20527270 Genome browser AA seq 422 aa AA seqDB search MAAAAVVEFQRAQSLLSTDREASIDILHSIVKRDIQENDEEAVQVKEQSILELGSLLAKT GQAAELGGLLKYVRPFLNSISKAKAARLVRSLLDLFLDMEAATGQEVELCLECIEWAKSE KRTFLRQALEARLVSLYFDTKRYQEALHLGSQLLRELKKMDDKALLVEVQLLESKTYHAL SNLPKARAALTSARTTANAIYCPPKLQATLDMQSGIIHAAEEKDWKTAYSYFYEAFEGYD SIDSPKAITSLKYMLLCKIMLNTPEDVQALVSGKLALRYAGRQTEALKCVAQASKNRSLA DFEKALTDYRAELRDDPIISTHLAKLYDNLLEQNLIRVIEPFSRVQIEHISSLIKLSKAD VERKLSQMILDKKFHGILDQGEGVLIIFDEPPVDKTYEAALETIQNMSKVVDSLYNKAKK LT NT seq 1269 nt NT seq  +upstreamnt  +downstreamnt atggcggcggcggcggtggtggagttccagagagcccagtctctactcagcaccgaccgg gaggcctccatcgacattctccactccatcgtgaagcgtgacattcaggagaatgatgag gaggcagtgcaggtcaaagagcagagtatcctggaactcgggtctctcttggcgaagact ggacaagctgcagagcttggaggactcctgaagtatgtgcgacccttcttgaattccatc agcaaggctaaggcagctcgtctggtccgatctcttcttgatctgtttcttgatatggaa gcagctacagggcaggaggtcgagttgtgtttagagtgcatcgaatgggccaaatcagag aaaagaactttcttacgccaagctttggaggcaagactggtgtctttgtactttgatacc aagaggtaccaggaagcattgcatttgggttctcagctgctgcgggagttgaaaaagatg gatgacaaagcccttttggtggaagtacagcttttagaaagcaaaacataccatgccctg agcaacctgccgaaagcccgagctgccttaacctctgctcgaactacagcaaatgctatc tactgcccccctaaattgcaggccacattggatatgcaatcaggtattatccatgcagca gaggagaaggattggaaaactgcatactcatatttctatgaggcatttgagggttatgat tccatcgatagccccaaggccatcacatctctgaagtacatgttgctgtgcaaaattatg ctcaacaccccagaagatgtccaggctttggtgagcgggaaacttgcgcttcggtatgca gggaggcagacagaagcattaaaatgtgtggctcaggctagcaagaacagatcactggca gattttgaaaaggccctgacagattaccgggcagagctccgggatgacccaatcatcagt acacacttggccaagttgtatgacaacttgctggaacagaatctgatccgggtcattgag cctttttcccgagttcagattgaacacatatctagcctcatcaaactctccaaggccgac gtggaaaggaaattatcacagatgattcttgacaagaaatttcatgggatcttggaccag ggggagggtgtcttgattattttcgatgaacccccagtagataaaacttatgaagctgct ctggaaacaattcagaacatgagtaaagtagtggattccctctacaacaaagccaagaaa ctgacatag

Felis catus (domestic cat): 101094025 Help Entry 101094025         CDS       T02385                                  Symbol PSMC1 Name (RefSeq) 26S proteasome regulatory subunit 4   KO K03062   26S proteasome regulatory subunit T2 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05165   Human papillomavirus infection fca05169   Epstein-Barr virus infection fca05203   Viral carcinogenesis Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101094025 (PSMC1)  09160 Human Diseases   09161 Cancer: overview    05203 Viral carcinogenesis     101094025 (PSMC1)   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101094025 (PSMC1)    05165 Human papillomavirus infection     101094025 (PSMC1)   09164 Neurodegenerative disease    05010 Alzheimer disease     101094025 (PSMC1)    05012 Parkinson disease     101094025 (PSMC1)    05014 Amyotrophic lateral sclerosis     101094025 (PSMC1)    05016 Huntington disease     101094025 (PSMC1)    05017 Spinocerebellar ataxia     101094025 (PSMC1)    05020 Prion disease     101094025 (PSMC1)    05022 Pathways of neurodegeneration - multiple diseases     101094025 (PSMC1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101094025 (PSMC1) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     ATPase subunits      101094025 (PSMC1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  AAA AAA_lid_3 Prot_ATP_ID_OB AAA_2 AAA_22 DUF815 RuvB_N AAA_5 AAA_16 AAA_18 AAA_25 AAA_33 ATPase IstB_IS21 AAA_28 RNA_helicase AAA_3 AAA_14 Mg_chelatase TIP49 AAA_7 Prot_ATP_OB_N NACHT PhoH AAA_24 AAA_30 NB-ARC ABC_tran Parvo_NS1 TsaE Sigma54_activat Motif Other DBs NCBI-GeneID:  101094025 NCBI-ProteinID:  XP_003987959 Ensembl:  ENSFCAG00000011310 UniProt:  A0A2I2UUT8 LinkDB All DBs Position B3:136031469..136045101 Genome browser AA seq 440 aa AA seqDB search MGQSQSGGHGPGGGKKDDKDKKKKYEPPVPTRVGKKKKKTKGPDAASKLPLVTPHTQCRL KLLKLERIKDYLLMEEEFIRNQEQMKPLEEKQEEERSKVDDLRGTPMSVGTLEEIIDDNH AIVSTSVGSEHYVSILSFVDKDLLEPGCSVLLNHKVHAVIGVLMDDTDPLVTVMKVEKAP QETYADIGGLDNQIQEIKESVELPLTHPEYYEEMGIKPPKGVILYGPPGTGKTLLAKAVA NQTSATFLRVVGSELIQKYLGDGPKLVRELFRVAEEHAPSIVFIDEIDAIGTKRYDSNSG GEREIQRTMLELLNQLDGFDSRGDVKVIMATNRIETLDPALIRPGRIDRKIEFPLPDEKT KRRIFQIHTSRMTLADDVTLDDLIMAKDDLSGADIKAICTEAGLMALRERRMKVTNEDFK KSKENVLYKKQEGTPEGLYL NT seq 1323 nt NT seq  +upstreamnt  +downstreamnt atgggtcaaagtcagagtggtggtcatggccctggaggtggcaagaaggatgacaaggat aagaaaaagaagtacgaacctcctgtaccaaccagagtggggaaaaagaagaagaaaaca aagggaccggatgctgccagcaagctgccactggtgacacctcacactcagtgccgctta aaattactgaagttagagagaattaaagactatcttctcatggaggaagaattcattaga aatcaggaacaaatgaagcctttagaagaaaagcaagaggaggagagatcaaaggtggat gatctgagggggaccccgatgtcggtaggaacgttggaagagatcattgatgacaatcac gccatcgtgtccacgtctgtgggctcagaacactacgtcagcattctctcctttgtagac aaggacctgctggagccaggctgttcggtcctgctcaaccacaaggtacatgccgtcata ggggtgctcatggatgacacggatcccttggtcacagtgatgaaagtagaaaaggccccc caggaaacctatgctgatattggggggctggacaaccaaatccaggaaattaaggaatct gtggagcttcctctcactcatcctgaatattatgaagagatgggtataaagcccccaaaa ggggtcattctctatggaccacctggcacaggtaaaaccttattagccaaagcagtagca aaccaaacctcagccactttcctaagagtggttggctctgaacttattcagaagtaccta ggtgatgggcccaaactcgttcgggagttatttcgagttgcagaagaacacgcgccatcc atcgtgtttattgatgaaattgatgccattggaacaaaaagatacgattcaaattccggt ggtgaaagagaaatccagcgaacaatgttggaactgttgaaccagttggatggatttgat tcaaggggtgacgtgaaagttatcatggccacaaaccgaatagaaactttggatccagca cttatcagaccaggccgcattgacaggaaaattgagttccccctgcccgatgaaaagacc aagaggcgcatctttcagatccacacaagcaggatgacgctggccgatgatgtgaccctg gacgacttgatcatggctaaagatgacctctctggggccgacatcaaggcgatctgtaca gaagctggtctgatggccttgagagaacgcagaatgaaagtaacaaatgaagacttcaaa aaatcgaaagaaaacgttctttataaaaaacaagaaggtacccctgaagggctctacttg tag

Felis catus (domestic cat): 101094305 Help Entry 101094305         CDS       T02385                                  Symbol PSMD3 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 3 isoform X2   KO K03033   26S proteasome regulatory subunit N3 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101094305 (PSMD3)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101094305 (PSMD3)   09164 Neurodegenerative disease    05010 Alzheimer disease     101094305 (PSMD3)    05012 Parkinson disease     101094305 (PSMD3)    05014 Amyotrophic lateral sclerosis     101094305 (PSMD3)    05016 Huntington disease     101094305 (PSMD3)    05017 Spinocerebellar ataxia     101094305 (PSMD3)    05020 Prion disease     101094305 (PSMD3)    05022 Pathways of neurodegeneration - multiple diseases     101094305 (PSMD3)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101094305 (PSMD3) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101094305 (PSMD3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Rpn3_C PCI TPR_2 CSN8_PSD8_EIF3K Motif Other DBs NCBI-GeneID:  101094305 NCBI-ProteinID:  XP_003996842 Ensembl:  ENSFCAG00000014991 UniProt:  M3WLR0 LinkDB All DBs Position E1:41012225..41027037 Genome browser AA seq 532 aa AA seqDB search MKQEGSGRRRGADKAKPPPGGGEQEPPPPPTPQDVEMKEEAAAGGASAGEADSKTAAAEH SQRELDTVTLEDIKEHVKQLEKAVSGKEPRFVLRALRMLPSTSRRLNHYVLYKAVHGFFT SNNATRDFLLPFLEEPMDTEADLQFRPRTGKAASAPLLPEVEAYLQLLVVIFLMNSKRYK EAQKISDDLMQKISTQNRRALDLVAAKCYYYHARVYEFLDKLDVVRSFLHARLRTATLRH DADGQATLLNLLLRNYLHYSLYDQAEKLVSKSVFPEQANNNEWARYLYYTGRIKAIQLEY SEARRTMTNALRKAPQHTAVGFKQTVHKLLIVVELLLGEIPDRLQFRQPSLKRSLMPYFL LTQAVRTGNLAKFNQVLDQFGEKFQADGTYTLIIRLRHNVIKTGVRMISLSYSRISLADI AQKLQLDSPEDAEFIVAKAIRDGVIEASINHEKGYVQSKEMIDIYSTREPQLAFHQRISF CLDIHNMSVKAMRFPPKSYNKDLESAEERREREQQDLEFAKEMAEDDDDSFP NT seq 1599 nt NT seq  +upstreamnt  +downstreamnt atgaaacaggagggctcggggcgccgccgcggcgcggacaaggcaaagccgccgccgggc ggaggggagcaagaaccaccgccgcccccgactccccaggatgtggagatgaaagaggag gcggcggcgggtggcgcgtcagcgggagaagctgacagcaaaacggcggcggctgagcac tcccagcgagagctggacaccgtcaccttggaggacattaaagagcatgtgaaacagctg gagaaggcagtttcgggcaaggagcctcgatttgtgctgagggccctgcggatgctccct tccacatcacgtcgcctcaaccactacgttctgtataaggctgtacatggcttcttcacc tcaaataatgccactcgagacttcttgctacccttcctggaagagcccatggacaccgaa gctgatttacagttccgtccccgaacaggaaaagctgcatcggcacccctcctgcctgag gtggaagcctatctacagctcctcgtggtcatcttcctgatgaacagcaaacgctacaaa gaggcacagaagatctctgatgacctaatgcagaagatcagcactcagaaccgccgggcc ctggaccttgtggccgcaaagtgttactactatcatgcccgggtctatgagttcctggac aagctggatgtggtgcgcagcttcttgcatgctcggctccggacagccacccttcggcat gatgcggatgggcaggccaccctgctgaacctcctgctgcggaactacctacactacagc ttgtacgaccaggctgagaagctggtgtccaagtccgtgttccccgagcaggccaacaac aatgagtgggccaggtacctctactacacagggcgaatcaaagctattcagttggagtac tcagaggcccggagaacaatgaccaatgcccttcgcaaggcccctcagcacacagctgtc ggcttcaaacagacggtgcacaagcttctgattgtggtggagctgctgcttggggagatc ccagaccggctacagttccgtcagccatctctcaagcgctcgctcatgccctacttcctt cttactcaagctgtcaggaccggaaaccttgccaagttcaaccaggtcctggaccagttt ggagagaagtttcaagcagatgggacctataccctaatcatccgactacggcacaacgtc attaagacaggtgtgcgcatgatcagcctttcctattcccgaatctccctggctgacatc gcccagaagctgcagctggatagcccagaggatgcagagttcattgttgccaaggccatc cgggatggtgtcattgaggccagcatcaaccacgagaagggctacgtccagtccaaggag atgattgatatctactccacccgtgagccccagctggccttccaccagcgcatctccttc tgtctagatatccacaacatgtccgtcaaggccatgaggtttcctcccaaatcgtacaac aaggacttggagtctgcagaggaacggcgcgagcgagagcagcaggacttggagtttgcc aaggagatggccgaagatgatgatgacagcttcccttga

Felis catus (domestic cat): 101094744 Help Entry 101094744         CDS       T02385                                  Symbol SEM1 Name (RefSeq) 26S proteasome complex subunit SEM1   KO K10881   26 proteasome complex subunit DSS1 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca03440   Homologous recombination fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101094744 (SEM1)   09124 Replication and repair    03440 Homologous recombination     101094744 (SEM1)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101094744 (SEM1)   09164 Neurodegenerative disease    05010 Alzheimer disease     101094744 (SEM1)    05012 Parkinson disease     101094744 (SEM1)    05014 Amyotrophic lateral sclerosis     101094744 (SEM1)    05016 Huntington disease     101094744 (SEM1)    05017 Spinocerebellar ataxia     101094744 (SEM1)    05020 Prion disease     101094744 (SEM1)    05022 Pathways of neurodegeneration - multiple diseases     101094744 (SEM1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03019 Messenger RNA biogenesis [BR:fca03019]     101094744 (SEM1)    04131 Membrane trafficking [BR:fca04131]     101094744 (SEM1)    03051 Proteasome [BR:fca03051]     101094744 (SEM1)    03400 DNA repair and recombination proteins [BR:fca03400]     101094744 (SEM1) Messenger RNA biogenesis [BR:fca03019]  Eukaryotic type   mRNA surveillance and transport factors    Transport factors     TREX-2 complex      101094744 (SEM1) Membrane trafficking [BR:fca04131]  Exocytosis   Tethering complex    Exocyst complex assembly proteins     101094744 (SEM1) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101094744 (SEM1) DNA repair and recombination proteins [BR:fca03400]  Eukaryotic type   DSBR (double strand breaks repair)    HR (homologous recombination)     Other HR factors      101094744 (SEM1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  DSS1_SEM1 Motif Other DBs NCBI-GeneID:  101094744 NCBI-ProteinID:  XP_023106137 Ensembl:  ENSFCAG00000023254 LinkDB All DBs Position A2:complement(101428521..101452925) Genome browser AA seq 70 aa AA seqDB search MSEKKQPVDLGLLEEDDEFEEFPAEDWAGLDEDEDAHVWEDNWDDDNVEDDFSNQLRAEL EKHGYKMETS NT seq 213 nt NT seq  +upstreamnt  +downstreamnt atgtcagagaaaaagcagccagtagatttgggtctcttggaggaggacgacgagttcgag gagttccctgcggaagactgggctggtttggatgaggatgaagatgcacatgtctgggag gataattgggatgatgacaatgtagaggatgacttctccaatcagttacgagctgaacta gagaaacatggttataagatggagacttcatag

Felis catus (domestic cat): 101095118 Help Entry 101095118         CDS       T02385                                  Symbol PSMD14 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 14   KO K03030   26S proteasome regulatory subunit N11 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101095118 (PSMD14)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101095118 (PSMD14)   09164 Neurodegenerative disease    05010 Alzheimer disease     101095118 (PSMD14)    05012 Parkinson disease     101095118 (PSMD14)    05014 Amyotrophic lateral sclerosis     101095118 (PSMD14)    05016 Huntington disease     101095118 (PSMD14)    05017 Spinocerebellar ataxia     101095118 (PSMD14)    05020 Prion disease     101095118 (PSMD14)    05022 Pathways of neurodegeneration - multiple diseases     101095118 (PSMD14)  09180 Brite Hierarchies   09181 Protein families: metabolism    01002 Peptidases and inhibitors [BR:fca01002]     101095118 (PSMD14)   09182 Protein families: genetic information processing    04121 Ubiquitin system [BR:fca04121]     101095118 (PSMD14)    03051 Proteasome [BR:fca03051]     101095118 (PSMD14) Peptidases and inhibitors [BR:fca01002]  Metallo peptidases   Family M67    101095118 (PSMD14) Ubiquitin system [BR:fca04121]  Deubiquitinating enzyme (DUB)   Ubiquitin-specific proteases (UBPs)    JAMM     101095118 (PSMD14) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101095118 (PSMD14) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  JAB MitMem_reg Prok-JAB DUF4525 Motif Other DBs NCBI-GeneID:  101095118 NCBI-ProteinID:  XP_006935378 Ensembl:  ENSFCAG00000030865 UniProt:  A0A337S6G5 LinkDB All DBs Position C1:153254771..153351676 Genome browser AA seq 310 aa AA seqDB search MDRLLRLGGGMPGLGQGPPTDAPAVDTAEQVYISSLALLKMLKHGRAGVPMEVMGLMLGE FVDDYTVRVIDVFAMPQSGTGVSVEAVDPVFQAKMLDMLKQTGRPEMVVGWYHSHPGFGC WLSGVDINTQQSFEALSERAVAVVVDPIQSVKGKVVIDAFRLINANMMVLGHEPRQTTSN LGHLNKPSIQALIHGLNRHYYSITINYRKNELEQKMLLNLHKKSWMEGLTLQDYSEHCKH NESVVKEMLELAKNYNKAVEEEDKMTPEQLAIKNVGKQDPKRHLEEHVDVLMTSNIVQCL AAMLDTVVFK NT seq 933 nt NT seq  +upstreamnt  +downstreamnt atggacagacttcttagacttggaggaggtatgcctggactgggccaggggccacccaca gatgctcctgcagtggacacagcagagcaagtatatatttcttcccttgcactgttaaaa atgttaaagcatggtcgtgctggagttccaatggaagttatgggtcttatgcttggagaa tttgttgatgattacaccgtcagagtgattgatgtgtttgctatgccacagtcaggaaca ggtgtcagtgtggaggcagttgatccagtgttccaagccaaaatgttagatatgttgaag cagacaggaaggcctgagatggttgttggttggtatcacagtcaccctggctttggttgt tggctttctggtgtggatatcaacactcagcagagctttgaagccttgtcggagagagct gtggcagtggttgtggatcccattcagagtgtaaaaggaaaggttgttatcgatgccttc agattgatcaatgctaatatgatggtcttaggacatgaaccaagacaaacaacctcaaat ctgggtcatttaaacaagccatctatccaggcgttaattcacggactaaacagacactac tactccattactattaactaccgaaaaaatgaactggaacagaagatgttgctaaatttg cataagaagagttggatggaaggtttgacacttcaggactacagtgaacactgtaaacac aatgaatcagtggtaaaagagatgttggaattagccaagaattacaataaggctgtagaa gaagaagataagatgacacctgaacagctggcaataaagaatgttggcaagcaggacccc aaacgtcatttggaggaacatgtggatgtacttatgacttcaaatatcgtccagtgttta gcagctatgttggatactgtcgtatttaaataa

Felis catus (domestic cat): 101095190 Help Entry 101095190         CDS       T02385                                  Symbol PSMD2 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 2   KO K03028   26S proteasome regulatory subunit N1 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101095190 (PSMD2)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101095190 (PSMD2)   09164 Neurodegenerative disease    05010 Alzheimer disease     101095190 (PSMD2)    05012 Parkinson disease     101095190 (PSMD2)    05014 Amyotrophic lateral sclerosis     101095190 (PSMD2)    05016 Huntington disease     101095190 (PSMD2)    05017 Spinocerebellar ataxia     101095190 (PSMD2)    05020 Prion disease     101095190 (PSMD2)    05022 Pathways of neurodegeneration - multiple diseases     101095190 (PSMD2)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101095190 (PSMD2) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101095190 (PSMD2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RPN1_RPN2_N RPN1_C PC_rep THAP Motif Other DBs NCBI-GeneID:  101095190 NCBI-ProteinID:  XP_006936288 Ensembl:  ENSFCAG00000007793 UniProt:  M3W8D9 LinkDB All DBs Position C2:complement(85245906..85255070) Genome browser AA seq 908 aa AA seqDB search MEEGGRDKAPLQPQQPPATAPGIADEKPGGKERRDAGDKDKEQELSEEDKQLQDELEMLV ERLGEKDTSLYRPALEELRRQIRSSTTSMTSVPKPLKFLRPHYGKLKEIYENMPPGENKR FAADIISVLAMTMSGERECLKYRLVGSQEELASWGHEYVRHLAGEVAKEWQELDDAEKTQ REPLLTLVKEIVPYNMAHNAEHEACDLLMEIEQVDMLEKDIDENAYAKVCLYLTSCVNYV PEPENSALLRCALGVFRKFSRFPEALRLALMLNDMELVEDIFTSCKDVVVQKQMAFMLGR HGVFLELSEDVEEYEDLTEIMSNVQLNSNFLALARELDIMEPKVPDDIYKTHLENNRFGG SGSQVDSARMNLASSFVNGFVNAAFGQDKLLTDDGNKWLYKNKDHGMLSAAASLGMILLW DVDGGLTQIDKYLYSSEDYIKSGALLACGIVNSGVRNECDPALALLSDYVLHNSNTMRLG SIFGLGLAYAGSNREDVLTLLLPVMGDSKSSMEVAGVTALACGMIAVGSCNGDVTSTILQ TIMEKSETELKDTYARWLPLGLGLNHLGKGEAIEAILAALEVVSEPFRSFANTLVDVCAY AGSGNVLKVQQLLHICSEHFDSKEKEEDKDKKEKKDKDKKEAPADMGAHQGVAVLGIALI AMGEEIGAEMALRTFGHLLRYGEPTLRRAVPLALALISVSNPRLNILDTLSKFSHDADPE VSYNSIFAMGMVGSGTNNARLAAMLRQLAQYHAKDPNNLFMVRLAQGLTHLGKGTLTLCP YHSDRQLMSQVAVAGLLTVLVSFLDVRNIILGKSHYVLYGLVAAMQPRMLVTFDEELRPL PVSVRVGQAVDVVGQAGKPKTITGFQTHTTPVLLAHGERAELATEEFLPVTPILEGFVIL RKNPNYDL NT seq 2727 nt NT seq  +upstreamnt  +downstreamnt atggaggagggtggccgggataaggctccgctgcagcctcagcagcctccggcgacggca ccgggcatcgcggacgagaagccgggcggcaaggagcggcgggatgctggcgacaaggac aaagagcaggagctgtctgaggaggacaaacaacttcaggatgaactggagatgctcgtg gaacgactgggggagaaggacacatctctgtaccgaccagccctcgaggaactgcggagg caaatccgatcttctacaacttccatgacttcagtgcccaagcctctcaaatttctgcgt ccacactatggcaaactgaaggaaatctatgagaacatgccccctggggagaataagcgt tttgctgctgacatcatctctgttctggctatgaccatgagtggggaacgtgagtgtctc aagtatcggctggtgggctcccaagaggaattggcatcatggggtcatgagtatgtgagg catctcgcaggggaagtggctaaggagtggcaggaactagatgacgcggaaaagacacaa cgggagccactgctgaccctggtgaaggagatcgtcccctacaacatggcccacaacgcg gagcacgaggcctgtgacctgctcatggaaattgagcaggtagacatgctggagaaggac attgatgagaatgcatatgccaaggtctgcctctatcttaccagctgtgtgaattatgtg cccgagcctgagaattctgcactactgcgctgtgctttgggtgtgttccgaaagttcagt cgttttcctgaagctctgagattggcattgatgctcaatgacatggagctggtagaagat atcttcacctcctgcaaggacgtggtagtacagaagcagatggcattcatgcttggccgt catggggtgtttctggagcttagtgaagacgtggaggagtatgaggacctgacagagatc atgtccaatgtgcagctcaacagcaacttcttggcattagctcgggagctggatattatg gagcccaaggtgcctgatgacatctataaaacccatctagagaacaacagatttgggggc agtggctctcaagtggactctgcccgcatgaacctggcctcttcttttgtgaatggcttt gtgaatgcagcctttggtcaggacaagctgctgactgatgatggcaacaaatggctttac aagaacaaagaccatggaatgttgagtgcagctgcgtcccttggcatgattctgctgtgg gatgtggatggtggcctcacgcagattgacaagtacttgtactcctctgaggactacatc aagtcaggagcccttctggcctgtggcattgtgaactctggagtccggaatgaatgtgac cccgcactagcactgctctcagactatgttctccacaacagcaacactatgagacttggt tccatttttgggctaggcttggcttacgctggctccaatcgtgaagatgtgctaacactg ctgctccctgtgatgggagattccaagtctagtatggaggtggcaggtgtgacagctcta gcctgtggaatgatagcagtgggatcctgcaatggagatgttacttccactatccttcag accatcatggagaaatcagagactgagctcaaggacacctatgcccgttggcttcctctt ggactgggcctcaaccacttggggaagggtgaggccatcgaggcaatcctggctgcgctg gaggttgtgtcagagccattccgcagttttgccaacacattagtggatgtgtgtgcctat gcaggctctgggaatgtactgaaggtgcagcagctgctccacatttgtagtgaacacttt gactccaaggaaaaagaggaagacaaggacaagaaggaaaagaaggacaaggacaagaag gaagcccctgccgacatgggagcacatcagggagtggctgtgctggggattgcccttatt gctatgggggaggagattggagcagagatggcattacgaaccttcggccacctgctgaga tatggggagccaacactccgacgggctgtgcctttagcactggctctaatctctgtttca aatccacgactcaacatcctggataccctaagcaaattctcccatgatgctgacccagaa gtttcctacaactccatttttgccatgggcatggtgggcagtggtaccaataatgcccgt ctggctgcaatgctgcgccagttagcccagtatcatgccaaggaccccaacaacctcttt atggtgcgcttggcacagggcctgacacatttagggaagggcacactcaccctctgtccc taccacagtgaccggcagcttatgagtcaagtggcagtggcggggctgcttactgtgctt gtctctttcctggatgtccgtaacatcatcctaggcaaatcacattatgtattgtatggg ctggtggctgccatgcagccccgaatgctggttacattcgatgaggagctgcggccactg ccggtgtcggtccgtgtgggccaggcagtggatgtggtgggccaggctggcaagcctaag actatcacagggttccagacacacacaaccccagtattgttggcccacggggagcgggca gaattggccactgaggaatttcttcctgtcacccccattctggaaggttttgttatcctt cggaagaaccccaactatgacctctaa

Felis catus (domestic cat): 101095435 Help Entry 101095435         CDS       T02385                                  Symbol PSMC3 Name (RefSeq) 26S proteasome regulatory subunit 6A   KO K03065   26S proteasome regulatory subunit T5 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101095435 (PSMC3)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101095435 (PSMC3)   09164 Neurodegenerative disease    05010 Alzheimer disease     101095435 (PSMC3)    05012 Parkinson disease     101095435 (PSMC3)    05014 Amyotrophic lateral sclerosis     101095435 (PSMC3)    05016 Huntington disease     101095435 (PSMC3)    05017 Spinocerebellar ataxia     101095435 (PSMC3)    05020 Prion disease     101095435 (PSMC3)    05022 Pathways of neurodegeneration - multiple diseases     101095435 (PSMC3)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101095435 (PSMC3) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     ATPase subunits      101095435 (PSMC3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  AAA Prot_ATP_ID_OB AAA_lid_3 AAA_5 AAA_16 RuvB_N AAA_2 AAA_22 AAA_33 Mg_chelatase AAA_11 DUF815 PhoH Sigma54_activat DUF5827 IstB_IS21 AAA_24 ATPase AAA_7 DUF3713 RNA_helicase Motif Other DBs NCBI-GeneID:  101095435 NCBI-ProteinID:  XP_003993291 UniProt:  A0A337SBG2 LinkDB All DBs Position D1:complement(101393545..101399661) Genome browser AA seq 439 aa AA seqDB search MNLLPELESPVTRQEKMATVWDEAEQDGIGEEVLKMSTEEIIQRTRLLDSEIKIMKSEVL RVTHELQAMKDKIKENSEKIKVNKTLPYLVSNVIELLDVDPNDQEEDGANIDLDSQRKGK CAVIKTSTRQTYFLPVIGLVDAEKLKPGDLVGVNKDSYLILETLPTEYDSRVKAMEVDER PTEQYSDIGGLDKQIQELVEAIVLPMNHKEKFENLGIQPPKGVLMYGPPGTGKTLLARAC AAQTKATFLKLAGPQLVQMFIGDGAKLVRDAFALAKEKAPSIIFIDELDAIGTKRFDSEK AGDREVQRTMLELLNQLDGFQPNTQVKVIAATNRVDILDPALLRSGRLDRKIEFPMPNEE ARARIMQIHSRKMNVSPDVNYEELARCTDDFNGAQCKAVCVEAGMIALRRGATELTHEDY MEGILEVQAKKKANLQYYA NT seq 1320 nt NT seq  +upstreamnt  +downstreamnt atgaatctgctgccggaactggagagtccagtgactcggcaggagaagatggctaccgtg tgggatgaagctgagcaagatggaatcggggaggaggtgctcaagatgtccacagaagag attatccagcgcacacggctgctggacagtgagatcaagatcatgaagagtgaagtattg cgagttacccacgaactccaggccatgaaggacaagatcaaagagaacagtgagaaaatc aaagtgaacaagaccctgccgtaccttgtctccaacgtcatcgagcttctagatgttgat cccaatgaccaagaggaggatggtgccaatattgacctggattcccagaggaagggtaaa tgtgcagtgatcaaaacctctacccgacagacatacttcctgcctgtgattgggttggtg gatgctgaaaagctaaagcccggagacttggtgggtgtgaacaaagactcctatctgatc ctggagaccctgcctacagagtatgactcacgggtgaaggccatggaggtggatgagagg cccacagaacaatacagtgacattgggggcctggacaaacagattcaggagctggtggag gccattgtcctgccaatgaaccacaaggagaagtttgagaacttggggatccagcctcca aaaggggtgttgatgtatggacctccaggtacggggaagaccctgctggcccgggcctgt gctgcacagaccaaggctaccttcctgaagctggctggcccacagctggtgcagatgttc attggggatggtgccaagctggtccgcgatgcctttgccctggctaaggagaaagctcca tccattatcttcattgatgagctggatgccatcggcactaagcgctttgacagtgagaag gctggagaccgggaggtacagaggacaatgttggagcttctgaaccaactggacgggttc cagcccaacactcaagtaaaggtaattgcagccaccaacagggtggacatcttggacccc gcacttctccgctcaggccgtctggaccgaaagattgaatttccgatgcccaacgaggag gcccgggccagaatcatgcagatccactcccgcaagatgaacgtcagtcctgacgtcaac tatgaggagctggcccgctgtacggatgacttcaatggggcccagtgcaaggccgtgtgt gtggaggcgggcatgatcgcgctgcgcaggggcgccacagagctcacccacgaggactac atggagggcatcctggaggtgcaggccaagaagaaagccaacctgcagtactacgcctag

Felis catus (domestic cat): 101095457 Help Entry 101095457         CDS       T02385                                  Symbol PSMD8 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 8   KO K03031   26S proteasome regulatory subunit N12 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101095457 (PSMD8)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101095457 (PSMD8)   09164 Neurodegenerative disease    05010 Alzheimer disease     101095457 (PSMD8)    05012 Parkinson disease     101095457 (PSMD8)    05014 Amyotrophic lateral sclerosis     101095457 (PSMD8)    05016 Huntington disease     101095457 (PSMD8)    05017 Spinocerebellar ataxia     101095457 (PSMD8)    05020 Prion disease     101095457 (PSMD8)    05022 Pathways of neurodegeneration - multiple diseases     101095457 (PSMD8)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101095457 (PSMD8) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101095457 (PSMD8) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  CSN8_PSD8_EIF3K Motif Other DBs NCBI-GeneID:  101095457 NCBI-ProteinID:  XP_011288167 LinkDB All DBs Position E2:complement(15573870..15581270) Genome browser AA seq 351 aa AA seqDB search MFIKGRAPRAPPRERLNANRGVAGPAAVAPPPALGSTFRPHFRRARGFRRRCRKSGRRFA ASRKMAAAAVNGSPGASGSGPAAASGAVLQVAAGMYEQLKGEWNRKSPNLSKCGEELGRL KLVLLELNFLPTTGTKLTKQQLILARDILEIGAQWSILRKDIPSFERYMAQLKCYYFDYK EQLPESAYMHQLLGLNLLFLLSQNRVAEFHTELERLPAKDIQTNVYIKHPVSLEQYLMEG SYNKVFLAKGNIPAESYTFFIDILLDTIRDEIAGCIEKAYEKILFTEATRILFFNTPKKM TDYAKKRGWVLGLNNYYSFASQQQKPEDTTIPSTELAKQVIEYARQLEMIV NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atgttcattaagggccgggctccaagggcaccgccccgagagcgactgaacgctaaccgc ggcgtggcggggccggcagccgtagccccgcccccggctctgggctccacctttcggccc cacttccgccgggcgagaggctttaggcgtcgctgccgtaagtcggggaggaggtttgcc gcatcacggaagatggcggccgcggcggtgaacgggtcgcccggcgcctctggctcaggg cctgcggcggcctcgggcgcagtcctgcaggtcgcggccggcatgtacgagcaacttaag ggcgagtggaaccgcaaaagccccaatcttagcaagtgcggtgaagagctgggccgtctc aagctggttctgctggagctcaacttcttgccaaccacagggaccaaactgaccaaacag cagctcattctggcccgtgacattctggagattggggcccagtggagcatcctgcgcaag gacatcccttccttcgaacgctacatggcccagctcaaatgctactactttgattacaag gagcagctccccgagtcagcctacatgcaccagctcttgggcctcaacctcctcttcctg ctgtcccagaaccgggtggctgagttccacacggagttggagaggctgcctgccaaggac atccaaaccaatgtgtacatcaagcatcctgtgtccctggagcagtacctgatggagggc agctataacaaggtgttcctggccaaaggcaacatccctgctgagagctacactttcttc attgacatcctgcttgacactatcagggatgagattgctgggtgcatcgagaaggcctat gagaaaatccttttcactgaggccacccggatcctcttcttcaacacacccaaaaagatg acggactacgccaagaagcgagggtgggttctgggcctcaacaactactacagttttgcc agccagcagcagaagccagaagataccaccatcccctccacggaactggccaaacaggtc atcgagtatgcccggcagctggagatgatcgtctga

Felis catus (domestic cat): 101097227 Help Entry 101097227         CDS       T02385                                  Symbol ADRM1 Name (RefSeq) proteasomal ubiquitin receptor ADRM1   KO K06691   26S proteasome regulatory subunit N13 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101097227 (ADRM1)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101097227 (ADRM1)   09164 Neurodegenerative disease    05010 Alzheimer disease     101097227 (ADRM1)    05012 Parkinson disease     101097227 (ADRM1)    05014 Amyotrophic lateral sclerosis     101097227 (ADRM1)    05016 Huntington disease     101097227 (ADRM1)    05017 Spinocerebellar ataxia     101097227 (ADRM1)    05020 Prion disease     101097227 (ADRM1)    05022 Pathways of neurodegeneration - multiple diseases     101097227 (ADRM1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101097227 (ADRM1) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101097227 (ADRM1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  RPN13_C Proteasom_Rpn13 ASXH GerD Motif Other DBs NCBI-GeneID:  101097227 NCBI-ProteinID:  XP_023106803 Ensembl:  ENSFCAG00000003252 LinkDB All DBs Position A3:complement(1882691..1888982) Genome browser AA seq 406 aa AA seqDB search MTTSGALFPSLVPGSRGSSNKYLVEFRAGKMSLKGTTVTPDKRKGLVYIQQTDDSLIHFC WKDRTSGNVEDDLIIFPDDCEFKRVPQCPSGRVYVLKFKAGSKRLFFWMQEPKTDQDEEH CRKVNEYLNNPPMPGALGASGSGGHELSALGGEGGLQSLLGNMSHSQLMQLIGPAGLGGL GGLGALTGPGLASLLGSGGPPASSSSSSSRSQSAAVTPSSTTSSTRATPAPSAPAAASVT SPSPAPSSGNGTSTAASPTQPIQLSDLQSILATMNVPAGPGGGQQVDLASVLTPEIMAPI LANADVQERLLPYLPSGESLPQTAEEIQNTLTSPQFQQALGMFSAALASGQLGPLMCQFG LPAEAVEAANKGDVEAFAKAMQNSARSEQEGDGKDKKDEEEDMSLD NT seq 1221 nt NT seq  +upstreamnt  +downstreamnt atgacgacttcaggcgctctgtttccaagcctggtgccaggctcccgaggctcctccaac aagtatctggtggagtttcgtgcaggaaagatgtcgctaaaaggaactactgtcacccca gataaacggaaagggctcgtgtacattcagcagacggatgactccctcattcacttctgc tggaaggacaggacatctgggaacgtggaggacgatttgatcatctttcctgacgactgt gagttcaagcgcgtgccgcagtgccccagcgggagggtctacgtgctcaagtttaaggca gggtccaagcggctcttcttctggatgcaggagcccaagacggaccaggacgaggagcac tgccgcaaggtcaacgagtatctgaacaaccccccgatgcctggagcgctgggggcgagt gggagtggaggccacgagctctctgcactgggcggcgagggcggcctgcagagtctgctg gggaacatgagccacagccagctcatgcagctcatcggacccgccggccttggaggactg gggggactgggggccctgaccgggccgggcctggccagcttactggggagtggagggcct ccggcgagcagctcttcgtccagctcgcggagccagtcggcagcagtcaccccgtcctcc accacctcttctacccgagccacccccgccccttccgctccagcagctgcctcggtgacc agtcccagccccgcacccagttcaggtaatggaaccagcacggcagccagcccaacccag cccatccagctgagcgaccttcagagcattctagctactatgaacgtgccggcagggcca ggaggcggccagcaagttgacctggccagtgttctgacgcccgagatcatggcccctatc ctcgccaacgcggacgtccaggagcgcctcttgccctacctgccctctggggagtcactg ccacagacggcagaggagatccagaacacgctgacctcgccccagttccagcaggccctg ggcatgttcagtgcagccctggcctctgggcagctgggccccctcatgtgccagtttggc ctgcctgcagaggccgtggaggcggccaacaaaggcgatgtggaagcatttgccaaagcc atgcagaacagtgccagatccgagcaggagggcgacgggaaggacaagaaggacgaagag gaggacatgagcttagattaa

Felis catus (domestic cat): 101097360 Help Entry 101097360         CDS       T02385                                  Symbol PSMC5 Name (RefSeq) 26S proteasome regulatory subunit 8 isoform X2   KO K03066   26S proteasome regulatory subunit T6 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101097360 (PSMC5)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101097360 (PSMC5)   09164 Neurodegenerative disease    05010 Alzheimer disease     101097360 (PSMC5)    05012 Parkinson disease     101097360 (PSMC5)    05014 Amyotrophic lateral sclerosis     101097360 (PSMC5)    05016 Huntington disease     101097360 (PSMC5)    05017 Spinocerebellar ataxia     101097360 (PSMC5)    05020 Prion disease     101097360 (PSMC5)    05022 Pathways of neurodegeneration - multiple diseases     101097360 (PSMC5)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101097360 (PSMC5) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     ATPase subunits      101097360 (PSMC5) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  AAA AAA_lid_3 Prot_ATP_ID_OB AAA_2 AAA_5 AAA_16 AAA_22 RuvB_N TIP49 AAA_33 AAA_18 AAA_3 Mg_chelatase ATPase FapA PhoH IstB_IS21 AAA_28 AAA_24 AAA_14 Sigma54_activat AAA_7 AAA_17 DUF815 bpMoxR AAA_25 Parvo_NS1 Zeta_toxin RNA_helicase HR1 TsaE AAA_19 AAA_11 Motif Other DBs NCBI-GeneID:  101097360 NCBI-ProteinID:  XP_003997107 Ensembl:  ENSFCAG00000003501 UniProt:  M3W0G3 LinkDB All DBs Position E1:48100687..48105079 Genome browser AA seq 406 aa AA seqDB search MALDGPEQMELEEGKAGSGLRQYYLSKIEELQLIVNDKSQNLRRLQAQRNELNAKVRLLR EELQLLQEQGSYVGEVVRAMDKKKVLVKVHPEGKFVVDVDKNIDINDVTPNCRVALRNDS YTLHKILPNKVDPLVSLMMVEKVPDSTYEMIGGLDKQIKEIKEVIELPVKHPELFEALGI AQPKGVLLYGPPGTGKTLLARAVAHHTDCTFIRVSGSELVQKFIGEGARMVRELFVMARE HAPSIIFMDEIDSIGSSRLEGGSGGDSEVQRTMLELLNQLDGFEATKNIKVIMATNRIDI LDSALLRPGRIDRKIEFPPPNEEARLDILKIHSRKMNLTRGINLRKIAELMPGASGAEVK GVCTEAGMYALRERRVHVTQEDFEMAVAKVMQKDSEKNMSIKKLWK NT seq 1221 nt NT seq  +upstreamnt  +downstreamnt atggcgcttgacggaccggagcagatggagctggaagagggaaaagcaggcagtggactc cgccagtattatctgtccaagattgaagaattgcagctgattgtgaatgacaagagccag aatctccggaggctgcaggcacagaggaatgagctcaatgcgaaagttcgcctactgcgg gaagagctacagctgctccaggaacagggctcctatgtaggagaagtagtccgggccatg gataagaagaaagtgttggttaaggtgcatcccgaaggcaagtttgtcgtagatgtggac aagaacatcgacatcaacgatgtgacacccaattgccgagtggctctaagaaacgacagc tacactctgcacaagatattgcccaacaaggtggaccccctggtgtcactgatgatggtg gagaaagtgccagattcaacctatgagatgatcggtggactggacaagcagataaaggag atcaaagaagtgatcgagctgcctgtcaagcatcctgagctctttgaagcgctgggcatt gcacagcccaagggggtgctgctatatgggcccccaggcactgggaagacactgttggcc cgggctgtggctcatcatacagactgtacctttattcgtgtctctggctctgaattggta cagaaattcatcggggaaggggcaagaatggtgagggagctgtttgtcatggcacgagaa catgctccttctatcatcttcatggatgaaatcgactccattggctcctcacggctggag gggggttccggaggggacagtgaggtgcagcgcacaatgctggagctgctcaaccagctg gatggctttgaggccaccaagaatatcaaggttatcatggctactaacaggattgacatc ctggactcggcgctgctccgccctgggcgcatcgacaggaaaattgaattcccacccccc aatgaggaggcccggctggacattttgaagattcattctcggaaaatgaacctgacccgg gggatcaacctgcggaagattgctgagctcatgcctggagcgtcaggggctgaagtaaag ggcgtgtgcaccgaagccggcatgtatgccctgcgggagcggcgagtccacgtcacgcag gaggactttgagatggcagtggccaaggtcatgcagaaggacagcgagaagaacatgtct atcaagaagctatggaagtga

Felis catus (domestic cat): 101098564 Help Entry 101098564         CDS       T02385                                  Symbol PSMD4 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 4 isoform X2   KO K03029   26S proteasome regulatory subunit N10 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101098564 (PSMD4)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101098564 (PSMD4)   09164 Neurodegenerative disease    05010 Alzheimer disease     101098564 (PSMD4)    05012 Parkinson disease     101098564 (PSMD4)    05014 Amyotrophic lateral sclerosis     101098564 (PSMD4)    05016 Huntington disease     101098564 (PSMD4)    05017 Spinocerebellar ataxia     101098564 (PSMD4)    05020 Prion disease     101098564 (PSMD4)    05022 Pathways of neurodegeneration - multiple diseases     101098564 (PSMD4)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101098564 (PSMD4) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101098564 (PSMD4) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  VWA_2 VWA Ssl1 UIM RAP80_UIM Motif Other DBs NCBI-GeneID:  101098564 NCBI-ProteinID:  XP_011283441 Ensembl:  ENSFCAG00000005564 UniProt:  A0A2I2V018 LinkDB All DBs Position C1:106332194..106341233 Genome browser AA seq 377 aa AA seqDB search MVLESTMVCVDNSEYMRNGDFLPTRLQAQQDAVNIVCHSKTRSNPENNVGLITLANDCEV LTTLTPDTGRILSKLHTVQPKGKITFCTGIRVAHLALKHRQGKNHKMRIIAFVGSPVEDN EKDLVKLAKRLKKEKVNVDIINFGEEEVNTEKLTAFVNTLNGKDGTGSHLVTVPPGPSLA DALISSPILAGEGGAMLGLGASDFEFGVDPSADPELALALRVSMEEQRQRQEEEARRAAA ASAAEAGIATAGAEDSDDALLKMTISQQEFGRTGLPDLSSMTEEEQIAYAMQMSLQGAEF GQAESADIDASSAMDTSEPAKEEEDYDVMQDPEFLQSVLENLPGVDPNNEAIRNAMGSLA SQANKDGKKDKKEEDKK NT seq 1134 nt NT seq  +upstreamnt  +downstreamnt atggtgttggaaagcactatggtctgtgtggacaacagtgaatatatgcggaatggggac ttcttacccacccggctgcaggcccagcaggacgctgtcaacatagtgtgtcactccaag acccgcagcaaccctgagaacaacgtgggcctcatcacactggccaatgactgtgaagtg ctgaccaccctcacccctgacaccggccgcatcctttccaagcttcacactgtccaaccc aagggcaagatcaccttctgcactggcatccgcgtggcccacctggcgttgaagcaccga cagggcaagaatcacaagatgcgcatcattgcctttgtgggaagtccagtggaggacaat gagaaggatctggtgaagctggctaaacgtctcaagaaggaaaaagtgaatgttgacatt atcaactttggggaagaggaagtgaacacagaaaagctgacagcgtttgtaaacacactg aatggcaaagatggtaccggttctcatctggtgacagtgccccccgggcccagcttggcc gatgccctcatcagttctccgattctggctggtgaaggtggtgccatgctgggacttggt gccagtgactttgaatttggagtggatcccagtgctgatcctgagctggccctggccctc cgtgtctctatggaagagcagcggcagcggcaggaggaggaggcccggcgggcagctgca gcctctgctgctgaggctgggattgctacagccggggccgaagactcggatgatgccctg ctgaagatgaccatcagccagcaggagtttggccgcaccgggctccccgacctgagcagt atgaccgaggaagagcagattgcctacgccatgcagatgtccctacagggtgcagagttt ggccaggcagaatcagccgacattgatgccagttcagccatggacacatctgagcccgcc aaggaggaggaggattatgatgtgatgcaggaccccgagttccttcagagtgtcctggag aacctgccaggagtggatcccaacaatgaagctattcgaaatgccatggggtccctcgcc tcccaggccaacaaggatggcaagaaagacaagaaggaggaggacaagaaatga

Felis catus (domestic cat): 101098797 Help Entry 101098797         CDS       T02385                                  Symbol PSMC6 Name (RefSeq) 26S proteasome regulatory subunit 10B   KO K03064   26S proteasome regulatory subunit T4 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101098797 (PSMC6)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101098797 (PSMC6)   09164 Neurodegenerative disease    05010 Alzheimer disease     101098797 (PSMC6)    05012 Parkinson disease     101098797 (PSMC6)    05014 Amyotrophic lateral sclerosis     101098797 (PSMC6)    05016 Huntington disease     101098797 (PSMC6)    05017 Spinocerebellar ataxia     101098797 (PSMC6)    05020 Prion disease     101098797 (PSMC6)    05022 Pathways of neurodegeneration - multiple diseases     101098797 (PSMC6)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101098797 (PSMC6) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     ATPase subunits      101098797 (PSMC6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  AAA AAA_lid_3 Prot_ATP_ID_OB AAA_16 AAA_5 AAA_22 AAA_2 RuvB_N AAA_33 AAA_18 Prot_ATP_OB_N DUF815 AAA_7 AAA_14 DUF5906 AAA_3 TPR_MLP1_2 RNA_helicase TIP49 bpMoxR Mg_chelatase AAA_11 Wtap TsaE AAA_24 AAA_25 ATPase NACHT AAA_19 AAA_28 IstB_IS21 Med4 DUF4140 Motif Other DBs NCBI-GeneID:  101098797 NCBI-ProteinID:  XP_003987690 Ensembl:  ENSFCAG00000012975 UniProt:  M3WNQ7 LinkDB All DBs Position B3:102543627..102566461 Genome browser AA seq 403 aa AA seqDB search MAIPGIPYERRLLIMADPRDKALQDYRKKLLEHKEIDGRLKELREQLKELTKQYEKSEND LKALQSVGQIVGEVLKQLTEEKFIVKATNGPRYVVGCRRQLDKSKLKPGTRVALDMTTLT IMRYLPREVDPLVYNMSHEDPGNVSYSEIGGLSEQIRELREVIELPLTNPELFQRVGIIP PKGCLLYGPPGTGKTLLARAVASQLDCNFLKVVSSSIVDKYIGESARLIREMFNYARDHQ PCIIFMDEIDAIGGRRFSEGTSADREIQRTLMELLNQMDGFDTLHRVKMIMATNRPDTLD PALLRPGRLDRKIHIDLPNEQARLDILKIHAGPITKHGEIDYEAIVKLSDGFNGADLRNV CTEAGMFAIRADHDFVVQEDFMKAVRKVADSKKLESKLDYKPV NT seq 1212 nt NT seq  +upstreamnt  +downstreamnt atggccattcccggcatcccctatgagcgacggcttctcatcatggcggaccctagagat aaggcgcttcaggactaccgcaagaagctgctggagcacaaggagatcgacggccgtctc aaggagttaagggaacaattaaaagaacttaccaagcagtatgaaaagtctgaaaatgat ctgaaggccctacaaagtgttgggcagattgtaggtgaagtacttaagcaactaactgaa gaaaaattcattgttaaagccacaaatggaccacgatatgttgtgggttgtcgtcgacag cttgacaaaagtaagctgaagccaggaacaagagttgctttggatatgactacactaact atcatgagatatttgccaagagaggtggatccactggtctacaacatgtctcatgaggac cctgggaatgtttcttattctgagattggaggactatcagaacagattcgggaattgaga gaggtgatagaattacctcttacaaacccagaattattccagcgtgtgggaataatacct ccaaaaggctgtttgttatatggaccaccaggtacaggaaaaacacttttggcaagagct gttgctagccagctggactgcaatttcttaaaggttgtatctagttctattgtagacaag tacattggtgaaagtgctcgtttgatcagagaaatgtttaattatgccagggatcatcaa ccatgcatcatttttatggatgaaatagatgctattggtggtcgtcggttttctgagggt acttcagctgatagagagattcagagaactttaatggagttactcaatcaaatggatgga tttgatactctacatagagttaaaatgatcatggctacaaacagaccggatacactggat cctgctttgcttcgtccaggaagattagatagaaaaatacatattgatttaccaaatgag caagcaagattagatatattgaaaatccatgcaggtcccattacaaagcatggtgaaata gattatgaagcaattgtgaagctttcagatggctttaatggagcagacctgagaaatgtt tgtactgaagcaggtatgtttgcaattcgtgctgatcatgattttgtagtacaggaagac ttcatgaaagcagtcagaaaagtggctgattctaagaagctagagtctaaattggactac aaacctgtgtaa

Felis catus (domestic cat): 101098912 Help Entry 101098912         CDS       T02385                                  Symbol PSMD7 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 7   KO K03038   26S proteasome regulatory subunit N8 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101098912 (PSMD7)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101098912 (PSMD7)   09164 Neurodegenerative disease    05010 Alzheimer disease     101098912 (PSMD7)    05012 Parkinson disease     101098912 (PSMD7)    05014 Amyotrophic lateral sclerosis     101098912 (PSMD7)    05016 Huntington disease     101098912 (PSMD7)    05017 Spinocerebellar ataxia     101098912 (PSMD7)    05020 Prion disease     101098912 (PSMD7)    05022 Pathways of neurodegeneration - multiple diseases     101098912 (PSMD7)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101098912 (PSMD7) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101098912 (PSMD7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  MitMem_reg JAB Connexin Coilin_N RPA43_OB Motif Other DBs NCBI-GeneID:  101098912 NCBI-ProteinID:  XP_003998254 Ensembl:  ENSFCAG00000022878 UniProt:  M3WTN9 LinkDB All DBs Position E2:complement(47317851..47326798) Genome browser AA seq 324 aa AA seqDB search MPELAVQKVVVHPLVLLSVVDHFNRIGKVGNQKRVVGVLLGSWQKKVLDVSNSFAVPFDE DDKDDSVWFLDHDYLENMYGMFKKVNARERIVGWYHTGPKLHKNDIAINELMKRYCPNSV LVIIDVKPKDLGLPTEAYISVEEVHDDGTPTSKTFEHVTSEIGAEEAEEVGVEHLLRDIK DTTVGTLSQRITNQVHGLKGLNSKLLDIRSYLEKVATGKLPINHQIIYQLQDVFNLLPDV SLQEFVKAFYLKTNDQMVVVYLASLIRSVVALHNLINNKIANRDAEKKEGQEKEESKKDR KDDKEKEKEKEKSDGKKEEKKEKK NT seq 975 nt NT seq  +upstreamnt  +downstreamnt atgccggagctggctgtgcagaaggtggtagttcaccccttggtgctgctcagtgtggtg gatcatttcaaccgaataggcaaggttggaaaccagaaacgtgtcgttggtgtgcttttg gggtcatggcaaaagaaagtacttgatgtatccaacagttttgcagtaccttttgatgaa gatgacaaagatgattctgtctggtttttagaccatgattatttggaaaacatgtatgga atgtttaagaaggtcaatgccagagaaagaatcgttgggtggtaccacacaggccctaaa ctacacaagaatgacatcgccattaatgaacttatgaagagatactgccctaactcagta ctggtcattattgacgtgaagccaaaggacctgggactgcccacagaagcatatatttca gtggaagaagttcacgatgatggaactccaacctcaaaaacatttgagcacgtgaccagt gaaattggagcagaggaagctgaggaagtcggagtggagcacttgttacgagacatcaaa gacactacagtgggcactctttcccagcggatcacaaaccaggtccatggtttgaaggga ctgaactccaagcttctggatatcaggagctacctggagaaagtggccacgggcaagctg cccatcaaccaccagatcatctaccagctacaggacgtcttcaacctgctgccggatgtc agcctccaggagtttgtcaaggccttttacctgaagaccaacgaccagatggtagtggtg tatttggcctcgttgatccgttctgtggttgccctgcacaacctcatcaacaacaaaatt gccaaccgggatgcagagaagaaagaaggtcaggaaaaagaagaaagcaaaaaggatagg aaagatgacaaagagaaagaaaaagagaaggaaaagagtgacggaaagaaagaagagaaa aaggagaaaaaataa

Felis catus (domestic cat): 101100851 Help Entry 101100851         CDS       T02385                                  Symbol PSMD12 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 12   KO K03035   26S proteasome regulatory subunit N5 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101100851 (PSMD12)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101100851 (PSMD12)   09164 Neurodegenerative disease    05010 Alzheimer disease     101100851 (PSMD12)    05012 Parkinson disease     101100851 (PSMD12)    05014 Amyotrophic lateral sclerosis     101100851 (PSMD12)    05016 Huntington disease     101100851 (PSMD12)    05017 Spinocerebellar ataxia     101100851 (PSMD12)    05020 Prion disease     101100851 (PSMD12)    05022 Pathways of neurodegeneration - multiple diseases     101100851 (PSMD12)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101100851 (PSMD12) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101100851 (PSMD12) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PCI RPN5_C SIX1_SD Motif Other DBs NCBI-GeneID:  101100851 NCBI-ProteinID:  XP_003997122 Ensembl:  ENSFCAG00000027374 UniProt:  M3X366 LinkDB All DBs Position E1:49438883..49467284 Genome browser AA seq 456 aa AA seqDB search MADGGSERADGRIVKMEVDYSATVDQRLPECEKLAKEGRLQEVIETLLSLEKQTRTASDM VSTSRILVAVVKMCYEAKEWDLLNENIMLLSKRRSQLKQAVAKMVQQCCTYVEEITDLPI KLRLIDTLRMVTEGKIYVEIERARLTKTLATIKEQNGDVKEAASILQELQVETYGSMEKK ERVEFILEQMRLCLAVKDYIRTQIISKKINTKFFQEENTEKLKLKYYNLMIQLDQHEGSY LSICKHYRAIYDTPCIQAESEKWQQALKSVVLYVILAPFDNEQSDLVHRISGDKKLEEIP KYKDLLKLFTTMELMRWSTLVEDYGLELRKGSPESPATDVFGSTEEGERRWKDLKNRVVE HNIRIMAKYYTRITMTRMAQLLDLSVDESEAFLSNLVVNKTIFAKVDRLAGIINFQRPKD PNNLLNDWSQKLNSLMSLVNKTTHLIAKEEMIHNLQ NT seq 1371 nt NT seq  +upstreamnt  +downstreamnt atggcggacggcggctcagagcgggctgatgggcgcatcgtcaagatggaggtggactac agcgccacggtggatcagcgactgccagagtgcgagaagctggccaaggaaggaagactt caagaagtcattgaaacccttctctctttggagaaacagacccgcaccgcttctgatatg gtgtctacatcccgtatcctagttgcagtggtgaagatgtgctatgaggctaaagaatgg gatttacttaatgaaaatattatgcttttgtcaaaaagacggagccaattaaagcaagct gttgcaaaaatggttcaacagtgctgtacttacgtcgaggaaatcacagaccttccgatc aagcttcgattaattgatactctgcgaatggttacagaaggcaagatttatgttgaaatt gagcgtgctcgactgactaaaacgttagcaaccataaaagaacaaaatggtgatgtgaaa gaggcagcctccattttacaagagttacaggtggaaacctacggatcaatggaaaagaaa gagcgagtggagtttattttggagcagatgaggctctgtctagctgtgaaggattacatt cgtacacaaatcatcagcaagaaaataaacaccaaatttttccaggaagaaaatacagag aaattaaagttgaaatattataacttaatgattcagctggatcaacatgaggggtcctat ttgtctatttgtaagcactacagagcaatatatgatactccctgtatacaggcagaaagt gaaaagtggcaacaggctctgaaaagtgttgtcctctatgtgatcttggctccttttgac aatgaacagtcagatttggttcaccgaataagtggcgacaagaagttagaagaaattcct aaatacaaggatcttttaaagctttttaccacaatggagctgatgcgctggtccacgctt gttgaagactatggactggaattaaggaaagggtctcccgagagtccggcaactgatgtg tttggttctacggaggaaggtgaaagaaggtggaaagacctgaagaacagagtcgttgaa cataatattagaataatggccaagtattacacgaggataacaatgacgaggatggcccag cttctcgatctgtctgttgatgagtcagaagcttttctttcgaatctagtagttaacaag accatctttgctaaagtagacaggttggcaggaattatcaacttccagagacccaaggat ccaaataatttattaaatgactggtctcagaaactgaactcactgatgtctctcgttaac aaaactacacacctcatagccaaagaggagatgatacataatctacaatag

Felis catus (domestic cat): 101101591 Help Entry 101101591         CDS       T02385                                  Symbol PSMD13 Name (RefSeq) 26S proteasome non-ATPase regulatory subunit 13   KO K03039   26S proteasome regulatory subunit N9 Organism fca  Felis catus (domestic cat) Pathway fca03050   Proteasome fca05010   Alzheimer disease fca05012   Parkinson disease fca05014   Amyotrophic lateral sclerosis fca05016   Huntington disease fca05017   Spinocerebellar ataxia fca05020   Prion disease fca05022   Pathways of neurodegeneration - multiple diseases fca05169   Epstein-Barr virus infection Brite KEGG Orthology (KO) [BR:fca00001]  09120 Genetic Information Processing   09123 Folding, sorting and degradation    03050 Proteasome     101101591 (PSMD13)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     101101591 (PSMD13)   09164 Neurodegenerative disease    05010 Alzheimer disease     101101591 (PSMD13)    05012 Parkinson disease     101101591 (PSMD13)    05014 Amyotrophic lateral sclerosis     101101591 (PSMD13)    05016 Huntington disease     101101591 (PSMD13)    05017 Spinocerebellar ataxia     101101591 (PSMD13)    05020 Prion disease     101101591 (PSMD13)    05022 Pathways of neurodegeneration - multiple diseases     101101591 (PSMD13)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03051 Proteasome [BR:fca03051]     101101591 (PSMD13) Proteasome [BR:fca03051]  Eukaryotic proteasome   Regulatory particles    PA700 (19S proteasome)     non-ATPase subunits      101101591 (PSMD13) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PCI Rpn9_C Motif Other DBs NCBI-GeneID:  101101591 NCBI-ProteinID:  XP_003993868 Ensembl:  ENSFCAG00000002669 UniProt:  M3VYX6 LinkDB All DBs Position D1:116952324..116964982 Genome browser AA seq 376 aa AA seqDB search MKDVPGFLQQSQSSGPGQAAVWHRLEELYTKKLWHQLTLQVLDFVQDPCFAQGDGLIKLY ENFISEFEHRVNPLSLVEIILHVVRQMTDPNVALTFLEKTREKVKSSDEAVILCKTAIGA LKLNIGDLQVTKETIEDVEEMLNNLPGVTSVHSRFYDLSSKYYQTIGNHASYYKDALRFL GCVDIKDLPVSEQQERAFTLGLAGLLGEGVFNFGELLMHPVLESLRNTDRQWLIDTLYAF NSGNVERFQTLKTSWGQQPDLAANEAQLLRKIQLLCLMEMTFTRPANHRQLTFEEIAKSA KITVNEVELLVMKALSVGLVKGSIDEVDKRVHMTWVQPRVLDLQQIAGMKDRLEFWCTDV RSMEMLVEHQAHDILT NT seq 1131 nt NT seq  +upstreamnt  +downstreamnt atgaaggacgtacctggctttctgcagcagagccagagctccgggcccggccaggccgcc gtgtggcaccgtctggaggagctctacacgaagaagttgtggcatcaactgacacttcag gtgcttgattttgtgcaggacccatgctttgcccaaggagatggcctcattaagctttat gaaaacttcatcagtgaatttgaacacagggtgaatcctttgtccctggtagaaatcatt cttcatgtagttagacagatgactgatcccaacgtggctcttacttttctggaaaagact cgtgaaaaggtgaaaagcagtgatgaggcagtgatcctgtgtaaaaccgcaatcggagct ctgaaattaaacatcggggacctacaggttacaaaggagacaattgaagacgttgaagag atgctcaacaacctccctggcgtgacatcagttcacagtcgtttctacgatctctctagt aaatactatcaaacaatcggaaaccacgcatcctactacaaagatgctctgcggtttcta ggctgtgtcgacatcaaggatcttccagtgtctgagcagcaggagagagctttcacgctg ggactagcaggacttcttggcgagggagtttttaactttggagaactcctcatgcacccc gtgctggaatcactgaggaacaccgaccgccagtggctgattgacaccctttatgccttt aacagtggcaacgtagagagattccagaccctgaagacctcgtggggccagcagcctgac ttggcagccaatgaagcccagcttctgaggaaaattcagctgttgtgcctcatggagatg actttcacacgacctgccaatcacagacaactcacttttgaagaaattgccaaaagtgct aaaatcaccgtgaacgaggtggagttgctggtgatgaaggcgctctcagtggggctggtg aaaggcagtattgatgaagtggataagcgggttcacatgacctgggtgcagccccgcgtg ttggatttgcaacagatcgcgggcatgaaggaccgcctggagttctggtgcaccgacgtc aggagcatggagatgctggtggagcaccaggcccacgacatcctcacctag

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