Puma concolor (puma): 112855785 Help Entry 112855785         CDS       T08890                                  Symbol ACTR10 Name (RefSeq) actin-related protein 10   KO K16576   actin-related protein 10 Organism pcoo  Puma concolor (puma) Pathway pcoo04814   Motor proteins pcoo05014   Amyotrophic lateral sclerosis pcoo05016   Huntington disease pcoo05022   Pathways of neurodegeneration - multiple diseases pcoo05132   Salmonella infection Brite KEGG Orthology (KO) [BR:pcoo00001]  09140 Cellular Processes   09142 Cell motility    04814 Motor proteins     112855785 (ACTR10)  09160 Human Diseases   09171 Infectious disease: bacterial    05132 Salmonella infection     112855785 (ACTR10)   09164 Neurodegenerative disease    05014 Amyotrophic lateral sclerosis     112855785 (ACTR10)    05016 Huntington disease     112855785 (ACTR10)    05022 Pathways of neurodegeneration - multiple diseases     112855785 (ACTR10)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03036 Chromosome and associated proteins [BR:pcoo03036]     112855785 (ACTR10)   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:pcoo04812]     112855785 (ACTR10) Chromosome and associated proteins [BR:pcoo03036]  Eukaryotic type   Centrosome formation proteins    Microtubules and associated factors     Dynactin complex      112855785 (ACTR10) Cytoskeleton proteins [BR:pcoo04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actins     Actin-related proteins      112855785 (ACTR10) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Actin DUF2124 Motif Other DBs NCBI-GeneID:  112855785 NCBI-ProteinID:  XP_025775115 UniProt:  A0A6P6HH31 LinkDB All DBs Position Unknown AA seq 337 aa AA seqDB search MPLYEGLGSGGEKTAVVIDLGEAFTKCGFAGETGPRCIIPSVIKKAGLPKPIKVVQYNIN TEELYSYLKEFIHILYFRHLLVNPRDRRVVVIESVLCPSHFRETLTRVLFKYFEKISVLG SIPEGVLEDIKVRTCFVSDLKRGLKIQAAKFNIDGNTERPSPPPNVDYPLDGEKILHVLG SIRDSVVEILFEQDNEEKSVATLILDSLIQCPIDTRKQLAENLVVIGGTSMLPGFLHRLL AEIRYLVEKPKYKKVLGTKTFRIHTPPAKANCVAWLGGAIFGALQDILGSRSVSKEYYNQ TGRIPDWCSLNNPPLEMMFDVGKAQPPLMKRAFSTEK NT seq 1014 nt NT seq  +upstreamnt  +downstreamnt atgcctctgtatgaaggcctggggagcggcggggagaaaacggcagtcgtgatagaccta ggagaggcttttaccaagtgtggatttgctggagaaactggtccaagatgcataattcct agtgtgataaaaaaagctggcttgcctaagcctatcaaagttgttcaatataatatcaat acagaagaattatattcctacttaaaggaattcatccacatcctgtatttcaggcatcta ttggtgaatcctagagaccgccgagttgtggttatcgagtcggtattatgtccttcccac ttcagagagacactcactcgtgttcttttcaagtattttgagaaaatttctgttttaggt tcaattccagaaggtgtcctagaggacattaaagtgcgcacttgctttgtaagtgatctg aaacgtggattaaaaatccaagcagcaaaatttaatattgatgggaatactgagcgtccc tcaccacccccaaatgttgactacccattagatggagagaagattttacatgttcttgga tcaatcagagattcggttgtggaaattctttttgaacaagataatgaagagaaatcagtt gccactttaatactggattctcttatacagtgcccaatagacaccagaaagcagctcgca gagaatttggtagtcataggtggcacgtcgatgttgccaggatttctccacagattgctg gcggaaataaggtatttggtagaaaaaccaaaatataaaaaagtactcggcaccaagaca ttccgaatccatactccacccgcaaaggccaattgtgtggcgtggttgggaggagctatt tttggtgcactacaagacatacttgggagccgttcagtctcaaaggaatattataatcag acaggccgtatacctgattggtgttctcttaacaaccctccgttggagatgatgtttgat gtcggaaaagctcagccacctctgatgaagagagcattttccactgagaaataa

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