KEGG   Neogale vison (American mink): 122894431
Entry
122894431         CDS       T08764                                 
Symbol
PSMC6
Name
(RefSeq) 26S proteasome regulatory subunit 10B
  KO
K03064  26S proteasome regulatory subunit T4
Organism
nvs  Neogale vison (American mink)
Pathway
nvs03050  Proteasome
nvs05010  Alzheimer disease
nvs05012  Parkinson disease
nvs05014  Amyotrophic lateral sclerosis
nvs05016  Huntington disease
nvs05017  Spinocerebellar ataxia
nvs05020  Prion disease
nvs05022  Pathways of neurodegeneration - multiple diseases
nvs05169  Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   03050 Proteasome
    122894431 (PSMC6)
 09160 Human Diseases
  09172 Infectious disease: viral
   05169 Epstein-Barr virus infection
    122894431 (PSMC6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122894431 (PSMC6)
   05012 Parkinson disease
    122894431 (PSMC6)
   05014 Amyotrophic lateral sclerosis
    122894431 (PSMC6)
   05016 Huntington disease
    122894431 (PSMC6)
   05017 Spinocerebellar ataxia
    122894431 (PSMC6)
   05020 Prion disease
    122894431 (PSMC6)
   05022 Pathways of neurodegeneration - multiple diseases
    122894431 (PSMC6)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03051 Proteasome [BR:nvs03051]
    122894431 (PSMC6)
Proteasome [BR:nvs03051]
 Eukaryotic proteasome
  Regulatory particles
   PA700 (19S proteasome)
    ATPase subunits
     122894431 (PSMC6)
SSDB
Motif
Pfam: AAA Prot_ATP_ID_OB_C AAA_lid_3 AAA_16 AAA_2 AAA_5 AAA_22 RuvB_N PRS7_OB nSTAND3 Prot_ATP_ID_OB_N AAA_14 DUF815 AAA_7 AAA_11 TIP49 AAA_33 RNA_helicase AAA_3 NPHP3_N Csa3_N AAA_18 Mg_chelatase TPR_MLP1_2 bpMoxR AAA_lid_PRS2_C AAA_28 DUF5906 TsaE AAA_24 DUF3829_2nd ATPase NACHT AAA_25 AAA_17 Occludin_ELL ATPase_2 Parvo_NS1 IstB_IS21 DUF4140 Med4
Other DBs
NCBI-GeneID: 122894431
NCBI-ProteinID: XP_044088153
LinkDB
Position
13:complement(46565291..46587055)
AA seq 389 aa
MADPRDKALQDYRKKLLEHKEIDGRLKELREQLKELTKQYEKSENDLKALQSVGQIVGEV
LKQLTEEKFIVKATNGPRYVVGCRRQLDKSKLKPGTRVALDMTTLTIMRYLPREVDPLVY
NMSHEDPGNVSYSEIGGLSEQIRELREVIELPLTNPELFQRVGIIPPKGCLLYGPPGTGK
TLLARAVASQLDCNFLKVVSSSIVDKYIGESARLIREMFNYARDHQPCIIFMDEIDAIGG
RRFSEGTSADREIQRTLMELLNQMDGFDTLHRVKMIMATNRPDTLDPALLRPGRLDRKIH
IDLPNEQARLDILKIHAGPITKHGEIDYEAIVKLSDGFNGADLRNVCTEAGMFAIRADHD
FVVQEDFMKAVRKVADSKKLESKLDYKPV
NT seq 1170 nt   +upstreamnt  +downstreamnt
atggcggaccctagagataaggcgcttcaggactaccgcaagaagctactggagcacaag
gagatcgacggccgtctcaaggagttaagggaacaattaaaagaacttaccaagcagtat
gaaaaatctgaaaatgatctgaaggccttacagagtgttgggcagattgtgggtgaagta
cttaagcaactaactgaggaaaaattcattgttaaagctacaaatggaccaagatatgtt
gtgggttgtcgtcgacagcttgacaaaagtaagctgaagccaggaacaagagttgctttg
gatatgactacactaacaatcatgagatatttgccaagagaggtggatccattggtctac
aacatgtctcatgaggaccctgggaatgtttcttattctgaaattggaggactatcagaa
cagattcgggaattaagagaggtgatagaattgcctcttacaaacccagaattattccag
cgtgtaggaataatacctccaaaaggctgtttgttatatggaccaccaggcacaggaaaa
acactcttggcacgagctgttgctagccagctggactgcaatttcttaaaggttgtatct
agttctattgtagacaagtacattggtgaaagtgctcgtttgatcagagaaatgtttaat
tatgccagggatcatcaaccatgcattatttttatggatgaaatagatgccattggtggt
cgtcggttttctgagggtacttcagctgatagagagattcagagaactttgatggagtta
ctgaatcaaatggatggatttgatactctacatagagttaaaatgatcatggctacaaac
agaccagatacactggatcctgccttgcttcgtcctggaagattagacagaaaaatacat
attgacttaccaaatgaacaagcaagattagacatattgaaaatccatgcaggtcccatt
acaaagcatggtgaaatagattatgaagcaattgtgaagctttcagatggctttaatgga
gcagacctgagaaatgtttgtactgaagcaggtatgtttgcaattcgtgctgatcatgat
tttgtagtacaggaagacttcatgaaagcagtcagaaaagtggctgattctaagaagcta
gagtctaaattggactacaaacctgtgtga

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