KEGG   Pan paniscus (bonobo): 100995677
Entry
100995677         CDS       T02283                                 
Name
(RefSeq) 26S proteasome regulatory subunit 10B-like
  KO
K03064  26S proteasome regulatory subunit T4
Organism
pps  Pan paniscus (bonobo)
Pathway
pps03050  Proteasome
pps05010  Alzheimer disease
pps05012  Parkinson disease
pps05014  Amyotrophic lateral sclerosis
pps05016  Huntington disease
pps05017  Spinocerebellar ataxia
pps05020  Prion disease
pps05022  Pathways of neurodegeneration - multiple diseases
pps05169  Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:pps00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   03050 Proteasome
    100995677
 09160 Human Diseases
  09172 Infectious disease: viral
   05169 Epstein-Barr virus infection
    100995677
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100995677
   05012 Parkinson disease
    100995677
   05014 Amyotrophic lateral sclerosis
    100995677
   05016 Huntington disease
    100995677
   05017 Spinocerebellar ataxia
    100995677
   05020 Prion disease
    100995677
   05022 Pathways of neurodegeneration - multiple diseases
    100995677
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03051 Proteasome [BR:pps03051]
    100995677
Proteasome [BR:pps03051]
 Eukaryotic proteasome
  Regulatory particles
   PA700 (19S proteasome)
    ATPase subunits
     100995677
SSDB
Motif
Pfam: AAA AAA_lid_3 Prot_ATP_ID_OB_C AAA_16 AAA_22 AAA_5 AAA_2 RuvB_N PRS7_OB nSTAND3 RNA_helicase AAA_14 Prot_ATP_ID_OB_N DUF815 AAA_7 TIP49 AAA_11 AAA_3 Mg_chelatase AAA_33 NPHP3_N AAA_18 Parvo_NS1 TsaE DUF5906 AAA_28 NACHT bpMoxR Phage_GP20 AAA_24 Csa3_N AAA_lid_PRS2_C ATPase Cep57_CLD_2 ATPase_2 IstB_IS21 AAA_17 AAA_25 AAA_19 GP41 ABC_tran DUF4140 Med4
Other DBs
NCBI-GeneID: 100995677
NCBI-ProteinID: XP_034822007
Ensembl: ENSPPAG00000000942
LinkDB
Position
7:complement(71707844..71709371)
AA seq 389 aa
MADPRDKALGDYRKKVLEHKEIDGRLKELREQLKELTKQYEKSENDLKALRSVGQIVGEV
FKQLTEEKFIVKATNGPRYVVGCRRQLDKSKLKPGTRVALDMTTLTIMRYLPREVDPLIY
NMSHEDPENVSYSEIGGLSEQIRELREGIELPLTNPELFQRVGIIPPKGCLLYGPPGTGK
TLLARAIASQLDCNFLKVVSSSIVDKYIGESAHLIREMFNYARDHQPCIIFMDEIDAIGG
RRFSEGTSADREIQRTLMELLNQMDGFDTLHRVKMIMATNRPDTLDPALLCPGRLDRKIH
IDLPNEQARLDILKIHAGPITKHGEIDYEAIVKLSDGFNGADLRNVCTEAGMFAIRADHD
FVVQEDFMKAVRKVADSKKLESKLDYKPV
NT seq 1170 nt   +upstreamnt  +downstreamnt
atggcggaccctagagataaggcgcttggggactaccgcaagaaggtgcttgagcacaag
gagattgacggccgtcttaaggagttaagggaacaattaaaagaacttaccaagcagtat
gaaaagtctgaaaatgatctgaaggccctacgaagtgttgggcagattgtgggtgaagtg
tttaaacagttaactgaagaaaaattcattgttaaagctaccaatggaccaagatatgtt
gtgggttgtcgtcgacagcttgacaaaagtaagctgaagccaggaacaagagttgctttg
gatatgactacactaactatcatgagatatttgccaagagaggtggatccactgatttat
aacatgtctcatgaggaccctgagaatgtttcttattctgagattggagggctatcagaa
cagatccgggaattaagagaggggatagaattacctcttacaaacccagagttatttcag
cgtgtaggaataatacctccaaaaggctgtttgttatatggaccaccaggtacgggaaaa
acactcttggcacgagccattgctagccagctggactgcaatttcttaaaggttgtatct
agttctattgtagacaagtacattggtgaaagtgctcatttgatcagagaaatgtttaat
tatgctagagatcatcaaccatgcatcatttttatggatgaaatagatgctattggtggt
cgtcggttttctgagggtacttcagctgacagagagattcagagaacgttaatggagtta
ctgaatcaaatggatggatttgatactctgcatagagttaaaatgatcatggctacaaac
agaccagatacactggatcctgctttgctgtgtccaggaagattagatagaaaaatacat
attgatttgccaaatgaacaagcaagattagacatactgaaaatccatgcaggtcccatt
acaaagcatggtgaaatagattatgaagcaattgtgaagctttcagatggctttaatgga
gcagacctgagaaatgtttgtactgaagcaggtatgttcgcaattcgtgctgatcatgat
tttgtagtacaggaagacttcatgaaagcagtcagaaaagtggctgattctaagaagctg
gagtctaaattggactacaaacctgtgtaa

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