KEGG   Rhinopithecus roxellana (golden snub-nosed monkey): 104658937
Entry
104658937         CDS       T03989                                 
Symbol
ATP5PB
Name
(RefSeq) ATP synthase F(0) complex subunit B1, mitochondrial isoform X1
  KO
K02127  F-type H+-transporting ATPase subunit b
Organism
rro  Rhinopithecus roxellana (golden snub-nosed monkey)
Pathway
rro00190  Oxidative phosphorylation
rro01100  Metabolic pathways
rro04714  Thermogenesis
rro05010  Alzheimer disease
rro05012  Parkinson disease
rro05014  Amyotrophic lateral sclerosis
rro05016  Huntington disease
rro05020  Prion disease
rro05022  Pathways of neurodegeneration - multiple diseases
rro05208  Chemical carcinogenesis - reactive oxygen species
rro05415  Diabetic cardiomyopathy
Module
rro_M00158  F-type ATPase, eukaryotes
Brite
KEGG Orthology (KO) [BR:rro00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    104658937 (ATP5PB)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    104658937 (ATP5PB)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    104658937 (ATP5PB)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    104658937 (ATP5PB)
   05012 Parkinson disease
    104658937 (ATP5PB)
   05014 Amyotrophic lateral sclerosis
    104658937 (ATP5PB)
   05016 Huntington disease
    104658937 (ATP5PB)
   05020 Prion disease
    104658937 (ATP5PB)
   05022 Pathways of neurodegeneration - multiple diseases
    104658937 (ATP5PB)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    104658937 (ATP5PB)
SSDB
Motif
Pfam: Mt_ATP-synt_B DUF5752 DUF2105
Other DBs
NCBI-GeneID: 104658937
NCBI-ProteinID: XP_010357388
Position
8:33802759..33814705
AA seq 256 aa
MLSRVVLSAAATAAPSLKNAAFLGPGVLQATRTFHTGQPHLAPVPPLPEYGGKVRYGLIP
EEFFQFLYPKTGVTGPYVLGTGLILYALSKEIYVITAETFTAMSLIGIMVYGIKKYGPSV
AEYADKLNEQKLAQLEEAKQASIQQIQNAIDMEKSQQALTQKRHYLFDVQRNNIAMALEV
TYRERLYRVYKEVKNRLDYHIAVQNMTRRKEQEHMINWVEKHVVQSISAQQEKETVAKCI
ADLKLLAKKAQAQPVM
NT seq 771 nt   +upstreamnt  +downstreamnt
atgctgtcccgggtggtactttccgccgccgccacagcggccccgtctctgaagaatgca
gccttcctaggtccaggagtattgcaggcaacaaggaccttccatacagggcagccacac
cttgcccctgtaccacctcttcctgaatatggaggaaaagttcgctatggactgatccct
gaggaattcttccagtttctttatcctaaaactggtgtaacaggaccctatgtgctcgga
actgggcttatcttgtatgctttatccaaagaaatatatgtgattaccgcagagaccttc
actgccatgtcattaatagggataatggtctatggaattaaaaaatatggtccttctgtt
gcagaatatgctgataaactcaatgagcaaaaacttgcccaactagaagaggcgaagcag
gcttccatccagcaaatccagaatgcaattgatatggagaagtcgcagcaggcactgact
cagaagcgccattacctttttgatgtgcaaaggaataacattgctatggctttggaggtt
acttaccgggaacgactatatagagtatataaggaagtaaagaatcgcctggactatcat
atagctgtgcagaacatgacgcgtcgaaaggaacaagagcacatgataaattgggtggag
aagcacgtggtgcaaagcatctccgcacagcaggaaaaggagacagttgccaagtgcatt
gcggacctaaagctgctggcaaagaaggctcaagcacagccggttatgtaa

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