KEGG   Homo sapiens (human): 539Help
Entry
539               CDS       H.sapiens                              

Gene name ATP5O
Definition ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit
(EC:3.6.3.14)
Orthology K02137  F-type H+-transporting ATPase oligomycin sensitivity
        conferral protein [EC:3.6.3.14]
Pathway hsa00190  Oxidative phosphorylation
hsa01100  Metabolic pathways
hsa05010  Alzheimer's disease
hsa05012  Parkinson's disease
hsa05016  Huntington's disease
Class Metabolism; Energy Metabolism; Oxidative phosphorylation
[PATH:hsa00190]
Human Diseases; Neurodegenerative Diseases; Alzheimer's disease
[PATH:hsa05010]
Human Diseases; Neurodegenerative Diseases; Parkinson's disease
[PATH:hsa05012]
Human Diseases; Neurodegenerative Diseases; Huntington's disease
[PATH:hsa05016]
BRITE hierarchy
SSDB OrthologParalogGene clusterGFIT
Motif Pfam: OSCP
PROSITE: ATPASE_DELTA
Motif
Other DBs NCBI-GI: 4502303
NCBI-GeneID: 539
OMIM: 600828
HGNC: 850
HPRD: 02899
Ensembl: ENSG00000159147
UniProt: P48047
Position 21q22.1-q22.2; 21q22.11
AA seq 213 aa AA seqDB search
MAAPAVSGLSRQVRCFSTSVVRPFAKLVRPPVQVYGIEGRYATALYSAASKQNKLEQVEK
ELLRVAQILKEPKVAASVLNPYVKRSIKVKSLNDITAKERFSPLTTNLINLLAENGRLSN
TQGVVSAFSTMMSVHRGEVPCTVTSASPLEEATLSELKTVLKSFLSQGQVLKLEAKTDPS
ILGGMIVRIGEKYVDMSVKTKIQKLGRAMREIV
NT seq 642 nt NT seq  +upstreamnt  +downstreamnt
atggctgccccagcagtgtccgggctctcccggcaggtgcgatgcttcagtacctctgtg
gtcagaccatttgccaagcttgtgaggcctcctgttcaggtatacggtattgaaggtcgc
tatgccacagctctttattctgctgcatcaaaacagaataagctggagcaagtagaaaag
gagttgttgagagtagcacaaatcctgaaggaacccaaagtggctgcttctgttttgaat
ccctatgtgaagcgttccattaaagtgaaaagcctaaatgacatcacagcaaaagagagg
ttctctcccctcactaccaatctgatcaatttgcttgctgaaaatggtcgattaagcaat
acccaaggagtcgtttctgccttttctaccatgatgagtgtccatcgcggagaggtacct
tgcacagtgacctctgcatctcctttagaagaagccacactctctgaattaaaaactgtc
ctcaagagcttcctaagtcaaggccaagtattgaaattggaggctaagactgatccgtca
atcttgggtggaatgattgtgcgcattggcgagaaatatgttgacatgtctgtcaagacc
aagattcagaagctgggcagggctatgcgggagattgtctaa

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