KEGG   Homo sapiens (human): 513Help
Entry
513               CDS       H.sapiens                              

Gene name ATP5D
Definition ATP synthase, H+ transporting, mitochondrial F1 complex, delta
subunit (EC:3.6.1.14)
Orthology K02134  F-type H+-transporting ATPase subunit delta [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: ATP-synt_DE_N
Motif
Other DBs NCBI-GI: 50345991
NCBI-GeneID: 513
OMIM: 603150
HGNC: 837
HPRD: 04397
Ensembl: ENSG00000099624
UniProt: P30049
Position 19p13.3
AA seq 168 aa AA seqDB search
MLPAALLRRPGLGRLVRHARAYAEAAAAPAAASGPNQMSFTFASPTQVFFNGANVRQVDV
PTLTGAFGILAAHVPTLQVLRPGLVVVHAEDGTTSKYFVSSGSIAVNADSSVQLLAEEAV
TLDMLDLGAAKANLEKAQAELVGTADEATRAEIQIRIEANEALVKALE
NT seq 507 nt NT seq  +upstreamnt  +downstreamnt
atgctgcccgccgcgctgctccgccgcccgggacttggccgcctcgtccgccacgcccgt
gcctatgccgaggccgccgccgccccggctgccgcctctggccccaaccagatgtccttc
accttcgcctctcccacgcaggtgttcttcaacggtgccaacgtccggcaggtggacgtg
cccacgctgaccggagccttcggcatcctggcggcccacgtgcccacgctgcaggtcctg
cggccggggctggtcgtggtgcatgcagaggacggcaccacctccaaatactttgtgagc
agcggttccatcgcagtgaacgccgactcttcggtgcagttgttggccgaagaggccgtg
acgctggacatgttggacctgggggcagccaaggcaaacttggagaaggcccaggcggag
ctggtggggacagctgacgaggccacgcgggcagagatccagatccgaatcgaggccaac
gaggccctggtgaaggccctggagtag

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