KEGG   Equus asinus (ass): 106831232
Entry
106831232         CDS       T04645                                 
Symbol
ATP5F1C
Name
(RefSeq) ATP synthase subunit gamma, mitochondrial isoform X1
  KO
K02136  F-type H+-transporting ATPase subunit gamma
Organism
eai  Equus asinus (ass)
Pathway
eai00190  Oxidative phosphorylation
eai01100  Metabolic pathways
eai04714  Thermogenesis
eai05010  Alzheimer disease
eai05012  Parkinson disease
eai05014  Amyotrophic lateral sclerosis
eai05016  Huntington disease
eai05020  Prion disease
eai05022  Pathways of neurodegeneration - multiple diseases
eai05208  Chemical carcinogenesis - reactive oxygen species
eai05415  Diabetic cardiomyopathy
Module
eai_M00158  F-type ATPase, eukaryotes
Brite
KEGG Orthology (KO) [BR:eai00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    106831232 (ATP5F1C)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    106831232 (ATP5F1C)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    106831232 (ATP5F1C)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    106831232 (ATP5F1C)
   05012 Parkinson disease
    106831232 (ATP5F1C)
   05014 Amyotrophic lateral sclerosis
    106831232 (ATP5F1C)
   05016 Huntington disease
    106831232 (ATP5F1C)
   05020 Prion disease
    106831232 (ATP5F1C)
   05022 Pathways of neurodegeneration - multiple diseases
    106831232 (ATP5F1C)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    106831232 (ATP5F1C)
SSDB
Motif
Pfam: ATP-synt
Other DBs
NCBI-GeneID: 106831232
NCBI-ProteinID: XP_014696797
UniProt: A0A8C4MN46
LinkDB
Position
29:complement(22102923..22121219)
AA seq 298 aa
MFSRAGVAGLSALAVQPQWIQVRNMATLKDITRRLKSIRNIQKITKSMKMVAAAKYARAE
RELKPARVYGIGSLALYEKADIKAPEDKKKHLLIGVSSDRGLCGAIHSSVAKQMKSEVAT
LTAAGKEVMIVGVGDKIRGILQRTHSDQFLVTFKEVGRKPPTFGDASVIALELLNSGYEF
DEGSIIFNRFRSVISYKTEEKPIFSLDTIASAESMSIYDDIDADVLKNYQEYSLANIIYY
SLKESTTSEQSARMTAMDNASKNASEMIDKLTLTFNRTRQAVITKELIEIISGAAALE
NT seq 897 nt   +upstreamnt  +downstreamnt
atgttctctcgggcgggtgtcgctgggctgtcggccttggccgtgcagccgcaatggatc
caagttcgaaatatggcaactttgaaagatattaccaggcgactgaagtccatcagaaac
atccagaaaattaccaagtctatgaaaatggtagccgcagccaaatatgcccgagccgag
agggagctgaaaccagcccgagtgtatggaatagggtctctggctctgtatgaaaaagct
gatattaaggcgcctgaagacaagaagaaacacctccttattggtgtgtcctcagatcga
gggctttgtggtgctattcattcctcggttgctaagcagatgaagagtgaagtggccacg
ctcacagcagccgggaaagaagttatgattgttggagttggtgataaaatcaggggtata
cttcaaaggactcactctgaccagtttctggtgacattcaaagaagtgggaagaaaaccc
cctacttttggagatgcgtcggtcattgccctggaattattaaattctggatatgaattt
gatgagggatctatcatctttaatcgattcaggtctgtcatctcctacaagacggaagaa
aagcccatcttttccctcgacaccattgcaagtgctgagagcatgagtatctacgatgat
attgatgctgacgtgctgaagaattaccaagaatacagtctggccaacatcatctactat
tcgctaaaggaatccaccacgagtgagcagagtgcccggatgacggccatggacaacgct
agcaagaacgcttctgagatgattgacaaactgactttgacattcaatcgcacccgccaa
gctgtcatcacgaaggagttgattgaaatcatctctggtgctgcagctctggagtaa

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