KEGG   Puma concolor (puma): 112867261
Entry
112867261         CDS       T08890                                 
Symbol
ATP5F1C
Name
(RefSeq) ATP synthase subunit gamma, mitochondrial isoform X1
  KO
K02136  F-type H+-transporting ATPase subunit gamma
Organism
pcoo  Puma concolor (puma)
Pathway
pcoo00190  Oxidative phosphorylation
pcoo01100  Metabolic pathways
pcoo04714  Thermogenesis
pcoo05010  Alzheimer disease
pcoo05012  Parkinson disease
pcoo05014  Amyotrophic lateral sclerosis
pcoo05016  Huntington disease
pcoo05020  Prion disease
pcoo05022  Pathways of neurodegeneration - multiple diseases
pcoo05208  Chemical carcinogenesis - reactive oxygen species
pcoo05415  Diabetic cardiomyopathy
Module
pcoo_M00158  F-type ATPase, eukaryotes
Brite
KEGG Orthology (KO) [BR:pcoo00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    112867261 (ATP5F1C)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    112867261 (ATP5F1C)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    112867261 (ATP5F1C)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    112867261 (ATP5F1C)
   05012 Parkinson disease
    112867261 (ATP5F1C)
   05014 Amyotrophic lateral sclerosis
    112867261 (ATP5F1C)
   05016 Huntington disease
    112867261 (ATP5F1C)
   05020 Prion disease
    112867261 (ATP5F1C)
   05022 Pathways of neurodegeneration - multiple diseases
    112867261 (ATP5F1C)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    112867261 (ATP5F1C)
SSDB
Motif
Pfam: ATP-synt ACT_4
Other DBs
NCBI-GeneID: 112867261
NCBI-ProteinID: XP_025786009
UniProt: A0A6P6IE53
LinkDB
Position
Unknown
AA seq 298 aa
MFSRAGVAGLSAWAVQPQWIQVRNMATLKDITRRLKSIKNIQKITKSMKMVAAAKYARAE
RELKPARVYGVGSLALYEKADIKAPEDKKKHLLIGVSSDRGLCGAIHSSVAKQMKNEVAT
LTAAGKEVMLVGIGDKIRGILHRTHSDQFLVSFKEVGRKPPTFGDASVIALELLNSGYEF
DEGSIIFNRFRSVISYKTEEKPIFSLDTVASAESMSVYDDIDADVLRNYQEYALANIIYY
SLKESTTSEQSARMTAMDNASKNASEMIDKLTLTFNRTRQAVITKELIEIISGAAALD
NT seq 897 nt   +upstreamnt  +downstreamnt
atgttctctcgggcgggcgtcgcggggctctcggcctgggccgtgcagccgcaatggatc
caagttcgaaatatggcaacattaaaagatattaccagacggctaaagtcgatcaaaaac
atccagaaaattaccaagtctatgaaaatggtggcagcagcaaaatacgcccgagccgag
agggagctgaaaccagcacgagtgtatggagtaggatctttggctctgtatgagaaagct
gatattaaggcgcctgaagacaagaagaaacacctcctaattggcgtgtcctctgatcga
gggctctgtggtgctattcattcctcggttgccaaacagatgaaaaatgaggtggccaca
ctcacggcagctgggaaagaagttatgcttgttggaattggtgataaaatcaggggtata
cttcacaggactcactctgaccagtttctggtgtccttcaaagaagtgggaagaaaacct
cctacttttggagatgcgtctgtcattgcccttgaactactaaattccggatatgaattt
gatgaagggtctatcatctttaatcggttcaggtctgtcatctcctacaagacagaagaa
aagcccatcttttccctggataccgttgcaagtgccgagagcatgagtgtctatgatgat
atcgatgctgacgtgctgcgcaattaccaagaatacgccttggccaacatcatctactat
tctctaaaggagtccaccacgagtgagcagagtgcgaggatgacggccatggacaacgcc
agcaagaatgcctcggagatgattgacaaactgactttgacattcaaccgcacccgccag
gccgtcatcacgaaggagctgatcgaaatcatctccggcgccgcggctctggattaa

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