KEGG   Homo sapiens (human): 514
Entry
514               CDS       T01001                                 
Symbol
ATP5F1E, ATP5E, ATPE, MC5DN3
Name
(RefSeq) ATP synthase F1 subunit epsilon
  KO
K02135  F-type H+-transporting ATPase subunit epsilon
Organism
hsa  Homo sapiens (human)
Pathway
hsa00190  Oxidative phosphorylation
hsa01100  Metabolic pathways
hsa04714  Thermogenesis
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
hsa05014  Amyotrophic lateral sclerosis
hsa05016  Huntington disease
hsa05020  Prion disease
hsa05022  Pathways of neurodegeneration - multiple diseases
hsa05208  Chemical carcinogenesis - reactive oxygen species
hsa05415  Diabetic cardiomyopathy
Module
hsa_M00158  F-type ATPase, eukaryotes
Network
nt06529  Thermogenesis
  Element
N01691  mitochondrial complex - UCP1 in Thermogenesis
Disease
H01369  ATP synthase deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    514 (ATP5F1E)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    514 (ATP5F1E)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    514 (ATP5F1E)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    514 (ATP5F1E)
   05012 Parkinson disease
    514 (ATP5F1E)
   05014 Amyotrophic lateral sclerosis
    514 (ATP5F1E)
   05016 Huntington disease
    514 (ATP5F1E)
   05020 Prion disease
    514 (ATP5F1E)
   05022 Pathways of neurodegeneration - multiple diseases
    514 (ATP5F1E)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    514 (ATP5F1E)
SSDB
Motif
Pfam: ATP-synt_Eps
Other DBs
NCBI-GeneID: 514
NCBI-ProteinID: NP_008817
OMIM: 606153
HGNC: 838
Ensembl: ENSG00000124172
UniProt: P56381
Structure
LinkDB
Position
20:complement(59025475..59032335)
AA seq 51 aa
MVAYWRQAGLSYIRYSQICAKAVRDALKTEFKANAEKTSGSNVKIVKVKKE
NT seq 156 nt   +upstreamnt  +downstreamnt
atggtggcctactggagacaggctggactcagctacatccgatactcccagatctgtgca
aaagcagtgagagatgcactgaagacagaattcaaagcaaatgctgagaagacttctggc
agcaacgtaaaaattgtgaaagtaaagaaggaataa

KEGG   Homo sapiens (human): 498
Entry
498               CDS       T01001                                 
Symbol
ATP5F1A, ATP5A, ATP5A1, ATP5AL2, ATPM, COXPD22, HEL-S-123m, MC5DN4, MC5DN4A, MC5DN4B, MOM2, OMR, ORM, hATP1
Name
(RefSeq) ATP synthase F1 subunit alpha
  KO
K02132  F-type H+-transporting ATPase subunit alpha
Organism
hsa  Homo sapiens (human)
Pathway
hsa00190  Oxidative phosphorylation
hsa01100  Metabolic pathways
hsa04714  Thermogenesis
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
hsa05014  Amyotrophic lateral sclerosis
hsa05016  Huntington disease
hsa05020  Prion disease
hsa05022  Pathways of neurodegeneration - multiple diseases
hsa05208  Chemical carcinogenesis - reactive oxygen species
hsa05415  Diabetic cardiomyopathy
Module
hsa_M00158  F-type ATPase, eukaryotes
Network
nt06529  Thermogenesis
  Element
N01691  mitochondrial complex - UCP1 in Thermogenesis
Disease
H00891  Combined oxidative phosphorylation deficiency
H01369  ATP synthase deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    498 (ATP5F1A)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    498 (ATP5F1A)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    498 (ATP5F1A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    498 (ATP5F1A)
   05012 Parkinson disease
    498 (ATP5F1A)
   05014 Amyotrophic lateral sclerosis
    498 (ATP5F1A)
   05016 Huntington disease
    498 (ATP5F1A)
   05020 Prion disease
    498 (ATP5F1A)
   05022 Pathways of neurodegeneration - multiple diseases
    498 (ATP5F1A)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    498 (ATP5F1A)
SSDB
Motif
Pfam: ATP-synt_ab ATP-synt_ab_C ATP-synt_ab_N DUF4142
Other DBs
NCBI-GeneID: 498
NCBI-ProteinID: NP_001001937
OMIM: 164360
HGNC: 823
Ensembl: ENSG00000152234
UniProt: P25705 V9HW26
Structure
LinkDB
Position
18:complement(46080248..46104227)
AA seq 553 aa
MLSVRVAAAVVRALPRRAGLVSRNALGSSFIAARNFHASNTHLQKTGTAEMSSILEERIL
GADTSVDLEETGRVLSIGDGIARVHGLRNVQAEEMVEFSSGLKGMSLNLEPDNVGVVVFG
NDKLIKEGDIVKRTGAIVDVPVGEELLGRVVDALGNAIDGKGPIGSKTRRRVGLKAPGII
PRISVREPMQTGIKAVDSLVPIGRGQRELIIGDRQTGKTSIAIDTIINQKRFNDGSDEKK
KLYCIYVAIGQKRSTVAQLVKRLTDADAMKYTIVVSATASDAAPLQYLAPYSGCSMGEYF
RDNGKHALIIYDDLSKQAVAYRQMSLLLRRPPGREAYPGDVFYLHSRLLERAAKMNDAFG
GGSLTALPVIETQAGDVSAYIPTNVISITDGQIFLETELFYKGIRPAINVGLSVSRVGSA
AQTRAMKQVAGTMKLELAQYREVAAFAQFGSDLDAATQQLLSRGVRLTELLKQGQYSPMA
IEEQVAVIYAGVRGYLDKLEPSKITKFENAFLSHVVSQHQALLGTIRADGKISEQSDAKL
KEIVTNFLAGFEA
NT seq 1662 nt   +upstreamnt  +downstreamnt
atgctgtccgtgcgcgttgctgcggccgtggtccgcgcccttcctcggcgggccggactg
gtctccagaaatgctttgggttcatctttcattgctgcaaggaacttccatgcctctaac
actcatcttcaaaagactgggactgctgagatgtcctctattcttgaagagcgtattctt
ggagctgatacctctgttgatcttgaagaaactgggcgtgtcttaagtattggtgatggt
attgcccgcgtacatgggctgaggaatgttcaagcagaagaaatggtagagttttcttca
ggcttaaagggtatgtccttgaacttggaacctgacaatgttggtgttgtcgtgtttgga
aatgataaactaattaaggaaggagatatagtgaagaggacaggagccattgtggacgtt
ccagttggtgaggagctgttgggtcgtgtagttgatgcccttggtaatgctattgatgga
aagggtccaattggttccaagacgcgtaggcgagttggtctgaaagcccccggtatcatt
cctcgaatttcagtgcgggaaccaatgcagactggcattaaggctgtggatagcttggtg
ccaattggtcgtggtcagcgtgaactgattattggtgaccgacagactgggaaaacctca
attgctattgacacaatcattaaccagaaacgtttcaatgatggatctgatgaaaagaag
aagctgtactgtatttatgttgctattggtcaaaagagatccactgttgcccagttggtg
aagagacttacagatgcagatgccatgaagtacaccattgtggtgtcggctacggcctcg
gatgctgccccacttcagtacctggctccttactctggctgttccatgggagagtatttt
agagacaatggcaaacatgctttgatcatctatgacgacttatccaaacaggctgttgct
taccgtcagatgtctctgttgctccgccgaccccctggtcgtgaggcctatcctggtgat
gtgttctacctacactcccggttgctggagagagcagccaaaatgaacgatgcttttggt
ggtggctccttgactgctttgccagtcatagaaacacaggctggtgatgtgtctgcttac
attccaacaaatgtcatttccatcactgacggacagatcttcttggaaacagaattgttc
tacaaaggtatccgccctgcaattaacgttggtctgtctgtatctcgtgtcggatccgct
gcccaaaccagggctatgaagcaggtagcaggtaccatgaagctggaattggctcagtat
cgtgaggttgctgcttttgcccagttcggttctgacctcgatgctgccactcaacaactt
ttgagtcgtggcgtgcgtctaactgagttgctgaagcaaggacagtattctcccatggct
attgaagaacaagtggctgttatctatgcgggtgtaaggggatatcttgataaactggag
cccagcaagattacaaagtttgagaatgctttcttgtctcatgtcgtcagccagcaccaa
gccttgttgggcactatcagggctgatggaaagatctcagaacaatcagatgcaaagctg
aaagagattgtaacaaatttcttggctggatttgaagcttaa

KEGG   Homo sapiens (human): 513
Entry
513               CDS       T01001                                 
Symbol
ATP5F1D, ATP5D, MC5DN5
Name
(RefSeq) ATP synthase F1 subunit delta
  KO
K02134  F-type H+-transporting ATPase subunit delta
Organism
hsa  Homo sapiens (human)
Pathway
hsa00190  Oxidative phosphorylation
hsa01100  Metabolic pathways
hsa04714  Thermogenesis
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
hsa05014  Amyotrophic lateral sclerosis
hsa05016  Huntington disease
hsa05020  Prion disease
hsa05022  Pathways of neurodegeneration - multiple diseases
hsa05208  Chemical carcinogenesis - reactive oxygen species
hsa05415  Diabetic cardiomyopathy
Module
hsa_M00158  F-type ATPase, eukaryotes
Network
nt06529  Thermogenesis
  Element
N01691  mitochondrial complex - UCP1 in Thermogenesis
Disease
H01369  ATP synthase deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    513 (ATP5F1D)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    513 (ATP5F1D)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    513 (ATP5F1D)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    513 (ATP5F1D)
   05012 Parkinson disease
    513 (ATP5F1D)
   05014 Amyotrophic lateral sclerosis
    513 (ATP5F1D)
   05016 Huntington disease
    513 (ATP5F1D)
   05020 Prion disease
    513 (ATP5F1D)
   05022 Pathways of neurodegeneration - multiple diseases
    513 (ATP5F1D)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    513 (ATP5F1D)
SSDB
Motif
Pfam: ATPD_C_metazoa ATP-synt_DE_N
Other DBs
NCBI-GeneID: 513
NCBI-ProteinID: NP_001001975
OMIM: 603150
HGNC: 837
Ensembl: ENSG00000099624
UniProt: P30049
Structure
LinkDB
Position
19:1241751..1244825
AA seq 168 aa
MLPAALLRRPGLGRLVRHARAYAEAAAAPAAASGPNQMSFTFASPTQVFFNGANVRQVDV
PTLTGAFGILAAHVPTLQVLRPGLVVVHAEDGTTSKYFVSSGSIAVNADSSVQLLAEEAV
TLDMLDLGAAKANLEKAQAELVGTADEATRAEIQIRIEANEALVKALE
NT seq 507 nt   +upstreamnt  +downstreamnt
atgctgcccgccgcgctgctccgccgcccgggacttggccgcctcgtccgccacgcccgt
gcctatgccgaggccgccgccgccccggctgccgcctctggccccaaccagatgtccttc
accttcgcctctcccacgcaggtgttcttcaacggtgccaacgtccggcaggtggacgtg
cccacgctgaccggagccttcggcatcctggcggcccacgtgcccacgctgcaggtcctg
cggccggggctggtcgtggtgcatgcagaggacggcaccacctccaaatactttgtgagc
agcggttccatcgcagtgaacgccgactcttcggtgcagttgttggccgaagaggccgtg
acgctggacatgttggacctgggggcagccaaggcaaacttggagaaggcccaggcggag
ctggtggggacagctgacgaggccacgcgggcagagatccagatccgaatcgaggccaac
gaggccctggtgaaggccctggagtag

KEGG   Homo sapiens (human): 539
Entry
539               CDS       T01001                                 
Symbol
ATP5PO, ATP5O, ATPO, HMC08D05, MC5DN7, OSCP
Name
(RefSeq) ATP synthase peripheral stalk subunit OSCP
  KO
K02137  F-type H+-transporting ATPase subunit O
Organism
hsa  Homo sapiens (human)
Pathway
hsa00190  Oxidative phosphorylation
hsa01100  Metabolic pathways
hsa04714  Thermogenesis
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
hsa05014  Amyotrophic lateral sclerosis
hsa05016  Huntington disease
hsa05020  Prion disease
hsa05022  Pathways of neurodegeneration - multiple diseases
hsa05208  Chemical carcinogenesis - reactive oxygen species
hsa05415  Diabetic cardiomyopathy
Module
hsa_M00158  F-type ATPase, eukaryotes
Network
nt06529  Thermogenesis
  Element
N01691  mitochondrial complex - UCP1 in Thermogenesis
Disease
H01369  ATP synthase deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    539 (ATP5PO)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    539 (ATP5PO)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    539 (ATP5PO)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    539 (ATP5PO)
   05012 Parkinson disease
    539 (ATP5PO)
   05014 Amyotrophic lateral sclerosis
    539 (ATP5PO)
   05016 Huntington disease
    539 (ATP5PO)
   05020 Prion disease
    539 (ATP5PO)
   05022 Pathways of neurodegeneration - multiple diseases
    539 (ATP5PO)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    539 (ATP5PO)
SSDB
Motif
Pfam: OSCP GASH CNOT11
Other DBs
NCBI-GeneID: 539
NCBI-ProteinID: NP_001688
OMIM: 600828
HGNC: 850
Ensembl: ENSG00000241837
UniProt: P48047
Structure
LinkDB
Position
21:complement(33903453..33915804)
AA seq 213 aa
MAAPAVSGLSRQVRCFSTSVVRPFAKLVRPPVQVYGIEGRYATALYSAASKQNKLEQVEK
ELLRVAQILKEPKVAASVLNPYVKRSIKVKSLNDITAKERFSPLTTNLINLLAENGRLSN
TQGVVSAFSTMMSVHRGEVPCTVTSASPLEEATLSELKTVLKSFLSQGQVLKLEAKTDPS
ILGGMIVRIGEKYVDMSVKTKIQKLGRAMREIV
NT seq 642 nt   +upstreamnt  +downstreamnt
atggctgccccagcagtgtccgggctctcccggcaggtgcgatgcttcagtacctctgtg
gtcagaccatttgccaagcttgtgaggcctcctgttcaggtatacggtattgaaggtcgc
tatgccacagctctttattctgctgcatcaaaacagaataagctggagcaagtagaaaag
gagttgttgagagtagcacaaatcctgaaggaacccaaagtggctgcttctgttttgaat
ccctatgtgaagcgttccattaaagtgaaaagcctaaatgacatcacagcaaaagagagg
ttctctcccctcactaccaatctgatcaatttgcttgctgaaaatggtcgattaagcaat
acccaaggagtcgtttctgccttttctaccatgatgagtgtccatcgcggagaggtacct
tgcacagtgacctctgcatctcctttagaagaagccacactctctgaattaaaaactgtc
ctcaagagcttcctaagtcaaggccaagtattgaaattggaggctaagactgatccgtca
atcttgggtggaatgattgtgcgcattggcgagaaatatgttgacatgtctgtcaagacc
aagattcagaagctgggcagggctatgcgggagattgtctaa

KEGG   Homo sapiens (human): 4508
Entry
4508              CDS       T01001                                 
Symbol
ATP6, ATPase6, MTATP6, MT-ATP6, RP
Name
(RefSeq) ATP synthase F0 subunit 6
  KO
K02126  F-type H+-transporting ATPase subunit a
Organism
hsa  Homo sapiens (human)
Pathway
hsa00190  Oxidative phosphorylation
hsa01100  Metabolic pathways
hsa04714  Thermogenesis
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
hsa05014  Amyotrophic lateral sclerosis
hsa05016  Huntington disease
hsa05020  Prion disease
hsa05022  Pathways of neurodegeneration - multiple diseases
hsa05208  Chemical carcinogenesis - reactive oxygen species
hsa05415  Diabetic cardiomyopathy
Module
hsa_M00158  F-type ATPase, eukaryotes
Network
nt06529  Thermogenesis
  Element
N01691  mitochondrial complex - UCP1 in Thermogenesis
Disease
H00068  Leber hereditary optic atrophy
H01177  Infantile bilateral striatal necrosis
H01355  Kearns-Sayre syndrome
H01363  NARP syndrome
H01369  ATP synthase deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    4508 (ATP6)
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    4508 (ATP6)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    4508 (ATP6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    4508 (ATP6)
   05012 Parkinson disease
    4508 (ATP6)
   05014 Amyotrophic lateral sclerosis
    4508 (ATP6)
   05016 Huntington disease
    4508 (ATP6)
   05020 Prion disease
    4508 (ATP6)
   05022 Pathways of neurodegeneration - multiple diseases
    4508 (ATP6)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    4508 (ATP6)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    4508 (ATP6)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial DNA-encoded proteins
   F-type ATPase
    4508 (ATP6)
SSDB
Motif
Pfam: ATP-synt_A
Other DBs
NCBI-GeneID: 4508
NCBI-ProteinID: YP_003024031
OMIM: 516060
HGNC: 7414
UniProt: P00846 Q0ZFE3
Structure
LinkDB
Position
MT:8527..9207
AA seq 226 aa
MNENLFASFIAPTILGLPAAVLIILFPPLLIPTSKYLINNRLITTQQWLIKLTSKQMMTM
HNTKGRTWSLMLVSLIIFIATTNLLGLLPHSFTPTTQLSMNLAMAIPLWAGTVIMGFRSK
IKNALAHFLPQGTPTPLIPMLVIIETISLLIQPMALAVRLTANITAGHLLMHLIGSATLA
MSTINLPSTLIIFTILILLTILEIAVALIQAYVFTLLVSLYLHDNT
NT seq 681 nt   +upstreamnt  +downstreamnt
atgaacgaaaatctgttcgcttcattcattgcccccacaatcctaggcctacccgccgca
gtactgatcattctatttccccctctattgatccccacctccaaatatctcatcaacaac
cgactaatcaccacccaacaatgactaatcaaactaacctcaaaacaaatgataaccata
cacaacactaaaggacgaacctgatctcttatactagtatccttaatcatttttattgcc
acaactaacctcctcggactcctgcctcactcatttacaccaaccacccaactatctata
aacctagccatggccatccccttatgagcgggcacagtgattataggctttcgctctaag
attaaaaatgccctagcccacttcttaccacaaggcacacctacaccccttatccccata
ctagttattatcgaaaccatcagcctactcattcaaccaatagccctggccgtacgccta
accgctaacattactgcaggccacctactcatgcacctaattggaagcgccaccctagca
atatcaaccattaaccttccctctacacttatcatcttcacaattctaattctactgact
atcctagaaatcgctgtcgccttaatccaagcctacgttttcacacttctagtaagcctc
tacctgcacgacaacacataa

DBGET integrated database retrieval system