KEGG   Homo sapiens (human): 56997
Entry
56997             CDS       T01001                                 
Symbol
COQ8A, ADCK3, ARCA2, CABC1, COQ10D4, COQ8, SCAR9
Name
(RefSeq) coenzyme Q8A
  KO
K08869  aarF domain-containing kinase
Organism
hsa  Homo sapiens (human)
Disease
H00999  Coenzyme Q10 deficiency
H01891  Autosomal recessive spinocerebellar ataxias
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01001 Protein kinases [BR:hsa01001]
    56997 (COQ8A)
Protein kinases [BR:hsa01001]
 Serine/threonine kinases: Other
  ABC1 family
   56997 (COQ8A)
SSDB
Motif
Pfam: ABC1 CbtA
Other DBs
NCBI-GeneID: 56997
NCBI-ProteinID: NP_064632
OMIM: 606980
HGNC: 16812
Ensembl: ENSG00000163050
UniProt: Q8NI60
Structure
Position
1:226940294..226987544
AA seq 647 aa
MAAILGDTIMVAKGLVKLTQAAVETHLQHLGIGGELIMAARALQSTAVEQIGMFLGKVQG
QDKHEEYFAENFGGPEGEFHFSVPHAAGASTDFSSASAPDQSAPPSLGHAHSEGPAPAYV
ASGPFREAGFPGQASSPLGRANGRLFANPRDSFSAMGFQRRFFHQDQSPVGGLTAEDIEK
ARQAKARPENKQHKQTLSEHARERKVPVTRIGRLANFGGLAVGLGFGALAEVAKKSLRSE
DPSGKKAVLGSSPFLSEANAERIVRTLCKVRGAALKLGQMLSIQDDAFINPHLAKIFERV
RQSADFMPLKQMMKTLNNDLGPNWRDKLEYFEERPFAAASIGQVHLARMKGGREVAMKIQ
YPGVAQSINSDVNNLMAVLNMSNMLPEGLFPEHLIDVLRRELALECDYQREAACARKFRD
LLKGHPFFYVPEIVDELCSPHVLTTELVSGFPLDQAEGLSQEIRNEICYNILVLCLRELF
EFHFMQTDPNWSNFFYDPQQHKVALLDFGATREYDRSFTDLYIQIIRAAADRDRETVRAK
SIEMKFLTGYEVKVMEDAHLDAILILGEAFASDEPFDFGTQSTTEKIHNLIPVMLRHRLV
PPPEETYSLHRKMGGSFLICSKLKARFPCKAMFEEAYSNYCKRQAQQ
NT seq 1944 nt   +upstreamnt  +downstreamnt
atggctgccatattgggagacaccatcatggtggctaaaggccttgtcaagctgacccag
gcggccgtggaaacccacctgcagcacttgggcatcggaggggagctgatcatggcggcc
agggccctgcagtccacggctgtggagcagattggcatgttcttggggaaggtgcagggt
caggataaacatgaagaatattttgctgagaacttcggcggcccagaaggggagttccac
ttctcagtcccgcatgcagccggagcctccacagacttctcttcagcctccgctcccgac
cagtcagcgcccccatccctgggtcatgcccacagcgagggcccagctcctgcctacgtg
gccagtggaccctttagagaagccgggttccccggccaggcctcctcccctctgggcagg
gccaacgggaggctctttgcaaaccccagagactcattctctgccatgggctttcagcga
aggttcttccaccaggaccaatcccctgttgggggcctcacagccgaggacattgagaag
gcccggcaggctaaggctcgccccgagaacaagcagcacaaacagacgctcagcgagcat
gcccgggagcggaaggtgcctgtgacgaggattggccggctggccaacttcggaggtctg
gccgtgggcctgggcttcggggcactggcagaggtcgccaagaagagcctgcgctccgag
gacccctcagggaagaaggccgtgctgggttccagtcctttcctgtccgaggccaatgca
gagcggatcgtgcgcacgctctgcaaggtgcgtggtgcggcactcaagctgggccagatg
ctgagcatccaggatgatgcctttatcaacccccacctggctaagatcttcgagcgggtg
cggcagagcgcggacttcatgccactgaagcagatgatgaaaactctcaacaacgacctg
ggccccaactggcgggacaagttggaatacttcgaggagcggcccttcgccgccgcatcc
attgggcaggtgcacttggcccgaatgaagggcggccgcgaggtggccatgaagatccag
taccctggcgtggcccagagcatcaacagtgatgtcaacaacctcatggccgtgttgaac
atgagcaacatgcttccagaaggcctgttccccgagcacctgatcgacgtgctgaggcgg
gagctggccctggagtgtgactaccagcgagaggccgcctgtgcccgcaagttcagggac
ctgctgaagggccaccccttcttctatgtgcctgagattgtggatgagctctgcagccca
catgtgctgaccacagagctggtgtctggcttccccctggaccaggccgaagggctcagc
caggagattcggaacgagatctgctacaacatcctggttctgtgcctgagggagctgttc
gagttccacttcatgcaaacagaccccaactggtccaacttcttctatgacccccagcag
cacaaggtggctcttttggattttggggcaacgcgggaatatgacagatccttcaccgac
ctctacattcagatcatcagggctgctgccgacagggacagggagactgtgcgggcgaaa
tccatagagatgaagttcctcaccggctacgaggtcaaggtcatggaagacgcccacttg
gatgccatcctcatcctgggggaggccttcgcctctgatgagccttttgattttggcact
cagagcaccaccgagaagatccacaacctgattcccgtcatgctgaggcaccgtctcgtc
cccccacccgaggaaacctactccctgcacaggaagatggggggctccttcctcatctgc
tccaagctgaaggcccgcttcccctgcaaggccatgttcgaggaggcctacagcaactac
tgcaagaggcaggcccagcagtag

  All links  
Disease (2)   
   OMIM (2)   
Gene (9)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (21)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (19)   
DNA sequence (53)   
   RefSeq(nuc) (19)   
   GenBank (17)   
   EMBL (17)   
3D Structure (4)   
   PDB (4)   
Protein domain (2)   
   Pfam (2)   
All databases (91)   

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