KEGG   Homo sapiens (human): 51126
Entry
51126             CDS       T01001                                 
Symbol
NAA20, MRT73, NAT3, NAT3P, NAT5, NAT5P, dJ1002M8.1
Name
(RefSeq) N-alpha-acetyltransferase 20, NatB catalytic subunit
  KO
K17972  N-terminal acetyltransferase B complex catalytic subunit [EC:2.3.1.254]
Organism
hsa  Homo sapiens (human)
Disease
H00768  Autosomal recessive intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    51126 (NAA20)
Enzymes [BR:hsa01000]
 2. Transferases
  2.3  Acyltransferases
   2.3.1  Transferring groups other than aminoacyl groups
    2.3.1.254  N-terminal methionine Nalpha-acetyltransferase NatB
     51126 (NAA20)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial quality control factors
  Mitochondrial dynamics
   Actin cytoskeleton organization
    51126 (NAA20)
SSDB
Motif
Pfam: Acetyltransf_1 Acetyltransf_7 Acetyltransf_10 FR47 Acetyltransf_9
Other DBs
NCBI-GeneID: 51126
NCBI-ProteinID: NP_057184
OMIM: 610833
HGNC: 15908
Ensembl: ENSG00000173418
UniProt: P61599
Structure
Position
20:20017290..20033655
AA seq 178 aa
MTTLRAFTCDDLFRFNNINLDPLTETYGIPFYLQYLAHWPEYFIVAEAPGGELMGYIMGK
AEGSVAREEWHGHVTALSVAPEFRRLGLAAKLMELLEEISERKGGFFVDLFVRVSNQVAV
NMYKQLGYSVYRTVIEYYSASNGEPDEDAYDMRKALSRDTEKKSIIPLPHPVRPEDIE
NT seq 537 nt   +upstreamnt  +downstreamnt
atgaccacgctacgggcctttacctgcgacgacctgttccgcttcaacaacattaacttg
gatccacttacagaaacttatgggattcctttctacctacaatacctcgcccactggcca
gagtatttcattgttgcagaggcacctggtggagaattaatgggttatattatgggtaaa
gcagaaggctcagtagctagggaagaatggcacgggcacgtcacagctctgtctgttgcc
ccagaatttcgacgccttggtttggctgctaaacttatggagttactagaggagatttca
gaaagaaagggtggattttttgtggatctctttgtaagagtatctaaccaagttgcagtt
aacatgtacaagcagttgggctacagtgtatataggacggtcatagagtactattcggcc
agcaacggggagcctgatgaggacgcttatgatatgaggaaagcactttccagggatact
gagaagaaatccatcataccattacctcatcctgtgaggcctgaagacattgaataa

  All links  
Ontology (3)   
   KEGG BRITE (3)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Chemical reaction (1)   
   KEGG ENZYME (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (23)   
   KEGG ORTHOLOGY (1)   
   RefGene (11)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (5)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (25)   
   RefSeq(nuc) (3)   
   GenBank (11)   
   EMBL (11)   
3D Structure (3)   
   PDB (3)   
Protein domain (5)   
   Pfam (5)   
All databases (69)   

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