KEGG T01001: 51126

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

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:

NCBI-ProteinID:

OMIM:

HGNC:

Ensembl:

UniProt:

Structure

LinkDB

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

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