1. Gene
  2. KAT2A - lysine acetyltransferase 2A Gene

KAT2A - lysine acetyltransferase 2A Gene

Homo sapiens

Also known as GCN5; hGCN5; GCN5L2; PCAF-b

Gene ID: 2648 | Gene type: protein coding

About KAT2A

Cytogenetic location: 17q21.2 Genomic coordinates (GRCh38): 17:42,113,111-42,121,367 (from NCBI)

This gene has 5 transcripts (splice variants), 209 orthologues and 11 paralogues. Ubiquitous expression in ovary (RPKM 41.6), adrenal (RPKM 30.6) and 25 other tissues.

Summary

KAT2A, or GCN5, is a Histone Acetyltransferase (HAT) that functions primarily as a transcriptional activator. It also functions as a repressor of NF-kappa-B (see MIM 164011) by promoting ubiquitination of the NF-kappa-B subunit RELA (MIM 164014) in a HAT-independent manner (Mao et al., 2009 [PubMed 19339690]).[supplied by OMIM, Sep 2009]

KAT2A Products(3)

mRNA Protein Name
XM_006721818.5 XP_006721881.1 histone acetyltransferase KAT2A isoform X1
NM_021078.3 NP_066564.2 histone acetyltransferase KAT2A isoform 1
NM_001376227.1 NP_001363156.1 histone acetyltransferase KAT2A isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
17301242 GOA
enables chromatin binding IDA
IDA: Inferred from direct assay
29211711 GOA
enables histone H3 acetyltransferase activity IDA
IDA: Inferred from direct assay
18838386 GOA
enables histone H3K9 acetyltransferase activity IDA
IDA: Inferred from direct assay
21131905 GOA
enables histone acetyltransferase activity IDA
IDA: Inferred from direct assay
10373431 GOA
enables histone deacetylase binding IPI
IPI: Inferred from physical interaction
12887892 GOA
enables histone glutaryltransferase activity IDA
IDA: Inferred from direct assay
31542297 GOA
enables histone succinyltransferase activity IDA
IDA: Inferred from direct assay
29211711 GOA
enables peptide-lysine-N-acetyltransferase activity IDA
IDA: Inferred from direct assay
16753578 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17664281 GOA
enables transcription coactivator activity IDA
IDA: Inferred from direct assay
11564863 GOA
Biological Process GO Annotation Evidence Reference Source
involved in internal peptidyl-lysine acetylation IDA
IDA: Inferred from direct assay
27796307 GOA
involved in negative regulation of centriole replication IDA
IDA: Inferred from direct assay
27796307 GOA
involved in negative regulation of gluconeogenesis IDA
IDA: Inferred from direct assay
16753578 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
18838386 GOA
involved in peptidyl-lysine glutarylation IDA
IDA: Inferred from direct assay
31542297 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
29973595 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
29211711 GOA
involved in regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
19936620 GOA
involved in regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
19103755 GOA
involved in regulation of cell division IDA
IDA: Inferred from direct assay
20562830 GOA
acts upstream of or within regulation of protein stability IMP
IMP: Inferred from mutant phenotype
20562830 GOA
involved in regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
9603525 GOA
involved in regulation of tubulin deacetylation IMP
IMP: Inferred from mutant phenotype
20562830 GOA
Cellular Component GO Annotation Evidence Reference Source
part of ATAC complex IDA
IDA: Inferred from direct assay
18838386 GOA
part of SAGA complex IDA
IDA: Inferred from direct assay
11564863 GOA
located in centrosome IDA
IDA: Inferred from direct assay
27796307 GOA
part of histone acetyltransferase complex IDA
IDA: Inferred from direct assay
29973595 GOA
located in nucleus IDA
IDA: Inferred from direct assay
11564863 GOA
part of oxoglutarate dehydrogenase complex IDA
IDA: Inferred from direct assay
29211711 GOA
part of transcription factor TFTC complex IDA
IDA: Inferred from direct assay
10373431 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

KAT2A Protein Structure

PCAF_N

PCAF_N: PCAF (P300/CBP-associated factor) N-terminal domain (86 - 337)

Acetyltransf_7

Acetyltransf_7: Acetyltransferase (GNAT) domain (547 - 628)

Bromodomain

Bromodomain: Bromodomain (738 - 818)

  • 0
  • 200
  • 400
  • 600
  • 837 a.a.
Protein Preferred Names Protein Names

histone acetyltransferase KAT2A

GCN5 (general control of amino-acid synthesis, yeast, homolog)-like 2

General control of amino acid synthesis, yeast, homolog-like 2

K(lysine) acetyltransferase 2A

STAF97

general control of amino acid synthesis protein 5-like 2

histone acetyltransferase GCN5

histone glutaryltransferase KAT2A

histone succinyltransferase KAT2A

hsGCN5

KAT2A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Cross
KAT2A Q92830 N SARS-CoV-2 P0DTC9
Acetylase Assay
33894414
Intra
KAT2A Q92830 ZZZ3 Homo sapiens Q8IYH5
Anti Bait CoIP
20562830
Intra
KAT2A Q92830 AATF Homo sapiens Q9NY61
Y2H
29232376
Intra
KAT2A Q92830 WDHD1 Homo sapiens O75717
Anti Bait CoIP
21725360
Cross: Cross-species interaction Intra: Intraspecies interaction

KAT2A Antibodies

Cat. No. Product Name Application Reactivity
HY-P83155 KAT2A Antibody (YA2900) WB, IP Human

Related Diseases

Diseases Alias
Retinal Degeneration

Degeneration Of Retina

Chromosome 16p13.3 Deletion Syndrome, Proximal

Rubinstein-Taybi Syndrome

Broad Thumb-Hallux Syndrome

Chromosome 16p13.3 Deletion Syndrome

Rubinstein-Taybi Syndrome Due To 16p13.3 Microdeletion

Rubinstein Syndrome

Broad Thumbs-Halluces Syndrome

Rsts

Rubinstein-Taybi Deletion Syndrome

Rsts Deletion Syndrome

Proximal Chromosome 16p13.3 Deletion Syndrome

16p13.3 Deletion Syndrome

Broad Thumbs And Great Toes, Characteristic Facies, And Mental Retardation

Rts

Spinocerebellar Ataxia 7

Spinocerebellar Ataxia Type 7

SCA7

Opca3

Opca Iii

Olivopontocerebellar Atrophy Iii

Opca With Retinal Degeneration

Opca With Macular Degeneration And External Ophthalmoplegia

Adca, Type Ii

Autosomal Dominant Cerebellar Ataxia Type 2

Olivopontocerebellar Atrophy 3

Autosomal Dominant Cerebellar Ataxia, Type Ii

Autosomal Dominant Cerebellar Ataxia Type Ii

Adca2

Adcaii

Ataxia With Pigmentary Retinopathy

Cerebellar Syndrome-Pigmentary Maculopathy Syndrome

Olivopontocerebellar Atrophy With Retinal Degeneration

Spinocerebellar Ataxia-7

Ataxia, Spinocerebellar, Type 7

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus KAT2A RGD RGD:1307242
Canis familiaris KAT2A VGNC VGNC:42209
Felis catus KAT2A VGNC VGNC:63023
Mus musculus KAT2A MGD MGI:1343101
Bos taurus KAT2A VGNC VGNC:30398
Others KAT2A NCBI