NAA60 - N-alpha-acetyltransferase 60, NatF catalytic subunit Gene
Also Known as HAT4; NatF; NAT15; hNaa60
Species: Homo sapiens
About NAA60
This gene has 40 transcripts (splice variants) and 202 orthologues. Ubiquitous expression in kidney (RPKM 15.2), duodenum (RPKM 14.4) and 25 other tissues.
Summary
This gene encodes an enzyme that localizes to the Golgi apparatus, where it transfers an acetyl group to the N-terminus of free proteins. This enzyme acts on histones, and its activity is important for chromatin assembly and chromosome integrity. Alternative splicing and the use of alternative promoters results in multiple transcript variants. The upstream promoter is located in a differentially methylated region (DMR) and undergoes imprinting; transcript variants originating from this position are expressed from the maternal allele. [provided by RefSeq, Nov 2015]
NAA60 Products (9)
| mRNA | Protein | Name |
|---|---|---|
| NM_001083600.3 | NP_001077069.1 | N-alpha-acetyltransferase 60 isoform a |
| NM_001083601.3 | NP_001077070.1 | N-alpha-acetyltransferase 60 isoform a |
| NM_001317093.1 | NP_001304022.1 | N-alpha-acetyltransferase 60 isoform b |
| NM_001317094.2 | NP_001304023.1 | N-alpha-acetyltransferase 60 isoform c |
| NM_001317095.2 | NP_001304024.1 | N-alpha-acetyltransferase 60 isoform d |
| NM_001317096.2 | NP_001304025.1 | N-alpha-acetyltransferase 60 isoform e |
| NM_001317097.2 | NP_001304026.1 | N-alpha-acetyltransferase 60 isoform f |
| NM_001317098.2 | NP_001304027.1 | N-alpha-acetyltransferase 60 isoform f |
| NM_024845.4 | NP_079121.1 | N-alpha-acetyltransferase 60 isoform a |
| Molecular Function GO Annotation | Evidence | Verweise | Source |
|---|---|---|---|
| enables histone H4 acetyltransferase activity |
IDA
IDA: Inferred from direct assay
|
21981917 | GOA |
| enables peptide alpha-N-acetyltransferase activity |
IDA
IDA: Inferred from direct assay
|
21750686 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32296183 | GOA |
| enables protein homodimerization activity |
IDA
IDA: Inferred from direct assay
|
27320834 | GOA |
| Biological Process GO Annotation | Evidence | Verweise | Source |
|---|---|---|---|
| involved in N-terminal peptidyl-methionine acetylation |
IDA
IDA: Inferred from direct assay
|
21750686 | GOA |
| involved in N-terminal protein amino acid acetylation |
IDA
IDA: Inferred from direct assay
|
25732826 | GOA |
| involved in cell population proliferation |
IMP
IMP: Inferred from mutant phenotype
|
21981917 | GOA |
| involved in nucleosome assembly |
IDA
IDA: Inferred from direct assay
|
21981917 | GOA |
| Cellular Component GO Annotation | Evidence | Verweise | Source |
|---|---|---|---|
| located in Golgi membrane |
IDA
IDA: Inferred from direct assay
|
21981917 | GOA |
NAA60 Protein Structure
Acetyltransf_1: Acetyltransferase (GNAT) family (60 - 156)
- 0
- 100
- 200
- 242 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
N-alpha-acetyltransferase 60 |
|
NAA60 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | Verweise |
|---|---|---|---|---|---|---|---|
|
Intra
|
NAA60 | Q9H7X0 | MEOX2 | Homo sapiens | Q6FHY5 | 32296183 | |
|
Intra
|
NAA60 | Q9H7X0 | MEOX2 | Homo sapiens | Q6FHY5 | 32296183 | |
|
Intra
|
NAA60 | Q9H7X0 | LAMP2 | Homo sapiens | P13473-2 | 32814053 | |
|
Intra
|
NAA60 | Q9H7X0 | LAMP2 | Homo sapiens | P13473-2 | 32814053 | |
|
Intra
|
NAA60 | Q9H7X0 | LAMP2 | Homo sapiens | P13473-2 | 32814053 | |
|
Intra
|
NAA60 | Q9H7X0 | SH3GLB1 | Homo sapiens | Q9Y371 | 32814053 | |
|
Intra
|
NAA60 | Q9H7X0 | SH3GLB1 | Homo sapiens | Q9Y371 | 32814053 | |
|
Intra
|
NAA60 | Q9H7X0 | SH3GLB1 | Homo sapiens | Q9Y371 | 32814053 | |
|
Intra
|
NAA60 | Q9H7X0 | CASP6 | Homo sapiens | P55212 | 32814053 | |
|
Intra
|
NAA60 | Q9H7X0 | CASP6 | Homo sapiens | P55212 | 32814053 | |
|
Intra
|
NAA60 | Q9H7X0 | CASP6 | Homo sapiens | P55212 | 32814053 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Scheuermann Disease |
|
|
| Microphthalmia, Syndromic 1 |
|
|
| Temple Syndrome |
|
|