METAP1D - methionyl aminopeptidase type 1D, mitochondrial Gene
Also Known as MAP1D; MAP 1D; Metap1l; MetAP 1D
Species: Homo sapiens
About METAP1D
This gene has 7 transcripts (splice variants), 204 orthologues and 7 paralogues. Ubiquitous expression in ovary (RPKM 4.2), endometrium (RPKM 2.3) and 25 other tissues.
Summary
The N-terminal methionine excision pathway is an essential process in which the N-terminal methionine is removed from many proteins, thus facilitating subsequent protein modification. In mitochondria, Enzymes that catalyze this reaction are celled methionine aminopeptidases (MetAps, or MAPs; EC 3.4.11.18) (Serero et al., 2003 [PubMed 14532271]).[supplied by OMIM, Mar 2008]
METAP1D Products (3)
| mRNA | Protein | Name |
|---|---|---|
| NM_001322278.2 | NP_001309207.1 | methionine aminopeptidase 1D, mitochondrial isoform 2 |
| NM_001322279.2 | NP_001309208.1 | methionine aminopeptidase 1D, mitochondrial isoform 2 |
| NM_199227.3 | NP_954697.1 | methionine aminopeptidase 1D, mitochondrial isoform 1 precursor |
| Molecular Function GO Annotation | Evidence | Références | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
33961781 | GOA |
| Cellular Component GO Annotation | Evidence | Références | Source |
|---|---|---|---|
| located in mitochondrion |
IDA
IDA: Inferred from direct assay
|
14532271 | GOA |
METAP1D Protein Structure
Peptidase_M24: Metallopeptidase family M24 (97 - 321)
- 0
- 100
- 200
- 300
- 335 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
methionine aminopeptidase 1D, mitochondrial |
|
METAP1D Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | Références |
|---|---|---|---|---|---|---|---|
|
Intra
|
METAP1D | Q6UB28 | PRICKLE4 | Homo sapiens | Q2TBC4 | 33961781 |
Recombinant METAP1D Proteins
| Cat. No. | Nom du produit | Accession | Pureté |
|---|---|---|---|
| HY-P70862 | METAP1D/Methionine aminopeptidase 1D Protein, Human (His) | Q6UB28 (R44-A335) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Spinocerebellar Ataxia 28 |
|
|
| Perrault Syndrome |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Rattus norvegicus | METAP1D | RGD | RGD:1307413 |
| Mus musculus | METAP1D | MGD | MGI:1913809 |
| Macaca mulatta | METAP1D | VGNC | VGNC:74632 |
| Bos taurus | METAP1D | VGNC | VGNC:31396 |
| Canis familiaris | METAP1D | VGNC | VGNC:53100 |
| Felis catus | METAP1D | VGNC | VGNC:63455 |
| Others | METAP1D | NCBI |