Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10988
Gene name Gene Name - the full gene name approved by the HGNC.
Methionyl aminopeptidase 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
METAP2
Synonyms (NCBI Gene) Gene synonyms aliases
MAP2, MNPEP, p67eIF2
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q22
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the methionyl aminopeptidase family. The encoded protein functions both by protecting the alpha subunit of eukaryotic initiation factor 2 from inhibitory phosphorylation and by removing the amino-terminal me
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020542 hsa-miR-155-5p Proteomics 18668040
MIRT022163 hsa-miR-124-3p Microarray 18668037
MIRT030371 hsa-miR-24-3p Microarray 19748357
MIRT031408 hsa-miR-16-5p Proteomics 18668040
MIRT051737 hsa-let-7c-5p CLASH 23622248
Transcription factors
Transcription factor Regulation Reference
PLAGL2 Activation 17462995
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22658674
GO:0004177 Function Aminopeptidase activity IDA 8858118
GO:0005515 Function Protein binding IPI 32814053
GO:0005737 Component Cytoplasm IDA 15102683
GO:0005829 Component Cytosol IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601870 16672 ENSG00000111142
Protein
UniProt ID P50579
Protein name Methionine aminopeptidase 2 (MAP 2) (MetAP 2) (EC 3.4.11.18) (Initiation factor 2-associated 67 kDa glycoprotein) (p67) (p67eIF2) (Peptidase M)
Protein function Cotranslationally removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). The catalyt
PDB 1B59 , 1B6A , 1BN5 , 1BOA , 1KQ0 , 1KQ9 , 1QZY , 1R58 , 1R5G , 1R5H , 1YW7 , 1YW8 , 1YW9 , 2ADU , 2EA2 , 2EA4 , 2GA2 , 2OAZ , 5CLS , 5D6E , 5D6F , 5JFR , 5JHU , 5JI6 , 5LYW , 5LYX , 6QED , 6QEF , 6QEG , 6QEH , 6QEI , 6QEJ , 7A12 , 7A13 , 7A14 , 7A15 , 7A16 , 8ONY , 8OXG , 9FPZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00557 Peptidase_M24 167 466 Metallopeptidase family M24 Domain
Sequence
Sequence length 478
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Inactivation, recovery and regulation of the phototransduction cascade
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 26935506
Astrocytoma Associate 23161775
Autoimmune Diseases Associate 34143178
Carcinoma Non Small Cell Lung Associate 26935506
Carcinoma Ovarian Epithelial Associate 32922205
Carcinoma Squamous Cell Associate 26935506
Cholangiocarcinoma Associate 23480755, 23480758, 30880771
Colorectal Neoplasms Associate 19703310
Communicable Diseases Associate 29579063
Graves Ophthalmopathy Associate 36076300