METAP2


Summary: 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 methionine residue from nascent proteins. Increased expression of this gene is associated with various forms of cancer, and the anti-cancer drugs fumagillin and ovalicin inhibit the protein by irreversibly binding to its active site. Inhibitors of this gene have also been shown to be effective for the treatment of obesity. A pseudogene of this gene is located on chromosome 2. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:601870
PHARMGKB IDPA30765
Map Location12q22

GO terms in METAP2


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Term Type
Evidence Type
GO Term ID
GO Des.
MF HDA GO:0003723 RNA binding
MF IDA GO:0004177 aminopeptidase activity
MF TAS GO:0004177 aminopeptidase activity
MF IDA GO:0008235 metalloexopeptidase activity
MF IEA GO:0046872 metal ion binding
CC IDA GO:0005737 cytoplasm
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Gene expression in normal tissue: METAP2

Gene-model tissue-cancer distribution: Bubble Plot

undefinetissue: undefine cancer: undefined model num: 0undefinedtissue: undefined cancer: PANCAN model num: 1

Gene-drug pathway distribution

Metabolic pathways1

Pathways in METAP2


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Database
Pathway ID
Pathway Des.
reactome R-HSA-162582 Signal Transduction
reactome R-HSA-2187338 Visual phototransduction
reactome R-HSA-2514856 The phototransduction cascade
reactome R-HSA-2514859 Inactivation, recovery and regulation of the phototransduction cascade
reactome R-HSA-372790 Signaling by GPCR
reactome R-HSA-388396 GPCR downstream signalling
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD68 Paclitaxel 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in METAP2

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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