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MME (NM_007289) - membrane metalloendopeptidase

Neprilysin Isoform A

Mutations Visualisation

Protein summary

This is an alternative isoform of MME protein. View all 4 isoforms
MME: neprilysin isoform a
Description:

The protein encoded by this gene is a type II transmembrane glycoprotein and a common acute lymphocytic leukemia antigen that is an important cell surface marker in the diagnosis of human acute lymphocytic leukemia (ALL). The encoded protein is present on leukemic cells of pre-B phenotype, which represent 85% of cases of ALL. This protein is not restricted to leukemic cells, however, and is found on a variety of normal tissues. The protein is a neutral endopeptidase that cleaves peptides at the amino side of hydrophobic residues and inactivates several peptide hormones including glucagon, enkephalins, substance P, neurotensin, oxytocin, and bradykinin. [provided by RefSeq, Aug 2017].

Strand
+
Chromosome
3
Protein
750 residues
All mutations
204
PTM sites
13
CDS
154,801,956 - 154,898,248
Transcription
154,798,078 - 154,901,518
6.4% of sequence is predicted to be disordered

External references

Mappings retrieved from NCBI & UniProt.
RefSeq
Entrez
gene: 4311
UniProt
Ensembl