Homo sapiens Gene: MMP3
Summary
InnateDB Gene IDBG-69254.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MMP3
Gene Name matrix metallopeptidase 3 (stromelysin 1, progelatinase)
Synonyms CHDS6; MMP-3; SL-1; STMY; STMY1; STR1
Species Homo sapiens
Ensembl Gene ENSG00000149968
Encoded Proteins
matrix metallopeptidase 3 (stromelysin 1, progelatinase)
matrix metallopeptidase 3 (stromelysin 1, progelatinase)
matrix metallopeptidase 3 (stromelysin 1, progelatinase)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. This gene encodes an enzyme which degrades fibronectin, laminin, collagens III, IV, IX, and X, and cartilage proteoglycans. The enzyme is thought to be involved in wound repair, progression of atherosclerosis, and tumor initiation. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3. [provided by RefSeq, Jul 2008]
Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP\'s are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. This gene encodes an enzyme which degrades fibronectin, laminin, collagens III, IV, IX, and X, and cartilage proteoglycans. The enzyme is thought to be involved in wound repair, progression of atherosclerosis, and tumor initiation. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:102835801-102843803
Strand Reverse strand
Band q22.2
Transcripts
ENST00000299855 ENSP00000299855
ENST00000434103 ENSP00000398346
ENST00000524478 ENSP00000435255
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 10 [view]
Protein-Protein 9 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004175 endopeptidase activity
GO:0004222 metalloendopeptidase activity
GO:0005509 calcium ion binding
GO:0008237 metallopeptidase activity
GO:0008270 zinc ion binding
Biological Process
GO:0006508 proteolysis
GO:0010727 negative regulation of hydrogen peroxide metabolic process
GO:0022617 extracellular matrix disassembly
GO:0030198 extracellular matrix organization
GO:0030334 regulation of cell migration
GO:0030574 collagen catabolic process
GO:0071230 cellular response to amino acid stimulus
Cellular Component
GO:0005576 extracellular region
GO:0005578 proteinaceous extracellular matrix
GO:0005615 extracellular space
GO:0031012 extracellular matrix
Orthologs
Species
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
EGFR Transactivation by Gastrin pathway
Gastrin-CREB signalling pathway via PKC and MAPK pathway
Assembly of collagen fibrils and other multimeric structures pathway
Activation of Matrix Metalloproteinases pathway
Collagen degradation pathway
Extracellular matrix organization pathway
Signaling by GPCR pathway
Degradation of the extracellular matrix pathway
Signal Transduction pathway
Collagen formation pathway
KEGG
INOH
PID NCI
Urokinase-type plasminogen activator (uPA) and uPAR-mediated signaling
p75(NTR)-mediated signaling
Posttranslational regulation of adherens junction stability and dissassembly
Cross-References
SwissProt
TrEMBL E9PKX2
UniProt Splice Variant
Entrez Gene 4314
UniGene Hs.375129 Hs.645710
RefSeq NM_002422
HUGO HGNC:7173
OMIM 185250
CCDS CCDS8323
HPRD 01703
IMGT
EMBL AP000789
GenPept
RNA Seq Atlas 4314