Homo sapiens Protein: ADAM9
Summary
InnateDB Protein IDBP-18371.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ADAM9
Protein Name ADAM metallopeptidase domain 9
Synonyms CORD9; MCMP; MDC9; Mltng;
Species Homo sapiens
Ensembl Protein ENSP00000369249
InnateDB Gene IDBG-18369 (ADAM9)
Protein Structure
UniProt Annotation
Function Probable zinc protease. May mediate cell-cell or cell- matrix interactions. Isoform 2 displays alpha-secretase activity for APP. {ECO:0000269PubMed:12054541}.
Subcellular Localization Isoform 1: Cell membrane; Single-pass type I membrane protein.Isoform 2: Secreted.
Disease Associations Cone-rod dystrophy 9 (CORD9) [MIM:612775]: An inherited retinal dystrophy characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa. {ECO:0000269PubMed:19409519}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Widely expressed. Expressed in chondrocytes. Isoform 2 is highly expressed in liver and heart. {ECO:0000269PubMed:12054541, ECO:0000269PubMed:7584026, ECO:0000269PubMed:8647900, ECO:0000269PubMed:9016778}.
Comments
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 2 interaction(s) predicted by orthology.
Experimentally validated
Total 10 [view]
Protein-Protein 10 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004222 metalloendopeptidase activity
GO:0005080 protein kinase C binding
GO:0005178 integrin binding
GO:0005515 protein binding
GO:0005518 collagen binding
GO:0008237 metallopeptidase activity
GO:0008270 zinc ion binding
GO:0017124 SH3 domain binding
GO:0043236 laminin binding
Biological Process
GO:0000186 activation of MAPKK activity
GO:0006508 proteolysis
GO:0006509 membrane protein ectodomain proteolysis
GO:0007155 cell adhesion
GO:0007160 cell-matrix adhesion
GO:0007179 transforming growth factor beta receptor signaling pathway
GO:0007229 integrin-mediated signaling pathway
GO:0010042 response to manganese ion
GO:0022617 extracellular matrix disassembly
GO:0030198 extracellular matrix organization
GO:0030216 keratinocyte differentiation
GO:0030574 collagen catabolic process
GO:0033627 cell adhesion mediated by integrin
GO:0033630 positive regulation of cell adhesion mediated by integrin
GO:0033631 cell-cell adhesion mediated by integrin
GO:0034241 positive regulation of macrophage fusion
GO:0034612 response to tumor necrosis factor
GO:0042117 monocyte activation
GO:0042542 response to hydrogen peroxide
GO:0050714 positive regulation of protein secretion
GO:0051044 positive regulation of membrane protein ectodomain proteolysis
GO:0051088 PMA-inducible membrane protein ectodomain proteolysis
GO:0051384 response to glucocorticoid
GO:0051549 positive regulation of keratinocyte migration
GO:0051592 response to calcium ion
GO:0071222 cellular response to lipopolysaccharide
Cellular Component
GO:0005615 extracellular space
GO:0009986 cell surface
GO:0016021 integral component of membrane
GO:0031233 intrinsic to external side of plasma membrane
Protein Structure and Domains
PDB ID
InterPro IPR001590 Peptidase M12B, ADAM/reprolysin
IPR001762 Blood coagulation inhibitor, Disintegrin
IPR002870 Peptidase M12B, propeptide
IPR006586 ADAM, cysteine-rich
PFAM PF01421
PF00200
PF01562
PF08516
PRINTS PR00289
PIRSF
SMART SM00050
SM00608
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q13443
PhosphoSite PhosphoSite-Q13443
TrEMBL
UniProt Splice Variant
Entrez Gene 8754
UniGene Hs.618683
RefSeq
HUGO HGNC:216
OMIM 602713
CCDS
HPRD 04091
IMGT
EMBL AF495383 BC143923 CH471080 D14665 U41766
GenPept AAC50403 AAI43924 AAM49575 BAA03499 EAW63284