Homo sapiens Protein: ADAM28
Summary
InnateDB Protein IDBP-364051.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ADAM28
Protein Name ADAM metallopeptidase domain 28
Synonyms ADAM 28; ADAM23; eMDC II; eMDCII; MDC-L; MDC-Lm; MDC-Ls; MDCL;
Species Homo sapiens
Ensembl Protein ENSP00000393699
InnateDB Gene IDBG-12310 (ADAM28)
Protein Structure
UniProt Annotation
Function May play a role in the adhesive and proteolytic events that occur during lymphocyte emigration or may function in ectodomain shedding of lymphocyte surface target proteins, such as FASL and CD40L. May be involved in sperm maturation.
Subcellular Localization Isoform 1: Cell membrane; Single-pass type I membrane protein.Isoform 2: Secreted.
Disease Associations
Tissue Specificity Expressed predominantly in secondary lymphoid tissues, such as lymph node, spleen, small intestine, stomach, colon, appendix and trachea. The lymphocyte population is responsible for expression of this protein in these tissues. Isoform 2 is expressed preferentially in spleen.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0004222 metalloendopeptidase activity
GO:0008237 metallopeptidase activity
GO:0008270 zinc ion binding
Biological Process
GO:0006508 proteolysis
GO:0007229 integrin-mediated signaling pathway
GO:0007283 spermatogenesis
Cellular Component
GO:0005576 extracellular region
GO:0005886 plasma membrane
GO:0016021 integral component of 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 Q9UKQ2
PhosphoSite PhosphoSite-Q9UKQ2
TrEMBL E5RGY1
UniProt Splice Variant
Entrez Gene 10863
UniGene Hs.639953
RefSeq NP_068547
HUGO HGNC:206
OMIM 606188
CCDS CCDS47830
HPRD 08391
IMGT
EMBL AC044891 AC120193 AF137334 AF137335 AJ242015 AK293382 BC136478 CH471080
GenPept AAD25099 AAD25100 AAI36479 BAG56894 CAB42085 EAW63609