Homo sapiens Protein: LAMP2
Summary
InnateDB Protein IDBP-84403.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LAMP2
Protein Name lysosomal-associated membrane protein 2
Synonyms CD107b; LAMP-2; LAMPB; LGP110;
Species Homo sapiens
Ensembl Protein ENSP00000200639
InnateDB Gene IDBG-84399 (LAMP2)
Protein Structure
UniProt Annotation
Function Implicated in tumor cell metastasis. May function in protection of the lysosomal membrane from autodigestion, maintenance of the acidic environment of the lysosome, adhesion when expressed on the cell surface (plasma membrane), and inter- and intracellular signal transduction. Protects cells from the toxic effects of methylating mutagens. {ECO:0000269PubMed:8407947}.
Subcellular Localization Cell membrane {ECO:0000269PubMed:17897319}; Single-pass type I membrane protein {ECO:0000255PROSITE- ProRule:PRU00740, ECO:0000269PubMed:17897319}. Endosome membrane {ECO:0000269PubMed:17897319}; Single-pass type I membrane protein {ECO:0000255PROSITE-ProRule:PRU00740, ECO:0000269PubMed:17897319}. Lysosome membrane {ECO:0000255PROSITE-ProRule:PRU00740, ECO:0000269PubMed:17897319}; Single-pass type I membrane protein {ECO:0000255PROSITE-ProRule:PRU00740, ECO:0000269PubMed:17897319}. Note=This protein shuttles between lysosomes, endosomes, and the plasma membrane.
Disease Associations Danon disease (DAND) [MIM:300257]: DAND is a lysosomal glycogen storage disease characterized by the clinical triad of cardiomyopathy, vacuolar myopathy and mental retardation. It is often associated with an accumulation of glycogen in muscle and lysosomes. {ECO:0000269PubMed:15673802, ECO:0000269PubMed:15907287}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Isoform LAMP-2A is highly expressed in placenta, lung and liver, less in kidney and pancreas, low in brain and skeletal muscle. Isoform LAMP-2B is highly expressed in skeletal muscle, less in brain, placenta, lung, kidney and pancreas, very low in liver.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 48 experimentally validated interaction(s) in this database.
They are also associated with 4 interaction(s) predicted by orthology.
Experimentally validated
Total 48 [view]
Protein-Protein 48 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 4 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0019899 enzyme binding
Biological Process
GO:0002576 platelet degranulation
GO:0007596 blood coagulation
GO:0030168 platelet activation
GO:0050821 protein stabilization
Cellular Component
GO:0005764 lysosome
GO:0005765 lysosomal membrane
GO:0005770 late endosome
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0031088 platelet dense granule membrane
GO:0031902 late endosome membrane
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR002000 Lysosome-associated membrane glycoprotein
PFAM PF01299
PRINTS PR00336
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P13473
PhosphoSite PhosphoSite-P13473
TrEMBL
UniProt Splice Variant
Entrez Gene 3920
UniGene Hs.703553
RefSeq NP_002285
HUGO HGNC:6501
OMIM 309060
CCDS CCDS14599
HPRD 02396
IMGT
EMBL AC002476 AK291090 AY561849 BC002965 CH471107 J04183 L09709 L09710 L09711 L09712 L09713 L09714 L09715 L09716 L09717 S79873 U36336 X77196
GenPept AAA60383 AAA91149 AAB35426 AAB41647 AAB67313 AAB67314 AAH02965 AAS67876 BAF83779 CAA54416 EAX11881 EAX11882 EAX11883 EAX11884