Homo sapiens Protein: LOXL2
Summary
InnateDB Protein IDBP-11847.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol LOXL2
Protein Name lysyl oxidase-like 2
Synonyms LOR2; WS9-14;
Species Homo sapiens
Ensembl Protein ENSP00000373783
InnateDB Gene IDBG-11841 (LOXL2)
Protein Structure
UniProt Annotation
Function Mediates the post-translational oxidative deamination of lysine residues on target proteins leading to the formation of deaminated lysine (allysine). When secreted in extracellular matrix, promotes cross-linking of extracellular matrix proteins by mediating oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin. Acts as a regulator of sprouting angiogenesis, probably via collagen IV scaffolding. When nuclear, acts as a transcription corepressor and specifically mediates deamination of trimethylated 'Lys-4' of histone H3 (H3K4me3), a specific tag for epigenetic transcriptional activation. Involved in epithelial to mesenchymal transition (EMT) via interaction with SNAI1 and participates in repression of E- cadherin, probably by mediating deamination of histone H3. Also involved in E-cadherin repression following hypoxia, a hallmark of epithelial to mesenchymal transition believed to amplify tumor aggressiveness, suggesting that it may play a role in tumor progression. Acts as a regulator of chondrocyte differentiation, probably by regulating expression of factors that control chondrocyte differentiation. {ECO:0000269PubMed:16096638, ECO:0000269PubMed:20026874, ECO:0000269PubMed:21233336, ECO:0000269PubMed:21732535, ECO:0000269PubMed:21835952, ECO:0000269PubMed:22483618}.
Subcellular Localization Secreted, extracellular space, extracellular matrix, basement membrane {ECO:0000250}. Nucleus. Chromosome. Note=Associated with chromatin. It is unclear how LOXL2 is nuclear: it contains a clear signal sequence and is predicted to localize in the extracellular medium. However, different reports confirmed the intracellular location and its key role in transcription regulation.
Disease Associations
Tissue Specificity Expressed in many tissues. Highest expression in reproductive tissues, placenta, uterus and prostate. Up- regulated in a number of cancers cells and tissues.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003682 chromatin binding
GO:0003714 transcription corepressor activity
GO:0004720 protein-lysine 6-oxidase activity
GO:0005044 scavenger receptor activity
GO:0005507 copper ion binding
GO:0005515 protein binding
GO:0009055 electron carrier activity
GO:0016641 oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor
GO:0035064 methylated histone binding
GO:0070492 oligosaccharide binding
Biological Process
GO:0001666 response to hypoxia
GO:0001837 epithelial to mesenchymal transition
GO:0001935 endothelial cell proliferation
GO:0002040 sprouting angiogenesis
GO:0006351 transcription, DNA-templated
GO:0006464 cellular protein modification process
GO:0006898 receptor-mediated endocytosis
GO:0007155 cell adhesion
GO:0007568 aging
GO:0016570 histone modification
GO:0018277 protein deamination
GO:0030199 collagen fibril organization
GO:0032332 positive regulation of chondrocyte differentiation
GO:0043542 endothelial cell migration
GO:0045892 negative regulation of transcription, DNA-templated
GO:0046688 response to copper ion
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005604 basement membrane
GO:0005615 extracellular space
GO:0005634 nucleus
GO:0005694 chromosome
GO:0016020 membrane
Protein Structure and Domains
PDB ID
InterPro IPR001190 SRCR domain
IPR001695 Lysyl oxidase
IPR017448 SRCR-like domain
PFAM PF00530
PF01186
PRINTS PR00258
PR00074
PIRSF
SMART SM00202
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9Y4K0
PhosphoSite PhosphoSite-Q9Y4K0
TrEMBL E5RJL2
UniProt Splice Variant
Entrez Gene 4017
UniGene Hs.736854
RefSeq NP_002309
HUGO HGNC:6666
OMIM 606663
CCDS CCDS34864
HPRD 09446
IMGT
EMBL AC090197 AC104561 AF117949 AK222477 AK312266 BC000594 U89942
GenPept AAB49697 AAD34343 AAH00594 BAD96197 BAG35197