Homo sapiens Protein: PLAU
Summary
InnateDB Protein IDBP-78891.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PLAU
Protein Name plasminogen activator, urokinase
Synonyms ATF; BDPLT5; QPD; u-PA; UPA; URK;
Species Homo sapiens
Ensembl Protein ENSP00000361850
InnateDB Gene IDBG-78889 (PLAU)
Protein Structure
UniProt Annotation
Function Specifically cleaves the zymogen plasminogen to form the active enzyme plasmin.
Subcellular Localization Secreted.
Disease Associations Quebec platelet disorder (QPD) [MIM:601709]: An autosomal dominant bleeding disorder due to a gain-of-function defect in fibrinolysis. Although affected individuals do not exhibit systemic fibrinolysis, they show delayed onset bleeding after challenge, such as surgery. The hallmark of the disorder is markedly increased PLAU levels within platelets, which causes intraplatelet plasmin generation and secondary degradation of alpha-granule proteins. {ECO:0000269PubMed:20007542}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed in the prostate gland and prostate cancers. {ECO:0000269PubMed:15988036}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 24 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 24 [view]
Protein-Protein 20 [view]
Protein-DNA 2 [view]
Protein-RNA 0
DNA-DNA 2 [view]
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004252 serine-type endopeptidase activity
GO:0005515 protein binding
Biological Process
GO:0001666 response to hypoxia
GO:0006508 proteolysis
GO:0006935 chemotaxis
GO:0007165 signal transduction
GO:0007596 blood coagulation
GO:0010469 regulation of receptor activity
GO:0014909 smooth muscle cell migration
GO:0014910 regulation of smooth muscle cell migration
GO:0033628 regulation of cell adhesion mediated by integrin
GO:0042127 regulation of cell proliferation
GO:0042730 fibrinolysis
GO:0061041 regulation of wound healing
GO:2000097 regulation of smooth muscle cell-matrix adhesion
Cellular Component
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005886 plasma membrane
GO:0009986 cell surface
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR000001 Kringle
IPR000742 Epidermal growth factor-like domain
IPR001254 Peptidase S1
IPR001314 Peptidase S1A, chymotrypsin-type
IPR009003 Trypsin-like cysteine/serine peptidase domain
IPR013806 Kringle-like fold
PFAM PF00051
PF00008
PF00089
PRINTS PR00722
PIRSF
SMART SM00130
SM00181
SM00020
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P00749
PhosphoSite PhosphoSite-P00749
TrEMBL S4R3G7
UniProt Splice Variant
Entrez Gene 5328
UniGene Hs.77274
RefSeq NP_002649
HUGO HGNC:9052
OMIM 191840
CCDS CCDS7339
HPRD 01883
IMGT
EMBL AF377330 AK298560 AL596247 AY029537 BC013575 BT007391 CH471083 D00244 D11143 K02286 K03027 K03226 M15476 X02419 X02760
GenPept AAA61252 AAA61253 AAA61257 AAC97138 AAH13575 AAK38734 AAK53822 AAP36055 BAA00175 BAA01919 BAG60754 CAA26268 CAA26535 CAI13969 EAW54544