Homo sapiens Protein: KLK8
Summary
InnateDB Protein IDBP-65299.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol KLK8
Protein Name kallikrein-related peptidase 8
Synonyms HNP; NP; NRPN; PRSS19; TADG14;
Species Homo sapiens
Ensembl Protein ENSP00000291726
InnateDB Gene IDBG-65297 (KLK8)
Protein Structure
UniProt Annotation
Function Serine protease which is capable of degrading a number of proteins such as casein, fibrinogen, kininogen, fibronectin and collagen type IV. Also cleaves L1CAM in response to increased neural activity. Induces neurite outgrowth and fasciculation of cultured hippocampal neurons. Plays a role in the formation and maturation of orphan and small synaptic boutons in the Schaffer- collateral pathway, regulates Schaffer-collateral long-term potentiation in the hippocampus and is required for memory acquisition and synaptic plasticity. Involved in skin desquamation and keratinocyte proliferation. Plays a role in the secondary phase of pathogenesis following spinal cord injury. {ECO:0000269PubMed:16337200}.
Subcellular Localization Secreted {ECO:0000269PubMed:17761692}. Cytoplasm {ECO:0000269PubMed:17761692}. Note=Shows a cytoplasmic distribution in the keratinocytes.
Disease Associations
Tissue Specificity Isoform 1 is predominantly expressed in the pancreas. Isoform 2 is expressed in adult brain and hippocampus. Isoform 1 and isoform 2 are found in fetal brain and placenta. Detected in salivary gland, uterus, thymus, breast, testis and kidney but not in spleen, liver, lung or normal ovarian tissue. Displays an 11.5-fold increase in Alzheimer disease hippocampus compared to controls and is overexpressed in some ovarian carcinomas. Expressed at low levels in normal skin while high levels are found in psoriasis vulgaris, seborrheic keratosis, lichen planus and squamous cell carcinoma skin samples. Expressed in the keratinocytes. {ECO:0000269PubMed:11309326, ECO:0000269PubMed:11522960, ECO:0000269PubMed:12147714, ECO:0000269PubMed:17761692}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
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:0006508 proteolysis
GO:0007613 memory
GO:0008219 cell death
GO:0009611 response to wounding
GO:0031642 negative regulation of myelination
GO:0043616 keratinocyte proliferation
GO:0048681 negative regulation of axon regeneration
GO:0048812 neuron projection morphogenesis
GO:0050807 regulation of synapse organization
Cellular Component
GO:0005615 extracellular space
GO:0005737 cytoplasm
Protein Structure and Domains
PDB ID
InterPro IPR001254 Peptidase S1
IPR009003 Trypsin-like cysteine/serine peptidase domain
PFAM PF00089
PRINTS
PIRSF
SMART SM00020
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt O60259
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 11202
UniGene Hs.104570
RefSeq NP_001268360
HUGO HGNC:6369
OMIM 605644
CCDS CCDS74433
HPRD 05733
IMGT
EMBL AB008390 AB008927 AB009849 AB010780 AB012761 AC011473 AC011483 AF055982 AF095742 AF095743 AF243527 AF251125 AY359036 AY563055 AY563056 AY563057 AY563058 AY563059 AY563060 AY563061 AY563062 AY563063 AY563064 AY563065 AY563066 AY563067 BC040887 CH471135 DQ267420
GenPept AAD25979 AAD29574 AAD56050 AAF79144 AAF79145 AAG23254 AAG33361 AAH40887 AAQ89395 AAT76913 AAT76914 AAT76915 AAT76916 AAT76917 AAT76918 AAT76919 AAT76920 AAT76921 AAT76922 AAT76923 AAT76924 AAT76925 AAT76926 AAT76927 AAT76928 AAT76929 AAT76930 AAT76931 AAT76932 AAT76933 AAT76934 AAT76935 AAT76936 AAT76937 AAT76938 ABB83339 BAA28673 BAA28676 BAA82665 BAA82666 BAA88684 EAW71962