Kallikrein-5

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Kallikrein-5, formerly known as stratum corneum tryptic enzyme (SCTE), is a serine protease expressed in the epidermis. In humans it is encoded by the KLK5 gene.[5][6][7][8][9][10] This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Its expression is up-regulated by estrogens and progestins. Alternative splicing results in multiple transcript variants encoding the same protein.[10]

PDBHuman UniProt search: PDBe RCSB
AliasesKLK5, KLK-L2, KLKL2, SCTE, kallikrein related peptidase 5
Quick facts KLK5, Available structures ...
KLK5
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesKLK5, KLK-L2, KLKL2, SCTE, kallikrein related peptidase 5
External IDsOMIM: 605643; MGI: 1915918; HomoloGene: 75000; GeneCards: KLK5; OMA:KLK5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001077491
NM_001077492
NM_012427

NM_026806

RefSeq (protein)

NP_001070959
NP_001070960
NP_036559

n/a

Location (UCSC)Chr 19: 50.94 – 50.95 MbChr 7: 43.49 – 43.5 Mb
PubMed search[3][4]
Wikidata
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KLK5 has been suggested to regulate cell shedding (desquamation) in conjunction with KLK7 and KLK14, given its ability to degrade proteins which form the extracellular component of cell junctions in the stratum corneum. It is proposed that KLK5 regulates this process since it is able to self-activate in addition to activating KLK7 and KLK14.[11]

References

Further reading

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