KLK1

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

Kallikrein-1 is a protein that in humans is encoded by the KLK1 gene.[5][6][7] KLK1 is a member of the peptidase S1 family.

PDBOrtholog search: PDBe RCSB
AliasesKLK1, KLKR, Klk6, hK1, kallikrein 1
Quick facts Available structures, PDB ...
KLK1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKLK1, KLKR, Klk6, hK1, kallikrein 1
External IDsOMIM: 147910; MGI: 102850; HomoloGene: 110727; GeneCards: KLK1; OMA:KLK1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002257

NM_010639
NM_001320331
NM_001320332

RefSeq (protein)

NP_002248

NP_001307260
NP_001307261
NP_034769

Location (UCSC)Chr 19: 50.82 – 50.82 MbChr 7: 43.87 – 43.88 Mb
PubMed search[3][4]
Wikidata
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Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. This protein is functionally conserved in its capacity to release the vasoactive peptide, Lys-bradykinin, from low molecular weight kininogen.[8]

See also

References

Further reading

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