PCSK5 (original) (raw)

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Protein-coding gene in the species Homo sapiens

PCSK5
Identifiers
Aliases PCSK5, PC5, PC6, PC6A, SPC6, proprotein convertase subtilisin/kexin type 5
External IDs OMIM: 600488; MGI: 97515; HomoloGene: 21244; GeneCards: PCSK5; OMA:PCSK5 - orthologs
Gene location (Human)Chromosome 9 (human)Chr.Chromosome 9 (human)[1]Chromosome 9 (human)Genomic location for PCSK5Genomic location for PCSK5Band9q21.13Start75,890,644 bp[1]End76,362,975 bp[1]
Gene location (Mouse)Chromosome 19 (mouse)Chr.Chromosome 19 (mouse)[2]Chromosome 19 (mouse)Genomic location for PCSK5Genomic location for PCSK5Band19 B|19 12.86 cMStart17,409,683 bp[2]End17,814,996 bp[2]
RNA expression patternBgeeHuman Mouse (ortholog)Top expressed inbuccal mucosa cellsaphenous veinsural nervepericardiumpancreatic ductal cellsecondary oocytevisceral pleuramucosa of paranasal sinusduodenumparietal pleuraTop expressed inexternal carotid arteryinternal carotid arterygastrulaPaneth cellvas deferenslumbar spinal ganglionadrenal glandGonadal ridgebody of femurvestibular sensory epitheliumMore reference expression dataBioGPSMore reference expression data
Gene ontologyMolecular function serine-type endopeptidase activity peptidase activity hydrolase activity serine-type peptidase activity peptide binding protein binding endopeptidase activity Cellular component integral component of membrane endomembrane system Golgi lumen membrane secretory granule Golgi apparatus extracellular region extracellular space trans-Golgi network integral component of Golgi membrane Biological process viral life cycle proteolysis female pregnancy cell-cell signaling coronary vasculature development renin secretion into blood stream heart development cardiac septum development determination of left/right symmetry protein processing signal peptide processing limb morphogenesis respiratory tube development peptide biosynthetic process embryo implantation peptide hormone processing kidney development embryonic skeletal system development embryonic digestive tract development anterior/posterior pattern specification regulation of lipoprotein lipase activity nerve growth factor processing Sources:Amigo / QuickGO
OrthologsSpeciesHuman MouseEntrez512518552EnsemblENSG00000099139ENSMUSG00000024713UniProtQ92824Q04592RefSeq (mRNA)NM_001190482NM_006200NM_001372043NM_001163144NM_001190483RefSeq (protein)NP_001177411NP_006191NP_001358972NP_001156616NP_001177412Location (UCSC)Chr 9: 75.89 – 76.36 MbChr 19: 17.41 – 17.81 MbPubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Proprotein convertase subtilisin/kexin type 5 is an enzyme that in humans is encoded by the PCSK5 gene, found in chromosome 9q21.3[5][6][7] Two alternatively spliced transcripts are described for this gene but only one has its full length nature known.

The protein encoded by this gene belongs to the subtilisin-like proprotein convertase family. The members of this family are proprotein convertases that process latent precursor proteins into their biologically active products. This encoded protein mediates posttranslational endoproteolytic processing for several integrin alpha subunits. It is thought to process prorenin, pro-membrane type-1 matrix metalloproteinase and HIV-1 glycoprotein gp160.[7]

Clinical significance

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Mutations in this gene have been associated with Currarino syndrome-like malformations.[8]

PCSK5 expression has been linked to higher survival rates for lung cancer patients.[9]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000099139Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024713Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ van de Loo JW, Creemers JW, Kas K, Roebroek AJ, Van de Ven WJ (1996). "Assignment of the human proprotein convertase gene PCSK5 to chromosome 9q21.3". Cytogenetic and Genome Research. 75 (4): 227–229. doi:10.1159/000134489. PMID 9067430.
  6. ^ Mbikay M, Seidah NG, Chrétien M, Simpson EM (Jul 1995). "Chromosomal assignment of the genes for proprotein convertases PC4, PC5, and PACE 4 in mouse and human". Genomics. 26 (1): 123–9. doi:10.1016/0888-7543(95)80090-9. PMID 7782070.
  7. ^ a b "Entrez Gene: PCSK5 proprotein convertase subtilisin/kexin type 5".
  8. ^ Szumska D, Pieles G, Essalmani R, Bilski M, Mesnard D, Kaur K, Franklyn A, El Omari K, Jefferis J, Bentham J, Taylor JM, Schneider JE, Arnold SJ, Johnson P, Tymowska-Lalanne Z, Stammers D, Clarke K, Neubauer S, Morris A, Brown SD, Shaw-Smith C, Cama A, Capra V, Ragoussis J, Constam D, Seidah NG, Prat A, Bhattacharya S (June 2008). "VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5". Genes Dev. 22 (11): 1465–77. doi:10.1101/gad.479408. PMC 2418583. PMID 18519639.
  9. ^ "Research update from the MCM team (January 2024)". World Community Grid. 16 January 2024. Retrieved 21 May 2024.