PCSK5 - proprotein convertase subtilisin/kexin type 5 Gene

Also Known as PC5; PC6; PC6A; SPC6

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5125

About PCSK5

Cytogenetic location: 9q21.13 Genomic coordinates (GRCh38): 9:75,889,809-76,362,975 (from NCBI)

This gene has 7 transcripts (splice variants), 271 orthologues and 9 paralogues. Broad expression in small intestine (RPKM 6.4), duodenum (RPKM 5.8) and 20 other tissues.

Summary

This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER. It then sorts to the trans-Golgi network where a second autocatalytic event takes place and the catalytic activity is acquired. This encoded protein is widely expressed and one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It mediates posttranslational endoproteolytic processing for several Integrin alpha subunits and is thought to process prorenin, pro-membrane type-1 matrix metalloproteinase and HIV-1 glycoprotein gp160. Alternative splicing results in multiple transcript variants, some of which encode distinct isoforms, including a protease packaged into dense core granules (PC5A) and a type 1 membrane bound protease (PC5B). [provided by RefSeq, May 2014]

PCSK5 Products (3)

mRNA Protein Name
NM_001190482.2 NP_001177411.1 proprotein convertase subtilisin/kexin type 5 isoform PC6B preproprotein
NM_001372043.1 NP_001358972.1 proprotein convertase subtilisin/kexin type 5 isoform 3 precursor
NM_006200.6 NP_006191.2 proprotein convertase subtilisin/kexin type 5 isoform PC6A preproprotein
Molecular Function GO Annotation Evidence References Source
enables endopeptidase activity EXP
EXP: Inferred from Experiment
16109723 GOA
enables peptidase activity IDA
IDA: Inferred from direct assay
15606899 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables serine-type endopeptidase activity IDA
IDA: Inferred from direct assay
8901832 GOA
Biological Process GO Annotation Evidence References Source
involved in anterior/posterior pattern specification IMP
IMP: Inferred from mutant phenotype
18519639 GOA
involved in embryonic digestive tract development IMP
IMP: Inferred from mutant phenotype
18519639 GOA
involved in embryonic skeletal system development IMP
IMP: Inferred from mutant phenotype
18519639 GOA
involved in kidney development IMP
IMP: Inferred from mutant phenotype
18519639 GOA
involved in peptide biosynthetic process IDA
IDA: Inferred from direct assay
8901832 GOA
involved in peptide hormone processing IDA
IDA: Inferred from direct assay
8901832 GOA
acts upstream of or within protein processing IDA
IDA: Inferred from direct assay
15606899 GOA
involved in protein processing IDA
IDA: Inferred from direct assay
8901832 GOA
involved in renin secretion into blood stream IEP
IEP: Inferred from expression pattern
8901832 GOA
involved in signal peptide processing IDA
IDA: Inferred from direct assay
16912035 GOA
involved in viral life cycle IEP
IEP: Inferred from expression pattern
8940009 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PCSK5 Protein Structure

Peptidase_S8

Peptidase_S8: Subtilase family (166 - 453)

P_proprotein

P_proprotein: Proprotein convertase P-domain (505 - 595)

GF_recep_IV

GF_recep_IV: Growth factor receptor domain IV (636 - 750)

  • 0
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  • 1200
  • 1500
  • 1860 a.a.
Protein Preferred Names Protein Names

proprotein convertase subtilisin/kexin type 5

  • prohormone convertase 5

PCSK5 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PCSK5 Q92824 KRTAP10-8 Homo sapiens P60410 25416956
Intra
PCSK5 Q92824 KRTAP10-7 Homo sapiens P60409 25416956
Intra
PCSK5 Q92824 KRTAP10-7 Homo sapiens P60409 25416956
Intra
PCSK5 Q92824 LCE3C Homo sapiens Q5T5A8 25416956
Intra
PCSK5 Q92824 LCE3C Homo sapiens Q5T5A8 25416956
Intra
PCSK5 Q92824 LCE3C Homo sapiens Q5T5A8 25416956
Intra
PCSK5 Q92824 NUFIP2 Homo sapiens Q7Z417 25416956
Intra
PCSK5 Q92824 GLRX3 Homo sapiens O76003 25416956
Intra
PCSK5 Q92824 GLRX3 Homo sapiens O76003 25416956
Intra
PCSK5 Q92824 KRTAP4-12 Homo sapiens Q9BQ66 25416956
Intra
PCSK5 Q92824 MEOX2 Homo sapiens P50222 25416956
Intra
PCSK5 Q92824 MEOX2 Homo sapiens P50222 25416956
Intra
PCSK5 Q92824 STK16 Homo sapiens O75716 25416956
Intra
PCSK5 Q92824 STK16 Homo sapiens O75716 25416956
Intra
PCSK5 Q92824 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
PCSK5 Q92824 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Motion Sickness
  • Airsickness

  • Carsickness

  • Seasickness

  • Travel Sickness

  • Riders' Vertigo

Currarino Syndrome
  • Currarino Triad

  • Partial Sacral Agenesis With Intact First Sacral Vertebra, Presacral Mass And Anorectal Malformation

  • CURRAS

Cataract 38
  • CTRCT38

  • Catc5

  • Autosomal Recessive Congenital Cataract 5

  • Cataract, Autosomal Recessive Congenital 5

  • Cataract 38, Autosomal Recessive

  • Cataract, Type 38

Epilepsy, Idiopathic Generalized 2
  • EIG2

  • Epilepsy, Idiopathic Generalized, Susceptibility To, 2

  • Idiopathic Generalized Epilepsy 2

  • Epilepsy, Idiopathic Generalized Locus On Chromosome 14

  • Epilepsy, Idiopathic Generalized, Susceptibility To, Locus On Chromosome 14

Sacral Defect With Anterior Meningocele
  • Caudal Regression Syndrome

  • Caudal Regression Sequence

  • Sacral Agenesis

  • Caudal Dysgenesis Syndrome

  • SDAM

  • Caudal Dysplasia Sequence

  • Caudal Dysplasia

  • Sacral Agenesis Syndrome

  • Sacral Regression Syndrome

  • Sacral Defect And Anterior Sacral Meningocele

  • Rudd Klimek Syndrome

  • Sirenomelia

Vacterl Association
  • Vater Association

  • Vater Syndrome

Somatization Disorder
  • Somatoform Disorders

  • Briquet'S Disorder

  • Polysomatising Disorder

  • Somatisation Disorder

  • Somatoform Disorder

Neurotic Disorder
  • Neurosis

  • Reactive Depression

  • Adjustment Disorders

  • Neurotic Disorders

  • Depressive Neurosis

  • Neurotic Depression

  • Neurotic Depression Reactive Type

  • Neurotic Depressive State

  • Psychoneurosis

  • Depressive Disorder

  • Depression, Neurotic

Pachyonychia Congenita 1
  • Pachyonychia Congenita

  • Jadassohn-Lewandowsky Syndrome

  • Pachyonychia Congenita Syndrome

  • PC1

  • Pachyonychia Congenita, Jadassohn-Lewandowsky Type

  • Congenital Pachyonychia

  • Pachyonychia Congenita, Type 1

  • Pachyonychia Congenita, Jadassohn-Lewandowsky Type, Formerly

  • Jadassohn-Lewandowsky Syndrome, Formerly

  • Jackson-Lawler Type Pachyonychia Congenita

  • Pachyonychia Congenita Type 1

  • Jackson-Lawler Syndrome

  • Jadassohn-Lewandowski Syndrome

  • Pc

  • Pachyonychia Congenita Jackson-Lawler Type

  • Pachyonychia Congenita Jadassohn-Lewandowsky Type

  • Pachyonychia Congenita Jackson Lawler Type

  • Pc-1

  • Pachyonychia Congenita, Jadassohn Lewandowsky Type

  • Pachyonychia Congenita, Type 2

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus PCSK5 VGNC VGNC:102961
Canis familiaris PCSK5 VGNC VGNC:44324
Rattus norvegicus PCSK5 RGD RGD:620326
Macaca mulatta PCSK5 VGNC VGNC:75787
Bos taurus PCSK5 VGNC VGNC:56979
Mus musculus PCSK5 MGD MGI:97515
Others PCSK5 NCBI