PCSK5 - proprotein convertase subtilisin/kexin type 5 Gene
Also Known as PC5; PC6; PC6A; SPC6
Species: Homo sapiens
About PCSK5
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 |
PCSK5 Protein Structure
Peptidase_S8: Subtilase family (166 - 453)
P_proprotein: Proprotein convertase P-domain (505 - 595)
GF_recep_IV: Growth factor receptor domain IV (636 - 750)
- 0
- 300
- 600
- 900
- 1200
- 1500
- 1860 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
proprotein convertase subtilisin/kexin type 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 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Motion Sickness |
|
|
| Currarino Syndrome |
|
|
| Cataract 38 |
|
|
| Epilepsy, Idiopathic Generalized 2 |
|
|
| Sacral Defect With Anterior Meningocele |
|
|
| Vacterl Association |
|
|
| Somatization Disorder |
|
|
| Neurotic Disorder |
|
|
| Pachyonychia Congenita 1 |
|
|
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 |