GP5
Platelet glycoprotein V
Also known as: CD42d, GPV_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P40197
- Gene
- GP5
- Ensembl
- ENSG00000178732
- Chromosome
- 3
- Canonical length
- 560 aa
- Protein class
- CD markers, Plasma proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Human platelet glycoprotein V (GP5) is a part of the Ib-V-IX system of surface glycoproteins that constitute the receptor for von Willebrand factor (VWF; MIM 613160) and mediate the adhesion of platelets to injured vascular surfaces in the arterial circulation, a critical initiating event in hemostasis. The main portion of the receptor is a heterodimer composed of 2 polypeptide chains, an alpha chain (GP1BA; MIM 606672) and a beta chain (GP1BB; MIM 138720), that are linked by disulfide bonds. The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX (GP9; MIM 173515) and GP5. Mutations in GP1BA, GP1BB, and GP9 have been shown to cause Bernard-Soulier syndrome (MIM 231200), a bleeding disorder (review by Lopez et al., 1998 [PubMed 9616133]).[supplied by OMIM, Nov 2010]
Canonical amino-acid sequenceUniProt
560 residues, UniProt reviewed canonical sequence.
>P40197|GP5
1 MLRGTLLCAV LGLLRAQPFP CPPACKCVFR DAAQCSGGDV ARISALGLPT NLTHILLFGM
61 GRGVLQSQSF SGMTVLQRLM ISDSHISAVA PGTFSDLIKL KTLRLSRNKI THLPGALLDK
121 MVLLEQLFLD HNALRGIDQN MFQKLVNLQE LALNQNQLDF LPASLFTNLE NLKLLDLSGN
181 NLTHLPKGLL GAQAKLERLL LHSNRLVSLD SGLLNSLGAL TELQFHRNHI RSIAPGAFDR
241 LPNLSSLTLS RNHLAFLPSA LFLHSHNLTL LTLFENPLAE LPGVLFGEMG GLQELWLNRT
301 QLRTLPAAAF RNLSRLRYLG VTLSPRLSAL PQGAFQGLGE LQVLALHSNG LTALPDGLLR
361 GLGKLRQVSL RRNRLRALPR ALFRNLSSLE SVQLDHNQLE TLPGDVFGAL PRLTEVLLGH
421 NSWRCDCGLG PFLGWLRQHL GLVGGEEPPR CAGPGAHAGL PLWALPGGDA ECPGPRGPPP
481 RPAADSSSEA PVHPALAPNS SEPWVWAQPV TTGKGQDHSP FWGFYFLLLA VQAMITVIIV
541 FAMIKIGQLF RKLIRERALGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GP5 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 1 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 1 nTPM
- appendix: 0.6 nTPM
- fallopian tube: 0.6 nTPM
- bone marrow: 0.5 nTPM
- tonsil: 0.5 nTPM
- spleen: 0.4 nTPM
Single-cell type
- platelets: 25 nCPM
- megakaryocytes: 19 nCPM
- thymocytes: 3.4 nCPM
- fallopian tube ciliated cells: 2 nCPM
- ependymal cells: 1.8 nCPM
- megakaryocyte progenitors: 1.7 nCPM
Immune cell
- naive CD8 T-cell: 0.4 nTPM
- naive CD4 T-cell: 0.3 nTPM
- plasmacytoid DC: 0.2 nTPM
- memory CD4 T-cell: 0.1 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- midbrain: 0.6 nTPM
- cerebral cortex: 0.5 nTPM
- hypothalamus: 0.5 nTPM
- medulla oblongata: 0.5 nTPM
- spinal cord: 0.5 nTPM
- cerebellum: 0.4 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.63
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.12
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- blood coagulation
- blood coagulation, intrinsic pathway
- cell adhesion
- megakaryocyte development
- positive regulation of platelet activation
- release of sequestered calcium ion into cytosol
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GP5 as an antibody target. Whether an autoantibody or antibody against GP5 could matter depends on whether native GP5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GP5 is annotated at the cell surface, where native GP5 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label GP5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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