PTPRC
Receptor-type tyrosine-protein phosphatase C
Also known as: CD45, GP180, LCA, PTPRC_HUMAN, T200
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P08575
- Gene
- PTPRC
- Ensembl
- ENSG00000081237
- Chromosome
- 1
- Canonical length
- 1306 aa
- Protein class
- Cancer-related genes, CD markers, Disease related genes, Enzymes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoplasm,Vesicles
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitosis, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus is classified as a receptor type PTP. This PTP has been shown to be an essential regulator of T- and B-cell antigen receptor signaling. It functions through either direct interaction with components of the antigen receptor complexes, or by activating various Src family kinases required for the antigen receptor signaling. This PTP also suppresses JAK kinases, and thus functions as a regulator of cytokine receptor signaling. Alternatively spliced transcripts variants of this gene, which encode distinct isoforms, have been reported. [provided by RefSeq, Jun 2012]
Canonical amino-acid sequenceUniProt
1306 residues, UniProt reviewed canonical sequence.
>P08575|PTPRC
1 MTMYLWLKLL AFGFAFLDTE VFVTGQSPTP SPTGLTTAKM PSVPLSSDPL PTHTTAFSPA
61 STFERENDFS ETTTSLSPDN TSTQVSPDSL DNASAFNTTG VSSVQTPHLP THADSQTPSA
121 GTDTQTFSGS AANAKLNPTP GSNAISDVPG ERSTASTFPT DPVSPLTTTL SLAHHSSAAL
181 PARTSNTTIT ANTSDAYLNA SETTTLSPSG SAVISTTTIA TTPSKPTCDE KYANITVDYL
241 YNKETKLFTA KLNVNENVEC GNNTCTNNEV HNLTECKNAS VSISHNSCTA PDKTLILDVP
301 PGVEKFQLHD CTQVEKADTT ICLKWKNIET FTCDTQNITY RFQCGNMIFD NKEIKLENLE
361 PEHEYKCDSE ILYNNHKFTN ASKIIKTDFG SPGEPQIIFC RSEAAHQGVI TWNPPQRSFH
421 NFTLCYIKET EKDCLNLDKN LIKYDLQNLK PYTKYVLSLH AYIIAKVQRN GSAAMCHFTT
481 KSAPPSQVWN MTVSMTSDNS MHVKCRPPRD RNGPHERYHL EVEAGNTLVR NESHKNCDFR
541 VKDLQYSTDY TFKAYFHNGD YPGEPFILHH STSYNSKALI AFLAFLIIVT SIALLVVLYK
601 IYDLHKKRSC NLDEQQELVE RDDEKQLMNV EPIHADILLE TYKRKIADEG RLFLAEFQSI
661 PRVFSKFPIK EARKPFNQNK NRYVDILPYD YNRVELSEIN GDAGSNYINA SYIDGFKEPR
721 KYIAAQGPRD ETVDDFWRMI WEQKATVIVM VTRCEEGNRN KCAEYWPSME EGTRAFGDVV
781 VKINQHKRCP DYIIQKLNIV NKKEKATGRE VTHIQFTSWP DHGVPEDPHL LLKLRRRVNA
841 FSNFFSGPIV VHCSAGVGRT GTYIGIDAML EGLEAENKVD VYGYVVKLRR QRCLMVQVEA
901 QYILIHQALV EYNQFGETEV NLSELHPYLH NMKKRDPPSE PSPLEAEFQR LPSYRSWRTQ
961 HIGNQEENKS KNRNSNVIPY DYNRVPLKHE LEMSKESEHD SDESSDDDSD SEEPSKYINA
1021 SFIMSYWKPE VMIAAQGPLK ETIGDFWQMI FQRKVKVIVM LTELKHGDQE ICAQYWGEGK
1081 QTYGDIEVDL KDTDKSSTYT LRVFELRHSK RKDSRTVYQY QYTNWSVEQL PAEPKELISM
1141 IQVVKQKLPQ KNSSEGNKHH KSTPLLIHCR DGSQQTGIFC ALLNLLESAE TEEVVDIFQV
1201 VKALRKARPG MVSTFEQYQF LYDVIASTYP AQNGQVKKNN HQEDKIEFDN EVDKVKQDAN
1261 CVNPLGAPEK LPEAKEQAEG SEPTSGTEGP EHSVNGPASP ALNQGSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PTPRC 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)
- 0.37
- Highest tissue expression
- 274 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 274 nTPM
- appendix: 229 nTPM
- thymus: 213 nTPM
- tonsil: 210 nTPM
- spleen: 170 nTPM
- bone marrow: 78 nTPM
Single-cell type
- neutrophils: 4,182 nCPM
- nk-cells: 962 nCPM
- monocytes: 938 nCPM
- t-cells: 915 nCPM
- microglia: 863 nCPM
- neutrophil progenitors: 816 nCPM
Immune cell
- total PBMC: 1,158 nTPM
- non-classical monocyte: 908 nTPM
- intermediate monocyte: 799 nTPM
- neutrophil: 717 nTPM
- gdT-cell: 574 nTPM
- memory CD8 T-cell: 545 nTPM
Brain region
- white matter: 38 nTPM
- medulla oblongata: 34 nTPM
- pons: 26 nTPM
- midbrain: 25 nTPM
- spinal cord: 24 nTPM
- thalamus: 22 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PTPRC.
Disease | AllUniProt
Conditions PTPRC is implicated in, by any mechanism.
- Multiple sclerosis (MS) MIM:126200
- Immunodeficiency 105, severe combined (IMD105) MIM:619924
Disease | GeneticClinVar
40 pathogenic / likely-pathogenic of 1,300 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Immunodeficiency 104
- Immunodeficiency 105
- Severe combined immunodeficiency disease
Disease | AutoantibodyPubMed
Conditions in which antibodies against PTPRC are reported. Each links to that disease's full target list.
ReferencesPubMed · IEDB
Publications for PTPRC from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
11 publications
- Efficacy and safety of anti-CD45-saporin as conditioning agent for RAG deficiency.
2021 · J Allergy Clin Immunol · RCR 1.9 · 34 citations - Autoantibodies specific for different isoforms of CD45 in systemic lupus erythematosus.
1990 · J Exp Med · RCR 1.3 · 54 citations - Cell-type specificity of anti-CD45 autoantibodies in systemic lupus erythematosus.
1996 · Arthritis Rheum · RCR 0.3 · 14 citations - A natural neonatal hybridoma autoantibody to the T200 antigen.
1989 · J Immunol · RCR 0.2 · 7 citations - Autoantibodies to CD45 in systemic lupus erythematosus.
1992 · Int J Clin Lab Res · RCR 0.2 · 7 citations
Show 6 more
- Carbohydrate specificity of IgM autoantibodies to CD45 in systemic lupus erythematosus.
1994 · Mol Biol Rep · RCR 0.2 · 7 citations - Expression of the sialosyl-Tn epitope on CD45 derived from activated peripheral blood T cells.
1998 · Immunol Invest · RCR 0.1 · 6 citations - CD45 autoantibodies mediate neutralization of activated T cells from lupus patients through anergy or apoptosis.
2000 · Lupus · RCR 0.1 · 4 citations - Autoantibodies to CD45 in systemic lupus erythematosus.
1998 · J Autoimmun · RCR 0.1 · 4 citations - Antibodies to CD45 and other cell membrane antigens in systemic lupus erythematosus.
1994 · Springer Semin Immunopathol · RCR 0.1 · 3 citations - [Clinical and hematological significance of antigranulocyte autoantibodies].
1998 · Klin Lab Diagn
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 0.21
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.17
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
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
- alpha-beta T cell proliferation
- B cell differentiation
- B cell proliferation
- B cell receptor signaling pathway
- bone marrow development
- cell cycle phase transition
- cell surface receptor signaling pathway
- defense response to virus
- dephosphorylation
- DN2 thymocyte differentiation
- extrinsic apoptotic signaling pathway
- gamma-delta T cell differentiation
- hematopoietic progenitor cell differentiation
- heterotypic cell-cell adhesion
- leukocyte cell-cell adhesion
- MAPK cascade
- natural killer cell differentiation
- negative regulation of cell adhesion involved in substrate-bound cell migration
- negative regulation of cytokine-mediated signaling pathway
- negative regulation of ERK1 and ERK2 cascade
- negative regulation of interleukin-2 production
- negative regulation of interleukin-4-mediated signaling pathway
- negative regulation of microglial cell activation
- negative regulation of protein kinase activity
- negative regulation of receptor signaling pathway via JAK-STAT
- negative regulation of T cell mediated cytotoxicity
- negative regulation of transcription by RNA polymerase II
- negative thymic T cell selection
- positive regulation of alpha-beta T cell proliferation
- positive regulation of B cell proliferation
- positive regulation of calcium-mediated signaling
- positive regulation of ERK1 and ERK2 cascade
- positive regulation of extrinsic apoptotic signaling pathway
- positive regulation of Fc receptor mediated stimulatory signaling pathway
- positive regulation of gamma-delta T cell differentiation
- positive regulation of hematopoietic stem cell migration
- positive regulation of humoral immune response mediated by circulating immunoglobulin
- positive regulation of immunoglobulin production
- positive regulation of interleukin-2 production
- positive regulation of isotype switching to IgG isotypes
- positive regulation of MAPK cascade
- positive regulation of phagocytosis
- positive regulation of protein kinase activity
- positive regulation of stem cell proliferation
- positive regulation of T cell mediated cytotoxicity
- positive regulation of T cell proliferation
- positive regulation of tumor necrosis factor production
- positive thymic T cell selection
- protein dephosphorylation
- regulation of cell cycle
- regulation of gene expression
- regulation of interleukin-8 production
- regulation of phagocytosis
- regulation of T cell receptor signaling pathway
- release of sequestered calcium ion into cytosol
- response to aldosterone
- response to gamma radiation
- signal transduction
- stem cell development
- T cell activation
- T cell differentiation
- T cell receptor signaling pathway
- plasma membrane raft distribution
- positive regulation of antigen receptor-mediated signaling pathway
Molecular functions
- ankyrin binding
- heparan sulfate proteoglycan binding
- heparin binding
- protein kinase binding
- protein tyrosine kinase inhibitor activity
- protein tyrosine phosphatase activity
- signaling receptor binding
- spectrin binding
- transmembrane receptor protein tyrosine phosphatase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Tyrosine-specific protein phosphatase, PTPase domain
- Tyrosine-specific protein phosphatases domain
- Protein-tyrosine phosphatase, catalytic
- Fibronectin type III
- Immunoglobulin-like fold
- Protein-tyrosine phosphatase, active site
- Protein-tyrosine phosphatase-like
- Fibronectin type III superfamily
- Protein-Tyrosine Phosphatase
- Fibronectin type III domain
- Protein-tyrosine phosphatase
- Receptor-type tyrosine-protein phosphatase C
- Protein tyrosine phosphatase, receptor type, N-terminal
- Protein tyrosine phosphatase N terminal
- Leukocyte receptor CD45
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PTPRC in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PTPRC as an antibody target. Whether an autoantibody or antibody against PTPRC could matter depends on whether native PTPRC is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PTPRC is annotated at the cell surface, where native PTPRC 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 PTPRC as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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