Matches in SemOpenAlex for { <https://semopenalex.org/work/W2034163119> ?p ?o ?g. }
- W2034163119 endingPage "2516" @default.
- W2034163119 startingPage "2512" @default.
- W2034163119 abstract "We have identified cDNA clones encoding a chondroitin sulfate proteoglycan of rat brain (previously designated 3F8 and now named phosphacan) that binds to neurons and neural cell-adhesion molecules. A sequence of 1616 amino acids deduced from a 4.8-kb open reading frame contains the N-terminal amino acid sequence of the 3F8 core glycoprotein as well as four internal CNBr, tryptic, and endoproteinase Lys-C peptide sequences from the proteoglycan. The deduced amino acid sequence, beginning with a 24-amino acid signal peptide, reveals an N-terminal domain of 255 amino acids homologous to carbonic anhydrases. The entire amino acid sequence deduced from our cDNA clones corresponds to the extracellular portion of a human receptor-type protein tyrosine phosphatase (RPTP zeta/beta) with which it has 76% identity, and the proteoglycan may represent an mRNA splicing variant of the larger transmembrane protein. RNA analysis demonstrated that a probe to the N-terminal carbonic anhydrase domain of the proteoglycan hybridizes with rat brain mRNA of 9.5, 8.4, and 6.4 kb, whereas probes to the phosphatase domains hybridize with only the 9.5-kb message and with the 6.4-kb message (which corresponds to a previously identified variant of the transmembrane protein in which half of the extracellular domain is deleted). The 30 N-terminal amino acids of the 3H1 chondroitin/keratan sulfate proteoglycan of brain are identical to those of the 3F8 proteoglycan, and six internal tryptic peptide sequences also matched those found in sequenced peptides of the 3F8 proteoglycan and/or amino acid sequences deduced from the cDNA clones. We therefore conclude that the 3H1 chondroitin/keratan sulfate proteoglycan and the 3F8 chondroitin sulfate proteoglycan represent glycosylation and possible extracellular splicing variants of a receptor-type protein tyrosine phosphatase. These proteoglycans may modulate cell interactions and other developmental processes in nervous tissue through heterophilic binding to cell-surface and extracellular matrix molecules, and by competition with ligands of the transmembrane phosphatase." @default.
- W2034163119 created "2016-06-24" @default.
- W2034163119 creator A5042408023 @default.
- W2034163119 creator A5049647908 @default.
- W2034163119 creator A5063217842 @default.
- W2034163119 creator A5069087434 @default.
- W2034163119 creator A5088206488 @default.
- W2034163119 date "1994-03-29" @default.
- W2034163119 modified "2023-10-11" @default.
- W2034163119 title "Phosphacan, a chondroitin sulfate proteoglycan of brain that interacts with neurons and neural cell-adhesion molecules, is an extracellular variant of a receptor-type protein tyrosine phosphatase." @default.
- W2034163119 cites W1502661652 @default.
- W2034163119 cites W1531779321 @default.
- W2034163119 cites W1598171890 @default.
- W2034163119 cites W1608455044 @default.
- W2034163119 cites W1674557579 @default.
- W2034163119 cites W1979993280 @default.
- W2034163119 cites W2046527737 @default.
- W2034163119 cites W2058852380 @default.
- W2034163119 cites W2059452371 @default.
- W2034163119 cites W2070925035 @default.
- W2034163119 cites W2090373637 @default.
- W2034163119 cites W2094636679 @default.
- W2034163119 cites W2096372770 @default.
- W2034163119 cites W2112984407 @default.
- W2034163119 cites W2118513878 @default.
- W2034163119 cites W2126658684 @default.
- W2034163119 cites W2160421139 @default.
- W2034163119 cites W2341359047 @default.
- W2034163119 doi "https://doi.org/10.1073/pnas.91.7.2512" @default.
- W2034163119 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/43399" @default.
- W2034163119 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/7511813" @default.
- W2034163119 hasPublicationYear "1994" @default.
- W2034163119 type Work @default.
- W2034163119 sameAs 2034163119 @default.
- W2034163119 citedByCount "271" @default.
- W2034163119 countsByYear W20341631192012 @default.
- W2034163119 countsByYear W20341631192013 @default.
- W2034163119 countsByYear W20341631192014 @default.
- W2034163119 countsByYear W20341631192015 @default.
- W2034163119 countsByYear W20341631192016 @default.
- W2034163119 countsByYear W20341631192017 @default.
- W2034163119 countsByYear W20341631192018 @default.
- W2034163119 countsByYear W20341631192019 @default.
- W2034163119 countsByYear W20341631192020 @default.
- W2034163119 countsByYear W20341631192021 @default.
- W2034163119 countsByYear W20341631192022 @default.
- W2034163119 countsByYear W20341631192023 @default.
- W2034163119 crossrefType "journal-article" @default.
- W2034163119 hasAuthorship W2034163119A5042408023 @default.
- W2034163119 hasAuthorship W2034163119A5049647908 @default.
- W2034163119 hasAuthorship W2034163119A5063217842 @default.
- W2034163119 hasAuthorship W2034163119A5069087434 @default.
- W2034163119 hasAuthorship W2034163119A5088206488 @default.
- W2034163119 hasBestOaLocation W20341631191 @default.
- W2034163119 hasConcept C104317684 @default.
- W2034163119 hasConcept C10858879 @default.
- W2034163119 hasConcept C118892022 @default.
- W2034163119 hasConcept C153911025 @default.
- W2034163119 hasConcept C167625842 @default.
- W2034163119 hasConcept C170493617 @default.
- W2034163119 hasConcept C185592680 @default.
- W2034163119 hasConcept C187882448 @default.
- W2034163119 hasConcept C189165786 @default.
- W2034163119 hasConcept C24530287 @default.
- W2034163119 hasConcept C2775895372 @default.
- W2034163119 hasConcept C2776165026 @default.
- W2034163119 hasConcept C2779335624 @default.
- W2034163119 hasConcept C515207424 @default.
- W2034163119 hasConcept C55493867 @default.
- W2034163119 hasConcept C85528070 @default.
- W2034163119 hasConcept C86803240 @default.
- W2034163119 hasConceptScore W2034163119C104317684 @default.
- W2034163119 hasConceptScore W2034163119C10858879 @default.
- W2034163119 hasConceptScore W2034163119C118892022 @default.
- W2034163119 hasConceptScore W2034163119C153911025 @default.
- W2034163119 hasConceptScore W2034163119C167625842 @default.
- W2034163119 hasConceptScore W2034163119C170493617 @default.
- W2034163119 hasConceptScore W2034163119C185592680 @default.
- W2034163119 hasConceptScore W2034163119C187882448 @default.
- W2034163119 hasConceptScore W2034163119C189165786 @default.
- W2034163119 hasConceptScore W2034163119C24530287 @default.
- W2034163119 hasConceptScore W2034163119C2775895372 @default.
- W2034163119 hasConceptScore W2034163119C2776165026 @default.
- W2034163119 hasConceptScore W2034163119C2779335624 @default.
- W2034163119 hasConceptScore W2034163119C515207424 @default.
- W2034163119 hasConceptScore W2034163119C55493867 @default.
- W2034163119 hasConceptScore W2034163119C85528070 @default.
- W2034163119 hasConceptScore W2034163119C86803240 @default.
- W2034163119 hasIssue "7" @default.
- W2034163119 hasLocation W20341631191 @default.
- W2034163119 hasLocation W20341631192 @default.
- W2034163119 hasLocation W20341631193 @default.
- W2034163119 hasLocation W20341631194 @default.
- W2034163119 hasOpenAccess W2034163119 @default.
- W2034163119 hasPrimaryLocation W20341631191 @default.
- W2034163119 hasRelatedWork W1972574335 @default.
- W2034163119 hasRelatedWork W1998618531 @default.
- W2034163119 hasRelatedWork W2003782406 @default.