Statements in which the resource exists.
SubjectPredicateObjectContext
http://www.reactome.org/bio...rdf:typebiopax3:BiochemicalReactionlld:biopax3
http://www.reactome.org/bio...biopax3:commentAuthored: Garapati, P V, 2011-07-11lld:biopax3
http://www.reactome.org/bio...biopax3:commentEdited: Garapati, P V, 2011-07-11lld:biopax3
http://www.reactome.org/bio...biopax3:commentReviewed: Rönnstrand, L, 2011-08-22lld:biopax3
http://www.reactome.org/bio...biopax3:commentTwo human isoforms of KIT have been identified, resulting from alternative splicing. They are characterized by the presence or absence of a tetrapeptide sequence (GNNK 510-513 aa) in the extracellular part of the juxtamembrane region and designated GNNK+ (Kit) or GNNK- (KitA) (Piao et al. 1994). The isoforms are co-expressed in most tisuues, with the GNNK- form predominating (Reith et al. 1991). No difference in ligand affinity was observed (Caruana et al. 1999). <br>KIT belongs to the type III tyrosine kinase receptor family, with five extracellular immunoglobulin (Ig)-like domains, a single transmembrane region, an inhibitory cytoplasmic juxtamembrane domain, and a split cytoplasmic kinase domain separated by a kinase insert segment and a cytoplasmic tail (Mol et al. 2003). <br>Signaling by KIT occurs following SCF binding. SCF homodimers binds to the first three Ig-like domains of KIT in the regions between aa L104-D122 and R146-D153 (Mendiaz et al. 1996, Matous et al. 1996) which leads to dimerization which is further stabilized by Ig-like domains 3-4 (Yuzawa et al., 2007).lld:biopax3
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http://www.reactome.org/bio...biopax3:xrefurn:biopax:UnificationXref:...lld:biopax3
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http://www.reactome.org/bio...biopax3:displayNameInteraction of KIT and sSCFlld:biopax3
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