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All rights reserved. http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel http://purl.org/dc/elements/1.1/title BEL Framework Large Corpus Document http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel http://purl.org/pav/authoredBy http://www.tkuhn.ch/bel2nanopub/RAGLC0SPKMNoZq8NjZzWIKsxuL8-AyihJuo31Oj7nZ5aQ#_6 http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel http://purl.org/pav/version 1.4 http://www.tkuhn.ch/bel2nanopub/RAGLC0SPKMNoZq8NjZzWIKsxuL8-AyihJuo31Oj7nZ5aQ#_5 http://www.w3.org/ns/prov#value From full text...Phosphorylation of the T286 cyclin D1 residue allows it to be recognized by the nuclear exporter CRM1, which transports it to the cytoplasm where it is rapidly degraded. Glycogen synthase kinase-3 (GSK-3) phosphorylates T286 of cyclin D1, and activation of GSK-3 has been shown to result in cyclin D1 nuclear export and degradation [Diehl et al., [1998]]. Other kinases also phosphorylate cyclin D1 at the T286 position, including p38SAPK2 and ERK2, as reviewed [Alao, [2007]]. 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