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http://www.tkuhn.ch/bel2nanopub/RA9gaJ9_AN5wopIUOLm4AOOiX588-38bpvTK3RvcTqRQQ#_1
http://semanticscience.org/resource/SIO_000139
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http://www.tkuhn.ch/bel2nanopub/RA9gaJ9_AN5wopIUOLm4AOOiX588-38bpvTK3RvcTqRQQ#_1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://amigo.geneontology.org/amigo/term/GO:0016301
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http://purl.obolibrary.org/obo/RO_0002204
http://resource.belframework.org/belframework/20131211/namespace/selventa-protein-families/AKT%20Family
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http://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI_36080
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http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.ebi.ac.uk/ontology-lookup/?termId=MOD:00000
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http://www.w3.org/2000/01/rdf-schema#label
kin(p(SFAM:"AKT Family")) => p(HGNC:CREB1,pmod(P,S))
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Approximately 61,000 statements.
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Copyright (c) 2011-2012, Selventa. All rights reserved.
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BEL Framework Large Corpus Document
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The best characterized of the AGC kinases is phosphoinositide-dependent kinase 1 (PDK1), one of the serine kinases that phosphorylates and activates the serine/threonine kinase Akt/PKB37. Akt possesses a PH domain that also interacts directly with PtdIns(3,4,5)P3, promoting membrane targeting of the protein and catalytic activation. Akt has been suggested to be important in transmission of the insulin signal, by phosphorylation of the enzyme GSK-3 (see below), the forkhead transcription factors and cAMP response element-binding protein
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http://www.ncbi.nlm.nih.gov/pubmed/11742412
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Selventa
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2014-07-03T14:31:45.376+02:00
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