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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/RAWU8I7bEVc1KhCJv2g9Q90fhsnLIEWl5UQOmmZXNnntY#_6 http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel http://purl.org/pav/version 1.4 http://www.tkuhn.ch/bel2nanopub/RAWU8I7bEVc1KhCJv2g9Q90fhsnLIEWl5UQOmmZXNnntY#_5 http://www.w3.org/ns/prov#value PRAS40 was phosphorylated in vitro by purified Akt on the same site that was phosphorylated in insulin-treated cells. (From Results section) -- To determine whether the predicted Akt consensus phosphorylation site (Thr-246) was in fact the site recognized by the anti-pAkt substrate antibody, a mutant form of the HA-tagged PRAS40 (T246A) was expressed in which this site was changed to Ala. 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