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Src42A myri has a point mutation in codon 2, which causes an amino acid substitution from Gly 2 to Asp. Gly 2 is conserved in all members of the Src family and must be myristylated for localization of Src to the cellular membrane in mammals (10 ).
Source: wiktionary
Similarly, FRS2, which is myristylated and has a potential PTB domain, is specifically phosphorylated by receptors for fibroblast growth factor (FGF) and nerve growth factor (NGF) (39 ).
Source: wiktionary
Data sourced from Wiktionary, WordNet, CMU, and other open linguistic databases. Updated March 2026.