Activating mutations in RAS proto-oncogenes encode proteins with great
er GTP binding. Such mutant proteins are responsible for many human ca
ncers. Six new amino acids were discovered that can yield an activated
Saccharomyces cerevisiae RAS2 protein when they are altered. These ne
w RAS2 alleles were found among a collection of 35 random mutations th
at exhibit a dominant reduction of glycogen accumulation. The RAS2-P41
S and RAS2-E99K alleles encode proteins that have lost responsiveness
to GTPase activating proteins. They affect amino acids in loop 2 and h
elix 3 respectively and illustrate that GTPase activating proteins rec
ognize a larger portion of the RAS structure than previously realized.
RAS2 mutations E130K, S153F, A154T, and A157S alter amino acids proxi
mal to the guanine binding site and probably influence nucleotide bind
ing either directly or indirectly.