... Xiaocheng Gu1, Ming Luo1,3and Xiaofeng Zheng1,21 National Laboratory of Protein Engineering and Plant Genetic Engineering, Peking University, Beijing, China2 Department of Biochemistry and ... con-taining 0.4 mL of the respective crystallization solution. Tofully saturate the enzyme binding site, GMP was added in a4 : 1 molar ratio with respect to wild-type and mutantHGPRTs. Single crystals ... to crystallization screening. The crystal structure of one mutant, L160I, was determined at 1.7 A˚resolution.Surprisingly, the active site is occupied by a peptide from the N-terminus of a...