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Results 1 - 10 of 12 > >>
EC Number Protein Variants Commentary Reference
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.237W the mutant shows severely reduced specific activity compared to the wild type enzyme 727023
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2C102A totally devoid of glutamine-dependent activity. Kinetic constants for NH4Cl, ATP, and XMP obtained for the ammonia-dependent activity are similar to that of the wild-type enzyme 714242
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2C95A mutant defective in glutamine hydrolysis. The phenotype of ectopic coexpression of USP7 witheither S242L or C95A is similar to that resulting from the coexpression of WT GMPS. Ectopic overexpression of only mutation S242L, mutation C95A, or USP7 mutation C250A has no effect on eye development 705708
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2E383A 8fold decrease in glutaminase activity 744157
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2G388D reduces the activity of GMP synthase Gua1 in budding yeast and the total G-nucleotide pool, leading to precipitous reductions in the GDP/GTP ratio and ATP level in vivo. G388D strongly reduces the rate of growth, impairs general protein synthesis, and derepresses translation of GCN4 mRNA, encoding a transcriptional activator of diverse amino acid biosynthetic enzymes. Although processing of pre-tRNAi Met and other tRNA precursors, and the aminoacylation of tRNAi Met are also strongly impaired in G388D cells, tRNAi Met-containing complexes with the macromolecular composition of the eIF2tRNAi Met.GTP complex and the multifactor complex required for translation initiation accumulate 10-fold in G388D cells and, to a lesser extent, in wild-type cells treated with 6-azauracil 715121
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2GP-1 psicofuranine, decoyinine and adenosine strongly inhibit wild type enzyme. Mutant enzyme GP-1 shows decreased inhibition with adenosine and psicofuranine, but inhibition by decoyinine does not vary, complete loss of inhibition in mutant MG-1 1379
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2H186A 30-50 fold decrease in Km value for glutamine 744157
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2H186A/E383A mutant exhibits poor solubility and basal glutaminase activity 744157
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2H186E/E383H interchange of the amino acids of the salt bridge, significant decrease in catalytic activity 744157
Show all pathways known for 6.3.5.2Display the word mapDisplay the reaction diagram Show all sequences 6.3.5.2more construction of disruption mutants, the heterozygote GUA1/gua1 strain is hypersensitive to 6-azauracil, a known inhibitor of the IMP dehydrogenase involved in GMP biosynthesis. In a murine model of systemic candidiasis, the virulence of the heterozygous strain is marginally attenuated, while the homozygous mutant gua1/gua1 strain is completely avirulent -, 703766
Results 1 - 10 of 12 > >>