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1 the G359F (small subunit) mutant protein of carbamoyl phosphate synthetase.
2 is similar to the folding of this domain in carbamoyl phosphate synthetase.
3 ransferase type I domain of Escherichia coli carbamoyl phosphate synthetase.
4 r the tunneling of ammonia within the native carbamoyl phosphate synthetase.
5 specifying the small subunit of Arg-specific carbamoyl phosphate synthetase.
6 codes the small subunit of arginine-specific carbamoyl phosphate synthetase.
8 the mitochondrial matrix and interacts with carbamoyl phosphate synthetase 1 (CPS1), an enzyme, cata
10 ylates and activates a mitochondrial enzyme, carbamoyl phosphate synthetase 1, which mediates the fir
13 proteins 70 and 90 (HSP-70; HSP-90), and the carbamoyl phosphate synthetase 2/aspartate transcarbamyl
15 which directly phosphorylates S1859 on CAD (carbamoyl-phosphate synthetase 2, aspartate transcarbamo
16 hatidylinositol 4-kinases (PI4KA and PI4KB), carbamoyl-phosphate synthetase 2, aspartate transcarbamy
19 he inhibitor UTP and the activator PRPP, the carbamoyl phosphate synthetase activity is controlled by
21 uted to altered allosteric regulation of the carbamoyl-phosphate synthetase activity of CAD (carbamoy
22 , cytidine 5'-triphosphate (CTP) synthetase, carbamoyl phosphate synthetase, and phosphoribosyl pyrop
23 bamoyl-phosphate synthetase activity of CAD (carbamoyl-phosphate synthetase-aspartate carbamoyltransf
24 an carbamoyl-phosphate synthetase is part of carbamoyl-phosphate synthetase-aspartate carbamoyltransf
25 d c-myc, dihydrofolate reductase (DHFR), and carbamoyl-phosphate synthetase-aspartate transcarbamoyl-
26 ned a 240 kDa protein that was identified as carbamoyl phosphate synthetase/aspartate transcarbamoyla
27 l phosphate synthetase II (CPSII) is part of carbamoyl phosphate synthetase/aspartate transcarbamoyla
33 imiting step in this pathway is catalysed by carbamoyl phosphate synthetase (CPS II), part of the mul
35 DP and carbamoyl phosphate, Escherichia coli carbamoyl phosphate synthetase (CPS) binds MgADP with a
39 analysis of the allosteric responsiveness of carbamoyl phosphate synthetase (CPS) from E. coli was pe
40 rt of carbamate through the large subunit of carbamoyl phosphate synthetase (CPS) from Escherichia co
52 st three enzymes in pyrimidine biosynthesis, carbamoyl phosphate synthetase (CPS), aspartate transcar
53 individual mutant lines deficient in either carbamoyl phosphate synthetase (CPS), the first enzyme i
57 l phosphate generated in situ by A. aeolicus carbamoyl phosphate synthetase (CPSase) was channeled to
58 a large multifunctional protein that carries carbamoyl phosphate synthetase (CPSase), aspartate trans
59 he kinetics of the coupled reactions between carbamoyl-phosphate synthetase (CPSase) and both asparta
62 hyperthermophile, has neither a full-length carbamoyl-phosphate synthetase (CPSase) resembling the e
70 ribe the X-ray crystallographic structure of carbamoyl phosphate synthetase from E. coli in which His
73 x-ray crystal structure of the heterodimeric carbamoyl phosphate synthetase from Escherichia coli has
75 mensional structures of tryptophan synthase, carbamoyl phosphate synthetase, glutamine phosphoribosyl
78 arginine serum levels on chromosome 2 at the carbamoyl phosphate synthetase I locus, on chromosome 5
80 ferential plasma proteins detected by iTRAQ, carbamoyl-phosphate synthetase I (CPSI, related to urea
81 ine nucleotide synthesis is catalyzed by the carbamoyl phosphate synthetase II (CPSase) domain of CAD
83 the virulence of T. gondii mutants that lack carbamoyl phosphate synthetase II (uracil auxotrophs) to
84 d enzymes ornithine carbamoyltransferase and carbamoyl-phosphate synthetase III (CPSase III) are indu
86 the first enzyme in the urea cycle pathway, carbamoyl-phosphate synthetase III (CPSase III), is too
87 e thioester intermediate of Escherichia coli carbamoyl-phosphate synthetase, indicates that the subst
89 mately 25 A in length, whereas the tunnel in carbamoyl phosphate synthetase is nearly 100 A long.
92 Ser(44) GLN domain and the Escherichia coli carbamoyl-phosphate synthetase large subunit had little
93 urea cycle--in particular, the efficiency of carbamoyl-phosphate synthetase--may contribute to the av
95 n some cases, such as biotin carboxylase and carbamoyl phosphate synthetase, the B-domains move signi
96 skewed distribution of the genotypes for the carbamoyl-phosphate synthetase variants at position 1405
97 trations of amino acids and genotypes of the carbamoyl-phosphate synthetase variants were determined
98 for threonine at position 1405 [T1405N]) in carbamoyl-phosphate synthetase, which controls the rate-
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