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1 se), rluE (pseudouridine synthase), and pta (phosphotransacetylase).
2 orylation or inactivation of the pta-encoded phosphotransacetylase.
3 y without affecting key TCA cycle enzymes or phosphotransacetylase.
4 ress protein, a ferritin-like protein, and a phosphotransacetylase.
5 e in the culture medium, suggesting that the phosphotransacetylase-acetate kinase (Pta-AckA) pathway
6 e broth, these cells excrete acetate via the phosphotransacetylase-acetate kinase (Pta-AckA) pathway.
7    Conversion of pyruvate to acetate via the phosphotransacetylase-acetate kinase pathway generates A
8 ntially, these cells excrete acetate via the phosphotransacetylase-acetate kinase pathway.
9 inated elevated levels of acetate kinase and phosphotransacetylase activities in response to phosphat
10 upstream of the genes (pta and ack) encoding phosphotransacetylase and acetate kinase and is transcri
11  mutants with lesions in the operon encoding phosphotransacetylase and acetate kinase failed to use e
12 es AcP by the conventional pathway involving phosphotransacetylase and acetate kinase, encoded by pta
13                     We propose that the EutD phosphotransacetylase and EutG alcohol dehydrogenase are
14  that it is adjacent to pta, which codes for phosphotransacetylase, and that these two genes are part
15                                              Phosphotransacetylase catalyzes the following reaction:
16                                              Phosphotransacetylase (EC 2.3.1.8) catalyzes reversible
17                                              Phosphotransacetylase (EC 2.3.1.8) catalyzes the reversi
18                                              Phosphotransacetylase (EC 2.3.1.8) catalyzes the reversi
19 in ( approximately 350 residues) of the Pta (phosphotransacetylase) enzyme of Salmonella enterica is
20       A steady-state kinetic analysis of the phosphotransacetylase from Methanosarcina thermophila in
21 logous production in Escherichia coli of the phosphotransacetylase from Methanosarcina thermophila, a
22 f arginine residues was investigated for the phosphotransacetylase from Methanosarcina thermophila.
23                    Two crystal structures of phosphotransacetylase from the methanogenic archaeon Met
24 ant with deletions of the acetate kinase and phosphotransacetylase genes (ackA-pta) was deficient in
25  the LetA/LetS two-component system, but not phosphotransacetylase or acetyl kinase, two enzymes that
26 D-serine is catabolized into acetate via the phosphotransacetylase (pta) and acetate kinase (ackA) ge
27 direct competition, on the one hand, between phosphotransacetylase (PTA) and alpha-ketoglutarate dehy
28 e activities of the propionate kinase (PduW)/phosphotransacetylase (Pta) enzyme system and the CobB s
29 is homologous to the catalytic domain of the phosphotransacetylase (Pta) enzyme.
30 he bacterial enzymes acetate kinase (AK) and phosphotransacetylase (PTA) form a key pathway for synth
31                                            A phosphotransacetylase (pta) mutant of Salmonella enteric
32 at acetyl phosphate, the intermediate of the phosphotransacetylase (Pta)-acetate kinase (AckA) pathwa
33 utilize acetate via acetate kinase (Ack) and phosphotransacetylase (Pta).
34                    Activity of the unaltered phosphotransacetylase was sensitive to N-ethylmaleimide.

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