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1 etabolite chorismate into salicylic acid via isochorismate.
2 l to allow formation of a hydrogen bond with isochorismate.
3 njugate addition of alpha-ketoglutarate with isochorismate.
4 cular Arg106 are critical for recognition of isochorismate.
5 om chorismate and water via the intermediate isochorismate.
6 of the inactive D38A variant in complex with isochorismate.
7 e enzymatic hydroxymutation of chorismate to isochorismate.
8 tic data indicate that for the production of isochorismate, a high magnesium ion concentration suppre
9 initiated by the conversion of chorismate to isochorismate, a reaction that is catalyzed by the menaq
11 se two residues are important for binding of isochorismate and for stabilizing the cofactor position.
12 he crystal structure of EntC in complex with isochorismate and Mg(2+)at 2.3 A resolution, the first s
13 s to establish the kinetic mechanisms of the isochorismate and salicylate synthase enzymes of siderop
15 residues in the conversion of chorismate to isochorismate and to obtaining clues about the pyruvate
17 lyzes hydrolysis of the related vinyl ethers isochorismate, chorismate, and 4-amino-4-deoxychorismate
18 orders of magnitude higher affinity for the isochorismate complex relative to the chorismate complex
19 lyzed activities, as well as the uncatalyzed isochorismate decomposition, are reported from temperatu
20 ismate synthase (ICS) converts chorismate to isochorismate for the biosynthesis of phylloquinone, an
21 ically produces salicylate and pyruvate from isochorismate for ultimate incorporation of the salicyla
22 , catalyzing the conversion of chorismate to isochorismate (IC) in a reaction that operates near equi
27 btI at 2.5 A resolution and demonstrate that isochorismate is a kinetically competent intermediate in
28 dicates that the methylene pyruvyl carbon of isochorismate is adjacent to the side chain carboxylate
32 encoded by angB and designated AngB, has an isochorismate lyase activity necessary for the synthesis
34 show that EntB, previously described as the isochorismate lyase required for production of 2,3-DHB,
35 monophosphate ligase, VibB is a bifunctional isochorismate lyase-aryl carrier protein (ArCP), and Vib
36 the enzymes of phylloquinone synthesis from isochorismate may form a complex in the chloroplast stro
37 ntC, MenF and Irp9 all convert chorismate to isochorismate, only Irp9 subsequently exhibits isochoris
39 lant Arabidopsis, it was discovered that the isochorismate pathway is the major source of SA during S
40 -ketoglutarate and with the second substrate isochorismate positioned to accept nucleophilic attack h
41 ochorismate, only Irp9 subsequently exhibits isochorismate pyruvate lyase activity resulting in the f
42 o this class is the enzyme PchB, an 11.4-kDa isochorismate pyruvate lyase from Pseudomonas aeruginosa
43 smate mutase activity similar to that of the isochorismate pyruvate lyase, PchB, from Pseudomonas aer
49 ase (MenF) is distinct from the entC-encoded isochorismate synthase (EntC) involved in enterobactin b
53 induced SA biosynthesis proceeds through the isochorismate synthase (ICS) pathway, with cold inductio
55 ing that SA synthesized via PAL, and not via isochorismate synthase (ICS), mediates lesion developmen
57 ed in chloroplasts from chorismic acid by an isochorismate synthase (ICS1); SA biosynthesis is negati
58 so inhibit two other enzymes in this family, isochorismate synthase (IS) and anthranilate synthase (A
59 hsis and shares a common core mechanism with isochorismate synthase (IS) and anthranilate synthase (A
60 amino-4-deoxychorismate synthase (ADCS), and isochorismate synthase (IS) are homologous enzymes that
61 (AS), aminodeoxychorismate synthase (ADCS), isochorismate synthase (IS), and salicylate synthase (SS
69 he role of magnesium ions, which inhibit the isochorismate synthase enzymes but not the salicylate sy
70 is of SA and Ybt by DC3000 requires pchA, an isochorismate synthase gene in the Ybt genomic cluster,
73 lts led to the demonstration of an alternate isochorismate synthase specifically involved in menaquin
75 35% identical to the Bs menaquinone-specific isochorismate synthase, MenF, illustrating an example of
77 ther chorismate-utilizing enzymes, including isochorismate synthase, suggests that they too may bind
78 ing for wild-type and SA biosynthetic mutant isochorismate synthase1 (ics1) Arabidopsis from 0 to 7 d
82 njugate addition of alpha-ketoglutarate with isochorismate to release 2-succinyl-5-enolpyruvyl-6-hydr
83 tamin K2) is the conversion of chorismate to isochorismate, which is mediated by an isochorismate syn
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