ライフサイエンスコーパス: phenylglyoxal

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1 espectively, may explain their resistance to phenylglyoxal.

2 100, and sensitivity to N-ethylmaleimide and phenylglyoxal.

3 ese altered enzymes were also insensitive to phenylglyoxal.

4 nophenyl)pyrimidin-2-amine (3) and 4-methoxy-phenylglyoxal (4), while eudistidine B (2) was synthesiz

5 Modification with [14C]phenylglyoxal allowed the identification of two nitrite

6 The arginine-specific reagents phenylglyoxal and butane-2,3-dione irreversibly inactiva

7 onding location (Arg187), was susceptible to phenylglyoxal and butane-2,3-dione.

8 ondrial GPAT with arginine-modifying agents, phenylglyoxal and cyclohexanedione, inactivated the enzy

9 odification of arginines and histidines with phenylglyoxal and diethyl pyrocarbonate, respectively, r

10 hly purified enzyme to N-ethylmaleimide, F-, phenylglyoxal, and diethylpyrocarbonate, both substrates

11 M; and 4) was sensitive to N-ethylmaleimide, phenylglyoxal, and diethylpyrocarbonate.

12 ATP and CTP), N-ethylmaleimide, propranolol, phenylglyoxal, and divalent cations (Ca(2+), Mn(2+), and

13 date, sodium fluoride, N-ethylmaleimide, and phenylglyoxal but was not significantly affected by lipi

14 ics in presence of alpha,beta-diones such as phenylglyoxal, cyclohaxanedione, and 2,3-butadione sugge

15 inactivation of the tritrichomonal enzyme by phenylglyoxal follows time-dependent and concentration-d

16 After incubation with 2 mM phenylglyoxal for 1 h, the modified enzyme had a 10-fold

17 astinal, iodoacetamide, iodoacetic acid, and phenylglyoxal gave substantial inhibition, and methyl bo

18 ted alpha-ketoesters and cyclic ketones with phenylglyoxal hydrates were realized with cinchona alkal

19 om the cyanobacterium Anabaena PCC 7120 with phenylglyoxal in 50 mM Hepes, pH 8.0, at 25 degrees C re

20 Phenylglyoxal inactivates the R336Q variant at over half

21 Phenylglyoxal inhibition and substrate protection experi

22 Phenylglyoxal is an arginine-specific reagent that inact

23 This may explain why phenylglyoxal labeling of Arg155 inactivates the enzyme

24 ctrometry (MS/MS) was used to identify three phenylglyoxal-modified Arg residues in monomeric rabbit

25 ospray ionizaton Fourier-transform MS of the phenylglyoxal-modified CK that had lost approximately 80

26 Digestion of [7-(14)C]phenylglyoxal-modified enzyme with trypsin and separatio

27 synthetase by the arginine-specific reagents phenylglyoxal or p-hydroxyphenylglyoxal inactivates the

28 to 2,4,6-trinitrobenzenesulfonate (TNBS) and phenylglyoxal (PG).

29 e pyrophosphorylase with the arginyl reagent phenylglyoxal resulted in complete desensitization to fr

30 itrulline-specific chemical probe, rhodamine-phenylglyoxal (Rh-PG), which we show can be used to inve

31 esC, and less susceptible to inactivation by phenylglyoxal, than RN.

32 rg155 as the target site of two molecules of phenylglyoxal that is protected by the substrates.

33 Phenylglyoxal treatment of the protein indicates that ar

34 inine-specific modifiers 2,3-butanedione and phenylglyoxal were found to be inactivators, and inactiv

35 e sulfite oxidase was rapidly inactivated by phenylglyoxal, yielding a modified protein with kinetic

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