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Random pathway mechanism involving parallel one- and two- substrate branches for glyoxalase I from yeast.

作者信息

Mannervik B, Bartfai T, Górna-Hall B

出版信息

J Biol Chem. 1974 Feb 10;249(3):901-3.

PMID:4590692
Abstract
摘要

相似文献

1
Random pathway mechanism involving parallel one- and two- substrate branches for glyoxalase I from yeast.酵母乙二醛酶I涉及平行单底物和双底物分支的随机途径机制。
J Biol Chem. 1974 Feb 10;249(3):901-3.
2
Discrimination between steady-state kinetic models of the Mechanism of action of yeast glyoxalase I.酵母乙二醛酶I作用机制的稳态动力学模型之间的区分。
Biochemistry. 1973 Jan 30;12(3):387-91. doi: 10.1021/bi00727a004.
3
The steady-state kinetics of glyoxalase I from porcine erythrocytes. Evidence for a random-pathway mechanism involving one- and two-substrate branches.猪红细胞乙二醛酶I的稳态动力学。关于涉及单底物和双底物分支的随机途径机制的证据。
Eur J Biochem. 1973 Aug 17;37(2):270-81. doi: 10.1111/j.1432-1033.1973.tb02985.x.
4
Deuterium isotope effects and chemically modified coenzymes as mechanism probes of yeast glyoxalase-I.氘同位素效应与化学修饰辅酶作为酵母乙二醛酶-I的机制探针
Biochemistry. 1973 Dec 4;12(25):5161-7. doi: 10.1021/bi00749a022.
5
Nonstereospecific substrate usage by glyoxalase I.乙二醛酶I的非立体特异性底物利用
Biochemistry. 1983 Jun 7;22(12):2945-51. doi: 10.1021/bi00281a025.
6
Effects of pH and thiols on the kinetics of yeast glyoxalase I. An evaluation of the random pathway mechanism.pH值和硫醇对酵母乙二醛酶I动力学的影响。随机途径机制的评估。
Biochemistry. 1975 Aug 12;14(16):3669-75. doi: 10.1021/bi00687a024.
7
The stereochemical configuration of the lactoyl group of S-lactoylglutathionine formed by the action of glyoxalase I from porcine erythrocytes and yeast.由猪红细胞和酵母中的乙二醛酶I作用形成的S-乳酰谷胱甘肽的乳酰基团的立体化学构型。
Biochim Biophys Acta. 1973 Feb 28;297(2):297-9. doi: 10.1016/0304-4165(73)90076-7.
8
Inactivation of glyoxalase I from porcine erythrocytes and yeast by amino-group reagents.氨基试剂对猪红细胞和酵母中乙二醛酶I的失活作用。
Eur J Biochem. 1975 May 6;53(2):327-33. doi: 10.1111/j.1432-1033.1975.tb04072.x.
9
Deuterium isotope effects on the product partitioning of fluoromethylglyoxal by glyoxalase I. Proof of a proton transfer mechanism.氘同位素对乙二醛酶I催化氟代甲基乙二醛产物分配的影响。质子转移机制的证据。
J Biol Chem. 1981 Oct 10;256(19):9785-8.
10
Hydrophobic binding is not an independent stereochemical determinant in the yeast glyoxalase I reaction.
Biophys Chem. 1980 Apr;11(2):265-9. doi: 10.1016/0301-4622(80)80029-9.

引用本文的文献

1
Nonredox nickel enzymes.非氧化还原镍酶
Chem Rev. 2014 Apr 23;114(8):4206-28. doi: 10.1021/cr4004488. Epub 2013 Dec 26.
2
Probing the active site of glyoxalase I from human erythrocytes by use of the strong reversible inhibitor S-p-bromobenzylglutathione and metal substitutions.利用强可逆抑制剂S-对溴苄基谷胱甘肽和金属置换探究人红细胞乙二醛酶I的活性位点。
Biochem J. 1981 Jul 1;197(1):67-75. doi: 10.1042/bj1970067.
3
Patterns of apparent co-operativity in a simple random non-equilibrium enzyme--substrate--modifier mechanism. Comparison with equilibrium allosteric models.
简单随机非平衡酶-底物-调节剂机制中的表观协同模式。与平衡别构模型的比较。
Biochem J. 1979 Feb 1;177(2):631-9. doi: 10.1042/bj1770631.
4
Comparison of glyoxalase I purified from yeast (Saccharomyces cerevisiae) with the enzyme from mammalian sources.从酵母(酿酒酵母)中纯化得到的乙二醛酶I与来自哺乳动物源的该酶的比较。
Biochem J. 1979 Oct 1;183(1):23-30. doi: 10.1042/bj1830023.
5
A steady-state-kinetic model for formaldehyde dehydrogenase from human liver. A mechanism involving NAD+ and the hemimercaptal adduct of glutathione and formaldehyde as substrates and free glutathione as an allosteric activator of the enzyme.人肝脏甲醛脱氢酶的稳态动力学模型。一种机制,涉及以NAD⁺、谷胱甘肽与甲醛的半硫醇加合物作为底物,以及游离谷胱甘肽作为该酶的变构激活剂。
Biochem J. 1979 Mar 1;177(3):869-78. doi: 10.1042/bj1770869.