Literature DB >> 1346570

Nature of the intermediate in the 3-oxo-delta 5-steroid isomerase reaction.

B F Zeng1, P L Bounds, R F Steiner, R M Pollack.   

Abstract

The role of Tyr-14 of 3-oxo-delta 5-steroid isomerase (KSI) was probed by analysis of the spectra of 3-amino-1,3,5(10)-estratrien-17 beta-ol (4) and equilenin (5) bound to the active site of KSI. The ultraviolet spectrum of 4 bound to KSI is identical to that for 4 in neutral solution. This observation indicates that Tyr-14 does not protonate the amine group of 4 at the active site. By analogy, it is argued that the 3-oxo group of steroid substrates for KSI is not protonated during the reaction. In contrast, the fluorescence excitation spectra of 5 bound to KSI show characteristics of an ionized phenol, even at pH values as low as 3.8. It is concluded that the pKa of equilenin is perturbed from its value in solution of 9 to less than or equal to 3.5 at the active site of KSI. Similarly, the pKa of the intermediate dienol in the KSI reaction should be lowered to less than or equal to 4.5 when it is bound to KSI. Thus, the function of Tyr-14 as an electrophilic catalyst is likely the stabilization of the anion of the dienol by hydrogen bonding rather than by proton transfer.

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Year:  1992        PMID: 1346570     DOI: 10.1021/bi00120a032

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  10 in total

1.  Evaluation of the energetics of the concerted acid-base mechanism in enzymatic catalysis: the case of ketosteroid isomerase.

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Journal:  J Phys Chem B       Date:  2011-12-28       Impact factor: 2.991

2.  On roads not taken in the evolution of protein catalysts: antibody steroid isomerases that use an enamine mechanism.

Authors:  C H Lin; T Z Hoffman; P Wirsching; C F Barbas; K D Janda; R A Lerner
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

3.  Thermodynamic framework for identifying free energy inventories of enzyme catalytic cycles.

Authors:  Stephen D Fried; Steven G Boxer
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-09       Impact factor: 11.205

4.  Ketosteroid isomerase provides further support for the idea that enzymes work by electrostatic preorganization.

Authors:  Shina C L Kamerlin; Pankaz K Sharma; Zhen T Chu; Arieh Warshel
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-11       Impact factor: 11.205

5.  The isomerization of Δ5-androstene-3,17-dione by the human glutathione transferase A3-3 proceeds via a conjugated heteroannular diene intermediate.

Authors:  Jonathan L Daka; Ikechukwu Achilonu; Heini W Dirr
Journal:  J Biol Chem       Date:  2014-09-23       Impact factor: 5.157

6.  NMR evidence for the participation of a low-barrier hydrogen bond in the mechanism of delta 5-3-ketosteroid isomerase.

Authors:  Q Zhao; C Abeygunawardana; P Talalay; A S Mildvan
Journal:  Proc Natl Acad Sci U S A       Date:  1996-08-06       Impact factor: 11.205

7.  Water in the active site of ketosteroid isomerase.

Authors:  Philip Hanoian; Sharon Hammes-Schiffer
Journal:  Biochemistry       Date:  2011-07-13       Impact factor: 3.162

Review 8.  Electric Fields and Enzyme Catalysis.

Authors:  Stephen D Fried; Steven G Boxer
Journal:  Annu Rev Biochem       Date:  2017-03-24       Impact factor: 23.643

Review 9.  Oriented internal electrostatic fields: an emerging design element in coordination chemistry and catalysis.

Authors:  Alexander B Weberg; Ryan P Murphy; Neil C Tomson
Journal:  Chem Sci       Date:  2022-04-20       Impact factor: 9.969

10.  Testing electrostatic complementarity in enzyme catalysis: hydrogen bonding in the ketosteroid isomerase oxyanion hole.

Authors:  Daniel A Kraut; Paul A Sigala; Brandon Pybus; Corey W Liu; Dagmar Ringe; Gregory A Petsko; Daniel Herschlag
Journal:  PLoS Biol       Date:  2006-03-28       Impact factor: 8.029

  10 in total

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