Literature DB >> 15895975

Why enzymes are proficient catalysts: beyond the Pauling paradigm.

Xiyun Zhang1, K N Houk.   

Abstract

Pauling proposed that "enzymes are molecules that are complementary in structure to the activated complexes of the reactions that they catalyze, ..., [rather than] entering into reactions". This paradigm has dominated thinking in the field. While complementarity of the type proposed by Pauling can account for acceleration up to 11 orders of magnitude, most enzymes exceed that proficiency. Enzymes with proficiencies ((k(cat)/K(M))/k(uncat)) > 10(11) M(-1) achieve over 15 kcal/mol of "transition state binding" not merely by a concatenation of noncovalent effects but by covalent bond formation between enzyme or cofactor and transition state, involving a change in mechanism from that in aqueous solution. Enzymes enter into reactions with substrates and do not merely complement the transition states of the uncatalyzed reactions.

Mesh:

Substances:

Year:  2005        PMID: 15895975     DOI: 10.1021/ar040257s

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  48 in total

1.  Evaluation and ranking of enzyme designs.

Authors:  Gert Kiss; Daniela Röthlisberger; David Baker; K N Houk
Journal:  Protein Sci       Date:  2010-09       Impact factor: 6.725

Review 2.  Mechanisms and free energies of enzymatic reactions.

Authors:  Jiali Gao; Shuhua Ma; Dan T Major; Kwangho Nam; Jingzhi Pu; Donald G Truhlar
Journal:  Chem Rev       Date:  2006-08       Impact factor: 60.622

Review 3.  Multidimensional tunneling, recrossing, and the transmission coefficient for enzymatic reactions.

Authors:  Jingzhi Pu; Jiali Gao; Donald G Truhlar
Journal:  Chem Rev       Date:  2006-08       Impact factor: 60.622

4.  Why urea eliminates ammonia rather than hydrolyzes in aqueous solution.

Authors:  Anastassia N Alexandrova; William L Jorgensen
Journal:  J Phys Chem B       Date:  2007-02-01       Impact factor: 2.991

5.  A kinetic analysis of DNA ejection from tailed phages revealing the prerequisite activation energy.

Authors:  Eric Raspaud; Thomas Forth; Carlos São-José; Paulo Tavares; Marta de Frutos
Journal:  Biophys J       Date:  2007-08-03       Impact factor: 4.033

6.  EMBM - a new enzyme mechanism-based method for rational design of chemical sites of covalent inhibitors.

Authors:  Tamar Traube; Subramaniam Vijayakumar; Michal Hirsch; Neta Uritsky; Michael Shokhen; Amnon Albeck
Journal:  J Chem Inf Model       Date:  2010-11-19       Impact factor: 4.956

7.  Cooperativity in the self-assembly of porphyrin ladders.

Authors:  Amaya Camara-Campos; Christopher A Hunter; Salvador Tomas
Journal:  Proc Natl Acad Sci U S A       Date:  2006-02-21       Impact factor: 11.205

8.  How similar are enzyme active site geometries derived from quantum mechanical theozymes to crystal structures of enzyme-inhibitor complexes? Implications for enzyme design.

Authors:  Jason Dechancie; Fernando R Clemente; Adam J T Smith; Hakan Gunaydin; Yi-Lei Zhao; Xiyun Zhang; K N Houk
Journal:  Protein Sci       Date:  2007-09       Impact factor: 6.725

9.  Geometric curvature controls the chemical patchiness and self-assembly of nanoparticles.

Authors:  David A Walker; Emily K Leitsch; Rikkert J Nap; Igal Szleifer; Bartosz A Grzybowski
Journal:  Nat Nanotechnol       Date:  2013-08-18       Impact factor: 39.213

Review 10.  Free energies of chemical reactions in solution and in enzymes with ab initio quantum mechanics/molecular mechanics methods.

Authors:  Hao Hu; Weitao Yang
Journal:  Annu Rev Phys Chem       Date:  2008       Impact factor: 12.703

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.