Literature DB >> 7664067

Why have mutagenesis studies not located the general base in ras p21.

T Schweins1, R Langen, A Warshel.   

Abstract

Ras p21 plays a major role in the control of cell growth, and oncogenic mutations of this protein have been found in human cancers. Unfortunately, the detailed mode of action of Ras p21 is still unclear, in spite of the great interest in this protein and the availability of its X-ray crystal structure. In particular, mutagenesis studies of different active site residues could not identify the general base for GTP hydrolysis. Here we tackle this question using a computer simulation approach with clear and reliable energy considerations and conclude that the most likely general base is the bound GTP itself. Obviously, the identification of such a general base cannot be easily accomplished by mutagenesis experiments.

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Year:  1994        PMID: 7664067     DOI: 10.1038/nsb0794-476

Source DB:  PubMed          Journal:  Nat Struct Biol        ISSN: 1072-8368


  33 in total

Review 1.  Substrate-assisted catalysis: molecular basis and biological significance.

Authors:  W Dall'Acqua; P Carter
Journal:  Protein Sci       Date:  2000-01       Impact factor: 6.725

Review 2.  Biological phosphoryl-transfer reactions: understanding mechanism and catalysis.

Authors:  Jonathan K Lassila; Jesse G Zalatan; Daniel Herschlag
Journal:  Annu Rev Biochem       Date:  2011       Impact factor: 23.643

3.  The Role of Gln61 in HRas GTP hydrolysis: a quantum mechanics/molecular mechanics study.

Authors:  Fernando Martín-García; Jesús Ignacio Mendieta-Moreno; Eduardo López-Viñas; Paulino Gómez-Puertas; Jesús Mendieta
Journal:  Biophys J       Date:  2012-01-03       Impact factor: 4.033

4.  Influence of key residues on the reaction mechanism of the cAMP-dependent protein kinase.

Authors:  M C Hutter; V Helms
Journal:  Protein Sci       Date:  1999-12       Impact factor: 6.725

5.  The active site histidines of creatine kinase. A critical role of His 61 situated on a flexible loop.

Authors:  M Forstner; A Müller; M Stolz; T Wallimann
Journal:  Protein Sci       Date:  1997-02       Impact factor: 6.725

6.  Active site comparisons highlight structural similarities between myosin and other P-loop proteins.

Authors:  C A Smith; I Rayment
Journal:  Biophys J       Date:  1996-04       Impact factor: 4.033

7.  Phosphoryl transfer by a concerted reaction mechanism in UMP/CMP-kinase.

Authors:  M C Hutter; V Helms
Journal:  Protein Sci       Date:  2000-11       Impact factor: 6.725

8.  Quantitative exploration of the molecular origin of the activation of GTPase.

Authors:  Ram Prasad B; Nikolay V Plotnikov; Jeronimo Lameira; Arieh Warshel
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-26       Impact factor: 11.205

9.  Overview of simulation studies on the enzymatic activity and conformational dynamics of the GTPase Ras.

Authors:  Priyanka Prakash; Alemayehu A Gorfe
Journal:  Mol Simul       Date:  2014-03-19       Impact factor: 2.178

Review 10.  Progress in ab initio QM/MM free-energy simulations of electrostatic energies in proteins: accelerated QM/MM studies of pKa, redox reactions and solvation free energies.

Authors:  Shina C L Kamerlin; Maciej Haranczyk; Arieh Warshel
Journal:  J Phys Chem B       Date:  2009-02-05       Impact factor: 2.991

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