Literature DB >> 6239374

Conformational variability of NAD+ in the free and bound states: a nicotinamide sandwich in NAD+ crystals.

R Parthasarathy, S M Fridey.   

Abstract

X-ray analysis of the free-acid crystal form of the coenzyme nicotinamide adenine dinucleotide (NAD+) revealed a conformational difference between the free NAD+ molecule and one bound in enzymes or complexed to Li+ ions. The pyrophosphate group showed asymmetry in the phosphate-oxygen bonds of the phosphate-oxygen-phosphate link; this bond at the nicotinamide side of the link is longer than that at the adenosine side by 0.04 angstrom. The crystal structure showed a novel intermolecular stacking of adenine and water molecules on opposite sides of nicotinamide that gives rise to a nicotinamide sandwich.

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Year:  1984        PMID: 6239374     DOI: 10.1126/science.6239374

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  4 in total

1.  A molecular model for the active site of S-adenosyl-L-homocysteine hydrolase.

Authors:  J C Yeh; R T Borchardt; A Vedani
Journal:  J Comput Aided Mol Des       Date:  1991-06       Impact factor: 3.686

2.  Structural and Molecular Dynamics of Mycobacterium tuberculosis Malic Enzyme, a Potential Anti-TB Drug Target.

Authors:  Kalistyn H Burley; Bonnie J Cuthbert; Piyali Basu; Jane Newcombe; Ervin M Irimpan; Robert Quechol; Ilona P Foik; David L Mobley; Dany J V Beste; Celia W Goulding
Journal:  ACS Infect Dis       Date:  2020-12-23       Impact factor: 5.084

3.  Electron Paramagnetic Resonance and Electron Spin Echo Studies of Co2+ Coordination by Nicotinamide Adenine Dinucleotide (NAD+) in Water Solution.

Authors:  Stanisław K Hoffmann; Janina Goslar; Stefan Lijewski
Journal:  Appl Magn Reson       Date:  2013-02-24       Impact factor: 0.831

4.  The NADPH binding site on beef liver catalase.

Authors:  I Fita; M G Rossmann
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

  4 in total

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