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Ultrahigh resolution drug design I: Details of interactions in human aldose reductase–inhibitor complex at 0.66 Å
Author(s) -
Howard E.I.,
Sanishvili R.,
Cachau R.E.,
Mitschler A.,
Chevrier B.,
Barth P.,
Lamour V.,
Van Zandt M.,
Sibley E.,
Bon C.,
Moras D.,
Schneider T.R.,
Joachimiak A.,
Podjarny A.
Publication year - 2004
Publication title -
proteins: structure, function, and bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.699
H-Index - 191
eISSN - 1097-0134
pISSN - 0887-3585
DOI - 10.1002/prot.20015
Subject(s) - aldose reductase inhibitor , chemistry , aldose reductase , hydrogen bond , protonation , drug design , stereochemistry , active site , cofactor , crystallography , rational design , resolution (logic) , computational chemistry , catalysis , enzyme , ion , molecule , materials science , nanotechnology , biochemistry , organic chemistry , artificial intelligence , computer science
The first subatomic resolution structure of a 36 kDa protein [aldose reductase (AR)] is presented. AR was cocrystallized at pH 5.0 with its cofactor NADP + and inhibitor IDD 594, a therapeutic candidate for the treatment of diabetic complications. X‐ray diffraction data were collected up to 0.62 Å resolution and treated up to 0.66 Å resolution. Anisotropic refinement followed by a blocked matrix inversion produced low standard deviations (<0.005 Å). The model was very well ordered overall (CA atoms' mean B factor is 5.5 Å 2 ). The model and the electron‐density maps revealed fine features, such as H‐atoms, bond densities, and significant deviations from standard stereochemistry. Other features, such as networks of hydrogen bonds (H bonds), a large number of multiple conformations, and solvent structure were also better defined. Most of the atoms in the active site region were extremely well ordered (mean B ∼3 Å 2 ), leading to the identification of the protonation states of the residues involved in catalysis. The electrostatic interactions of the inhibitor's charged carboxylate head with the catalytic residues and the charged coenzyme NADP + explained the inhibitor's noncompetitive character. Furthermore, a short contact involving the IDD 594 bromine atom explained the selectivity profile of the inhibitor, important feature to avoid toxic effects. The presented structure and the details revealed are instrumental for better understanding of the inhibition mechanism of AR by IDD 594, and hence, for the rational drug design of future inhibitors. This work demonstrates the capabilities of subatomic resolution experiments and stimulates further developments of methods allowing the use of the full potential of these experiments. Proteins 2004. © 2004 Wiley‐Liss, Inc.