IsoStar: A library of information about nonbonded interactions

被引:273
作者
Bruno, IJ [1 ]
Cole, JC [1 ]
Lommerse, JPM [1 ]
Rowland, RS [1 ]
Taylor, R [1 ]
Verdonk, ML [1 ]
机构
[1] Cambridge Crystallog Data Ctr, Cambridge CB2 1EZ, England
关键词
nonbonded interactions; Cambridge Structural Database; Brookhaven Protein Databank; intermolecular perturbation theory;
D O I
10.1023/A:1007934413448
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Crystallographic and theoretical tab initio) data on intermolecular nonbonded interactions have been gathered together in a computerised library ('IsoStar'). The library contains information about the nonbonded contacts formed by some 250 chemical groupings. The data can be displayed visually-and used to aid protein-ligand docking or the identification of bioisosteric 'replacements. Data from the library show that there is great variability in the geometrical preferences of different types of hydrogen bonds, although in general there is a tendency for H-bonds to form along lone-pair directions. The H-bond acceptor abilities of oxygen and sulphur atoms are highly dependent on intramolecular environments. The nonbonded contacts formed by many hydrophobic groups show surprisingly strong directional preferences. Many unusual nonbonded interactions are to be found in the library-and are of potential value for designing novel biologically active molecules.
引用
收藏
页码:525 / 537
页数:13
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