IsoStar: A library of information about nonbonded interactions
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Robin Taylor | Jason C. Cole | Marcel L. Verdonk | Ian J. Bruno | Jos P. M. Lommerse | R. Scott Rowland | I. Bruno | Robin Taylor | M. Verdonk | J. Cole | R. Rowland | J. Lommerse
[1] J. Thornton,et al. Amino/aromatic interactions in proteins: is the evidence stacked against hydrogen bonding? , 1994, Journal of molecular biology.
[2] John K. Ousterhout,et al. Tcl and the Tk Toolkit , 1994 .
[3] J. Dunitz,et al. Directional preferences of nonbonded atomic contacts with divalent sulfur. 1. Electrophiles and nucleophiles , 1977 .
[4] Frank H. Allen,et al. The Nature and Geometry of Intermolecular Interactions between Halogens and Oxygen or Nitrogen , 1996 .
[5] G. A. Jeffrey,et al. A survey of O-H⋯O hydrogen bond geometries determined by neutron diffraction , 1981 .
[6] Philip M. Dean,et al. Three-dimensional hydrogen-bond geometry and probability information from a crystal survey , 1996, J. Comput. Aided Mol. Des..
[7] Peter Murray-Rust,et al. Iodine⋯X(O, N, S) intermolecular contacts: models of thyroid hormoneprotein binding interactions using information from the cambridge crystallographic data files , 1984 .
[8] Marina Tintelnot,et al. Geometries of functional group interactions in enzyme-ligand complexes: Guides for receptor modelling , 1989, J. Comput. Aided Mol. Des..
[9] Peter Murray-Rust,et al. Computer retrieval and analysis of molecular geometry. 4. Intermolecular interactions , 1979 .
[10] A. Bondi. van der Waals Volumes and Radii , 1964 .
[11] R. Cramer,et al. Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins. , 1988, Journal of the American Chemical Society.
[12] D. M. F. Aalten,et al. PRODRG, a program for generating molecular topologies and unique molecular descriptors from coordinates of small molecules , 1996, J. Comput. Aided Mol. Des..
[13] Olga Kennard,et al. Geometry of the imino-carbonyl (N-H...O:C) hydrogen bond. 1. Lone-pair directionality , 1983 .
[14] Anthony J. Stone,et al. Distributed multipole analysis, or how to describe a molecular charge distribution , 1981 .
[15] J. Lommerse,et al. Characterising non-covalent interactions with the Cambridge Structural Database. , 1997, Journal of enzyme inhibition.
[16] J. Singh,et al. The geometries of interacting arginine‐carboxyls in proteins , 1987, FEBS letters.
[17] Gerhard Klebe,et al. A fast and efficient method to generate biologically relevant conformations , 1994, J. Comput. Aided Mol. Des..
[18] G J Williams,et al. The Protein Data Bank: a computer-based archival file for macromolecular structures. , 1977, Journal of molecular biology.
[19] Owen Johnson,et al. The development of versions 3 and 4 of the Cambridge Structural Database System , 1991, J. Chem. Inf. Comput. Sci..
[20] J. Glusker. Structural aspects of metal liganding to functional groups in proteins. , 1991, Advances in protein chemistry.
[21] A. Gavezzotti,et al. Statistical analysis of some structural properties of solid hydrocarbons , 1989 .
[22] B Pullman,et al. ELECTRON-DONOR AND -ACCEPTOR PROPERTIES OF BIOLOGICALLY IMPORTANT PURINES, PYRIMIDINES, PTERIDINES, FLAVINS, AND AROMATIC AMINO ACIDS. , 1958, Proceedings of the National Academy of Sciences of the United States of America.
[23] S. Price,et al. On the electrostatic directionality of NH…OC hydrogen bonding , 1989 .
[24] Anthony J. Stone,et al. An intermolecular perturbation theory for the region of moderate overlap , 1984 .
[25] G. A. Jeffrey,et al. Cooperative aspects of hydrogen bonding in carbohydrates , 1978 .
[26] Gautam R. Desiraju,et al. Crystal engineering : the design of organic solids , 1989 .
[27] J. Thornton,et al. Atlas of protein side-chain interactions , 1992 .
[28] Robin Taylor,et al. Hydrogen bonding of carbonyl, ether, and ester oxygen atoms with alkanol hydroxyl groups , 1997 .
[29] Jack D. Dunitz,et al. Geometrical reaction coordinates. II. Nucleophilic addition to a carbonyl group , 1973 .
[30] G. Klebe. The use of composite crystal-field environments in molecular recognition and the de novo design of protein ligands. , 1994, Journal of molecular biology.
[31] P Willett,et al. Development and validation of a genetic algorithm for flexible docking. , 1997, Journal of molecular biology.
[32] Peter Murray-Rust,et al. Directional hydrogen bonding to sp2- and sp3-hybridized oxygen atoms and its relevance to ligand-macromolecule interactions , 1984 .
[33] Peter Murray-Rust,et al. Mapping the atomic environment of functional groups: turning 3D scatter plots into pseudo-density contours , 1984 .
[34] Anthony J. Stone,et al. Computation of charge-transfer energies by perturbation theory , 1993 .
[35] Olga Kennard,et al. Crystallographic evidence for the existence of CH.cntdot..cntdot..cntdot.O, CH.cntdot..cntdot..cntdot.N and CH.cntdot..cntdot..cntdot.Cl hydrogen bonds , 1982 .
[36] G. M. Smith,et al. Electronic distributions within protein phenylalanine aromatic rings are reflected by the three-dimensional oxygen atom environments. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[37] F. Temple Burling,et al. Computational studies of nonbonded sulfur-oxygen and selenium-oxygen interactions in the thiazole and selenazole nucleosides , 1992 .
[38] B. Katz,et al. Binding to protein targets of peptidic leads discovered by phage display: crystal structures of streptavidin-bound linear and cyclic peptide ligands containing the HPQ sequence. , 1995, Biochemistry.
[39] Margaret C. Etter,et al. Encoding and decoding hydrogen-bond patterns of organic compounds , 1990 .
[40] Jan Kroon,et al. O-H · O Hydrogen bonds in molecular crystals a statistical and quantum-chemical analysis , 1975 .
[41] Sarah L. Price,et al. Role of electrostatic interactions in determining the crystal structures of polar organic molecules. A distributed multipole study , 1996 .
[42] Olga Kennard,et al. Hydrogen-bond geometry in organic crystals , 1984 .
[43] Gerhard Klebe,et al. What Can We Learn from Molecular Recognition in Protein–Ligand Complexes for the Design of New Drugs? , 1996 .
[44] Gautam R. Desiraju,et al. The role of Cl.cntdot..cntdot..cntdot.Cl and C-H.cntdot..cntdot..cntdot.O interactions in the crystal engineering of 4-.ANG. short-axis structures , 1986 .
[45] Gerhard Klebe,et al. Oxygen and Nitrogen in Competitive Situations: Which is the Hydrogen‐Bond Acceptor? , 1996 .
[46] Frank H. Allen,et al. Resonance-induced hydrogen bonding at sulfur acceptors in R1R2C=S and R1CS2- systems , 1997 .
[47] Kaddour Lamara,et al. 3H-Azepines and related systems. Part 5. Photo-induced ring expansions of o-Azidobenzonitriles to 3-Cyano- and 7-Cyano-3H- azepin-2(1H)-ones , 1994 .
[48] D. A. Dougherty,et al. Cation-π Interactions in Chemistry and Biology: A New View of Benzene, Phe, Tyr, and Trp , 1996, Science.
[49] Robin Taylor,et al. Use of crystallographic data in searching for isosteric replacements: Composite crystal-field environments of nitro and carbonyl groups† , 1990 .
[50] J. Goodfellow,et al. Solvent interactions with pi ring systems in proteins. , 1995, Protein engineering.