Literature DB >> 7876900

Electrostatic complementarity between proteins and ligands. 3. Structural basis.

P L Chau1, P M Dean.   

Abstract

Electrostatic potential complementarity between ligands and their receptor sites is evaluated by the superposition of the electrostatic potential, generated by the receptor, onto the ligand potential over the ligand van der Waals surface. We would like to examine which structural factors generate this pattern of superposition. Example studies suggest that in many ligand-protein pairs, there exist principal formal charges on each molecule, largely responsible for the electrostatic potential complementarity observed. Electrostatic potential complementarity depends on the relative disposition of these principal charges and the ligand van der Waals surface. Simple mathematical models were constructed to predict the complementarity solely from structural considerations. The essential conditions for electrostatic potential complementarity were elucidated. These can be used in ligand design strategies to obtain an electrostatically optimal ligand.

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Year:  1994        PMID: 7876900     DOI: 10.1007/bf00123665

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  9 in total

1.  Crystal structures of Escherichia coli dihydrofolate reductase: the NADP+ holoenzyme and the folate.NADP+ ternary complex. Substrate binding and a model for the transition state.

Authors:  C Bystroff; S J Oatley; J Kraut
Journal:  Biochemistry       Date:  1990-04-03       Impact factor: 3.162

2.  Structure of a complex of catabolite gene activator protein and cyclic AMP refined at 2.5 A resolution.

Authors:  I T Weber; T A Steitz
Journal:  J Mol Biol       Date:  1987-11-20       Impact factor: 5.469

3.  Electrostatic complementarity between proteins and ligands. 2. Ligand moieties.

Authors:  P L Chau; P M Dean
Journal:  J Comput Aided Mol Des       Date:  1994-10       Impact factor: 3.686

4.  Electrostatic complementarity between proteins and ligands. 1. Charge disposition, dielectric and interface effects.

Authors:  P L Chau; P M Dean
Journal:  J Comput Aided Mol Des       Date:  1994-10       Impact factor: 3.686

5.  Structures of product and inhibitor complexes of Streptomyces griseus protease A at 1.8 A resolution. A model for serine protease catalysis.

Authors:  M N James; A R Sielecki; G D Brayer; L T Delbaere; C A Bauer
Journal:  J Mol Biol       Date:  1980-11-25       Impact factor: 5.469

6.  Crystal structures of recombinant human dihydrofolate reductase complexed with folate and 5-deazafolate.

Authors:  J F Davies; T J Delcamp; N J Prendergast; V A Ashford; J H Freisheim; J Kraut
Journal:  Biochemistry       Date:  1990-10-09       Impact factor: 3.162

7.  Crystal structure of p-hydroxybenzoate hydroxylase complexed with its reaction product 3,4-dihydroxybenzoate.

Authors:  H A Schreuder; J M van der Laan; W G Hol; J Drenth
Journal:  J Mol Biol       Date:  1988-02-20       Impact factor: 5.469

8.  Three-dimensional structure of the ribonuclease T1 2'-GMP complex at 1.9-A resolution.

Authors:  R Arni; U Heinemann; R Tokuoka; W Saenger
Journal:  J Biol Chem       Date:  1988-10-25       Impact factor: 5.157

9.  Atomic structure of ferredoxin-NADP+ reductase: prototype for a structurally novel flavoenzyme family.

Authors:  P A Karplus; M J Daniels; J R Herriott
Journal:  Science       Date:  1991-01-04       Impact factor: 47.728

  9 in total
  4 in total

1.  A branch-and-bound method for optimal atom-type assignment in de novo ligand design.

Authors:  N P Todorov; P M Dean
Journal:  J Comput Aided Mol Des       Date:  1998-07       Impact factor: 3.686

2.  The atom assignment problem in automated de novo drug design. 1. Transferability of molecular fragment properties.

Authors:  M T Barakat; P M Dean
Journal:  J Comput Aided Mol Des       Date:  1995-08       Impact factor: 3.686

3.  Electrostatic complementarity between proteins and ligands. 2. Ligand moieties.

Authors:  P L Chau; P M Dean
Journal:  J Comput Aided Mol Des       Date:  1994-10       Impact factor: 3.686

4.  Electrostatic complementarity between proteins and ligands. 1. Charge disposition, dielectric and interface effects.

Authors:  P L Chau; P M Dean
Journal:  J Comput Aided Mol Des       Date:  1994-10       Impact factor: 3.686

  4 in total

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