Literature DB >> 10651278

Locating interaction sites on proteins: the crystal structure of thermolysin soaked in 2% to 100% isopropanol.

A C English1, S H Done, L S Caves, C R Groom, R E Hubbard.   

Abstract

Multiple-solvent crystal structure determination (MSCS) allows the position and orientation of bound solvent fragments to be identified by determining the structure of protein crystals soaked in organic solvents. We have extended this technique by the determination of high-resolution crystal structures of thermolysin (TLN), generated from crystals soaked in 2% to 100% isopropanol. The procedure causes only minor changes to the conformation of the protein, and an increasing number of isopropanol interaction sites could be identified as the solvent concentration is increased. Isopropanol occupies all four of the main subsites in the active site, although this was only observed at very high concentrations of isopropanol for three of the four subsites. Analysis of the isopropanol positions shows little correlation with interaction energy computed using a molecular mechanics force field, but the experimentally determined positions of isopropanol are consistent with the structures of known protein-ligand complexes of TLN.

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Year:  1999        PMID: 10651278

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  39 in total

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5.  Relationship between hot spot residues and ligand binding hot spots in protein-protein interfaces.

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Review 7.  The multi-copy simultaneous search methodology: a fundamental tool for structure-based drug design.

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8.  Fragment-based identification of druggable 'hot spots' of proteins using Fourier domain correlation techniques.

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9.  Improving protocols for protein mapping through proper comparison to crystallography data.

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10.  Analysis of substructural variation in families of enzymatic proteins with applications to protein function prediction.

Authors:  Drew H Bryant; Mark Moll; Brian Y Chen; Viacheslav Y Fofanov; Lydia E Kavraki
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