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Ligand Access Channels in Cytochrome P450 Enzymes: A Review

Quantitative structure-activity relationships may bring invaluable information on structural elements of both enzymes and substrates that, together, govern substrate specificity. Buried active sites in cytochrome P450 enzymes are connected to the solvent by a network of channels exiting at the dista...

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Autores principales: Urban, Philippe, Lautier, Thomas, Pompon, Denis, Truan, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032366/
https://www.ncbi.nlm.nih.gov/pubmed/29848998
http://dx.doi.org/10.3390/ijms19061617
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author Urban, Philippe
Lautier, Thomas
Pompon, Denis
Truan, Gilles
author_facet Urban, Philippe
Lautier, Thomas
Pompon, Denis
Truan, Gilles
author_sort Urban, Philippe
collection PubMed
description Quantitative structure-activity relationships may bring invaluable information on structural elements of both enzymes and substrates that, together, govern substrate specificity. Buried active sites in cytochrome P450 enzymes are connected to the solvent by a network of channels exiting at the distal surface of the protein. This review presents different in silico tools that were developed to uncover such channels in P450 crystal structures. It also lists some of the experimental evidence that actually suggest that these predicted channels might indeed play a critical role in modulating P450 functions. Amino acid residues at the entrance of the channels may participate to a first global ligand recognition of ligands by P450 enzymes before they reach the buried active site. Moreover, different P450 enzymes show different networks of predicted channels. The plasticity of P450 structures is also important to take into account when looking at how channels might play their role.
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spelling pubmed-60323662018-07-13 Ligand Access Channels in Cytochrome P450 Enzymes: A Review Urban, Philippe Lautier, Thomas Pompon, Denis Truan, Gilles Int J Mol Sci Review Quantitative structure-activity relationships may bring invaluable information on structural elements of both enzymes and substrates that, together, govern substrate specificity. Buried active sites in cytochrome P450 enzymes are connected to the solvent by a network of channels exiting at the distal surface of the protein. This review presents different in silico tools that were developed to uncover such channels in P450 crystal structures. It also lists some of the experimental evidence that actually suggest that these predicted channels might indeed play a critical role in modulating P450 functions. Amino acid residues at the entrance of the channels may participate to a first global ligand recognition of ligands by P450 enzymes before they reach the buried active site. Moreover, different P450 enzymes show different networks of predicted channels. The plasticity of P450 structures is also important to take into account when looking at how channels might play their role. MDPI 2018-05-30 /pmc/articles/PMC6032366/ /pubmed/29848998 http://dx.doi.org/10.3390/ijms19061617 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Urban, Philippe
Lautier, Thomas
Pompon, Denis
Truan, Gilles
Ligand Access Channels in Cytochrome P450 Enzymes: A Review
title Ligand Access Channels in Cytochrome P450 Enzymes: A Review
title_full Ligand Access Channels in Cytochrome P450 Enzymes: A Review
title_fullStr Ligand Access Channels in Cytochrome P450 Enzymes: A Review
title_full_unstemmed Ligand Access Channels in Cytochrome P450 Enzymes: A Review
title_short Ligand Access Channels in Cytochrome P450 Enzymes: A Review
title_sort ligand access channels in cytochrome p450 enzymes: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032366/
https://www.ncbi.nlm.nih.gov/pubmed/29848998
http://dx.doi.org/10.3390/ijms19061617
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