TY - JOUR
T1 - AFAL
T2 - A web service for profiling amino acids surrounding ligands in proteins
AU - Arenas-Salinas, Mauricio
AU - Ortega-Salazar, Samuel
AU - Gonzales-Nilo, Fernando
AU - Pohl, Ehmke
AU - Holmes, David S.
AU - Quatrini, Raquel
N1 - Funding Information:
Acknowledgments The authors wish to thank the anonymous reviewers, and Dr. Jaime Henriquez, Alejandro Valdes, Melisa Ale-gría, Osvaldo Yañez, Wladimir Morales, Daniel Aguayo, Raúl Arias and Francisco Correa for many valuable scientific discussions. Funding is gratefully acknowledged from FONDECYT Grants (Fondo Nacional de Desarrollo Científico y Tecnológico) 1140048 and 1130683, CONICYT Grant (Comisión Nacional de Investigación Científica y Tecnológica) Basal CCTE PFB16 and a Santander Mobility Grant for collaboration with Durham University.
Publisher Copyright:
© 2014 The Author(s).
PY - 2014/11
Y1 - 2014/11
N2 - With advancements in crystallographic technology and the increasing wealth of information populating structural databases, there is an increasing need for prediction tools based on spatial information that will support the characterization of proteins and protein-ligand interactions. Herein, a new web service is presented termed amino acid frequency around ligand (AFAL) for determining amino acids type and frequencies surrounding ligands within proteins deposited in the Protein Data Bank and for assessing the atoms and atom-ligand distances involved in each interaction (availability: http://structuralbio.utalca.cl/AFAL/index.html). AFAL allows the user to define a wide variety of filtering criteria (protein family, source organism, resolution, sequence redundancy and distance) in order to uncover trends and evolutionary differences in amino acid preferences that define interactions with particular ligands. Results obtained from AFAL provide valuable statistical information about amino acids that may be responsible for establishing particular ligand-protein interactions. The analysis will enable investigators to compare ligand-binding sites of different proteins and to uncover general as well as specific interaction patterns from existing data. Such patterns can be used subsequently to predict ligand binding in proteins that currently have no structural information and to refine the interpretation of existing protein models. The application of AFAL is illustrated by the analysis of proteins interacting with adenosine-5′-triphosphate.
AB - With advancements in crystallographic technology and the increasing wealth of information populating structural databases, there is an increasing need for prediction tools based on spatial information that will support the characterization of proteins and protein-ligand interactions. Herein, a new web service is presented termed amino acid frequency around ligand (AFAL) for determining amino acids type and frequencies surrounding ligands within proteins deposited in the Protein Data Bank and for assessing the atoms and atom-ligand distances involved in each interaction (availability: http://structuralbio.utalca.cl/AFAL/index.html). AFAL allows the user to define a wide variety of filtering criteria (protein family, source organism, resolution, sequence redundancy and distance) in order to uncover trends and evolutionary differences in amino acid preferences that define interactions with particular ligands. Results obtained from AFAL provide valuable statistical information about amino acids that may be responsible for establishing particular ligand-protein interactions. The analysis will enable investigators to compare ligand-binding sites of different proteins and to uncover general as well as specific interaction patterns from existing data. Such patterns can be used subsequently to predict ligand binding in proteins that currently have no structural information and to refine the interpretation of existing protein models. The application of AFAL is illustrated by the analysis of proteins interacting with adenosine-5′-triphosphate.
KW - AFAL
KW - Bioinformatics
KW - Drug design
KW - Enzyme engineering
KW - PDB
KW - Protein-ligand interactions
UR - http://www.scopus.com/inward/record.url?scp=84936753182&partnerID=8YFLogxK
U2 - 10.1007/s10822-014-9783-6
DO - 10.1007/s10822-014-9783-6
M3 - Article
C2 - 25085083
AN - SCOPUS:84936753182
SN - 0920-654X
VL - 28
SP - 1069
EP - 1076
JO - Journal of Computer-Aided Molecular Design
JF - Journal of Computer-Aided Molecular Design
IS - 11
ER -