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MolProbity: all-atom contacts and structure validation for proteins and nucleic acids

MolProbity is a general-purpose web server offering quality validation for 3D structures of proteins, nucleic acids and complexes. It provides detailed all-atom contact analysis of any steric problems within the molecules as well as updated dihedral-angle diagnostics, and it can calculate and displa...

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Autores principales: Davis, Ian W., Leaver-Fay, Andrew, Chen, Vincent B., Block, Jeremy N., Kapral, Gary J., Wang, Xueyi, Murray, Laura W., Arendall, W. Bryan, Snoeyink, Jack, Richardson, Jane S., Richardson, David C.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1933162/
https://www.ncbi.nlm.nih.gov/pubmed/17452350
http://dx.doi.org/10.1093/nar/gkm216
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author Davis, Ian W.
Leaver-Fay, Andrew
Chen, Vincent B.
Block, Jeremy N.
Kapral, Gary J.
Wang, Xueyi
Murray, Laura W.
Arendall, W. Bryan
Snoeyink, Jack
Richardson, Jane S.
Richardson, David C.
author_facet Davis, Ian W.
Leaver-Fay, Andrew
Chen, Vincent B.
Block, Jeremy N.
Kapral, Gary J.
Wang, Xueyi
Murray, Laura W.
Arendall, W. Bryan
Snoeyink, Jack
Richardson, Jane S.
Richardson, David C.
author_sort Davis, Ian W.
collection PubMed
description MolProbity is a general-purpose web server offering quality validation for 3D structures of proteins, nucleic acids and complexes. It provides detailed all-atom contact analysis of any steric problems within the molecules as well as updated dihedral-angle diagnostics, and it can calculate and display the H-bond and van der Waals contacts in the interfaces between components. An integral step in the process is the addition and full optimization of all hydrogen atoms, both polar and nonpolar. New analysis functions have been added for RNA, for interfaces, and for NMR ensembles. Additionally, both the web site and major component programs have been rewritten to improve speed, convenience, clarity and integration with other resources. MolProbity results are reported in multiple forms: as overall numeric scores, as lists or charts of local problems, as downloadable PDB and graphics files, and most notably as informative, manipulable 3D kinemage graphics shown online in the KiNG viewer. This service is available free to all users at http://molprobity.biochem.duke.edu.
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spelling pubmed-19331622007-07-31 MolProbity: all-atom contacts and structure validation for proteins and nucleic acids Davis, Ian W. Leaver-Fay, Andrew Chen, Vincent B. Block, Jeremy N. Kapral, Gary J. Wang, Xueyi Murray, Laura W. Arendall, W. Bryan Snoeyink, Jack Richardson, Jane S. Richardson, David C. Nucleic Acids Res Articles MolProbity is a general-purpose web server offering quality validation for 3D structures of proteins, nucleic acids and complexes. It provides detailed all-atom contact analysis of any steric problems within the molecules as well as updated dihedral-angle diagnostics, and it can calculate and display the H-bond and van der Waals contacts in the interfaces between components. An integral step in the process is the addition and full optimization of all hydrogen atoms, both polar and nonpolar. New analysis functions have been added for RNA, for interfaces, and for NMR ensembles. Additionally, both the web site and major component programs have been rewritten to improve speed, convenience, clarity and integration with other resources. MolProbity results are reported in multiple forms: as overall numeric scores, as lists or charts of local problems, as downloadable PDB and graphics files, and most notably as informative, manipulable 3D kinemage graphics shown online in the KiNG viewer. This service is available free to all users at http://molprobity.biochem.duke.edu. Oxford University Press 2007-07 2007-04-22 /pmc/articles/PMC1933162/ /pubmed/17452350 http://dx.doi.org/10.1093/nar/gkm216 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Davis, Ian W.
Leaver-Fay, Andrew
Chen, Vincent B.
Block, Jeremy N.
Kapral, Gary J.
Wang, Xueyi
Murray, Laura W.
Arendall, W. Bryan
Snoeyink, Jack
Richardson, Jane S.
Richardson, David C.
MolProbity: all-atom contacts and structure validation for proteins and nucleic acids
title MolProbity: all-atom contacts and structure validation for proteins and nucleic acids
title_full MolProbity: all-atom contacts and structure validation for proteins and nucleic acids
title_fullStr MolProbity: all-atom contacts and structure validation for proteins and nucleic acids
title_full_unstemmed MolProbity: all-atom contacts and structure validation for proteins and nucleic acids
title_short MolProbity: all-atom contacts and structure validation for proteins and nucleic acids
title_sort molprobity: all-atom contacts and structure validation for proteins and nucleic acids
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1933162/
https://www.ncbi.nlm.nih.gov/pubmed/17452350
http://dx.doi.org/10.1093/nar/gkm216
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