Show simple item record

dc.contributor.authorMartin, BP
dc.contributor.authorBrandon, CJ
dc.contributor.authorStewart, JJP
dc.contributor.authorBraun-Sand, SB
dc.date.accessioned2020-12-22T05:51:49Z
dc.date.available2020-12-22T05:51:49Z
dc.date.issued2015-08
dc.identifier.citationMartin, B. P., Brandon, C. J., Stewart, J. J. P. & Braun-Sand, S. B. (2015). Accuracy issues involved in modeling in vivo protein structures using PM7.. Proteins, 83 (8), pp.1427-1435. https://doi.org/10.1002/prot.24826.
dc.identifier.issn0887-3585
dc.identifier.urihttp://hdl.handle.net/11343/258372
dc.description.abstractUsing the semiempirical method PM7, an attempt has been made to quantify the error in prediction of the in vivo structure of proteins relative to X-ray structures. Three important contributory factors are the experimental limitations of X-ray structures, the difference between the crystal and solution environments, and the errors due to PM7. The geometries of 19 proteins from the Protein Data Bank that had small R values, that is, high accuracy structures, were optimized and the resulting drop in heat of formation was calculated. Analysis of the changes showed that about 10% of this decrease in heat of formation was caused by faults in PM7, the balance being attributable to the X-ray structure and the difference between the crystal and solution environments. A previously unknown fault in PM7 was revealed during tests to validate the geometries generated using PM7. Clashscores generated by the Molprobity molecular mechanics structure validation program showed that PM7 was predicting unrealistically close contacts between nonbonding atoms in regions where the local geometry is dominated by very weak noncovalent interactions. The origin of this fault was traced to an underestimation of the core-core repulsion between atoms at distances smaller than the equilibrium distance.
dc.languageeng
dc.publisherWiley
dc.titleAccuracy issues involved in modeling in vivo protein structures using PM7.
dc.typeJournal Article
dc.identifier.doi10.1002/prot.24826
melbourne.affiliation.departmentSir Peter MacCallum Department of Oncology
melbourne.source.titleProteins: Structure, Function, and Bioinformatics
melbourne.source.volume83
melbourne.source.issue8
melbourne.source.pages1427-1435
dc.rights.licenseCC BY
melbourne.elementsid1196028
melbourne.openaccess.pmchttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744657
melbourne.contributor.authorMARTIN, BEN PAUL
dc.identifier.eissn1097-0134
melbourne.accessrightsOpen Access


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record