Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2008-2-21
pubmed:abstractText
Protein cysteine thiols can be divided into four groups based on their reactivities: those that form permanent structural disulfide bonds, those that coordinate with metals, those that remain in the reduced state, and those that are susceptible to reversible oxidation. Physicochemical parameters of oxidation-susceptible protein thiols were organized into a database named the Balanced Oxidation Susceptible Cysteine Thiol Database (BALOSCTdb). BALOSCTdb contains 161 cysteine thiols that undergo reversible oxidation and 161 cysteine thiols that are not susceptible to oxidation. Each cysteine was represented by a set of 12 parameters, one of which was a label (1/0) to indicate whether its thiol moiety is susceptible to oxidation. A computer program (the C4.5 decision tree classifier re-implemented as the J48 classifier) segregated cysteines into oxidation-susceptible and oxidation-non-susceptible classes. The classifier selected three parameters critical for prediction of thiol oxidation susceptibility: (1) distance to the nearest cysteine sulfur atom, (2) solvent accessibility, and (3) pKa. The classifier was optimized to correctly predict 136 of the 161 cysteine thiols susceptible to oxidation. Leave-one-out cross-validation analysis showed that the percent of correctly classified cysteines was 80.1% and that 16.1% of the oxidation-susceptible cysteine thiols were incorrectly classified. The algorithm developed from these parameters, named the Cysteine Oxidation Prediction Algorithm (COPA), is presented here. COPA prediction of oxidation-susceptible sites can be utilized to locate protein cysteines susceptible to redox-mediated regulation and identify possible enzyme catalytic sites with reactive cysteine thiols.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-10339558, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-10869018, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-11256959, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-11301006, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-11916965, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-11964141, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-11983871, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-12033454, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-12119021, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-12354231, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-12381855, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-12524212, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-12648682, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-12714747, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-12714748, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-13678530, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-14744249, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-14977531, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-15215411, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-15980492, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-16231289, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-16246123, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-16290020, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-16415107, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-16749919, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-16819828, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-16844986, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-16844987, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-17172268, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-17215875, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-2231712, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-3567225, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-5551392, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-7771771, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-8369304, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-9497290, http://linkedlifedata.com/resource/pubmed/commentcorrection/18287280-9917330
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0961-8368
pubmed:author
pubmed:issnType
Print
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
473-81
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
Prediction of reversibly oxidized protein cysteine thiols using protein structure properties.
pubmed:affiliation
Department of Chemistry and Biochemistry, California State University, Los Angeles, California 90032, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, N.I.H., Extramural