Publication:
Protein-protein interactions: hot spots and structurally conserved residues often locate in complemented pockets that pre-organized in the unbound states: implications for docking

dc.contributor.coauthorLi, X
dc.contributor.coauthorMa, BY
dc.contributor.coauthorNussinov, R
dc.contributor.coauthorLiang, J
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.kuauthorKeskin, Özlem
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.contributor.yokid26605
dc.date.accessioned2024-11-09T23:02:36Z
dc.date.issued2004
dc.description.abstractEnergetic hot spots account for a significant portion of the total binding free energy and correlate with structurally conserved interface residues. Here, we map experimentally determined hot spots and structurally conserved residues to investigate their geometrical organization. Unfilled pockets are pockets that remain unfilled after protein-protein complexation, while complemented pockets are pockets that disappear upon binding, representing tightly fit regions. We find that structurally conserved residues and energetic hot spots are strongly favored to be located in complemented pockets, and are disfavored in unfilled pockets. For the three available protein-protein complexes with complemented pockets where both members of the complex were alanine-scanned, 62% of all hot spots (DeltaDeltaG > 2 kcal/mol) are within these pockets, and 60% of the residues in the complemented pockets are hot spots. 93% of all red-hot residues (DeltaDeltaG greater than or equal to 4 kcal/mol) either protrude into or are located in complemented pockets. The occurrence of hot spots and conserved residues in complemented pockets highlights the role of local tight packing in protein associations, and rationalizes their energetic contribution and conservation. Complemented pockets and their corresponding protruding residues emerge among the most important geometric features in protein-protein interactions. By screening the solvent, this organization shields backbone hydrogen bonds and charge-charge interactions. Complemented pockets often pre-exist binding. For 18 protein-protein complexes with complemented pockets whose unbound structures are available, in 16 the pockets are identified to pre-exist in the unbound structures. The root-mean-squared deviations of the atoms lining the pockets between the bound and unbound states is as small as 0.9 Angstrom, suggesting that such pockets constitute features of the populated native state that may be used in docking.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue3
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipThis work is supported by grants from National Science Foundation (CAREER DBI013356, DBI0078270), and National Institute of Health (GM68958). The research of R.N. in Israel has been supported, in part, by the Center of Excellence in Geometric Computing and its Applications funded by the Israel Science Foundation (administered by the Israel Academy of Sciences). This project has been funded in whole or in part with Federal funds from the National Cancer Institute, National Institutes of Health, under contract number NO1-CO-12400.
dc.description.volume344
dc.identifier.doi10.1016/j.jmb.2004.09.051
dc.identifier.eissn1089-8638
dc.identifier.issn0022-2836
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-7944225979
dc.identifier.urihttp://dx.doi.org/10.1016/j.jmb.2004.09.051
dc.identifier.urihttps://hdl.handle.net/20.500.14288/8326
dc.identifier.wos225304500015
dc.keywordsProtein-protein interactions
dc.keywordsResidue hot spots
dc.keywordsProtein docking
dc.keywordsResidue conservation
dc.keywordsBinding and folding
dc.languageEnglish
dc.publisherElsevier
dc.sourceJournal of Molecular Biology
dc.subjectBiochemistry and molecular biology
dc.titleProtein-protein interactions: hot spots and structurally conserved residues often locate in complemented pockets that pre-organized in the unbound states: implications for docking
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0002-4202-4049
local.contributor.kuauthorKeskin, Özlem
relation.isOrgUnitOfPublicationc747a256-6e0c-4969-b1bf-3b9f2f674289
relation.isOrgUnitOfPublication.latestForDiscoveryc747a256-6e0c-4969-b1bf-3b9f2f674289

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