Publication:
The contribution of the Trp/Met/Phe residues to physical interactions of p53 with cellular proteins

dc.contributor.coauthorMa, BY
dc.contributor.coauthorPan, YP
dc.contributor.coauthorGunasekaran, K
dc.contributor.coauthorVenkataraghavan, RB
dc.contributor.coauthorLevine, AJ
dc.contributor.coauthorNussinov, R
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.departmentCCBB (The Center for Computational Biology and Bioinformatics)
dc.contributor.kuauthorKeskin, Özlem
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2024-11-09T23:22:19Z
dc.date.issued2005
dc.description.abstractDynamic molecular interaction networks underlie biological phenomena. Among the many genes which are involved, p53 plays a central role in networks controlling cellular life and death. It not only operates as a tumor suppressor, but also helps regulate hundreds of genes in response to various types of stress. To accomplish these functions as a guardian of the genome, p53 interacts extensively with both nucleic acids and proteins. This paper examines the physical interfaces of the p53 protein with cellular proteins. Previously, in the analysis of the structures of protein-protein complexes, we have observed that amino acids Trp, Met and Phe are important for protein-protein interactions in general. Here we show that these residues are critical for the many functions of p53. Several clusters of the Trp/Met/Phe residues are involved in the p53 protein-protein interactions. Phe19/Trp23 in the TA1 region extensively binds to the transcriptional factors and the MDM2 protein. Trp53/Phe54 in the TA2 region is crucial for transactivation and DNA replication. Met243 in the core domain interacts with 53BP1, 53BP2 and Rad 51 proteins. Met384/Phe385 in the C-terminal region interacts with the S100B protein and the Bromodomain of the CBP protein. Thus, these residues may assist in elucidating the p53 interactions when structural data are not available.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue2
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipNCI NIH HHS [N01-CO-12400] Funding Source: Medline
dc.description.volume2
dc.identifier.doi10.1088/1478-3975/2/2/S06
dc.identifier.eissn1478-3975
dc.identifier.issn1478-3967
dc.identifier.quartileQ3
dc.identifier.scopus2-s2.0-22244490043
dc.identifier.urihttps://doi.org/10.1088/1478-3975/2/2/S06
dc.identifier.urihttps://hdl.handle.net/20.500.14288/11053
dc.identifier.wos234992400007
dc.keywordsTumor-suppressor
dc.keywordsTranscriptional activation
dc.keywordsCrystal-structure
dc.language.isoeng
dc.publisherInstitute of Physics (IOP) Publishing
dc.relation.ispartofPhysical Biology
dc.subjectBiochemistry
dc.subjectMolecular biology
dc.subjectBiophysics
dc.titleThe contribution of the Trp/Met/Phe residues to physical interactions of p53 with cellular proteins
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorKeskin, Özlem
local.publication.orgunit1College of Engineering
local.publication.orgunit1Research Center
local.publication.orgunit2Department of Chemical and Biological Engineering
local.publication.orgunit2CCBB (The Center for Computational Biology and Bioinformatics)
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