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001-es BibID:BIBFORM076309
035-os BibID:(cikkazonosító)3315 (scopus)85055616152 (wos)000451528500031
Első szerző:Pancsa Rita
Cím:Co-Evolution of Intrinsically Disordered Proteins with Folded Partners Witnessed by Evolutionary Couplings / Rita Pancsa, Fruzsina Zsolyomi, Peter Tompa
Dátum:2018
ISSN:1661-6596 1422-0067
Megjegyzések:Although improved strategies for the detection and analysis of evolutionary couplings (ECs) between protein residues already enable the prediction of protein structures and interactions, they are mostly restricted to conserved and well-folded proteins. Whereas intrinsically disordered proteins (IDPs) are central to cellular interaction networks, due to the lack of strict structural constraints, they undergo faster evolutionary changes than folded domains. This makes the reliable identification and alignment of IDP homologs difficult, which led to IDPs being omitted in most large-scale residue co-variation analyses. By preforming a dedicated analysis of phylogenetically widespread bacterial IDP⁻partner interactions, here we demonstrate that partner binding imposes constraints on IDP sequences that manifest in detectable interprotein ECs. These ECs were not detected for interactions mediated by short motifs, rather for those with larger IDP⁻partner interfaces. Most identified coupled residue pairs reside close (<10 Å) to each other on the interface, with a third of them forming multiple direct atomic contacts. EC-carrying interfaces of IDPs are enriched in negatively charged residues, and the EC residues of both IDPs and partners preferentially reside in helices. Our analysis brings hope that IDP⁻partner interactions difficult to study could soon be successfully dissected through residue co-variation analysis.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
co-evolution
correlated mutations
disordered protein
evolutionary couplings
interaction surface
intrinsically disordered
residue co-variation
residue contact network
structural disorder
Megjelenés:International Journal of Molecular Sciences. - 19 : 11 (2018), p. 1-16. -
További szerzők:Zsólyomi Fruzsina (1988-) Tompa Péter
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