A computationally directed screen identifying interacting coiled coils from Saccharomyces cerevisiae
- 21 November 2000
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 97 (24) , 13203-13208
- https://doi.org/10.1073/pnas.97.24.13203
Abstract
Computational methods can frequently identify protein-interaction motifs in otherwise uncharacterized open reading frames. However, the identification of candidate ligands for these motifs (e.g., so that partnering can be determined experimentally in a directed manner) is often beyond the scope of current computational capabilities. One exception is provided by the coiled-coil interaction motif, which consists of two or more alpha helices that wrap around each other: the ligands for coiled-coil sequences are generally other coiled-coil sequences, thereby greatly simplifying the motif/ligand recognition problem. Here, we describe a two-step approach to identifying protein-protein interactions mediated by two-stranded coiled coils that occur in Saccharomyces cerevisiae. Coiled coils from the yeast genome are first predicted computationally, by using the multicoil program, and associations between coiled coils are then determined experimentally by using the yeast two-hybrid assay. We report 213 unique interactions between 162 putative coiled-coil sequences. We evaluate the resulting interactions, focusing on associations identified between components of the spindle pole body (the yeast centrosome).Keywords
This publication has 60 references indexed in Scilit:
- LearnCoil-VMF: computational evidence for coiled-coil-like motifs in many viral membrane-fusion proteinsJournal of Molecular Biology, 1999
- Analysis of the Saccharomyces Spindle Pole by Matrix-assisted Laser Desorption/Ionization (MALDI) Mass SpectrometryThe Journal of cell biology, 1998
- MultiCoil: A program for predicting two‐and three‐stranded coiled coilsProtein Science, 1997
- Life with 6000 GenesScience, 1996
- A spring-loaded mechanism for the conformational change of influenza hemagglutininCell, 1993
- SH2 domains recognize specific phosphopeptide sequencesPublished by Elsevier ,1993
- A new approach to protein fold recognitionNature, 1992
- X-Ray Structure of the GCN4 Leucine Zipper, a Two-Stranded, Parallel Coiled CoilScience, 1991
- Predicting Coiled Coils from Protein SequencesScience, 1991
- A novel genetic system to detect protein–protein interactionsNature, 1989