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Short Linear Sequence Motif LxxPTPh Targets Diverse Proteins to Growing Microtubule Ends.
- Source :
-
Structure (London, England : 1993) [Structure] 2017 Jun 06; Vol. 25 (6), pp. 924-932.e4. Date of Electronic Publication: 2017 May 25. - Publication Year :
- 2017
-
Abstract
- Microtubule plus-end tracking proteins (+TIPs) are involved in virtually all microtubule-based processes. End-binding (EB) proteins are considered master regulators of +TIP interaction networks, since they autonomously track growing microtubule ends and recruit a plethora of proteins to this location. Two major EB-interacting elements have been described: CAP-Gly domains and linear SxIP sequence motifs. Here, we identified LxxPTPh as a third EB-binding motif that enables major +TIPs to interact with EBs at microtubule ends. In contrast to EB-SxIP and EB-CAP-Gly, the EB-LxxPTPh binding mode does not depend on the C-terminal tail region of EB. Our study reveals that +TIPs developed additional strategies besides CAP-Gly and SxIP to target EBs at growing microtubule ends. They further provide a unique basis to discover novel +TIPs, and to dissect the role of key interaction nodes and their differential regulation for hierarchical +TIP network organization and function in eukaryotic organisms.<br /> (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Subjects :
- Amino Acid Motifs
Animals
Binding Sites
COS Cells
Cell Cycle Proteins chemistry
Cell Cycle Proteins genetics
Cell Cycle Proteins metabolism
Chlorocebus aethiops
Crystallography, X-Ray
Fluorescence Polarization
Microtubule Proteins chemistry
Microtubule Proteins genetics
Microtubule Proteins metabolism
Microtubule-Associated Proteins chemistry
Microtubule-Associated Proteins genetics
Models, Molecular
Nuclear Proteins genetics
Protein Domains
Saccharomyces cerevisiae Proteins genetics
Microtubule-Associated Proteins metabolism
Microtubules metabolism
Nuclear Proteins chemistry
Nuclear Proteins metabolism
Saccharomyces cerevisiae Proteins chemistry
Saccharomyces cerevisiae Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1878-4186
- Volume :
- 25
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Structure (London, England : 1993)
- Publication Type :
- Academic Journal
- Accession number :
- 28552577
- Full Text :
- https://doi.org/10.1016/j.str.2017.04.010