β-Tubulin C354 Mutations that Severely Decrease Microtubule Dynamics Do Not Prevent Nuclear Migration in Yeast
Author:
Affiliation:
1. Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas 66045; and
2. Department of Biology, University of North Carolina, Chapel Hill, North Carolina 27599
Abstract
Publisher
American Society for Cell Biology (ASCB)
Subject
Cell Biology,Molecular Biology
Reference54 articles.
1. Microtubule Interactions with the Cell Cortex Causing Nuclear Movements in Saccharomyces cerevisiae
2. Dominant-Lethal α-Tubulin Mutants Defective in Microtubule Depolymerization in Yeast
3. Identification of the cysteine residue of .beta.-tubulin alkylated by the antimitotic agent 2,4-dichlorobenzyl thiocyanate, facilitated by separatio of the protein subunits of tubulin by hydrophobic column chromatography
4. Identification of Cysteine 354 of β-Tubulin as Part of the Binding Site for the A Ring of Colchicine
5. Direct Photoaffinity Labeling of Cysteine 211 or a Nearby Amino Acid Residue of β-Tubulin by Guanosine 5′-Diphosphate Bound in the Exchangeable Site
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