Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous Abstract"Extension of reproductive suppression by pheromonal cues in subordinate female marmoset monkeys, Callithrix jacchus"    Next Abstract"Chemical and biological assessment of an urban, estuarine marsh in northeastern New Jersey USA" »

Mol Biol Cell


Title:The Kar3p kinesin-related protein forms a novel heterodimeric structure with its associated protein Cik1p
Author(s):Barrett JG; Manning BD; Snyder M;
Address:"Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103, USA"
Journal Title:Mol Biol Cell
Year:2000
Volume:11
Issue:7
Page Number:2373 - 2385
DOI: 10.1091/mbc.11.7.2373
ISSN/ISBN:1059-1524 (Print) 1059-1524 (Linking)
Abstract:"Proteins that physically associate with members of the kinesin superfamily are critical for the functional diversity observed for these microtubule motor proteins. However, quaternary structures of complexes between kinesins and kinesin-associated proteins are poorly defined. We have analyzed the nature of the interaction between the Kar3 motor protein, a minus-end-directed kinesin from yeast, and its associated protein Cik1. Extraction experiments demonstrate that Kar3p and Cik1p are tightly associated. Mapping of the interaction domains of the two proteins by two-hybrid analyses indicates that Kar3p and Cik1p associate in a highly specific manner along the lengths of their respective coiled-coil domains. Sucrose gradient velocity centrifugation and gel filtration experiments were used to determine the size of the Kar3-Cik1 complex from both mating pheromone-treated cells and vegetatively growing cells. These experiments predict a size for this complex that is consistent with that of a heterodimer containing one Kar3p subunit and one Cik1p subunit. Finally, immunoprecipitation of epitope-tagged and untagged proteins confirms that only one subunit of Kar3p and Cik1p are present in the Kar3-Cik1 complex. These findings demonstrate that the Kar3-Cik1 complex has a novel heterodimeric structure not observed previously for kinesin complexes"
Keywords:"Amino Acid Sequence Centrifugation, Density Gradient Chemical Fractionation Dimerization Fungal Proteins/genetics/*metabolism Kinesins/genetics/*metabolism *Microtubule Proteins *Microtubule-Associated Proteins Molecular Sequence Data Molecular Weight Phe;"
Notes:"MedlineBarrett, J G Manning, B D Snyder, M eng R01 GM036494/GM/NIGMS NIH HHS/ GM36494/GM/NIGMS NIH HHS/ GM52197/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. 2000/07/11 Mol Biol Cell. 2000 Jul; 11(7):2373-85. doi: 10.1091/mbc.11.7.2373"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 16-11-2024