Loop L5 assumes three distinct orientations during the ATPase cycle of the mitotic kinesin Eg5: A transient and time-resolved fluorescence study

Journal of Biological Chemistry

Volumn 288, Issue 48, 2013, Pages 34839-34849

  Muretta, Joseph M ^a   Behnke Parks, William M ^b   Major, Jennifer ^c   Petersen, Karl J ^a   Goulet, Adeline ^d   Moores, Carolyn A ^d   Thomas, David D ^a   Rosenfeld, Steven S ^c  

^a UNIVERSITY OF MINNESOTA   (United States)

^b Och Spine at New York Presbyterian Hospitals   (United States)

^c LERNER RESEARCH INSTITUTE   (United States)

^d UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EQUILIBRIUM MIXTURES; FLUORESCENCE STUDIES; MICROTUBULE COMPLEX; MITOTIC KINESIN EG5; REVERSIBLE INTERACTIONS; TIME-RESOLVED FLUORESCENCE; TIME-RESOLVED METHODS; TRANSIENT STATE KINETICS;

FLUORESCENCE; MEDICAL IMAGING; MIXTURES; NUCLEOTIDES;

LINEAR MOTORS;

ADENOSINE TRIPHOSPHATASE; FLUORESCENT DYE; KINESIN; MITOTIC KINESIN EG5; UNCLASSIFIED DRUG;

ALPHA HELIX; ARTICLE; BINDING KINETICS; COMPLEX FORMATION; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; FLUORESCENCE; MICROTUBULE; MITOSIS; PRIORITY JOURNAL; PROTEIN MOTIF; STEADY STATE;

EID: 84889008365     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.518845     Document Type: Article

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