A structural study of CESA1 catalytic domain of arabidopsis cellulose synthesis complex: Evidence for CESA trimers

Plant Physiology

Volumn 170, Issue 1, 2016, Pages 123-135

  Vandavasi, Venu Gopal ^a   Putnam, Daniel K ^b   Zhang, Qiu ^a   Petridis, Loukas ^a   Heller, William T ^a   Tracy Nixon, B ^d   Haigler, Candace H ^e   Kalluri, Udaya ^a   Coates, Leighton ^a   Langan, Paul ^a   Smith, Jeremy C ^a,f   Meiler, Jens ^b,c   O’Neill, Hugh ^a,f  

^a OAK RIDGE NATIONAL LABORATORY   (United States)

^b VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^c VANDERBILT UNIVERSITY   (United States)

^d PENNSYLVANIA STATE UNIVERSITY   (United States)

^e NORTH CAROLINA STATE UNIVERSITY   (United States)

^f UNIVERSITY OF TENNESSEE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS PROTEIN; CELLULOSE; CESA1 PROTEIN, ARABIDOPSIS; GLUCOSYLTRANSFERASE; MULTIPROTEIN COMPLEX; RECOMBINANT PROTEIN;

ARABIDOPSIS; BIOSYNTHESIS; CHEMISTRY; ENZYME ACTIVE SITE; ESCHERICHIA COLI; GENETICS; ISOLATION AND PURIFICATION; METABOLISM; MOLECULAR MODEL; PROTEIN MULTIMERIZATION; PROTEIN SECONDARY STRUCTURE; SMALL ANGLE SCATTERING; TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION;

ARABIDOPSIS; ARABIDOPSIS PROTEINS; CATALYTIC DOMAIN; CELLULOSE; ESCHERICHIA COLI; GLUCOSYLTRANSFERASES; MICROSCOPY, ELECTRON, TRANSMISSION; MODELS, MOLECULAR; MULTIPROTEIN COMPLEXES; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, SECONDARY; RECOMBINANT PROTEINS; SCATTERING, SMALL ANGLE; X-RAY DIFFRACTION;

EID: 84953297154     PISSN: 00320889     EISSN: 15322548     Source Type: Journal    
DOI: 10.1104/pp.15.01356     Document Type: Article

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