Conserved tertiary couplings stabilize elements in the PDZ fold, leading to characteristic patterns of domain conformational flexibility

doi:10.1002/pro.318

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Conserved tertiary couplings stabilize elements in the PDZ fold, leading to characteristic patterns of domain conformational flexibility

Bosco K. Ho^*,
David A. Agard

Article first published online: 5 JAN 2010

DOI: 10.1002/pro.318

Issue

Protein Science

Volume 19, Issue 3, pages 398–411, March 2010

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How to Cite

Ho, B. K. and Agard, D. A. (2010), Conserved tertiary couplings stabilize elements in the PDZ fold, leading to characteristic patterns of domain conformational flexibility. Protein Science, 19: 398–411. doi: 10.1002/pro.318

Author Information

Department of Biochemistry and Biophysics, Howard Hughes Medical Institute, University of California, San Francisco, California 94158-2517

Email: Bosco K. Ho (boscoh@gmail.com)

^*Department of Biochemistry and Biophysics, Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158-2517

Publication History

Issue published online: 22 FEB 2010
Article first published online: 5 JAN 2010
Manuscript Accepted: 10 DEC 2009
Manuscript Received: 23 SEP 2009

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Conserved tertiary couplings stabilize elements in the PDZ fold, leading to characteristic patterns of domain conformational flexibility

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Conserved tertiary couplings stabilize elements in the PDZ fold, leading to characteristic patterns of domain conformational flexibility

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