Using the experimentally determined components of the overall rotational diffusion tensor to restrain molecular shape and size in NMR structure determination of globular proteins and protein-protein complexes

Journal of the American Chemical Society

Volumn 131, Issue 27, 2009, Pages 9522-9531

  Ryabov, Yaroslav ^a   Suh, Jeong Yong ^b   Grishaev, Alexander ^b   Clore, G Marius ^b   Schwieters, Charles D ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL SHIFT PERTURBATION MAPPING; CORRECT SOLUTION; DOCKING COMPLEXES; GLOBULAR PROTEINS; HIV-1 PROTEASE; HYDROPHOBIC CONTACT; LOWEST ENERGY STRUCTURE; MACROMOLECULAR COMPLEXES; MOLECULAR SHAPES; N-TERMINAL DOMAINS; NMR RELAXATION; NMR RESTRAINTS; NMR STRUCTURES; PROTEIN STRUCTURES; PROTEIN-PROTEIN COMPLEXES; ROTATIONAL DIFFUSION; SHAPE AND SIZE; SMALL ANGLE X-RAY SCATTERING; STRUCTURAL INFORMATION; STRUCTURE DETERMINATION;

DIFFUSION IN SOLIDS; MACROMOLECULES; MECHANICAL VARIABLES MEASUREMENT; NUCLEAR MAGNETIC RESONANCE; SCATTERING; X RAY SCATTERING;

TENSORS;

BACTERIAL ENZYME; BACTERIAL PROTEIN; HISTIDINE PHOSPHOCARRIER PROTEIN; PHOSPHOENOLPYRUVATE PROTEIN PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ARTICLE; COMPLEX FORMATION; MOLECULAR SIZE; NUCLEAR MAGNETIC RESONANCE; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; X RAY;

BACTERIAL PROTEINS; COMPUTER SIMULATION; DIFFUSION; DIMERIZATION; HIV PROTEASE; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; PROTEIN STRUCTURE, TERTIARY;

EID: 67650477385     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja902336c     Document Type: Article

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