Energy-based de novo protein folding by conformational space annealing and an off-lattice united-residue force field: Application to the 10-55 fragment of staphylococcal protein A and to apo calbindin D9K

Proceedings of the National Academy of Sciences of the United States of America

Volumn 96, Issue 5, 1999, Pages 2025-2030

  Lee, Jooyoung ^a   Liwo, Adam ^a,b   Scheraga, Harold A ^a  

^a Cornell University ^*  (United States)

^b UNIVERSITY OF GDA SK   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

CALBINDIN; POLYPEPTIDE; PROTEIN; STAPHYLOCOCCUS PROTEIN A;

ALGORITHM; ARTICLE; ENERGY; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN FOLDING; PROTEIN STRUCTURE;

AMINO ACID SUBSTITUTION; APOPROTEINS; BINDING SITES; CALCIUM-BINDING PROTEIN, VITAMIN D-DEPENDENT; CALORIMETRY; MODELS, MOLECULAR; NERVE TISSUE PROTEINS; PEPTIDE FRAGMENTS; PROTEIN CONFORMATION; PROTEIN FOLDING; RECOMBINANT PROTEINS; STAPHYLOCOCCAL PROTEIN A; THERMODYNAMICS;

BACTERIA (MICROORGANISMS); STAPHYLOCOCCUS;

EID: 0033514939     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.5.2025     Document Type: Article

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