CHARMM36m: An improved force field for folded and intrinsically disordered proteins

Nature Methods

Volumn 14, Issue 1, 2016, Pages 71-73

  Huang, Jing ^a   Rauscher, Sarah ^b   Nawrocki, Grzegorz ^c   Ran, Ting ^a   Feig, Michael ^c   De Groot, Bert L ^b   Grubmüller, Helmut ^b   MacKerell, Alexander D ^a  

^a UNIVERSITY OF MARYLAND SCHOOL OF PHARMACY   (United States)

^b MAX PLANCK INSTITUTE FOR BIOPHYSICAL CHEMISTRY   (Germany)

^c Michigan State University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHARMM36 PROTEIN; INTRINSICALLY DISORDERED PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; HUMAN; MOLECULAR DYNAMICS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN FOLDING; PROTEIN SECONDARY STRUCTURE; X RAY CRYSTALLOGRAPHY; CHEMICAL PHENOMENA; CHEMISTRY; HYDROGEN BOND;

HUMANS; HYDROGEN BONDING; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; INTRINSICALLY DISORDERED PROTEINS; MOLECULAR DYNAMICS SIMULATION; PROTEIN CONFORMATION; PROTEIN FOLDING;

EID: 84994682451     PISSN: 15487091     EISSN: 15487105     Source Type: Journal    
DOI: 10.1038/nmeth.4067     Document Type: Article

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