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OSPREY 3.0: Open‐source protein redesign for you, with powerful new features.

Authors :
Hallen, Mark A.
Martin, Jeffrey W.
Ojewole, Adegoke
Jou, Jonathan D.
Lowegard, Anna U.
Frenkel, Marcel S.
Gainza, Pablo
Nisonoff, Hunter M.
Mukund, Aditya
Wang, Siyu
Holt, Graham T.
Zhou, David
Dowd, Elizabeth
Donald, Bruce R.
Source :
Journal of Computational Chemistry. 11/15/2018, Vol. 39 Issue 30, p2494-2507. 14p.
Publication Year :
2018

Abstract

We present osprey 3.0, a new and greatly improved release of the osprey protein design software. Osprey 3.0 features a convenient new Python interface, which greatly improves its ease of use. It is over two orders of magnitude faster than previous versions of osprey when running the same algorithms on the same hardware. Moreover, osprey 3.0 includes several new algorithms, which introduce substantial speedups as well as improved biophysical modeling. It also includes GPU support, which provides an additional speedup of over an order of magnitude. Like previous versions of osprey, osprey 3.0 offers a unique package of advantages over other design software, including provable design algorithms that account for continuous flexibility during design and model conformational entropy. Finally, we show here empirically that osprey 3.0 accurately predicts the effect of mutations on protein–protein binding. Osprey 3.0 is available at http://www.cs.duke.edu/donaldlab/osprey.php as free and open‐source software. © 2018 Wiley Periodicals, Inc. We present the third major release of the OSPREY protein design software, along with comparisons to experimental data that confirm its ability to optimize protein mutants for desired functions. Osprey 3.0 has significant efficiency, ease‐of‐use, and algorithmic improvements over previous versions, including GPU acceleration and a new Python interface. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01928651
Volume :
39
Issue :
30
Database :
Academic Search Index
Journal :
Journal of Computational Chemistry
Publication Type :
Academic Journal
Accession number :
133070918
Full Text :
https://doi.org/10.1002/jcc.25522