4.7 Article

Generalized dead-end elimination algorithms make large-scale protein side-chain structure prediction tractable: Implications for protein design and structural genomics

期刊

JOURNAL OF MOLECULAR BIOLOGY
卷 307, 期 1, 页码 429-445

出版社

ACADEMIC PRESS LTD
DOI: 10.1006/jmbi.2000.4424

关键词

dead-end elimination; protein design; structural genomics; homology modeling

资金

  1. NIGMS NIH HHS [R01GM49871] Funding Source: Medline
  2. PHS HHS [5T32-GN08487] Funding Source: Medline

向作者/读者索取更多资源

The dead-end elimination (DEE) theorems are powerful tools for the combinatorial optimization of protein side-chain placement in protein design and homology modeling. In order to reach their full potential, the theorems must be extended to handle very hard problems. We present a suite of new algorithms within the DEE paradigm that significantly extend its range of convergence and reduce run time. As a demonstration, we show that a total protein design problem of 10(115) combinations, a hydrophobic core design problem of 10(244) combinations, and a side-chain placement problem of 10(1044) combinations are solved in less than two weeks, a day and a half, and an hour of CPU time, respectively. This extends the range of the method by approximately 53, 144 and 851 log-units, respectively, using modest computational resources. Small to average-sized protein domains can now be designed automatically, and side-chain placement calculations can be solved for nearly all sizes of proteins and protein complexes in the growing field of structural genomics. (C) 2001 Academic Press.

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