Computational protein design continues to experience a variety of methodological advances. Several improvements have been suggested for the objective functions used to quantify sequence/structure compatibility. Disparate design strategies based upon dead-end elimination, simulated annealing and statistical design have each recently yielded striking successes involving de novo designed proteins with sizes on the order of 100 residues or greater. Such methods may be used to design new proteins, as well as to redesign natural proteins to facilitate structural and biophysical studies.
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SASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur, Tamil Nadu, IndiaSASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur, Tamil Nadu, India
Srikanth, Srimari
Srinivasan, Thamarai Selvi
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SASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur, Tamil Nadu, IndiaSASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur, Tamil Nadu, India
Srinivasan, Thamarai Selvi
Prabhu, Dhamodharan
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Sree Balaji Med Coll & Hosp BIHER, Res & Dev Wing, Chennai, Tamil Nadu, IndiaSASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur, Tamil Nadu, India
Prabhu, Dhamodharan
Kadhirvel, Saraboji
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Cent Univ Punjab, Dept Computat Sci, Bathinda, Punjab, IndiaSASTRA Deemed Univ, Sch Chem & Biotechnol, Thanjavur, Tamil Nadu, India
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Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94158 USA
UCSF, Calif Quantitat Biosci Inst QBI, San Francisco, CA 94158 USAUniv Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94158 USA
Kretschmer, Simon
Kortemme, Tanja
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Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94158 USA
UCSF, Calif Quantitat Biosci Inst QBI, San Francisco, CA 94158 USAUniv Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94158 USA