Using a residue clash map to functionally characterize protein recombination hybrids

Protein Engineering

Volumn 16, Issue 12, 2003, Pages 1025-1034

  Saraf, Manish C ^a   Maranas, Costas D ^a  

^a The Center for Nanotechnology Education and Utilization   (United States)

Author keywords

Bioinformatics; Directed evolution; Protein engineering; Residue residue clash

Indexed keywords

BETA LACTAMASE; BETA LACTAMASE PSE 4; BETA LACTAMASE TEM 1; BIPHENYL DIOXYGENASE; CATECHOL 2,3 DIOXYGENASE; CATECHOL 2,3 OXYGENASE NAHH; CATECHOL 2,3 OXYGENASE XYLE; GLUTATHIONE S TRANSFERASE M1 1; GLUTATHIONE S TRANSFERASE M2 2; GLUTATHIONE TRANSFERASE; HYBRID PROTEIN; OXYGENASE; PHOSPHORIBOSYLGLYCINAMIDE FORMYLTRANSFERASE; RECOMBINANT PROTEIN; TETRACHLOROBENZENE DIOXYGENASE; TOLUENE DIOXYGENASE; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; GENETIC VARIABILITY; HYDROGEN BOND; MOLECULAR EVOLUTION; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FAMILY; PROTEIN INTERACTION; PROTEIN STRUCTURE;

ESCHERICHIA COLI;

EID: 1442286044     PISSN: 02692139     EISSN: None     Source Type: Journal    
DOI: 10.1093/protein/gzg129     Document Type: Article

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