Pages that link to "Q28259812"
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The following pages link to Comparison of random mutagenesis and semi-rational designed libraries for improved cytochrome P450 BM3-catalyzed hydroxylation of small alkanes (Q28259812):
Displayed 21 items.
- Human P450-like oxidation of diverse proton pump inhibitor drugs by 'gatekeeper' mutants of flavocytochrome P450 BM3 (Q27689400) (← links)
- Crystal Structure of a Putative Cytochrome P450 Alkane Hydroxylase (CYP153D17) from Sphingomonas sp. PAMC 26605 and Its Conformational Substrate Binding (Q28818591) (← links)
- Structure-based redesign of the binding specificity of anti-apoptotic Bcl-x(L). (Q30423652) (← links)
- High-throughput enzyme evolution in Saccharomyces cerevisiae using a synthetic RNA switch. (Q34255120) (← links)
- Improvement of biocatalysts for industrial and environmental purposes by saturation mutagenesis (Q35196065) (← links)
- Structure-based design of combinatorial mutagenesis libraries (Q35547152) (← links)
- Enantioselective enzymes by computational design and in silico screening (Q35555046) (← links)
- Semirational Directed Evolution of Loop Regions in Aspergillus japonicus β-Fructofuranosidase for Improved Fructooligosaccharide Production (Q35740340) (← links)
- A mix-and-read drop-based in vitro two-hybrid method for screening high-affinity peptide binders (Q35945330) (← links)
- Orthogonal Luciferase-Luciferin Pairs for Bioluminescence Imaging (Q36255155) (← links)
- Enriching Peptide Libraries for Binding Affinity and Specificity Through Computationally Directed Library Design. (Q36290587) (← links)
- Investigating models of protein function and allostery with a widespread mutational analysis of a light-activated protein (Q37117487) (← links)
- Computational design gains momentum in enzyme catalysis engineering (Q38104437) (← links)
- Recent advances in engineering proteins for biocatalysis (Q38209808) (← links)
- Improved conversion of ginsenoside Rb1 to compound K by semi-rational design of Sulfolobus solfataricus β-glycosidase (Q42370315) (← links)
- Stabilization of the Reductase Domain in the Catalytically Self-Sufficient Cytochrome P450BM3 via Consensus-Guided Mutagenesis. (Q47220251) (← links)
- Semi-rational engineering of CYP153A35 to enhance ω-hydroxylation activity toward palmitic acid (Q47363058) (← links)
- Rational and Semirational Protein Design (Q47396971) (← links)
- CYP116B5: a new class VII catalytically self-sufficient cytochrome P450 from Acinetobacter radioresistens that enables growth on alkanes (Q47969550) (← links)
- Protein engineering: Chemistry gets the assist. (Q50885257) (← links)
- The full-length cytochrome P450 enzyme CYP102A1 dimerizes at its reductase domains and has flexible heme domains for efficient catalysis. (Q52331920) (← links)