Karl Gruber
molekularbiologie.uni-graz.at
0000-0002-3485-9740
University of Graz
128 papers found
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Atomic Resolution Crystal Structures and Quantum Chemistry Meet to Reveal Subtleties of Hydroxynitrile Lyase Catalysis
Bioactivation of Nitroglycerin by Purified Mitochondrial and Cytosolic Aldehyde Dehydrogenases*
Asymmetric Bioreduction of CC Bonds using Enoate Reductases OPR1, OPR3 and YqjM: Enzyme-Based Stereocontrol
Structure-Function Correlations of Two Highly Conserved Motifs in Saccharomyces cerevisiae Squalene Epoxidase
Laboratory Evolved Biocatalysts for Stereoselective Syntheses of Substituted Benzaldehyde Cyanohydrins
The solution structure of ParD, the antidote of the ParDE toxin–antitoxin module, provides the structural basis for DNA and toxin binding
Stereoselective Biocatalytic Synthesis of (S)-2-Hydroxy-2-Methylbutyric Acid via Substrate Engineering by Using “Thio-Disguised” Precursors and Oxynitrilase Catalysis
Serine scanning—A tool to prove the consequences of N-glycosylation of proteins
Structural determinants of the enantioselectivity of the hydroxynitrile lyase from Hevea brasiliensis
Inverting enantioselectivity of Burkholderia gladioli esterase EstB by directed and designed evolution
Characterization of Squalene Epoxidase of Saccharomyces cerevisiae by Applying Terbinafine-Sensitive Variants
A Biocatalytic Henry Reaction—The Hydroxynitrile Lyase fromHevea brasiliensis Also Catalyzes Nitroaldol Reactions
Vitamin B12: A Methyl Group without a Job?
Structure and Function of YcnD fromBacillus subtilis,a Flavin-Containing Oxidoreductase†,‡
Asymmetric biocatalytic hydrocyanation of pyrrole carboxaldehydes
B12-retro-Riboswitches: Constitutional Switching of B12Coenzymes Induced by Nucleotides
Homocoenzyme B12and Bishomocoenzyme B12: Covalent Structural Mimics for Homolyzed, Enzyme-Bound Coenzyme B12
Hydroxynitrile lyase catalysed synthesis of heterocyclic (R)- and (S)-cyanohydrins
2,6,9-Trioxabicyclo[3.3.1]nona-3,7-dien-4-oyl and tetraoxaadamantan-9-oyl functionalized aromatic di- and triamines: Synthesis, stereochemistry and complexation
The Cofactor of Tetrachloroethene Reductive Dehalogenase ofDehalospirillum multivorans Is Norpseudo-B12, a New Type of a Natural Corrinoid
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