ENZYME-INHIBITORS - GROUND-STATE TRANSITION-STATE ANALOGS

[1] SUICIDE ENZYME INACTIVATORS [J]. CHEMICAL & ENGINEERING NEWS, 1983, 61 (38) : 48 - 56

[2] MEVINOLIN - A HIGHLY POTENT COMPETITIVE INHIBITOR OF HYDROXYMETHYLGLUTARYL-COENZYME-A REDUCTASE AND A CHOLESTEROL-LOWERING AGENT [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07): : 3957 - 3961

[3] 3-DIMENSIONAL STRUCTURE OF THE COMPLEX BETWEEN PANCREATIC SECRETORY TRYPSIN-INHIBITOR (KAZAL TYPE) AND TRYPSINOGEN AT 1-8 A RESOLUTION - STRUCTURE SOLUTION, CRYSTALLOGRAPHIC REFINEMENT AND PRELIMINARY STRUCTURAL INTERPRETATION [J]. JOURNAL OF MOLECULAR BIOLOGY, 1982, 162 (04) : 839 - 868

[4] BINDING OF SPECIFIC AND NONSPECIFIC ALDEHYDE SUBSTRATE ANALOGS TO ALPHA-CHYMOTRYPSIN [J]. FEBS LETTERS, 1975, 56 (01) : 81 - 84

[5] BRODBECK U, 1979, BIOCHIM BIOPHYS ACTA, V567, P357, DOI 10.1016/0005-2744(79)90122-0

[6] TIGHT-BINDING INHIBITORS .1. KINETIC-BEHAVIOR [J]. BIOCHEMICAL PHARMACOLOGY, 1975, 24 (23) : 2177 - 2185

[7] EVIDENCE FOR HEMIACETAL FORMATION BETWEEN N-ACYL-L-PHENYLALANINALS AND ALPHA-CHYMOTRYPSIN BY CROSS-SATURATION NUCLEAR MAGNETIC-RESONANCE SPECTROSCOPY [J]. BIOCHEMISTRY, 1979, 18 (05) : 921 - 926

[8] PYRAZOLE BINDING IN CRYSTALLINE BINARY AND TERNARY COMPLEXES WITH LIVER ALCOHOL-DEHYDROGENASE [J]. BIOCHEMISTRY, 1982, 21 (20) : 4858 - 4866

[9] COMPETITIVE INHIBITION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE BY ML-236A AND ML-236B FUNGAL METABOLITES, HAVING HYPOCHOLESTEROLEMIC ACTIVITY [J]. FEBS LETTERS, 1976, 72 (02) : 323 - 326

[10] LEAVING GROUP SPECIFICITY IN CHYMOTRYPSIN-CATALYZED HYDROLYSIS OF PEPTIDES - STEREOCHEMICAL INTERPRETATION [J]. BIOCHEMISTRY, 1973, 12 (11) : 2035 - 2041

[1] SUICIDE ENZYME INACTIVATORS [J]. CHEMICAL & ENGINEERING NEWS, 1983, 61 (38) : 48 - 56

[2] MEVINOLIN - A HIGHLY POTENT COMPETITIVE INHIBITOR OF HYDROXYMETHYLGLUTARYL-COENZYME-A REDUCTASE AND A CHOLESTEROL-LOWERING AGENT [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07): : 3957 - 3961

[3] 3-DIMENSIONAL STRUCTURE OF THE COMPLEX BETWEEN PANCREATIC SECRETORY TRYPSIN-INHIBITOR (KAZAL TYPE) AND TRYPSINOGEN AT 1-8 A RESOLUTION - STRUCTURE SOLUTION, CRYSTALLOGRAPHIC REFINEMENT AND PRELIMINARY STRUCTURAL INTERPRETATION [J]. JOURNAL OF MOLECULAR BIOLOGY, 1982, 162 (04) : 839 - 868

[4] BINDING OF SPECIFIC AND NONSPECIFIC ALDEHYDE SUBSTRATE ANALOGS TO ALPHA-CHYMOTRYPSIN [J]. FEBS LETTERS, 1975, 56 (01) : 81 - 84

[5] BRODBECK U, 1979, BIOCHIM BIOPHYS ACTA, V567, P357, DOI 10.1016/0005-2744(79)90122-0

[6] TIGHT-BINDING INHIBITORS .1. KINETIC-BEHAVIOR [J]. BIOCHEMICAL PHARMACOLOGY, 1975, 24 (23) : 2177 - 2185

[7] EVIDENCE FOR HEMIACETAL FORMATION BETWEEN N-ACYL-L-PHENYLALANINALS AND ALPHA-CHYMOTRYPSIN BY CROSS-SATURATION NUCLEAR MAGNETIC-RESONANCE SPECTROSCOPY [J]. BIOCHEMISTRY, 1979, 18 (05) : 921 - 926

[8] PYRAZOLE BINDING IN CRYSTALLINE BINARY AND TERNARY COMPLEXES WITH LIVER ALCOHOL-DEHYDROGENASE [J]. BIOCHEMISTRY, 1982, 21 (20) : 4858 - 4866

[9] COMPETITIVE INHIBITION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE BY ML-236A AND ML-236B FUNGAL METABOLITES, HAVING HYPOCHOLESTEROLEMIC ACTIVITY [J]. FEBS LETTERS, 1976, 72 (02) : 323 - 326

[10] LEAVING GROUP SPECIFICITY IN CHYMOTRYPSIN-CATALYZED HYDROLYSIS OF PEPTIDES - STEREOCHEMICAL INTERPRETATION [J]. BIOCHEMISTRY, 1973, 12 (11) : 2035 - 2041