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Results: 1-10 |
Results: 10
Quantitation of rate enhancements attained by the binding of cobalamin to methionine synthase
Authors: Bandarian, V Matthews, RG
Citation: V. Bandarian et Rg. Matthews, Quantitation of rate enhancements attained by the binding of cobalamin to methionine synthase, BIOCHEM, 40(16), 2001, pp. 5056-5064
5 '-deoxyadenosine contacts the substrate radical intermediate in the active site of ethanolamine ammonia-lyase: H-2 and C-13 electron nuclear doubleresonance studies
Authors: LoBrutto, R Bandarian, V Magnusson, OT Chen, XY Schramm, VL Reed, GH
Citation: R. Lobrutto et al., 5 '-deoxyadenosine contacts the substrate radical intermediate in the active site of ethanolamine ammonia-lyase: H-2 and C-13 electron nuclear doubleresonance studies, BIOCHEM, 40(1), 2001, pp. 9-14
Inhibition of lysine 2,3-aminomutase by the alternative substrate 4-thialysine and characterization of the 4-thialysyl radical intermediate
Authors: Miller, J Bandarian, V Reed, GH Frey, PA
Citation: J. Miller et al., Inhibition of lysine 2,3-aminomutase by the alternative substrate 4-thialysine and characterization of the 4-thialysyl radical intermediate, ARCH BIOCH, 387(2), 2001, pp. 281-288
Isotope effects in the transient phases of the reaction catalyzed by ethanolamine ammonia-lyase: Determination of the number of exchangeable hydrogens in the enzyme-cofactor complex
Authors: Bandarian, V Reed, GH
Citation: V. Bandarian et Gh. Reed, Isotope effects in the transient phases of the reaction catalyzed by ethanolamine ammonia-lyase: Determination of the number of exchangeable hydrogens in the enzyme-cofactor complex, BIOCHEM, 39(39), 2000, pp. 12069-12075
Lysine 2,3-aminomutase and trans-4,5-dehydrolysine: Characterization of anallylic analogue of a substrate-based radical in the catalytic mechanism?
Authors: Wu, WM Booker, S Lieder, KW Bandarian, V Reed, GH Frey, PA
Citation: Wm. Wu et al., Lysine 2,3-aminomutase and trans-4,5-dehydrolysine: Characterization of anallylic analogue of a substrate-based radical in the catalytic mechanism?, BIOCHEM, 39(31), 2000, pp. 9561-9570
Identification of cis-ethanesemidione as the organic radical derived from glycolaldehyde in the suicide inactivation of dioldehydrase and of ethanolamine ammonia-lyase
Authors: Abend, A Bandarian, V Reed, GH Frey, PA
Citation: A. Abend et al., Identification of cis-ethanesemidione as the organic radical derived from glycolaldehyde in the suicide inactivation of dioldehydrase and of ethanolamine ammonia-lyase, BIOCHEM, 39(20), 2000, pp. 6250-6257
Characterization of a unique coenzyme B-6 radical in the ascarylose biosynthetic pathway
Authors: Chang, CWT Johnson, DA Bandarian, V Zhou, HQ LoBrutto, R Reed, GH Liu, HW
Citation: Cwt. Chang et al., Characterization of a unique coenzyme B-6 radical in the ascarylose biosynthetic pathway, J AM CHEM S, 122(17), 2000, pp. 4239-4240
Hydrazine cation radical in the active site of ethanolamine ammonia-lyase:Mechanism-based inactivation by hydroxyethylhydrazine
Authors: Bandarian, V Reed, GH
Citation: V. Bandarian et Gh. Reed, Hydrazine cation radical in the active site of ethanolamine ammonia-lyase:Mechanism-based inactivation by hydroxyethylhydrazine, BIOCHEM, 38(38), 1999, pp. 12394-12402
Hydrogen atom exchange between 5 '-deoxyadenosine and hydroxyethylhydrazine during the single turnover inactivation of ethanolamine ammonia-lyase
Authors: Bandarian, V Poyner, RR Reed, GH
Citation: V. Bandarian et al., Hydrogen atom exchange between 5 '-deoxyadenosine and hydroxyethylhydrazine during the single turnover inactivation of ethanolamine ammonia-lyase, BIOCHEM, 38(38), 1999, pp. 12403-12407
Ethanolamine ammonia-lyase has a "base-on" binding mode for coenzyme B-12
Authors: Abend, A Bandarian, V Nitsche, R Stupperich, E Retey, J Reed, GH
Citation: A. Abend et al., Ethanolamine ammonia-lyase has a "base-on" binding mode for coenzyme B-12, ARCH BIOCH, 370(1), 1999, pp. 138-141
Risultati: 1-10 |