-
1
-
-
0032475836
-
The low barrier hydrogen bond in enzymatic catalysis
-
Cleland WW, Frey PA, Gerlt JA (1998) The low barrier hydrogen bond in enzymatic catalysis. J Biol Chem 273(40):25529-25532.
-
(1998)
J Biol Chem
, vol.273
, Issue.40
, pp. 25529-25532
-
-
Cleland, W.W.1
Frey, P.A.2
Gerlt, J.A.3
-
2
-
-
0343006258
-
Site-directed mutagenesis and the role of the oxyanion hole in subtilisin
-
Bryan P, Pantoliano MW, Quill SG, Hsiao HY, Poulos T (1986) Site-directed mutagenesis and the role of the oxyanion hole in subtilisin. Proc Natl Acad Sci USA 83(11):3743-3745.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, Issue.11
, pp. 3743-3745
-
-
Bryan, P.1
Pantoliano, M.W.2
Quill, S.G.3
Hsiao, H.Y.4
Poulos, T.5
-
3
-
-
0028918401
-
A proficient enzyme
-
Radzicka A, Wolfenden R (1995) A proficient enzyme. Science 267(5194):90-93.
-
(1995)
Science
, vol.267
, Issue.5194
, pp. 90-93
-
-
Radzicka, A.1
Wolfenden, R.2
-
4
-
-
38849119713
-
Carbon isotope effect study on orotidine 5′-monophosphate decarboxylase: Support for an anionic intermediate
-
Van Vleet JL, Reinhardt LA, Miller BG, Sievers A, Cleland WW (2008) Carbon isotope effect study on orotidine 5′-monophosphate decarboxylase: Support for an anionic intermediate. Biochemistry 47(2):798-803.
-
(2008)
Biochemistry
, vol.47
, Issue.2
, pp. 798-803
-
-
Van Vleet, J.L.1
Reinhardt, L.A.2
Miller, B.G.3
Sievers, A.4
Cleland, W.W.5
-
5
-
-
0034102419
-
Electrostatic stress in catalysis: Structure and mechanism of the enzyme orotidine monophosphate decarboxylase
-
Wu N, Mo Y, Gao J, Pai EF (2000) Electrostatic stress in catalysis: Structure and mechanism of the enzyme orotidine monophosphate decarboxylase. Proc Natl Acad Sci USA 97(5):2017-2022.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, Issue.5
, pp. 2017-2022
-
-
Wu, N.1
Mo, Y.2
Gao, J.3
Pai, E.F.4
-
6
-
-
8844240654
-
OMP decarboxylase: An experimental test of electrostatic destabilization of the enzyme-substrate complex
-
Callahan BP, Wolfenden R (2004) OMP decarboxylase: An experimental test of electrostatic destabilization of the enzyme-substrate complex. J Am Chem Soc 126(45):14698-14699.
-
(2004)
J Am Chem Soc
, vol.126
, Issue.45
, pp. 14698-14699
-
-
Callahan, B.P.1
Wolfenden, R.2
-
7
-
-
0035805488
-
Dissecting a charged network at the active site of orotidine-5′-phosphate decarboxylase
-
Miller BG, Snider MJ, Wolfenden R, Short SA (2001) Dissecting a charged network at the active site of orotidine-5′-phosphate decarboxylase. J Biol Chem 276(18):15174-15176.
-
(2001)
J Biol Chem
, vol.276
, Issue.18
, pp. 15174-15176
-
-
Miller, B.G.1
Snider, M.J.2
Wolfenden, R.3
Short, S.A.4
-
8
-
-
80053406780
-
Mechanism of the orotidine 5′-monophosphate decarboxylase-catalyzed reaction: Importance of residues in the orotate binding site
-
Iiams V, et al. (2011) Mechanism of the orotidine 5′-monophosphate decarboxylase-catalyzed reaction: Importance of residues in the orotate binding site. Biochemistry 50(39):8497-8507.
-
(2011)
Biochemistry
, vol.50
, Issue.39
, pp. 8497-8507
-
-
Iiams, V.1
-
9
-
-
67649210974
-
Mechanism of the orotidine 5′-monophosphate decarboxylase-catalyzed reaction: Evidence for substrate destabilization
-
Chan KK, et al. (2009) Mechanism of the orotidine 5′-monophosphate decarboxylase-catalyzed reaction: Evidence for substrate destabilization. Biochemistry 48(24):5518-5531.
-
(2009)
Biochemistry
, vol.48
, Issue.24
, pp. 5518-5531
-
-
Chan, K.K.1
-
10
-
-
84888355894
-
Substrate distortion contributes to the catalysis of orotidine 5′-monophosphate decarboxylase
-
Fujihashi M, et al. (2013) Substrate distortion contributes to the catalysis of orotidine 5′-monophosphate decarboxylase. J Am Chem Soc 135(46):17432-17443.
-
(2013)
J Am Chem Soc
, vol.135
, Issue.46
, pp. 17432-17443
-
-
Fujihashi, M.1
-
11
-
-
0035793646
-
Crystal structures of orotidine monophosphate decarboxylase: Does the structure reveal the mechanism of nature's most proficient enzyme?
-
Houk KN, Lee JK, Tantillo DJ, Bahmanyar S, Hietbrink BN (2001) Crystal structures of orotidine monophosphate decarboxylase: Does the structure reveal the mechanism of nature's most proficient enzyme? ChemBioChem 2(2):113-118.
-
(2001)
ChemBioChem
, vol.2
, Issue.2
, pp. 113-118
-
-
Houk, K.N.1
Lee, J.K.2
Tantillo, D.J.3
Bahmanyar, S.4
Hietbrink, B.N.5
-
12
-
-
35848965479
-
Product deuterium isotope effect for orotidine 5′-monophosphate decarboxylase: Evidence for the existence of a short-lived carbanion intermediate
-
Toth K, et al. (2007) Product deuterium isotope effect for orotidine 5′-monophosphate decarboxylase: Evidence for the existence of a short-lived carbanion intermediate. J Am Chem Soc 129(43):12946-12947.
-
(2007)
J Am Chem Soc
, vol.129
, Issue.43
, pp. 12946-12947
-
-
Toth, K.1
-
13
-
-
38949172353
-
Formation and stability of a vinyl carbanion at the active site of orotidine 5′-monophosphate decarboxylase: PKa of the C-6 proton of enzyme-bound UMP
-
Amyes TL, Wood BM, Chan K, Gerlt JA, Richard JP (2008) Formation and stability of a vinyl carbanion at the active site of orotidine 5′-monophosphate decarboxylase: pKa of the C-6 proton of enzyme-bound UMP. J Am Chem Soc 130(5):1574-1575.
-
(2008)
J Am Chem Soc
, vol.130
, Issue.5
, pp. 1574-1575
-
-
Amyes, T.L.1
Wood, B.M.2
Chan, K.3
Gerlt, J.A.4
Richard, J.P.5
-
14
-
-
77952556805
-
Product deuterium isotope effects for orotidine 5′-monophosphate decarboxylase: Effect of changing substrate and enzyme structure on the partitioning of the vinyl carbanion reaction intermediate
-
Toth K, et al. (2010) Product deuterium isotope effects for orotidine 5′-monophosphate decarboxylase: Effect of changing substrate and enzyme structure on the partitioning of the vinyl carbanion reaction intermediate. J Am Chem Soc 132(20):7018-7024.
-
(2010)
J Am Chem Soc
, vol.132
, Issue.20
, pp. 7018-7024
-
-
Toth, K.1
-
15
-
-
0030912339
-
A proficient enzyme revisited: The predicted mechanism for orotidine monophosphate decarboxylase
-
Lee JK, Houk KN (1997) A proficient enzyme revisited: The predicted mechanism for orotidine monophosphate decarboxylase. Science 276(5314):942-945.
-
(1997)
Science
, vol.276
, Issue.5314
, pp. 942-945
-
-
Lee, J.K.1
Houk, K.N.2
-
16
-
-
37149000703
-
Synthesis of polyester by means of genetic code reprogramming
-
Ohta A, Murakami H, Higashimura E, Suga H (2007) Synthesis of polyester by means of genetic code reprogramming. Chem Biol 14(12):1315-1322.
-
(2007)
Chem Biol
, vol.14
, Issue.12
, pp. 1315-1322
-
-
Ohta, A.1
Murakami, H.2
Higashimura, E.3
Suga, H.4
-
17
-
-
79958158209
-
Flexizymes for genetic code reprogramming
-
Goto Y, Katoh T, Suga H (2011) Flexizymes for genetic code reprogramming. Nat Protoc 6(6):779-790.
-
(2011)
Nat Protoc
, vol.6
, Issue.6
, pp. 779-790
-
-
Goto, Y.1
Katoh, T.2
Suga, H.3
-
18
-
-
27844574242
-
Activation of orotidine 5′-monophosphate decarboxylase by phosphite dianion: The whole substrate is the sum of two parts
-
Amyes TL, Richard JP, Tait JJ (2005) Activation of orotidine 5′-monophosphate decarboxylase by phosphite dianion: The whole substrate is the sum of two parts. J Am Chem Soc 127(45):15708-15709.
-
(2005)
J Am Chem Soc
, vol.127
, Issue.45
, pp. 15708-15709
-
-
Amyes, T.L.1
Richard, J.P.2
Tait, J.J.3
-
19
-
-
67649173263
-
Mechanism of the orotidine 5′-monophosphate decarboxylase-catalyzed reaction: Effect of solvent viscosity on kinetic constants
-
Wood BM, Chan KK, Amyes TL, Richard JP, Gerlt JA (2009) Mechanism of the orotidine 5′-monophosphate decarboxylase-catalyzed reaction: Effect of solvent viscosity on kinetic constants. Biochemistry 48(24):5510-5517.
-
(2009)
Biochemistry
, vol.48
, Issue.24
, pp. 5510-5517
-
-
Wood, B.M.1
Chan, K.K.2
Amyes, T.L.3
Richard, J.P.4
Gerlt, J.A.5
-
20
-
-
6444229663
-
QM/MM studies of the enzyme-catalyzed dechlorination of 4-chlor-obenzoyl-CoA provide insight into reaction energetics
-
Xu D, et al. (2004) QM/MM studies of the enzyme-catalyzed dechlorination of 4-chlor-obenzoyl-CoA provide insight into reaction energetics. J Am Chem Soc 126(42):13649-13658.
-
(2004)
J Am Chem Soc
, vol.126
, Issue.42
, pp. 13649-13658
-
-
Xu, D.1
-
21
-
-
72749112569
-
The thiolase reaction mechanism: The importance of Asn316 and His348 for stabilizing the enolate intermediate of the Claisen condensation
-
Meriläinen G, Poikela V, Kursula P, Wierenga RK (2009) The thiolase reaction mechanism: The importance of Asn316 and His348 for stabilizing the enolate intermediate of the Claisen condensation. Biochemistry 48(46):11011-11025.
-
(2009)
Biochemistry
, vol.48
, Issue.46
, pp. 11011-11025
-
-
Meriläinen, G.1
Poikela, V.2
Kursula, P.3
Wierenga, R.K.4
-
22
-
-
77951677267
-
Conformational changes in orotidine 5′-monophosphate decarboxylase: "Remote" residues that stabilize the active conformation
-
Wood BM, et al. (2010) Conformational changes in orotidine 5′-monophosphate decarboxylase: "Remote" residues that stabilize the active conformation. Biochemistry 49(17):3514-3516.
-
(2010)
Biochemistry
, vol.49
, Issue.17
, pp. 3514-3516
-
-
Wood, B.M.1
-
23
-
-
0034904102
-
Cell-free translation reconstituted with purified components
-
Shimizu Y, et al. (2001) Cell-free translation reconstituted with purified components. Nat Biotechnol 19(8):751-755.
-
(2001)
Nat Biotechnol
, vol.19
, Issue.8
, pp. 751-755
-
-
Shimizu, Y.1
-
24
-
-
80054854782
-
RF1 knockout allows ribosomal incorporation of unnatural amino acids at multiple sites
-
Johnson DB, et al. (2011) RF1 knockout allows ribosomal incorporation of unnatural amino acids at multiple sites. Nat Chem Biol 7(11):779-786.
-
(2011)
Nat Chem Biol
, vol.7
, Issue.11
, pp. 779-786
-
-
Johnson, D.B.1
-
25
-
-
84865206196
-
Release factor one is nonessential in Escherichia coli
-
Johnson DB, et al. (2012) Release factor one is nonessential in Escherichia coli. ACS Chem Biol 7(8):1337-1344.
-
(2012)
ACS Chem Biol
, vol.7
, Issue.8
, pp. 1337-1344
-
-
Johnson, D.B.1
-
26
-
-
33646044708
-
A highly flexible tRNA acylation method for non-natural polypeptide synthesis
-
Murakami H, Ohta A, Ashigai H, Suga H (2006) A highly flexible tRNA acylation method for non-natural polypeptide synthesis. Nat Methods 3(5):357-359.
-
(2006)
Nat Methods
, vol.3
, Issue.5
, pp. 357-359
-
-
Murakami, H.1
Ohta, A.2
Ashigai, H.3
Suga, H.4
-
27
-
-
84868089459
-
Conformational changes in orotidine 5′-monophosphate decarboxylase: A structure-based explanation for how the 5′-phosphate group activates the enzyme
-
Desai BJ, et al. (2012) Conformational changes in orotidine 5′-monophosphate decarboxylase: A structure-based explanation for how the 5′-phosphate group activates the enzyme. Biochemistry 51(43):8665-8678.
-
(2012)
Biochemistry
, vol.51
, Issue.43
, pp. 8665-8678
-
-
Desai, B.J.1
-
28
-
-
0842341771
-
Development and use of quantum mechanical molecular models. 76. AM1: A new general purpose quantum mechanical molecular model
-
Dewar MJS, Zoebisch EG, Healy EF, Stewart JJP (1985) Development and use of quantum mechanical molecular models. 76. AM1: A new general purpose quantum mechanical molecular model. J Am Chem Soc 107(13):3902-3909.
-
(1985)
J Am Chem Soc
, vol.107
, Issue.13
, pp. 3902-3909
-
-
Dewar, M.J.S.1
Zoebisch, E.G.2
Healy, E.F.3
Stewart, J.J.P.4
-
29
-
-
84986512474
-
CHARMM: A program for macromolecular energy, minimization, and dynamics calculations
-
Brooks BR, et al. (1983) CHARMM: A program for macromolecular energy, minimization, and dynamics calculations. J Comput Chem 4(2):187-217.
-
(1983)
J Comput Chem
, vol.4
, Issue.2
, pp. 187-217
-
-
Brooks, B.R.1
-
30
-
-
4444221565
-
UCSF Chimera - A visualization system for exploratory research and analysis
-
Pettersen EF, et al. (2004) UCSF Chimera - a visualization system for exploratory research and analysis. J Comput Chem 25(13):1605-1612.
-
(2004)
J Comput Chem
, vol.25
, Issue.13
, pp. 1605-1612
-
-
Pettersen, E.F.1
-
31
-
-
84987419408
-
Proposal for a common nomenclature for sequence ions in mass spectra of peptides
-
Roepstorff P, Fohlman J (1984) Proposal for a common nomenclature for sequence ions in mass spectra of peptides. Biomed Mass Spectrom 11(11):601.
-
(1984)
Biomed Mass Spectrom
, vol.11
, Issue.11
, pp. 601
-
-
Roepstorff, P.1
Fohlman, J.2
-
32
-
-
0025617140
-
Appendix 5. Nomenclature for peptide fragment ions (positive ions)
-
Biemann K (1990) Appendix 5. Nomenclature for peptide fragment ions (positive ions). Methods Enzymol 193:886-887.
-
(1990)
Methods Enzymol
, vol.193
, pp. 886-887
-
-
Biemann, K.1
|