-
1
-
-
0028930481
-
Mechanism-Based Enzyme Inactivators
-
Silverman, R. B. Mechanism-Based Enzyme Inactivators. Methods Enzymol. 1995, 249, 240-283.
-
(1995)
Methods Enzymol
, vol.249
, pp. 240-283
-
-
Silverman, R.B.1
-
3
-
-
10644266789
-
Mediators of Chronic Obstructive Pulmonary Disease
-
(b) Barnes, P. J. Mediators of Chronic Obstructive Pulmonary Disease. Pharmacol. Rev. 2004, 56, 515-548.
-
(2004)
Pharmacol. Rev
, vol.56
, pp. 515-548
-
-
Barnes, P.J.1
-
4
-
-
20444480168
-
COPD: Current Therapeutic Interventions and Future Approaches
-
(c) Barnes, P. J.; Stockley, R. A. COPD: Current Therapeutic Interventions and Future Approaches. Eur. Respir. J. 2005, 25, 1984-1106.
-
(2005)
Eur. Respir. J
, vol.25
, pp. 1984-1106
-
-
Barnes, P.J.1
Stockley, R.A.2
-
6
-
-
0344413022
-
Neutrophil Elastase Contributes to Cigarette Smoke-Induced Emphysema in Mice
-
(e) Shapiro, S. D.; Goldstein, N. M.; Houghton, A. M.; Kobayashi, D. K.; Kelley, D.; Belaaouaj, A. Neutrophil Elastase Contributes to Cigarette Smoke-Induced Emphysema in Mice. Am. J. Pathol. 2003, 163, 2329-2335.
-
(2003)
Am. J. Pathol
, vol.163
, pp. 2329-2335
-
-
Shapiro, S.D.1
Goldstein, N.M.2
Houghton, A.M.3
Kobayashi, D.K.4
Kelley, D.5
Belaaouaj, A.6
-
7
-
-
0031443570
-
Inhibition of Neutrophil Elastase in CF Sputum by L-658,758
-
(f) Rees, D. D.; Brain, J. D.; Wohl, M. E.; Humes, J. L.; Mumford, R. A. Inhibition of Neutrophil Elastase in CF Sputum by L-658,758. J. Pharmacol. Exp. Ther. 1997, 283, 1201-1206.
-
(1997)
J. Pharmacol. Exp. Ther
, vol.283
, pp. 1201-1206
-
-
Rees, D.D.1
Brain, J.D.2
Wohl, M.E.3
Humes, J.L.4
Mumford, R.A.5
-
9
-
-
0032930510
-
The Protease-Antiprotease Battle in the Cystic Fibrosis Lung
-
(h) Balfour-Lynn, I. M. The Protease-Antiprotease Battle in the Cystic Fibrosis Lung. J. R. Soc. Med. 1999, 92, S23-S30.
-
(1999)
J. R. Soc. Med
, vol.92
-
-
Balfour-Lynn, I.M.1
-
10
-
-
0035117026
-
Proteinase 3, Wegener's Autoantigen: From Gene to Antigen
-
(i) Van Der Geld, Y. M.; Limburg, P. C.; Kallenberg, C. G. Proteinase 3, Wegener's Autoantigen: From Gene to Antigen. J. Leuk. Biol. 2001, 69, 177-190.
-
(2001)
J. Leuk. Biol
, vol.69
, pp. 177-190
-
-
Van Der Geld, Y.M.1
Limburg, P.C.2
Kallenberg, C.G.3
-
11
-
-
0030993410
-
Structure-Based Design of a General Class of Mechanism-Based Inhibitors of the Serine Proteinases Employing a Novel Amino Acid-Derived Heterocyclic Scaffold
-
(a) Groutas, W. C.; Kuang, R.; Venkataraman, R.; Epp, J. B.; Ruan, S.; Prakash, O. Structure-Based Design of a General Class of Mechanism-Based Inhibitors of the Serine Proteinases Employing a Novel Amino Acid-Derived Heterocyclic Scaffold. Biochemistry 1997, 36, 4739-4750.
-
(1997)
Biochemistry
, vol.36
, pp. 4739-4750
-
-
Groutas, W.C.1
Kuang, R.2
Venkataraman, R.3
Epp, J.B.4
Ruan, S.5
Prakash, O.6
-
12
-
-
0031835168
-
Potent and Specific Inhibition of Human Leukocyte Elastase, Cathepsin G and Proteinase 3 by Sulfone Derivatives Employing the 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide Scaffold
-
(b) Groutas, W. C.; Kuang, R.; Ruan, S.; Epp, J. B.; Venkataraman, R.; Truong, T. M. Potent and Specific Inhibition of Human Leukocyte Elastase, Cathepsin G and Proteinase 3 by Sulfone Derivatives Employing the 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide Scaffold. Bioorg. Med. Chem. 1998, 6, 661-671.
-
(1998)
Bioorg. Med. Chem
, vol.6
, pp. 661-671
-
-
Groutas, W.C.1
Kuang, R.2
Ruan, S.3
Epp, J.B.4
Venkataraman, R.5
Truong, T.M.6
-
13
-
-
0032478061
-
Use of the 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide and Isothiazolidin-3-one 1,1-Dioxide Scaffolds in the Design of Potent Inhibitors of Serine Proteinases
-
(c) Kuang, R.; Venkataraman, R.; Ruan, S.; Groutas, W. C. Use of the 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide and Isothiazolidin-3-one 1,1-Dioxide Scaffolds in the Design of Potent Inhibitors of Serine Proteinases. Bioorg. Med. Chem. Lett. 1998, 8, 539-544.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 539-544
-
-
Kuang, R.1
Venkataraman, R.2
Ruan, S.3
Groutas, W.C.4
-
14
-
-
0034088325
-
Utilization of the 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide Scaffold in the Design of Potent Inhibitors of Serine Proteases: SAR Studies Using Carboxylates
-
(d) Kuang, R.; Epp, J. B.; Ruan, S.; Chong, L. S.; Venkataraman, R.; Tu, J.; He, S.; Truong, T. M.; Groutas, W. C. Utilization of the 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide Scaffold in the Design of Potent Inhibitors of Serine Proteases: SAR Studies Using Carboxylates. Bioorg. Med. Chem. 2000, 8, 1005-1016.
-
(2000)
Bioorg. Med. Chem
, vol.8
, pp. 1005-1016
-
-
Kuang, R.1
Epp, J.B.2
Ruan, S.3
Chong, L.S.4
Venkataraman, R.5
Tu, J.6
He, S.7
Truong, T.M.8
Groutas, W.C.9
-
15
-
-
0033919340
-
Potent Inhibition of Serine Proteases by Heterocyclic Sulfide Derivatives of 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide
-
(e) He, S.; Kuang, R.; Venkataraman, R.; Tu, J.; Truong, T. M.; Chan, H-K.; Groutas, W. C. Potent Inhibition of Serine Proteases by Heterocyclic Sulfide Derivatives of 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide. Bioorg. Med. Chem. 2000, 8, 1713-1717.
-
(2000)
Bioorg. Med. Chem
, vol.8
, pp. 1713-1717
-
-
He, S.1
Kuang, R.2
Venkataraman, R.3
Tu, J.4
Truong, T.M.5
Chan, H.-K.6
Groutas, W.C.7
-
16
-
-
14744287476
-
1,2,5-Thiadiazolidin-3-one 1,1-Dioxide-Based Heterocyclic Sulfides are Potent Inhibitors of Human Tryptase
-
(f) Wong, T.; Groutas, C. S.; Mohan, S.; Lai, Z.; Alliston, K. R.; Vu, N.; Schechter, N. M.; Groutas, W. C. 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide-Based Heterocyclic Sulfides are Potent Inhibitors of Human Tryptase. Arch. Biochem. Biophys. 2005, 436, 1-7.
-
(2005)
Arch. Biochem. Biophys
, vol.436
, pp. 1-7
-
-
Wong, T.1
Groutas, C.S.2
Mohan, S.3
Lai, Z.4
Alliston, K.R.5
Vu, N.6
Schechter, N.M.7
Groutas, W.C.8
-
17
-
-
3543002291
-
Mechanism-Based Inactivation of Human Leukocyte Elastase via an Enzyme-Induced Sulfonamide Fragmentation Process
-
(g) Wei, L.; Lai, Z.; Gan, X.; Alliston, K. R.; Zhong, J.; Epp, J. B.; Tu, J.; Perera, A. B.; Van Sipdonk, M.; Groutas, W. C. Mechanism-Based Inactivation of Human Leukocyte Elastase via an Enzyme-Induced Sulfonamide Fragmentation Process. Arch. Biochem. Biophys. 2004, 429, 60-70.
-
(2004)
Arch. Biochem. Biophys
, vol.429
, pp. 60-70
-
-
Wei, L.1
Lai, Z.2
Gan, X.3
Alliston, K.R.4
Zhong, J.5
Epp, J.B.6
Tu, J.7
Perera, A.B.8
Van Sipdonk, M.9
Groutas, W.C.10
-
18
-
-
4143055869
-
Potent Inhibition of Human Leukocyte Elastase by 1,2,5-Thiadiazolidin-one 1,1-Dioxide-Based Sulfonamide Derivatives
-
(h) Lai, Z.; Gan, X.; Wei, L.; Alliston, K. R.; Yu, H.; Li, Y. H.; Groutas, W. C. Potent Inhibition of Human Leukocyte Elastase by 1,2,5-Thiadiazolidin-one 1,1-Dioxide-Based Sulfonamide Derivatives. Arch. Biochem. Biophys. 2004, 429, 191-197.
-
(2004)
Arch. Biochem. Biophys
, vol.429
, pp. 191-197
-
-
Lai, Z.1
Gan, X.2
Wei, L.3
Alliston, K.R.4
Yu, H.5
Li, Y.H.6
Groutas, W.C.7
-
19
-
-
0014211618
-
-
Nomenclature used is that of Schechterzp, I, Berger, A. xx. Biochem. Biophys. Res. Commun. 1967, 27, 157-162, where S 1, S2, S3, S n and S1′, S2′, S3′, Sn′ correspond to the enzyme subsites on either side of the scissile bond. Each subsite accommodates a corresponding amino acid residue side chain designated P1, P2, P3, Pn and P1′, P2′, P 3′, Pn′ of the substrate or inhibitor, S1 is the primary substrate specificity subsite, and P1-P1′ is the scissile bond
-
1′ is the scissile bond.
-
-
-
-
20
-
-
0034780680
-
1,2,5-Thiadiazolidin-3-one 1,1-Dioxide: A Powerful Scaffold for Probing the S′ Subsites of (Chymo)trypsin-like Serine Proteases
-
(a) Groutas, W. C.; Epp, J. B.; Kuang, R.; Ruan, S.; Chong, L. S.; Venkataraman, R.; Tu, J.; He, S.; Yu, H.; Fu, Q.; Li, Y-H.; Truong, T. M.; Vu, N. T. 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide: A Powerful Scaffold for Probing the S′ Subsites of (Chymo)trypsin-like Serine Proteases. Arch. Biochem. Biophys. 2001, 385, 162-169.
-
(2001)
Arch. Biochem. Biophys
, vol.385
, pp. 162-169
-
-
Groutas, W.C.1
Epp, J.B.2
Kuang, R.3
Ruan, S.4
Chong, L.S.5
Venkataraman, R.6
Tu, J.7
He, S.8
Yu, H.9
Fu, Q.10
Li, Y.-H.11
Truong, T.M.12
Vu, N.T.13
-
21
-
-
0034942070
-
Inhibition of Serine Proteases by Functionalized Sulfonamides Coupled to the 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide Scaffold
-
(b) Groutas, W. C.; He, S.; Kuang, R.; Ruan, S.; Tu, J.; Chan, H-K. Inhibition of Serine Proteases by Functionalized Sulfonamides Coupled to the 1,2,5-Thiadiazolidin-3-one 1,1-Dioxide Scaffold. Bioorg. Med. Chem. 2001, 9, 1543-1548.
-
(2001)
Bioorg. Med. Chem
, vol.9
, pp. 1543-1548
-
-
Groutas, W.C.1
He, S.2
Kuang, R.3
Ruan, S.4
Tu, J.5
Chan, H.-K.6
-
22
-
-
0033536494
-
A General Inhibitor Scaffold for Serine Proteases with a (Chymo)trypsin-like Fold: Solution-Phase Construction of the First Series of Libraries of Mechanism-Based Inhibitors
-
Kuang, R.; Epp, J. B.; Ruan, S.; Yu, H.; Huang, P.; He, S.; Tu, J.; Schechter, N. M.; Turbov, J.; Froelich, C. J.; Groutas, W. C. A General Inhibitor Scaffold for Serine Proteases with a (Chymo)trypsin-like Fold: Solution-Phase Construction of the First Series of Libraries of Mechanism-Based Inhibitors. J. Am. Chem. Soc. 1999, 121, 8128-8129.
-
(1999)
J. Am. Chem. Soc
, vol.121
, pp. 8128-8129
-
-
Kuang, R.1
Epp, J.B.2
Ruan, S.3
Yu, H.4
Huang, P.5
He, S.6
Tu, J.7
Schechter, N.M.8
Turbov, J.9
Froelich, C.J.10
Groutas, W.C.11
-
23
-
-
0025314849
-
Degradation of Basement Laminin by Human Neutrophil Elastase
-
(a) Abrahamson, D. R.; Irvin, M. H.; Blackburn, W. D.; Heck, L. W. Degradation of Basement Laminin by Human Neutrophil Elastase. Am. J. Pathol. 1990, 136, 1267-1274.
-
(1990)
Am. J. Pathol
, vol.136
, pp. 1267-1274
-
-
Abrahamson, D.R.1
Irvin, M.H.2
Blackburn, W.D.3
Heck, L.W.4
-
24
-
-
0032030785
-
Cleavage of Native Type I Collagen by Human Neutrophil Elastase
-
(b) Kafienah, W.; Buttle, D.; Hollander, A. P. Cleavage of Native Type I Collagen by Human Neutrophil Elastase. Biochem. J. 1998, 330, 897-902.
-
(1998)
Biochem. J
, vol.330
, pp. 897-902
-
-
Kafienah, W.1
Buttle, D.2
Hollander, A.P.3
-
25
-
-
0025776716
-
Characterization of Proteinase 3, A Neutrophil Serine Proteinase. Structural and Functional Properties
-
(c) Rao, N. V.; Wehner, N. G.; Marshall, B. C.; Gary, W. R.; Gray, B. H.; Hoidal, J. R. Characterization of Proteinase 3, A Neutrophil Serine Proteinase. Structural and Functional Properties. J. Biol. Chem. 1991, 266, 9540-9548.
-
(1991)
J. Biol. Chem
, vol.266
, pp. 9540-9548
-
-
Rao, N.V.1
Wehner, N.G.2
Marshall, B.C.3
Gary, W.R.4
Gray, B.H.5
Hoidal, J.R.6
-
26
-
-
0024571818
-
Human Leukocyte Elastase and Porcine Pancreatic Elastase: X-ray Crystal Structures, Mechanism, Substrate Specificity, and Mechanism-Based Inhibition
-
Bode, W.; Meyer, E.; Powers, J. C. Human Leukocyte Elastase and Porcine Pancreatic Elastase: X-ray Crystal Structures, Mechanism, Substrate Specificity, and Mechanism-Based Inhibition. Biochemistry 1989, 28, 1951-1963.
-
(1989)
Biochemistry
, vol.28
, pp. 1951-1963
-
-
Bode, W.1
Meyer, E.2
Powers, J.C.3
-
27
-
-
0029833222
-
The Crystal Structure of PR 3, A Neutrophil Serine Proteinase Antigen of Wegener's Granulomatosis Antibodies
-
Fujinaga, M.; Chenaia, M. M.; Halenbeck, R.; Koths, K.; James, M. N. G. The Crystal Structure of PR 3, A Neutrophil Serine Proteinase Antigen of Wegener's Granulomatosis Antibodies. J. Mol. Biol. 1996, 261, 267-278.
-
(1996)
J. Mol. Biol
, vol.261
, pp. 267-278
-
-
Fujinaga, M.1
Chenaia, M.M.2
Halenbeck, R.3
Koths, K.4
James, M.N.G.5
-
28
-
-
0026486812
-
Human Neutrophil Proteinase 3: Mapping of the Substrate Binding Site Using Peptidyl Thiobenzyl Esters
-
Brubaker, M. J.; Groutas, W. C.; Hoidal, J. R.; Rao, N. V. Human Neutrophil Proteinase 3: Mapping of the Substrate Binding Site Using Peptidyl Thiobenzyl Esters. Biochem. Biophys. Res. Comm. 1992, 188, 1318-1324.
-
(1992)
Biochem. Biophys. Res. Comm
, vol.188
, pp. 1318-1324
-
-
Brubaker, M.J.1
Groutas, W.C.2
Hoidal, J.R.3
Rao, N.V.4
-
29
-
-
0026516023
-
Substrate and Inhibitor Studies on Proteinase 3
-
Kam, C. M.; Kerrigan, J. E.; Dolman, K. M.; Goldschmeding, R.; Von dem Borne, A. E.; Powers, J. C. Substrate and Inhibitor Studies on Proteinase 3. FEBS Lett. 1992, 297, 119-123.
-
(1992)
FEBS Lett
, vol.297
, pp. 119-123
-
-
Kam, C.M.1
Kerrigan, J.E.2
Dolman, K.M.3
Goldschmeding, R.4
Von dem Borne, A.E.5
Powers, J.C.6
-
30
-
-
0038306865
-
Compared Action of Neutrophil Proteinase 3 and Elastase on Model Substrates. Favorable Effect of S′-P′ Interactions on Proteinase 3 Catalysis
-
Korkmaz, B.; Knight, G.; Bieth, J. Compared Action of Neutrophil Proteinase 3 and Elastase on Model Substrates. Favorable Effect of S′-P′ Interactions on Proteinase 3 Catalysis. J. Biol. Chem. 2003, 278, 12609-12612.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 12609-12612
-
-
Korkmaz, B.1
Knight, G.2
Bieth, J.3
-
31
-
-
33144464593
-
Inspection of the Binding Sites of Proteinase 3 for the Design of a Highly Specific Substrate
-
Hajjar, E.; Korkmaz, B.; Gautheir, F.; Brandsdal, B. O.; Witko-Sarsat, V.; Reuter, N. Inspection of the Binding Sites of Proteinase 3 for the Design of a Highly Specific Substrate. J. Med. Chem. 2006, 49, 1248-1260.
-
(2006)
J. Med. Chem
, vol.49
, pp. 1248-1260
-
-
Hajjar, E.1
Korkmaz, B.2
Gautheir, F.3
Brandsdal, B.O.4
Witko-Sarsat, V.5
Reuter, N.6
-
32
-
-
0023728105
-
The Behaviour and Significance of Slow Binding Inhibitors
-
(a) Morrison, J. F.; Walsh, C. T. The Behaviour and Significance of Slow Binding Inhibitors. Adv. Enzymol. 1988, 61, 201-301.
-
(1988)
Adv. Enzymol
, vol.61
, pp. 201-301
-
-
Morrison, J.F.1
Walsh, C.T.2
-
33
-
-
0027270445
-
New Mechanism-Based Inhibitors of Trypsin-like Proteinases. Selective Inhibition of Urokinase by Functionalized Cyclopeptides Incorporating a Sulfonomethyl-Substituted m-Aminobenzoic Acid
-
(b) Wakselman, M.; Xie, J.; Mazaleyrat, J. P. New Mechanism-Based Inhibitors of Trypsin-like Proteinases. Selective Inhibition of Urokinase by Functionalized Cyclopeptides Incorporating a Sulfonomethyl-Substituted m-Aminobenzoic Acid. J. Med. Chem. 1993, 36, 1539-1547.
-
(1993)
J. Med. Chem
, vol.36
, pp. 1539-1547
-
-
Wakselman, M.1
Xie, J.2
Mazaleyrat, J.P.3
-
34
-
-
0032510807
-
Novel Natural Product 5,5-trans-Lactone Inhibitors of Human alpha-Thrombin: Mechanism of Action and Structural Studies
-
(c) Weir, M. P.; Bethell, S. S.; Cleasby, A.; Campbell, C. J.; Dennis, R. J.; Dix, C. J.; Finch, H.; Jhoti, H.; Mooney, C. J.; Patel, S.; Tang, C-M.; Ward, M.; Wonacott, A. J.; Wharton, C. W. Novel Natural Product 5,5-trans-Lactone Inhibitors of Human alpha-Thrombin: Mechanism of Action and Structural Studies. Biochemistry 1998, 37, 6645-6657.
-
(1998)
Biochemistry
, vol.37
, pp. 6645-6657
-
-
Weir, M.P.1
Bethell, S.S.2
Cleasby, A.3
Campbell, C.J.4
Dennis, R.J.5
Dix, C.J.6
Finch, H.7
Jhoti, H.8
Mooney, C.J.9
Patel, S.10
Tang, C.-M.11
Ward, M.12
Wonacott, A.J.13
Wharton, C.W.14
-
35
-
-
84863247738
-
Evaluation of Enzyme Inhibitors
-
Wiley: New York
-
(d) Copeland, R. A. Evaluation of Enzyme Inhibitors. In Drug Discovery; Wiley: New York, 2005.
-
(2005)
Drug Discovery
-
-
Copeland, R.A.1
-
36
-
-
33845339435
-
Protease Inhibitors in the Clinic
-
(a) Abbenante, G.; Fairlie, D. P. Protease Inhibitors in the Clinic. Med. Chem. 2005, 1, 71-104.
-
(2005)
Med. Chem
, vol.1
, pp. 71-104
-
-
Abbenante, G.1
Fairlie, D.P.2
-
37
-
-
0003567457
-
-
Smith, H. J, Simons, C, Eds, Taylor and Francis: London
-
(b) Edwards, P. D. In Proteinase and Peptidase Inhibition; Smith, H. J., Simons, C., Eds.; Taylor and Francis: London, 2002.
-
(2002)
Proteinase and Peptidase Inhibition
-
-
Edwards, P.D.1
-
38
-
-
0037009199
-
Clarification of the Mechanism of Human Sputum Elastase Inhibition by a New Inhibitor, ONO-5046, Using Electrospray Ionization Mass Spectrometry
-
(a) Nakayama, Y.; Odakagi, Y.; Fujita, S.; Matsuoka, S.; Kamanaka, N.; Nakai, H.; Toda, M. Clarification of the Mechanism of Human Sputum Elastase Inhibition by a New Inhibitor, ONO-5046, Using Electrospray Ionization Mass Spectrometry. Bioorg. Med. Chem. 2002, 12, 2349-2353.
-
(2002)
Bioorg. Med. Chem
, vol.12
, pp. 2349-2353
-
-
Nakayama, Y.1
Odakagi, Y.2
Fujita, S.3
Matsuoka, S.4
Kamanaka, N.5
Nakai, H.6
Toda, M.7
-
39
-
-
0027405045
-
Electrospray Ionization Mass Spectrometry as a Mechanistic Tool: Mass of Human Leukocyte Elastase and a β-Lactam-Derived E-I Complex
-
(b) Knight, W. B.; Swiderek, K. M.; Sakuma, T.; Calaycay, J.; Shively, J. E.; Lee, T. D.; Covey, T. R.; Shushan, B.; Green, B. G.; Chabin, R.; Shah, S.; Mumford, R.; Dickinson, T. A.; Griffin, P. R. Electrospray Ionization Mass Spectrometry as a Mechanistic Tool: Mass of Human Leukocyte Elastase and a β-Lactam-Derived E-I Complex. Biochemistry 1993, 32, 2031-2035.
-
(1993)
Biochemistry
, vol.32
, pp. 2031-2035
-
-
Knight, W.B.1
Swiderek, K.M.2
Sakuma, T.3
Calaycay, J.4
Shively, J.E.5
Lee, T.D.6
Covey, T.R.7
Shushan, B.8
Green, B.G.9
Chabin, R.10
Shah, S.11
Mumford, R.12
Dickinson, T.A.13
Griffin, P.R.14
-
40
-
-
0031059866
-
Processing of X-ray Diffraction Data Collected in Oscillation Mode
-
Otwinowski, Z.; Minor, W. Processing of X-ray Diffraction Data Collected in Oscillation Mode. Methods Enzymol. 1997, 276, 307-326.
-
(1997)
Methods Enzymol
, vol.276
, pp. 307-326
-
-
Otwinowski, Z.1
Minor, W.2
-
41
-
-
0035788107
-
Pushing the Boundaries of Molecular Replacement with Maximum Likelihood
-
Read, R. J. Pushing the Boundaries of Molecular Replacement with Maximum Likelihood. Acta Crystallogr. 2001, D57, 1373-1382.
-
(2001)
Acta Crystallogr
, vol.D57
, pp. 1373-1382
-
-
Read, R.J.1
-
42
-
-
84889120137
-
Improved Methods for Building Protein Models in Electron Density Maps and the Location of Errors in These Models
-
Jones, T. A.; Zhou, J. Y.; Cowan, S. W.; Kjelgaard, M. Improved Methods for Building Protein Models in Electron Density Maps and the Location of Errors in These Models. Acta Crystallogr. 1991, 47, 110-119.
-
(1991)
Acta Crystallogr
, vol.47
, pp. 110-119
-
-
Jones, T.A.1
Zhou, J.Y.2
Cowan, S.W.3
Kjelgaard, M.4
-
43
-
-
3543012707
-
Crystallography and NMR System: A New Software Suite for Macromolecular Structure determination
-
Brünger, A. T.; Adams, P. D.; Clore, G. M.; Delano, W. L.; Gros, P.; Grosse-Kunstleve, R. W. Crystallography and NMR System: A New Software Suite for Macromolecular Structure determination. Acta Crystallogr. 1998, 54, 905-921.
-
(1998)
Acta Crystallogr
, vol.54
, pp. 905-921
-
-
Brünger, A.T.1
Adams, P.D.2
Clore, G.M.3
Delano, W.L.4
Gros, P.5
Grosse-Kunstleve, R.W.6
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