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Lu, SM
Lu, WY
Qasim, MA
Anderson, S
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Ardelt, W
Bigler, T
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Cook, J
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Lin, TY
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Park, SJ
Qasim, S
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Tashiro, M
Warne, N
Whatley, H
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Wieczorek, M
Wilusz, T
Wynn, R
Zhang, WL
Laskowski, M
Citation: Sm. Lu et al., Predicting the reactivity of proteins from their sequence alone: Kazal family of protein inhibitors of serine proteinases, P NAS US, 98(4), 2001, pp. 1410-1415
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Anderson, S
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Qasim, MA
Laskowski, M
James, MNG
Citation: Ks. Bateman et al., Contribution of peptide bonds to inhibitor-protease binding: Crystal structures of the turkey ovomucoid third domain backbone variants OMTYK3-Pro18l and OMTKY3-psi[COO]-Leu18l in complex with Streptomyces griseus proteinase B (SGPB) and the structure of the free inhibitor, OMTKY3-psi[CH2NH2+]-Asp19l, J MOL BIOL, 305(4), 2001, pp. 839-849
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Toyota, E
Ng, KKS
Sekizaki, H
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Citation: E. Toyota et al., X-ray crystallographic analyses of complexes between bovine beta-trypsin and Schiff base copper(II) or iron(III) chelates, J MOL BIOL, 305(3), 2001, pp. 471-479
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Maynes, JT
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Citation: Jt. Maynes et al., Crystal structure of the tumor-promoter okadaic acid bound to protein phosphatase-1, J BIOL CHEM, 276(47), 2001, pp. 44078-44082
Authors:
Mark, BL
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Citation: Bl. Mark et al., Biochemical and structural assessment of the 1-N-azasugar GalNAc-isofagomine as a potent family 20 beta-N-acetylhexosaminidase inhibitor, J BIOL CHEM, 276(45), 2001, pp. 42131-42137
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Mark, BL
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Citation: Bl. Mark et al., Crystallographic evidence for substrate-assisted catalysis in a bacterial beta-hexosaminidase, J BIOL CHEM, 276(13), 2001, pp. 10330-10337
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Bateman, KS
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Laskowski, M
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Citation: Ks. Bateman et al., Deleterious effects of beta-branched residues in the S-1 specificity pocket of Streptomyces griseus proteinase B (SGPB): Crystal structures of the turkey ovomucoid third domain variants Ile18I, Val18I, Thr18I, and Ser18I in complex with SGPB, PROTEIN SCI, 9(1), 2000, pp. 83-94
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Fujinaga, M
Cherney, MM
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Citation: M. Fujinaga et al., Structural study of the complex between human pepsin and a phosphorus-containing peptidic transition-state analog, ACT CRYST D, 56, 2000, pp. 272-279
Authors:
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Citation: Jc. Rochet et al., Pig heart CoA transferase exists as two oligomeric forms separated by a large kinetic barrier, BIOCHEM, 39(37), 2000, pp. 11291-11302
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Citation: Ma. Joyce et al., ADP-binding site of Escherichia coli succinyl-CoA synthetase revealed by X-ray crystallography, BIOCHEM, 39(1), 2000, pp. 17-25
Authors:
Bernstein, NK
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Citation: Nk. Bernstein et al., Crystal structure of the novel aspartic proteinase zymogen proplasmepsin II from Plasmodium falciparum, NAT ST BIOL, 6(1), 1999, pp. 32-37
Authors:
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Citation: Jfw. Petersen et al., The structure of the 2A proteinase from a common cold virus: a proteinase responsible for the shut-off of host-cell protein synthesis, EMBO J, 18(20), 1999, pp. 5463-5475
Authors:
Bergmann, EM
Cherney, MM
Mckendrick, J
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Citation: Em. Bergmann et al., Crystal structure of an inhibitor complex of the 3C proteinase from hepatitis a virus (HAV) and implications for the polyprotein processing in HAV, VIROLOGY, 265(1), 1999, pp. 153-163
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Citation: Ar. Khan et al., Structural aspects of activation pathways of aspartic protease zymogens and viral 3C protease precursors, P NAS US, 96(20), 1999, pp. 10968-10975
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Fraser, ME
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Wolodko, WT
Citation: Dl. Bailey et al., A dimeric form of Escherichia coli succinyl-CoA synthetase produced by site-directed mutagenesis, J MOL BIOL, 285(4), 1999, pp. 1655-1666
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Lu, SM
Ding, JH
Bateman, KS
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Anderson, S
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Markley, JL
Ganz, PJ
Saunders, CW
Laskowski, M
Citation: Ma. Qasim et al., Thermodynamic criterion for the conformation of P-1 residues of substratesand of inhibitors in complexes with serine proteinases, BIOCHEM, 38(22), 1999, pp. 7142-7150