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BU of 1bey by Molmil

ANTIBODY TO CAMPATH-1H HUMANIZED FAB
Descriptor:	CAMPATH-1H ANTIBODY
Authors:	Cheetham, G.M.T, Hale, G, Waldmann, H, Bloomer, A.C.
Deposit date:	1998-05-18
Release date:	1999-01-27
Last modified:	2023-08-02
Method:	X-RAY DIFFRACTION (3.25 Å)
Cite:	Crystal structures of a rat anti-CD52 (CAMPATH-1) therapeutic antibody Fab fragment and its humanized counterpart. J.Mol.Biol., 284, 1998

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BU of 1bfo by Molmil

CAMPATH-1G IGG2B RAT MONOCLONAL FAB
Descriptor:	CAMPATH-1G ANTIBODY
Authors:	Cheetham, G.M.T, Hale, G, Waldmann, H, Bloomer, A.C.
Deposit date:	1998-05-20
Release date:	1999-03-16
Last modified:	2024-04-03
Method:	X-RAY DIFFRACTION (2.6 Å)
Cite:	Crystal structures of a rat anti-CD52 (CAMPATH-1) therapeutic antibody Fab fragment and its humanized counterpart. J.Mol.Biol., 284, 1998

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BU of 1ce1 by Molmil

1.9A STRUCTURE OF THE THERAPEUTIC ANTIBODY CAMPATH-1H FAB IN COMPLEX WITH A SYNTHETIC PEPTIDE ANTIGEN
Descriptor:	PROTEIN (CAMPATH-1H:HEAVY CHAIN), PROTEIN (CAMPATH-1H:LIGHT CHAIN), PROTEIN (PEPTIDE ANTIGEN)
Authors:	James, L.C, Hale, G, Waldmann, H, Bloomer, A.C.
Deposit date:	1999-03-12
Release date:	1999-06-25
Last modified:	2023-12-27
Method:	X-RAY DIFFRACTION (1.9 Å)
Cite:	1.9 A structure of the therapeutic antibody CAMPATH-1H fab in complex with a synthetic peptide antigen. J.Mol.Biol., 289, 1999

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BU of 4hws by Molmil

Crystal structure of E. coli Threonyl-tRNA synthetase bound to a novel inhibitor
Descriptor:	N-{[3-(4-amino-2-chloroquinazolin-7-yl)phenyl]sulfonyl}-L-threoninamide, Threonine--tRNA ligase, ZINC ION
Authors:	Hilgers, M.T.
Deposit date:	2012-11-08
Release date:	2013-09-18
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (1.7 Å)
Cite:	Identification of bacteria-selective threonyl-tRNA synthetase substrate inhibitors by structure-based design. J.Med.Chem., 56, 2013

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BU of 4hwp by Molmil

Crystal structure of E. coli Threonyl-tRNA synthetase bound to a novel inhibitor
Descriptor:	N-{[3-(4-amino-2-methylquinazolin-7-yl)phenyl]sulfonyl}-L-threoninamide, Threonine--tRNA ligase, ZINC ION
Authors:	Hilgers, M.T.
Deposit date:	2012-11-08
Release date:	2013-09-18
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (1.807 Å)
Cite:	Identification of bacteria-selective threonyl-tRNA synthetase substrate inhibitors by structure-based design. J.Med.Chem., 56, 2013

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BU of 4hwt by Molmil

Crystal structure of human Threonyl-tRNA synthetase bound to a novel inhibitor
Descriptor:	N-{[3-(2H-indazol-5-yl)phenyl]sulfonyl}-L-threoninamide, Threonine--tRNA ligase, cytoplasmic, ...
Authors:	Hilgers, M.T.
Deposit date:	2012-11-08
Release date:	2013-09-18
Method:	X-RAY DIFFRACTION (2.3 Å)
Cite:	Identification of bacteria-selective threonyl-tRNA synthetase substrate inhibitors by structure-based design. J.Med.Chem., 56, 2013

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BU of 4hwo by Molmil

Crystal structure of E. coli Threonyl-tRNA synthetase bound to a novel inhibitor
Descriptor:	N-{[3-(4-aminoquinazolin-7-yl)phenyl]sulfonyl}-L-threoninamide, Threonine--tRNA ligase, ZINC ION
Authors:	Hilgers, M.T.
Deposit date:	2012-11-08
Release date:	2013-09-18
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (1.907 Å)
Cite:	Identification of bacteria-selective threonyl-tRNA synthetase substrate inhibitors by structure-based design. J.Med.Chem., 56, 2013

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BU of 4hwr by Molmil

Crystal structure of E. coli Threonyl-tRNA synthetase bound to a novel inhibitor
Descriptor:	N-{[3-(2H-indazol-5-yl)phenyl]sulfonyl}-L-threoninamide, Threonine--tRNA ligase, ZINC ION
Authors:	Hilgers, M.T.
Deposit date:	2012-11-08
Release date:	2013-09-18
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (1.9 Å)
Cite:	Identification of bacteria-selective threonyl-tRNA synthetase substrate inhibitors by structure-based design. J.Med.Chem., 56, 2013

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