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REDUCED DSBA AT 2.7 ANGSTROMS RESOLUTION
Descriptor:	DISULFIDE BOND FORMATION PROTEIN
Authors:	Martin, J.L, Guddat, L.W.
Deposit date:	1998-01-06
Release date:	1998-07-08
Last modified:	2024-05-22
Method:	X-RAY DIFFRACTION (2.7 Å)
Cite:	Crystal structures of reduced and oxidized DsbA: investigation of domain motion and thiolate stabilization. Structure, 6, 1998

1BQ7

DSBA MUTANT P151A, ROLE OF THE CIS-PROLINE IN THE ACTIVE SITE OF DSBA
Descriptor:	PROTEIN (DISULFIDE OXIDOREDUCTASE)
Authors:	Charbonnier, J.-B, Stura, E.A.
Deposit date:	1998-08-21
Release date:	1999-08-20
Last modified:	2024-10-30
Method:	X-RAY DIFFRACTION (2.8 Å)
Cite:	On the role of the cis-proline residue in the active site of DsbA. Protein Sci., 8, 1999

3CTI

RELAXATION MATRIX REFINEMENT OF THE SOLUTION STRUCTURE OF SQUASH TRYPSIN INHIBITOR
Descriptor:	TRYPSIN INHIBITOR
Authors:	Nilges, M, Habazettl, J, Bruenger, A.T, Holak, T.A.
Deposit date:	1991-03-27
Release date:	1992-04-15
Last modified:	2024-10-23
Method:	SOLUTION NMR
Cite:	Relaxation matrix refinement of the solution structure of squash trypsin inhibitor. J.Mol.Biol., 219, 1991

9GSS

HUMAN GLUTATHIONE S-TRANSFERASE P1-1, COMPLEX WITH S-HEXYL GLUTATHIONE
Descriptor:	2-(N-MORPHOLINO)-ETHANESULFONIC ACID, GLUTATHIONE S-TRANSFERASE P1-1, S-HEXYLGLUTATHIONE, ...
Authors:	Oakley, A, Parker, M.
Deposit date:	1997-08-14
Release date:	1998-09-16
Last modified:	2024-05-22
Method:	X-RAY DIFFRACTION (1.97 Å)
Cite:	The structures of human glutathione transferase P1-1 in complex with glutathione and various inhibitors at high resolution. J.Mol.Biol., 274, 1997

1ADZ

THE SOLUTION STRUCTURE OF THE SECOND KUNITZ DOMAIN OF TISSUE FACTOR PATHWAY INHIBITOR, NMR, 30 STRUCTURES
Descriptor:	TISSUE FACTOR PATHWAY INHIBITOR
Authors:	Burgering, M.J.M, Orbons, L.P.M.
Deposit date:	1997-02-19
Release date:	1998-02-25
Last modified:	2024-10-30
Method:	SOLUTION NMR
Cite:	The second Kunitz domain of human tissue factor pathway inhibitor: cloning, structure determination and interaction with factor Xa. J.Mol.Biol., 269, 1997

6ATQ

Crystal structure of apo-hGSTA1-1 exhibiting a new conformation of C-terminal helix
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, Glutathione S-transferase A1
Authors:	Kumari, V, Ji, X.
Deposit date:	2017-08-29
Release date:	2018-09-12
Last modified:	2023-10-04
Method:	X-RAY DIFFRACTION (2 Å)
Cite:	The dynamic nature of hGSTA1-1 C-terminal helix To be published

6ATO

Crystal structure of hGSTA1-1 complexed with GSH and MPD in each subunit
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, GLUTATHIONE, Glutathione S-transferase A1
Authors:	Kumari, V, Ji, X.
Deposit date:	2017-08-29
Release date:	2018-09-12
Last modified:	2023-10-04
Method:	X-RAY DIFFRACTION (1.55 Å)
Cite:	The dynamic nature of hGSTA1-1 C-terminal helix To be published

6ATR

Crystal structure of hGSTA1-1 complexed with two GSH analogues in each subunit
Descriptor:	1,2-ETHANEDIOL, 2-AMINO-5-[1-(CARBOXYLATOMETHYLCARBAMOYL)-2-NITROSOSULFANYL-ETHYL]AMINO-5-OXO-PENTANOATE, Glutathione S-transferase A1, ...
Authors:	Kumari, V, Ji, X.
Deposit date:	2017-08-29
Release date:	2018-09-12
Last modified:	2023-10-04
Method:	X-RAY DIFFRACTION (1.29 Å)
Cite:	hGSTA1 apo structure and dynamic c-terminus helix To be published

5GSS

HUMAN GLUTATHIONE S-TRANSFERASE P1-1, COMPLEX WITH GLUTATHIONE
Descriptor:	2-(N-MORPHOLINO)-ETHANESULFONIC ACID, GLUTATHIONE, GLUTATHIONE S-TRANSFERASE P1-1
Authors:	Oakley, A, Parker, M.
Deposit date:	1997-08-11
Release date:	1998-09-16
Last modified:	2024-05-22
Method:	X-RAY DIFFRACTION (1.95 Å)
Cite:	The structures of human glutathione transferase P1-1 in complex with glutathione and various inhibitors at high resolution. J.Mol.Biol., 274, 1997

6ATP

Crystal structure of apo-hGSTA1-1 exhibiting a new conformation of C-terminal helix
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, Glutathione S-transferase A1
Authors:	Kumari, V, Ji, X.
Deposit date:	2017-08-29
Release date:	2018-09-12
Last modified:	2023-10-04
Method:	X-RAY DIFFRACTION (1.7 Å)
Cite:	The dynamic nature of hGSTA1-1 C-terminal helix To be published

2WSN

Structure of Enhanced Cyan Fluorescent Protein at physiological pH
Descriptor:	GREEN FLUORESCENT PROTEIN
Authors:	Lelimousin, M, Noirclerc-Savoye, M, Lazareno-Saez, C, Paetzold, B, Le Vot, S, Chazal, R, Macheboeuf, P, Field, M.J, Bourgeois, D, Royant, A.
Deposit date:	2009-09-08
Release date:	2009-09-29
Last modified:	2024-10-16
Method:	X-RAY DIFFRACTION (1.37 Å)
Cite:	Intrinsic Dynamics in Ecfp and Cerulean Control Fluorescence Quantum Yield. Biochemistry, 48, 2009

1FVJ

THE 2.06 ANGSTROM STRUCTURE OF THE H32Y MUTANT OF THE DISULFIDE BOND FORMATION PROTEIN (DSBA)
Descriptor:	DISULFIDE BOND FORMATION PROTEIN
Authors:	Martin, J.L, Guddat, L.W.
Deposit date:	1996-08-28
Release date:	1997-05-15
Last modified:	2024-10-23
Method:	X-RAY DIFFRACTION (2.06 Å)
Cite:	Structural analysis of three His32 mutants of DsbA: support for an electrostatic role of His32 in DsbA stability. Protein Sci., 6, 1997

1FVK

THE 1.7 ANGSTROM STRUCTURE OF WILD TYPE DISULFIDE BOND FORMATION PROTEIN (DSBA)
Descriptor:	DISULFIDE BOND FORMATION PROTEIN
Authors:	Martin, J.L, Guddat, L.W.
Deposit date:	1996-08-28
Release date:	1997-08-20
Last modified:	2024-10-30
Method:	X-RAY DIFFRACTION (1.7 Å)
Cite:	Structural analysis of three His32 mutants of DsbA: support for an electrostatic role of His32 in DsbA stability. Protein Sci., 6, 1997

2HNT

CRYSTALLOGRAPHIC STRUCTURE OF HUMAN GAMMA-THROMBIN
Descriptor:	GAMMA-THROMBIN
Authors:	Tulinsky, A.
Deposit date:	1994-08-23
Release date:	1994-11-30
Last modified:	2024-10-23
Method:	X-RAY DIFFRACTION (2.5 Å)
Cite:	Crystallographic structure of human gamma-thrombin. J.Biol.Chem., 269, 1994

1BTH

STRUCTURE OF THROMBIN COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR
Descriptor:	BOVINE PANCREATIC TRYPSIN INHIBITOR, THROMBIN
Authors:	Van De Locht, A, Bode, W, Stubbs, M.T.
Deposit date:	1996-12-03
Release date:	1997-12-24
Last modified:	2024-11-20
Method:	X-RAY DIFFRACTION (2.3 Å)
Cite:	The thrombin E192Q-BPTI complex reveals gross structural rearrangements: implications for the interaction with antithrombin and thrombomodulin. EMBO J., 16, 1997

6GSS

HUMAN GLUTATHIONE S-TRANSFERASE P1-1, COMPLEX WITH GLUTATHIONE
Descriptor:	2-(N-MORPHOLINO)-ETHANESULFONIC ACID, GLUTATHIONE, GLUTATHIONE S-TRANSFERASE P1-1
Authors:	Oakley, A, Parker, M.
Deposit date:	1997-08-13
Release date:	1998-09-16
Last modified:	2024-05-22
Method:	X-RAY DIFFRACTION (1.9 Å)
Cite:	The structures of human glutathione transferase P1-1 in complex with glutathione and various inhibitors at high resolution. J.Mol.Biol., 274, 1997

1A5I

CATALYTIC DOMAIN OF VAMPIRE BAT (DESMODUS ROTUNDUS) SALIVA PLASMINOGEN ACTIVATOR IN COMPLEX WITH EGR-CMK (GLU-GLY-ARG CHLOROMETHYL KETONE)
Descriptor:	L-alpha-glutamyl-N-{(1S)-4-{[amino(iminio)methyl]amino}-1-[(1S)-2-chloro-1-hydroxyethyl]butyl}glycinamide, PLASMINOGEN ACTIVATOR
Authors:	Renatus, M, Stubbs, M.T, Bode, W.
Deposit date:	1998-02-17
Release date:	1999-03-23
Last modified:	2024-10-30
Method:	X-RAY DIFFRACTION (2.9 Å)
Cite:	Catalytic domain structure of vampire bat plasminogen activator: a molecular paradigm for proteolysis without activation cleavage. Biochemistry, 36, 1997

1BDA

CATALYTIC DOMAIN OF HUMAN SINGLE CHAIN TISSUE PLASMINOGEN ACTIVATOR IN COMPLEX WITH DANSYL-EGR-CMK (DANSYL-GLU-GLY-ARG CHLOROMETHYL KETONE)
Descriptor:	N-{[5-(dimethylamino)naphthalen-2-yl]sulfonyl}-L-alpha-glutamyl-N-[(1S)-4-{[amino(iminio)methyl]amino}-1-(chloroacetyl) butyl]glycinamide, SINGLE CHAIN TISSUE TYPE PLASMINOGEN ACTIVATOR
Authors:	Bode, W, Renatus, M, Engh, R.A.
Deposit date:	1998-05-07
Release date:	1999-05-11
Last modified:	2024-10-16
Method:	X-RAY DIFFRACTION (3.35 Å)
Cite:	Lysine 156 promotes the anomalous proenzyme activity of tPA: X-ray crystal structure of single-chain human tPA. EMBO J., 16, 1997

5JCU

Crystal Structure of hGSTA1-1 with Glutathione Adduct of Phenethyl Isothiocyanate and Cystein Adduct of Phenethyl Isothiocyanate
Descriptor:	1,2-ETHANEDIOL, Glutathione S-transferase A1, L-gamma-glutamyl-S-[(2-phenylethyl)carbamothioyl]-L-cysteinylglycine
Authors:	Kumari, V, Ji, X.
Deposit date:	2016-04-15
Release date:	2016-10-12
Last modified:	2023-09-27
Method:	X-RAY DIFFRACTION (1.93 Å)
Cite:	Irreversible Inhibition of Glutathione S-Transferase by Phenethyl Isothiocyanate (PEITC), a Dietary Cancer Chemopreventive Phytochemical. Plos One, 11, 2016

1C9P

COMPLEX OF BDELLASTASIN WITH PORCINE TRYPSIN
Descriptor:	BDELLASTASIN, CALCIUM ION, TRYPSIN
Authors:	Rester, U.
Deposit date:	1999-08-03
Release date:	2000-08-03
Last modified:	2024-10-16
Method:	X-RAY DIFFRACTION (2.8 Å)
Cite:	Structure of the complex of the antistasin-type inhibitor bdellastasin with trypsin and modelling of the bdellastasin-microplasmin system. J.Mol.Biol., 293, 1999

1LKT

CRYSTAL STRUCTURE OF THE HEAD-BINDING DOMAIN OF PHAGE P22 TAILSPIKE PROTEIN
Descriptor:	TAILSPIKE PROTEIN
Authors:	Steinbacher, S.
Deposit date:	1997-10-17
Release date:	1998-01-28
Last modified:	2024-02-14
Method:	X-RAY DIFFRACTION (2.6 Å)
Cite:	Phage P22 tailspike protein: crystal structure of the head-binding domain at 2.3 A, fully refined structure of the endorhamnosidase at 1.56 A resolution, and the molecular basis of O-antigen recognition and cleavage. J.Mol.Biol., 267, 1997

1AST

STRUCTURE OF ASTACIN AND IMPLICATIONS FOR ACTIVATION OF ASTACINS AND ZINC-LIGATION OF COLLAGENASES
Descriptor:	ASTACIN, ZINC ION
Authors:	Bode, W, Gomis-Rueth, F.X, Stoecker, W.
Deposit date:	1993-04-21
Release date:	1994-07-31
Last modified:	2024-10-30
Method:	X-RAY DIFFRACTION (1.8 Å)
Cite:	Structure of astacin and implications for activation of astacins and zinc-ligation of collagenases. Nature, 358, 1992

1A5H

CATALYTIC DOMAIN OF HUMAN TWO-CHAIN TISSUE PLASMINOGEN ACTIVATOR COMPLEX OF A BIS-BENZAMIDINE
Descriptor:	2,7-BIS-(4-AMIDINOBENZYLIDENE)-CYCLOHEPTAN-1-ONE, TISSUE PLASMINOGEN ACTIVATOR
Authors:	Renatus, M, Bode, W, Stubbs, M.T.
Deposit date:	1998-02-17
Release date:	1999-04-20
Last modified:	2024-11-06
Method:	X-RAY DIFFRACTION (2.9 Å)
Cite:	Structural mapping of the active site specificity determinants of human tissue-type plasminogen activator. Implications for the design of low molecular weight substrates and inhibitors. J.Biol.Chem., 272, 1997

4TPI

THE REFINED 2.2-ANGSTROMS (0.22-NM) X-RAY CRYSTAL STRUCTURE OF THE TERNARY COMPLEX FORMED BY BOVINE TRYPSINOGEN, VALINE-VALINE AND THE ARG15 ANALOGUE OF BOVINE PANCREATIC TRYPSIN INHIBITOR
Descriptor:	BOVINE PANCREATIC TRYPSIN INHIBITOR, CALCIUM ION, SULFATE ION, ...
Authors:	Bode, W, Walter, J.
Deposit date:	1985-06-11
Release date:	1985-11-08
Last modified:	2024-10-23
Method:	X-RAY DIFFRACTION (2.2 Å)
Cite:	The refined 2.2-A (0.22-nm) X-ray crystal structure of the ternary complex formed by bovine trypsinogen, valine-valine and the Arg15 analogue of bovine pancreatic trypsin inhibitor Eur.J.Biochem., 144, 1984

9QZT

Room temperature structure of Glycine max phyA in Pfr/Pr ensemble
Descriptor:	PHYCOCYANOBILIN, Phytochrome A-2
Authors:	Nagano, S, Hughes, J.
Deposit date:	2025-04-24
Release date:	2025-06-04
Last modified:	2025-07-02
Method:	X-RAY DIFFRACTION (2.2 Å)
Cite:	Pr and Pfr structures of plant phytochrome A. Nat Commun, 16, 2025

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