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Atomic Resolution (0.98A) Structure of Eosinophil-Derived Neurotoxin
Descriptor:	ACETATE ION, EOSINOPHIL-DERIVED NEUROTOXIN
Authors:	Swaminathan, G.J, Holloway, D.E, Veluraja, K, Acharya, K.R.
Deposit date:	2001-12-05
Release date:	2002-03-08
Last modified:	2023-12-13
Method:	X-RAY DIFFRACTION (0.98 Å)
Cite:	Atomic Resolution (0.98 A) Structure of Eosinophil-Derived Neurotoxin Biochemistry, 41, 2002

2VV4

hPPARgamma Ligand binding domain in complex with 6-oxoOTE
Descriptor:	(8E,10S,12Z)-10-hydroxy-6-oxooctadeca-8,12-dienoic acid, (8R,9Z,12Z)-8-hydroxy-6-oxooctadeca-9,12-dienoic acid, PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA
Authors:	Itoh, T, Fairall, L, Schwabe, J.W.R.
Deposit date:	2008-06-02
Release date:	2008-08-19
Last modified:	2023-12-13
Method:	X-RAY DIFFRACTION (2.35 Å)
Cite:	Structural Basis for the Activation of Pparg by Oxidised Fatty Acids Nat.Struct.Mol.Biol., 15, 2008

2VST

hPPARgamma Ligand binding domain in complex with 13-(S)-HODE
Descriptor:	(9Z,11E,13S)-13-hydroxyoctadeca-9,11-dienoic acid, PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA
Authors:	Itoh, T, Fairall, L, Schwabe, J.W.R.
Deposit date:	2008-04-29
Release date:	2008-08-19
Last modified:	2023-12-13
Method:	X-RAY DIFFRACTION (2.35 Å)
Cite:	Structural Basis for the Activation of Pparg by Oxidised Fatty Acids Nat.Struct.Mol.Biol., 15, 2008

2VV3

hPPARgamma Ligand binding domain in complex with 4-oxoDHA
Descriptor:	(6E,10Z,13Z,16Z,19Z)-4-oxodocosa-6,10,13,16,19-pentaenoic acid, PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA
Authors:	Itoh, T, Fairall, L, Schwabe, J.W.R.
Deposit date:	2008-06-02
Release date:	2008-08-19
Last modified:	2023-12-13
Method:	X-RAY DIFFRACTION (2.85 Å)
Cite:	Structural Basis for the Activation of Ppargamma by Oxidized Fatty Acids. Nat.Struct.Mol.Biol., 15, 2008

2VV0

hPPARgamma Ligand binding domain in complex with DHA
Descriptor:	DOCOSA-4,7,10,13,16,19-HEXAENOIC ACID, PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA
Authors:	Itoh, T, Fairall, L, Schwabe, J.W.R.
Deposit date:	2008-06-02
Release date:	2008-08-19
Last modified:	2023-12-13
Method:	X-RAY DIFFRACTION (2.55 Å)
Cite:	Structural Basis for the Activation of Pparg by Oxidised Fatty Acids Nat.Struct.Mol.Biol., 15, 2008

3UB6

Periplasmic portion of the Helicobacter pylori chemoreceptor TlpB with urea bound
Descriptor:	DI(HYDROXYETHYL)ETHER, GLYCEROL, SULFATE ION, ...
Authors:	Henderson, J.N, Sweeney, E.G, Goers, J, Wreden, C, Hicks, K.G, Parthasarathy, R, Guillemin, K.J, Remington, S.J.
Deposit date:	2011-10-23
Release date:	2012-06-27
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (1.38 Å)
Cite:	Structure and proposed mechanism for the pH-sensing Helicobacter pylori chemoreceptor TlpB. Structure, 20, 2012

4D8P

Structural and functional studies of the trans-encoded HLA-DQ2.3 (DQA103:01/DQB102:01) molecule
Descriptor:	GLYCEROL, HLA-DQA1 protein, Peptide from Gamma-gliadin,HLA class II histocompatibility antigen, ...
Authors:	Kim, C.-Y, Hotta, K, Mathews, I.I, Chen, X.
Deposit date:	2012-01-11
Release date:	2012-03-14
Last modified:	2023-11-08
Method:	X-RAY DIFFRACTION (3.05 Å)
Cite:	*Structural and functional studies of trans-encoded HLA-DQ2.3 (DQA103:01/DQB102:01) protein molecule* J.Biol.Chem., 287, 2012

3UB7

Periplasmic portion of the Helicobacter pylori chemoreceptor TlpB with acetamide bound
Descriptor:	ACETAMIDE, GLYCEROL, SULFATE ION, ...
Authors:	Henderson, J.N, Sweeney, E.G, Goers, J, Wreden, C, Hicks, K.G, Parthasarathy, R, Guillemin, K.J, Remington, S.J.
Deposit date:	2011-10-23
Release date:	2012-06-27
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (1.4 Å)
Cite:	Structure and proposed mechanism for the pH-sensing Helicobacter pylori chemoreceptor TlpB. Structure, 20, 2012

3VSD

Crystal Structure of the K127A Mutant of O-Phosphoserine Sulfhydrylase Complexed with External Schiff Base of Pyridoxal 5'-Phosphate with O-Acetyl-L-Serine
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, O-ACETYLSERINE, PYRIDOXAL-5'-PHOSPHATE, ...
Authors:	Nakamura, T, Kawai, Y, Kataoka, M, Ishikawa, K.
Deposit date:	2012-04-24
Release date:	2012-05-16
Last modified:	2017-11-22
Method:	X-RAY DIFFRACTION (2.09 Å)
Cite:	Structural analysis of the substrate recognition mechanism in O-phosphoserine sulfhydrylase from the hyperthermophilic archaeon Aeropyrum pernix K1 J.Mol.Biol., 422, 2012

3VSC

Crystal Structure of the K127A Mutant of O-Phosphoserine Sulfhydrylase Complexed with External Schiff Base of Pyridoxal 5'-Phosphate with O-Phospho-L-Serine
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, PHOSPHOSERINE, PYRIDOXAL-5'-PHOSPHATE, ...
Authors:	Nakamura, T, Kawai, Y, Kataoka, M, Ishikawa, K.
Deposit date:	2012-04-24
Release date:	2012-05-16
Last modified:	2017-11-22
Method:	X-RAY DIFFRACTION (2.07 Å)
Cite:	Structural analysis of the substrate recognition mechanism in O-phosphoserine sulfhydrylase from the hyperthermophilic archaeon Aeropyrum pernix K1 J.Mol.Biol., 422, 2012

3VSA

Crystal Structure of O-phosphoserine sulfhydrylase without acetate
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, PYRIDOXAL-5'-PHOSPHATE, Protein CysO
Authors:	Nakamura, T, Kawai, Y, Kataoka, M, Ishikawa, K.
Deposit date:	2012-04-24
Release date:	2012-05-16
Last modified:	2017-11-22
Method:	X-RAY DIFFRACTION (2.07 Å)
Cite:	Structural analysis of the substrate recognition mechanism in O-phosphoserine sulfhydrylase from the hyperthermophilic archaeon Aeropyrum pernix K1 J.Mol.Biol., 422, 2012

2VV2

hPPARgamma Ligand binding domain in complex with 5-HEPA
Descriptor:	(5R,6E,8Z,11Z,14Z,17Z)-5-hydroxyicosa-6,8,11,14,17-pentaenoic acid, PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA
Authors:	Itoh, T, Fairall, L, Schwabe, J.W.R.
Deposit date:	2008-06-02
Release date:	2008-08-19
Last modified:	2023-12-13
Method:	X-RAY DIFFRACTION (2.75 Å)
Cite:	Structural Basis for the Activation of Pparg by Oxidised Fatty Acids Nat.Struct.Mol.Biol., 15, 2008

3UB8

Periplasmic portion of the Helicobacter pylori chemoreceptor TlpB with formamide bound
Descriptor:	FORMAMIDE, GLYCEROL, SULFATE ION, ...
Authors:	Henderson, J.N, Sweeney, E.G, Goers, J, Wreden, C, Hicks, K.G, Parthasarathy, R, Guillemin, K.J, Remington, S.J.
Deposit date:	2011-10-23
Release date:	2012-06-27
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (1.42 Å)
Cite:	Structure and proposed mechanism for the pH-sensing Helicobacter pylori chemoreceptor TlpB. Structure, 20, 2012

4FJZ

Crystal structure of PI3K-gamma in complex with pyrrolo-pyridine inhibitor 63
Descriptor:	1'-[7-fluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-yl]-6'-(morpholin-4-yl)-1',2,2',3,5,6-hexahydrospiro[pyran-4,3'-pyrrolo[3,2-b]pyridine], Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, SULFATE ION
Authors:	Whittington, D.A, Tang, J, Yakowec, P.
Deposit date:	2012-06-12
Release date:	2012-10-24
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (3 Å)
Cite:	Discovery and in Vivo Evaluation of Dual PI3K-beta/delta inhibitors J.Med.Chem., 55, 2012

4FJY

Crystal structure of PI3K-gamma in complex with quinoline-indoline inhibitor 24f
Descriptor:	4-[3,3-dimethyl-6-(morpholin-4-yl)-2,3-dihydro-1H-indol-1-yl]-7-fluoro-3-methyl-2-(pyridin-3-yl)quinoline, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform, SULFATE ION
Authors:	Whittington, D.A, Tang, J, Yakowec, P.
Deposit date:	2012-06-12
Release date:	2012-10-24
Last modified:	2024-02-28
Method:	X-RAY DIFFRACTION (2.9 Å)
Cite:	Discovery and in Vivo Evaluation of Dual PI3K-beta/delta inhibitors J.Med.Chem., 55, 2012

2PIE

Crystal structure of the FHA domain of RNF8 in complex with its optimal phosphopeptide
Descriptor:	E3 ubiquitin-protein ligase RNF8, phosphopeptide
Authors:	Grant, R.A, Yaffe, M.B.
Deposit date:	2007-04-13
Release date:	2007-12-11
Last modified:	2023-08-30
Method:	X-RAY DIFFRACTION (1.35 Å)
Cite:	RNF8 Transduces the DNA-Damage Signal via Histone Ubiquitylation and Checkpoint Protein Assembly. Cell(Cambridge,Mass.), 131, 2007

3PIS

Crystal Structure of Carcinoscorpius rotundicauda Serine Protease Inhibitor Domain 1
Descriptor:	Kazal-type serine protease inhibitor SPI-1
Authors:	Giri, P.K, Tang, X.H, Sivaraman, J.
Deposit date:	2010-11-08
Release date:	2010-12-08
Last modified:	2011-07-13
Method:	X-RAY DIFFRACTION (2 Å)
Cite:	Modifying the Substrate Specificity of Carcinoscorpius rotundicauda Serine Protease Inhibitor Domain 1 to Target Thrombin To be Published

3RI4

Ets1 cooperative binding to widely separated sites on promoter DNA
Descriptor:	Isoform Ets-1 p27 of Protein C-ets-1, TCR alpha promoter DNA
Authors:	Babayeva, N.D, Mino, K, Tahirov, T.H.
Deposit date:	2011-04-12
Release date:	2012-04-04
Last modified:	2023-09-13
Method:	X-RAY DIFFRACTION (3 Å)
Cite:	Structural basis of ets1 cooperative binding to widely separated sites on promoter DNA. Plos One, 7, 2012

2E7A

TNF Receptor Subtype One-selective TNF Mutant with Antagonistic Activity
Descriptor:	Tumor necrosis factor
Authors:	Mukai, Y, Yamagata, Y, Tsutsumi, Y.
Deposit date:	2007-01-09
Release date:	2007-11-13
Last modified:	2023-10-25
Method:	X-RAY DIFFRACTION (1.8 Å)
Cite:	Creation and X-ray structure analysis of the tumor necrosis factor receptor-1-selective mutant of a tumor necrosis factor-alpha antagonist J.Biol.Chem., 283, 2008

2E5C

Crystal structure of Human NMPRTase complexed with 5'-phosphoribosyl-1'-pyrophosphate
Descriptor:	1-O-pyrophosphono-5-O-phosphono-alpha-D-ribofuranose, Nicotinamide phosphoribosyltransferase
Authors:	Takahashi, R, Nakamura, S, Kobayashi, Y, Ohkubo, T.
Deposit date:	2006-12-20
Release date:	2007-12-25
Last modified:	2023-10-25
Method:	X-RAY DIFFRACTION (2.2 Å)
Cite:	Structure and reaction mechanism of human nicotinamide phosphoribosyltransferase J.Biochem., 147, 2010

3B2R

Crystal Structure of PDE5A1 catalytic domain in complex with Vardenafil
Descriptor:	2-{2-ETHOXY-5-[(4-ETHYLPIPERAZIN-1-YL)SULFONYL]PHENYL}-5-METHYL-7-PROPYLIMIDAZO[5,1-F][1,2,4]TRIAZIN-4(1H)-ONE, cGMP-specific 3',5'-cyclic phosphodiesterase
Authors:	Huanchen, W, Mengchun, Y, Howard, R, Sharron, H.F, Hengming, K.
Deposit date:	2007-10-19
Release date:	2008-05-20
Last modified:	2024-04-03
Method:	X-RAY DIFFRACTION (2.07 Å)
Cite:	Conformational variations of both phosphodiesterase-5 and inhibitors provide the structural basis for the physiological effects of vardenafil and sildenafil. Mol.Pharmacol., 73, 2008

2AQL

Crystal Structure of the MRG15 MRG domain
Descriptor:	Mortality factor 4-like protein 1
Authors:	Quiocho, F.A, Bowman, B.R.
Deposit date:	2005-08-18
Release date:	2006-02-28
Last modified:	2024-02-14
Method:	X-RAY DIFFRACTION (2.3 Å)
Cite:	Multipurpose MRG domain involved in cell senescence and proliferation exhibits structural homology to a DNA-interacting domain. Structure, 14, 2006

2E5B

Crystal structure of Human NMPRTase as free-form
Descriptor:	Nicotinamide phosphoribosyltransferase
Authors:	Takahashi, R, Nakamura, S, Kobayashi, Y, Ohkubo, T.
Deposit date:	2006-12-20
Release date:	2007-12-25
Last modified:	2023-10-25
Method:	X-RAY DIFFRACTION (2 Å)
Cite:	Structure and reaction mechanism of human nicotinamide phosphoribosyltransferase J.Biochem., 147, 2010

2E5D

Crystal structure of Human NMPRTase complexed with nicotinamide
Descriptor:	NICOTINAMIDE, Nicotinamide phosphoribosyltransferase
Authors:	Takahashi, R, Nakamura, S, Kobayashi, Y, Ohkubo, T.
Deposit date:	2006-12-20
Release date:	2007-12-25
Last modified:	2023-10-25
Method:	X-RAY DIFFRACTION (2 Å)
Cite:	Structure and reaction mechanism of human nicotinamide phosphoribosyltransferase J.Biochem., 147, 2010

1BD8

STRUCTURE OF CDK INHIBITOR P19INK4D
Descriptor:	P19INK4D CDK4/6 INHIBITOR
Authors:	Baumgartner, R, Fernandez-Catalan, C, Winoto, A, Huber, R, Engh, R, Holak, T.A.
Deposit date:	1998-05-12
Release date:	1998-10-14
Last modified:	2024-02-07
Method:	X-RAY DIFFRACTION (1.8 Å)
Cite:	Structure of human cyclin-dependent kinase inhibitor p19INK4d: comparison to known ankyrin-repeat-containing structures and implications for the dysfunction of tumor suppressor p16INK4a. Structure, 6, 1998

<2 3 4 5 6 7 89

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Displayed results:	25
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