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HPT + HMTT
分子名称:	6-{[4-(HYDROXYMETHYL)-5-METHYL-2,6-DIOXOHEXAHYDROPYRIMIDIN-5-YL]METHYL}-5-METHYLPYRIMIDINE-2,4(1H,3H)-DIONE, SULFATE ION, THYMIDINE KINASE
著者	Vogt, J, Scapozza, L, Schulz, G.E.
登録日	2000-05-23
公開日	2001-03-31
最終更新日	2023-12-06
実験手法	X-RAY DIFFRACTION (2.2 Å)
主引用文献	The Effect of Substrate Binding on the Conformation and Structural Stability of Herpes Simplex Virus Type 1 Thymidine Kinase Protein Sci., 10, 2001

1E2M

HPT + HMTT
分子名称:	6-HYDROXYPROPYLTHYMINE, SULFATE ION, THYMIDINE KINASE
著者	Vogt, J, Scapozza, L, Schulz, G.E.
登録日	2000-05-23
公開日	2001-03-31
最終更新日	2023-12-06
実験手法	X-RAY DIFFRACTION (2.2 Å)
主引用文献	The Effect of Substrate Binding on the Conformation and Structural Stability of Herpes Simplex Virus Type 1 Thymidine Kinase Protein Sci., 10, 2001

1E2K

Kinetics and crystal structure of the wild-type and the engineered Y101F mutant of Herpes simplex virus type 1 thymidine kinase interacting with (North)-methanocarba-thymidine
分子名称:	1-[4-HYDROXY-5-(HYDROXYMETHYL)BICYCLO[3.1.0]HEX-2-YL]-5-METHYLPYRIMIDINE-2,4(1H,3H)-DIONE, SULFATE ION, THYMIDINE KINASE
著者	Vogt, J, Scapozza, L, Schulz, G.E.
登録日	2000-05-23
公開日	2000-08-19
最終更新日	2023-12-06
実験手法	X-RAY DIFFRACTION (1.7 Å)
主引用文献	Kinetics and Crystal Structure of the Wild-Type and the Engineered Y101F Mutant of Herpes Simplex Virus Type 1 Thymidine Kinase Interacting with (North)-Methanocarba-Thymidine Biochemistry, 39, 2000

1E2L

Kinetics and crystal structure of the wild-type and the engineered Y101F mutant of Herpes simplex virus type 1 thymidine kinase interacting with (North)-methanocarba-thymidine
分子名称:	1-[4-HYDROXY-5-(HYDROXYMETHYL)BICYCLO[3.1.0]HEX-2-YL]-5-METHYLPYRIMIDINE-2,4(1H,3H)-DIONE, SULFATE ION, THYMIDINE KINASE
著者	Vogt, J, Scapozza, L, Schulz, G.E.
登録日	2000-05-23
公開日	2000-08-18
最終更新日	2023-12-06
実験手法	X-RAY DIFFRACTION (2.4 Å)
主引用文献	Kinetics and Crystal Structure of the Wild-Type and the Engineered Y101F Mutant of Herpes Simplex Virus Type 1 Thymidine Kinase Interacting with (North)-Methanocarba-Thymidine Biochemistry, 39, 2000

1E2I

The nucleoside binding site of Herpes simplex type 1 thymidine kinase analyzed by X-ray crystallography
分子名称:	9-HYDROXYPROPYLADENINE, R-ISOMER, S-ISOMER, ...
著者	Vogt, J, Scapozza, L, Schulz, G.E.
登録日	2000-05-23
公開日	2000-11-06
最終更新日	2023-12-06
実験手法	X-RAY DIFFRACTION (1.9 Å)
主引用文献	Nucleoside Binding Site of Herpes Simplex Type 1 Thymidine Kinase Analyzed by X-Ray Crystallography Proteins, 41, 2000

1E2J

The nucleoside binding site of Herpes simplex type 1 thymidine kinase analyzed by X-ray crystallography
分子名称:	SULFATE ION, THYMIDINE, THYMIDINE KINASE
著者	Vogt, J, Scapozza, L, Schulz, G.E.
登録日	2000-05-23
公開日	2000-11-06
最終更新日	2023-12-06
実験手法	X-RAY DIFFRACTION (2.5 Å)
主引用文献	Nucleoside Binding Site of Herpes Simplex Type 1 Thymidine Kinase Analyzed by X-Ray Crystallography Proteins: Struct.,Funct., Genet., 41, 2000

1E2H

The nucleoside binding site of Herpes simplex type 1 thymidine kinase analyzed by X-ray crystallography
分子名称:	SULFATE ION, THYMIDINE KINASE
著者	Vogt, J, Scapozza, L, Schulz, G.E.
登録日	2000-05-23
公開日	2000-11-06
最終更新日	2023-12-06
実験手法	X-RAY DIFFRACTION (1.9 Å)
主引用文献	Nucleoside Binding Site of Herpes Simplex Type 1 Thymidine Kinase Analyzed by X-Ray Crystallography Proteins: Struct.,Funct., Genet., 41, 2000

1OJR

L-rhamnulose-1-phosphate aldolase from Escherichia coli (mutant E192A)
分子名称:	1,4-DIETHYLENE DIOXIDE, Dihydroxyacetone, GLYCEROL, ...
著者	Kroemer, M, Merkel, I, Schulz, G.E.
登録日	2003-07-15
公開日	2003-09-11
最終更新日	2023-12-13
実験手法	X-RAY DIFFRACTION (1.35 Å)
主引用文献	Structure and Catalytic Mechanism of L-Rhamnulose-1-Phosphate Aldolase. Biochemistry, 42, 2003

1FUA

L-FUCULOSE 1-PHOSPHATE ALDOLASE CRYSTAL FORM T
分子名称:	BETA-MERCAPTOETHANOL, L-FUCULOSE-1-PHOSPHATE ALDOLASE, SULFATE ION, ...
著者	Dreyer, M.K, Schulz, G.E.
登録日	1996-02-14
公開日	1996-10-14
最終更新日	2011-11-16
実験手法	X-RAY DIFFRACTION (1.92 Å)
主引用文献	Refined high-resolution structure of the metal-ion dependent L-fuculose-1-phosphate aldolase (class II) from Escherichia coli. Acta Crystallogr.,Sect.D, 52, 1996

1H37

Structures of Human Oxidosqualene Cyclase Inhibitors Bound to an Homologous Enzyme
分子名称:	(HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, SQUALENE--HOPENE CYCLASE, {4-[((1S,2S)-2-{[ALLYL(CYCLOPROPYL)AMINO]METHYL}CYCLOPROPYL)METHOXY]PHENYL}(4-BROMOPHENYL)METHANONE
著者	Lenhart, A, Reinert, D.J, Weihofen, W.A, Aebi, J.D, Dehmlow, H, Morand, O.H, Schulz, G.E.
登録日	2002-08-24
公開日	2003-08-21
最終更新日	2024-05-08
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem., 46, 2003

1H36

Structures of Human Oxidosqualene Cyclase Inhibitors Bound to an Homologous Enzyme
分子名称:	(4-BROMOPHENYL)[4-({(2E)-4-[CYCLOPROPYL(METHYL)AMINO]BUT-2-ENYL}OXY)PHENYL]METHANONE, (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, SQUALENE--HOPENE CYCLASE
著者	Lenhart, A, Reinert, D.J, Weihofen, W.A, Aebi, J.D, Dehmlow, H, Morand, O.H, Schulz, G.E.
登録日	2002-08-24
公開日	2003-08-21
最終更新日	2024-05-08
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem., 46, 2003

1H35

Structures of Human Oxidosqualene Cyclase Inhibitors Bound to an Homologous Enzyme
分子名称:	(4'-{[ALLYL(METHYL)AMINO]METHYL}-1,1'-BIPHENYL-4-YL)(4-BROMOPHENYL)METHANONE, (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, SQUALENE--HOPENE CYCLASE
著者	Lenhart, A, Reinert, D.J, Weihofen, W.A, Aebi, J.D, Dehmlow, H, Morand, O.H, Schulz, G.E.
登録日	2002-08-24
公開日	2003-08-21
最終更新日	2024-05-08
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem., 46, 2003

1H3B

Squalene-Hopene Cyclase
分子名称:	(HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, N-{6-[4-(6-BROMO-1,2-BENZISOTHIAZOL-3-YL)PHENOXY]HEXYL}-N-METHYL-2-PROPEN-1-AMINE, SQUALENE--HOPENE CYCLASE
著者	Lenhart, A, Reinert, D.J, Weihofen, W.A, Aebi, J.D, Dehmlow, H, Morand, O.H, Schulz, G.E.
登録日	2002-08-25
公開日	2003-08-21
最終更新日	2024-05-08
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem., 46, 2003

1H3A

Structures of Human Oxidosqualene Cyclase Inhibitors Bound to an Homologous Enzyme
分子名称:	(2E)-N-ALLYL-4-{[3-(4-BROMOPHENYL)-5-FLUORO-1-METHYL-1H-INDAZOL-6-YL]OXY}-N-METHYL-2-BUTEN-1-AMINE, (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, SQUALENE--HOPENE CYCLASE
著者	Lenhart, A, Reinert, D.J, Weihofen, W.A, Aebi, J.D, Dehmlow, H, Morand, O.H, Schulz, G.E.
登録日	2002-08-24
公開日	2003-08-21
最終更新日	2024-05-08
実験手法	X-RAY DIFFRACTION (2.85 Å)
主引用文献	Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem., 46, 2003

1H39

Structures of Human Oxidosqualene Cyclase Inhibitors Bound to an Homologous Enzyme
分子名称:	(HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, ALLYL-{6-[3-(4-BROMO-PHENYL)-1-METHYL-1H-INDAZOL-6-YL]OXY}HEXYL)-N-METHYLAMINE, SQUALENE--HOPENE CYCLASE
著者	Lenhart, A, Reinert, D.J, Weihofen, W.A, Aebi, J.D, Dehmlow, H, Morand, O.H, Schulz, G.E.
登録日	2002-08-24
公開日	2003-08-21
最終更新日	2024-05-08
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem., 46, 2003

1GSZ

Crystal Structure of a Squalene Cyclase in Complex with the Potential Anticholesteremic Drug Ro48-8071
分子名称:	(HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, SQUALENE--HOPENE CYCLASE, [4-({6-[ALLYL(METHYL)AMINO]HEXYL}OXY)-2-FLUOROPHENYL](4-BROMOPHENYL)METHANONE
著者	Lenhart, A, Weihofen, W.A, Pleschke, A.E.W, Schulz, G.E.
登録日	2002-01-09
公開日	2003-01-16
最終更新日	2024-05-08
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Crystal Structure of a Squalene Cyclase in Complex with the Potential Anticholesteremic Drug Ro48-8071 Chem.Biol., 9, 2002

1H3C

Structures of Human Oxidosqualene Cyclase Inhibitors Bound to an Homologous Enzyme
分子名称:	(HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, N-(6-{[3-(4-BROMOPHENYL)-1,2-BENZISOTHIAZOL-6-YL]OXY}HEXYL)-N-METHYLPROP-2-EN-1-AMINE, SQUALENE--HOPENE CYCLASE
著者	Lenhart, A, Reinert, D.J, Weihofen, W.A, Aebi, J.D, Dehmlow, H, Morand, O.H, Schulz, G.E.
登録日	2002-08-25
公開日	2003-08-21
最終更新日	2024-05-08
実験手法	X-RAY DIFFRACTION (2.9 Å)
主引用文献	Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem., 46, 2003

1VTK

THYMIDINE KINASE FROM HERPES SIMPLEX VIRUS TYPE 1 IN COMPLEX WITH ADP AND DEOXYTHYMIDINE-MONOPHOSPHATE
分子名称:	ADENOSINE-5'-DIPHOSPHATE, THYMIDINE KINASE, THYMIDINE-5'-PHOSPHATE
著者	Wild, K, Schulz, G.E.
登録日	1997-04-01
公開日	1997-10-22
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.75 Å)
主引用文献	The structures of thymidine kinase from herpes simplex virus type 1 in complex with substrates and a substrate analogue. Protein Sci., 6, 1997

2AK2

ADENYLATE KINASE ISOENZYME-2
分子名称:	ADENYLATE KINASE ISOENZYME-2, SULFATE ION
著者	Schlauderer, G.J, Schulz, G.E.
登録日	1995-12-29
公開日	1996-06-10
最終更新日	2011-07-13
実験手法	X-RAY DIFFRACTION (2.1 Å)
主引用文献	The structure of bovine mitochondrial adenylate kinase: comparison with isoenzymes in other compartments. Protein Sci., 5, 1996

1MPR

MALTOPORIN FROM SALMONELLA TYPHIMURIUM
分子名称:	CALCIUM ION, MALTOPORIN
著者	Meyer, J.E.W, Schulz, G.E.
登録日	1996-12-18
公開日	1997-03-12
最終更新日	2023-08-09
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Structure of maltoporin from Salmonella typhimurium ligated with a nitrophenyl-maltotrioside. J.Mol.Biol., 266, 1997

1NKS

ADENYLATE KINASE FROM SULFOLOBUS ACIDOCALDARIUS
分子名称:	ADENOSINE MONOPHOSPHATE, ADENOSINE-5'-DIPHOSPHATE, ADENYLATE KINASE
著者	Vonrhein, C, Schulz, G.E.
登録日	1998-07-16
公開日	1998-12-09
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.57 Å)
主引用文献	The structure of a trimeric archaeal adenylate kinase. J.Mol.Biol., 282, 1998

1O9G

rRNA methyltransferase aviRa from Streptomyces viridochromogenes at 1.5A
分子名称:	RRNA METHYLTRANSFERASE
著者	Mosbacher, T.G, Schulz, G.E.
登録日	2002-12-13
公開日	2003-05-16
最終更新日	2019-07-24
実験手法	X-RAY DIFFRACTION (1.5 Å)
主引用文献	Crystal Structure of the Avilamycin Resistance-Conferring Methyltransferase Avira from Streptomyces Viridochromogenes J.Mol.Biol., 329, 2003

1O9H

rRNA methyltransferase aviRa from Streptomyces viridochromogenes at 2.4A
分子名称:	RRNA METHYLTRANSFERASE
著者	Mosbacher, T.G, Schulz, G.E.
登録日	2002-12-13
公開日	2003-05-16
最終更新日	2023-12-13
実験手法	X-RAY DIFFRACTION (2.4 Å)
主引用文献	Crystal Structure of the Avilamycin Resistance-Conferring Methyltransferase Avira from Streptomyces Viridochromogenes J.Mol.Biol., 329, 2003

1OG4

Crystal Structure of the Eucaryotic Mono-ADP-Ribosyltransferase ART2.2 Mutant E189A in Complex with NADH
分子名称:	1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE, T-CELL ECTO-ADP-RIBOSYLTRANSFERASE 2
著者	Ritter, H, Koch-Nolte, F, Marquez, V.E, Schulz, G.E.
登録日	2003-04-24
公開日	2003-08-28
最終更新日	2023-12-13
実験手法	X-RAY DIFFRACTION (2.6 Å)
主引用文献	Substrate Binding and Catalysis of Ecto-Adp-Ribosyltransferase 2.2 From Rat Biochemistry, 42, 2003

1OKX

Binding Structure of Elastase Inhibitor Scyptolin A
分子名称:	ELASTASE 1, SCYPTOLIN A
著者	Matern, U, Schleberger, C, Jelakovic, S, Weckesser, J, Schulz, G.E.
登録日	2003-07-31
公開日	2003-10-24
最終更新日	2023-12-13
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Binding Structure of Elastase Inhibitor Scyptolin A Chem.Biol., 10, 2003

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