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C123aT Mutant of E. coli Succinyl-CoA Synthetase
分子名称:	COENZYME A, GLYCEROL, PHOSPHATE ION, ...
著者	Fraser, M.E.
登録日	2006-11-08
公開日	2007-07-24
最終更新日	2023-08-30
実験手法	X-RAY DIFFRACTION (2.15 Å)
主引用文献	Participation of Cys 123alpha of Escherichia coli Succinyl-CoA Synthetase in Catalysis ACTA CRYSTALLOGR.,SECT.D, 63, 2007

2NUA

C123aV Mutant of E. coli Succinyl-CoA Synthetase
分子名称:	COENZYME A, PHOSPHATE ION, SULFATE ION, ...
著者	Fraser, M.E.
登録日	2006-11-08
公開日	2007-07-24
最終更新日	2023-08-30
実験手法	X-RAY DIFFRACTION (2.95 Å)
主引用文献	Participation of Cys 123alpha of Escherichia coli Succinyl-CoA Synthetase in Catalysis ACTA CRYSTALLOGR.,SECT.D, 63, 2007

1ALQ

CIRCULARLY PERMUTED BETA-LACTAMASE FROM STAPHYLOCOCCUS AUREUS PC1
分子名称:	CARBONATE ION, CP254 BETA-LACTAMASE, SULFATE ION
著者	Pieper, U, Herzberg, O.
登録日	1997-06-02
公開日	1997-09-26
最終更新日	2024-05-22
実験手法	X-RAY DIFFRACTION (1.8 Å)
主引用文献	Circularly permuted beta-lactamase from Staphylococcus aureus PC1. Biochemistry, 36, 1997

1APW

CRYSTALLOGRAPHIC ANALYSIS OF TRANSITION STATE MIMICS BOUND TO PENICILLOPEPSIN: DIFLUOROSTATINE-AND DIFLUOROSTATONE-CONTAINING PEPTIDES
分子名称:	DIMETHYLFORMAMIDE, INHIBITOR ISOVALERYL (IVA)-VAL-VAL-DIFLUOROSTATINE-N-METHYLAMINE, PENICILLOPEPSIN, ...
著者	Sielecki, A.R, James, M.N.G.
登録日	1991-12-16
公開日	1994-01-31
最終更新日	2020-07-29
実験手法	X-RAY DIFFRACTION (1.8 Å)
主引用文献	Crystallographic analysis of transition state mimics bound to penicillopepsin: difluorostatine- and difluorostatone-containing peptides. Biochemistry, 31, 1992

1APV

CRYSTALLOGRAPHIC ANALYSIS OF TRANSITION STATE MIMICS BOUND TO PENICILLOPEPSIN: DIFLUOROSTATINE-AND DIFLUOROSTATONE-CONTAINING PEPTIDES
分子名称:	DIMETHYLFORMAMIDE, INHIBITOR ISOVALERYL (IVA)-VAL-VAL-HYDRATED DIFLUOROSTATONE-N-METHYLAMINE, PENICILLOPEPSIN, ...
著者	Sielecki, A.R, James, M.N.G.
登録日	1991-12-16
公開日	1994-01-31
最終更新日	2020-07-29
実験手法	X-RAY DIFFRACTION (1.8 Å)
主引用文献	Crystallographic analysis of transition state mimics bound to penicillopepsin: difluorostatine- and difluorostatone-containing peptides. Biochemistry, 31, 1992

1DZO

Truncated PAK pilin from Pseudomonas aeruginosa
分子名称:	TYPE IV PILIN
著者	Hazes, B, Read, R.J.
登録日	2000-03-06
公開日	2000-06-11
最終更新日	2019-05-08
実験手法	X-RAY DIFFRACTION (1.63 Å)
主引用文献	Crystal Structure of Pseudomonas Aeruginosa Pak Pilin Suggests a Main-Chain-Dominated Mode of Receptor Binding J.Mol.Biol., 299, 2000

2ESM

Crystal Structure of ROCK 1 bound to fasudil
分子名称:	5-(1,4-DIAZEPAN-1-SULFONYL)ISOQUINOLINE, Rho-associated protein kinase 1
著者	Jacobs, M.
登録日	2005-10-26
公開日	2005-11-08
最終更新日	2023-08-23
実験手法	X-RAY DIFFRACTION (3.2 Å)
主引用文献	The Structure of Dimeric ROCK I Reveals the Mechanism for Ligand Selectivity. J.Biol.Chem., 281, 2006

2ETK

Crystal Structure of ROCK 1 bound to hydroxyfasudil
分子名称:	1-(1-HYDROXY-5-ISOQUINOLINESULFONYL)HOMOPIPERAZINE, Rho-associated protein kinase 1
著者	Jacobs, M.
登録日	2005-10-27
公開日	2005-11-08
最終更新日	2023-08-23
実験手法	X-RAY DIFFRACTION (2.96 Å)
主引用文献	The Structure of Dimeric ROCK I Reveals the Mechanism for Ligand Selectivity. J.Biol.Chem., 281, 2006

2ETR

Crystal Structure of ROCK I bound to Y-27632
分子名称:	(R)-TRANS-4-(1-AMINOETHYL)-N-(4-PYRIDYL) CYCLOHEXANECARBOXAMIDE, Rho-associated protein kinase 1
著者	Jacobs, M.
登録日	2005-10-27
公開日	2005-11-08
最終更新日	2023-08-23
実験手法	X-RAY DIFFRACTION (2.6 Å)
主引用文献	The Structure of Dimeric ROCK I Reveals the Mechanism for Ligand Selectivity. J.Biol.Chem., 281, 2006

2ERZ

Crystal Structure of c-AMP Dependent Kinase (PKA) bound to hydroxyfasudil
分子名称:	1-(1-HYDROXY-5-ISOQUINOLINESULFONYL)HOMOPIPERAZINE, cAMP-dependent protein kinase inhibitor, alpha form, ...
著者	Jacobs, M.
登録日	2005-10-25
公開日	2005-11-08
最終更新日	2023-08-23
実験手法	X-RAY DIFFRACTION (2.2 Å)
主引用文献	The Structure of Dimeric ROCK I Reveals the Mechanism for Ligand Selectivity. J.Biol.Chem., 281, 2006

3SGB

STRUCTURE OF THE COMPLEX OF STREPTOMYCES GRISEUS PROTEASE B AND THE THIRD DOMAIN OF THE TURKEY OVOMUCOID INHIBITOR AT 1.8 ANGSTROMS RESOLUTION
分子名称:	PROTEINASE B (SGPB), TURKEY OVOMUCOID INHIBITOR (OMTKY3)
著者	Read, R.J, Fujinaga, M, Sielecki, A.R, James, M.N.G.
登録日	1983-01-21
公開日	1983-07-12
最終更新日	2017-11-29
実験手法	X-RAY DIFFRACTION (1.8 Å)
主引用文献	Structure of the complex of Streptomyces griseus protease B and the third domain of the turkey ovomucoid inhibitor at 1.8-A resolution. Biochemistry, 22, 1983

4YVC

ROCK 1 bound to thiazole inhibitor
分子名称:	2-fluoro-N-[4-(pyridin-4-yl)-1,3-thiazol-2-yl]benzamide, Rho-associated protein kinase 1
著者	Jacobs, M.D.
登録日	2015-03-19
公開日	2015-06-10
最終更新日	2023-09-27
実験手法	X-RAY DIFFRACTION (3.2 Å)
主引用文献	Design, Synthesis, and Structure-Activity Relationships of Pyridine-Based Rho Kinase (ROCK) Inhibitors. J.Med.Chem., 58, 2015

4YVE

ROCK 1 bound to methoxyphenyl thiazole inhibitor
分子名称:	2-(3-methoxyphenyl)-N-[4-(pyridin-4-yl)-1,3-thiazol-2-yl]acetamide, Rho-associated protein kinase 1
著者	Jacobs, M.D.
登録日	2015-03-19
公開日	2015-06-10
最終更新日	2023-09-27
実験手法	X-RAY DIFFRACTION (3.4 Å)
主引用文献	Design, Synthesis, and Structure-Activity Relationships of Pyridine-Based Rho Kinase (ROCK) Inhibitors. J.Med.Chem., 58, 2015

5BML

ROCK 1 bound to a pyridine thiazole inhibitor
分子名称:	N-[4-(2-fluoropyridin-4-yl)thiophen-2-yl]-2-{3-[(methylsulfonyl)amino]phenyl}acetamide, Rho-associated protein kinase 1
著者	Jacobs, M.D.
登録日	2015-05-22
公開日	2015-06-10
最終更新日	2024-03-06
実験手法	X-RAY DIFFRACTION (2.95 Å)
主引用文献	Design, Synthesis, and Structure-Activity Relationships of Pyridine-Based Rho Kinase (ROCK) Inhibitors. J.Med.Chem., 58, 2015

5TNC

REFINED CRYSTAL STRUCTURE OF TROPONIN C FROM TURKEY SKELETAL MUSCLE AT 2.0 ANGSTROMS RESOLUTION
分子名称:	CALCIUM ION, TROPONIN-C
著者	Herzberg, O, James, M.N.G.
登録日	1988-05-27
公開日	1988-10-09
最終更新日	2024-03-06
実験手法	X-RAY DIFFRACTION (2 Å)
主引用文献	Refined crystal structure of troponin C from turkey skeletal muscle at 2.0 A resolution. J.Mol.Biol., 203, 1988

2WEC

ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL(2S)-[1-(((N-(1-NAPHTHALENEACETYL))-L-VALYL)AMINOMETHYL)HYDROXY PHOSPHINYLOXY]-3-PHENYLPROPANOATE, SODIUM SALT
分子名称:	METHYL (2S)-[1-((N-(NAPHTHALENEACETYL))-L-VALYL)AMINOMETHYL)HYDROXYPHOSPHINYLOXY]-3-PHENYL PROPANOATE, PENICILLOPEPSIN, SULFATE ION, ...
著者	Ding, J, Fraser, M.E, James, M.N.G.
登録日	1998-02-03
公開日	1998-05-27
最終更新日	2020-07-29
実験手法	X-RAY DIFFRACTION (1.5 Å)
主引用文献	Macrocyclic Inhibitors of Penicillopepsin. II. X-Ray Crystallographic Analyses of Penicillopepsin Complexed with a P3-P1 Macrocyclic Peptidyl Inhibitor and with its Two Acyclic Analogues J.Am.Chem.Soc., 120, 1998

2WED

ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE MACROCYCLIC INHIBITOR:METHYL[CYCLO-7[(2R)-((N-VALYL)AMINO)-2-(HYDROXYL-(1S)-1-METHYOXYCARBONYL-2-PHENYLETHOXY)PHOSPHINYLOXY-ETHYL]-1-NAPHTHALENEACETAMIDE], SODIUM SALT
分子名称:	METHYL[CYCLO-7[(2R)-((N-VALYL)AMINO)-2-(HYDROXYL-(1S)-1-METHYLOXYCARBONYL-2-PHENYLETHOXY)PHOSPHINYLOXY-ETHYL]-1-NAPHTHALENEACETAMIDE], PENICILLOPEPSIN, SULFATE ION, ...
著者	Ding, J, Fraser, M.E, James, M.N.G.
登録日	1998-02-03
公開日	1998-05-27
最終更新日	2020-07-29
実験手法	X-RAY DIFFRACTION (1.5 Å)
主引用文献	Macrocyclic Inhibitors of Penicillopepsin. II. X-Ray Crystallographic Analyses of Penicillopepsin Complexed with a P3-P1 Macrocyclic Peptidyl Inhibitor and with its Two Acyclic Analogues J.Am.Chem.Soc., 120, 1998

2WEA

ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL[CYCLO-7[(2R)-((N-VALYL) AMINO)-2-(HYDROXYL-(1S)-1-METHYOXYCARBONYL-2-PHENYLETHOXY) PHOSPHINYLOXY-ETHYL]-1-NAPHTHALENEACETAMIDE], SODIUM SALT
分子名称:	METHYL[CYCLO-7[(2R)-((N-VALYL)AMINO)-2-(HYDROXYL-(1S)-1-METHYLOXYCARBONYL-2-PHENYLETHOXY)PHOSPHINYLOXY-ETHYL]-1-NAPHTHALENEACETAMIDE], PENICILLOPEPSIN, SULFATE ION, ...
著者	Ding, J, Fraser, M.E, James, M.N.G.
登録日	1998-02-03
公開日	1998-05-27
最終更新日	2020-07-29
実験手法	X-RAY DIFFRACTION (1.25 Å)
主引用文献	Macrocyclic Inhibitors of Penicillopepsin. II. X-Ray Crystallographic Analyses of Penicillopepsin Complexed with a P3-P1 Macrocyclic Peptidyl Inhibitor and with its Two Acyclic Analogues J.Am.Chem.Soc., 120, 1998

1QNU

Shiga-Like Toxin I B Subunit Complexed with the Bridged-Starfish Inhibitor
分子名称:	ETHYL-CARBAMIC ACID METHYL ESTER, METHYL-CARBAMIC ACID ETHYL ESTER, Shiga toxin 1 variant B subunit, ...
著者	Pannu, N.S, Hayakawa, K, Read, R.J.
登録日	1999-10-21
公開日	2000-04-11
最終更新日	2023-12-13
実験手法	X-RAY DIFFRACTION (2.23 Å)
主引用文献	Shiga-like toxins are neutralized by tailored multivalent carbohydrate ligands. Nature, 403, 2000

2WEB

ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL(2S)-[1-(((N-FORMYL)-L-VALYL)AMINO-2-(2-NAPHTHYL)ETHYL)HYDROXYPHOSPHINYLOXY]-3-PHENYLPROPANOATE, SODIUM SALT
分子名称:	METHYL (2S)-[1-((N-FORMYL)-L-VALYL)AMINO-2-(2-NAPHTHYL)ETHYL)HYDROXYPHOSPHINYLOXY]-3-PHENYL PROPANOATE, PENICILLOPEPSIN, SULFATE ION, ...
著者	Ding, J, Fraser, M.E, James, M.N.G.
登録日	1998-02-03
公開日	1998-05-27
最終更新日	2020-07-29
実験手法	X-RAY DIFFRACTION (1.5 Å)
主引用文献	Macrocyclic Inhibitors of Penicillopepsin. II. X-Ray Crystallographic Analyses of Penicillopepsin Complexed with a P3-P1 Macrocyclic Peptidyl Inhibitor and with its Two Acyclic Analogues J.Am.Chem.Soc., 120, 1998

1TON

RAT SUBMAXILLARY GLAND SERINE PROTEASE, TONIN. STRUCTURE SOLUTION AND REFINEMENT AT 1.8 ANGSTROMS RESOLUTION
分子名称:	TONIN, ZINC ION
著者	Fujinaga, M, James, M.N.G.
登録日	1987-06-03
公開日	1988-01-16
最終更新日	2017-11-29
実験手法	X-RAY DIFFRACTION (1.8 Å)
主引用文献	Rat submaxillary gland serine protease, tonin. Structure solution and refinement at 1.8 A resolution. J.Mol.Biol., 195, 1987

1RNE

THE CRYSTAL STRUCTURE OF RECOMBINANT GLYCOSYLATED HUMAN RENIN ALONE AND IN COMPLEX WITH A TRANSITION STATE ANALOG INHIBITOR
分子名称:	2-acetamido-2-deoxy-beta-D-glucopyranose, RENIN, [[[3-(2-METHYL-PROPANE-2-SULFONYL)-1-BENZENYL]-2-PROPYL]-CARBONYL-HISTIDYL]-AMINO-[CYCLOHEXYLMETHYL]-[2-HYDROXY-4-ISOPROPYL]-PENTAN-5-OIC ACID BUTYLAMIDE
著者	Gruetter, M.G, Rahuel, J, Priestle, J.P.
登録日	1991-12-12
公開日	1993-10-31
最終更新日	2020-10-21
実験手法	X-RAY DIFFRACTION (2.4 Å)
主引用文献	The crystal structures of recombinant glycosylated human renin alone and in complex with a transition state analog inhibitor. J.Struct.Biol., 107, 1991

1APU

Crystallographic analysis of a pepstatin analogue binding to the aspartyl proteinase penicillopepsin at 1.8 angstroms resolution
分子名称:	PEPSTATIN ANALOGUE ISOVALERYL-VAL-VAL-STA-O-ET, PROTEIN (PENICILLOPEPSIN), alpha-D-mannopyranose
著者	Sielecki, A.R, James, M.N.G.
登録日	1991-12-16
公開日	1994-01-31
最終更新日	2020-07-29
実験手法	X-RAY DIFFRACTION (1.8 Å)
主引用文献	Crystallographic Analysis of Transition State Mimics Bound to Penicillopepsin: Difluorostatine-and Difluorostatone-Containing Peptides Biochemistry, 31, 1992

1APT

CRYSTALLOGRAPHIC ANALYSIS OF A PEPSTATIN ANALOGUE BINDING TO THE ASPARTYL PROTEINASE PENICILLOPEPSIN AT 1.8 ANGSTROMS RESOLUTION
分子名称:	INHIBITOR ISOVALERYL (IVA)-VAL-VAL-LYSTA-O-ET (LYSTA IS A LYSYL SIDE CHAIN ANALOGUE OF STATIN, PENICILLOPEPSIN, alpha-D-mannopyranose
著者	Sielecki, A.R, James, M.N.G.
登録日	1991-12-16
公開日	1994-01-31
最終更新日	2020-07-29
実験手法	X-RAY DIFFRACTION (1.8 Å)
主引用文献	Crystallographic Analysis of a Pepstatin Analogue Binding to the Aspartyl Proteinase Penicillopepsin at 1.8 Angstroms Resolution Peptides: Structure and Function, Proceedings of the of the Eighth American Peptide Symposium, 1, 1983

2CI2

CRYSTAL AND MOLECULAR STRUCTURE OF THE SERINE PROTEINASE INHIBITOR CI-2 FROM BARLEY SEEDS
分子名称:	CHYMOTRYPSIN INHIBITOR 2
著者	Mcphalen, C.A, James, M.N.G.
登録日	1988-09-05
公開日	1988-09-07
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2 Å)
主引用文献	Crystal and molecular structure of the serine proteinase inhibitor CI-2 from barley seeds. Biochemistry, 26, 1987

<12

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表示件数:	25
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