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Human serum albumin complexed with sodium 4-phenylbutyrate
Descriptor:	4-PHENYL-BUTANOIC ACID, PHOSPHATE ION, Serum albumin
Authors:	Kawai, A, Otagiri, M.
Deposit date:	2017-10-30
Release date:	2018-02-07
Last modified:	2023-11-22
Method:	X-RAY DIFFRACTION (2.65 Å)
Cite:	Crystal structure analysis of human serum albumin complexed with sodium 4-phenylbutyrate. Biochem Biophys Rep, 13, 2018

3ACJ

Crystal structure of imidazo pyrimidine derivative bound to the kinase domain of human LCK, (Auto-phosphorylated on TYR394)
Descriptor:	7-(3,4-dimethoxyphenyl)-5-(ethylsulfanyl)imidazo[1,2-c]pyrimidine, DIMETHYL SULFOXIDE, Proto-oncogene tyrosine-protein kinase LCK, ...
Authors:	Tsuji, E.
Deposit date:	2010-01-05
Release date:	2010-06-30
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.2 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

3ACK

Crystal structure of Pyrrolo pyrazine derivative bound to the kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	6-(5-methoxy-1-methyl-1H-indol-3-yl)-5H-pyrrolo[2,3-b]pyrazine, DIMETHYL SULFOXIDE, Proto-oncogene tyrosine-protein kinase LCK, ...
Authors:	Tsuji, E.
Deposit date:	2010-01-05
Release date:	2010-06-30
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.6 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

3AD4

Crystal Structure of Methoxy Benzofuran Derivative bound to the Kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	(4-chlorophenyl)(5-methoxy-1-benzofuran-2-yl)methanone, (4S)-2-METHYL-2,4-PENTANEDIOL, DIMETHYL SULFOXIDE, ...
Authors:	Tsuji, E.
Deposit date:	2010-01-14
Release date:	2011-01-19
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.2 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

3AC4

Crystal structure of triazolo pyrimidine derivative bound to the kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	5-[(2-amino-1,1-dimethylethyl)amino]-7-[(3,5-dimethoxyphenyl)amino][1,2,4]triazolo[4,3-c]pyrimidine-8-carboxamide, DIMETHYL SULFOXIDE, Proto-oncogene tyrosine-protein kinase LCK, ...
Authors:	Tsuji, E.
Deposit date:	2009-12-28
Release date:	2010-06-30
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.7 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

3AD6

Crystal structure of Pyrazolo pyrimidine derivative bound to the kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	7-[(cyclopropylmethyl)amino]-2-[(4-methoxyphenyl)amino]-5-methylpyrazolo[1,5-a]pyrimidine-3-carboxamide, DIMETHYL SULFOXIDE, Proto-oncogene tyrosine-protein kinase LCK, ...
Authors:	Tsuji, E.
Deposit date:	2010-01-14
Release date:	2011-01-19
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.15 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

3AFB

Crystal structures of catalytic site mutants of active domain 2 of chitinase from Pyrococcus furiosus
Descriptor:	GLYCEROL, MAGNESIUM ION, Putative chitinase, ...
Authors:	Tsuji, H.
Deposit date:	2010-02-25
Release date:	2010-06-09
Last modified:	2024-03-13
Method:	X-RAY DIFFRACTION (1.76 Å)
Cite:	Kinetic and crystallographic analyses of the catalytic domain of chitinase from Pyrococcus furiosus- the role of conserved residues in the active site Febs J., 277, 2010

3AD5

Crystal structure of Triazolone derivative bound to the kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, 4-[4-(benzyloxy)phenyl]-5-{[2-(4-chlorophenyl)-2-oxoethyl]sulfanyl}-2,4-dihydro-3H-1,2,4-triazol-3-one, DIMETHYL SULFOXIDE, ...
Authors:	Tsuji, E.
Deposit date:	2010-01-14
Release date:	2011-01-19
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

2ZIR

Crystal Structure of rat protein farnesyltransferase complexed with a benzofuran inhibitor and FPP
Descriptor:	2-[(S)-(4-chlorophenyl)(hydroxy)(1-methyl-1H-imidazol-5-yl)methyl]-N-morpholin-4-yl-7-phenyl-1-benzofuran-5-carboxamide, FARNESYL DIPHOSPHATE, GLYCEROL, ...
Authors:	Fukami, T.A, Sogabe, S, Nagata, Y, Kondoh, O, Ishii, N.
Deposit date:	2008-02-22
Release date:	2009-02-24
Last modified:	2023-11-01
Method:	X-RAY DIFFRACTION (2.4 Å)
Cite:	Synthesis and structure-activity relationships of novel benzofuran farnesyltransferase inhibitors Bioorg.Med.Chem.Lett., 19, 2009

2ZTH

Crystal structure of holo form of rat catechol-o-methyltransferase
Descriptor:	Catechol O-methyltransferase, MAGNESIUM ION, S-ADENOSYLMETHIONINE
Authors:	Tsuji, E.
Deposit date:	2008-10-01
Release date:	2009-01-13
Last modified:	2023-11-01
Method:	X-RAY DIFFRACTION (2.6 Å)
Cite:	Crystal structures of the Apo and Holo form of rat catechol-O-methyltransferase J.Struct.Biol., 165, 2009

2ZIS

Crystal Structure of rat protein farnesyltransferase complexed with a bezoruran inhibitor and FPP
Descriptor:	3-{2-[(S)-(4-cyanophenyl)(hydroxy)(1-methyl-1H-imidazol-5-yl)methyl]-5-nitro-1-benzofuran-7-yl}benzonitrile, ACETIC ACID, FARNESYL DIPHOSPHATE, ...
Authors:	Fukami, T.A, Sogabe, S, Nagata, Y, Kondoh, O, Ishii, N.
Deposit date:	2008-02-22
Release date:	2009-02-24
Last modified:	2023-11-01
Method:	X-RAY DIFFRACTION (2.6 Å)
Cite:	Synthesis and structure-activity relationships of novel benzofuran farnesyltransferase inhibitors Bioorg.Med.Chem.Lett., 19, 2009

3AC1

Crystal structure of pyrazin derivative bound to the kinase domain of Human LCK, (Auto-phosphorylated on TYR394)
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, 5-{[(1R,2S)-2-aminocyclohexyl]amino}-3-[(3,5-dimethoxyphenyl)amino]pyrazine-2-carboxamide, DIMETHYL SULFOXIDE, ...
Authors:	Tsuji, E.
Deposit date:	2009-12-28
Release date:	2010-06-30
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (1.99 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

3AC5

Crystal structure of triazolo pyrimidine derivative bound to the kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	5-{[(1R,2S)-2-aminocyclohexyl]amino}-7-[(3,5-dimethoxyphenyl)amino]-2-(3-hydroxyphenyl)[1,2,4]triazolo[1,5-c]pyrimidine-8-carboxamide, DIMETHYL SULFOXIDE, Proto-oncogene tyrosine-protein kinase LCK, ...
Authors:	Tsuji, E.
Deposit date:	2009-12-28
Release date:	2010-06-30
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.5 Å)
Cite:	Ab initio molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

3AC3

Crystal structure of pyrazolo pyrimidine derivative bound to the kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	2-[(3,5-dimethoxyphenyl)amino]-5-ethyl-7-[(2R)-2-(hydroxymethyl)pyrrolidin-1-yl]pyrazolo[1,5-a]pyrimidine-3-carboxamide, Proto-oncogene tyrosine-protein kinase LCK, SULFATE ION
Authors:	Tsuji, E.
Deposit date:	2009-12-28
Release date:	2010-06-30
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.55 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

1XJD

Crystal Structure of PKC-theta complexed with Staurosporine at 2A resolution
Descriptor:	Protein kinase C, theta type, STAUROSPORINE
Authors:	Xu, Z.B.
Deposit date:	2004-09-23
Release date:	2004-10-19
Last modified:	2023-08-23
Method:	X-RAY DIFFRACTION (2 Å)
Cite:	Catalytic domain crystal structure of protein kinase C-theta (PKCtheta) J.Biol.Chem., 279, 2004

3AC2

Crystal structure of pyrazolo pyrimidine derivative bound to the kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	(4S)-2-METHYL-2,4-PENTANEDIOL, 7-[(2-amino-2-methylpropyl)amino]-2-[(3,5-dimethoxyphenyl)amino]-5-methylpyrazolo[1,5-a]pyrimidine-3-carboxamide, DIMETHYL SULFOXIDE, ...
Authors:	Tsuji, E.
Deposit date:	2009-12-28
Release date:	2010-06-30
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.1 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

3AC8

Crystal structure of pyrazolo pyrimidine derivative bound to the kinase domain of human LCK, (auto-phosphorylated on TYR394)
Descriptor:	7-[(2-amino-2-methylpropyl)amino]-5-cyclopropyl-2-[(3,5-dimethoxyphenyl)amino]pyrazolo[1,5-a]pyrimidine-3-carboxamide, Proto-oncogene tyrosine-protein kinase LCK, SULFATE ION
Authors:	Tsuji, E.
Deposit date:	2009-12-29
Release date:	2010-06-30
Last modified:	2023-11-15
Method:	X-RAY DIFFRACTION (2.3 Å)
Cite:	Ab initio fragment molecular orbital study of ligand binding to leukocyte-specific protein tyrosine (LCK) kinase To be Published

1V7R

Structure of nucleotide triphosphate pyrophosphatase from pyrococcus horikoshii OT3
Descriptor:	CITRIC ACID, hypothetical protein PH1917
Authors:	Lokanath, N.K, Kunishima, N, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
Deposit date:	2003-12-22
Release date:	2003-12-30
Last modified:	2023-10-25
Method:	X-RAY DIFFRACTION (1.4 Å)
Cite:	Structures of dimeric nonstandard nucleotide triphosphate pyrophosphatase from Pyrococcus horikoshii OT3: functional significance of interprotomer conformational changes. J.Mol.Biol., 375, 2008

2ZLB

Crystal structure of APO form of rat catechol-O-methyltransferase
Descriptor:	Catechol O-methyltransferase, SULFATE ION
Authors:	Tsuji, E.
Deposit date:	2008-04-04
Release date:	2008-10-07
Last modified:	2023-11-01
Method:	X-RAY DIFFRACTION (2.2 Å)
Cite:	Crystal structures of the Apo and Holo form of rat catechol-O-methyltransferase J.Struct.Biol., 165, 2009

2ZVJ

Crystal structures of rat Catechol-O-Methyltransferase complexed with coumarine-based inhibitor
Descriptor:	7,8-dihydroxy-4-phenyl-2H-chromen-2-one, Catechol O-methyltransferase, MAGNESIUM ION, ...
Authors:	Tsuji, E.
Deposit date:	2008-11-07
Release date:	2009-01-06
Last modified:	2023-11-01
Method:	X-RAY DIFFRACTION (2.3 Å)
Cite:	Crystal structures of rat catechol-O-methyltransferase complexed with coumarine-based inhibitor Biochem.Biophys.Res.Commun., 378, 2009

7CU2

CRYSTAL STRUCTURE OF STREPTOMYCES ALBOGRISEOLUS FLAVIN-DEPENDENT TRYPTOPHAN 6-HALOGENASE THAL IN COMPLEX WITH REDUCED FAD
Descriptor:	DIHYDROFLAVINE-ADENINE DINUCLEOTIDE, Tryptophan 6-halogenase
Authors:	Chitnumsub, P, Jaruwat, A, Phintha, A, Chaiyen, P.
Deposit date:	2020-08-20
Release date:	2020-11-25
Last modified:	2023-11-29
Method:	X-RAY DIFFRACTION (2.4 Å)
Cite:	Dissecting the low catalytic capability of flavin-dependent halogenases. J.Biol.Chem., 296, 2020

7WBK

Crystal structure of Legionella pneumophila effector protein Lpg0081
Descriptor:	Lpg0081, SULFATE ION
Authors:	Lee, J, Kim, H, Oh, B.H.
Deposit date:	2021-12-16
Release date:	2022-06-15
Method:	X-RAY DIFFRACTION (2.74 Å)
Cite:	Reversible modification of mitochondrial ADP/ATP translocases by paired Legionella effector proteins. Proc.Natl.Acad.Sci.USA, 119, 2022

7WBM

Crystal structure of Legionella pneumophila effector protein Lpg0081
Descriptor:	Lpg0081, [(2R,3S,4R,5R)-5-(6-AMINOPURIN-9-YL)-3,4-DIHYDROXY-OXOLAN-2-YL]METHYL [HYDROXY-[[(2R,3S,4R,5S)-3,4,5-TRIHYDROXYOXOLAN-2-YL]METHOXY]PHOSPHORYL] HYDROGEN PHOSPHATE
Authors:	Lee, J, Kim, H, Oh, B.H.
Deposit date:	2021-12-17
Release date:	2022-06-15
Last modified:	2023-11-29
Method:	X-RAY DIFFRACTION (2.7 Å)
Cite:	Reversible modification of mitochondrial ADP/ATP translocases by paired Legionella effector proteins. Proc.Natl.Acad.Sci.USA, 119, 2022

7CU0

Crystal structure of Streptomyces albogriseolus flavin-dependent tryptophan 6-halogenase Thal in complex with tryptophan
Descriptor:	TRYPTOPHAN, Tryptophan 6-halogenase
Authors:	Chitnumsub, P, Jaruwat, A, Phintha, A, Chaiyen, P.
Deposit date:	2020-08-20
Release date:	2020-11-25
Last modified:	2023-11-29
Method:	X-RAY DIFFRACTION (1.95 Å)
Cite:	Dissecting the low catalytic capability of flavin-dependent halogenases. J.Biol.Chem., 296, 2020

7W3O

Crystal structure of human CYB5R3
Descriptor:	FLAVIN-ADENINE DINUCLEOTIDE, NADH-cytochrome b5 reductase 3 soluble form
Authors:	Noda, N.N.
Deposit date:	2021-11-25
Release date:	2022-12-07
Last modified:	2023-11-29
Method:	X-RAY DIFFRACTION (2.46 Å)
Cite:	The UFM1 system regulates ER-phagy through the ufmylation of CYB5R3. Nat Commun, 13, 2022

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