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1QK1
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BU of 1qk1 by Molmil
CRYSTAL STRUCTURE OF HUMAN UBIQUITOUS MITOCHONDRIAL CREATINE KINASE
Descriptor: CREATINE KINASE, UBIQUITOUS MITOCHONDRIAL, PHOSPHATE ION
Authors:Eder, M, Schlattner, U, Fritz-Wolf, K, Wallimann, T, Kabsch, W.
Deposit date:1999-07-08
Release date:2000-04-11
Last modified:2023-12-13
Method:X-RAY DIFFRACTION (2.7 Å)
Cite:Crystal Structure of Human Ubiquitous Mitochondrial Creatine Kinase
Proteins: Struct.,Funct., Genet., 39, 2000
1QH4
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BU of 1qh4 by Molmil
CRYSTAL STRUCTURE OF CHICKEN BRAIN-TYPE CREATINE KINASE AT 1.41 ANGSTROM RESOLUTION
Descriptor: ACETATE ION, CALCIUM ION, CREATINE KINASE
Authors:Eder, M, Schlattner, U, Becker, A, Wallimann, T, Kabsch, W, Fritz-Wolf, K.
Deposit date:1999-05-11
Release date:1999-11-19
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (1.41 Å)
Cite:Crystal structure of brain-type creatine kinase at 1.41 A resolution.
Protein Sci., 8, 1999
7P22
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BU of 7p22 by Molmil
Thaumatin-like protein of Amycolatopsis rifamycinica
Descriptor: Thaumatin pathogenesis-like protein
Authors:Eder, M, Hofer, G, Odabas, M, Keller, W.
Deposit date:2021-07-03
Release date:2022-07-13
Last modified:2024-01-31
Method:X-RAY DIFFRACTION (1.87 Å)
Cite:The structure of Thaumatin-like proteins of a bacterial, a fungal and an animal origin
To Be Published
7P23
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BU of 7p23 by Molmil
Thaumatin-like protein of Puccinia graminis
Descriptor: SODIUM ION, Thaumatin-like protein of Puccinia graminis
Authors:Eder, M, Hofer, G, Odabas, M, Keller, W.
Deposit date:2021-07-03
Release date:2022-07-13
Last modified:2024-01-31
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:The structure of Thaumatin-like proteins of a bacterial, a fungal and an animal origin
To Be Published
7QEH
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BU of 7qeh by Molmil
LTA-binding domain of SlpA, the S-layer protein from Lactobacillus amylovorus
Descriptor: PHOSPHATE ION, S-layer
Authors:Eder, M, Dordic, A, Sagmeister, T, Pavkov-Keller, T.
Deposit date:2021-12-03
Release date:2022-12-14
Method:X-RAY DIFFRACTION (1.67 Å)
Cite:The binding of the lactobacilli S-layer protein to the bacterial cell through interaction with LTA
to be published
7P20
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BU of 7p20 by Molmil
High resolution structure of the Juniperus ashei allergen - Jun a 3
Descriptor: CHLORIDE ION, Pathogenesis-related 5 protein Jun a 3.0101
Authors:Eder, M, Hofer, G, Keller, W.
Deposit date:2021-07-03
Release date:2022-07-13
Last modified:2024-01-31
Method:X-RAY DIFFRACTION (1.4 Å)
Cite:Crystal structure of the allergen Jun a 3 the Thaumatin-like protein of Juniperus ashei
To Be Published
2VIN
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BU of 2vin by Molmil
Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
Descriptor: (2R)-1-(2,6-dimethylphenoxy)propan-2-amine, ACETATE ION, SULFATE ION, ...
Authors:Frederickson, M, Callaghan, O, Chessari, G, Congreve, M, Cowan, S.R, Matthews, J.E, McMenamin, R, Smith, D, Vinkovic, M, Wallis, N.G.
Deposit date:2007-12-05
Release date:2008-01-22
Last modified:2017-07-05
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
J.Med.Chem., 51, 2008
2VIQ
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BU of 2viq by Molmil
Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
Descriptor: 4-(2-aminoethoxy)-N-(2,5-diethoxyphenyl)-3,5-dimethylbenzamide, ACETATE ION, UROKINASE-TYPE PLASMINOGEN ACTIVATOR CHAIN B
Authors:Frederickson, M, Callaghan, O, Chessari, G, Congreve, M, Cowan, S.R, Matthews, J.E, McMenamin, R, Smith, D, Vinkovic, M, Wallis, N.G.
Deposit date:2007-12-05
Release date:2008-01-22
Last modified:2017-07-05
Method:X-RAY DIFFRACTION (2 Å)
Cite:Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator.
J.Med.Chem., 51, 2008
2VIP
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BU of 2vip by Molmil
Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
Descriptor: 4-(2-AMINOETHOXY)-3,5-DICHLORO-N-[3-(1-METHYLETHOXY)PHENYL]BENZAMIDE, ACETATE ION, SULFATE ION, ...
Authors:Frederickson, M, Callaghan, O, Chessari, G, Congreve, M, Cowan, S.R, Matthews, J.E, McMenamin, R, Smith, D, Vinkovic, M, Wallis, N.G.
Deposit date:2007-12-05
Release date:2008-01-22
Last modified:2017-07-05
Method:X-RAY DIFFRACTION (1.72 Å)
Cite:Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
J.Med.Chem., 51, 2008
4HD4
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BU of 4hd4 by Molmil
Crystal Structure of Tyrosinase from Bacillus megaterium V218F mutant
Descriptor: COPPER (II) ION, Tyrosinase
Authors:Goldfeder, M, Kanteev, M, Adir, N, Fishman, A.
Deposit date:2012-10-02
Release date:2013-01-23
Last modified:2024-02-28
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Influencing the monophenolase/diphenolase activity ratio in tyrosinase.
Biochim.Biophys.Acta, 1834, 2013
2VIW
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BU of 2viw by Molmil
Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
Descriptor: 4-(2-aminoethoxy)-N-(3-chloro-2-ethoxy-5-piperidin-1-ylphenyl)-3,5-dimethylbenzamide, ACETATE ION, UROKINASE-TYPE PLASMINOGEN ACTIVATOR CHAIN B
Authors:Frederickson, M, Callaghan, O, Chessari, G, Congreve, M, Cowan, S.R, Matthews, J.E, McMenamin, R, Smith, D, Vinkovic, M, Wallis, N.G.
Deposit date:2007-12-05
Release date:2008-01-22
Last modified:2017-07-05
Method:X-RAY DIFFRACTION (2.05 Å)
Cite:Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator.
J.Med.Chem., 51, 2008
2VIV
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BU of 2viv by Molmil
Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
Descriptor: 4-(2-aminoethoxy)-N-(3-chloro-5-piperidin-1-ylphenyl)-3,5-dimethylbenzamide, ACETATE ION, UROKINASE-TYPE PLASMINOGEN ACTIVATOR CHAIN B
Authors:Frederickson, M, Callaghan, O, Chessari, G, Congreve, M, Cowan, S.R, Matthews, J.E, McMenamin, R, Smith, D, Vinkovic, M, Wallis, N.G.
Deposit date:2007-12-05
Release date:2008-01-22
Last modified:2017-07-05
Method:X-RAY DIFFRACTION (1.72 Å)
Cite:Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator.
J.Med.Chem., 51, 2008
4HD7
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BU of 4hd7 by Molmil
Crystal Structure of Tyrosinase from Bacillus megaterium V218G mutant soaked in CuSO4
Descriptor: COPPER (II) ION, Tyrosinase
Authors:Goldfeder, M, Kanteev, M, Adir, N, Fishman, A.
Deposit date:2012-10-02
Release date:2013-01-23
Last modified:2024-02-28
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:Influencing the monophenolase/diphenolase activity ratio in tyrosinase.
Biochim.Biophys.Acta, 1834, 2013
2VIO
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BU of 2vio by Molmil
Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
Descriptor: 4-(2-aminoethoxy)-3,5-dichlorobenzoic acid, ACETATE ION, UROKINASE-TYPE PLASMINOGEN ACTIVATOR CHAIN B
Authors:Frederickson, M, Callaghan, O, Chessari, G, Congreve, M, Cowan, S.R, Matthews, J.E, McMenamin, R, Smith, D, Vinkovic, M, Wallis, N.G.
Deposit date:2007-12-05
Release date:2008-01-22
Last modified:2017-07-05
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Fragment-Based Discovery of Mexiletine Derivatives as Orally Bioavailable Inhibitors of Urokinase-Type Plasminogen Activator
J.Med.Chem., 51, 2008
4HD6
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BU of 4hd6 by Molmil
Crystal Structure of Tyrosinase from Bacillus megaterium V218F mutant soaked in CuSO4
Descriptor: COPPER (II) ION, Tyrosinase
Authors:Goldfeder, M, Kanteev, M, Adir, N, Fishman, A.
Deposit date:2012-10-02
Release date:2013-01-23
Last modified:2024-02-28
Method:X-RAY DIFFRACTION (2 Å)
Cite:Influencing the monophenolase/diphenolase activity ratio in tyrosinase.
Biochim.Biophys.Acta, 1834, 2013
7PQS
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BU of 7pqs by Molmil
SRPK1 in complex with MSC2711186
Descriptor: 1,2-ETHANEDIOL, CHLORIDE ION, CITRIC ACID, ...
Authors:Schroeder, M, Leiendecker, M, Knapp, S, Structural Genomics Consortium (SGC)
Deposit date:2021-09-20
Release date:2021-12-15
Last modified:2024-01-31
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:SRPK1 in complex with MSC2711186
To Be Published
4P6R
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BU of 4p6r by Molmil
Crystal Structure of tyrosinase from Bacillus megaterium with tyrosine in the active site
Descriptor: TYROSINE, Tyrosinase, ZINC ION
Authors:Goldfeder, M, Kanteev, M, Adir, N, Fishman, A.
Deposit date:2014-03-25
Release date:2014-07-30
Last modified:2023-12-27
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Determination of tyrosinase substrate-binding modes reveals mechanistic differences between type-3 copper proteins.
Nat Commun, 5, 2014
4P6S
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BU of 4p6s by Molmil
Crystal Structure of tyrosinase from Bacillus megaterium with L-DOPA in the active site
Descriptor: 3,4-DIHYDROXYPHENYLALANINE, Tyrosinase, ZINC ION
Authors:Goldfeder, M, Kanteev, M, Adir, N, Fishman, A.
Deposit date:2014-03-25
Release date:2014-07-30
Last modified:2023-12-27
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Determination of tyrosinase substrate-binding modes reveals mechanistic differences between type-3 copper proteins.
Nat Commun, 5, 2014
4P6T
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BU of 4p6t by Molmil
Crystal Structure of tyrosinase from Bacillus megaterium with p-tyrosol in the active site
Descriptor: 4-(2-hydroxyethyl)phenol, COPPER (II) ION, Tyrosinase
Authors:Goldfeder, M, Kanteev, M, Adir, N, Fishman, A.
Deposit date:2014-03-25
Release date:2014-07-30
Last modified:2023-12-27
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:Determination of tyrosinase substrate-binding modes reveals mechanistic differences between type-3 copper proteins.
Nat Commun, 5, 2014
6SFO
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BU of 6sfo by Molmil
MAPK14 with bound inhibitor SR-318
Descriptor: 5-azanyl-~{N}-[[4-(3-cyclohexylpropylcarbamoyl)phenyl]methyl]-1-phenyl-pyrazole-4-carboxamide, GLYCEROL, Mitogen-activated protein kinase 14, ...
Authors:Schroeder, M, Edwards, A.M, Arrowsmith, C.H, Bountra, C, Knapp, S, Structural Genomics Consortium (SGC)
Deposit date:2019-08-01
Release date:2019-09-11
Last modified:2024-01-24
Method:X-RAY DIFFRACTION (1.75 Å)
Cite:MAPK14 with bound inhibitor SR-318
To Be Published
6RAA
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BU of 6raa by Molmil
CLK1 Kinase domain with bound imidazopyridin inhibitor TP003
Descriptor: 1,2-ETHANEDIOL, 4-[2-methyl-1-(4-methylpiperazin-1-yl)-1-oxidanylidene-propan-2-yl]-~{N}-(6-pyridin-4-ylimidazo[1,2-a]pyridin-2-yl)benzamide, Dual specificity protein kinase CLK1
Authors:Schroeder, M, Arrowsmith, C, Knapp, S, Bountra, C, Edwards, A, Structural Genomics Consortium (SGC)
Deposit date:2019-04-05
Release date:2019-04-24
Last modified:2024-01-24
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:CLK1 Kinase domain with bound imidazopyridin inhibitor TP003
To Be Published
8ALU
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BU of 8alu by Molmil
Crystal structure of the teichoic acid binding domain of SlpA, S-layer protein from Lactobacillus acidophilus (aa. 314-444)
Descriptor: PHOSPHATE ION, S-layer protein
Authors:Eder, M, Dordic, A, Sagmeister, T, Vejzovic, D, Pavkov-Keller, T.
Deposit date:2022-08-01
Release date:2023-08-16
Method:X-RAY DIFFRACTION (2.09 Å)
Cite:The binding of the lactobacilli S-layer protein to the bacterial cell through interaction with teichoic acids
To Be Published
7QEC
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BU of 7qec by Molmil
Crystal structure of SlpA - domain II, domain that is involved in the self-assembly of the S-layer from Lactobacillus amylovorus
Descriptor: S-layer
Authors:Eder, M, Dordic, A, Millan, C, Sagmeister, T, Uson, I, Pavkov-Keller, T.
Deposit date:2021-12-02
Release date:2022-12-14
Method:X-RAY DIFFRACTION (1.95 Å)
Cite:The self-assembly of the S-layer protein from lactobacilli
to be published
7QFG
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BU of 7qfg by Molmil
Crystal structure of S-layer protein SlpA from Lactobacillus acidophilus, domain III (aa 309-444)
Descriptor: 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, CHLORIDE ION, S-layer protein
Authors:Sagmeister, T, Eder, M, Pavkov-Keller, T.
Deposit date:2021-12-06
Release date:2022-12-21
Last modified:2024-01-31
Method:X-RAY DIFFRACTION (1.65 Å)
Cite:The binding of the lactobacilli S-layer protein to the bacterial cell through interaction with LTA
To be published
4UIR
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BU of 4uir by Molmil
Structure of oleate hydratase from Elizabethkingia meningoseptica
Descriptor: FLAVIN-ADENINE DINUCLEOTIDE, HEXAETHYLENE GLYCOL, OLEATE HYDRATASE, ...
Authors:Pavkov-Keller, T, Hromic, A, Engleder, M, Emmerstorfer, A, Steinkellner, G, Schrempf, S, Wriessnegger, T, Leitner, E, Strohmeier, G.A, Kaluzna, I, Mink, D, Schuermann, M, Wallner, S, Macheroux, P, Pichler, H, Gruber, K.
Deposit date:2015-04-02
Release date:2015-07-01
Last modified:2024-01-10
Method:X-RAY DIFFRACTION (2.75 Å)
Cite:Structure-Based Mechanism of Oleate Hydratase from Elizabethkingia Meningoseptica.
Chembiochem, 16, 2015

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