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PDB: 17822 件

3CQG
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Nucleoporin Nup107/Nup133 interaction complex, delta finger mutant
分子名称: Nuclear pore complex protein Nup107, Nuclear pore complex protein Nup133
著者Jeudy, S, Boehmer, T, Berke, I, Schwartz, T.U.
登録日2008-04-02
公開日2008-07-01
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献Structural and functional studies of Nup107/Nup133 interaction and its implications for the architecture of the nuclear pore complex.
Mol.Cell, 30, 2008
5EQG
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Human GLUT1 in complex with inhibitor (2~{S})-3-(4-fluorophenyl)-2-[2-(3-hydroxyphenyl)ethanoylamino]-~{N}-[(1~{S})-1-phenylethyl]propanamide
分子名称: (2~{S})-3-(4-fluorophenyl)-2-[2-(3-hydroxyphenyl)ethanoylamino]-~{N}-[(1~{S})-1-phenylethyl]propanamide, Solute carrier family 2, facilitated glucose transporter member 1
著者Kapoor, K, Finer-Moore, J, Pedersen, B.P, Caboni, L, Waight, A.B, Hillig, R, Bringmann, P, Heisler, I, Muller, T, Siebeneicher, H, Stroud, R.M.
登録日2015-11-12
公開日2016-04-13
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Mechanism of inhibition of human glucose transporter GLUT1 is conserved between cytochalasin B and phenylalanine amides.
Proc.Natl.Acad.Sci.USA, 113, 2016
3V19
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Forestalling insulin fibrillation by insertion of a chiral clamp mechanism-based application of protein engineering to global health
分子名称: CHLORIDE ION, Insulin, PHENOL, ...
著者Wan, Z.L, Hua, Q.X, Wickramasinghe, N.P, Huang, K, Petkova, A.T, Hu, S.Q, Phillips, N.B, Yeh, I.J, Whittake, J, Ismail-Beigi, F, Katsoyyannis, P.G, Tycko, R, Weiss, M.A.
登録日2011-12-09
公開日2012-12-12
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Forestalling insulin fibrillation by insertion of a chiral clamp mechanism-based application of protein engineering to global health
To be Published
1RNO
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RIBONUCLEASE A CRYSTALLIZED FROM 80% AMMONIUM SULPHATE
分子名称: RIBONUCLEASE A, SULFATE ION
著者Fedorov, A.A, Josef-Mccarthy, D, Graf, I, Anguelova, D, Fedorov, E.V, Almo, S.C.
登録日1995-11-08
公開日1996-04-03
最終更新日2019-08-14
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Ionic interactions in crystalline bovine pancreatic ribonuclease A.
Biochemistry, 35, 1996
6GBR
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Crystal Structure of the oligomerization domain of VP35 from Reston virus, mercury derivative
分子名称: MERCURIBENZOIC ACID, Polymerase cofactor VP35
著者Zinzula, L, Nagy, I, Orsini, M, Weyher-Stingl, E, Baumeister, W, Bracher, A.
登録日2018-04-16
公開日2018-10-10
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (3.15 Å)
主引用文献Structures of Ebola and Reston Virus VP35 Oligomerization Domains and Comparative Biophysical Characterization in All Ebolavirus Species.
Structure, 27, 2019
3SJB
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Crystal structure of S. cerevisiae Get3 in the open state in complex with Get1 cytosolic domain
分子名称: ATPase GET3, Golgi to ER traffic protein 1, PHOSPHATE ION, ...
著者Reitz, S, Wild, K, Sinning, I.
登録日2011-06-21
公開日2011-07-06
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (3.3 Å)
主引用文献Structural basis for tail-anchored membrane protein biogenesis by the Get3-receptor complex.
Science, 333, 2011
2OSZ
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Structure of Nup58/45 suggests flexible nuclear pore diameter by intermolecular sliding
分子名称: Nucleoporin p58/p45
著者Melcak, I, Hoelz, A, Blobel, G.
登録日2007-02-06
公開日2007-04-10
最終更新日2024-02-21
実験手法X-RAY DIFFRACTION (2.85 Å)
主引用文献Structure of Nup58/45 suggests flexible nuclear pore diameter by intermolecular sliding.
Science, 315, 2007
1TA2
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Crystal structure of thrombin in complex with compound 1
分子名称: 1-(2-AMINO-3,3-DIPHENYL-PROPIONYL)-PYRROLIDINE-3-CARBOXYLIC ACID 2,5-DICHLORO-BENZYLAMIDE, Hirudin, thrombin
著者Tucker, T.J, Brady, S.F, Lumma, W.C, Lewis, S.D, Gardel, S.J, Naylor-Olsen, A.M, Yan, Y, Sisko, J.T, Stauffer, K.J, Lucas, B.Y, Lynch, J.J, Cook, J.J, Stranieri, M.T, Holahan, M.A, Lyle, E.A, Baskin, E.P, Chen, I.-W, Dancheck, K.B, Krueger, J.A, Cooper, C.M, Vacca, J.P.
登録日2004-05-19
公開日2004-06-08
最終更新日2017-10-11
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Design and synthesis of a series of potent and orally bioavailable noncovalent thrombin inhibitors that utilize nonbasic groups in the P1 position
J.Med.Chem., 41, 1998
5EK8
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Crystal structure of a 9R-lipoxygenase from Cyanothece PCC8801 at 2.7 Angstroms
分子名称: FE (II) ION, Lipoxygenase, SODIUM ION
著者Feussner, I, Ficner, R, Neumann, P, Newie, J, Andreou, A, Einsle, O.
登録日2015-11-03
公開日2015-12-23
最終更新日2024-05-08
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Crystal structure of a lipoxygenase from Cyanothece sp. may reveal novel features for substrate acquisition.
J.Lipid Res., 57, 2016
5EKJ
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Human Carbonic Anhydrase II complexed with a two-faced guest
分子名称: 2-(butylamino)-~{N}-[2-(4-sulfamoylphenyl)ethyl]ethanamide, Carbonic anhydrase 2, GLYCEROL, ...
著者Roose, B.W, Dmochowski, I.J.
登録日2015-11-03
公開日2016-01-06
最終更新日2024-03-06
実験手法X-RAY DIFFRACTION (1.129 Å)
主引用文献Programming A Molecular Relay for Ultrasensitive Biodetection through (129) Xe NMR.
Angew.Chem.Int.Ed.Engl., 55, 2016
2UYA
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DEL162-163 mutant of Bacillus subtilis Oxalate Decarboxylase OxdC
分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, CHLORIDE ION, GLYCEROL, ...
著者Just, V.J, Burrell, M.R, Bowater, L, McRobbie, I, Stevenson, C.E.M, Lawson, D.M, Bornemann, S.
登録日2007-04-03
公開日2007-08-21
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献The Identity of the Active Site of Oxalate Decarboxylase and the Importance of the Stability of Active-Site Lid Conformations.
Biochem.J., 407, 2007
1SSJ
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A DNA DUPLEX CONTAINING A CHOLESTEROL ADDUCT (BETA-ANOMER)
分子名称: 5'-D(*CP*CP*AP*CP*(HOB)P*GP*GP*AP*AP*C)-3', 5'-D(GP*TP*TP*CP*CP*GP*GP*TP*GP*G)-3'
著者Gomez-Pinto, I, Cubero, E, Kalko, S.G, Monaco, V, van der Marel, G, van Boom, J.H, Orozco, M, Gonzalez, C.
登録日2004-03-24
公開日2004-06-01
最終更新日2024-05-01
実験手法SOLUTION NMR
主引用文献Effect of bulky lesions on DNA: Solution structure of a DNA duplex containing a cholesterol adduct.
J.Biol.Chem., 279, 2004
2UYB
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S161A mutant of Bacillus subtilis Oxalate Decarboxylase OxdC
分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, FORMIC ACID, MANGANESE (II) ION, ...
著者Just, V.J, Burrell, M.R, Bowater, L, McRobbie, I, Stevenson, C.E.M, Lawson, D.M, Bornemann, S.
登録日2007-04-03
公開日2007-08-21
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献The Identity of the Active Site of Oxalate Decarboxylase and the Importance of the Stability of Active-Site Lid Conformations.
Biochem.J., 407, 2007
2OSN
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An alternate description of a crystal structure of phospholipase A2 from Bungarus caeruleus
分子名称: CHLORIDE ION, Phospholipase A2 isoform 3
著者Stenkamp, R.E, Le Trong, I.
登録日2007-02-06
公開日2007-03-06
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献An alternate description of two crystal structures of phospholipase A(2) from Bungarus caeruleus.
Acta Crystallogr.,Sect.D, 63, 2007
1SW0
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Triosephosphate isomerase from Gallus gallus, loop 6 hinge mutant K174L, T175W
分子名称: 2-PHOSPHOGLYCOLIC ACID, Triosephosphate isomerase
著者Kursula, I, Salin, M, Sun, J, Norledge, B.V, Haapalainen, A.M, Sampson, N.S, Wierenga, R.K.
登録日2004-03-30
公開日2004-08-24
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (1.71 Å)
主引用文献Understanding protein lids: structural analysis of active hinge mutants in triosephosphate isomerase
Protein Eng.Des.Sel., 17, 2004
1SW3
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Triosephosphate isomerase from Gallus gallus, loop 6 mutant T175V
分子名称: 2-PHOSPHOGLYCOLIC ACID, Triosephosphate isomerase
著者Kursula, I, Salin, M, Sun, J, Norledge, B.V, Haapalainen, A.M, Sampson, N.S, Wierenga, R.K.
登録日2004-03-30
公開日2004-08-24
最終更新日2023-10-25
実験手法X-RAY DIFFRACTION (2.03 Å)
主引用文献Understanding protein lids: structural analysis of active hinge mutants in triosephosphate isomerase
Protein Eng.Des.Sel., 17, 2004
2W5U
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Flavodoxin from Helicobacter pylori in complex with the C3 inhibitor
分子名称: FLAVIN MONONUCLEOTIDE, Flavodoxin, [2-(5-amino-4-cyano-1H-pyrazol-1-yl)-5-(trifluoromethyl)phenyl](hydroxy)oxoammonium
著者Cremades, N, Perez-Dorado, I, Hermoso, J.A, Martinez-Julvez, M, Sancho, J.
登録日2008-12-12
公開日2009-12-22
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.62 Å)
主引用文献Discovery of Specific Flavodoxin Inhibitors as Potential Therapeutic Agents Against Helicobacter Pylori Infection.
Acs Chem.Biol., 4, 2009
1T40
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Crystal structure of human aldose reductase complexed with NADP and IDD552 at ph 5
分子名称: Aldose reductase, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, [5-FLUORO-2-({[(4,5,7-TRIFLUORO-1,3-BENZOTHIAZOL-2-YL)METHYL]AMINO}CARBONYL)PHENOXY]ACETIC ACID
著者Ruiz, F, Hazemann, I, Mitschler, A, Chevrier, B, Schneider, T, Joachimiak, A, Karplus, M, Podjarny, A.
登録日2004-04-28
公開日2004-08-03
最終更新日2024-03-13
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献The crystallographic structure of the aldose reductase-IDD552 complex shows direct proton donation from tyrosine 48.
Acta Crystallogr.,Sect.D, 60, 2004
3RXR
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Crystal structure of Trypsin complexed with cycloheptanamine (F01 and F03, cocktail experiment)
分子名称: CALCIUM ION, Cationic trypsin, DIMETHYL SULFOXIDE, ...
著者Yamane, J, Yao, M, Zhou, Y, Tanaka, I.
登録日2011-05-10
公開日2011-08-24
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (1.72 Å)
主引用文献In-crystal affinity ranking of fragment hit compounds reveals a relationship with their inhibitory activities
J.Appl.Crystallogr., 44, 2011
6C4Q
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1.16 Angstrom Resolution Crystal Structure of Acyl Carrier Protein Domain (residues 1-100) of Polyketide Synthase Pks13 from Mycobacterium tuberculosis
分子名称: (4S)-2-METHYL-2,4-PENTANEDIOL, 1,2-ETHANEDIOL, Polyketide synthase Pks13
著者Minasov, G, Shuvalova, L, Dubrovska, I, Kiryukhina, O, Grimshaw, S, Kwon, K, Anderson, W.F, Satchell, K.J.F, Joachimiak, A, Center for Structural Genomics of Infectious Diseases (CSGID)
登録日2018-01-12
公開日2018-01-24
実験手法X-RAY DIFFRACTION (1.16 Å)
主引用文献1.16 Angstrom Resolution Crystal Structure of Acyl Carrier Protein Domain (residues 1-100) of Polyketide Synthase Pks13 from Mycobacterium tuberculosis.
To Be Published
7X9S
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Crystal structure of a complex between the antirepressor GmaR and the transcriptional repressor MogR
分子名称: GmaR, Motility gene repressor MogR
著者Cho, S.Y, Na, H.W, Oh, H.B, Kwak, Y.M, Song, W.S, Park, S.C, Yoon, S.I.
登録日2022-03-16
公開日2022-11-23
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (3.11 Å)
主引用文献Structural basis of flagellar motility regulation by the MogR repressor and the GmaR antirepressor in Listeria monocytogenes.
Nucleic Acids Res., 50, 2022
5OPE
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Robo1 Ig1-4 crystals form 2
分子名称: PHOSPHATE ION, Roundabout homolog 1
著者Aleksandrova, N, Gutsche, I, Kandiah, E, Avilov, S.V, Petoukhov, M.V, Seiradake, E, McCarthy, A.A.
登録日2017-08-09
公開日2018-01-17
最終更新日2024-01-17
実験手法X-RAY DIFFRACTION (2.54 Å)
主引用文献Robo1 Forms a Compact Dimer-of-Dimers Assembly.
Structure, 26, 2018
7XHY
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Crystal structure of MerTK Kinase domain with BMS794833
分子名称: CHLORIDE ION, DIMETHYL SULFOXIDE, Tyrosine-protein kinase Mer, ...
著者Kim, J.H, Lee, B.I.
登録日2022-04-11
公開日2022-11-30
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (2.16 Å)
主引用文献BMS794833 inhibits macrophage efferocytosis by directly binding to MERTK and inhibiting its activity.
Exp.Mol.Med., 54, 2022
3DPR
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Human rhinovirus 2 bound to a concatamer of the VLDL receptor module V3
分子名称: CALCIUM ION, LAURIC ACID, LDL-receptor class A 3, ...
著者Querol-Audi, J, Pous, J, Fita, I, Verdaguer, N.
登録日2008-07-09
公開日2009-04-07
最終更新日2017-10-25
実験手法X-RAY DIFFRACTION (3.5 Å)
主引用文献Minor group human rhinovirus-receptor interactions: geometry of multimodular attachment and basis of recognition
Febs Lett., 583, 2009
1T4Z
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Solution structure of the N-terminal domain of Synechococcus elongatus SasA (25-structures ensemble)
分子名称: Adaptive-response sensory-kinase sasA
著者Vakonakis, I, Klewer, D.A, LiWang, A.C.
登録日2004-04-30
公開日2004-11-16
最終更新日2024-05-01
実験手法SOLUTION NMR
主引用文献Structure of the N-terminal domain of the circadian clock-associated histidine kinase SasA.
J.Mol.Biol., 342, 2004

223790

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