6AEZ
| Crystal structure of human CCL5 trimer | Descriptor: | C-C motif chemokine 5, SULFATE ION | Authors: | Chen, Y.C, Li, K.M, Chen, P.J, Zarivach, R, Sun, Y.J, Sue, S.C. | Deposit date: | 2018-08-07 | Release date: | 2019-08-07 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (1.63 Å) | Cite: | Integrative Model to Coordinate the Oligomerization and Aggregation Mechanisms of CCL5. J.Mol.Biol., 432, 2020
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6LSQ
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6LOG
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2PJG
| Solution structure of rhodostomin D51E mutant | Descriptor: | Rhodostoxin-disintegrin rhodostomin | Authors: | Chuang, W.J, Chen, Y.C, Chen, C.Y, Chou, L.J. | Deposit date: | 2007-04-16 | Release date: | 2007-05-08 | Last modified: | 2021-11-10 | Method: | SOLUTION NMR | Cite: | Effect of D to E mutation of the RGD motif in rhodostomin on its activity, structure, and dynamics: Importance of the interactions between the D residue and integrin Proteins, 2009
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2PJF
| Solution structure of rhodostomin | Descriptor: | Rhodostoxin-disintegrin rhodostomin | Authors: | Chuang, W.J, Chen, Y.C, Chen, C.Y, Chang, Y.T. | Deposit date: | 2007-04-16 | Release date: | 2007-05-08 | Last modified: | 2022-03-16 | Method: | SOLUTION NMR | Cite: | Effect of D to E mutation of the RGD motif in rhodostomin on its activity, structure, and dynamics: Importance of the interactions between the D residue and integrin Proteins, 2009
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3CLH
| Crystal structure of 3-dehydroquinate synthase (DHQS)from Helicobacter pylori | Descriptor: | 3-dehydroquinate synthase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, ZINC ION | Authors: | Wang, W.C, Liu, J.S, Cheng, W.C, Wang, H.J, Chen, Y.C. | Deposit date: | 2008-03-19 | Release date: | 2009-03-24 | Last modified: | 2023-11-01 | Method: | X-RAY DIFFRACTION (2.4 Å) | Cite: | Structure-based inhibitor discovery of Helicobacter pylori dehydroquinate synthase. Biochem.Biophys.Res.Commun., 373, 2008
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2LA1
| Expression in Pichia pastoris and backbone dynamics of dendroaspin, a three finger toxin | Descriptor: | Mambin | Authors: | Chuang, W.J, Cheng, C.H, Chen, Y.C, Shiu, J.H. | Deposit date: | 2011-03-01 | Release date: | 2012-03-07 | Last modified: | 2023-06-14 | Method: | SOLUTION NMR | Cite: | Dynamics and functional differences between dendroaspin and rhodostomin: Insights into protein scaffolds in integrin recognition Protein Sci., 21, 2012
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4V93
| Fitted coordinates for Lumbricus terrestris hemoglobin cryo-EM complex (EMD-2627) | Descriptor: | EXTRACELLULAR GLOBIN-2, EXTRACELLULAR GLOBIN-3, EXTRACELLULAR GLOBIN-4, ... | Authors: | Chen, W.T, Chen, Y.C, Liou, H.H, Chao, C.Y. | Deposit date: | 2014-04-16 | Release date: | 2014-07-09 | Last modified: | 2019-12-11 | Method: | ELECTRON MICROSCOPY (8.1 Å) | Cite: | Structural Basis for Cooperative Oxygen Binding and Bracelet-Assisted Assembly of Lumbricus Terrestris Hemoglobin To be Published
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1Q7J
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1Q7I
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3UCI
| Crystal structure of Rhodostomin ARLDDL mutant | Descriptor: | disintegrin | Authors: | Shiu, J.H, Chen, C.Y, Chen, Y.C, Chang, Y.T, Chang, Y.S, Huang, C.H, Chuang, W.J. | Deposit date: | 2011-10-27 | Release date: | 2012-11-21 | Last modified: | 2023-11-01 | Method: | X-RAY DIFFRACTION (1.35 Å) | Cite: | Design of Integrin AlphaVbeta3-Specific Disintegrin for Cancer Therapy To be Published
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5GO3
| Crystal structure of a di-nucleotide cyclase Vibrio mutant | Descriptor: | Cyclic GMP-AMP synthase | Authors: | Ming, Z.H, Wang, W, Xie, Y.C, Chen, Y.C, Yan, L.M, Lou, Z.Y. | Deposit date: | 2016-07-26 | Release date: | 2016-11-02 | Method: | X-RAY DIFFRACTION (2.2 Å) | Cite: | Crystal structure of a di-nucleotide cyclase Vibrio mutant To Be Published
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6KY5
| Crystal structure of a hydrolase mutant | Descriptor: | PET hydrolase, SULFATE ION | Authors: | Cui, Y.L, Chen, Y.C, Liu, X.Y, Dong, S.J, Han, J, Xiang, H, Chen, Q, Liu, H.Y, Han, X, Liu, W.D, Tang, S.Y, Wu, B. | Deposit date: | 2019-09-16 | Release date: | 2020-09-23 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (1.631 Å) | Cite: | Computational redesign of PETase for plasticbiodegradation by GRAPE strategy. Biorxiv, 2020
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2LUN
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4P5U
| Crystal structure of TatD | Descriptor: | Tat-linked quality control protein TatD | Authors: | Chen, Y, Li, C.-L, Hsiao, Y.-Y, Duh, Y, Yuan, H.S. | Deposit date: | 2014-03-20 | Release date: | 2014-08-27 | Last modified: | 2023-09-27 | Method: | X-RAY DIFFRACTION (2 Å) | Cite: | Structure and function of TatD exonuclease in DNA repair. Nucleic Acids Res., 42, 2014
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4PE8
| Crystal structure of TatD in complex with trinucleotide DNA | Descriptor: | DNA (5'-D(*GP*CP*T)-3'), Tat-linked quality control protein TatD | Authors: | Chen, Y, Li, C.-L, Hsiao, Y.-Y, Duh, Y, Yuan, H.S. | Deposit date: | 2014-04-23 | Release date: | 2014-08-27 | Last modified: | 2023-09-27 | Method: | X-RAY DIFFRACTION (2.894 Å) | Cite: | Structure and function of TatD exonuclease in DNA repair. Nucleic Acids Res., 42, 2014
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5YAM
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3K53
| Crystal Structure of NFeoB from P. furiosus | Descriptor: | Ferrous iron transport protein b | Authors: | Eng, E.T, Dong, G, Unger, V.M. | Deposit date: | 2009-10-06 | Release date: | 2010-05-26 | Last modified: | 2017-11-01 | Method: | X-RAY DIFFRACTION (2.7 Å) | Cite: | Structural fold, conservation and Fe(II) binding of the intracellular domain of prokaryote FeoB. J.Struct.Biol., 170, 2010
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5MJB
| Kinase domain of human EphB1, G703C mutant, covalently bound to a quinazoline-based inhibitor | Descriptor: | 2-chloranyl-~{N}-[4-[(2-chloranyl-5-oxidanyl-phenyl)amino]quinazolin-7-yl]ethanamide, Ephrin type-B receptor 1, SULFATE ION | Authors: | Kung, A, Schimpl, M, Chen, Y.-C, Overman, R.C, Zhang, C. | Deposit date: | 2016-11-30 | Release date: | 2017-05-17 | Last modified: | 2024-01-17 | Method: | X-RAY DIFFRACTION (2.23 Å) | Cite: | A Chemical-Genetic Approach to Generate Selective Covalent Inhibitors of Protein Kinases. ACS Chem. Biol., 12, 2017
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5MJA
| Kinase domain of human EphB1 bound to a quinazoline-based inhibitor | Descriptor: | 2-chloranyl-~{N}-[4-[(2-chloranyl-5-oxidanyl-phenyl)amino]quinazolin-7-yl]ethanamide, Ephrin type-B receptor 1, SULFATE ION | Authors: | Kung, A, Schimpl, M, Chen, Y.-C, Overman, R.C, Zhang, C. | Deposit date: | 2016-11-30 | Release date: | 2017-05-17 | Last modified: | 2024-01-17 | Method: | X-RAY DIFFRACTION (2.14 Å) | Cite: | A Chemical-Genetic Approach to Generate Selective Covalent Inhibitors of Protein Kinases. ACS Chem. Biol., 12, 2017
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6OQI
| CDK2 in complex with Cpd14 (5-fluoro-4-(4-methyl-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepin-3-yl)-N-(5-(4-methylpiperazin-1-yl)pyridin-2-yl)pyrimidin-2-amine) | Descriptor: | 5-fluoro-N-[5-(4-methylpiperazin-1-yl)pyridin-2-yl]-4-[(4S)-4-methyl-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepin-3-yl]pyrimidin-2-amine, Cyclin-dependent kinase 2 | Authors: | Murray, J.M. | Deposit date: | 2019-04-26 | Release date: | 2020-07-29 | Last modified: | 2023-10-11 | Method: | X-RAY DIFFRACTION (2 Å) | Cite: | Design of a brain-penetrant CDK4/6 inhibitor for glioblastoma. Bioorg.Med.Chem.Lett., 29, 2019
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1JXS
| Solution Structure of the DNA-Binding Domain of Interleukin Enhancer Binding Factor | Descriptor: | interleukin enhancer binding factor | Authors: | Chuang, W.J, Liu, P.P, Li, C, Hsieh, Y.H, Chen, S.W, Chen, S.H, Jeng, W.Y. | Deposit date: | 2001-09-08 | Release date: | 2003-03-11 | Last modified: | 2024-05-29 | Method: | SOLUTION NMR | Cite: | Solution structure of the DNA-binding domain of interleukin enhancer binding factor 1 (FOXK1a) PROTEINS: STRUCT.,FUNCT.,GENET., 49, 2002
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1BC4
| THE SOLUTION STRUCTURE OF A CYTOTOXIC RIBONUCLEASE FROM THE OOCYTES OF RANA CATESBEIANA (BULLFROG), NMR, 15 STRUCTURES | Descriptor: | RIBONUCLEASE | Authors: | Chang, C.-F, Chen, C, Chen, Y.-C, Hom, K, Huang, R.-F, Huang, T. | Deposit date: | 1998-05-05 | Release date: | 1998-10-14 | Last modified: | 2019-12-25 | Method: | SOLUTION NMR | Cite: | The solution structure of a cytotoxic ribonuclease from the oocytes of Rana catesbeiana (bullfrog). J.Mol.Biol., 283, 1998
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1PSJ
| ACIDIC PHOSPHOLIPASE A2 FROM AGKISTRODON HALYS PALLAS | Descriptor: | CALCIUM ION, PHOSPHOLIPASE A2 | Authors: | Wang, X.Q, Lin, Z.J. | Deposit date: | 1995-05-24 | Release date: | 1996-07-11 | Last modified: | 2024-06-05 | Method: | X-RAY DIFFRACTION (2 Å) | Cite: | Crystal structure of an acidic phospholipase A2 from the venom of Agkistrodon halys pallas at 2.0 A resolution. J.Mol.Biol., 255, 1996
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5L6P
| EphB3 kinase domain covalently bound to an irreversible inhibitor (compound 6) | Descriptor: | 1,4-DIETHYLENE DIOXIDE, Ephrin type-B receptor 3, ~{N}-(4-phenylazanylquinazolin-7-yl)ethanamide | Authors: | Schimpl, M, Overman, R, Kung, A, Chen, Y.-C, Ni, F, Zhu, J, Turner, M, Molina, H, Zhang, C. | Deposit date: | 2016-05-30 | Release date: | 2016-08-10 | Last modified: | 2024-01-10 | Method: | X-RAY DIFFRACTION (2.26 Å) | Cite: | Development of Specific, Irreversible Inhibitors for a Receptor Tyrosine Kinase EphB3. J.Am.Chem.Soc., 138, 2016
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