8Z0L
| Cryo-EM structure of Cas8-HNH system at partial R-loop state | Descriptor: | DNA (32-MER), DNA (5'-D(P*GP*TP*GP*CP*GP*GP*A)-3'), HNH endonuclease, ... | Authors: | Zhang, H, Zhu, H, Li, X, Liu, Y. | Deposit date: | 2024-04-09 | Release date: | 2024-10-02 | Last modified: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (2.57 Å) | Cite: | Structural basis for the type I-F Cas8-HNH system. Embo J., 43, 2024
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8Z0K
| Cryo-EM structure of Cas8-HNH system at full R-loop state | Descriptor: | DNA (37-MER), DNA (5'-D(P*GP*TP*GP*CP*GP*GP*A)-3'), HNH endonuclease, ... | Authors: | Zhang, H, Zhu, H, Li, X, Liu, Y. | Deposit date: | 2024-04-09 | Release date: | 2024-10-02 | Last modified: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (2.51 Å) | Cite: | Structural basis for the type I-F Cas8-HNH system. Embo J., 43, 2024
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8ZDY
| Cryo-EM structure of Cas8-HNH system at target free state | Descriptor: | RNA (58-MER), a protein | Authors: | Zhang, H, Zhu, H, Li, X, Liu, Y. | Deposit date: | 2024-05-03 | Release date: | 2024-10-02 | Last modified: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (3.6 Å) | Cite: | Structural basis for the type I-F Cas8-HNH system. Embo J., 43, 2024
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8ZNR
| Cryo-EM structure of Cas8-HNH system at ssDNA-bound state | Descriptor: | DNA (35-MER), RNA (56-MER), protein structure | Authors: | Zhang, H, Zhu, H, Li, X, Liu, Y. | Deposit date: | 2024-05-28 | Release date: | 2024-10-02 | Last modified: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (2.9 Å) | Cite: | Structural basis for the type I-F Cas8-HNH system. Embo J., 43, 2024
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6OMV
| CryoEM structure of the LbCas12a-crRNA-AcrVA4-DNA complex | Descriptor: | AcrVA4, Cpf1, DNA (5'-D(*CP*GP*TP*CP*CP*TP*TP*TP*AP*GP*GP*A)-3'), ... | Authors: | Chang, L, Li, Z, Zhang, H. | Deposit date: | 2019-04-19 | Release date: | 2019-06-12 | Last modified: | 2024-03-20 | Method: | ELECTRON MICROSCOPY (3.9 Å) | Cite: | Structural Basis for the Inhibition of CRISPR-Cas12a by Anti-CRISPR Proteins. Cell Host Microbe, 25, 2019
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6KX2
| Crystal structure of GDP bound RhoA protein | Descriptor: | GUANOSINE-5'-DIPHOSPHATE, Transforming protein RhoA | Authors: | Zhang, H, Luo, C. | Deposit date: | 2019-09-09 | Release date: | 2020-08-19 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (1.454 Å) | Cite: | Covalent Inhibitors Allosterically Block the Activation of Rho Family Proteins and Suppress Cancer Cell Invasion. Adv Sci, 7, 2020
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6KX3
| Crystal structure of RhoA protein with covalent inhibitor DC-Rhoin | Descriptor: | GUANOSINE-5'-DIPHOSPHATE, Transforming protein RhoA, prop-2-enyl (3R)-1,1-bis(oxidanylidene)-2,3-dihydro-1-benzothiophene-3-carboxylate | Authors: | Zhang, H, Luo, C. | Deposit date: | 2019-09-09 | Release date: | 2020-08-19 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (1.981 Å) | Cite: | Covalent Inhibitors Allosterically Block the Activation of Rho Family Proteins and Suppress Cancer Cell Invasion. Adv Sci, 7, 2020
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8YHE
| Cryo-EM structure of CTR-bound type VII CRISPR-Cas complex at post-state II | Descriptor: | RNA (29-MER), RNA (46-MER), ZINC ION, ... | Authors: | Zhang, H, Deng, Z, Li, X. | Deposit date: | 2024-02-28 | Release date: | 2024-08-21 | Last modified: | 2024-09-25 | Method: | ELECTRON MICROSCOPY (3.07 Å) | Cite: | Structural basis for the activity of the type VII CRISPR-Cas system. Nature, 633, 2024
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8Z4L
| Cryo-EM structure of CTR-bound type VII CRISPR-Cas complex at substrate-engaged state I | Descriptor: | RNA (40-MER), RNA (49-MER), ZINC ION, ... | Authors: | Zhang, H, Deng, Z, Li, X. | Deposit date: | 2024-04-17 | Release date: | 2024-08-21 | Last modified: | 2024-09-25 | Method: | ELECTRON MICROSCOPY (2.85 Å) | Cite: | Structural basis for the activity of the type VII CRISPR-Cas system. Nature, 633, 2024
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8Z9C
| Cryo-EM structure of NTR-bound type VII CRISPR-Cas complex at substrate-engaged state I | Descriptor: | Protein structure, RNA (41-MER), RNA (48-MER), ... | Authors: | Zhang, H, Deng, Z, Li, X. | Deposit date: | 2024-04-23 | Release date: | 2024-08-21 | Last modified: | 2024-09-25 | Method: | ELECTRON MICROSCOPY (3.01 Å) | Cite: | Structural basis for the activity of the type VII CRISPR-Cas system. Nature, 633, 2024
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8Z4J
| Cryo-EM structure of CTR-bound type VII CRISPR-Cas complex at substrate-engaged state II | Descriptor: | Protein structure, RNA (34-MER), RNA (38-MER), ... | Authors: | Zhang, H, Deng, Z, Li, X. | Deposit date: | 2024-04-17 | Release date: | 2024-08-21 | Last modified: | 2024-09-25 | Method: | ELECTRON MICROSCOPY (2.97 Å) | Cite: | Structural basis for the activity of the type VII CRISPR-Cas system. Nature, 633, 2024
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8Z9E
| Cryo-EM structure of NTR-bound type VII CRISPR-Cas complex at substrate-engaged state II | Descriptor: | Protein structure, RNA (34-MER), RNA (39-MER), ... | Authors: | Zhang, H, Deng, Z, Li, X. | Deposit date: | 2024-04-23 | Release date: | 2024-08-21 | Last modified: | 2024-09-25 | Method: | ELECTRON MICROSCOPY (3.13 Å) | Cite: | Structural basis for the activity of the type VII CRISPR-Cas system. Nature, 633, 2024
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8Z99
| Cryo-EM structure of NTR-bound type VII CRISPR-Cas complex at substrate-engaged state +I | Descriptor: | RNA (49-MER), RNA (54-MER), ZINC ION, ... | Authors: | Zhang, H, Deng, Z, Li, X. | Deposit date: | 2024-04-22 | Release date: | 2024-08-21 | Last modified: | 2024-10-16 | Method: | ELECTRON MICROSCOPY (3.2 Å) | Cite: | Structural basis for the activity of the type VII CRISPR-Cas system. Nature, 633, 2024
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8YHD
| Cryo-EM structure of CTR-bound type VII CRISPR-Cas complex at post-state I | Descriptor: | RNA (35-MER), RNA (53-MER), ZINC ION, ... | Authors: | Zhang, H, Deng, Z, Li, X. | Deposit date: | 2024-02-28 | Release date: | 2024-08-21 | Last modified: | 2024-09-25 | Method: | ELECTRON MICROSCOPY (2.93 Å) | Cite: | Structural basis for the activity of the type VII CRISPR-Cas system. Nature, 633, 2024
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4TMF
| Crystal structure of human CD38 in complex with hydrolysed compound JMS713 | Descriptor: | 5-O-[(R)-{[(S)-[4-(8-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)butoxy](hydroxy)phosphoryl]oxy}(hydroxy)phosphoryl]-alpha-D- ribofuranose, ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 | Authors: | Zhang, H, Swarbrick, J, Potter, B, Hao, Q. | Deposit date: | 2014-06-01 | Release date: | 2015-05-13 | Last modified: | 2023-09-27 | Method: | X-RAY DIFFRACTION (2.05 Å) | Cite: | Cyclic adenosine 5'-diphosphate ribose analogs without a "southern" ribose inhibit ADP-ribosyl cyclase-hydrolase CD38. J.Med.Chem., 57, 2014
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6JYJ
| Crystal structure of FAM46B (TENT5B) | Descriptor: | CITRATE ANION, Terminal nucleotidyltransferase 5B | Authors: | Zhang, H, Hu, J.L, Gao, S. | Deposit date: | 2019-04-26 | Release date: | 2020-03-04 | Last modified: | 2024-04-03 | Method: | X-RAY DIFFRACTION (2.693199 Å) | Cite: | FAM46B is a prokaryotic-like cytoplasmic poly(A) polymerase essential in human embryonic stem cells. Nucleic Acids Res., 48, 2020
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3NSN
| Crystal Structure of insect beta-N-acetyl-D-hexosaminidase OfHex1 complexed with TMG-chitotriomycin | Descriptor: | 2-deoxy-2-(trimethylammonio)-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, N-acetylglucosaminidase | Authors: | Zhang, H, Liu, T, Liu, F, Yang, Q, Shen, X. | Deposit date: | 2010-07-02 | Release date: | 2010-11-24 | Last modified: | 2024-10-09 | Method: | X-RAY DIFFRACTION (2.1 Å) | Cite: | Structural Determinants of an Insect {beta}-N-Acetyl-D-hexosaminidase Specialized as a Chitinolytic Enzyme J.Biol.Chem., 286, 2011
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3H0Q
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3H0J
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3HFJ
| Bacillus anthracis nicotinate mononucleotide adenylytransferase (nadD) in complex with inhibitor CID 3289443 | Descriptor: | 3-amino-N-(3-fluorophenyl)-6-thiophen-2-ylthieno[2,3-b]pyridine-2-carboxamide, CALCIUM ION, Nicotinate (Nicotinamide) nucleotide adenylyltransferase | Authors: | Zhang, H, Huang, N, Eyobo, Y. | Deposit date: | 2009-05-11 | Release date: | 2009-09-08 | Last modified: | 2024-02-21 | Method: | X-RAY DIFFRACTION (2.02 Å) | Cite: | Targeting NAD biosynthesis in bacterial pathogens: Structure-based development of inhibitors of nicotinate mononucleotide adenylyltransferase NadD. Chem.Biol., 16, 2009
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5Z5T
| The first bromodomain of BRD4 with compound BDF-2141 | Descriptor: | 2-amino-4-(1H-imidazol-1-yl)quinolin-8-ol, Bromodomain-containing protein 4 | Authors: | Zhang, H, Luo, C. | Deposit date: | 2018-01-20 | Release date: | 2019-01-23 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (1.991 Å) | Cite: | Development and evaluation of a novel series of Nitroxoline-derived BET inhibitors with antitumor activity in renal cell carcinoma. Oncogenesis, 7, 2018
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5Z5V
| The first bromodomain of BRD4 with compound BDF-1253 | Descriptor: | Bromodomain-containing protein 4, N-{8-hydroxy-4-[(1H-imidazol-1-yl)methyl]quinolin-2-yl}acetamide | Authors: | Zhang, H, Luo, C. | Deposit date: | 2018-01-20 | Release date: | 2019-01-23 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (1.66 Å) | Cite: | Development and evaluation of a novel series of Nitroxoline-derived BET inhibitors with antitumor activity in renal cell carcinoma. Oncogenesis, 7, 2018
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5Z5U
| The first bromodomain of BRD4 with compound BDF-2254 | Descriptor: | 2-amino-4-(1H-imidazol-1-yl)quinoline-6,8-diol, Bromodomain-containing protein 4 | Authors: | Zhang, H, Luo, C. | Deposit date: | 2018-01-20 | Release date: | 2019-01-23 | Last modified: | 2023-11-22 | Method: | X-RAY DIFFRACTION (1.631 Å) | Cite: | Development and evaluation of a novel series of Nitroxoline-derived BET inhibitors with antitumor activity in renal cell carcinoma. Oncogenesis, 7, 2018
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3GBF
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4KTC
| NS3/NS4A protease with inhibitor | Descriptor: | (2R,6S,13aR,14aR,16aS)-6-{[(cyclopentyloxy)carbonyl]amino}-14a-[(cyclopropylsulfonyl)carbamoyl]-5,16-dioxooctadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-2-yl 3,4-dihydroisoquinoline-2(1H)-carboxylate, NS4A peptide, Serine protease NS3, ... | Authors: | Zhang, H, Ballard, J, Vigers, G.P.A, Brandhuber, B.J. | Deposit date: | 2013-05-20 | Release date: | 2013-08-07 | Last modified: | 2023-09-20 | Method: | X-RAY DIFFRACTION (2.3 Å) | Cite: | Discovery of Danoprevir (ITMN-191/R7227), a Highly Selective and Potent Inhibitor of Hepatitis C Virus (HCV) NS3/4A Protease. J.Med.Chem., 57, 2014
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