9D6C
| Gag CA-SP1 immature lattice bound with Lenacapavir and Bevirimat from enveloped virus like particles | Descriptor: | 3alpha-[(3-carboxy-3-methylbutanoyl)oxy]-8alpha,9beta,10alpha,13alpha,17alpha,19beta-lup-20(29)-en-28-oic acid, Gag, INOSITOL HEXAKISPHOSPHATE, ... | Authors: | Wu, C, Meuser, M.E, Xiong, Y. | Deposit date: | 2024-08-14 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (2.1 Å) | Cite: | Structural insights into inhibitor mechanisms on immature HIV-1 Gag lattice revealed by high-resolution in situ single-particle cryo-EM. Biorxiv, 2024
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9D6D
| Gag CA-SP1 immature lattice bound with Lenacapavir from enveloped virus like particles | Descriptor: | Gag polyprotein, INOSITOL HEXAKISPHOSPHATE, N-[(1S)-1-(3-{4-chloro-3-[(methylsulfonyl)amino]-1-(2,2,2-trifluoroethyl)-1H-indazol-7-yl}-6-[3-methyl-3-(methylsulfonyl)but-1-yn-1-yl]pyridin-2-yl)-2-(3,5-difluorophenyl)ethyl]-2-[(3bS,4aR)-5,5-difluoro-3-(trifluoromethyl)-3b,4,4a,5-tetrahydro-1H-cyclopropa[3,4]cyclopenta[1,2-c]pyrazol-1-yl]acetamide | Authors: | Wu, C, Meuser, M.E, Xiong, Y. | Deposit date: | 2024-08-14 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (2.18 Å) | Cite: | Structural insights into inhibitor mechanisms on immature HIV-1 Gag lattice revealed by high-resolution in situ single-particle cryo-EM. Biorxiv, 2024
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9D6E
| Gag CA-SP1 immature lattice bound with Bevirimat from enveloped virus like particles | Descriptor: | 3alpha-[(3-carboxy-3-methylbutanoyl)oxy]-8alpha,9beta,10alpha,13alpha,17alpha,19beta-lup-20(29)-en-28-oic acid, Gag polyprotein, INOSITOL HEXAKISPHOSPHATE | Authors: | Wu, C, Meuser, M.E, Xiong, Y. | Deposit date: | 2024-08-14 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (3.09 Å) | Cite: | Structural insights into inhibitor mechanisms on immature HIV-1 Gag lattice revealed by high-resolution in situ single-particle cryo-EM. Biorxiv, 2024
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9D88
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9DQC
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9DR0
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9DVA
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9DVF
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9DWD
| Gag CA-SP1 immature lattice bound with Lenacapavir from enveloped virus like particles (T8I) | Descriptor: | Gag, INOSITOL HEXAKISPHOSPHATE, N-[(1S)-1-(3-{4-chloro-3-[(methylsulfonyl)amino]-1-(2,2,2-trifluoroethyl)-1H-indazol-7-yl}-6-[3-methyl-3-(methylsulfonyl)but-1-yn-1-yl]pyridin-2-yl)-2-(3,5-difluorophenyl)ethyl]-2-[(3bS,4aR)-5,5-difluoro-3-(trifluoromethyl)-3b,4,4a,5-tetrahydro-1H-cyclopropa[3,4]cyclopenta[1,2-c]pyrazol-1-yl]acetamide | Authors: | Wu, C, Meuser, M.E, Xiong, Y. | Deposit date: | 2024-10-09 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (3.13 Å) | Cite: | Structural insights into inhibitor mechanisms on immature HIV-1 Gag lattice revealed by high-resolution in situ single-particle cryo-EM. Biorxiv, 2024
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9DZ8
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9DZE
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9E17
| Structure of RyR1 in the primed state in the presence of caffeine (reprocessed/reanalyzed from EMPIAR-10997, 7TZC, EMD-26205) | Descriptor: | (2S)-3-(octadecanoyloxy)-2-[(9Z)-octadec-9-enoyloxy]propyl 2-(trimethylammonio)ethyl phosphate, 4-[(7-methoxy-2,3-dihydro-1,4-benzothiazepin-4(5H)-yl)methyl]benzoic acid, ADENOSINE-5'-TRIPHOSPHATE, ... | Authors: | Miotto, M.C, Marks, A.R. | Deposit date: | 2024-10-21 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (2.45 Å) | Cite: | Targeting Ryanodine Receptors with Allopurinol and Xanthine Derivatives for the Treatment of Cardiac and Musculoskeletal Weakness Disorders To Be Published
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9E18
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9E19
| Structure of RyR1 in the open state in the presence of pentoxifylline | Descriptor: | 3,7-DIMETHYL-1-(5-OXOHEXYL)-3,7-DIHYDRO-1H-PURINE-2,6-DIONE, ADENOSINE-5'-TRIPHOSPHATE, CALCIUM ION, ... | Authors: | Miotto, M.C, Marks, A.R. | Deposit date: | 2024-10-21 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (4.04 Å) | Cite: | Targeting Ryanodine Receptors with Allopurinol and Xanthine Derivatives for the Treatment of Cardiac and Musculoskeletal Weakness Disorders To Be Published
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9E1A
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9E1B
| Structure of RyR1 in the open state in the presence of dyphylline | Descriptor: | ADENOSINE-5'-TRIPHOSPHATE, CALCIUM ION, Peptidyl-prolyl cis-trans isomerase FKBP1A, ... | Authors: | Miotto, M.C, Marks, A.R. | Deposit date: | 2024-10-21 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (4.49 Å) | Cite: | Targeting Ryanodine Receptors with Allopurinol and Xanthine Derivatives for the Treatment of Cardiac and Musculoskeletal Weakness Disorders To Be Published
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9E1C
| Structure of RyR1 in the primed state in the presence of IBMX | Descriptor: | 3-ISOBUTYL-1-METHYLXANTHINE, ADENOSINE-5'-TRIPHOSPHATE, CALCIUM ION, ... | Authors: | Miotto, M.C, Marks, A.R. | Deposit date: | 2024-10-21 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (2.63 Å) | Cite: | Targeting Ryanodine Receptors with Allopurinol and Xanthine Derivatives for the Treatment of Cardiac and Musculoskeletal Weakness Disorders To Be Published
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9E1D
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9E1E
| Structure of RyR1 in the primed state in the presence of uracil | Descriptor: | ADENOSINE-5'-TRIPHOSPHATE, CALCIUM ION, Peptidyl-prolyl cis-trans isomerase FKBP1A, ... | Authors: | Miotto, M.C, Marks, A.R. | Deposit date: | 2024-10-21 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (2.92 Å) | Cite: | Targeting Ryanodine Receptors with Allopurinol and Xanthine Derivatives for the Treatment of Cardiac and Musculoskeletal Weakness Disorders To Be Published
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9E1F
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9E1G
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9E1H
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9E1I
| Structure of RyR1 in the open state in the presence of oxopyricid | Descriptor: | ADENOSINE-5'-TRIPHOSPHATE, CALCIUM ION, Peptidyl-prolyl cis-trans isomerase FKBP1A, ... | Authors: | Miotto, M.C, Marks, A.R. | Deposit date: | 2024-10-21 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (3.2 Å) | Cite: | Targeting Ryanodine Receptors with Allopurinol and Xanthine Derivatives for the Treatment of Cardiac and Musculoskeletal Weakness Disorders To Be Published
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9EPR
| Cryo-EM Structure of Jumping Spider Rhodopsin-1 bound to a Gi heterotrimer | Descriptor: | Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(T) subunit gamma-T1, Guanine nucleotide-binding protein G(i) subunit alpha-1, ... | Authors: | Tejero, O, Pamula, F, Koyanagi, M, Nagata, T, Afanasyev, P, Das, I, Deupi, X, Sheves, M, Terakita, A, Schertler, G.F.X, Rodrigues, M.J, Tsai, C.-J. | Deposit date: | 2024-03-19 | Release date: | 2024-10-30 | Method: | ELECTRON MICROSCOPY (4.9 Å) | Cite: | Active state structures of a bistable visual opsin bound to G proteins. Nat Commun, 15, 2024
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9F2P
| Crystal structure of Keap1 kelch domain in complex with a fluorenone-based small molecule inhibitor at 1.36A resolution | Descriptor: | (R)-2-(3-(((4-methoxyphenyl)sulfonamido)methyl)phenyl)-2-(9-oxo-9H-fluorene-4-carboxamido)acetate, DIMETHYL SULFOXIDE, Kelch-like ECH-associated protein 1, ... | Authors: | Narayanan, D, Bach, A, Gajhede, M. | Deposit date: | 2024-04-23 | Release date: | 2024-10-30 | Method: | X-RAY DIFFRACTION (1.36 Å) | Cite: | Structure-Guided Conformational Restriction Leading to High-Affinity, Selective, and Cell-Active Tetrahydroisoquinoline-Based Noncovalent Keap1-Nrf2 Inhibitors. J.Med.Chem., 2024
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