6B9A
| Hsp90-alpha N-domain bound to NPCA | Descriptor: | Heat shock protein HSP 90-alpha, N-PROPYL CARBOXYAMIDO ADENOSINE | Authors: | Huck, J.D, Gewirth, D.T. | Deposit date: | 2017-10-10 | Release date: | 2018-10-17 | Last modified: | 2023-10-04 | Method: | X-RAY DIFFRACTION (1.65381 Å) | Cite: | Hsp90-alpha N-domain bound to NPCA To Be Published
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5ULS
| Structure of GRP94 in the active conformation | Descriptor: | Endoplasmin, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER | Authors: | Huck, J.D, Que, N.L.S, Gewirth, D.T. | Deposit date: | 2017-01-25 | Release date: | 2017-09-27 | Last modified: | 2023-10-04 | Method: | X-RAY DIFFRACTION (2.622 Å) | Cite: | Structural and Functional Analysis of GRP94 in the Closed State Reveals an Essential Role for the Pre-N Domain and a Potential Client-Binding Site. Cell Rep, 20, 2017
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6N8W
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6N8Y
| Hsp90-beta bound to PU-11-trans | Descriptor: | 9-[(2E)-but-2-en-1-yl]-8-[(3,4,5-trimethoxyphenyl)methyl]-9H-purin-6-amine, Heat shock protein HSP 90-beta | Authors: | Huck, J.D, Que, N.L.S, Gewirth, D.T. | Deposit date: | 2018-11-30 | Release date: | 2019-07-03 | Last modified: | 2023-10-11 | Method: | X-RAY DIFFRACTION (1.553908 Å) | Cite: | Structures of Hsp90 alpha and Hsp90 beta bound to a purine-scaffold inhibitor reveal an exploitable residue for drug selectivity. Proteins, 87, 2019
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6N8X
| Hsp90-alpha bound to PU-11-trans | Descriptor: | 9-[(2E)-but-2-en-1-yl]-8-[(3,4,5-trimethoxyphenyl)methyl]-9H-purin-6-amine, Heat shock protein HSP 90-alpha | Authors: | Huck, J.D, Que, N.L.S, Gewirth, D.T. | Deposit date: | 2018-11-30 | Release date: | 2019-07-03 | Last modified: | 2024-03-13 | Method: | X-RAY DIFFRACTION (1.49484479 Å) | Cite: | Structures of Hsp90 alpha and Hsp90 beta bound to a purine-scaffold inhibitor reveal an exploitable residue for drug selectivity. Proteins, 87, 2019
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6B99
| Hsp90-alpha N-domain bound to NECA | Descriptor: | Heat shock protein HSP 90-alpha, N-ETHYL-5'-CARBOXAMIDO ADENOSINE | Authors: | Huck, J.D, Gewirth, D.T. | Deposit date: | 2017-10-10 | Release date: | 2018-10-17 | Last modified: | 2023-10-04 | Method: | X-RAY DIFFRACTION (1.60237718 Å) | Cite: | Hsp90-alpha N-domain bound to NECA To Be Published
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6CYG
| Hsp90-alpha N-domain bound to NEOCA | Descriptor: | 5'-N-(2-HYDROXYL)ETHYL CARBOXYAMIDO ADENOSINE, Heat shock protein HSP 90-alpha, MAGNESIUM ION | Authors: | Huck, J.D, Campomizzi, C, Gewirth, D.T. | Deposit date: | 2018-04-05 | Release date: | 2019-04-10 | Last modified: | 2023-10-04 | Method: | X-RAY DIFFRACTION (1.503922 Å) | Cite: | NECA derivatives exploit the paralog-specific properties of the site 3 side pocket of Grp94, the endoplasmic reticulum Hsp90. J.Biol.Chem., 294, 2019
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6CYH
| Hsp90-alpha N-domain bound to NEACA | Descriptor: | 5'-N-[(2-AMINO)ETHYL CARBOXAMIDO] ADENOSINE, Heat shock protein HSP 90-alpha, MAGNESIUM ION | Authors: | Huck, J.D, Campomizzi, C, Gewirth, D.T. | Deposit date: | 2018-04-05 | Release date: | 2019-04-10 | Last modified: | 2023-10-04 | Method: | X-RAY DIFFRACTION (1.49 Å) | Cite: | NECA derivatives exploit the paralog-specific properties of the site 3 side pocket of Grp94, the endoplasmic reticulum Hsp90. J.Biol.Chem., 294, 2019
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6CYI
| Grp94 N-domain bound to NEOCA | Descriptor: | 5'-N-(2-HYDROXYL)ETHYL CARBOXYAMIDO ADENOSINE, Endoplasmin, TETRAETHYLENE GLYCOL, ... | Authors: | Huck, J.D, Aw, W.J, Gewirth, D.T. | Deposit date: | 2018-04-05 | Release date: | 2019-04-10 | Last modified: | 2023-10-04 | Method: | X-RAY DIFFRACTION (1.7565825 Å) | Cite: | NECA derivatives exploit the paralog-specific properties of the site 3 side pocket of Grp94, the endoplasmic reticulum Hsp90. J.Biol.Chem., 294, 2019
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6OLX
| Hsp90-alpha S52A bound to PU-11-trans | Descriptor: | 9-[(2E)-but-2-en-1-yl]-8-[(3,4,5-trimethoxyphenyl)methyl]-9H-purin-6-amine, Heat shock protein HSP 90-alpha | Authors: | Gewirth, D.T, Huck, J.D. | Deposit date: | 2019-04-17 | Release date: | 2019-07-03 | Last modified: | 2024-03-06 | Method: | X-RAY DIFFRACTION (1.43760586 Å) | Cite: | Structures of Hsp90 alpha and Hsp90 beta bound to a purine-scaffold inhibitor reveal an exploitable residue for drug selectivity. Proteins, 87, 2019
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