UniProt P26663
P26663
P26663 (UniProt P26663): 170 experimental structures on GenesisL1, 4 ligands bound. Binding sites, pockets, druggability and 3D structures in GL1X.
- UniProt
- P26663
- Experimental structures
- 170
- Predicted models
- 0
- Ligands
- 4
Structures
170 records of P26663 in the MolNFT archive: 170 experimental, 0 predicted.
| Entry | Title | Method | Chains | Ligands | Pockets |
|---|---|---|---|---|---|
| 1A1Q | Hepatitis C virus NS3 proteinase | x-ray diffraction | A, B, C | — | — |
| 1A1Q | Hepatitis C virus NS3 proteinase | x-ray diffraction | A, B, C | — | — |
| 1BT7 | The solution NMR structure of the N-terminal protease domain of the hepatitis C virus (HCV)… | solution nmr | A | — | — |
| 1BT7 | The solution NMR structure of the N-terminal protease domain of the hepatitis C virus (HCV)… | solution nmr | A | — | — |
| 1C2P | Hepatitis C virus NS5B RNA-dependent RNA polymerase | x-ray diffraction | A, B | — | — |
| 1C2P | Hepatitis C virus NS5B RNA-dependent RNA polymerase | x-ray diffraction | A, B | — | — |
| 1CSJ | Crystal structure of the RNA-dependent RNA polymerase of hepatitis C virus | x-ray diffraction | A, B | — | — |
| 1CSJ | Crystal structure of the RNA-dependent RNA polymerase of hepatitis C virus | x-ray diffraction | A, B | — | — |
| 1CU1 | Crystal structure of an enzyme complex from hepatitis C virus | x-ray diffraction | A, B | — | — |
| 1CU1 | Crystal structure of an enzyme complex from hepatitis C virus | x-ray diffraction | A, B | — | — |
| 1GX5 | Hepatitis C Virus RNA Polymerase in Complex with GTP and Manganese | x-ray diffraction | A | — | — |
| 1GX5 | Hepatitis C virus RNA polymerase in complex with GTP and manganese | x-ray diffraction | A | — | — |
| 1GX6 | Hepatitis C Virus RNA polymerase in complex with UTP and manganese | x-ray diffraction | A | — | — |
| 1GX6 | Hepatitis C virus RNA polymerase in complex with UTP and manganese | x-ray diffraction | A | — | — |
| 1JXP | Bk strain hepatitis C virus (HCV) NS3-NS4A | x-ray diffraction | A, C, B, D | — | — |
| 1JXP | Bk strain hepatitis C virus (HCV) NS3-NS4A | x-ray diffraction | A, C, B, D | — | — |
| 1NHU | Hepatitis C virus RNA polymerase in complex with non-nucleoside analogue inhibitor | x-ray diffraction | A, B | — | — |
| 1NHU | Hepatitis C virus RNA polymerase in complex with non-nucleoside analogue inhibitor | x-ray diffraction | A, B | — | — |
| 1NHV | Hepatitis C virus RNA polymerase in complex with non-nucleoside analogue inhibitor | x-ray diffraction | A, B | — | — |
| 1NHV | Hepatitis C virus RNA polymerase in complex with non-nucleoside analogue inhibitor | x-ray diffraction | A, B | — | — |
| 1NS3 | Structure of HCV protease (bk strain) | x-ray diffraction | A, B, C, D | — | — |
| 1NS3 | Structure of HCV protease (bk strain) | x-ray diffraction | A, B, C, D | — | — |
| 1OS5 | Crystal structure of HCV NS5B RNA polymerase complexed with a novel non-competitive inhibitor. | x-ray diffraction | A | — | — |
| 1OS5 | Crystal structure of HCV NS5B RNA polymerase complexed with a novel non-competitive inhibitor. | x-ray diffraction | A | — | — |
| 1QUV | Crystal structure of the RNA directed RNA polymerase of hepatitis C virus | x-ray diffraction | A | — | — |
| 1QUV | Crystal structure of the RNA directed RNA polymerase of hepatitis C virus | x-ray diffraction | A | — | — |
| 2AWZ | Hepatitis C Virus NS5b RNA Polymerase in complex with a covalent inhibitor (5h) | x-ray diffraction | A, B | — | — |
| 2AWZ | Hepatitis C virus NS5B RNA polymerase in complex with a covalent inhibitor (5H) | x-ray diffraction | A, B | — | — |
| 2AX0 | Hepatitis C Virus NS5b RNA Polymerase in complex with a covalent inhibitor (5x) | x-ray diffraction | A, B | — | — |
| 2AX0 | Hepatitis C virus NS5B RNA polymerase in complex with a covalent inhibitor (5X) | x-ray diffraction | A, B | — | — |
| 2AX1 | Hepatitis C Virus NS5b RNA Polymerase in complex with a covalent inhibitor (5ee) | x-ray diffraction | A, B | — | — |
| 2AX1 | Hepatitis C virus NS5B RNA polymerase in complex with a covalent inhibitor (5EE) | x-ray diffraction | A, B | — | — |
| 2BRK | Crystal structure of Hepatitis C virus polymerase in complex with an allosteric inhibitor (compound… | x-ray diffraction | A | — | — |
| 2BRK | Crystal structure of hepatitis C virus polymerase in complex with an allosteric inhibitor (compound… | x-ray diffraction | A | — | — |
| 2BRL | Crystal structure of Hepatitis C virus polymerase in complex with an allosteric inhibitor (compound… | x-ray diffraction | A | — | — |
| 2BRL | Crystal structure of hepatitis C virus polymerase in complex with an allosteric inhibitor (compound… | x-ray diffraction | A | — | — |
| 2DXS | Crystal structure of HCV NS5B RNA polymerase complexed with a tetracyclic inhibitor | x-ray diffraction | A, B | — | — |
| 2DXS | Crystal structure of HCV NS5B RNA polymerase complexed with a tetracyclic inhibitor | x-ray diffraction | A, B | — | — |
| 2GIQ | Hepatitis C virus RNA-dependent RNA polymerase NS5B with NNI-2 inhibitor | x-ray diffraction | A, B | — | — |
| 2GIQ | Hepatitis C virus RNA-dependent RNA polymerase NS5B with nni-2 inhibitor | x-ray diffraction | A, B | — | — |
| 2GIR | Hepatitis C virus RNA-dependent RNA polymerase NS5B with NNI-1 inhibitor | x-ray diffraction | A, B | — | — |
| 2GIR | Hepatitis C virus RNA-dependent RNA polymerase NS5B with nni-1 inhibitor | x-ray diffraction | A, B | — | — |
| 2HAI | Crystal structure of HCV NS5B RNA polymerase in complex with novel class of… | x-ray diffraction | A | — | — |
| 2HAI | Crystal structure of HCV NS5B RNA polymerase in complex with novel class of… | x-ray diffraction | A | — | — |
| 2HWH | HCV NS5B allosteric inhibitor complex | x-ray diffraction | A, B | — | — |
| 2HWH | HCV NS5B allosteric inhibitor complex | x-ray diffraction | A, B | — | — |
| 2HWI | HCV NS5B allosteric inhibitor complex | x-ray diffraction | A, B | — | — |
| 2HWI | HCV NS5B allosteric inhibitor complex | x-ray diffraction | A, B | — | — |
| 2I1R | Novel Thiazolones as HCV NS5B Polymerase Inhibitors: Further Designs, Synthesis, SAR and X-ray… | x-ray diffraction | A, B | — | — |
| 2I1R | Novel thiazolones as HCV NS5B polymerase inhibitors: further designs, synthesis, sar and X-ray… | x-ray diffraction | A, B | — | — |
| 2O5D | Thiazolone-acylsulfonamides as novel HCV NS5B polymerase allosteric inhibitors: Convergence of… | x-ray diffraction | A, B | — | — |
| 2O5D | Thiazolone-acylsulfonamides as novel HCV NS5B polymerase allosteric inhibitors: convergence of… | x-ray diffraction | A, B | — | — |
| 2WCX | Crystal Structure of Hepatitis C Virus NS5B Polymerase in Complex with Thienopyrrole-Based… | x-ray diffraction | A | — | — |
| 2WCX | Crystal structure of hepatitis C virus NS5B polymerase in complex with thienopyrrole-based… | x-ray diffraction | A | — | — |
| 2WHO | Crystal structure of hepatitis C virus NS5B polymerase from 1B genotype in complex with a… | x-ray diffraction | A, B | — | — |
| 2WHO | Crystal structure of hepatitis C virus NS5B polymerase from 1B genotype in complex with a… | x-ray diffraction | A, B | — | — |
| 2WRM | Identification of Novel Allosteric Inhibitors of Hepatitis C Virus NS5B Polymerase Thumb Domain… | x-ray diffraction | A | — | — |
| 2WRM | Identification of novel allosteric inhibitors of hepatitis C virus NS5B polymerase thumb domain… | x-ray diffraction | A | — | — |
| 2XWY | Structure of MK-3281, a Potent Non-Nucleoside Finger-Loop Inhibitor, in complex with the Hepatitis… | x-ray diffraction | A | — | — |
| 2XWY | Structure of mk-3281, a potent non-nucleoside finger-loop inhibitor, in complex with the hepatitis… | x-ray diffraction | A | — | — |
110 records more on the page itself.
Ligands
- 3VY · (1-methyl-1H-indol-3-yl)acetic acid · in 1 record
- 9VY · 2-(4-fluorophenyl)-5-(11-fluoro-6H-pyrido[2',3':5,6][1, 3]oxazino[3,4-a]indol-2-yl)-N-methyl-6-[methyl(methylsulfonyl)amino]-1-benzofuran-3-carboxamide · in 1 record
- K4S · (4-{[5-cyclopropyl-2-(4-fluorophenyl)-3-(methylcarbamoyl)-1-benzofuran-6-yl](methylsulfonyl) amino}phenyl)boronic acid · in 1 record
- SL4 · 5-[[(2~{S})-4-[1,1-bis(oxidanylidene)-1,2-benzothiazol-3-yl]-2-~{tert}-butyl-3-oxidanyl-5-oxidanylidene-2~{H}-pyrrol-1-yl]methyl]-2-fluoranyl-benzenecarbonitrile · in 1 record
Elsewhere
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