UniProt P04936
P04936
P04936 (UniProt P04936): 27 experimental structures on GenesisL1, 8 ligands bound. Binding sites, pockets, druggability and 3D structures in GL1X.
- UniProt
- P04936
- Experimental structures
- 27
- Predicted models
- 0
- Ligands
- 8
Structures
27 records of P04936 in the MolNFT archive: 27 experimental, 0 predicted.
| Entry | Title | Method | Chains | Ligands | Pockets |
|---|---|---|---|---|---|
| 1A3R | Fab fragment (antibody 8F5) complexed with peptide from human rhinovirus (serotype 2) viral capsid… | x-ray diffraction | P | — | — |
| 1A3R | Fab fragment (antibody 8F5) complexed with peptide from human rhinovirus (serotype 2) viral capsid… | x-ray diffraction | P | — | — |
| 1CQQ | Type 2 rhinovirus 3C protease with AG7088 inhibitor | x-ray diffraction | A | — | — |
| 1CQQ | Type 2 rhinovirus 3C protease with AG7088 inhibitor | x-ray diffraction | A | — | — |
| 1FPN | Human rhinovirus serotype 2 (HRV2) | x-ray diffraction | 1, 2, 3, 4 | — | — |
| 1FPN | Human rhinovirus serotype 2 (HRV2) | x-ray diffraction | 1, 2, 3, 4 | — | — |
| 1V9U | Human Rhinovirus 2 bound to a fragment of its cellular receptor protein | x-ray diffraction | 1, 2, 3, 4 | — | — |
| 1V9U | Human rhinovirus 2 bound to a fragment of its cellular receptor protein | x-ray diffraction | 1, 2, 3, 4 | — | — |
| 2HRV | 2A cysteine proteinase from human rhinovirus 2 | x-ray diffraction | A, B | — | — |
| 2HRV | 2A cysteine proteinase from human rhinovirus 2 | x-ray diffraction | A, B | — | — |
| 2XYA | Non-covalent inhibtors of rhinovirus 3C protease. | x-ray diffraction | A | — | — |
| 2XYA | Non-covalent inhibtors of rhinovirus 3C protease. | x-ray diffraction | A | — | — |
| 3DPR | Human rhinovirus 2 bound to a concatamer of the VLDL receptor module V3 | x-ray diffraction | A, B, C, D | — | — |
| 3DPR | Human rhinovirus 2 bound to a concatamer of the vldl receptor module V3 | x-ray diffraction | A, B, C, D | — | — |
| 3TN9 | X-ray structure of the HRV2 empty capsid (B-particle) | x-ray diffraction | 1, 2, 3 | — | — |
| 3TN9 | X-ray structure of the HRV2 empty capsid (B-particle) | x-ray diffraction | 1, 2, 3 | — | — |
| 3VDD | Structure of HRV2 capsid complexed with antiviral compound BTA798 | x-ray diffraction | A, B, C, D | — | — |
| 3VDD | Structure of HRV2 capsid complexed with antiviral compound BTA798 | x-ray diffraction | A, B, C, D | — | — |
| 4L3B | X-ray structure of the HRV2 A particle uncoating intermediate | x-ray diffraction | A, B, C | — | — |
| 4L3B | X-ray structure of the HRV2 a particle uncoating intermediate | x-ray diffraction | A, B, C | — | — |
| 5FX5 | Novel inhibitors of human rhinovirus 3C protease | x-ray diffraction | A | HOV | — |
| 5FX5 | Novel inhibitors of human rhinovirus 3C protease | x-ray diffraction | A | — | — |
| 5FX6 | Novel inhibitors of human rhinovirus 3C protease | x-ray diffraction | A | 6OY | — |
| 5FX6 | Novel inhibitors of human rhinovirus 3C protease | x-ray diffraction | A | — | — |
| 6FFN | Structure-based design and synthesis of macrocyclic human rhinovirus 3C protease inhibitors | x-ray diffraction | A | D8K, SO4 | — |
| 6FFS | Structure-based design and synthesis of macrocyclic human rhinovirus 3C protease inhibitors | x-ray diffraction | A | D8E, SO4 | — |
| 7ARA | Rhinovirus A2 2A protease in complex with ZVAM.FMK | x-ray diffraction | A, B | S7N, ZN, S7Q | — |
Ligands
- SO4 · Sulfate ion · in 2 records
- 6OY · ethyl (4R)-4-[[(2S,4S)-1-[(2S)-3-methyl-2-[(5-methyl-1,2-oxazol-3-yl)carbonylamino]butanoyl]-4-phenyl-pyrrolidin-2-yl]carbonylamino]-5-[(3S)-2-oxidanylidenepyrrolidin-3-yl]pentanoate · in 1 record
- D8E · ~{N}-[(2~{S},5~{S},14~{S})-2-[(4-fluorophenyl)methyl]-5-(hydroxymethyl)-9-methyl-3,8,15-tris(oxidanylidene)-1,4,9-triazacyclopentadec-14-yl]-5-methyl-1,2-oxazole-3-carboxamide · in 1 record
- D8K · ~{N}-[(5~{S},8~{S},11~{S},15~{R})-8-[(4-fluorophenyl) methyl]-5-(hydroxymethyl)-2,7,10,14-tetrakis(oxidanylidene)-1,6,9,13-tetrazabicyclo[13.3.0]octadecan-11-yl]-5-methyl-1,2-oxazole-3-carboxamide · in 1 record
- HOV · ethyl (4R)-4-[[(2S,3R)-1-[(2S)-3-methyl-2-[(5-methyl-1,2-oxazol-3-yl)carbonylamino]butanoyl]-3-phenyl-pyrrolidin-2-yl]carbonylamino]-5-[(3S)-2-oxidanylidenepyrrolidin-3-yl]pentanoate · in 1 record
- S7N · (phenylmethyl) ~{N}-[(2~{R})-3-methyl-1-[[(2~{S})-1-[[(3~{S})-1-methylsulfanyl-4-oxidanylidene-pentan-3-yl]amino]-1-oxidanylidene-propan-2-yl]amino]-1-oxidanylidene-butan-2-yl]carbamate · in 1 record
- S7Q · (phenylmethyl) ~{N}-[(2~{S})-3-methyl-1-[[(2~{R})-1-[[(3~{R})-1-methylsulfanyl-4-oxidanylidene-pentan-3-yl]amino]-1-oxidanylidene-propan-2-yl]amino]-1-oxidanylidene-butan-2-yl]carbamate · in 1 record
- ZN · Zinc ion · in 1 record
Elsewhere
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