Research workbench
Mutant P44S P169S M296I of foot-and-mouth disease virus RNA-dependent RNA polymerase
Analyse Mutant P44S P169S M296I of foot-and-mouth disease virus RNA-dependent RNA… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4IQX
- Type
- protein + RNA
- Length
- 488 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 3D polymerase; RNA (5'-R(*AP*UP*GP*GP*GP*CP*C)-3'); RNA (5'-R(*GP*GP*CP*CP*C)-3')
- UniProt
- Q9QCE4
- Pockets
- 2 · best druggability 0.77
Structure
x-ray diffraction · 3 distinct chains · 42% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | 3D polymerase | protein | 476 | 42% helix, 19% strand | Q9QCE4 |
| B | RNA (5'-R(*AP*UP*GP*GP*GP*CP*C)-3') | rna | 7 | — | — |
| C | RNA (5'-R(*GP*GP*CP*CP*C)-3') | rna | 5 | — | — |
Pockets
2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 938 | 0.77 | 0.80 | 70 | empty |
| 2 | 115 | 0.62 | 0.87 | 26 | empty |
Interfaces
3 interfaces between chains.
- A–B · 947 Ų buried · 25 hydrogen bonds · protein-nucleic
- A–C · 602 Ų buried · 7 hydrogen bonds · protein-nucleic
- B–C · 244 Ų buried · 27 hydrogen bonds · nucleic-nucleic
Compared structures
- 4IQX · Mutant P44S P169S M296I of Foot-and-mouth disease Virus RNA-dependent RNA polymerase · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt Q9QCE4
- Elsewhere: RCSB PDB 4IQX · PDBe 4IQX · UniProt Q9QCE4
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