MolNFT v1 · #173772 · protein + RNA
Structure of rig-I ctd (I875A) bound to P-RNA
7BAI · Antiviral innate immune response receptor rig-I: “Structure of rig-I ctd (I875A) bound to P-RNA”. X-ray diffraction, 1 ligand (ZN), 3 pockets (best druggability 0.70). MolNFT v1 #173772 on GenesisL1: 3D structure, binding sites and…
- PDB
- 7BAI
- Type
- protein + RNA
- Length
- 396 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Antiviral innate immune response receptor rig-I; RNA…
- EC
- 3.6.4.13
- UniProt
- O95786
- Ligands
- ZN
- Pockets
- 3 · best druggability 0.70
Structure
x-ray diffraction · 4 distinct chains · 12% helix, 49% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Antiviral innate immune response receptor rig-I (EC 3.6.4.13) | protein | 120 | 13% helix, 50% strand | O95786 |
| B | Antiviral innate immune response receptor rig-I (EC 3.6.4.13) | protein | 121 | 11% helix, 46% strand | O95786 |
| C, D, V | RNA (5'-R(*(GDP)P*AP*CP*GP*CP*UP*AP*GP*CP*GP*UP*C)-3') | rna | 12 | — | — |
| E | Antiviral innate immune response receptor rig-I (EC 3.6.4.13) | protein | 119 | 13% helix, 51% strand | O95786 |
Ligands and binding sites
- ZN · Zinc ion · metal · 5 copies · chains A, B, E
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 777 | 0.70 | 0.77 | 46 | empty |
| 2 | 496 | 0.67 | 0.78 | 47 | empty |
| 3 | 253 | 0.54 | 0.76 | 24 | empty |
Interfaces
10 interfaces between chains.
- C–D · 541 Ų buried · 38 hydrogen bonds · nucleic-nucleic
- E–V · 436 Ų buried · 10 hydrogen bonds · protein-nucleic
- A–C · 426 Ų buried · 6 hydrogen bonds · protein-nucleic
- B–D · 411 Ų buried · 8 hydrogen bonds · protein-nucleic
- B–E · 339 Ų buried · 4 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 3 modified (nucleotide modification).
Compared structures
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 O95786
- Elsewhere: RCSB PDB 7BAI · PDBe 7BAI · UniProt O95786
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