MolNFT v1 · #164318 · protein + RNA
Human REXO2 exonuclease in complex with RNA.
6STY · Oligoribonuclease, mitochondrial: “Human REXO2 exonuclease in complex with RNA.”. X-ray diffraction, 1 ligand (CA), 5 pockets (best druggability 0.66). MolNFT v1 #164318 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 6STY
- Type
- protein + RNA
- Length
- 771 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Oligoribonuclease, mitochondrial; RNA (5'-R(P*AP*UP*C)-3')
- EC
- 3.1.-.-
- UniProt
- Q9Y3B8
- Ligands
- CA
- Pockets
- 5 · best druggability 0.66
Structure
x-ray diffraction · 6 distinct chains · 49% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Oligoribonuclease, mitochondrial (EC 3.1.-.-) | protein | 198 | 46% helix, 18% strand | Q9Y3B8 |
| B | Oligoribonuclease, mitochondrial (EC 3.1.-.-) | protein | 190 | 49% helix, 18% strand | Q9Y3B8 |
| C | RNA (5'-R(P*AP*UP*C)-3') | rna | 3 | — | — |
| D | Oligoribonuclease, mitochondrial (EC 3.1.-.-) | protein | 197 | 49% helix, 20% strand | Q9Y3B8 |
| E | Oligoribonuclease, mitochondrial (EC 3.1.-.-) | protein | 181 | 50% helix, 22% strand | Q9Y3B8 |
| F | RNA (5'-R(P*AP*UP*C)-3') | rna | 2 | — | — |
Ligands and binding sites
- CA · Calcium ion · metal · chains B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 622 | 0.66 | 0.76 | 65 | empty |
| 2 | 127 | 0.61 | 0.86 | 24 | empty |
| 3 | 279 | 0.60 | 0.79 | 38 | empty |
| 4 | 309 | 0.54 | 0.75 | 32 | empty |
| 5 | 71 | 0.44 | 0.82 | 21 | empty |
Interfaces
6 interfaces between chains.
- A–B · 1916 Ų buried · 24 hydrogen bonds · protein-protein
- D–E · 1903 Ų buried · 21 hydrogen bonds · protein-protein
- B–C · 439 Ų buried · 10 hydrogen bonds · protein-nucleic
- E–F · 377 Ų buried · 14 hydrogen bonds · protein-nucleic
- A–C · 115 Ų buried · 3 hydrogen bonds · protein-nucleic
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 Q9Y3B8
- Elsewhere: RCSB PDB 6STY · PDBe 6STY · UniProt Q9Y3B8
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