Research workbench
M64V pnp +mepdr
Analyse M64V pnp +mepdr in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1OVG
- Type
- protein
- Length
- 711 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Purine nucleoside phosphorylase
- EC
- 2.4.2.1
- UniProt
- P0ABP8
- Ligands
- MDR, PO4
- Pockets
- 7 · best druggability 0.61
Structure
x-ray diffraction · 1 distinct chain · 35% helix, 28% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Purine nucleoside phosphorylase (EC 2.4.2.1) | protein | 237 | 35% helix, 28% strand | P0ABP8 |
Ligands and binding sites
- MDR · 9-(2-deoxy-beta-D-ribofuranosyl)-6-methylpurine · ligand · 3 copies · chains A, B, C
- PO4 · Phosphate ion · ion · 3 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
7 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 279 | 0.61 | 0.79 | 45 | PO4, MDR |
| 2 | 302 | 0.58 | 0.77 | 42 | PO4, MDR |
| 3 | 207 | 0.52 | 0.77 | 38 | PO4, MDR |
| 4 | 120 | 0.37 | 0.74 | 18 | empty |
| 5 | 71 | 0.34 | 0.76 | 14 | empty |
Interfaces
3 interfaces between chains.
- A–B · 130 Ų buried · 1 hydrogen bond · protein-protein
- A–C · 116 Ų buried · 1 hydrogen bond · protein-protein
- B–C · 105 Ų buried · 1 hydrogen bond · protein-protein
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 P0ABP8
- Elsewhere: RCSB PDB 1OVG · PDBe 1OVG · UniProt P0ABP8
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