Research workbench
Crystal structure of pml B1-box multimers
Analyse Crystal structure of pml B1-box multimers in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6IMQ
- Type
- protein
- Length
- 197 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein pml
- UniProt
- P29590
- Ligands
- ZN, CL
- Pockets
- 3 · best druggability 0.77
Structure
x-ray diffraction · 2 distinct chains · 20% helix, 30% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C, D | Protein pml | protein | 49 | 20% helix, 31% strand | P29590 |
| B | Protein pml | protein | 50 | 20% helix, 30% strand | P29590 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 685 | 0.77 | 0.82 | 45 | CL |
| 2 | 93 | 0.37 | 0.75 | 14 | empty |
| 3 | 70 | 0.33 | 0.75 | 14 | empty |
Interfaces
5 interfaces between chains.
- C–D · 954 Ų buried · 12 hydrogen bonds · protein-protein
- A–B · 949 Ų buried · 19 hydrogen bonds · protein-protein
- A–C · 237 Ų buried · 1 hydrogen bond · protein-protein
- B–C · 128 Ų buried · 1 hydrogen bond · protein-protein
- A–D · 105 Ų buried · 0 hydrogen bonds · 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 P29590
- Elsewhere: RCSB PDB 6IMQ · PDBe 6IMQ · UniProt P29590
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