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Crystal structure of sumo E3 ligase PIAS3
Analyse Crystal structure of sumo E3 ligase PIAS3 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4MVT
- Type
- protein
- Length
- 1,008 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- E3 sumo-protein ligase PIAS3
- EC
- 6.3.2.-
- UniProt
- Q9Y6X2
- Ligands
- ZN, UNX, CL
- Pockets
- 9 · best druggability 0.60
Structure
x-ray diffraction · 4 distinct chains · 22% helix, 32% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | E3 sumo-protein ligase PIAS3 (EC 6.3.2.-) | protein | 255 | 21% helix, 33% strand | Q9Y6X2 |
| B | E3 sumo-protein ligase PIAS3 (EC 6.3.2.-) | protein | 251 | 22% helix, 32% strand | Q9Y6X2 |
| C | E3 sumo-protein ligase PIAS3 (EC 6.3.2.-) | protein | 253 | 21% helix, 32% strand | Q9Y6X2 |
| D | E3 sumo-protein ligase PIAS3 (EC 6.3.2.-) | protein | 249 | 22% helix, 32% strand | Q9Y6X2 |
Ligands and binding sites
- ZN · Zinc ion · metal · 4 copies · chains A, B, C, D
- UNX · Unknown atom or ion · ion · 32 copies · chains A, D, B, C
- CL · Chloride ion · ion · 2 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
9 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 307 | 0.60 | 0.78 | 46 | CL, UNX |
| 2 | 338 | 0.59 | 0.77 | 38 | UNX |
| 3 | 255 | 0.57 | 0.78 | 30 | UNX |
| 4 | 257 | 0.56 | 0.77 | 35 | UNX |
| 5 | 255 | 0.56 | 0.77 | 30 | UNX |
Interfaces
3 interfaces between chains.
- A–D · 463 Ų buried · 2 hydrogen bonds · protein-protein
- C–D · 459 Ų buried · 17 hydrogen bonds · protein-protein
- A–B · 451 Ų buried · 20 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 Q9Y6X2
- Elsewhere: RCSB PDB 4MVT · PDBe 4MVT · UniProt Q9Y6X2
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