Research workbench
Crystal structure of ZN(II)-bound yjia GTPase from E. COLI
Analyse Crystal structure of ZN(II)-bound yjia GTPase from E. COLI in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4IXM
- Type
- protein
- Length
- 635 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Uncharacterized GTP-binding protein yjia
- UniProt
- P24203
- Ligands
- ZN, SO4
- Pockets
- 12 · best druggability 0.87
Structure
x-ray diffraction · 2 distinct chains · 30% helix, 30% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Uncharacterized GTP-binding protein yjia | protein | 318 | 30% helix, 30% strand | P24203 |
| B | Uncharacterized GTP-binding protein yjia | protein | 317 | 29% helix, 30% strand | P24203 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
12 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 557 | 0.87 | 0.92 | 61 | empty |
| 2 | 120 | 0.59 | 0.85 | 28 | empty |
| 3 | 213 | 0.53 | 0.77 | 33 | empty |
| 4 | 160 | 0.49 | 0.78 | 27 | empty |
| 5 | 171 | 0.49 | 0.77 | 26 | empty |
Interfaces
1 interface between chains.
- A–B · 1184 Ų buried · 21 hydrogen bonds · protein-protein
Compared structures
- 4IXM · Crystal structure of Zn(II)-bound YjiA GTPase from E. coli · the same entry in another collection · chain A against A, TM-score 1.00
- P24203 · AlphaFold monomer V2.0 prediction for P-loop guanosine triphosphatase yjia (P24203) · a predicted model of the same protein · chain A against A, TM-score 0.98
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 P24203
- Elsewhere: RCSB PDB 4IXM · PDBe 4IXM · UniProt P24203
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