MolNFT v1 · #53057 · protein
Crystal structure of the tyrosine phosphatase wzb from escherichia COLI K30 in complex with phosphate.
2WJA · Putative acid phosphatase wzb: “Crystal structure of the tyrosine phosphatase wzb from escherichia COLI K30 in complex with phosphate.”. X-ray diffraction, 2 ligands (NI, PO4), 1 pocket (best druggability 0.46). MolNFT v1 #53057 on…
- PDB
- 2WJA
- Type
- protein
- Length
- 284 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Putative acid phosphatase wzb
- UniProt
- Q9X4B8
- Ligands
- NI, PO4
- Pockets
- 1 · best druggability 0.46
Structure
x-ray diffraction · 2 distinct chains · 40% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Putative acid phosphatase wzb | protein | 146 | 41% helix, 14% strand | Q9X4B8 |
| B | Putative acid phosphatase wzb | protein | 138 | 39% helix, 16% strand | Q9X4B8 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 100 | 0.46 | 0.80 | 15 | empty |
Interfaces
1 interface between chains.
- A–B · 277 Ų buried · 2 hydrogen bonds · protein-protein
Compared structures
- 2WJA · Crystal structure of the tyrosine phosphatase Wzb from Escherichia coli K30 in complex… · the same entry in another collection · chain A against A, TM-score 1.00
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 Q9X4B8
- Elsewhere: RCSB PDB 2WJA · PDBe 2WJA · UniProt Q9X4B8
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.