Research workbench
Covalent complex of E. COLI transaldolase talb with tagatose-6- phosphate
Analyse Covalent complex of E. COLI transaldolase talb with tagatose-6- phosphate in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4S2B
- Type
- protein
- Length
- 632 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Transaldolase B
- EC
- 2.2.1.2
- UniProt
- P0A870
- Ligands
- 44S, SO4
- Pockets
- 5 · best druggability 0.82
Structure
x-ray diffraction · 1 distinct chain · 56% helix, 13% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Transaldolase B (EC 2.2.1.2) | protein | 316 | 56% helix, 13% strand | P0A870 |
Ligands and binding sites
- 44S · 2-deoxy-6-O-phosphono-beta-D-lyxo-hexofuranose · ligand · 2 copies · chains A, B
- SO4 · Sulfate ion · ion · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 171 | 0.82 | 0.97 | 26 | empty |
| 2 | 112 | 0.46 | 0.79 | 21 | 44S |
| 3 | 114 | 0.43 | 0.77 | 20 | 44S |
| 4 | 56 | 0.29 | 0.75 | 12 | empty |
| 5 | 53 | 0.27 | 0.74 | 15 | empty |
Interfaces
1 interface between chains.
- A–B · 823 Ų buried · 4 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 covalent (covalent ligand).
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 P0A870
- Elsewhere: RCSB PDB 4S2B · PDBe 4S2B · UniProt P0A870
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