Research workbench
Pseudomonas aeruginosa rmla in complex with allosteric inhibitor
Analyse Pseudomonas aeruginosa rmla in complex with allosteric inhibitor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4B2X
- Type
- protein
- Length
- 1,187 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Glucose-1-phosphate thymidylyltransferase
- EC
- 2.7.7.24
- UniProt
- Q9HU22
- Ligands
- NIQ, CL
- Pockets
- 20 · best druggability 0.80
Structure
x-ray diffraction · 3 distinct chains · 36% helix, 22% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Glucose-1-phosphate thymidylyltransferase (EC 2.7.7.24) | protein | 299 | 35% helix, 21% strand | Q9HU22 |
| B | Glucose-1-phosphate thymidylyltransferase (EC 2.7.7.24) | protein | 302 | 36% helix, 22% strand | Q9HU22 |
| C, D | Glucose-1-phosphate thymidylyltransferase (EC 2.7.7.24) | protein | 293 | 35% helix, 23% strand | Q9HU22 |
Ligands and binding sites
- NIQ · 6-amino-1-butyl-5-(cyclopentylamino)pyrimidine-2,4(1H,3H)-dione · ligand · 4 copies · chains A, B, C, D
- CL · Chloride ion · ion · 4 copies · chains A, B, C, D
- MES · 2-(N-morpholino)-ethanesulfonic acid · additive · chains D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 13 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 106 | 0.80 | 0.99 | 19 | empty |
| 2 | 78 | 0.77 | 0.99 | 15 | empty |
| 3 | 445 | 0.75 | 0.84 | 40 | empty |
| 4 | 467 | 0.74 | 0.83 | 42 | empty |
| 5 | 1063 | 0.74 | 0.77 | 107 | empty |
Interfaces
5 interfaces between chains.
- A–C · 1427 Ų buried · 19 hydrogen bonds · protein-protein
- B–D · 1306 Ų buried · 8 hydrogen bonds · protein-protein
- A–D · 592 Ų buried · 7 hydrogen bonds · protein-protein
- A–B · 369 Ų buried · 3 hydrogen bonds · protein-protein
- B–C · 338 Ų buried · 5 hydrogen bonds · protein-protein
Compared structures
- 4B2X · Pseudomonas aeruginosa RmlA in complex with allosteric inhibitor · 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 Q9HU22
- Elsewhere: RCSB PDB 4B2X · PDBe 4B2X · UniProt Q9HU22
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