Research workbench
Structure of Agrobacterium tumefaciens B6 strain PBP SocA complexed with Deoxyfructosylglutamine (DFG) at 1.8 A resolution
Analyse Structure of Agrobacterium tumefaciens B6 strain PBP SocA complexed with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6HQH
- Type
- protein
- Length
- 242 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 1.8
- Source
- Rhizobium radiobacter
- Molecule
- Membrane-bound lytic murein transglycosylase F
- UniProt
- A0A0F4FYR3
- Ligands
- SNW
- Pockets
- 2 · best druggability 0.80
Structure
x-ray diffraction · resolution 1.8 · 1 distinct chain · 37% helix, 24% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Membrane-bound lytic murein transglycosylase F | protein | 242 | 37% helix, 24% strand | A0A0F4FYR3 |
Ligands and binding sites
- SNW · Deoxyfructosylglutamine · ligand · chains A
- EDO · 1,2-ethanediol · additive · 6 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 183 | 0.80 | 0.94 | 41 | SNW |
| 2 | 89 | 0.32 | 0.73 | 19 | EDO |
Compared structures
- 6HQH · Structure of agrobacterium tumefaciens B6 strain pbp soca complexed with… · 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 A0A0F4FYR3
- Elsewhere: RCSB PDB 6HQH · PDBe 6HQH · UniProt A0A0F4FYR3
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