Research workbench
Crystal structure of a selenium-derivatized complex of the bacterial cellulose secretion regulators bcsr and bcsq, crystallized in the presence of appcp
Analyse Crystal structure of a selenium-derivatized complex of the bacterial cellulose… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6YAR
- Type
- protein
- Length
- 541 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Bacterial cellulose secretion regulator bcsq; Bacterial cellulose secretion regulator bcsr
- UniProt
- A0A0B1KWQ0, J7QAC9
- Ligands
- ATP, MG
- Pockets
- 3 · best druggability 0.89
Structure
x-ray diffraction · 4 distinct chains · 45% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Bacterial cellulose secretion regulator bcsq | protein | 242 | 44% helix, 17% strand | A0A0B1KWQ0 |
| B | Bacterial cellulose secretion regulator bcsq | protein | 240 | 45% helix, 18% strand | A0A0B1KWQ0 |
| C | Bacterial cellulose secretion regulator bcsr | protein | 32 | 50% helix, 6% strand | J7QAC9 |
| D | Bacterial cellulose secretion regulator bcsr | protein | 27 | 52% helix, 7% strand | J7QAC9 |
Ligands and binding sites
- ATP · Adenosine-5'-triphosphate · ligand · 2 copies · chains A, B
- MG · Magnesium ion · metal · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1150 | 0.89 | 0.90 | 119 | MG, ATP |
| 2 | 57 | 0.33 | 0.77 | 13 | empty |
| 3 | 55 | 0.30 | 0.76 | 12 | empty |
Interfaces
5 interfaces between chains.
- A–B · 1549 Ų buried · 23 hydrogen bonds · protein-protein
- B–C · 1084 Ų buried · 10 hydrogen bonds · protein-protein
- A–D · 994 Ų buried · 11 hydrogen bonds · protein-protein
- A–C · 446 Ų buried · 5 hydrogen bonds · protein-protein
- B–D · 415 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 modified (engineered).
Compared structures
- 6YAR · Crystal structure of a Selenium-derivatized complex of the bacterial cellulose secretion… · 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 A0A0B1KWQ0
- Every structure of UniProt J7QAC9
- Elsewhere: RCSB PDB 6YAR · PDBe 6YAR · UniProt A0A0B1KWQ0 · UniProt J7QAC9
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