MolNFT v1 · #118310 · protein
Crystal structure of cody from bacillus cereus
5EY2 · GTP-sensing transcriptional pleiotropic repressor cody: “Crystal structure of cody from bacillus cereus”. X-ray diffraction, 20 pockets (best druggability 0.78). MolNFT v1 #118310 on GenesisL1: 3D structure, binding sites and…
- PDB
- 5EY2
- Type
- protein
- Length
- 965 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- GTP-sensing transcriptional pleiotropic repressor cody
- UniProt
- Q819X8
- Pockets
- 20 · best druggability 0.78
Structure
x-ray diffraction · 3 distinct chains · 45% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | GTP-sensing transcriptional pleiotropic repressor cody | protein | 254 | 47% helix, 18% strand | Q819X8 |
| D | GTP-sensing transcriptional pleiotropic repressor cody | protein | 226 | 45% helix, 14% strand | Q819X8 |
| C | GTP-sensing transcriptional pleiotropic repressor cody | protein | 231 | 44% helix, 17% strand | Q819X8 |
Pockets
20 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 287 | 0.78 | 0.90 | 48 | empty |
| 2 | 916 | 0.77 | 0.80 | 112 | empty |
| 3 | 196 | 0.70 | 0.87 | 34 | empty |
| 4 | 114 | 0.65 | 0.88 | 24 | empty |
| 5 | 239 | 0.54 | 0.76 | 29 | empty |
Interfaces
6 interfaces between chains.
- A–B · 1344 Ų buried · 11 hydrogen bonds · protein-protein
- D–C · 1246 Ų buried · 12 hydrogen bonds · protein-protein
- A–D · 1008 Ų buried · 1 hydrogen bond · protein-protein
- B–C · 842 Ų buried · 2 hydrogen bonds · protein-protein
- B–D · 712 Ų buried · 8 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 29 modified (engineered).
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 Q819X8
- Elsewhere: RCSB PDB 5EY2 · PDBe 5EY2 · UniProt Q819X8
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