Research workbench
Cytochrome P450 BM3H-8C8 mri sensor, no ligand
Analyse Cytochrome P450 BM3H-8C8 mri sensor, no ligand in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4DTY
- Type
- protein
- Length
- 906 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cytochrome P450 BM3 variant 8C8
- EC
- 1.14.14.1
- UniProt
- P14779
- Ligands
- HEM, MG
- Pockets
- 12 · best druggability 0.86
Structure
x-ray diffraction · 1 distinct chain · 54% helix, 11% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B, A | Cytochrome P450 BM3 variant 8C8 (EC 1.14.14.1) | protein | 453 | 54% helix, 11% strand | P14779 |
Ligands and binding sites
- HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains B, A
- MG · Magnesium ion · metal · chains B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
12 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 822 | 0.86 | 0.88 | 90 | HEM |
| 2 | 861 | 0.86 | 0.88 | 92 | HEM |
| 3 | 296 | 0.55 | 0.75 | 39 | empty |
| 4 | 217 | 0.54 | 0.78 | 28 | empty |
| 5 | 214 | 0.54 | 0.77 | 26 | empty |
Interfaces
1 interface between chains.
- B–A · 1016 Ų buried · 17 hydrogen bonds · protein-protein
Compared structures
- 4DTY · cytochrome P450 BM3h-8C8 MRI sensor, no ligand · the same entry in another collection · chain A against A, TM-score 1.00
- P14779 · AlphaFold monomer V2.0 prediction for bifunctional cytochrome P450/NADPH--P450 reductase… · a predicted model of the same protein · chain B against A, TM-score 0.99
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 P14779
- Elsewhere: RCSB PDB 4DTY · PDBe 4DTY · UniProt P14779
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