Research workbench
1.25A resolution structure of rat type B cytochrome B5
Analyse 1.25A resolution structure of rat type B cytochrome B5 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4HIL
- Type
- protein
- Length
- 166 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cytochrome B5 type B
- UniProt
- P04166
- Ligands
- HEM, NA
- Pockets
- 5 · best druggability 0.71
Structure
x-ray diffraction · 2 distinct chains · 38% helix, 24% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Cytochrome B5 type B | protein | 85 | 35% helix, 24% strand | P04166 |
| B | Cytochrome B5 type B | protein | 81 | 41% helix, 25% strand | P04166 |
Ligands and binding sites
- HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
- NA · Sodium ion · metal · chains B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 118 | 0.71 | 0.92 | 28 | empty |
| 2 | 125 | 0.63 | 0.86 | 20 | HEM |
| 3 | 118 | 0.62 | 0.86 | 20 | HEM |
| 4 | 70 | 0.33 | 0.76 | 19 | empty |
| 5 | 62 | 0.33 | 0.76 | 20 | empty |
Interfaces
1 interface between chains.
- A–B · 650 Ų buried · 6 hydrogen bonds · protein-protein
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 P04166
- Elsewhere: RCSB PDB 4HIL · PDBe 4HIL · UniProt P04166
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