MolNFT v1 · #115428 · protein
Structure of CYP107L2
5CJE · Cytochrome P450 hydroxylase: “Structure of CYP107L2”. X-ray diffraction, 1 ligand (HEM), 3 pockets (best druggability 0.83). MolNFT v1 #115428 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 5CJE
- Type
- protein
- Length
- 390 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cytochrome P450 hydroxylase
- UniProt
- Q82LM3
- Ligands
- HEM
- Pockets
- 3 · best druggability 0.83
Structure
x-ray diffraction · 1 distinct chain · 56% helix, 9% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Cytochrome P450 hydroxylase | protein | 390 | 56% helix, 9% strand | Q82LM3 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 895 | 0.83 | 0.85 | 79 | HEM |
| 2 | 134 | 0.54 | 0.82 | 25 | empty |
| 3 | 74 | 0.34 | 0.76 | 16 | empty |
Compared structures
- 5CJE · Structure of CYP107L2 · 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 Q82LM3
- Elsewhere: RCSB PDB 5CJE · PDBe 5CJE · UniProt Q82LM3
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