MolNFT v1 · #2938 · protein
PHE161 and ARG166 variants of P-hydroxybenzoate hydroxylase. implications for NADPH recognition and structural stability.
1CC4 · Protein (P-hydroxybenzoate hydroxylase): “PHE161 and ARG166 variants of P-hydroxybenzoate hydroxylase. implications for NADPH recognition and…”. X-ray diffraction, 2 ligands (FAD, PHB), 2 pockets (best druggability 0.77). MolNFT v1…
- PDB
- 1CC4
- Type
- protein
- Length
- 391 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein (P-hydroxybenzoate hydroxylase)
- EC
- 1.14.13.2
- UniProt
- P00438
- Ligands
- FAD, PHB
- Pockets
- 2 · best druggability 0.77
Structure
x-ray diffraction · 1 distinct chain · 41% helix, 29% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Protein (P-hydroxybenzoate hydroxylase) (EC 1.14.13.2) | protein | 391 | 41% helix, 29% strand | P00438 |
Ligands and binding sites
- FAD · Flavin-adenine dinucleotide · ligand · chains A
- PHB · P-hydroxybenzoic acid · ligand · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 590 | 0.77 | 0.83 | 66 | FAD, PHB |
| 2 | 77 | 0.40 | 0.79 | 17 | empty |
Compared structures
- 1CC4 · PHE161 and ARG166 variants of P-hydroxybenzoate hydroxylase. implications for NADPH… · the same entry in another collection · chain A against A, TM-score 1.00
- P00438 · AlphaFold monomer V2.0 prediction for P-hydroxybenzoate hydroxylase (P00438) · a predicted model of the same protein · 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 P00438
- Elsewhere: RCSB PDB 1CC4 · PDBe 1CC4 · UniProt P00438
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