MolNFT v1 · #162260 · protein
Aspergillus niger ferric acid decarboxylase (fdc) L439G variant in complex with prfmn (purified in the radical form) and phenylpropiolic acid
6R3O · Ferulic acid decarboxylase 1: “Aspergillus niger ferric acid decarboxylase (fdc) L439G variant in complex with prfmn (purified in the…”. X-ray diffraction, 4 ligands (JQ8, 4LU, K), 2 pockets (best druggability 0.83). MolNFT v1…
- PDB
- 6R3O
- Type
- protein
- Length
- 500 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ferulic acid decarboxylase 1
- EC
- 4.1.1.102
- UniProt
- A0A3F3RNU4
- Ligands
- JQ8, 4LU, K, MN
- Pockets
- 2 · best druggability 0.83
Structure
x-ray diffraction · 1 distinct chain · 31% helix, 23% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Ferulic acid decarboxylase 1 (EC 4.1.1.102) | protein | 500 | 31% helix, 23% strand | A0A3F3RNU4 |
Ligands and binding sites
- JQ8 · phenylpropiolic acid · ligand · 3 copies · chains A
- 4LU · 1-deoxy-5-O-phosphono-1-(3,3,4,5-tetramethyl-9,11-dioxo-2,3,8,9,10,11-hexahydro-7H-quinolino[1,8-fg]pteridin-12-ium-7-yl)-D-ribitol · ligand · chains A
- K · Potassium ion · metal · 2 copies · chains A
- MN · Manganese (II) ion · metal · 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 | 586 | 0.83 | 0.88 | 74 | 4LU, K, JQ8 |
| 2 | 54 | 0.31 | 0.76 | 13 | empty |
Compared structures
- 6R3O · Aspergillus niger ferric acid decarboxylase (Fdc) L439G variant in complex with prFMN… · 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 A0A3F3RNU4
- Elsewhere: RCSB PDB 6R3O · PDBe 6R3O · UniProt A0A3F3RNU4
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