MolNFT v1 · #72525 · protein
Crystal structure of oxidized H88Q synechocystis sp. pcya
3NB8 · PHYCOCYANOBILIN:FERREDOXIN oxidoreductase: “Crystal structure of oxidized H88Q synechocystis sp. pcya”. X-ray diffraction, 1 ligand (BLA), 2 pockets (best druggability 0.72). MolNFT v1 #72525 on GenesisL1: 3D structure, binding…
- PDB
- 3NB8
- Type
- protein
- Length
- 242 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- PHYCOCYANOBILIN:FERREDOXIN oxidoreductase
- EC
- 1.3.7.5
- UniProt
- Q55891
- Ligands
- BLA
- Pockets
- 2 · best druggability 0.72
Structure
x-ray diffraction · 1 distinct chain · 42% helix, 24% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | PHYCOCYANOBILIN:FERREDOXIN oxidoreductase (EC 1.3.7.5) | protein | 242 | 42% helix, 24% strand | Q55891 |
Ligands and binding sites
- BLA · Biliverdine IX alpha · ligand · chains A
- EDO · 1,2-ethanediol · additive · 14 copies · 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 | 234 | 0.72 | 0.87 | 37 | BLA |
| 2 | 67 | 0.39 | 0.80 | 21 | empty |
Compared structures
- 3NB8 · Crystal structure of oxidized H88Q Synechocystis sp. PCYA · the same entry in another collection · chain A against A, TM-score 1.00
- Q55891 · AlphaFold monomer V2.0 prediction for PHYCOCYANOBILIN:FERREDOXIN oxidoreductase (Q55891) · a predicted model of the same protein · chain A against A, TM-score 0.98
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 Q55891
- Elsewhere: RCSB PDB 3NB8 · PDBe 3NB8 · UniProt Q55891
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