MolNFT v1 · #151759 · protein
Anti from P. luminescens catalyses terminal polyketide shortening in the biosynthesis of anthraquinones
6HXA: “Anti from P. luminescens catalyses terminal polyketide shortening in the biosynthesis of anthraquinones”. X-ray diffraction, 1 pocket (best druggability 0.69). MolNFT v1 #151759 on GenesisL1: 3D structure, binding sites and pockets…
- PDB
- 6HXA
- Type
- protein
- Length
- 375 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Anti
- UniProt
- Q7MZT8
- Pockets
- 1 · best druggability 0.69
Structure
x-ray diffraction · 1 distinct chain · 51% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Anti | protein | 375 | 51% helix, 16% strand | Q7MZT8 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 137 | 0.69 | 0.89 | 32 | empty |
Compared structures
- 6HXA · AntI from P. luminescens catalyses terminal polyketide shortening in the biosynthesis of… · 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 Q7MZT8
- Elsewhere: RCSB PDB 6HXA · PDBe 6HXA · UniProt Q7MZT8
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