MolNFT v1 · #152094 · protein
Sepiapterin reductase in complex with compound 4
6I79: “Sepiapterin reductase in complex with compound 4”. X-ray diffraction, 2 ligands (NAP, H5E), 5 pockets (best druggability 0.78). MolNFT v1 #152094 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 6I79
- Type
- protein
- Length
- 542 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Sepiapterin reductase
- EC
- 1.1.1.153
- UniProt
- P35270
- Ligands
- NAP, H5E
- Pockets
- 5 · best druggability 0.78
Structure
x-ray diffraction · 1 distinct chain · 49% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Sepiapterin reductase (EC 1.1.1.153) | protein | 271 | 49% helix, 16% strand | P35270 |
Ligands and binding sites
- NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
- H5E · 6-[(4-~{tert}-butyl-1,3-thiazol-2-yl)methyl]-4,6-diazaspiro[2.4]heptane-5,7-dione · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 507 | 0.78 | 0.85 | 48 | NAP, H5E |
| 2 | 575 | 0.76 | 0.83 | 60 | NAP, H5E |
| 3 | 79 | 0.35 | 0.76 | 19 | empty |
| 4 | 63 | 0.33 | 0.76 | 15 | empty |
| 5 | 64 | 0.31 | 0.74 | 12 | empty |
Interfaces
1 interface between chains.
- A–B · 1948 Ų buried · 18 hydrogen bonds · protein-protein
Compared structures
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 P35270
- Elsewhere: RCSB PDB 6I79 · PDBe 6I79 · UniProt P35270
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