MolNFT v1 · #188474 · protein
Stable-5-lox elongated HA2 (4 copies asu)
7TTL · Arachidonate 5-lipoxygenase: “Stable-5-lox elongated HA2 (4 copies asu)”. X-ray diffraction, 1 ligand (FE2), 20 pockets (best druggability 0.86). MolNFT v1 #188474 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7TTL
- Type
- protein
- Length
- 2,607 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Arachidonate 5-lipoxygenase
- EC
- 1.13.11.34
- UniProt
- P09917
- Ligands
- FE2
- Pockets
- 20 · best druggability 0.86
Structure
x-ray diffraction · 4 distinct chains · 44% helix, 14% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Arachidonate 5-lipoxygenase (EC 1.13.11.34) | protein | 674 | 44% helix, 13% strand | P09917 |
| C | Arachidonate 5-lipoxygenase (EC 1.13.11.34) | protein | 617 | 44% helix, 15% strand | P09917 |
| D | Arachidonate 5-lipoxygenase (EC 1.13.11.34) | protein | 673 | 44% helix, 14% strand | P09917 |
| B | Arachidonate 5-lipoxygenase (EC 1.13.11.34) | protein | 643 | 46% helix, 14% strand | P09917 |
Ligands and binding sites
- FE2 · Fe (II) ion · metal · 4 copies · chains A, C, D, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 18 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1019 | 0.86 | 0.87 | 104 | empty |
| 2 | 1082 | 0.86 | 0.86 | 101 | empty |
| 3 | 859 | 0.81 | 0.83 | 101 | empty |
| 4 | 142 | 0.80 | 0.97 | 36 | empty |
| 5 | 111 | 0.80 | 0.98 | 29 | empty |
Interfaces
4 interfaces between chains.
- D–B · 1118 Ų buried · 13 hydrogen bonds · protein-protein
- A–C · 1062 Ų buried · 14 hydrogen bonds · protein-protein
- A–B · 838 Ų buried · 10 hydrogen bonds · protein-protein
- C–D · 197 Ų buried · 1 hydrogen bond · 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 P09917
- Elsewhere: RCSB PDB 7TTL · PDBe 7TTL · UniProt P09917
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