MolNFT v1 · #17392 · protein
Dehydrated T6 human insulin at 295 K
1OS4: “Dehydrated T6 human insulin at 295 K”. X-ray diffraction, 1 ligand (ZN), 1 pocket (best druggability 0.79). MolNFT v1 #17392 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1OS4
- Type
- protein
- Length
- 294 residues
- Chains
- 12
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Insulin
- UniProt
- P01308
- Ligands
- ZN
- Pockets
- 1 · best druggability 0.79
Structure
x-ray diffraction · 4 distinct chains · 55% helix, 12% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C, E, I, K | Insulin | protein | 21 | 67% helix, 10% strand | P01308 |
| B | Insulin | protein | 29 | 52% helix, 14% strand | P01308 |
| D, F, H, J, L | Insulin | protein | 28 | 50% helix, 14% strand | P01308 |
| G | Insulin | protein | 20 | 55% helix, 10% strand | P01308 |
Ligands and binding sites
- ZN · Zinc ion · metal · 2 copies · chains B, F, J, D, H, L
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 | 673 | 0.79 | 0.83 | 72 | ZN |
Interfaces
33 interfaces between chains.
- K–L · 893 Ų buried · 9 hydrogen bonds · protein-protein
- C–D · 888 Ų buried · 9 hydrogen bonds · protein-protein
- G–H · 815 Ų buried · 10 hydrogen bonds · protein-protein
- I–J · 787 Ų buried · 8 hydrogen bonds · protein-protein
- E–F · 782 Ų buried · 10 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 18 disulfide (disulfide).
Compared structures
- 1OS4 · Dehydrated T6 human insulin at 295 K · 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 P01308
- Elsewhere: RCSB PDB 1OS4 · PDBe 1OS4 · UniProt P01308
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