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Insulin fibrillation is the janus face of induced fit. a chiral clamp stabilizes the native state at the expense of activity

Analyse Insulin fibrillation is the janus face of induced fit. a chiral clamp… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3P33
Type
protein
Length
204 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Insulin
UniProt
P01308
Ligands
IPH, ZN, CL
Pockets
3 · best druggability 0.59

Structure

x-ray diffraction · 2 distinct chains · 61% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, E, GInsulinprotein2148% helix, 5% strandP01308
B, D, F, HInsulinprotein3070% helix, 10% strandP01308

Ligands and binding sites

  • IPH · Phenol · ligand · 4 copies · chains A, B, C, D, E, F, G, H
  • ZN · Zinc ion · metal · 4 copies · chains B, D, F, H
  • CL · Chloride ion · ion · 4 copies · chains B, D, F, H

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13390.590.7736empty
2850.380.7715empty
3730.330.7512empty

Interfaces

13 interfaces between chains.

  • B–D · 736 Ų buried · 10 hydrogen bonds · protein-protein
  • F–H · 713 Ų buried · 8 hydrogen bonds · protein-protein
  • G–H · 654 Ų buried · 5 hydrogen bonds · protein-protein
  • E–F · 646 Ų buried · 3 hydrogen bonds · protein-protein
  • A–B · 624 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 disulfide (disulfide).

Compared structures

  • 3P33 · Insulin fibrillation is the Janus face of induced fit. A chiral clamp stabilizes the… · the same entry in another collection · chain A against A, TM-score 1.00

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