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Despentapeptide insulin in acetic acid (pH 2)

Analyse Despentapeptide insulin in acetic acid (pH 2) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2CEU
Type
protein
Length
90 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Insulin
UniProt
P01308
Ligands
SO4
Pockets
1 · best druggability 0.55

Structure

x-ray diffraction · 2 distinct chains · 53% helix, 4% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CInsulinprotein2157% helix, 5% strandP01308
B, DInsulinprotein2450% helix, 4% strandP01308

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 3 copies · chains A, C

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.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1750.550.8617empty

Interfaces

6 interfaces between chains.

  • A–B · 638 Ų buried · 12 hydrogen bonds · protein-protein
  • C–D · 636 Ų buried · 11 hydrogen bonds · protein-protein
  • B–D · 421 Ų buried · 0 hydrogen bonds · protein-protein
  • B–C · 112 Ų buried · 0 hydrogen bonds · protein-protein
  • A–D · 109 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 2CEU · Despentapeptide insulin in acetic acid (pH 2) · the same entry in another collection · chain A against A, TM-score 1.00

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