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Crystal structure of human insulin-degrading enzyme (ide) in complex with human atrial natriuretic peptide (anp)

Analyse Crystal structure of human insulin-degrading enzyme (ide) in complex with human… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3N57
Type
protein
Length
1,912 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Insulin-degrading enzyme; Atrial natriuretic factor
EC
3.4.24.56
UniProt
P14735, P01160
Ligands
ZN
Pockets
20 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 45% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BInsulin-degrading enzyme (EC 3.4.24.56)protein95345% helix, 20% strandP14735
C, DAtrial natriuretic factorprotein30% helix, 33% strandP01160

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains A, 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, 13 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19960.790.8095empty
28720.760.8095empty
36650.760.8276ZN
45730.680.7867empty
54020.670.8039empty

Interfaces

3 interfaces between chains.

  • A–B · 861 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 319 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 314 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 isopeptide (isopeptide).

Compared structures

  • 3N57 · Crystal Structure of human Insulin-degrading enzyme (IDE) in complex with human atrial… · the same entry in another collection · chain A against A, TM-score 1.00
  • P01160 · AlphaFold monomer V2.0 prediction for natriuretic peptides a (P01160) · a predicted model of the same protein · chain C against A, TM-score 1.00

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