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Crystal structure of human beta secretase in complex with nvp-BUR436, derived from a co-crystallization experiment

Analyse Crystal structure of human beta secretase in complex with nvp-BUR436, derived… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4D83
Type
protein
Length
1,131 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-secretase 1
EC
3.4.23.46
UniProt
P56817
Ligands
0GT
Pockets
9 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 14% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CBeta-secretase 1 (EC 3.4.23.46)protein37714% helix, 41% strandP56817

Ligands and binding sites

  • 0GT · (3R,4S,5S)-3-[(3-tert-butylbenzyl)amino]-5-{[3-(2,2-difluoroethyl)-1H-indol-5-yl]methyl}tetrahydro-2H-thiopyran-4-ol 1,1-dioxide · ligand · 3 copies · chains A, B, C

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

Pockets

9 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19840.750.78970GT
24140.670.80450GT
33980.670.80420GT
41700.580.8236empty
51340.550.8228empty

Interfaces

2 interfaces between chains.

  • A–C · 1058 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 560 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 4D83 · Crystal Structure of Human Beta Secretase in Complex with NVP-BUR436, derived from a… · the same entry in another collection · chain A against A, TM-score 1.00
  • P56817 · AlphaFold monomer V2.0 prediction for beta-secretase 1 (P56817) · a predicted model of the same protein · chain B against A, TM-score 0.99

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