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Crystal structure of macrocycles containing ABETA17-23 (LVF(MEA)AED) and ABETA30-36 (AIIGL(ORN)V)

Analyse Crystal structure of macrocycles containing ABETA17-23 (LVF(MEA)AED) and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4NW9
Type
protein
Length
192 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cyclic hexadecapeptide (ORN)LVF(MEA)AED(ORN)AIIGL(ORN)V
Ligands
NA, CL
Pockets
1 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 0% helix, 63% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, LCyclic hexadecapeptide (ORN)LVF(MEA)AED(ORN)AIIGL(ORN)Vprotein160% helix, 63% strand—

Ligands and binding sites

  • NA · Sodium ion · metal · 2 copies · chains D, L, K
  • CL · Chloride ion · ion · 3 copies · chains C, K, B, G, I, J

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
18350.670.7369empty

Interfaces

33 interfaces between chains.

  • G–I · 247 Ų buried · 3 hydrogen bonds · protein-protein
  • A–C · 247 Ų buried · 3 hydrogen bonds · protein-protein
  • J–L · 243 Ų buried · 2 hydrogen bonds · protein-protein
  • D–E · 243 Ų buried · 2 hydrogen bonds · protein-protein
  • K–L · 241 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 48 modified (nonstandard).

Compared structures

  • 4NW9 · Crystal structure of macrocycles containing Abeta17-23 (LVF(MEA)AED) and Abeta30-36… · the same entry in another collection · chain A against A, TM-score 1.00

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