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Crystal structure of mvl bound to MAN3GLCNAC2

Analyse Crystal structure of mvl bound to MAN3GLCNAC2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1ZHS
Type
protein
Length
904 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Mannan-binding lectin
Ligands
NAG, MAN, BMA, PO4
Pockets
6 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 24% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, HMannan-binding lectinprotein11324% helix, 50% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 32 copies · chains A, C, B, D, E, F, G, H
  • MAN · alpha-D-mannopyranose · sugar · 32 copies · chains A, B, C, D, E, F, G, H
  • BMA · beta-D-mannopyranose · sugar · 16 copies · chains A, B, C, D, E, F, G, H
  • PO4 · Phosphate ion · ion · 2 copies · chains G
  • EDO · 1,2-ethanediol · additive · 26 copies · chains A, B, E, C, D, F, G, H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110460.840.8590NAG, EDO
211830.830.8498NAG, EDO
311730.820.83138EDO
43560.750.8664EDO
52280.740.8946EDO

Interfaces

15 interfaces between chains.

  • G–H · 1985 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 1982 Ų buried · 11 hydrogen bonds · protein-protein
  • E–F · 1972 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 1966 Ų buried · 12 hydrogen bonds · protein-protein
  • D–G · 236 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 1ZHS · Crystal structure of MVL bound to Man3GlcNAc2 · the same entry in another collection · chain E against E, TM-score 1.00

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