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Crystal structure of cyanovirin-N complexed to a synthetic hexamannoside

Analyse Crystal structure of cyanovirin-N complexed to a synthetic hexamannoside in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3GXY
Type
protein
Length
202 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cyanovirin-N
UniProt
P81180
Ligands
OPM, MAN, MG
Pockets
1 · best druggability 0.54

Structure

x-ray diffraction · 1 distinct chain · 13% helix, 55% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BCyanovirin-Nprotein10113% helix, 55% strandP81180

Ligands and binding sites

  • OPM · pentyl alpha-D-mannopyranoside · ligand · 2 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 4 copies · chains A, B
  • MG · Magnesium ion · metal · chains A, B
  • NHE · 2-[N-cyclohexylamino]ethane sulfonic acid · additive · chains A, B

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
11620.540.8026empty

Interfaces

1 interface between chains.

  • A–B · 3287 Ų buried · 61 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 3GXY · Crystal structure of cyanovirin-n complexed to a synthetic hexamannoside · the same entry in another collection · chain A against A, TM-score 1.00
  • P81180 · AlphaFold monomer V2.0 prediction for cyanovirin-N (P81180) · a predicted model of the same protein · chain B against A, TM-score 0.49

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