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Crystal structure of norovirus GII.10 P domain in complex with nano-85

Analyse Crystal structure of norovirus GII.10 P domain in complex with nano-85 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4X7E
Type
protein
Length
847 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Capsid protein; Nano-85 nanobody
UniProt
Q5F4T5
Pockets
4 · best druggability 0.78

Structure

x-ray diffraction · 4 distinct chains · 7% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACapsid proteinprotein3047% helix, 37% strandQ5F4T5
CNano-85 nanobodyprotein1215% helix, 57% strand—
BCapsid proteinprotein3027% helix, 37% strandQ5F4T5
DNano-85 nanobodyprotein1205% helix, 58% strand—

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 6 copies · chains A, B
  • ACT · Acetate ion · additive · 3 copies · chains A, B, D

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19780.780.80112EDO, ACT
21720.550.8028empty
3640.370.7920empty
4590.320.7616empty

Interfaces

3 interfaces between chains.

  • A–B · 1897 Ų buried · 25 hydrogen bonds · protein-protein
  • A–C · 755 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 738 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 4X7E · Crystal structure of norovirus GII.10 P domain in complex with Nano-85 · the same entry in another collection · chain A against A, TM-score 1.00

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