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The crystal structure of macrobrachium rosenbergii nodavirus P-domain

Analyse The crystal structure of macrobrachium rosenbergii nodavirus P-domain in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5YKV
Type
protein
Length
996 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Capsid protein
UniProt
Q6XNL3
Pockets
7 · best druggability 0.66

Structure

x-ray diffraction · 2 distinct chains · 2% helix, 58% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, F, HCapsid proteinprotein1242% helix, 58% strandQ6XNL3
B, D, E, GCapsid proteinprotein1252% helix, 58% strandQ6XNL3

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16070.660.7665empty
26140.660.7665empty
31170.460.7919empty
4590.330.7711empty
5520.320.7811empty

Interfaces

10 interfaces between chains.

  • C–D · 1484 Ų buried · 22 hydrogen bonds · protein-protein
  • A–B · 1479 Ų buried · 23 hydrogen bonds · protein-protein
  • E–F · 1474 Ų buried · 25 hydrogen bonds · protein-protein
  • G–H · 1466 Ų buried · 23 hydrogen bonds · protein-protein
  • A–D · 680 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 5YKV · The crystal structure of Macrobrachium rosenbergii nodavirus P-domain · the same entry in another collection · chain A against A, TM-score 1.00

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