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Crystal structural analysis of 2A protease from coxsackievirus A16

Analyse Crystal structural analysis of 2A protease from coxsackievirus A16 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4MG3
Type
protein
Length
287 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protease 2A
EC
3.4.22.29
UniProt
Q9QF31
Ligands
ZN
Pockets
2 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 13% helix, 52% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtease 2A (EC 3.4.22.29)protein14212% helix, 52% strandQ9QF31
BProtease 2A (EC 3.4.22.29)protein14514% helix, 51% strandQ9QF31

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • 1PE · Pentaethylene glycol · additive · chains A, B
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14030.740.8460TRS
2620.290.7416empty

Interfaces

1 interface between chains.

  • A–B · 544 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 4MG3 · Crystal Structural Analysis of 2A Protease from Coxsackievirus A16 · the same entry in another collection · chain A against A, TM-score 1.00

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