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Crystal structure of the STX2A

Analyse Crystal structure of the STX2A in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7D6Q
Type
protein
Length
630 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
RRNA N-glycosylase; Shiga toxin 2 B subunit
EC
3.2.2.22
UniProt
Q8XBV2, Q7DJJ2
Ligands
1PS
Pockets
2 · best druggability 0.72

Structure

x-ray diffraction · 3 distinct chains · 31% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARRNA N-glycosylase (EC 3.2.2.22)protein28339% helix, 24% strandQ8XBV2
BShiga toxin 2 B subunitprotein6716% helix, 48% strandQ7DJJ2
C, D, E, FShiga toxin 2 B subunitprotein7016% helix, 46% strandQ7DJJ2

Ligands and binding sites

  • 1PS · 3-pyridinium-1-ylpropane-1-sulfonate · ligand · 4 copies · chains B, C, D, F

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
16840.720.7968empty
21480.440.7629empty

Interfaces

10 interfaces between chains.

  • E–F · 751 Ų buried · 15 hydrogen bonds · protein-protein
  • B–C · 743 Ų buried · 15 hydrogen bonds · protein-protein
  • D–E · 734 Ų buried · 16 hydrogen bonds · protein-protein
  • B–F · 729 Ų buried · 15 hydrogen bonds · protein-protein
  • A–E · 671 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 7D6Q · Crystal structure of the Stx2a · the same entry in another collection · chain A against A, TM-score 1.00

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