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Structure of CAN2 from sulfobacillus thermosulfidooxidans in complex with cyclic tetra-adenylate (CA4)

Analyse Structure of CAN2 from sulfobacillus thermosulfidooxidans in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7BDV
Type
protein + RNA
Length
1,387 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CAN2; Cyclic tetra-adenylate
Pockets
14 · best druggability 0.75

Structure

x-ray diffraction · 5 distinct chains · 42% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACAN2protein35542% helix, 22% strand—
BCAN2protein34242% helix, 22% strand—
CCAN2protein34142% helix, 22% strand—
DCAN2protein34144% helix, 22% strand—
F, HCyclic tetra-adenylaterna4——

Pockets

14 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19220.750.7964empty
211150.740.7798empty
310770.740.7774empty
4700.630.9216empty
5650.590.9020empty

Interfaces

7 interfaces between chains.

  • A–B · 1711 Ų buried · 25 hydrogen bonds · protein-protein
  • C–D · 1671 Ų buried · 26 hydrogen bonds · protein-protein
  • A–F · 607 Ų buried · 12 hydrogen bonds · protein-nucleic
  • C–H · 602 Ų buried · 11 hydrogen bonds · protein-nucleic
  • B–F · 601 Ų buried · 12 hydrogen bonds · protein-nucleic

Modifications

Observed in the structure: 12 modified (engineered).

Compared structures

  • 7BDV · Structure of Can2 from Sulfobacillus thermosulfidooxidans in complex with cyclic… · the same entry in another collection · chain A against A, TM-score 1.00

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