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Crystal structure of the C-terminal domain of Streptococcus mutans surface protein SpaP

Analyse Crystal structure of the C-terminal domain of Streptococcus mutans surface… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3OPU
Type
protein
Length
2,029 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.181
Source
Streptococcus mutans
Molecule
SpaP
Ligands
CA
Pockets
15 · best druggability 0.82

Structure

x-ray diffraction · resolution 2.181 · 3 distinct chains · 13% helix, 44% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, FSpaPprotein33813% helix, 44% strand—
CSpaPprotein33712% helix, 44% strand—
D, ESpaPprotein33913% helix, 44% strand—

Ligands and binding sites

  • CA · Calcium ion · metal · 12 copies · chains A, B, C, D, E, F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19490.820.83114empty
29520.780.81106empty
31550.740.9227empty
410250.730.76104empty
510280.720.76102empty

Interfaces

11 interfaces between chains.

  • A–C · 1267 Ų buried · 25 hydrogen bonds · protein-protein
  • B–D · 1200 Ų buried · 21 hydrogen bonds · protein-protein
  • A–B · 599 Ų buried · 9 hydrogen bonds · protein-protein
  • C–D · 566 Ų buried · 6 hydrogen bonds · protein-protein
  • D–F · 448 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 isopeptide (isopeptide).

Compared structures

  • 3OPU · Crystal structure of the C-terminal domain of streptococcus mutans surface protein spap · the same entry in another collection · chain A against A, TM-score 1.00

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