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Crystal structure of the srpa adhesin R347E mutant from streptococcus sanguinis

Analyse Crystal structure of the srpa adhesin R347E mutant from streptococcus sanguinis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5EQ4
Type
protein
Length
770 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Platelet-binding glycoprotein
UniProt
A3CM52
Ligands
CA
Pockets
3 · best druggability 0.75

Structure

x-ray diffraction · 4 distinct chains · 11% helix, 36% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APlatelet-binding glycoproteinprotein18812% helix, 35% strandA3CM52
BPlatelet-binding glycoproteinprotein19512% helix, 36% strandA3CM52
CPlatelet-binding glycoproteinprotein19310% helix, 36% strandA3CM52
DPlatelet-binding glycoproteinprotein19411% helix, 38% strandA3CM52

Ligands and binding sites

  • CA · Calcium ion · metal · 9 copies · chains A, B, C, D
  • ACT · Acetate ion · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17740.750.8083ACT
21090.370.7418empty
3760.310.7315empty

Interfaces

5 interfaces between chains.

  • A–B · 577 Ų buried · 13 hydrogen bonds · protein-protein
  • A–C · 455 Ų buried · 7 hydrogen bonds · protein-protein
  • C–D · 282 Ų buried · 10 hydrogen bonds · protein-protein
  • B–D · 154 Ų buried · 2 hydrogen bonds · protein-protein
  • B–C · 59 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 5EQ4 · Crystal structure of the SrpA adhesin R347E mutant from Streptococcus sanguinis · the same entry in another collection · chain A against A, TM-score 1.00

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