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Crystal structure of C-terminal domain of shaft pilin spaa from lactobacillus rhamnosus gg - P21212 space group with yb heavy atom

Analyse Crystal structure of C-terminal domain of shaft pilin spaa from lactobacillus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5FGR
Type
protein
Length
486 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cell surface protein spaa
UniProt
C7T9P4
Ligands
YB
Pockets
10 · best druggability 0.55

Structure

x-ray diffraction · 3 distinct chains · 5% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACell surface protein spaaprotein1212% helix, 46% strandC7T9P4
BCell surface protein spaaprotein1216% helix, 44% strandC7T9P4
C, DCell surface protein spaaprotein1226% helix, 48% strandC7T9P4

Ligands and binding sites

  • YB · Ytterbium (III) ion · metal · 10 copies · chains A, B, D, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12740.550.7644empty
22720.550.7645empty
31760.480.7733empty
41420.440.7630empty
5940.420.7816empty

Interfaces

4 interfaces between chains.

  • B–C · 574 Ų buried · 10 hydrogen bonds · protein-protein
  • B–D · 550 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 508 Ų buried · 8 hydrogen bonds · protein-protein
  • A–D · 452 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 isopeptide (isopeptide).

Compared structures

  • 5FGR · Crystal structure of C-terminal domain of shaft pilin spaA from Lactobacillus rhamnosus… · the same entry in another collection · chain A against A, TM-score 1.00

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