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Structural and biochemical characterization of CLFB:LIGAND interactions

Analyse Structural and biochemical characterization of CLFB:LIGAND interactions in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3ASW
Type
protein
Length
331 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Clumping factor B; Tail region derived peptide
UniProt
Q7A382, P13645
Pockets
2 · best druggability 0.55

Structure

x-ray diffraction · 2 distinct chains · 6% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AClumping factor Bprotein3207% helix, 49% strandQ7A382
BTail region derived peptideprotein110% helix, 64% strandP13645

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12990.550.7639empty
2980.420.7821empty

Interfaces

1 interface between chains.

  • A–B · 734 Ų buried · 29 hydrogen bonds · protein-protein

Compared structures

  • 3ASW · Structural and biochemical characterization of ClfB:ligand interactions · the same entry in another collection · chain A against A, TM-score 1.00
  • Q7A382 · AlphaFold monomer V2.0 prediction for clumping factor B (Q7A382) · a predicted model of the same protein · chain A against A, TM-score 0.99
  • P13645 · AlphaFold monomer V2.0 prediction for keratin, type I cytoskeletal 10 (P13645) · a predicted model of the same protein · chain B against A, TM-score 0.33

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