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Crystal structure of fv polyglutamine complex

Analyse Crystal structure of fv polyglutamine complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2OTW
Type
protein
Length
488 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fv light chain avriable domain vl; Fv heavy chain variable domain vh; Poly-gln peptide…
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · 3 distinct chains · 5% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CFv light chain avriable domain vlprotein1155% helix, 52% strand—
B, DFv heavy chain variable domain vhprotein1185% helix, 54% strand—
E, FPoly-gln peptide antigenprotein110% helix, 9% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111150.760.7887empty
21360.430.7619empty
3840.330.7420empty
4760.310.7418empty
5700.310.7417empty

Interfaces

11 interfaces between chains.

  • A–B · 935 Ų buried · 7 hydrogen bonds · protein-protein
  • C–D · 921 Ų buried · 5 hydrogen bonds · protein-protein
  • A–E · 479 Ų buried · 16 hydrogen bonds · protein-protein
  • C–F · 475 Ų buried · 20 hydrogen bonds · protein-protein
  • B–E · 472 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 2OTW · Crystal structure of Fv polyglutamine complex · the same entry in another collection · chain B against B, TM-score 1.00

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