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Single chain fv of C219 in complex with synthetic epitope peptide

Analyse Single chain fv of C219 in complex with synthetic epitope peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2AP2
Type
protein
Length
503 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Single chain fv; P-glycoprotein
UniProt
Q6KB05, Q505N9
Pockets
2 · best druggability 0.39

Structure

x-ray diffraction · 4 distinct chains · 9% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASingle chain fvprotein2385% helix, 47% strandQ6KB05, Q505N9
CSingle chain fvprotein2405% helix, 48% strandQ6KB05, Q505N9
PP-glycoproteinprotein1182% helix, 0% strand—
QP-glycoproteinprotein1479% helix, 0% strand—

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1890.390.7721empty
21030.360.7421empty

Interfaces

2 interfaces between chains.

  • C–Q · 556 Ų buried · 8 hydrogen bonds · protein-protein
  • A–P · 453 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 2AP2 · Single chain fv of C219 in complex with synthetic epitope peptide · the same entry in another collection · chain A against A, TM-score 1.00

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