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Crystal structure of VRC42.01 Fab in complex with T117-F mper scaffold

Analyse Crystal structure of VRC42.01 Fab in complex with T117-F mper scaffold in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6MTO
Type
protein
Length
588 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antibody VRC42.01 Fab light chain; Antibody VRC42.01 Fab heavy chain; VRC42 epitope…
Pockets
7 · best druggability 0.58

Structure

x-ray diffraction · 3 distinct chains · 17% helix, 44% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
LAntibody VRC42.01 Fab light chainprotein2128% helix, 50% strand—
HAntibody VRC42.01 Fab heavy chainprotein2197% helix, 54% strand—
TVRC42 epitope T117-F scaffoldprotein15743% helix, 22% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14460.580.7450empty
22190.540.7827empty
31300.430.7620empty
41300.420.7523empty
51080.390.7521empty

Interfaces

3 interfaces between chains.

  • L–H · 1725 Ų buried · 8 hydrogen bonds · protein-protein
  • H–T · 862 Ų buried · 6 hydrogen bonds · protein-protein
  • L–T · 197 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 6MTO · Crystal structure of VRC42.01 Fab in complex with T117-F MPER scaffold · the same entry in another collection · chain L against L, TM-score 1.00

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