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Ontogeny of recognition specificity and functionality for the anti-HIV neutralizing antibody 4E10

Analyse Ontogeny of recognition specificity and functionality for the anti-HIV… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4M8Q
Type
protein
Length
764 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
GEP1 fv heavy chain; GEP1 fv light chain; 4E10 epitope scaffold T117
UniProt
P18136
Pockets
11 · best druggability 0.56

Structure

x-ray diffraction · 5 distinct chains · 22% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGEP1 fv heavy chainprotein1252% helix, 56% strand—
B, LGEP1 fv light chainprotein1066% helix, 55% strandP18136
C4E10 epitope scaffold T117protein14845% helix, 24% strand—
HGEP1 fv heavy chainprotein1252% helix, 55% strand—
S4E10 epitope scaffold T117protein15443% helix, 23% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1860.560.8732empty
2850.480.8123empty
31520.440.7528empty
41240.430.7618empty
51070.420.7716empty

Interfaces

7 interfaces between chains.

  • A–S · 786 Ų buried · 7 hydrogen bonds · protein-protein
  • A–B · 720 Ų buried · 4 hydrogen bonds · protein-protein
  • H–L · 717 Ų buried · 6 hydrogen bonds · protein-protein
  • C–H · 703 Ų buried · 4 hydrogen bonds · protein-protein
  • B–L · 308 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 4M8Q · Ontogeny of recognition specificity and functionality for the anti-HIV neutralizing… · the same entry in another collection · chain A against A, TM-score 1.00

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