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MolNFT v1 · #70248 · protein

2F5 epitope scaffold elicited anti-HIV-1 monoclonal antibody 11F10 in complex with HIV-1 GP41

3LEX · 11F10 antibody heavy chain: “2F5 epitope scaffold elicited anti-HIV-1 monoclonal antibody 11F10 in complex with HIV-1 GP41”. X-ray diffraction, 1 ligand (NH2), 7 pockets (best druggability 0.60). MolNFT v1 #70248 on GenesisL1: 3D…

PDB
3LEX
Type
protein
Length
876 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
11F10 antibody heavy chain; 11F10 antibody light chain; Envelope glycoprotein GP41
UniProt
Q9IJQ0
Ligands
NH2
Pockets
7 · best druggability 0.60

Structure

x-ray diffraction · 3 distinct chains · 6% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
H, A11F10 antibody heavy chainprotein2126% helix, 54% strand—
L, B11F10 antibody light chainprotein2197% helix, 51% strand—
P, CEnvelope glycoprotein GP41protein70% helix, 0% strandQ9IJQ0

Ligands and binding sites

  • NH2 · Amino group · ion · 2 copies · chains P, C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

7 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15230.600.7451empty
25240.590.7455empty
31900.510.7726empty
4940.390.7726empty
51030.390.7626empty

Interfaces

8 interfaces between chains.

  • H–L · 1935 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 1935 Ų buried · 14 hydrogen bonds · protein-protein
  • L–B · 399 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 326 Ų buried · 6 hydrogen bonds · protein-protein
  • L–P · 325 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 3LEX · 2F5 Epitope scaffold elicited anti-HIV-1 monoclonal antibody 11F10 in complex with HIV-1… · the same entry in another collection · chain H against H, TM-score 1.00

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