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Crystal structure of DH511.2 Fab in complex with HIV-1 GP41 mper 670- 683 peptide

Analyse Crystal structure of DH511.2 Fab in complex with HIV-1 GP41 mper 670- 683… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5U3L
Type
protein
Length
912 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DH511.2 Fab heavy chain; DH511.2 Fab light chain; GP41 mper peptide
Pockets
6 · best druggability 0.65

Structure

x-ray diffraction · 5 distinct chains · 9% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HDH511.2 Fab heavy chainprotein2237% helix, 54% strand—
LDH511.2 Fab light chainprotein2147% helix, 50% strand—
ADH511.2 Fab heavy chainprotein22411% helix, 54% strand—
BDH511.2 Fab light chainprotein2136% helix, 50% strand—
P, CGP41 mper peptideprotein1963% helix, 0% strand—

Pockets

6 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16020.650.7674empty
23570.560.7562empty
31020.510.8223empty
42470.500.7537empty
5820.300.7317empty

Interfaces

7 interfaces between chains.

  • H–L · 1938 Ų buried · 15 hydrogen bonds · protein-protein
  • A–B · 1890 Ų buried · 19 hydrogen bonds · protein-protein
  • H–P · 773 Ų buried · 14 hydrogen bonds · protein-protein
  • A–C · 749 Ų buried · 15 hydrogen bonds · protein-protein
  • H–B · 369 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 disulfide (disulfide).

Compared structures

  • 5U3L · Crystal Structure of DH511.2 Fab in Complex with HIV-1 gp41 MPER 670-683 Peptide · the same entry in another collection · chain H against H, TM-score 1.00

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