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MolNFT v1 · #94219 · protein

Crystal structure of RV144-elicited antibody CH59 in complex with V2 peptide

4HPY · CH59 Fab heavy chain: “Crystal structure of RV144-elicited antibody CH59 in complex with V2 peptide”. X-ray diffraction, 4 pockets (best druggability 0.65). MolNFT v1 #94219 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
4HPY
Type
protein
Length
443 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
CH59 Fab heavy chain; CH59 Fab light chain; Envelope glycoprotein GP160
UniProt
Q9WLG7
Pockets
4 · best druggability 0.65

Structure

x-ray diffraction · 3 distinct chains · 8% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HCH59 Fab heavy chainprotein21910% helix, 50% strand—
LCH59 Fab light chainprotein2136% helix, 49% strand—
PEnvelope glycoprotein GP160protein1127% helix, 9% strandQ9WLG7

Ligands and binding sites

  • GOL · Glycerol · additive · 2 copies · chains H, L

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16890.650.7480empty
2510.490.8716empty
31020.420.7824GOL
41100.390.7524empty

Interfaces

3 interfaces between chains.

  • H–L · 1715 Ų buried · 11 hydrogen bonds · protein-protein
  • L–P · 513 Ų buried · 8 hydrogen bonds · protein-protein
  • H–P · 434 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 4HPY · Crystal structure of RV144-elicited antibody CH59 in complex with V2 peptide · the same entry in another collection · chain H against H, TM-score 1.00

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