GL1X · GenesisL1 explorer

MolNFT v1 · #152330 · protein

Structure of rvfv gn and human monoclonal antibody R13

6IEA · Nsmgngc: “Structure of rvfv gn and human monoclonal antibody R13”. X-ray diffraction, 8 pockets (best druggability 0.59). MolNFT v1 #152330 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6IEA
Type
protein
Length
728 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Nsmgngc; R13 L chain; R13 H chain
UniProt
H9BSP3
Pockets
8 · best druggability 0.59

Structure

x-ray diffraction · 3 distinct chains · 9% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANsmgngcprotein30012% helix, 32% strandH9BSP3
LR13 L chainprotein2187% helix, 50% strand—
HR13 H chainprotein2107% helix, 52% strand—

Ligands and binding sites

  • GOL · Glycerol · additive · chains A
  • PEG · Di(hydroxyethyl)ether · additive · chains A, L, H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15100.590.7449empty
23440.570.7639GOL
32040.540.7834empty
4740.520.8522PEG
51660.480.7619empty

Interfaces

3 interfaces between chains.

  • L–H · 1941 Ų buried · 24 hydrogen bonds · protein-protein
  • A–L · 442 Ų buried · 8 hydrogen bonds · protein-protein
  • A–H · 355 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 14 disulfide (disulfide).

Compared structures

  • 6IEA · Structure of RVFV Gn and human monoclonal antibody R13 · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.