GL1X · GenesisL1 explorer

MolNFT v1 · #152315 · protein

Peptide asparaginyl ligases from viola yedoensis

6IDV: “Peptide asparaginyl ligases from viola yedoensis”. X-ray diffraction, 3 ligands (SNN, NAG, FUC), 6 pockets (best druggability 0.62). MolNFT v1 #152315 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
6IDV
Type
protein
Length
850 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peptide asparaginyl ligases
Ligands
SNN, NAG, FUC
Pockets
6 · best druggability 0.62

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeptide asparaginyl ligasesprotein42544% helix, 11% strand—
BPeptide asparaginyl ligasesprotein42544% helix, 11% strand—

Ligands and binding sites

  • SNN · L-3-aminosuccinimide · ligand · 2 copies · chains A, B
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 9 copies · chains A, B
  • FUC · alpha-L-fucopyranose · sugar · 2 copies
  • EDO · 1,2-ethanediol · additive · 2 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1520.620.9325empty
22700.610.8037SNN
33000.590.7841empty
41840.530.7941empty
51650.500.7832empty

Interfaces

1 interface between chains.

  • A–B · 893 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 covalent, 4 disulfide, 4 glycan (covalent ligand, disulfide, N-glycosylation).

Compared structures

  • 6IDV · Peptide Asparaginyl Ligases from Viola yedoensis · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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