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Concanavalin A/15-mer peptide complex

Analyse Concanavalin A/15-mer peptide complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1JYC
Type
protein
Length
1,008 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Concanavalin-br; 15-mer peptide
UniProt
P55915
Ligands
MN, CA
Pockets
3 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 4% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DConcanavalin-brprotein2374% helix, 44% strandP55915
P, Q, R, S15-mer peptideprotein150% helix, 0% strand—

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 4 copies · chains A, B, C, D
  • CA · Calcium ion · metal · 4 copies · chains A, B, C, D

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

Pockets

3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1540.710.9817empty
2810.640.9125empty
3530.340.7816empty

Interfaces

6 interfaces between chains.

  • A–B · 1178 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 1161 Ų buried · 20 hydrogen bonds · protein-protein
  • A–P · 701 Ų buried · 12 hydrogen bonds · protein-protein
  • D–S · 693 Ų buried · 12 hydrogen bonds · protein-protein
  • C–R · 663 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 1JYC · CONCANAVALIN A/15-mer PEPTIDE COMPLEX · the same entry in another collection · chain S against S, TM-score 1.00
  • P55915 · AlphaFold monomer V2.0 prediction for concanavalin-br (P55915) · a predicted model of the same protein · chain C against A, TM-score 0.99

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