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SP2-SP3 - a complex of two storage proteins from bombyx mori hemolymph

Analyse SP2-SP3 - a complex of two storage proteins from bombyx mori hemolymph in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4L37
Type
protein
Length
1,341 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Silkworm storage protein; Arylphorin
UniProt
H9JHM9, Q1HPP4
Ligands
NAG, MAN, BMA, NA, SCN, SO4
Pockets
20 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASilkworm storage proteinprotein67442% helix, 19% strandH9JHM9
BArylphorinprotein66743% helix, 20% strandQ1HPP4

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B
  • MAN · alpha-D-mannopyranose · sugar · 4 copies · chains A, B
  • BMA · beta-D-mannopyranose · sugar · 2 copies
  • NA · Sodium ion · metal · 3 copies · chains A, B
  • SCN · Thiocyanate ion · ion · 5 copies · chains A, B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13020.820.9343empty
22080.810.9541empty
36690.780.8383NAG
47750.770.8164empty
52780.750.8731empty

Interfaces

1 interface between chains.

  • A–B · 2224 Ų buried · 20 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide, 2 glycan (disulfide, N-glycosylation).

Compared structures

  • 4L37 · SP2-SP3 - a complex of two storage proteins from Bombyx mori hemolymph · the same entry in another collection · chain A against A, TM-score 1.00

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