GL1X · GenesisL1 explorer

MolNFT v1 · #11546 · protein

Crystal structure of il-17F

1JPY · Interleukin 17F: “Crystal structure of il-17F”. X-ray diffraction, 3 ligands (NAG, NDG, SO4), 8 pockets (best druggability 0.83). MolNFT v1 #11546 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
1JPY
Type
protein
Length
479 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Interleukin 17F
Ligands
NAG, NDG, SO4
Pockets
8 · best druggability 0.83

Structure

x-ray diffraction · 3 distinct chains · 5% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BInterleukin 17Fprotein1218% helix, 50% strand—
XInterleukin 17Fprotein1170% helix, 48% strand—
YInterleukin 17Fprotein1206% helix, 48% strand—

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains B, X, A, Y
  • NDG · 2-acetamido-2-deoxy-alpha-D-glucopyranose · sugar
  • SO4 · Sulfate ion · ion · chains X

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110610.830.8478empty
21680.530.7922empty
31900.530.7825empty
41730.450.7534empty
5690.420.8016empty

Interfaces

5 interfaces between chains.

  • X–Y · 3534 Ų buried · 48 hydrogen bonds · protein-protein
  • A–B · 3486 Ų buried · 48 hydrogen bonds · protein-protein
  • B–X · 610 Ų buried · 4 hydrogen bonds · protein-protein
  • B–Y · 183 Ų buried · 1 hydrogen bond · protein-protein
  • A–X · 174 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 1JPY · Crystal structure of IL-17F · the same entry in another collection · chain A against A, TM-score 1.00

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