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Crystal structure of antigen TPF1 from treponema pallidum

Analyse Crystal structure of antigen TPF1 from treponema pallidum in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2FJC
Type
protein
Length
2,416 residues
Chains
16
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Antigen TPF1
UniProt
P16665
Ligands
FE
Pockets
20 · best druggability 0.74

Structure

x-ray diffraction · 3 distinct chains · 79% helix, 3% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, D, F, H, I, J, K, L, M, PAntigen TPF1protein15179% helix, 3% strandP16665
BAntigen TPF1protein15677% helix, 4% strandP16665
C, E, G, N, OAntigen TPF1protein15080% helix, 3% strandP16665

Ligands and binding sites

  • FE · Fe (III) ion · metal · 16 copies · chains A, D, B, C, E, H, F, G, I, L, J, K, M, N, O, P

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14620.740.8291empty
24390.720.8281empty
36330.710.78108empty
43010.660.8234empty
53060.650.8138empty

Interfaces

35 interfaces between chains.

  • F–G · 1311 Ų buried · 21 hydrogen bonds · protein-protein
  • B–C · 1310 Ų buried · 21 hydrogen bonds · protein-protein
  • M–N · 1306 Ų buried · 23 hydrogen bonds · protein-protein
  • J–K · 1304 Ų buried · 22 hydrogen bonds · protein-protein
  • E–H · 1300 Ų buried · 22 hydrogen bonds · protein-protein

Compared structures

  • 2FJC · Crystal structure of antigen TpF1 from Treponema pallidum · the same entry in another collection · chain P against P, TM-score 1.00

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