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1.4 a resolution structure of mouse tumor necrosis factor, towards modulation of its selectivity and trimerisation

Analyse 1.4 a resolution structure of mouse tumor necrosis factor, towards modulation… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2TNF
Type
protein
Length
444 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein (tumor necrosis factor alpha)
UniProt
P06804
Pockets
5 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 2% helix, 51% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CProtein (tumor necrosis factor alpha)protein1482% helix, 51% strandP06804

Ligands and binding sites

  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains A, B, C
  • IPA · Isopropyl alcohol · additive · chains A, B, C

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

Pockets

5 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16570.780.8356empty
2630.730.9820TRS
3880.590.8722empty
4600.550.8819empty
5990.480.8120empty

Interfaces

3 interfaces between chains.

  • B–C · 1018 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 992 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 989 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 2TNF · 1.4 a resolution structure of mouse tumor necrosis factor, towards modulation of its… · the same entry in another collection · chain A against A, TM-score 1.00
  • P06804 · AlphaFold monomer V2.0 prediction for tumor necrosis factor (P06804) · a predicted model of the same protein · chain A against A, TM-score 0.99

Analyse

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