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Phenethylisothiocyanate covalently bound to macrophage migration inhibitory factor (mif)

Analyse Phenethylisothiocyanate covalently bound to macrophage migration inhibitory… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3SMB
Type
protein
Length
342 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Macrophage migration inhibitory factor
EC
5.3.2.1, 5.3.3.12
UniProt
P14174
Ligands
LE2, NA, CL
Pockets
5 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 39% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CMacrophage migration inhibitory factor (EC 5.3.2.1, 5.3.3.12)protein11439% helix, 31% strandP14174

Ligands and binding sites

  • LE2 · N-(2-phenylethyl)thioformamide · ligand · 3 copies · chains A, C, B
  • NA · Sodium ion · metal · 3 copies · chains A, B, C
  • CL · Chloride ion · ion · 9 copies · 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
14320.830.9050empty
21000.600.8614LE2
3850.580.8714LE2
4870.570.8613LE2
51750.440.7418CL, NA

Interfaces

3 interfaces between chains.

  • A–B · 1162 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 1155 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 1146 Ų buried · 17 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 covalent (covalent ligand).

Compared structures

  • 3SMB · Phenethylisothiocyanate Covalently Bound to Macrophage Migration Inhibitory Factor (MIF) · the same entry in another collection · chain A against A, TM-score 1.00

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