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Macrophage migration inhibitory factor (mif) with covalently bound pitc

Analyse Macrophage migration inhibitory factor (mif) with covalently bound pitc in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6FVH
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
0FI, SO4
Pockets
5 · best druggability 0.82

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

  • 0FI · N-phenylthioformamide · ligand · 3 copies · chains A, B, C
  • SO4 · Sulfate ion · ion · 6 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
14810.820.8949empty
21000.560.84130FI
3670.530.86130FI
4810.510.84140FI
51460.400.7319empty

Interfaces

3 interfaces between chains.

  • A–C · 1153 Ų buried · 18 hydrogen bonds · protein-protein
  • B–C · 1146 Ų buried · 18 hydrogen bonds · protein-protein
  • A–B · 1144 Ų buried · 17 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 6FVH · Macrophage Migration Inhibitory Factor (MIF) with Covalently Bound PITC · the same entry in another collection · chain A against A, TM-score 1.00

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