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Crystal structure of the E153Q mutant of the cftr inhibitory factor cif containing the adducted styrene oxide hydrolysis intermediate

Analyse Crystal structure of the E153Q mutant of the cftr inhibitory factor cif… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5TNP
Type
protein
Length
1,172 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cftr inhibitory factor
UniProt
A0A0M3KL26
Ligands
FEH
Pockets
8 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 43% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DCftr inhibitory factorprotein29343% helix, 20% strandA0A0M3KL26

Ligands and binding sites

  • FEH · (1R)-1-phenylethane-1,2-diol · ligand · 8 copies · chains A, B, C, D

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

Pockets

8 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12810.800.9139empty
22830.790.9146empty
33090.640.8035empty
43700.640.7951empty
52610.620.8028empty

Interfaces

5 interfaces between chains.

  • A–B · 1418 Ų buried · 14 hydrogen bonds · protein-protein
  • C–D · 1409 Ų buried · 14 hydrogen bonds · protein-protein
  • B–C · 664 Ų buried · 7 hydrogen bonds · protein-protein
  • A–D · 635 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 426 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 covalent, 4 disulfide (covalent ligand, disulfide).

Compared structures

  • 5TNP · Crystal structure of the E153Q mutant of the CFTR inhibitory factor Cif containing the… · the same entry in another collection · chain A against A, TM-score 1.00

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