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MolNFT v1 · #135065 · protein

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

5TNP: “Crystal structure of the E153Q mutant of the cftr inhibitory factor cif containing the adducted styrene oxide…”. X-ray diffraction, 1 ligand (FEH), 8 pockets (best druggability 0.80). MolNFT v1 #135065 on GenesisL1: 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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