GL1X · GenesisL1 explorer

Research workbench

Crystal structure of the cftr inhibitory factor cif bound to tiratricol

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

PDB
4YX9
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
Q02P97
Ligands
4HY
Pockets
10 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 42% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DCftr inhibitory factorprotein29342% helix, 20% strandQ02P97

Ligands and binding sites

  • 4HY · [4-(4-hydroxy-3-iodo-phenoxy)-3,5-diiodo-phenyl]-acetic acid · ligand · 4 copies · chains A, B, C, D

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

Pockets

10 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17150.810.851024HY
22840.790.9142empty
32640.630.81434HY
42690.620.8029empty
52440.620.8130empty

Interfaces

5 interfaces between chains.

  • C–D · 1421 Ų buried · 16 hydrogen bonds · protein-protein
  • A–B · 1415 Ų buried · 16 hydrogen bonds · protein-protein
  • A–D · 623 Ų buried · 4 hydrogen bonds · protein-protein
  • B–C · 615 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 394 Ų buried · 5 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide, 3 covalent (disulfide, covalent ligand).

Compared structures

  • 4YX9 · Crystal structure of the CFTR inhibitory factor Cif bound to tiratricol · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.