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Neutron structure of human transthyretin (ttr) S52P mutant in complex with tafamidis at room temperature to 2A resolution (quasi-laue)

Analyse Neutron structure of human transthyretin (ttr) S52P mutant in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6FFT
Type
protein
Length
232 residues
Chains
2
Method
x-ray diffraction; neutron diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transthyretin
UniProt
P02766
Ligands
3MI
Pockets
3 · best druggability 0.32

Structure

x-ray diffraction; neutron diffraction · 1 distinct chain · 6% helix, 53% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BTransthyretinprotein1166% helix, 53% strandP02766

Ligands and binding sites

  • 3MI · 2-(3,5-dichlorophenyl)-1,3-benzoxazole-6-carboxylic acid · ligand · 2 copies · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1640.320.7616empty
2670.320.7514empty
3550.260.7317empty

Interfaces

1 interface between chains.

  • A–B · 931 Ų buried · 21 hydrogen bonds · protein-protein

Compared structures

  • 6FFT · Neutron structure of human transthyretin (TTR) S52P mutant in complex with tafamidis at… · the same entry in another collection · chain A against A, TM-score 1.00

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