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Crystal structure of sea bream transthyretin in complex with thyroxine at 1.9A resolution

Analyse Crystal structure of sea bream transthyretin in complex with thyroxine at 1.9A… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1SN0
Type
protein
Length
463 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transthyretin
UniProt
Q9PTT3
Ligands
T44, SO4
Pockets
4 · best druggability 0.65

Structure

x-ray diffraction · 4 distinct chains · 8% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATransthyretinprotein1187% helix, 46% strandQ9PTT3
BTransthyretinprotein1167% helix, 49% strandQ9PTT3
CTransthyretinprotein11510% helix, 50% strandQ9PTT3
DTransthyretinprotein11410% helix, 48% strandQ9PTT3

Ligands and binding sites

  • T44 · 3,5,3',5'-tetraiodo-L-thyronine · ligand · 2 copies · chains B, D, A, C
  • SO4 · Sulfate ion · ion · chains A

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13040.650.8135T44
23050.650.8139T44
3700.310.7419empty
4510.290.7515empty

Interfaces

6 interfaces between chains.

  • C–D · 922 Ų buried · 19 hydrogen bonds · protein-protein
  • A–B · 917 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 594 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 377 Ų buried · 2 hydrogen bonds · protein-protein
  • A–D · 352 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 1SN0 · Crystal Structure Of Sea Bream Transthyretin in complex with thyroxine At 1.9A Resolution · the same entry in another collection · chain A against A, TM-score 1.00

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