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Crystal structure of sea bream transthyretin in complex with triiodothyronine at 1.90A resolution

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

PDB
1SN5
Type
protein
Length
463 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transthyretin
UniProt
Q9PTT3
Ligands
T3, SO4
Pockets
4 · best druggability 0.65

Structure

x-ray diffraction · 4 distinct chains · 9% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATransthyretinprotein1188% helix, 46% strandQ9PTT3
BTransthyretinprotein1167% helix, 51% strandQ9PTT3
CTransthyretinprotein11510% helix, 48% strandQ9PTT3
DTransthyretinprotein11410% helix, 48% strandQ9PTT3

Ligands and binding sites

  • T3 · 3,5,3'triiodothyronine · ligand · 2 copies · chains A, C, B, D
  • 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
12950.650.8134T3
23030.640.8138T3
3710.300.7319empty
4560.260.7315empty

Interfaces

6 interfaces between chains.

  • C–D · 941 Ų buried · 23 hydrogen bonds · protein-protein
  • A–B · 910 Ų buried · 17 hydrogen bonds · protein-protein
  • A–C · 604 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 390 Ų buried · 2 hydrogen bonds · protein-protein
  • A–D · 354 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 1SN5 · Crystal Structure of Sea Bream Transthyretin in complex with Triiodothyronine at 1.90A… · the same entry in another collection · chain A against A, TM-score 1.00

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