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Human thyrotropin receptor bound by cs-17 inverse agonist FAB/ORG 274179-0 antagonist

Analyse Human thyrotropin receptor bound by cs-17 inverse agonist FAB/ORG 274179-0… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7T9M
Type
protein
Length
995 residues
Chains
3
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cs-17 heavy chain; Cs-17 light chain; Thyrotropin receptor
UniProt
A0A0A0MTJ0
Ligands
NAG
Pockets
13 · best druggability 0.84

Structure

electron microscopy · 3 distinct chains · 27% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HCs-17 heavy chainprotein2177% helix, 48% strand—
LCs-17 light chainprotein2137% helix, 46% strand—
RThyrotropin receptorprotein56542% helix, 12% strandA0A0A0MTJ0

Ligands and binding sites

  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 5 copies · chains H, R

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

Pockets

13 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111700.840.85128empty
24640.710.8148empty
3500.670.9516empty
4950.570.8624empty
5850.540.8524empty

Interfaces

3 interfaces between chains.

  • H–L · 1861 Ų buried · 16 hydrogen bonds · protein-protein
  • H–R · 662 Ų buried · 17 hydrogen bonds · protein-protein
  • L–R · 268 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 9 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 7T9M · Human Thyrotropin receptor bound by CS-17 Inverse Agonist Fab/Org 274179-0 Antagonist · the same entry in another collection · chain H against H, TM-score 1.00

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