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QRI7 and AMP complex

Analyse QRI7 and AMP complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3WUH
Type
protein
Length
694 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
TRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial
EC
2.3.1.-
UniProt
P43122
Ligands
AMP, ZN
Pockets
4 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial (EC 2.3.1.-)protein34442% helix, 21% strandP43122
BTRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial (EC 2.3.1.-)protein35041% helix, 21% strandP43122

Ligands and binding sites

  • AMP · Adenosine monophosphate · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17680.780.82103AMP
23980.660.8048AMP
3860.560.8615empty
4600.290.7418empty

Interfaces

1 interface between chains.

  • A–B · 1170 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 3WUH · Qri7 and AMP complex · the same entry in another collection · chain A against A, TM-score 1.00
  • P43122 · AlphaFold monomer V2.0 prediction for tRNA N6-adenosine threonylcarbamoyltransferase… · a predicted model of the same protein · chain B against A, TM-score 0.98

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