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Crystal structure of qdtc, the dtdp-3-amino-3,6-dideoxy-D- glucose N-acetyl transferase from thermoanaerobacterium thermosaccharolyticum in complex with CoA and dtdp-3-amino- quinovose

Analyse Crystal structure of qdtc, the dtdp-3-amino-3,6-dideoxy-D- glucose N-acetyl… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3FSB
Type
protein
Length
518 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Qdtc
UniProt
Q6TFC6
Ligands
COA, T3Q
Pockets
3 · best druggability 0.51

Structure

x-ray diffraction · 2 distinct chains · 7% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AQdtcprotein2607% helix, 30% strandQ6TFC6
BQdtcprotein2586% helix, 31% strandQ6TFC6

Ligands and binding sites

  • COA · Coenzyme A · ligand · 2 copies · chains A, B
  • T3Q · [(3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl][hydroxy-[[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy]phosphoryl] hydrogen phosphate · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12610.510.7532empty
2680.320.7412empty
3600.290.7311empty

Interfaces

1 interface between chains.

  • A–B · 151 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 3FSB · Crystal structure of QdtC, the dTDP-3-amino-3,6-dideoxy-D-glucose N-acetyl transferase… · the same entry in another collection · chain A against A, TM-score 1.00

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