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Crystal structure of udp-galactopyranose mutase from corynebacterium diphtheriae in complex with 2-[4-(4-chlorophenyl)-7-(2-thienyl)-2- thia-5,6,8,9-TETRAZABICYCLO[4.3.0]NONA-4,7,9-trien-3-YL]ACETIC

Analyse Crystal structure of udp-galactopyranose mutase from corynebacterium… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4XGK
Type
protein
Length
772 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Udp-galactopyranose mutase
EC
5.4.99.9
UniProt
Q6NER4
Ligands
40K, FDA, SO4
Pockets
6 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 39% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BUdp-galactopyranose mutase (EC 5.4.99.9)protein38639% helix, 18% strandQ6NER4

Ligands and binding sites

  • 40K · [(7S)-6-(4-chlorophenyl)-3-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl]acetic acid · ligand · 2 copies · chains A, B
  • FDA · Dihydroflavine-adenine dinucleotide · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 11 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110440.830.849440K, FDA
210110.810.829440K, FDA
34270.650.7945empty
43870.650.7936SO4
51080.360.7420empty

Interfaces

1 interface between chains.

  • A–B · 1017 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 4XGK · Crystal structure of UDP-galactopyranose mutase from Corynebacterium diphtheriae in… · the same entry in another collection · chain A against A, TM-score 1.00

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