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MolNFT v1 · #128935 · protein

Crystal structure of human udp-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1) (V264G mutant) in complex with tunicamycin

5O5E · Udp-N-acetylglucosamine--dolichyl-phosphate N…: “Crystal structure of human udp-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase…”. X-ray diffraction, 3 ligands (P6L, 9LH, UNL), 3 pockets (best…

PDB
5O5E
Type
protein
Length
381 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Udp-N-acetylglucosamine--dolichyl-phosphate N- acetylglucosaminephosphotransferase
EC
2.7.8.15
UniProt
Q9H3H5
Ligands
P6L, 9LH, UNL
Pockets
3 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 63% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUdp-N-acetylglucosamine--dolichyl-phosphate N- acetylglucosaminephosphotransferase (EC 2.7.8.15)protein38163% helix, 7% strandQ9H3H5

Ligands and binding sites

  • P6L · (2S)-3-{[{[(2S)-2,3-dihydroxypropyl]oxy}(hydroxy)phosphoryl]oxy}-2-[(6E)-hexadec-6-enoyloxy]propyl (8E)-octadec-8-enoate · ligand · chains A
  • 9LH · Tunicamycin · ligand · chains A
  • UNL · Unknown ligand · ligand · chains A

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
15750.760.83529LH
2920.420.7814empty
31020.360.7425empty

Compared structures

  • 5O5E · Crystal structure of human UDP-N-acetylglucosamine-dolichyl-phosphate… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9H3H5 · AlphaFold monomer V2.0 prediction for udp-N-acetylglucosamine-- dolichyl-phosphate… · a predicted model of the same protein · chain A against A, TM-score 0.99

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