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Crystal structure of the L780 udp-rhamnose synthase from acanthamoeba polyphaga mimivirus

Analyse Crystal structure of the L780 udp-rhamnose synthase from acanthamoeba polyphaga… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7JID
Type
protein
Length
574 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Udp-L-rhamnose synthase
UniProt
Q5UPS5
Ligands
AWU, NAP
Pockets
5 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUdp-L-rhamnose synthaseprotein28742% helix, 15% strandQ5UPS5
BUdp-L-rhamnose synthaseprotein28741% helix, 15% strandQ5UPS5

Ligands and binding sites

  • AWU · [[(2~{R},3~{S},4~{R},5~{R})-5-[2,4-bis(oxidanylidene) pyrimidin-1-yl]-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] [(2~{R},3~{R},4~{R},5~{R},6~{S})-6-methyl-3,4,5-tris(oxidanyl)oxan-2-yl] hydrogen phosphate · ligand · 2 copies · chains A, B
  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 9 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16350.820.8763AWU, NAP
26390.820.8768AWU, NAP
31910.530.7834empty
41080.400.7623empty
5850.350.7519empty

Interfaces

1 interface between chains.

  • A–B · 1041 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 7JID · Crystal structure of the L780 UDP-rhamnose synthase from Acanthamoeba polyphaga mimivirus · the same entry in another collection · chain A against A, TM-score 1.00

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