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X-ray structure of 1-deoxy-D-xylulose 5-phosphate reductoisomerase, dxr, RV2870C, from mycobacterium tuberculosis, in complex with a 3,4- dichlorophenyl-substituted fosmidomycin analogue and manganese.

Analyse X-ray structure of 1-deoxy-D-xylulose 5-phosphate reductoisomerase, dxr… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2Y1D
Type
protein
Length
738 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
1-deoxy-D-xylulose 5-phosphate reductoisomerase
EC
1.1.1.267
UniProt
A2VLK3
Ligands
34F, MN
Pockets
7 · best druggability 0.68

Structure

x-ray diffraction · 2 distinct chains · 47% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A1-deoxy-D-xylulose 5-phosphate reductoisomerase (EC 1.1.1.267)protein35948% helix, 16% strandA2VLK3
B1-deoxy-D-xylulose 5-phosphate reductoisomerase (EC 1.1.1.267)protein37947% helix, 16% strandA2VLK3

Ligands and binding sites

  • 34F · (1S)-1-(3,4-dichlorophenyl)-3-[formyl(hydroxy)amino]propyl}phosphonic acid · ligand · chains A
  • MN · Manganese (II) ion · metal · 2 copies · chains A, B

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

Pockets

7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15390.680.7859MN
25050.660.787334F
3590.430.8214empty
41050.410.7721empty
51050.380.7518empty

Interfaces

1 interface between chains.

  • A–B · 1691 Ų buried · 39 hydrogen bonds · protein-protein

Compared structures

  • 2Y1D · X-ray structure of 1-deoxy-D-xylulose 5-phosphate reductoisomerase, DXR, Rv2870c, from… · the same entry in another collection · chain A against A, TM-score 1.00

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