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Crystal Structure of a Pantothenate Synthetase from M. tuberculosis in complex with AMPCPP and pantoate

Analyse Crystal Structure of a Pantothenate Synthetase from M. tuberculosis in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1N2E
Type
protein
Length
569 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.6
Source
Mycobacterium tuberculosis
Molecule
pantothenate synthetase
EC
6.3.2.1
UniProt
P0A5R0
Ligands
APC, PAF, MG, SO4
Pockets
4 · best druggability 0.81

Structure

x-ray diffraction · resolution 1.6 · 2 distinct chains · 43% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
Apantothenate synthetase (EC 6.3.2.1)protein28843% helix, 22% strandP0A5R0
Bpantothenate synthetase (EC 6.3.2.1)protein28143% helix, 23% strandP0A5R0

Ligands and binding sites

  • APC · Diphosphomethylphosphonic acid adenosyl ester · ligand · 2 copies · chains A, B
  • PAF · Pantoate · ligand · chains A
  • MG · Magnesium ion · metal · chains B
  • SO4 · Sulfate ion · ion · 2 copies · chains A, B
  • EOH · Ethanol · additive · 4 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15270.810.8757MG, APC, GOL
25950.810.8657APC, PAF
32710.600.7928EOH
4600.320.7614empty

Interfaces

1 interface between chains.

  • A–B · 1219 Ų buried · 24 hydrogen bonds · protein-protein

Compared structures

  • 1N2E · Crystal structure of a pantothenate synthetase from M. tuberculosis in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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