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MolNFT v1 · #87122 · protein

Legionella pneumophila NTPDASE1 Q193E crystal form II, closed, mg amppnp complex

4BRD · Ectonucleoside triphosphate diphosphohydrolase I: “Legionella pneumophila NTPDASE1 Q193E crystal form II, closed, mg amppnp complex”. X-ray diffraction, 3 ligands (ANP, MG, CL), 8 pockets (best druggability 0.83). MolNFT v1 #87122…

PDB
4BRD
Type
protein
Length
717 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ectonucleoside triphosphate diphosphohydrolase I
EC
3.6.1.5
UniProt
Q5ZUA2
Ligands
ANP, MG, CL
Pockets
8 · best druggability 0.83

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEctonucleoside triphosphate diphosphohydrolase I (EC 3.6.1.5)protein35940% helix, 25% strandQ5ZUA2
BEctonucleoside triphosphate diphosphohydrolase I (EC 3.6.1.5)protein35840% helix, 26% strandQ5ZUA2

Ligands and binding sites

  • ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 5 copies · chains A, B
  • CL · Chloride ion · ion · 2 copies · chains A, B
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18530.830.8587MG, ANP
22430.720.8739ANP, MG
31910.550.7931MES, CL
42080.530.7826MES
5910.470.8121empty

Interfaces

1 interface between chains.

  • A–B · 1536 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 4BRD · Legionella pneumophila NTPDase1 Q193E crystal form II, closed, Mg AMPPNP complex · the same entry in another collection · chain A against A, TM-score 1.00

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