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Legionella pneumophila NTPDASE1 crystal form II (closed) in complex with mg umppnp

Analyse Legionella pneumophila NTPDASE1 crystal form II (closed) in complex with mg… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4BRI
Type
protein
Length
716 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
UNP, MG, CL
Pockets
9 · best druggability 0.85

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)protein35739% helix, 25% strandQ5ZUA2

Ligands and binding sites

  • UNP · 5'-O-[(R)-hydroxy{[(s)-hydroxy(phosphonoamino) phosphoryl]oxy}phosphoryl]uridine · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 2 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

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111350.850.86115UNP, MG
21920.550.7926MES, CL
32120.530.7829MES
41000.480.8021empty
5670.450.8218empty

Interfaces

1 interface between chains.

  • A–B · 1520 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide (disulfide).

Compared structures

  • 4BRI · Legionella pneumophila NTPDase1 crystal form II (closed) in complex with MG UMPPNP · the same entry in another collection · chain A against A, TM-score 1.00

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