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P4 protein from bacteriophage PHI12 S252A mutant in complex with ATP and mg

Analyse P4 protein from bacteriophage PHI12 S252A mutant in complex with ATP and mg in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2VHQ
Type
protein
Length
906 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NTPase P4
UniProt
Q94M05
Ligands
ATP, MG
Pockets
11 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 29% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CNTPase P4protein30229% helix, 32% strandQ94M05

Ligands and binding sites

  • ATP · Adenosine-5'-triphosphate · ligand · 3 copies · chains A, B, C
  • MG · Magnesium ion · metal · 3 copies · chains A, B, C

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

Pockets

11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18340.810.84102ATP, MG
23580.790.8953ATP, MG
36730.780.8364empty
46840.760.8266empty
53640.560.7451empty

Interfaces

2 interfaces between chains.

  • A–B · 2059 Ų buried · 27 hydrogen bonds · protein-protein
  • B–C · 2051 Ų buried · 33 hydrogen bonds · protein-protein

Compared structures

  • 2VHQ · P4 PROTEIN FROM BACTERIOPHAGE PHI12 S252A mutant in complex with ATP AND MG · the same entry in another collection · chain A against A, TM-score 1.00

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