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MolNFT v1 · #51773 · protein

P4 protein from bacteriophage PHI12 N234G mutant in complex with ampcpp and mn

2VHC · NTPase P4: “P4 protein from bacteriophage PHI12 N234G mutant in complex with ampcpp and mn”. X-ray diffraction, 2 ligands (APC, MN), 11 pockets (best druggability 0.79). MolNFT v1 #51773 on GenesisL1: 3D structure, binding sites and…

PDB
2VHC
Type
protein
Length
864 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NTPase P4
UniProt
Q94M05
Ligands
APC, MN
Pockets
11 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 30% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CNTPase P4protein28830% helix, 31% strandQ94M05

Ligands and binding sites

  • APC · Diphosphomethylphosphonic acid adenosyl ester · ligand · 3 copies · chains A, B, C
  • MN · Manganese (II) 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, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19840.790.8197empty
26900.770.8262empty
33280.750.8737APC, MN
42510.750.8933APC, MN
52670.590.7939empty

Interfaces

2 interfaces between chains.

  • A–B · 1929 Ų buried · 26 hydrogen bonds · protein-protein
  • B–C · 1808 Ų buried · 27 hydrogen bonds · protein-protein

Compared structures

  • 2VHC · P4 PROTEIN FROM BACTERIOPHAGE PHI12 N234G mutant in complex with AMPCPP and MN · the same entry in another collection · chain A against A, TM-score 1.00

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