GL1X · GenesisL1 explorer

Research workbench

Mutant S147M structure of PH0725 from pyrococcus horikoshii OT3

Analyse Mutant S147M structure of PH0725 from pyrococcus horikoshii OT3 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2ED5
Type
protein
Length
530 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Diphthine synthase
EC
2.1.1.98
UniProt
O58456
Ligands
SAH, NA
Pockets
7 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BDiphthine synthase (EC 2.1.1.98)protein26537% helix, 23% strandO58456

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · chains A
  • NA · Sodium ion · metal · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains B

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

Pockets

7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14640.740.8346empty
24410.740.8355SAH
31370.410.7419empty
41020.400.7616empty
5920.380.7616empty

Interfaces

1 interface between chains.

  • A–B · 2520 Ų buried · 31 hydrogen bonds · protein-protein

Compared structures

  • 2ED5 · Mutant S147M structure of PH0725 from Pyrococcus horikoshii OT3 · the same entry in another collection · chain A against A, TM-score 1.00
  • O58456 · AlphaFold monomer V2.0 prediction for diphthine synthase (O58456) · a predicted model of the same protein · chain B against A, TM-score 0.99

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.