GL1X · GenesisL1 explorer

Research workbench

Crystal structure of the pH domain of sharpin

Analyse Crystal structure of the pH domain of sharpin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4EMO
Type
protein
Length
426 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sharpin
UniProt
Q9H0F6
Pockets
4 · best druggability 0.67

Structure

x-ray diffraction · 4 distinct chains · 19% helix, 43% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASharpinprotein10419% helix, 43% strandQ9H0F6
BSharpinprotein10020% helix, 46% strandQ9H0F6
CSharpinprotein11719% helix, 41% strandQ9H0F6
DSharpinprotein10517% helix, 42% strandQ9H0F6

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13480.670.8152empty
22620.570.7842empty
31530.430.7526empty
4690.310.7416empty

Interfaces

5 interfaces between chains.

  • B–C · 929 Ų buried · 15 hydrogen bonds · protein-protein
  • A–C · 661 Ų buried · 4 hydrogen bonds · protein-protein
  • A–D · 632 Ų buried · 4 hydrogen bonds · protein-protein
  • B–D · 343 Ų buried · 7 hydrogen bonds · protein-protein
  • C–D · 127 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 9 modified (engineered).

Compared structures

  • 4EMO · Crystal structure of the PH domain of SHARPIN · the same entry in another collection · chain D against D, TM-score 1.00
  • Q9H0F6 · AlphaFold monomer V2.0 prediction for sharpin (Q9H0F6) · a predicted model of the same protein · chain A against A, TM-score 0.96

Analyse

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