GL1X · GenesisL1 explorer

Research workbench

Crystal structure of the type-I signal peptidase from staphylococcus aureus (spsb) in complex with a substrate peptide (PEP1).

Analyse Crystal structure of the type-I signal peptidase from staphylococcus aureus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4WVH
Type
protein
Length
525 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Maltose-binding periplasmic PROTEIN,SIGNAL peptidase ib; Substrate peptide (PEP1)
EC
3.4.21.89
UniProt
P0AEY0, Q5HHB9
Ligands
GLC
Pockets
3 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMaltose-binding periplasmic PROTEIN,SIGNAL peptidase ib (EC 3.4.21.89)protein51936% helix, 25% strandP0AEY0, Q5HHB9
CSubstrate peptide (PEP1)protein60% helix, 50% strand—

Ligands and binding sites

  • GLC · alpha-D-glucopyranose · sugar · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13240.700.8335GLC
22140.490.7531empty
3910.350.7423empty

Interfaces

1 interface between chains.

  • A–C · 473 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 4WVH · Crystal structure of the Type-I signal peptidase from Staphylococcus aureus (SpsB) in… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q5HHB9 · AlphaFold monomer V2.0 prediction for signal peptidase ib (Q5HHB9) · a predicted model of the same protein · chain A against A, TM-score 0.31

Analyse

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