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1.9A crystal structure of the protein isdg from staphylococcus aureus aureus, structural genomics, mcsg

Analyse 1.9A crystal structure of the protein isdg from staphylococcus aureus aureus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1XBW
Type
protein
Length
383 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hypothetical protein isdg
UniProt
Q8NX62
Pockets
5 · best druggability 0.71

Structure

x-ray diffraction · 4 distinct chains · 21% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHypothetical protein isdgprotein9926% helix, 45% strandQ8NX62
BHypothetical protein isdgprotein9616% helix, 47% strandQ8NX62
CHypothetical protein isdgprotein9017% helix, 50% strandQ8NX62
DHypothetical protein isdgprotein9824% helix, 45% strandQ8NX62

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17580.710.7769empty
21950.660.8529empty
31210.650.8820empty
41050.410.7616empty
5790.360.7514empty

Interfaces

6 interfaces between chains.

  • A–B · 1598 Ų buried · 30 hydrogen bonds · protein-protein
  • C–D · 1567 Ų buried · 23 hydrogen bonds · protein-protein
  • A–C · 244 Ų buried · 1 hydrogen bond · protein-protein
  • B–C · 111 Ų buried · 0 hydrogen bonds · protein-protein
  • B–D · 64 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 1XBW · 1.9A Crystal Structure of the protein isdG from Staphylococcus aureus aureus, Structural… · the same entry in another collection · chain D against D, TM-score 1.00
  • Q8NX62 · AlphaFold monomer V2.0 prediction for heme oxygenase (staphylobilin- producing) 1 (Q8NX62) · a predicted model of the same protein · chain D against A, TM-score 0.97

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