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Structure of P. aeruginosa ATCC27853 HORMA1:HORMA2:PEPTIDE 1 complex

Analyse Structure of P. aeruginosa ATCC27853 HORMA1:HORMA2:PEPTIDE 1 complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6P8S
Type
protein
Length
603 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Horma domain containing protein; HORMA1; Peptide 1
UniProt
Q8GQ50, A0A0F6RRN7
Ligands
CL
Pockets
2 · best druggability 0.60

Structure

x-ray diffraction · 4 distinct chains · 32% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHorma domain containing proteinprotein16231% helix, 36% strandQ8GQ50
C, DHORMA1protein13238% helix, 23% strandA0A0F6RRN7
EPeptide 1protein70% helix, 57% strand—
FPeptide 1protein80% helix, 50% strand—

Ligands and binding sites

  • CL · Chloride ion · ion · 3 copies · chains A, B
  • ACT · Acetate ion · additive · 2 copies · chains A
  • 1PE · Pentaethylene glycol · additive · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11900.600.8239empty
21510.460.7737empty

Interfaces

6 interfaces between chains.

  • B–D · 1028 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 984 Ų buried · 12 hydrogen bonds · protein-protein
  • B–F · 703 Ų buried · 12 hydrogen bonds · protein-protein
  • A–E · 657 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 439 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 6P8S · Structure of P. aeruginosa ATCC27853 HORMA1:HORMA2:Peptide 1 complex · the same entry in another collection · chain A against A, TM-score 1.00

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