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Synechococcus Olefin Synthase FAAL domain in complex with AMP and pyrophosphate

Analyse Synechococcus Olefin Synthase FAAL domain in complex with AMP and pyrophosphate in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7R7E
Type
protein
Length
1,134 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.99
Source
Synechococcus sp. PCC 7002
Molecule
Polyketide synthase
EC
6.2.1.20
UniProt
B1XKC6
Ligands
AMP, POP, MG
Pockets
8 · best druggability 0.86

Structure

x-ray diffraction · resolution 1.99 · 1 distinct chain · 35% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPolyketide synthase (EC 6.2.1.20)protein56735% helix, 28% strandB1XKC6

Ligands and binding sites

  • AMP · Adenosine monophosphate · ligand · 2 copies · chains A, B
  • POP · Pyrophosphate 2- · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 2 copies · chains A, B
  • ACT · Acetate ion · additive · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110860.860.87113AMP, POP, MG
211550.850.86115AMP, POP, MG
38310.700.7659ACT
41970.580.8127empty
51720.510.7829empty

Interfaces

1 interface between chains.

  • A–B · 635 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 7R7E · Synechococcus olefin synthase faal domain in complex with AMP and pyrophosphate · the same entry in another collection · chain A against A, TM-score 1.00

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