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Ternary cocrystal structure of alkanesulfonate monooxygenase msud from pseudomonas fluorescens

Analyse Ternary cocrystal structure of alkanesulfonate monooxygenase msud from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7JW9
Type
protein
Length
1,512 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alkanesulfonate monooxygenase
EC
1.14.14.5
UniProt
Q3K9A1
Ligands
03S, FMN, NA
Pockets
14 · best druggability 0.87

Structure

x-ray diffraction · 1 distinct chain · 41% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DAlkanesulfonate monooxygenase (EC 1.14.14.5)protein37841% helix, 19% strandQ3K9A1

Ligands and binding sites

  • 03S · methanesulfonic acid · ligand · 4 copies · chains A, B, C, D
  • FMN · Flavin mononucleotide · ligand · 4 copies · chains A, B, C, D
  • NA · Sodium ion · metal · chains A

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

Pockets

14 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14760.870.946103S, FMN
24840.870.935703S, FMN
34300.860.945303S, FMN
44220.860.945103S, FMN
511200.810.82101empty

Interfaces

6 interfaces between chains.

  • B–C · 2478 Ų buried · 51 hydrogen bonds · protein-protein
  • A–D · 2474 Ų buried · 47 hydrogen bonds · protein-protein
  • A–B · 2020 Ų buried · 26 hydrogen bonds · protein-protein
  • C–D · 2020 Ų buried · 27 hydrogen bonds · protein-protein
  • B–D · 668 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 7JW9 · Ternary cocrystal structure of alkanesulfonate monooxygenase MsuD from Pseudomonas… · the same entry in another collection · chain A against A, TM-score 1.00

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