Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 1.14.13.231 extracted from

  • Volkers, G.; Damas, J.M.; Palm, G.J.; Panjikar, S.; Soares, C.M.; Hinrichs, W.
    Putative dioxygen-binding sites and recognition of tigecycline and minocycline in the tetracycline-degrading monooxygenase TetX (2013), Acta Crystallogr. Sect. D, 69, 1758-1767.
    View publication on PubMed

Crystallization (Commentary)

Crystallization (Comment) Organism
in complex with tetracyclines minocycline and tigecycline at 2.18 and 2.30 A resolution, respectively. Both tetracyclines bind in a large tunnel-shaped active site in close contact to the cofactor FAD, preoriented for regioselective hydroxylation to 11alpha-hydroxytetracyclines. The bulky 9-tert-butylglycylamido substituent of tigecycline is solvent-exposed and does not interfere with TetX binding. In the TetX-minocycline complex a second binding site for a minocycline dimer is observed close to the active-site entrance. The putative dioxygen-binding cavities are located in the substrate-binding domain next to the active site Bacteroides thetaiotaomicron

Organism

Organism UniProt Comment Textmining
Bacteroides thetaiotaomicron Q93L51
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
minocycline + NADPH + H+ + O2
-
Bacteroides thetaiotaomicron 11a-hydroxyminocycline + NADP+ + H2O
-
?
tigecycline + NADPH + H+ + O2
-
Bacteroides thetaiotaomicron 11a-hydroxytigecycline + NADP+ + H2O
-
?

Synonyms

Synonyms Comment Organism
TetX family tetracycline inactivation enzyme
-
Bacteroides thetaiotaomicron
TetX2
-
Bacteroides thetaiotaomicron

Cofactor

Cofactor Comment Organism Structure
FAD
-
Bacteroides thetaiotaomicron