Journal:Acta Cryst D:S2059798324001360
From Proteopedia
(Difference between revisions)

Line 8: | Line 8: | ||
Here we focused on the characterisation of two mevalonate kinases. Mevalonate kinase enzymes phosphorylate a mevalonate compound. This step in the pathway is a key control point for some bacteria and eukaryotes, where the mevalonate kinase activity is inhibited in presence of long phosphorylated compounds, made downstream of the pathway. This is called feedback-inhibition and it is one of the many mechanisms preventing the over-production of some of the potent secondary metabolites this pathway can produce. In archaea, however, the mevalonate kinases appear totally resistant to inhibition in presence of phosphorylated compounds and the pathway is controlled using other mechanisms. | Here we focused on the characterisation of two mevalonate kinases. Mevalonate kinase enzymes phosphorylate a mevalonate compound. This step in the pathway is a key control point for some bacteria and eukaryotes, where the mevalonate kinase activity is inhibited in presence of long phosphorylated compounds, made downstream of the pathway. This is called feedback-inhibition and it is one of the many mechanisms preventing the over-production of some of the potent secondary metabolites this pathway can produce. In archaea, however, the mevalonate kinases appear totally resistant to inhibition in presence of phosphorylated compounds and the pathway is controlled using other mechanisms. | ||
- | We characterized two mevalonate kinases- one coming from a psychrophilic archaea, ''Methanococcoides burtonii'' (MKbur) and one coming from the tardigrade ''Ramazzottius varieornatus'' (MKvar). The tardigrade MKvar presents a classic feedback inhibition profile and is inhibited in presence of phosphorylated compounds such as farnesyl pyrophosphate (FPP) and geranyl pyrophosphate (GPP), whereas the MKbur is not. As expected MKbur is able to function at very low temperature as low as 4°C. The structures are resolved to 2 Å for MKvar and 2.2 Å for MKbur. | + | We characterized two mevalonate kinases- one coming from a psychrophilic archaea, ''Methanococcoides burtonii'' (MKbur) and one coming from the tardigrade ''Ramazzottius varieornatus'' (MKvar). <scene name='10/1033720/Mkvarb/1'>Cartoon representation of the monomer of MKvar (‘N-term’/‘C-term’ domains)</scene>. The tardigrade MKvar presents a classic feedback inhibition profile and is inhibited in presence of phosphorylated compounds such as farnesyl pyrophosphate (FPP) and geranyl pyrophosphate (GPP), whereas the MKbur is not. As expected MKbur is able to function at very low temperature as low as 4°C. The structures are resolved to 2 Å for MKvar and 2.2 Å for MKbur. |
<b>References</b><br> | <b>References</b><br> |
Revision as of 16:31, 6 March 2024
|
This page complements a publication in scientific journals and is one of the Proteopedia's Interactive 3D Complement pages. For aditional details please see I3DC.