Jump to content

4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase

From Wikipedia, the free encyclopedia
(Redirected from HMB-PP synthase)
4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase
Identifiers
EC no.1.17.7.1
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
Search
PMCarticles
PubMedarticles
NCBIproteins

In enzymology, a 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase (HMB-PP synthase, IspG, EC 1.17.7.1) is an enzyme that catalyzes the chemical reaction

2-C-methyl-D-erythritol 2,4-cyclodiphosphate + protein-dithiol (E)-4-hydroxy-3-methylbut-2-en-1-yl diphosphate + H2O + protein-disulfide

The substrate of this enzyme is 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (MEcPP) and the product is (E)-4-hydroxy-3-methylbut-2-en-1-yl diphosphate (HMB-PP). Electrons are donated by two reduced ferredoxin proteins per reaction.

This enzyme participates in the MEP pathway (non-mevalonate pathway) of Isoprenoid precursor biosynthesis.

Nomenclature

[edit]

This enzyme belongs to the family of oxidoreductases, specifically those acting on CH or CH2 groups with a disulfide as acceptor. The systematic name of this enzyme class is (E)-4-hydroxy-3-methylbut-2-en-1-yl-diphosphate:protein-disulfide oxidoreductase (hydrating).

References

[edit]

Further reading

[edit]
  • Hecht S, Eisenreich W, Adam P, Amslinger S, Kis K, Bacher A, Arigoni D, Rohdich F (December 2001). "Studies on the nonmevalonate pathway to terpenes: the role of the GcpE (IspG) protein". Proceedings of the National Academy of Sciences of the United States of America. 98 (26): 14837–42. Bibcode:2001PNAS...9814837H. doi:10.1073/pnas.201399298. PMC 64945. PMID 11752431.