Mannose phosphate isomerase
Mannose-6 phosphate isomerase | |||||||||
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MetaCyc | metabolic pathway | ||||||||
PRIAM | profile | ||||||||
PDB structures | RCSB PDB PDBe PDBsum | ||||||||
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Mannose-6 phosphate isomerase (MPI), alternately phosphomannose isomerase (PMI) (
Mechanism
MPI must convert an aldose (mannose) to a ketose (fructose), in addition to opening and closing the rings for these sugars.[4] In humans a mechanism has been suggested which involves a hydrogen transfer between C1 and C2, mediated by Tyr278, and the movement of a proton from O1 and O2 mediated by the associated Zn2+ ion.[5] The ring opening step may be catalyzed by His99 and Asp270, and isomerization is likely a cis-enediol mechanism.[6][7]
PMI shows a high degree of selectivity for the beta anomer of M6P, and the alpha anomer has no activity, and may in fact act as an inhibitor.[8] Phosphoglucose isomerase (PGI) has a very similar function to PMI, (as it catalyzes the interconversion of glucose 6-phosphate and F6P) however PGI can anomerize alpha and beta G6P, and may also catalyze the conversion of alpha M6P to beta M6P, while PMI may not anomerize M6P.[8] It is likely the cis-enediol intermediate formed by PMI is the same intermediate formed by PGI.[9]
Structure
MPI is composed of 440 amino acid residues, with one active site and one zinc ion (Zn2+) ligand. Amino acids GLN 111A, HIS 113A, GLU 138A, HIS 285A, and HOH 798A are involved with the zinc ligand bonding.[2] Structure differs from phosphoglucose isomerase by a threonine residue (Thr291) which creates extra space in the active site of PMI to accommodate the different stereochemistry of M6P. This increased space created by the threonine allows the rotation of the C2-C3 bond, which enables the necessary cis-enediol intermediate to be formed. Because mannose and glucose are stereoisomers at C2, which is crucial to the mechanism for both enzymes, PMI must allow extra space in the active site to allow for rotation of mannose to form the cis-enediol intermediate, which is the same intermediate formed by phosphoglucose isomerase.[10]
Biological relevance
PMI has several contributions to necessary metabolic pathways. It enables cells to transform M6P into F6P, which can then be entered into Glycolysis. PMI also allows cells to convert F6P into M6P, which is a common glycolytic cellular identifier for cellular transport and cell membrane identification in prokaryotic and eukaryotic organisms.[4]
Medical relevance
PMI may be helpful in the development of new antifungal treatments, as lack of PMI activity in yeast cells can lead to cell lysis and the enzyme may be a target for inhibition.
See also
Notes
- ^ EBI Database, IPRO16305 Mannose-6-phosphate Isomerase.
- ^ a b "1pmi". PDBe.
- PMID 16131071.
- ^ a b Berg JM, Tymoczko JL, Stryer L (2007). Biochemistry (6th ed.). New York, New York: W.H. Freeman & Co.
- PMID 16488169.
- PMID 19564693.
- PMID 4973622.
- ^ PMID 4570473.
- PMID 18470986.
- S2CID 40093771.
- PMID 8612079.
- S2CID 18282235.
External links
- GeneReviews/NCBI/NIH/UW entry on Congenital Disorders of Glycosylation Overview
- Mannose-6-Phosphate+Isomerase at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- http://www.ebi.ac.uk/interpro/IEntry?ac=IPR016305