Scyllo-inosamine-4-phosphate amidinotransferase

Scyllo-inosamine-4-phosphate amidinotransferase (EC 2.1.4.2) is an enzyme that catalyzes a chemical reaction in which the amino acid arginine transfers its guanidine group to a specific stereoisomer of an inositol phosphate containing an amino group, with the production of ornithine as a byproduct:[1]

Scyllo-inosamine-4-phosphate amidinotransferase
Identifiers
EC no.2.1.4.2
CAS no.52227-63-1
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
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PMCarticles
PubMedarticles
NCBIproteins
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2D representation of the chemical structure of Q27102726.
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Reversible left-right reaction arrow
 
 
 
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2D representation of the chemical structure of Q27098399.
(2)

1-amino-1-deoxy-scyllo-inositol 4-phosphate (1) is converted to 1-guanidino-1-deoxy-scyllo-inositol 4-phosphate (2). The enzyme was characterised from Streptomyces bluensis and is part of the biosynthetic pathway to streptomycin.[2]

Streptomycin

This enzyme belongs to the family of transferases that transfer one-carbon groups, specifically the amidinotransferases. The systematic name of this enzyme class is L-arginine:1-amino-1-deoxy-scyllo-inositol-4-phosphate amidinotransferase. Other names in common use include L-arginine:inosamine-P-amidinotransferase, inosamine-P amidinotransferase, L-arginine:inosamine phosphate amidinotransferase, and inosamine-phosphate amidinotransferase.[1]

Structural studies

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As of late 2007, only one structure has been solved for this class of enzymes, with the PDB accession code 1BWD.

References

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  1. 1 2 Enzyme 2.1.4.2 at KEGG Pathway Database.
  2. Walker MS, Walker JB (1966). "Enzymic studies on the biosynthesis of streptomycin, transamidation of inosamine and streptamine derivatives". J. Biol. Chem. 241 (6): 1262–1269. doi:10.1016/S0021-9258(18)96769-4. PMID 5935341.