Perosamine

Names
IUPAC name 4-Amino-4,6-dideoxy-D-mannose
Systematic IUPAC name (2S,3S,4R,5R)-4-Amino-2,3,5-trihydroxyhexanal
Identifiers
CAS Number	31348-80-8 Y
3D model (JSmol)	Interactive image
ChemSpider	142026 N
PubChem CID	161706
UNII	73JD8O473G Y
CompTox Dashboard (EPA)	DTXSID30185273
InChI InChI=1S/C6H13NO4/c1-3(9)5(7)6(11)4(10)2-8/h2-6,9-11H,7H2,1H3/t3-,4-,5-,6-/m1/s1 N Key: UEHGPSGGFKLPTD-KVTDHHQDSA-N N InChI=1/C6H13NO4/c1-3(9)5(7)6(11)4(10)2-8/h2-6,9-11H,7H2,1H3/t3-,4-,5-,6-/m1/s1 Key: UEHGPSGGFKLPTD-KVTDHHQDBX
SMILES C[C@H]([C@H]([C@@H]([C@@H](C=O)O)O)N)O
Properties
Chemical formula	C6H13NO4
Molar mass	163.172 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Perosamine (or GDP-perosamine) is a mannose-derived 4-aminodeoxysugar produced by some bacteria.

N-acetyl-perosamine is found in the O-antigen of Gram-negative bacteria such as Vibrio cholerae O1, E. coli O157:H7 and Caulobacter crescentus CB15.^[1] The sugar is also found in perimycin, an antibiotic produced by the Gram-positive organism Streptomyces coelicolor var. aminophilus.^[2]

Its biosynthesis from mannose-1-phosphate follows a pathway similar to that of colitose, but is different in that it is aminated and does not undergo 3-OH deoxygenation or C-5 epimerization.^[3]

GDP-perosamine synthase is a PLP-dependent enzyme that transfers a nitrogen from glutamate to the 4-keto position of GDP-4-keto-6-deoxymannose during the biosynthesis of GDP-perosamine.^[1]