Queuosine

Queuosine
Names
	IUPAC name 2-Amino-5-[[[(1S,4S,5R)-4,5-dihydroxy-1-cyclopent-2-enyl]amino]methyl]-7-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-tetrahydrofuranyl]-1H-pyrrolo[3,2-e]pyrimidin-4-one
Identifiers
CAS Number	57072-36-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	38409 ;
PubChem CID	42119;
CompTox Dashboard (EPA)	DTXSID50205684 ;
	InChI InChI=1S/C17H23N5O7/c18-17-20-14-10(15(28)21-17)6(3-19-7-1-2-8(24)11(7)25)4-22(14)16-13(27)12(26)9(5-23)29-16/h1-2,4,7-9,11-13,16,19,23-27H,3,5H2,(H3,18,20,21,28)/t7-,8-,9+,11+,12+,13+,16+/m0/s1 Key: QQXQGKSPIMGUIZ-AEZJAUAXSA-N ; InChI=1/C17H23N5O7/c18-17-20-14-10(15(28)21-17)6(3-19-7-1-2-8(24)11(7)25)4-22(14)16-13(27)12(26)9(5-23)29-16/h1-2,4,7-9,11-13,16,19,23-27H,3,5H2,(H3,18,20,21,28)/t7-,8-,9+,11+,12+,13+,16+/m0/s1 Key: QQXQGKSPIMGUIZ-AEZJAUAXBO;
	SMILES C1=C[C@@H]([C@@H]([C@H]1NCC2=CN(C3=C2C(=O)N=C(N3)N)[C@H]4[C@@H]([C@@H]([C@H](O4)CO)O)O)O)O;
Properties
Chemical formula	C17H23N5O7
Molar mass	409.399 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Queuosine is a modified nucleoside that is present in certain tRNAs in bacteria and eukaryotes.[1][2] It contains the nucleobase queuine. Originally identified in E. coli, queuosine was found to occupy the first anticodon position of tRNAs for histidine, aspartic acid, asparagine and tyrosine.[3] The first anticodon position pairs with the third "wobble" position in codons, and queuosine improves accuracy of translation compared to guanosine.[4][5][6] Synthesis of queuosine begins with GTP. In bacteria, three structurally unrelated classes of riboswitch are known to regulate genes that are involved in the synthesis or transport of pre-queuosine₁, a precursor to queuosine: PreQ1-I riboswitches, PreQ1-II riboswitches and PreQ1-III riboswitches.

References

Iwata-Reuyl D (2003). "Biosynthesis of the 7-deazaguanosine hypermodified nucleosides of transfer RNA". Bioorg. Chem. 31 (1): 24–43. doi:10.1016/S0045-2068(02)00513-8. PMID 12697167.
Morris RC, Elliott MS (2001). "Queuosine modification of tRNA: a case for convergent evolution". Mol. Genet. Metab. 74 (1–2): 147–159. doi:10.1006/mgme.2001.3216. PMID 11592812.
Harada F, Nishimura S (1972). "Possible anticodon sequences of tRNA^His, tRNA^Asm, and tRNA^Asp from Escherichia coli B. Universal presence of nucleoside Q in the first position of the anticondons of these transfer ribonucleic acids". Biochemistry. 11 (2): 301–308. doi:10.1021/bi00752a024. PMID 4550561.
Bienz M, Kubli E (1981). "Wild-type tRNA^Tyr_G reads the TMV RNA stop codon, but Q base-modified tRNA^Tyr_Q does not". Nature. 294 (5837): 188–190. Bibcode:1981Natur.294..188B. doi:10.1038/294188a0. PMID 29451243.
Meier F, Suter B, Grosjean H, Keith G, Kubli E (1985). "Queuosine modification of the wobble base in tRNAHis influences 'in vivo' decoding properties". EMBO J. 4 (3): 823–827. doi:10.1002/j.1460-2075.1985.tb03704.x. PMC 554263. PMID 2988936.
Urbonavicius J, Qian Q, Durand JM, Hagervall TG, Björk GR (2001). "Improvement of reading frame maintenance is a common function for several tRNA modifications". EMBO J. 20 (17): 4863–4873. doi:10.1093/emboj/20.17.4863. PMC 125605. PMID 11532950.

Wikigenes: Queuosine
Human Metabolome Database: Queuosine (HMDB11596)
Klepper, Florian; Jahn, Eva-Maria; Hickmann, Volker; Carell, Thomas (2007). "Synthesis of the Transfer-RNA Nucleoside Queuosine by Using a Chiral Allyl Azide Intermediate". Angewandte Chemie International Edition. 46 (13): 2325–2327. doi:10.1002/anie.200604579. PMID 17310487.

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