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. 2017 Mar 22;7(1):33. doi: 10.3390/biom7010033

Table 3.

Molecular masses of tRNA modifications dependent on sulfur metabolism and standards.

S-Dependent Modifications
Modification Name Monoisotopic Mass (amu) Observed Molecular Ion (m/z+) Major Fragment (m/z+) Standard **
s2C 2-thiocytidine 259.063 260.071 128.028 1
s2U 2-thiouridine 260.047 261.055 129.009 * 1
s4U 4-thiouridine 260.047 261.055 129.009 * 2
s2Um 2-thio-2′-O-methyluridine 274.062 275.067 129.008 *
m5s2U/s2T 5-methyl-2-thiouridine/2-thioribothymidine 274.062 275.062 143.019 1, 2
m2A N2-methyladenosine 281.112 282.114 150.071
nm5s2U 5-methylaminomethyl-2-thiouridine 289.073 290.081 158.038
mnm5s2U 5-methylaminomethyl-2-thiouridine 303.089 304.097 172.057 *
se2U 2-selenouridine 305.992 306.999 174.956
ms2m6A 2-methylthio-N6-methyladenosine 327.100 328.108 196.065
cmnm5s2U 5-carboxymethylaminomethyl-2-thiouridine 347.079 348.082 216.047 *
mnm5se2U 5-methylaminomethyl-2-selenouridine 349.034 350.034 217.991
inm5s2U 5-(isopentenylaminomethyl)-2-thiouridine 357.136 358.144 226.101
ms2i6A 2-methylthio-N6-isopentenyladenosine 381.147 382.155 250.108 * 1
cmnm5se2U 5-carboxymethylaminomethyl-2-selenouridine 393.024 394.032 261.989
ct6A cyclic N6-threonylcarbamoyladenosine 394.124 395.128 263.089 *
ges2U 2-geranylthiouridine 396.172 397.180 265.137
ms2io6A 2-methylthio-N6-(cis-hydroxyisopentenyl) adenosine 397.142 398.150 266.107
Q queuosine 409.160 410.168 278.125
nm5ges2U 5-methylaminomethyl-2-geranylthiouridine 425.198 426.206 294.163
mnm5ges2U 5-methylaminomethyl-2-geranylthiouridine 439.214 440.222 308.179
ms2ct6A 2-methylthio-cyclic-N6-threonyl carbamoyladenosine 440.111 441.119 309.076
ms2t6A 2-methylthio-N6-threonyl carbamoyladenosine 458.112 459.130 182.049 *
ms2hn6A 2-methylthio-N6-hydroxynorvalylcarbamoyladenosine 472.138 473.146 341.103
cmnm5ges2U 5-carboxymethylaminomethyl-2-geranylthiouridine 483.204 484.212 352.169
Precursor and Related Modifications
Modification Name Monoisotopic Mass (amu) Observed Molecular Ion (m/z+) Major Fragment (m/z+) Standard **
cmnm5Um 5-carboxymethylaminomethyl-2′-O-methyluridine 345.117 346.117 200.058 *
m6A N6-methyladenosine †,‡ 281.112 282.114 150.071 * 1
mnm5U 5-methylaminomethyluridine 287.112 288.120 156.074 *
i6A N6-isopentenyladenosine 335.159 336.167 204.119 * 1
inm5U 5-(isopentenylaminomethyl) uridine 341.159 342.167 210.135
io6A N6-(cis-hydroxyisopentenyl) adenosine 351.154 352.156 220.115 *
inm5Um 5-(isopentenylaminomethyl)-2′-O-methyluridine 355.174 356.182 224.139
t6A N6-threonylcarbamoyladenosine 412.134 413.142 136.062 * 3
oQ epoxyqueuosine 425.155 426.163 294.120
hn6A N6-hydroxynorvalylcarbamoyl adenosine 426.150 427.158 295.115
Common Internal Standards
Modification Name Monoisotopic Mass (amu) Observed Molecular Ion (m/z+) Major Fragment (m/z+) Standard **
I Inosine 268.081 269.088 137.047 * 2
Ψ Pseudouridine 244.070 245.078 209.052 * 2
D Dihydrouridine 246.085 247.092 115.050 * 4, 5

* major fragment masses have been experimentally validated [151]; ** commercially available standards: 1-Carbosynth Ltd., Berkshire, United Kingdom, 2-Sigma-Aldrich, St Louis, MO, USA, 3-BioLog Life Science Institute, Bremen, Germany, 4-Advanced Technology & Industrial Co., Ltd., Hong Kong, China, 5-Dalton Pharma Services, Toronto, Canada; Also found in bacterial ribosomal RNA; Has not been found in bacterial messenger RNA, but occurs in eukaryotic mRNA.