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. Author manuscript; available in PMC: 2011 Sep 30.
Published in final edited form as: Nature. 2011 Mar 31;471(7340):647–650. doi: 10.1038/nature09918

Table 1.

Effect of labeled lysine and D-ornithine on MtmB pyrrolysyl-peptide ionsa

K isotopeb D-orn Observed m/zc UAG Residue Formula Assignedb m/z error (ppm)d UAG-Residue Mass (Da)e Residue Identity (mass shift Da)
C6N2 783.40802+ C12H19N3O2 0.77 237.05 O
13C6 15N2 790.92252+ 13C12H19 15N3O2 2.53 252.05 O (+15)
α–l5N 792.40312+f C12H19 15N2NO2 0.25 239.14 O (+2)
ε-15N 783.90842+ C12H19 15NN2O2 1.27 238.16 O (+1)
C6N2 + 783.40652+ C12H19N3O2 3.06 237.15 O
776.39932+ C11H17N3O2 2.19 223.12 O*
13C6 15N2 + 790.92242+ 13C12H19 15N3O2 0.12 252.19 O (+15)
780.40992+ 13C6C5H17 15N2N1O2 0.26 231.16 O* (+8)
C6N2g + 776.40252+ C11H17N3O2 1.93 223.13 O*
a

194AGRPGMGV(O or O*)202GPETSL208 from chymotryptic digestion of MtmB produced in E. coli transformed with pylTSBCD (except where indicated) and mtmB1 supplemented with the listed isotopic form of lysine in the presence and absence of D-ornithine.

b

Isotopic composition is most abundant natural isotope, unless otherwise indicated.

c

Accurate mass measured with LTQ-Orbitrap.

d

Difference between observed and theoretical m/z calculated with indicated elemental formula for UAG-encoded residue.

e

Average calculated mass (Da) using y- and b-series ions from MS/MS analysis.

f

Mox replaces M.

g

Only pylTSCD present.