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. 2013 Dec;33(24):4872–4888. doi: 10.1128/MCB.00711-13

Table 2.

T. brucei aaRS enzyme classification, subcellular localization, and essentialitya

aaRS no. aaRS GeneDB accession no. Subclass IFA (reference) Mass spectrometry countb
Localization Growth defect (reference)d
WC MP
1 AlaRS Tb927.6.700 IIc 23 3 C/M Yes
2 ArgRS Tb927.11.1990 Ic 23 2 C/M
3 AsnRS Tb927.4.2310 IIb 10 3 C/M
4 AspRS-2 Tb927.10.1260 IIb M (26) 0 8 M Yes (26)
5 AspRS-1 Tb927.6.1880 IIb C (26 12 0 C Yes (26)
6 CysRS Tb927.6.950 Ia C 9 27 C/M
7 GlnRS Tb927.9.5210 Ic C/M (30)c 14 0 C/M Yes (30)
8 GluRS Tb927.6.4590 Ic C/M (30)c 10 8 C/M Yes (30)
9 GlyRS Tb927.11.9640 IIc C 25 13 C/M
10 HisRS Tb927.6.2060 IIa 8 0 C
11 IleRS Tb927.10.9190 Ia C/M (29) 31 70 C/M Yes (24, 29)
12 LeuRS Tb927.11.3730 Ia 28 13 C/M Yes
13 LysRS-1 Tb927.8.1600 IIb C (27) 13 4 C/M Yes (27)
14 LysRS-2 Tb927.6.1510 IIb M (27) 0 11 M Yes (27)
15 MetRS Tb927.10.1500 Ia C 22 19 C/M Yes (31)
16 PheRS-α Tb927.11.14120 IIc 8 4 C/M
17 PheRS-β Tb927.11.2360 IIc 10 13 C/M
18 ProRS Tb927.10.12890 IIa C/M 28 11 C/M Yes
19 SerRS Tb927.11.7170 IIa C 11 3 C/M Yes (28)
20 ThrRS Tb927.5.1090 IIa C 23 16 C/M Yes (Kalidas et al.)
21 TrpRS-1 Tb927.3.5580 Ib C (25) 0 0 C Yes (25)
22 TrpRS-2 Tb927.8.2240 Ib M (25) 0 39 M Yes (25, 70)
23 TyrRS Tb927.7.3620 Ib 6 2 C/M
24 ValRS Tb927.6.4480 Ia C 27 20 C/M
a

The enzyme classification is based on sequence and motif similarity (1, 2). The immunofluorescence assay (IFA) and growth defect results are reported here (Fig. 1 and 2) and elsewhere, as indicated by the citations in parentheses or as reported by S. Kalidas, I. Cestari, K. Stuart, and M. Phillips (unpublished data). Abbreviations: C, cytoplasmic localization; M, mitochondrial localization; C/M, dual localization; C/M, lower-confidence dual localization; −, not determined.

b

Total spectral counts for each aaRS identified by mass spectrometry of whole-cell (WC) or purified mitochondrial (MP) lysates. The mass spectrometry analyses were performed on procyclic forms.

c

GlnRS and GluRS were localized by Western analysis of cytosolic and mitochondrial subcellular fractions (30).

d

Growth defect data are from procyclic forms, except that data from references 24, 29, and 70 or presented in Fig. 2 are from bloodstream forms.