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. 2013 Aug 19;288(40):28913–28924. doi: 10.1074/jbc.M113.492108

TABLE 3.

Proteins significantly enriched in lysates from Aat+ cells compared with Aat cells

Cells were grown in LB to stationary phase (≤16 h). Proteins were judged to be Aat substrates if they were present in ClpS pulldowns from wild-type cells but were absent in the pulldowns from aat mutant cells. Of the 17 proteins selected by this criterion, 13 had been independently identified as Aat substrates based on N-terminal sequencing.

Protein ID Spectral count
G value p value N-terminal sequencea
Aat+ Aat
AccA 8 0 6.2 1.3 × 10−2 S2LNFLD
AccD 5 0 3 8.8 × 10−2 (L)K16ASIP
AldB 11 0 9.8 1.8 × 10−3
AtpA 11 0 9.8 1.8 × 10−3 M1QLNSTEISELIKb
AtpD 11 0 9.8 1.8 × 10−3
FhuF 6 0 3.9 4.6 × 10−2
GrpE 7 0 5 2.5 × 10−2
GyrB 12 0 11 9.2 × 10−4 (L)R394KGALDL
InfB 32 0 37 1.3 × 10−9 (L)K87KRTFV
(L)K88RTFVKR
Odo1/SucA 10 0 8.5 3.5 × 10−3 (L)R68LAKDAS
PatA (PATase) 20 0 21 4.4 × 10−6 (LLL)M1NRLPS
RecT 7 0 5 2.5 × 10−2
RsgA 9 0 7.3 6.7 × 10−3 (L)R21LKTS
Tig 25 0 28 1.5 × 10−7 (L)K46GKVP
TufA/TufB (EF-Tu) 18 0 19 1.7 × 10−5 (L)K5FERTK
YbaB 9 0 7.3 6.7 × 10−3 (L)K4GGLGNL
YggL 12 0 11 9.2 × 10−4

a N-terminal sequences were determined by Edman degradation with the exception of AtpA. The superscript indicates the position of the amino acid in the deduced open reading frame encoded by the corresponding gene. The (L) indicates a leucine residue added to the N terminus by Aat.

b N-terminal peptide for AtpA was determined by MS/MS.