Table II. Summary of proteins and phosphopeptides identified from soluble leaf extracts by 2D CN-PAGE and MS/MS analysis.
Spot Identifier and Change in pp2a-b′γa | Full Name | Gene | Score/Coverage | Phosphopeptidesb |
Defense and stress | ||||
TGG1 ↑ | Thioglucoside glucohydrolase 1 | AT5G26000 | 2,732/39% | R.GYALG(p)TDAPGR.CK.GFIFGVAS(p)SAYQVEGGR.GR.EYVGDRLPEF(p)SETEAALVK.GK.EKYE(p)TNPALYGELAK.G |
CA1 ↑ | Carbonic anhydrase1 | AT3G01500 | 1,224/27% | |
AtGSTF2 ↑ | Glutathione S-transferase F2 | AT4G02520 | 1,028/58% | |
CSD2 ↑ | Copper/zinc superoxide dismutase | AT2G28190 | 229/32% | |
Amino acid metabolism and Met cycle | ||||
OLD3 ↑ | Onset of leaf death 3/O-acetyl-Ser(thiol)lyase | AT4G14880 | 688/40% | |
SAHH1 ↑ | S-Adenosyl-l-homocysteine hydrolase 1 | AT4G13940 | 1,375/39% | R.LVGV(p)SEETTTGVK.RR.I(p)TIKPQTDR.Wc |
SAHH2 ↑ | S-Adenosyl-l-homocysteine hydrolase 2 | AT3G23810 | 265/18% | |
ADK1 ↑ | Adenosine kinase 1 | AT3G09820 | 484/39% | |
ADK2 ↑ | Adenosine kinase 2 | AT5G03300 | 482/35% | |
GS2 ↓ | Gln synthetase 2 | AT5G35630 | 694/24% | R.(p)TIEKPVEDPSELPK.W |
GS1.2 | Gln synthetase 1;2 | AT1G66200 | 143/10% | |
AtGLN1;1 ↑ | Gln synthetase 1;1 | AT5G37600 | 262/24% | |
AGT1 | Ala-glyoxylate aminotransferase | AT2G13360 | 499/25% | K.(p)TLLEDVKK.IK.L(p)SQDENHTIK.A |
Carbon metabolism | ||||
TKL ↑ | Transketolase | AT3G60750 | 902/30% | K.(p)TVTDKPTLIK.VK.(p)SIITGELPAGWEK.AK.AN(p)SYSVHGAALGEK.ER.HTPEGA(p)TLESDWSAK.F |
FBA | Fru bisphosphate aldolase | AT4G38970 | 582/30% | K.Y(p)TGEGESEEAK.ER.A(p)TPEQVAAYTLK.LK.DRA(p)TPEQVAAYTLK.LK.RLDSIGLEN(p)TEANR.Q |
MDH | Malate dehydrogenase | AT1G04410 | 774 | |
FBP | Fru-1,6-bisphosphatase | AT1G43670 | 681/46% | |
PRK ↑ | Phosphoribulokinase | AT1G32060 | 1,731/28% | K.FYGEV(p)TQQMLK.H |
IDH | Cytosolic NADP+-dependent isocitrate dehydrogenase | AT1G65930 | 711/17% | |
Other | ||||
CA2 | Carbonic anhydrase 2 | AT5G14740 | 642/50% | |
CRT1 | Calreticulin 1 | AT1G56340 | 587/33% | |
Cpn60α ↑ | Chaperonin-60α | AT2G28000 | 785/31% |
The spot identifications are as presented in Figure 4. Protein spots showing higher or lower intensity as compared with the wild type are indicated by arrows.
For identification of phosphopeptides, Mascot analysis of MS/MS spectra was conducted by restricting searches for the Arabidopsis database and allowing phosphorylation of Thr and Ser residues as possible modifications.
This peptide was detected with a score below the statistical limit for reliable identification.