EC Number |
Recommended Name |
Source Tissue |
Reference |
---|
6.3.4.10 | biotin-[propionyl-CoA-carboxylase (ATP-hydrolysing)] ligase |
leaf |
- |
1396 |
6.3.4.13 | phosphoribosylamine-glycine ligase |
leaf |
- |
1416 |
6.3.4.14 | biotin carboxylase |
leaf |
- |
1436, 716633 |
6.3.4.14 | biotin carboxylase |
leaf |
developing, 7 days old |
654339 |
6.3.4.3 | formate-tetrahydrofolate ligase |
leaf |
- |
1506, 1519, 1520 |
6.3.5.1 | NAD+ synthase (glutamine-hydrolysing) |
leaf |
wild-type Nicotiana sylvestris and the CMSII mutant that lacks respiratory complex I show different NADS mRNA expression pattern |
716646 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
- |
662720, 663157, 676655, 716548, 716577, 745003, 745465 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
expression of HvAS1, higher mRNA levels in younger leaves than in older leaves, induced by dark treatment, induction seems to require a dramatic change in the C/N ratio since no diurnal variation is observed and up-regulation of transcription only occurs after 10 h of darkness |
650394 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
expression of HvAS2 |
650394 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
first leaves, etiolated |
651553 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
high content of AS in leaf sheath at the second position from the fully expanded top leaf, the contents gradually decreases in leaf sheaths as a function of increasing age, in vascular tissues |
653466 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
of seedlings |
1703 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
OsAS2 mRNA is abundant in leaf blades and sheathes of rice |
746041 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
primary leaves |
1716 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
rosette leaves, of 35-day-old plants |
-, 743980 |
6.3.5.4 | asparagine synthase (glutamine-hydrolysing) |
leaf |
upregulation in leaves infected by the bacterial pathogen Pseudomonas syringae, high activity in phloem cells of the main vascular bundles and in secondary veins of the leaf blade |
663070 |
6.3.5.5 | carbamoyl-phosphate synthase (glutamine-hydrolysing) |
leaf |
- |
697908 |
6.4.1.2 | acetyl-CoA carboxylase |
leaf |
- |
37572, 37576, 37596, 37598, 37608, 37610, 37621, 666355, 676199, 694556, 716773 |
6.4.1.2 | acetyl-CoA carboxylase |
leaf |
2 isoforms: non-mesophyll chloroplast form and mesophyll chloroplast form |
37629 |
6.4.1.2 | acetyl-CoA carboxylase |
leaf |
young |
665262 |
6.4.1.3 | propionyl-CoA carboxylase |
leaf |
- |
1875 |
6.4.1.4 | methylcrotonoyl-CoA carboxylase |
leaf |
- |
1894, 1895, 1896 |
6.6.1.1 | magnesium chelatase |
leaf |
- |
644269, 644273, 661635, 716044, 716515, 716531, 747003, 747893, 748471, 748487, 749008 |
6.6.1.1 | magnesium chelatase |
leaf |
4-week-old |
644259 |
6.6.1.1 | magnesium chelatase |
leaf |
6-day-old |
644263 |
6.6.1.1 | magnesium chelatase |
leaf |
generation of transgenic tobacco lines with RNAi silenced expression of the glutamate 1-semialdehyde aminotransferase (GSA) gene does not cause a decrease in the transcript levels after inactivation of HEMA and GSA-expression. Enzyme activity for Mg chelatase is lower in parallel to the loss of chlorophyll and heme content |
676559 |
7.1.1.6 | plastoquinol-plastocyanin reductase |
leaf |
- |
395289, 395292, 395293, 395294, 395295, 395296, 395297, 395298, 395299, 395300, 395301, 395302, 395305, 395307, 395308, 395311, 395312, 395313, 395314, 395316, 676461, 676619, 712948 |
7.1.1.6 | plastoquinol-plastocyanin reductase |
leaf |
efficient cytochrome b6f complex biogenesis occurs only in young leaves. The capacity for de novo synthesis of the complex is very low in mature and aging leaves. Ontogenetic down-regulation of cytochrome b6f complex biogenesis occurs at the post-transcriptional level |
687683 |
7.1.1.8 | quinol-cytochrome-c reductase |
leaf |
- |
724452 |
7.1.1.9 | cytochrome-c oxidase |
leaf |
expression in leaves is only observed when cuts are produced, suggesting an induction by wounding |
694694 |
7.1.2.1 | P-type H+-exporting transporter |
leaf |
- |
718783, 720320, 734941, 747045, 747159, 748771, 748981 |
7.1.2.1 | P-type H+-exporting transporter |
leaf |
plasma membrane H+-ATPase transcript and protein level and activity related to unit surface area of plasma membrane are more than twice as high in growing compared with non-growing leaf tissue |
734852 |
7.1.2.1 | P-type H+-exporting transporter |
leaf |
two plasma membrane H+-ATPase genes are differentially expressed in iron-deficient cucumber plants. CsHA2 transcript is detected both in roots and leaves and is unaffected by Fe |
670608 |
7.1.2.2 | H+-transporting two-sector ATPase |
leaf |
- |
673361, 688635, 688653, 689637, 699765, 712374, 748478, 749414 |
7.1.2.2 | H+-transporting two-sector ATPase |
leaf |
young |
696385 |
7.1.3.1 | H+-exporting diphosphatase |
leaf |
- |
209832, 670567, 720685, 734385, 748775, 748997, 749407 |
7.2.2.10 | P-type Ca2+ transporter |
leaf |
- |
700805, 720773, 751803 |
7.2.2.10 | P-type Ca2+ transporter |
leaf |
low expression |
751094 |
7.2.2.12 | P-type Zn2+ transporter |
leaf |
- |
656971 |
7.2.2.12 | P-type Zn2+ transporter |
leaf |
rosette leaves and cauline leaves |
700757 |
7.2.2.14 | P-type Mg2+ transporter |
leaf |
vascular tissue |
697187 |
7.2.2.2 | ABC-type Cd2+ transporter |
leaf |
high expression level |
700809 |
7.2.2.21 | Cd2+-exporting ATPase |
leaf |
- |
655581 |
7.2.2.21 | Cd2+-exporting ATPase |
leaf |
high expression level |
754916 |
7.2.2.9 | P-type Cu2+ transporter |
leaf |
- |
688693 |
7.3.2.1 | ABC-type phosphate transporter |
leaf |
- |
-, 719540, 720506, 720741, 720826, 734020, 734879, 748950 |
7.3.2.1 | ABC-type phosphate transporter |
leaf |
high expression in mature leaves, lower expression in senescent leaves |
698749 |
7.3.2.1 | ABC-type phosphate transporter |
leaf |
of mycorrhiza plants and non-mycorrhiza plants |
689445 |
7.3.2.1 | ABC-type phosphate transporter |
leaf |
senescent |
670533 |
7.3.2.1 | ABC-type phosphate transporter |
leaf |
young |
720750 |
7.3.2.4 | ABC-type nitrate transporter |
leaf |
- |
713272 |
7.3.2.4 | ABC-type nitrate transporter |
leaf |
mature leaves |
734917 |
7.3.2.4 | ABC-type nitrate transporter |
leaf |
NRT1.4 and NRT1.7, the latter is expressed in the phloem of minor veins in older leaves |
721094 |
7.3.2.4 | ABC-type nitrate transporter |
leaf |
NRT1.7 is expressed in the phloem of the leaf minor vein. NRT1.7 is predominantly expressed in old leaves |
713270 |
7.3.2.5 | ABC-type molybdate transporter |
leaf |
- |
700871 |
7.4.2.1 | ABC-type polar-amino-acid transporter |
leaf |
up-regulation very early during rust development |
676106 |
7.4.2.10 | ABC-type glutathione transporter |
leaf |
- |
751856 |
7.4.2.4 | chloroplast protein-transporting ATPase |
leaf |
- |
733398, 734384 |
7.4.2.4 | chloroplast protein-transporting ATPase |
leaf |
first foliage leaf in seedlings |
700715 |
7.6.2.1 | P-type phospholipid transporter |
leaf |
- |
696218, 748976 |