|
CH_car_1 |
4.96411e-31 |
19 |
Ca_LG6_v3 |
GO:0009733 |
BP |
response to auxin |
|
CH_car_10 |
0.000000000296984 |
4 |
Ca_LG5_v3 |
GO:0008115 |
MF |
sarcosine oxidase activity |
|
CH_car_100 |
0.0000706032 |
3 |
Ca_LG8_v3 |
GO:0015934 |
CC |
large ribosomal subunit |
|
CH_car_101 |
0.0000720575 |
4 |
Ca_LG7_v3 |
GO:0045787 |
BP |
positive regulation of cell cycle |
|
CH_car_102 |
0.0000734603 |
3 |
Ca_LG3_v3 |
GO:0033506 |
BP |
glucosinolate biosynthetic process from homomethionine |
|
CH_car_103 |
0.0000750787 |
24 |
Ca_LG7_v3 |
GO:0005515 |
MF |
protein binding |
|
CH_car_104 |
0.0000766549 |
3 |
Ca_LG6_v3 |
GO:0000145 |
CC |
exocyst |
|
CH_car_105 |
0.0000778301 |
2 |
Ca_LG5_v3 |
GO:0052669 |
MF |
CTP:2-trans,-6-trans-farnesol kinase activity |
|
CH_car_106 |
0.0000778301 |
2 |
Ca_LG7_v3 |
GO:0070179 |
BP |
D-serine biosynthetic process |
|
CH_car_107 |
0.0000778301 |
2 |
Ca_LG1_v3 |
GO:0033234 |
BP |
negative regulation of protein sumoylation |
|
CH_car_108 |
0.0000778301 |
2 |
Ca_LG8_v3 |
GO:1901811 |
BP |
beta-carotene catabolic process |
|
CH_car_109 |
0.0000778301 |
2 |
Ca_LG2_v3 |
GO:0042906 |
BP |
xanthine transport |
|
CH_car_11 |
0.000000000392592 |
7 |
Ca_LG7_v3 |
GO:0043086 |
BP |
negative regulation of catalytic activity |
|
CH_car_110 |
0.0000778301 |
2 |
Ca_LG5_v3 |
GO:0003721 |
MF |
telomerase RNA reverse transcriptase activity |
|
CH_car_111 |
0.0000778301 |
2 |
Ca_LG2_v3 |
GO:0008108 |
MF |
UDP-glucose:hexose-1-phosphate uridylyltransferase activity |
|
CH_car_112 |
0.0000778301 |
2 |
Ca_LG6_v3 |
GO:0004198 |
MF |
calcium-dependent cysteine-type endopeptidase activity |
|
CH_car_113 |
0.0000778301 |
2 |
Ca_LG1_v3 |
GO:0005245 |
MF |
voltage-gated calcium channel activity |
|
CH_car_114 |
0.0000778301 |
2 |
Ca_LG1_v3 |
GO:0010241 |
BP |
ent-kaurene oxidation to kaurenoic acid |
|
CH_car_115 |
0.0000778301 |
2 |
Ca_LG6_v3 |
GO:0042306 |
BP |
regulation of protein import into nucleus |
|
CH_car_116 |
0.0000778301 |
2 |
Ca_LG1_v3 |
GO:0046865 |
BP |
terpenoid transport |
|
CH_car_117 |
0.0000778301 |
2 |
Ca_LG1_v3 |
GO:0003864 |
MF |
3-methyl-2-oxobutanoate hydroxymethyltransferase activity |
|
CH_car_118 |
0.0000778301 |
2 |
Ca_LG3_v3 |
GO:0004363 |
MF |
glutathione synthase activity |
|
CH_car_119 |
0.0000778301 |
2 |
Ca_LG6_v3 |
GO:0080184 |
BP |
response to phenylpropanoid |
|
CH_car_12 |
0.00000000101104 |
4 |
Ca_LG6_v3 |
GO:0004573 |
MF |
mannosyl-oligosaccharide glucosidase activity |
|
CH_car_120 |
0.0000778301 |
2 |
Ca_LG4_v3 |
GO:0045430 |
MF |
chalcone isomerase activity |
|
CH_car_121 |
0.0000778301 |
2 |
Ca_LG3_v3 |
GO:0090353 |
MF |
polygalacturonase inhibitor activity |
|
CH_car_122 |
0.0000778301 |
2 |
Ca_LG6_v3 |
GO:0046202 |
BP |
cyanide biosynthetic process |
|
CH_car_123 |
0.0000778301 |
2 |
Ca_LG4_v3 |
GO:0003796 |
MF |
lysozyme activity |
|
CH_car_124 |
0.0000889533 |
4 |
Ca_LG5_v3 |
GO:0072348 |
BP |
sulfur compound transport |
|
CH_car_125 |
0.000104156 |
3 |
Ca_LG8_v3 |
GO:0016629 |
MF |
12-oxophytodienoate reductase activity |
|
CH_car_126 |
0.000104162 |
4 |
Ca_LG7_v3 |
GO:0008643 |
BP |
carbohydrate transport |
|
CH_car_127 |
0.000107958 |
4 |
Ca_LG3_v3 |
GO:0012501 |
BP |
programmed cell death |
|
CH_car_128 |
0.000128939 |
3 |
Ca_LG4_v3 |
GO:0015299 |
MF |
solute:proton antiporter activity |
|
CH_car_129 |
0.000137935 |
3 |
Ca_LG1_v3 |
GO:0048544 |
BP |
recognition of pollen |
|
CH_car_13 |
0.00000000127709 |
6 |
Ca_LG4_v3 |
GO:0016796 |
MF |
exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters |
|
CH_car_130 |
0.00014448 |
3 |
Ca_LG3_v3 |
GO:0003872 |
MF |
6-phosphofructokinase activity |
|
CH_car_131 |
0.000148354 |
4 |
Ca_LG7_v3 |
GO:0015926 |
MF |
glucosidase activity |
|
CH_car_132 |
0.000163145 |
19 |
Ca_LG4_v3 |
GO:0034641 |
BP |
cellular nitrogen compound metabolic process |
|
CH_car_133 |
0.000174684 |
6 |
Ca_LG5_v3 |
GO:0060918 |
BP |
auxin transport |
|
CH_car_134 |
0.000175199 |
4 |
Ca_LG3_v3 |
GO:0016747 |
MF |
acyltransferase activity, transferring groups other than amino-acyl groups |
|
CH_car_135 |
0.000188456 |
28 |
Ca_LG4_v3 |
GO:0005515 |
MF |
protein binding |
|
CH_car_136 |
0.000189686 |
5 |
Ca_LG2_v3 |
GO:0016887 |
MF |
ATP hydrolysis activity |
|
CH_car_137 |
0.000199778 |
5 |
Ca_LG2_v3 |
GO:0045087 |
BP |
innate immune response |
|
CH_car_138 |
0.000233481 |
2 |
Ca_LG6_v3 |
GO:0070888 |
MF |
E-box binding |
|
CH_car_139 |
0.000233481 |
2 |
Ca_LG2_v3 |
GO:0018479 |
MF |
benzaldehyde dehydrogenase (NAD+) activity |
|
CH_car_14 |
0.00000000261874 |
7 |
Ca_LG6_v3 |
GO:0004553 |
MF |
hydrolase activity, hydrolyzing O-glycosyl compounds |
|
CH_car_140 |
0.000233481 |
2 |
Ca_LG4_v3 |
GO:0006424 |
BP |
glutamyl-tRNA aminoacylation |
|
CH_car_141 |
0.000233481 |
2 |
Ca_LG5_v3 |
GO:0004071 |
MF |
aspartate-ammonia ligase activity |
|
CH_car_142 |
0.000233481 |
2 |
Ca_LG4_v3 |
GO:0010309 |
MF |
acireductone dioxygenase [iron(II)-requiring] activity |
|
CH_car_143 |
0.000233481 |
2 |
Ca_LG6_v3 |
GO:0051745 |
MF |
4-hydroxy-3-methylbut-2-en-1-yl diphosphate reductase activity |
|
CH_car_144 |
0.000233481 |
2 |
Ca_LG7_v3 |
GO:0033214 |
BP |
siderophore-dependent iron import into cell |
|
CH_car_145 |
0.00023349 |
2 |
Ca_LG5_v3 |
GO:0002943 |
BP |
tRNA dihydrouridine synthesis |
|
CH_car_146 |
0.00023349 |
2 |
Ca_LG6_v3 |
GO:0071076 |
BP |
RNA 3' uridylation |
|
CH_car_147 |
0.00023349 |
2 |
Ca_LG1_v3 |
GO:0015864 |
BP |
pyrimidine nucleoside transport |
|
CH_car_148 |
0.00023349 |
2 |
Ca_LG7_v3 |
GO:0033730 |
MF |
arogenate dehydrogenase (NADP+) activity |
|
CH_car_149 |
0.00023349 |
2 |
Ca_LG2_v3 |
GO:0050403 |
MF |
trans-zeatin O-beta-D-glucosyltransferase activity |
|
CH_car_15 |
0.00000000333155 |
5 |
Ca_LG1_v3 |
GO:0042744 |
BP |
hydrogen peroxide catabolic process |
|
CH_car_150 |
0.00023349 |
2 |
Ca_LG2_v3 |
GO:0080045 |
MF |
quercetin 3'-O-glucosyltransferase activity |
|
CH_car_151 |
0.00023349 |
2 |
Ca_LG5_v3 |
GO:0005464 |
MF |
UDP-xylose transmembrane transporter activity |
|
CH_car_152 |
0.00023349 |
2 |
Ca_LG6_v3 |
GO:0030071 |
BP |
regulation of mitotic metaphase/anaphase transition |
|
CH_car_153 |
0.00023349 |
2 |
Ca_LG7_v3 |
GO:0007043 |
BP |
cell-cell junction assembly |
|
CH_car_154 |
0.00023349 |
2 |
Ca_LG5_v3 |
GO:0035671 |
MF |
enone reductase activity |
|
CH_car_155 |
0.00023349 |
2 |
Ca_LG6_v3 |
GO:0050062 |
MF |
long-chain-fatty-acyl-CoA reductase activity |
|
CH_car_156 |
0.00023349 |
2 |
Ca_LG2_v3 |
GO:0004046 |
MF |
aminoacylase activity |
|
CH_car_157 |
0.00023349 |
2 |
Ca_LG6_v3 |
GO:0010365 |
BP |
positive regulation of ethylene biosynthetic process |
|
CH_car_158 |
0.00023349 |
2 |
Ca_LG7_v3 |
GO:0090158 |
BP |
endoplasmic reticulum membrane organization |
|
CH_car_159 |
0.00023349 |
2 |
Ca_LG4_v3 |
GO:0015671 |
BP |
oxygen transport |
|
CH_car_16 |
0.00000000379475 |
5 |
Ca_LG5_v3 |
GO:0000981 |
MF |
DNA-binding transcription factor activity, RNA polymerase II-specific |
|
CH_car_160 |
0.00023349 |
2 |
Ca_LG3_v3 |
GO:0000126 |
CC |
transcription factor TFIIIB complex |
|
CH_car_161 |
0.00023349 |
2 |
Ca_LG8_v3 |
GO:0030123 |
CC |
AP-3 adaptor complex |
|
CH_car_162 |
0.00023349 |
2 |
Ca_LG6_v3 |
GO:0030845 |
BP |
phospholipase C-inhibiting G protein-coupled receptor signaling pathway |
|
CH_car_163 |
0.00023349 |
2 |
Ca_LG2_v3 |
GO:0010442 |
BP |
guard cell morphogenesis |
|
CH_car_164 |
0.00023349 |
2 |
Ca_LG1_v3 |
GO:0005542 |
MF |
folic acid binding |
|
CH_car_165 |
0.00023349 |
2 |
Ca_LG4_v3 |
GO:0000974 |
CC |
Prp19 complex |
|
CH_car_166 |
0.000255115 |
4 |
Ca_LG3_v3 |
GO:0008194 |
MF |
UDP-glycosyltransferase activity |
|
CH_car_167 |
0.000295398 |
3 |
Ca_LG4_v3 |
GO:0044093 |
BP |
positive regulation of molecular function |
|
CH_car_168 |
0.000301836 |
10 |
Ca_LG6_v3 |
GO:0051179 |
BP |
localization |
|
CH_car_169 |
0.00031137 |
23 |
Ca_LG3_v3 |
GO:0050789 |
BP |
regulation of biological process |
|
CH_car_17 |
0.0000000057868 |
5 |
Ca_LG8_v3 |
GO:0000250 |
MF |
lanosterol synthase activity |
|
CH_car_170 |
0.000312374 |
5 |
Ca_LG3_v3 |
GO:0004857 |
MF |
enzyme inhibitor activity |
|
CH_car_171 |
0.000331809 |
3 |
Ca_LG5_v3 |
GO:0006913 |
BP |
nucleocytoplasmic transport |
|
CH_car_172 |
0.000343657 |
3 |
Ca_LG3_v3 |
GO:0051607 |
BP |
defense response to virus |
|
CH_car_173 |
0.000350149 |
8 |
Ca_LG2_v3 |
GO:0016788 |
MF |
hydrolase activity, acting on ester bonds |
|
CH_car_174 |
0.000358702 |
3 |
Ca_LG3_v3 |
GO:0008408 |
MF |
3'-5' exonuclease activity |
|
CH_car_175 |
0.000382131 |
18 |
Ca_LG7_v3 |
GO:0043231 |
CC |
intracellular membrane-bounded organelle |
|
CH_car_176 |
0.000407745 |
3 |
Ca_LG8_v3 |
GO:0003953 |
MF |
NAD+ nucleosidase activity |
|
CH_car_177 |
0.000439117 |
7 |
Ca_LG6_v3 |
GO:2001141 |
BP |
regulation of RNA biosynthetic process |
|
CH_car_178 |
0.000466944 |
2 |
Ca_LG1_v3 |
GO:0004865 |
MF |
protein serine/threonine phosphatase inhibitor activity |
|
CH_car_179 |
0.000466944 |
2 |
Ca_LG4_v3 |
GO:0009974 |
MF |
zeinoxanthin epsilon hydroxylase activity |
|
CH_car_18 |
0.0000000103473 |
4 |
Ca_LG7_v3 |
GO:0016762 |
MF |
xyloglucan:xyloglucosyl transferase activity |
|
CH_car_180 |
0.000466944 |
2 |
Ca_LG2_v3 |
GO:0004157 |
MF |
dihydropyrimidinase activity |
|
CH_car_181 |
0.000466944 |
2 |
Ca_LG2_v3 |
GO:0090730 |
CC |
Las1 complex |
|
CH_car_182 |
0.000466944 |
2 |
Ca_LG5_v3 |
GO:0010234 |
BP |
anther wall tapetum cell fate specification |
|
CH_car_183 |
0.000466981 |
2 |
Ca_LG1_v3 |
GO:0008107 |
MF |
galactoside 2-alpha-L-fucosyltransferase activity |
|
CH_car_184 |
0.000466981 |
2 |
Ca_LG6_v3 |
GO:0008891 |
MF |
glycolate oxidase activity |
|
CH_car_185 |
0.000466981 |
2 |
Ca_LG4_v3 |
GO:0015185 |
MF |
gamma-aminobutyric acid transmembrane transporter activity |
|
CH_car_186 |
0.000466981 |
2 |
Ca_LG8_v3 |
GO:0055122 |
BP |
response to very low light intensity stimulus |
|
CH_car_187 |
0.000466981 |
2 |
Ca_LG5_v3 |
GO:0031314 |
CC |
extrinsic component of mitochondrial inner membrane |
|
CH_car_188 |
0.000480779 |
3 |
Ca_LG3_v3 |
GO:0097573 |
MF |
glutathione oxidoreductase activity |
|
CH_car_189 |
0.000494861 |
3 |
Ca_LG6_v3 |
GO:0009838 |
BP |
abscission |
|
CH_car_19 |
0.0000000207241 |
5 |
Ca_LG1_v3 |
GO:0140359 |
MF |
ABC-type transporter activity |
|
CH_car_190 |
0.000519347 |
3 |
Ca_LG4_v3 |
GO:0001558 |
BP |
regulation of cell growth |
|
CH_car_191 |
0.000542719 |
3 |
Ca_LG3_v3 |
GO:0002229 |
BP |
defense response to oomycetes |
|
CH_car_192 |
0.000545263 |
13 |
Ca_LG6_v3 |
GO:0005524 |
MF |
ATP binding |
|
CH_car_193 |
0.000551027 |
3 |
Ca_LG6_v3 |
GO:0048544 |
BP |
recognition of pollen |
|
CH_car_194 |
0.000565153 |
3 |
Ca_LG4_v3 |
GO:0030599 |
MF |
pectinesterase activity |
|
CH_car_195 |
0.000565153 |
3 |
Ca_LG3_v3 |
GO:0030599 |
MF |
pectinesterase activity |
|
CH_car_196 |
0.000587595 |
3 |
Ca_LG5_v3 |
GO:0015690 |
BP |
aluminum cation transport |
|
CH_car_197 |
0.000593564 |
3 |
Ca_LG3_v3 |
GO:0010584 |
BP |
pollen exine formation |
|
CH_car_198 |
0.000621055 |
3 |
Ca_LG7_v3 |
GO:0003954 |
MF |
NADH dehydrogenase activity |
|
CH_car_199 |
0.000700425 |
2 |
Ca_LG1_v3 |
GO:0006101 |
BP |
citrate metabolic process |
|
CH_car_2 |
1.49998e-17 |
9 |
Ca_LG2_v3 |
GO:0000145 |
CC |
exocyst |
|
CH_car_20 |
0.0000000207754 |
6 |
Ca_LG1_v3 |
GO:0003690 |
MF |
double-stranded DNA binding |
|
CH_car_200 |
0.000700425 |
2 |
Ca_LG6_v3 |
GO:0001561 |
BP |
fatty acid alpha-oxidation |
|
CH_car_201 |
0.000700425 |
2 |
Ca_LG5_v3 |
GO:0043486 |
BP |
histone exchange |
|
CH_car_202 |
0.000700425 |
2 |
Ca_LG2_v3 |
GO:0051754 |
BP |
meiotic sister chromatid cohesion, centromeric |
|
CH_car_203 |
0.000700425 |
2 |
Ca_LG3_v3 |
GO:0048283 |
BP |
indeterminate inflorescence morphogenesis |
|
CH_car_204 |
0.000704576 |
3 |
Ca_LG3_v3 |
GO:0004185 |
MF |
serine-type carboxypeptidase activity |
|
CH_car_205 |
0.000764924 |
3 |
Ca_LG2_v3 |
GO:0008171 |
MF |
O-methyltransferase activity |
|
CH_car_206 |
0.00077821 |
2 |
Ca_LG4_v3 |
GO:0046522 |
MF |
S-methyl-5-thioribose kinase activity |
|
CH_car_207 |
0.00077821 |
2 |
Ca_LG6_v3 |
GO:1900064 |
BP |
positive regulation of peroxisome organization |
|
CH_car_208 |
0.000778301 |
2 |
Ca_LG4_v3 |
GO:0000179 |
MF |
rRNA (adenine-N6,N6-)-dimethyltransferase activity |
|
CH_car_209 |
0.000778301 |
2 |
Ca_LG4_v3 |
GO:0008843 |
MF |
endochitinase activity |
|
CH_car_21 |
0.0000000216212 |
4 |
Ca_LG5_v3 |
GO:0005854 |
CC |
nascent polypeptide-associated complex |
|
CH_car_210 |
0.000778301 |
2 |
Ca_LG3_v3 |
GO:0010731 |
BP |
protein glutathionylation |
|
CH_car_211 |
0.000778301 |
2 |
Ca_LG7_v3 |
GO:0003997 |
MF |
acyl-CoA oxidase activity |
|
CH_car_212 |
0.000778301 |
2 |
Ca_LG1_v3 |
GO:0004618 |
MF |
phosphoglycerate kinase activity |
|
CH_car_213 |
0.000778301 |
2 |
Ca_LG4_v3 |
GO:0031116 |
BP |
positive regulation of microtubule polymerization |
|
CH_car_214 |
0.000778301 |
2 |
Ca_LG7_v3 |
GO:0000275 |
CC |
mitochondrial proton-transporting ATP synthase complex, catalytic sector F(1) |
|
CH_car_215 |
0.000778301 |
2 |
Ca_LG3_v3 |
GO:0032977 |
MF |
membrane insertase activity |
|
CH_car_216 |
0.000778301 |
2 |
Ca_LG8_v3 |
GO:0030527 |
MF |
structural constituent of chromatin |
|
CH_car_217 |
0.000828619 |
3 |
Ca_LG1_v3 |
GO:0042631 |
BP |
cellular response to water deprivation |
|
CH_car_218 |
0.000846598 |
26 |
Ca_LG8_v3 |
GO:0044238 |
BP |
primary metabolic process |
|
CH_car_219 |
0.000886799 |
3 |
Ca_LG1_v3 |
GO:0010215 |
BP |
cellulose microfibril organization |
|
CH_car_22 |
0.0000000216322 |
4 |
Ca_LG4_v3 |
GO:0010088 |
BP |
phloem development |
|
CH_car_220 |
0.000992623 |
10 |
Ca_LG6_v3 |
GO:0032991 |
CC |
protein-containing complex |
|
CH_car_23 |
0.0000000248251 |
4 |
Ca_LG7_v3 |
GO:0005085 |
MF |
guanyl-nucleotide exchange factor activity |
|
CH_car_24 |
0.0000000363451 |
3 |
Ca_LG1_v3 |
GO:0003862 |
MF |
3-isopropylmalate dehydrogenase activity |
|
CH_car_25 |
0.0000000363451 |
3 |
Ca_LG6_v3 |
GO:0010282 |
CC |
senescence-associated vacuole |
|
CH_car_26 |
0.0000000363466 |
3 |
Ca_LG4_v3 |
GO:0043564 |
CC |
Ku70:Ku80 complex |
|
CH_car_27 |
0.0000000387654 |
4 |
Ca_LG3_v3 |
GO:0004364 |
MF |
glutathione transferase activity |
|
CH_car_28 |
0.0000000485558 |
6 |
Ca_LG1_v3 |
GO:0050660 |
MF |
flavin adenine dinucleotide binding |
|
CH_car_29 |
0.0000000675023 |
4 |
Ca_LG4_v3 |
GO:0016274 |
MF |
protein-arginine N-methyltransferase activity |
|
CH_car_3 |
2.77498e-16 |
18 |
Ca_LG4_v3 |
GO:0006468 |
BP |
protein phosphorylation |
|
CH_car_30 |
0.0000000833234 |
4 |
Ca_LG7_v3 |
GO:0030145 |
MF |
manganese ion binding |
|
CH_car_31 |
0.0000000908664 |
3 |
Ca_LG7_v3 |
GO:0042946 |
BP |
glucoside transport |
|
CH_car_32 |
0.0000000908664 |
3 |
Ca_LG5_v3 |
GO:1990064 |
BP |
ground tissue pattern formation |
|
CH_car_33 |
0.000000121725 |
7 |
Ca_LG5_v3 |
GO:0016887 |
MF |
ATP hydrolysis activity |
|
CH_car_34 |
0.000000145376 |
3 |
Ca_LG6_v3 |
GO:0004657 |
MF |
proline dehydrogenase activity |
|
CH_car_35 |
0.000000162848 |
5 |
Ca_LG6_v3 |
GO:0030246 |
MF |
carbohydrate binding |
|
CH_car_36 |
0.000000181733 |
3 |
Ca_LG2_v3 |
GO:0004435 |
MF |
phosphatidylinositol phospholipase C activity |
|
CH_car_37 |
0.000000181733 |
3 |
Ca_LG5_v3 |
GO:0017040 |
MF |
N-acylsphingosine amidohydrolase activity |
|
CH_car_38 |
0.000000181733 |
3 |
Ca_LG6_v3 |
GO:0045471 |
BP |
response to ethanol |
|
CH_car_39 |
0.000000193474 |
4 |
Ca_LG3_v3 |
GO:0046938 |
BP |
phytochelatin biosynthetic process |
|
CH_car_4 |
6.85981e-16 |
7 |
Ca_LG1_v3 |
GO:0010427 |
MF |
abscisic acid binding |
|
CH_car_40 |
0.000000230831 |
4 |
Ca_LG1_v3 |
GO:0048544 |
BP |
recognition of pollen |
|
CH_car_41 |
0.000000313572 |
5 |
Ca_LG6_v3 |
GO:0050660 |
MF |
flavin adenine dinucleotide binding |
|
CH_car_42 |
0.000000318032 |
3 |
Ca_LG4_v3 |
GO:0008661 |
MF |
1-deoxy-D-xylulose-5-phosphate synthase activity |
|
CH_car_43 |
0.000000363416 |
3 |
Ca_LG7_v3 |
GO:0016618 |
MF |
hydroxypyruvate reductase activity |
|
CH_car_44 |
0.00000036343 |
3 |
Ca_LG2_v3 |
GO:0033897 |
MF |
ribonuclease T2 activity |
|
CH_car_45 |
0.000000433378 |
5 |
Ca_LG1_v3 |
GO:0003690 |
MF |
double-stranded DNA binding |
|
CH_car_46 |
0.00000043693 |
10 |
Ca_LG4_v3 |
GO:0006468 |
BP |
protein phosphorylation |
|
CH_car_47 |
0.000000726839 |
3 |
Ca_LG3_v3 |
GO:0030581 |
BP |
symbiont intracellular protein transport in host |
|
CH_car_48 |
0.000000763278 |
3 |
Ca_LG3_v3 |
GO:0042735 |
CC |
protein body |
|
CH_car_49 |
0.00000104647 |
6 |
Ca_LG6_v3 |
GO:0004190 |
MF |
aspartic-type endopeptidase activity |
|
CH_car_5 |
0.00000000000112395 |
7 |
Ca_LG7_v3 |
GO:0004869 |
MF |
cysteine-type endopeptidase inhibitor activity |
|
CH_car_50 |
0.0000010904 |
3 |
Ca_LG4_v3 |
GO:0019264 |
BP |
glycine biosynthetic process from serine |
|
CH_car_51 |
0.00000126532 |
24 |
Ca_LG3_v3 |
GO:0005886 |
CC |
plasma membrane |
|
CH_car_52 |
0.00000153963 |
4 |
Ca_LG1_v3 |
GO:0030599 |
MF |
pectinesterase activity |
|
CH_car_53 |
0.00000156278 |
4 |
Ca_LG6_v3 |
GO:0008171 |
MF |
O-methyltransferase activity |
|
CH_car_54 |
0.00000181687 |
3 |
Ca_LG1_v3 |
GO:0019139 |
MF |
cytokinin dehydrogenase activity |
|
CH_car_55 |
0.00000203364 |
6 |
Ca_LG1_v3 |
GO:0008194 |
MF |
UDP-glycosyltransferase activity |
|
CH_car_56 |
0.00000203503 |
3 |
Ca_LG1_v3 |
GO:0030915 |
CC |
Smc5-Smc6 complex |
|
CH_car_57 |
0.00000239752 |
4 |
Ca_LG2_v3 |
GO:0010369 |
CC |
chromocenter |
|
CH_car_58 |
0.00000259878 |
3 |
Ca_LG6_v3 |
GO:0030026 |
BP |
cellular manganese ion homeostasis |
|
CH_car_59 |
0.00000443305 |
8 |
Ca_LG8_v3 |
GO:0031225 |
CC |
anchored component of membrane |
|
CH_car_6 |
0.00000000000707269 |
4 |
Ca_LG5_v3 |
GO:0052861 |
MF |
glucan endo-1,3-beta-glucanase activity, C-3 substituted reducing group |
|
CH_car_60 |
0.00000610174 |
4 |
Ca_LG3_v3 |
GO:0009055 |
MF |
electron transfer activity |
|
CH_car_61 |
0.00000612335 |
29 |
Ca_LG7_v3 |
GO:0043167 |
MF |
ion binding |
|
CH_car_62 |
0.00000635743 |
3 |
Ca_LG5_v3 |
GO:0032039 |
CC |
integrator complex |
|
CH_car_63 |
0.00000635768 |
3 |
Ca_LG4_v3 |
GO:0070652 |
CC |
HAUS complex |
|
CH_car_64 |
0.00000786943 |
4 |
Ca_LG5_v3 |
GO:0043531 |
MF |
ADP binding |
|
CH_car_65 |
0.0000103917 |
3 |
Ca_LG7_v3 |
GO:0005544 |
MF |
calcium-dependent phospholipid binding |
|
CH_car_66 |
0.0000121247 |
6 |
Ca_LG7_v3 |
GO:0071669 |
BP |
plant-type cell wall organization or biogenesis |
|
CH_car_67 |
0.0000127168 |
4 |
Ca_LG3_v3 |
GO:0031267 |
MF |
small GTPase binding |
|
CH_car_68 |
0.0000133728 |
4 |
Ca_LG3_v3 |
GO:0097573 |
MF |
glutathione oxidoreductase activity |
|
CH_car_69 |
0.000015007 |
5 |
Ca_LG3_v3 |
GO:0008194 |
MF |
UDP-glycosyltransferase activity |
|
CH_car_7 |
0.0000000000202036 |
8 |
Ca_LG5_v3 |
GO:0009733 |
BP |
response to auxin |
|
CH_car_70 |
0.000015007 |
5 |
Ca_LG3_v3 |
GO:0008194 |
MF |
UDP-glycosyltransferase activity |
|
CH_car_71 |
0.0000161396 |
6 |
Ca_LG3_v3 |
GO:0016887 |
MF |
ATP hydrolysis activity |
|
CH_car_72 |
0.0000167855 |
8 |
Ca_LG7_v3 |
GO:0022857 |
MF |
transmembrane transporter activity |
|
CH_car_73 |
0.000018023 |
4 |
Ca_LG3_v3 |
GO:0009873 |
BP |
ethylene-activated signaling pathway |
|
CH_car_74 |
0.000018851 |
4 |
Ca_LG1_v3 |
GO:0016765 |
MF |
transferase activity, transferring alkyl or aryl (other than methyl) groups |
|
CH_car_75 |
0.0000199785 |
3 |
Ca_LG4_v3 |
GO:0032454 |
MF |
histone demethylase activity (H3-K9 specific) |
|
CH_car_76 |
0.0000208993 |
3 |
Ca_LG7_v3 |
GO:1990961 |
BP |
xenobiotic detoxification by transmembrane export across the plasma membrane |
|
CH_car_77 |
0.0000247046 |
3 |
Ca_LG2_v3 |
GO:0000775 |
CC |
chromosome, centromeric region |
|
CH_car_78 |
0.0000265536 |
3 |
Ca_LG3_v3 |
GO:0030628 |
MF |
pre-mRNA 3'-splice site binding |
|
CH_car_79 |
0.0000266919 |
3 |
Ca_LG3_v3 |
GO:0000776 |
CC |
kinetochore |
|
CH_car_8 |
0.0000000000990023 |
4 |
Ca_LG5_v3 |
GO:0070577 |
MF |
lysine-acetylated histone binding |
|
CH_car_80 |
0.0000270801 |
6 |
Ca_LG4_v3 |
GO:0048366 |
BP |
leaf development |
|
CH_car_81 |
0.000027443 |
17 |
Ca_LG7_v3 |
GO:0016740 |
MF |
transferase activity |
|
CH_car_82 |
0.0000286589 |
4 |
Ca_LG7_v3 |
GO:0030246 |
MF |
carbohydrate binding |
|
CH_car_83 |
0.0000294869 |
14 |
Ca_LG3_v3 |
GO:0006355 |
BP |
regulation of transcription, DNA-templated |
|
CH_car_84 |
0.0000298639 |
6 |
Ca_LG3_v3 |
GO:2000113 |
BP |
negative regulation of cellular macromolecule biosynthetic process |
|
CH_car_85 |
0.0000301243 |
4 |
Ca_LG4_v3 |
GO:0016667 |
MF |
oxidoreductase activity, acting on a sulfur group of donors |
|
CH_car_86 |
0.000039217 |
4 |
Ca_LG3_v3 |
GO:0043531 |
MF |
ADP binding |
|
CH_car_87 |
0.0000408444 |
3 |
Ca_LG2_v3 |
GO:0003953 |
MF |
NAD+ nucleosidase activity |
|
CH_car_88 |
0.0000426962 |
3 |
Ca_LG6_v3 |
GO:0004332 |
MF |
fructose-bisphosphate aldolase activity |
|
CH_car_89 |
0.0000436458 |
13 |
Ca_LG3_v3 |
GO:0006468 |
BP |
protein phosphorylation |
|
CH_car_9 |
0.000000000264971 |
5 |
Ca_LG4_v3 |
GO:0000977 |
MF |
RNA polymerase II transcription regulatory region sequence-specific DNA binding |
|
CH_car_90 |
0.0000482817 |
3 |
Ca_LG6_v3 |
GO:0016435 |
MF |
rRNA (guanine) methyltransferase activity |
|
CH_car_91 |
0.0000488945 |
7 |
Ca_LG4_v3 |
GO:0004190 |
MF |
aspartic-type endopeptidase activity |
|
CH_car_92 |
0.0000520916 |
5 |
Ca_LG6_v3 |
GO:0008194 |
MF |
UDP-glycosyltransferase activity |
|
CH_car_93 |
0.0000527138 |
8 |
Ca_LG4_v3 |
GO:0004672 |
MF |
protein kinase activity |
|
CH_car_94 |
0.0000584837 |
4 |
Ca_LG7_v3 |
GO:0008061 |
MF |
chitin binding |
|
CH_car_95 |
0.0000594721 |
3 |
Ca_LG8_v3 |
GO:0004866 |
MF |
endopeptidase inhibitor activity |
|
CH_car_96 |
0.0000618915 |
4 |
Ca_LG1_v3 |
GO:0004252 |
MF |
serine-type endopeptidase activity |
|
CH_car_97 |
0.0000642821 |
3 |
Ca_LG5_v3 |
GO:0004649 |
MF |
poly(ADP-ribose) glycohydrolase activity |
|
CH_car_98 |
0.0000692222 |
24 |
Ca_LG5_v3 |
GO:0071840 |
BP |
cellular component organization or biogenesis |
|
CH_car_99 |
0.0000706032 |
3 |
Ca_LG6_v3 |
GO:0004185 |
MF |
serine-type carboxypeptidase activity |