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ATP + (+)-jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
-
Substrates: very low activity
Products: -
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ATP + (+/-)-jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
-
Substrates: -
Products: -
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ATP + (-)-jasmonate + L-Gln
AMP + diphosphate + jasmonoyl-L-Gln
-
Substrates: -
Products: -
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ATP + (-)-jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
ATP + (-)-jasmonate + L-Leu
AMP + diphosphate + jasmonoyl-L-Leu
ATP + (-)-jasmonate + L-Phe
AMP + diphosphate + jasmonoyl-L-Phe
-
Substrates: -
Products: -
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ATP + (-)-jasmonate + L-Val
AMP + diphosphate + jasmonoyl-L-Val
ATP + 12-oxophytodienoate + L-Ile
AMP + diphosphate + 12-oxophytodienoyl-L-Ile
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Substrates: low activity
Products: -
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ATP + 13-hydroperoxylinolenoate + L-Ile
AMP + diphosphate + 13-hydroperoxylinolenoyl-L-Ile
-
Substrates: low activity
Products: -
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ATP + 3-oxocyclopentane octanoate + L-Ile
AMP + diphosphate + 3-oxocyclopentane octanoyl-L-Ile
-
Substrates: low activity
Products: -
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ATP + 9,10-dihydro-jasmonate + L-Ile
?
-
Substrates: -
Products: -
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ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
ATP + linolenate + L-Ile
AMP + diphosphate + linolenoyl-L-Ile
-
Substrates: low activity
Products: -
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additional information
?
-
ATP + (-)-jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
-
Substrates: L-Ile is the preferred amino acid
Products: -
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ATP + (-)-jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
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Substrates: the rate of synthesis of (-)-jasmonate is about 100fold faster than for (+)-jasmonate. Diadenosine tetraphosphate cannot substitute ATP
Products: -
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ATP + (-)-jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
-
Substrates: -
Products: -
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ATP + (-)-jasmonate + L-Leu
AMP + diphosphate + jasmonoyl-L-Leu
-
Substrates: -
Products: -
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ATP + (-)-jasmonate + L-Leu
AMP + diphosphate + jasmonoyl-L-Leu
-
Substrates: -
Products: -
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ATP + (-)-jasmonate + L-Val
AMP + diphosphate + jasmonoyl-L-Val
-
Substrates: -
Products: -
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ATP + (-)-jasmonate + L-Val
AMP + diphosphate + jasmonoyl-L-Val
-
Substrates: -
Products: -
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ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
-
Substrates: -
Products: -
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ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
Substrates: -
Products: -
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ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
Substrates: specific substrate
Products: -
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ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
-
Substrates: -
Products: -
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ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
-
Substrates: -
Products: -
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ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
Substrates: -
Products: -
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ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
-
Substrates: highest activity
Products: -
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ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
A1BNG5
Substrates: -
Products: -
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ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
Substrates: -
Products: -
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additional information
?
-
-
Substrates: the rate of conjugation with 12-hydroxy-jasmonate and 3-oxo-2-(2Z-pentenyl)cyclopentane-1-butyric acid is about 1-2% that for jasmonate. The enzyme shows no activity with (+/-)-12-oxo-phytodienoic acid, 3-oxo-2-(2Z-pentenyl)cyclopentane-1-hexanoate, and 3-oxo-2-(2Z-pentenyl)cyclopentane-1-octanoate
Products: -
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additional information
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-
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Substrates: no activity with 1-aminocyclopropane-1-carboxylic acid, L-Me, or L-Trp
Products: -
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ATP + (-)-jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
-
Substrates: L-Ile is the preferred amino acid
Products: -
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ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
-
Substrates: -
Products: -
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ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
Substrates: -
Products: -
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ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
Substrates: specific substrate
Products: -
?
ATP + jasmonate + an L-amino acid
AMP + diphosphate + a jasmonoyl-L-amino acid
-
Substrates: -
Products: -
?
ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
-
Substrates: -
Products: -
?
ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
Substrates: -
Products: -
?
ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
A1BNG5
Substrates: -
Products: -
?
ATP + jasmonate + L-Ile
AMP + diphosphate + jasmonoyl-L-Ile
Substrates: -
Products: -
?
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Guranowski, A.; Miersch, O.; Staswick, P.; Suza, W.; Wasternack, C.
Substrate specificity and products of side-reactions catalyzed by jasmonate amino acid synthetase (JAR1)
FEBS Lett.
581
815-820
2007
Arabidopsis thaliana
brenda
Swain, S.; Jiang, H.; Hsieh, H.
FAR-RED INSENSITIVE 219/JAR1 contributes to shade avoidance responses of Arabidopsis seedlings by modulating key shade signaling components
Front. Plant Sci.
8
1901
2017
Arabidopsis thaliana
brenda
Meesters, C.; Mönig, T.; Oeljeklaus, J.; Krahn, D.; Westfall, C.; Hause, B.; Jez, J.; Kaiser, M.; Kombrink, E.
A chemical inhibitor of jasmonate signaling targets JAR1 in Arabidopsis thaliana
Nat. Chem. Biol.
10
830-836
2014
Arabidopsis thaliana (Q9SKE2), Arabidopsis thaliana
brenda
Vandoorn, A.; Bonaventure, G.; Schmidt, D.; Baldwin, I.
Regulation of jasmonate metabolism and activation of systemic signaling in Solanum nigrum COI1 and JAR4 play overlapping yet distinct roles
New Phytol.
190
640-652
2011
Solanum nigrum (F6KIF4)
brenda
Staswick, P.; Tiryaki, I.; Rowe, M.
Jasmonate response locus JAR1 and several related Arabidopsis genes encode enzymes of the firefly luciferase superfamily that show activity on jasmonic, salicylic, and indole-3-acetic acids in an assay for adenylation
Plant Cell
14
1405-1415
2002
Arabidopsis thaliana (Q9SKE2)
brenda
Staswick, P.; Tiryaki, I.
The oxylipin signal jasmonic acid is activated by an enzyme that conjugate it to isoleucine in Arabidopsis W inside box sign
Plant Cell
16
2117-2127
2004
Arabidopsis thaliana
brenda
Kang, J.; Wang, L.; Giri, A.; Baldwin, I.
Silencing threonine deaminase and JAR4 in Nicotiana attenuata impairs jasmonic acid-isoleucine-mediated defenses against Manduca sexta
Plant Cell
18
3303-3320
2006
Nicotiana attenuata (A1BNG5)
brenda
Kawamura, Y.; Takenaka, S.; Hase, S.; Kubota, M.; Ichinose, Y.; Kanayama, Y.; Nakaho, K.; Klessig, D.; Takahashi, H.
Enhanced defense responses in Arabidopsis induced by the cell wall protein fractions from Pythium oligandrum require SGT1, RAR1, NPR1 and JAR1
Plant Cell Physiol.
50
924-934
2009
Arabidopsis thaliana (Q9SKE2)
brenda
Staswick, P.; Yuen, G.; Lehman, C.
Jasmonate signaling mutants of Arabidopsis are susceptible to the soil fungus Pythium irregulare
Plant J.
15
747-754
1998
Arabidopsis thaliana
brenda
Kishimoto, K.; Matsui, K.; Ozawa, R.; Takabayashi, J.
ETR1-, JAR1- and PAD2-dependent signaling pathways are involved in C6-aldehyde-induced defense responses of Arabidopsis
Plant Sci.
171
415-423
2006
Arabidopsis thaliana
brenda
Wang, L.; Halitschke, R.; Kang, J.; Berg, A.; Harnisch, F.; Baldwin, I.
Independently silencing two JAR family members impairs levels of trypsin proteinase inhibitors but not nicotine
Planta
226
159-167
2007
Nicotiana attenuata
brenda
Suza, W.; Staswick, P.
The role of JAR1 in jasmonoyl-L-isoleucine production during Arabidopsis wound response
Planta
227
1221-1232
2008
Arabidopsis thaliana
brenda