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A0A1D6GWD6 | Receptor-like protein kinase-like. (376 aa) | ||||
ZIM21 | ZIM transcription factor. (216 aa) | ||||
ZIM16 | ZIM motif family protein. (181 aa) | ||||
A0A096QX45 | TIFY19. (218 aa) | ||||
A0A1D6E1P4 | Sirohydrochlorin ferrochelatase chloroplastic. (212 aa) | ||||
A0A1D6E388 | Protein LAZ1. (498 aa) | ||||
A0A1D6E5Y8 | Phenylalanine ammonia-lyase. (715 aa) | ||||
A0A1D6E5Y9 | Phenylalanine ammonia-lyase. (789 aa) | ||||
Mlo3 | MLO-like protein; May be involved in modulation of pathogen defense and leaf cell death. (496 aa) | ||||
A0A1D6EEQ0 | Protein TIFY 10B. (98 aa) | ||||
EDS | Eudesmanediol synthase; Component of the volatile terpenes biosynthesis pathways. Dihydroxylated sesquiterpenoid synthase that generates dually hydroxylated products directly from (E,E)-farnesyl diphosphate, primarily eudesmane-2,11-diol, along with two closely related structural isomers. (557 aa) | ||||
A0A1D6EM25 | E3 ubiquitin-protein ligase RGLG1. (122 aa) | ||||
A0A1D6EWJ9 | Protein LAZ1. (167 aa) | ||||
A0A1D6EXK6 | Uncharacterized protein. (222 aa) | ||||
A0A1D6F1D1 | Protein TIFY 10B. (266 aa) | ||||
A0A1D6F256 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (368 aa) | ||||
Pco121700 | Jasmonic acid-amido synthetase JAR1. (576 aa) | ||||
A0A1D6FTB3 | Polyadenylate-binding protein RBP45C. (124 aa) | ||||
A0A1D6FUY8 | Peroxidase 2; Belongs to the peroxidase family. (187 aa) | ||||
A0A1D6FZK0 | Jasmonic acid-amido synthetase JAR1. (614 aa) | ||||
A0A1D6G2M7 | Kinase superfamily protein. (313 aa) | ||||
A0A1D6G2M8 | Kinase superfamily protein. (278 aa) | ||||
A0A1D6G6M1 | E3 ubiquitin-protein ligase RGLG1. (508 aa) | ||||
A0A1D6GR78 | Protein TIFY 10B. (184 aa) | ||||
A0A1D6GU51 | IAA-amino acid hydrolase ILR1-like 6. (481 aa) | ||||
A0A1D6H6Q7 | Protein TIFY 10B. (157 aa) | ||||
A0A1D6HDL5 | Phenylalanine ammonia-lyase. (719 aa) | ||||
A0A1D6HDL9 | Phenylalanine ammonia-lyase. (704 aa) | ||||
A0A1D6HKX5 | E3 ubiquitin-protein ligase ATL6. (419 aa) | ||||
A0A1D6HQ97 | Polyadenylate-binding protein RBP45C. (142 aa) | ||||
A0A1D6I689 | E3 ubiquitin-protein ligase ATL6. (398 aa) | ||||
A0A1D6ICF7 | Protein LAZ1. (351 aa) | ||||
A0A1D6IKV7 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (351 aa) | ||||
A0A1D6IKV9 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (391 aa) | ||||
A0A1D6IKW0 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (380 aa) | ||||
A0A1D6IKW1 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (350 aa) | ||||
A0A1D6IKW2 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (391 aa) | ||||
A0A1D6IKX3 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. These functions might be dependent on each isozyme/isoform in each plant tissue; Belongs to the peroxidase family. (560 aa) | ||||
A0A1D6IZC4 | Protein TIFY 10B. (60 aa) | ||||
A0A1D6JZU3 | Pathogenesis-related protein 10; Belongs to the BetVI family. (160 aa) | ||||
A0A1D6K433 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (336 aa) | ||||
A0A1D6K434 | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (337 aa) | ||||
A0A1D6K4X2 | E3 ubiquitin-protein ligase ATL6. (383 aa) | ||||
Myc7 | Myc transcription factor7. (705 aa) | ||||
A0A1D6KXF9 | Phenylalanine ammonia-lyase. (698 aa) | ||||
A0A1D6L5R0 | E3 ubiquitin-protein ligase RGLG1. (169 aa) | ||||
A0A1D6L8G4 | Protein TIFY 10B. (118 aa) | ||||
A0A1D6LAB5 | Protein LAZ1. (438 aa) | ||||
A0A1D6LMQ4 | Protein LAZ1. (480 aa) | ||||
A0A1D6LMX8 | Receptor-like protein kinase-like. (556 aa) | ||||
A0A1D6LS17 | E3 ubiquitin-protein ligase RGLG1. (458 aa) | ||||
A0A1D6LVF9 | Putative RING zinc finger domain superfamily protein. (421 aa) | ||||
A0A1D6MC49 | MACPF domain-containing protein NSL1. (630 aa) | ||||
Hir3 | Hypersensitive induced reaction3. (341 aa) | ||||
A0A1D6MEQ0 | WRKY transcription factor 6. (541 aa) | ||||
A0A1D6MTS9 | Protein TIFY 10B. (206 aa) | ||||
A0A1D6MV70 | E3 ubiquitin-protein ligase RGLG1. (107 aa) | ||||
A0A1D6N3Y9 | E3 ubiquitin-protein ligase RGLG1. (472 aa) | ||||
A0A1D6NF20 | Kinase superfamily protein. (266 aa) | ||||
A0A1D6NF21 | Kinase superfamily protein. (310 aa) | ||||
A0A1D6PQ30 | E3 ubiquitin-protein ligase RGLG1. (308 aa) | ||||
A0A1D6PQ63 | 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily protein. (196 aa) | ||||
A0A1D6PR86 | Hevein-like preproprotein. (152 aa) | ||||
A0A1D6PTB6 | Hevein-like preproprotein. (150 aa) | ||||
A0A1D6Q421 | Protein TIFY 10B. (202 aa) | ||||
A0A1D6Q5B1 | Phenylalanine ammonia-lyase. (703 aa) | ||||
A0A1D6Q5B7 | Phenylalanine ammonia-lyase 1. (157 aa) | ||||
A0A1D6QSQ3 | Peroxidase 3. (222 aa) | ||||
Pco137346 | TIFY transcription factor. (227 aa) | ||||
Pco080661a | Hevein-like preproprotein. (149 aa) | ||||
B4FQE1_MAIZE | Protein TIFY 10B. (233 aa) | ||||
B4FS23_MAIZE | Hevein-like preproprotein. (150 aa) | ||||
PR-5 | Pathogenesis related protein5. (174 aa) | ||||
B4FW68_MAIZE | Phenylalanine ammonia-lyase. (718 aa) | ||||
B4FWR0_MAIZE | Protein LAZ1. (407 aa) | ||||
B4G105_MAIZE | Type III polyketide synthase B; Belongs to the thiolase-like superfamily. Chalcone/stilbene synthases family. (417 aa) | ||||
B6SU27_MAIZE | NAC domain-containing protein 48. (295 aa) | ||||
B6T9S4_MAIZE | Chalcone synthase WHP1; Belongs to the thiolase-like superfamily. Chalcone/stilbene synthases family. (401 aa) | ||||
ZIM4 | Putative tify domain/CCT motif transcription factor family protein. (172 aa) | ||||
ZIM26 | ZIM motif family protein. (164 aa) | ||||
ZIM18 | ZIM motif family protein. (182 aa) | ||||
ZIM3 | ZIM motif family protein. (162 aa) | ||||
Pal3 | Phenylalanine ammonia-lyase. (703 aa) | ||||
TIDP2917 | Protein BONZAI 3. (589 aa) | ||||
C0HHL9_MAIZE | Protein TIFY 10B. (228 aa) | ||||
PAL | Phenylalanine ammonia-lyase. (715 aa) | ||||
C0P4B4_MAIZE | Protein TIFY 10B. (202 aa) | ||||
ZIM28 | ZIM-transcription factor 28. (218 aa) | ||||
IDP1683 | Putative tify domain/CCT motif transcription factor family protein isoform 1. (230 aa) | ||||
C0PL14_MAIZE | Phenylalanine ammonia-lyase. (716 aa) | ||||
Pco123637(113) | ZIM transcription factor. (216 aa) | ||||
C4J3S7_MAIZE | Protein LAZ1. (404 aa) | ||||
C4J4N2_MAIZE | E3 ubiquitin-protein ligase RGLG1. (541 aa) | ||||
RGD2 | Protein argonaute 7; Belongs to the argonaute family. (1032 aa) | ||||
Yuc | Defective18. (399 aa) | ||||
K7TMB0_MAIZE | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (338 aa) | ||||
K7TRU9_MAIZE | Laccase; Lignin degradation and detoxification of lignin-derived products; Belongs to the multicopper oxidase family. (591 aa) | ||||
K7U151_MAIZE | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (327 aa) | ||||
K7UFY8_MAIZE | Polyadenylate-binding protein RBP47B. (430 aa) | ||||
K7VFH6_MAIZE | Peroxidase; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. (330 aa) | ||||
ZIM14 | Putative tify domain/CCT motif transcription factor family protein. (183 aa) | ||||
rps2 | 30S ribosomal protein S2, chloroplastic. (236 aa) | ||||
C2 | Chalcone synthase C2; The primary product of this enzyme is 4,2',4',6'- tetrahydroxychalcone (also termed naringenin-chalcone or chalcone) which can under specific conditions spontaneously isomerize into naringenin. (400 aa) | ||||
A2 | Leucoanthocyanidin dioxygenase; Oxidation of leucoanthocyanidins into anthocyanidins. (395 aa) | ||||
A1 | Dihydroflavonol 4-reductase; Bifunctional enzyme involved in flavonoid metabolism. Belongs to the NAD(P)-dependent epimerase/dehydratase family. Dihydroflavonol-4-reductase subfamily. (357 aa) | ||||
TPS7 | Tau-cadinol synthase; Sesquiterpene synthase that catalyzes the formation of a blend of sesquiterpenes and sesquiterpenoid alcohols. Converts farnesyl diphosphate to tau-cadinol. (548 aa) | ||||
aoc | Allene oxide cyclase1. (238 aa) | ||||
TPS1 | Acyclic sesquiterpene synthase; Involved in the formation of (E)-beta-farnesene and (3E)-4,8- dimethyl-1,3,7-nonatriene, key signal molecules in induced plant defense mediated by the attraction of enemies of herbivores. In the presence of geranyl diphosphate, catalyzes the formation of the acyclic monoterpens (3R)-linalool and geraniol. However, the in vitro rate of sesquiterpene formation is about four times higher than the rate of monoterpene formation. Mediates the conversion of ent-copalyl diphosphate into ent-kaurene, thus having probably a role in gibberellin biosynthesis. (590 aa) | ||||
PER2 | Peroxidase 2; Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress. These functions might be dependent on each isozyme/isoform in each plant tissue. (335 aa) |