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G7JWX2_MEDTR | Putative salicylate carboxymethyltransferase. (421 aa) | ||||
G7IW74_MEDTR | Short-chain dehydrogenase/reductase. (280 aa) | ||||
G7ICD6_MEDTR | Sigma factor sigb regulation rsbq-like protein. (268 aa) | ||||
B7FHG6_MEDTR | Putative transcription factor C2H2 family. (155 aa) | ||||
A0A072V8S5 | Putative 9-cis-epoxycarotenoid dioxygenase. (610 aa) | ||||
A0A072V8C0 | Zeaxanthin epoxidase, putative. (217 aa) | ||||
G7KHF8_MEDTR | Indole-3-acetaldehyde oxidase. (1356 aa) | ||||
A0A072U6H5 | Putative neoxanthin synthase. (236 aa) | ||||
A0A072V5M6 | 2OG-Fe(II) oxygenase family oxidoreductase; Belongs to the iron/ascorbate-dependent oxidoreductase family. (363 aa) | ||||
A0A072UTU8 | AP2 domain class transcription factor. (425 aa) | ||||
A0A072UCL6 | Zeaxanthin epoxidase, chloroplastic; Converts zeaxanthin into antheraxanthin and subsequently violaxanthin. (699 aa) | ||||
D27 | Beta-carotene isomerase D27, chloroplastic; Involved in strigolactones biosynthesis by catalyzing the isomerization of the C9-C10 double bond in all-trans-beta-carotene leading to 9-cis-beta-carotene and providing the substrate for CCD7. Strigolactones are hormones that inhibit tillering and shoot branching through the MAX-dependent pathway, contribute to the regulation of shoot architectural response to phosphate-limiting conditions and function as rhizosphere signals that stimulate hyphal branching of arbuscular mycorrhizal fungi and trigger seed germination of root parasitic weeds. (252 aa) | ||||
G7ZY14_MEDTR | Putative neoxanthin synthase. (239 aa) | ||||
G7KU00_MEDTR | Carotenoid cleavage dioxygenase. (621 aa) | ||||
G7KP55_MEDTR | Neoxanthin synthase. (240 aa) | ||||
G7KHG0_MEDTR | Indole-3-acetaldehyde oxidase. (1372 aa) | ||||
G7K6P3_MEDTR | Zeaxanthin epoxidase, putative. (72 aa) | ||||
A0A072U3B7 | Putative beta-carotene isomerase. (248 aa) |