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AP22.17 | Late embryogenesis abundant (LEA) protein. (359 aa) | ||||
F4J573_ARATH | Late embryogenesis abundant protein (LEA) family protein. (298 aa) | ||||
T1G11.19 | AWPM-19-like family protein. (186 aa) | ||||
F21P24.17 | Similar to late embryogenesis abundant proteins. (92 aa) | ||||
F27G19.5 | Late embryogenesis abundant (LEA) protein-like protein. (341 aa) | ||||
GASA3 | Gibberellin-regulated protein 3; Gibberellin-regulated protein that may function in hormonal controlled steps of development such as seed germination, flowering and seed maturation; Belongs to the GASA family. (99 aa) | ||||
LEA6 | Late embryogenesis abundant protein 6; Involved dehydration tolerance. Involved in the adaptive response of vascular plants to withstand water deficit. May possess chaperone-like activity under water deficit (By similarity). (134 aa) | ||||
Y1465_ARATH | Late embryogenesis abundant protein At1g64065. (214 aa) | ||||
PV42B | SNF1-related protein kinase regulatory subunit gamma-like PV42b; Plays redundant role with PV42a in regulating male gametogenesis and pollen tube guidance. (357 aa) | ||||
SAG21 | Protein SENESCENCE-ASSOCIATED GENE 21, mitochondrial; Mediates tolerance to oxidative stresses (e.g. hydrogen peroxide H(2)O(2), diamide, menadione and tert-butyl hydroperoxide) by minimizing the negative effects of oxidation and monitoring photosynthesis during stress. Promotes root development. Prevents premature aging (e.g. senescence and flowering). Involved in resistance against compatible pathogens such as Botrytis cinerea and Pseudomonas syringae pv. tomato. (97 aa) | ||||
LEA | Probable dehydrin LEA; Belongs to the plant dehydrin family. (185 aa) | ||||
LEA7 | Late embryogenesis abundant protein 7; Involved in dehydration and freezing tolerance. Protects and stabilizes the enzyme activities of ADP-glucose-pyrophosphorylase (AGPase) and glucose-6-phosphate dehydrogenase (G6PDH) during drought stress and freezing. Prevents aggregation of leaf soluble proteins during drought stress. Does not stabilize liposomes during drying and rehydration; Belongs to the LEA type 4 family. (169 aa) | ||||
LEA18 | Late embryogenesis abundant protein 18; Involved dehydration tolerance. Involved in the adaptive response of vascular plants to withstand water deficit. May possess chaperone-like activity under water deficit. Binds to negatively charged membranes of liposomes. This binding induces partial folding of the largely unstructured LEA18 protein, vesicle aggregation, and leakage of soluble content from liposomes. (97 aa) | ||||
F13K9.9 | Transmembrane protein. (271 aa) | ||||
F28P5.13 | Late embryogenesis abundant domain-containing protein / LEA domain-containing protein. (480 aa) | ||||
T22E19.12 | At1g68250. (133 aa) | ||||
MRN17.10 | Late embryogenesis abundant (LEA) hydroxyproline-rich glycoprotein family. (207 aa) | ||||
LEA46 | Late embryogenesis abundant protein 46; Involved dehydration tolerance. Involved in the adaptive response of vascular plants to withstand water deficit. May possess chaperone-like activity under water deficit ; Belongs to the LEA type 1 family. (158 aa) | ||||
AGL81 | Agamous-like MADS-box protein AGL81; Probable transcription factor that may function in the maintenance of the proper function of the central cell in pollen tube attraction. (355 aa) | ||||
K9L2.18 | Berberine bridge enzyme-like 24. (541 aa) | ||||
K9L2.7 | Late embryogenesis abundant protein (LEA) family protein. (331 aa) | ||||
T24C10.2 | Late embryogenesis abundant (LEA) protein-like protein. (347 aa) | ||||
F8J2_210 | Late embryogenesis abundant protein At3g53040; May function in the proximal abscission zone cells to prevent water loss after floral organ shedding (Probable). May be involved in the reestablishment of desiccation tolerance in germinated seeds (Probable); Belongs to the LEA type 4 family. (479 aa) | ||||
ECP31 | Late embryogenesis abundant protein 32; LEA proteins are late embryonic proteins abundant in higher plant seed embryos. The function of those proteins is not known. Belongs to the LEA type SMP family. (256 aa) | ||||
CKL8 | Casein kinase 1-like protein 8; Casein kinases are operationally defined by their preferential utilization of acidic proteins such as caseins as substrates. It can phosphorylate a large number of proteins. (480 aa) | ||||
LEA29 | Late embryogenesis abundant protein 29; Involved dehydration tolerance. Belongs to the LEA type 4 family. (225 aa) | ||||
T2I1.40 | NFU1 iron-sulfur cluster protein. (165 aa) | ||||
F16B3.11 | Late embryogenesis abundant protein (LEA) family protein. (68 aa) | ||||
T12H1.23 | Glucose and ribitol dehydrogenase homolog 2; May act as a short alcohol-polyol-sugar dehydrogenase possibly related to carbohydrate metabolism and the acquisition of desiccation tolerance. May also be involved in signal transduction (By similarity). (289 aa) | ||||
RAB28-2 | Late embryogenesis abundant protein 3; LEA proteins are late embryonic proteins abundant in higher plant seed embryos. The function of those proteins is not known. Belongs to the LEA type SMP family. (182 aa) | ||||
F14N22.17 | Late embryogenesis abundant domain-containing protein / LEA domain-containing protein. (635 aa) | ||||
Q9SJ17_ARATH | Seed maturation protein. (78 aa) | ||||
F11F19.12 | Late embryogenesis abundant (LEA) hydroxyproline-rich glycoprotein family. (211 aa) | ||||
F12K8.5 | Late embryogenesis abundant protein (LEA) family protein. (385 aa) | ||||
ECP63 | Late embryogenesis abundant protein ECP63; May be involved in the BHLH109-mediated regulation of somatic embryogenesis; Belongs to the LEA type 4 family. (448 aa) | ||||
LEA2 | Late embryogenis abundant protein 2; Belongs to the LEA type 3 family. (91 aa) | ||||
F6D8.10 | Late embryogenesis abundant protein-like protein/LEA protein-like protein. (114 aa) | ||||
T13K14.180 | Late embryogenesis abundant protein (LEA) family protein. (266 aa) | ||||
T13M11.12 | Late embryogenesis abundant (LEA) hydroxyproline-rich glycoprotein family. (224 aa) |