Acer truncatum |
Atru.chr3.1801 |
|
chr3 |
+ |
View |
Actinidia chinensis |
Actinidia32951 |
|
Lachesis_group0 |
- |
View |
Cicer arietinum L. |
Ca_11422_v3 |
|
Ca_LG4_v3 |
+ |
View |
Citrus clementina |
Ciclev10018740m.g |
|
scaffold_3 |
- |
View |
Carya illinoinensis |
CiPaw.02G059800 |
PTHR10997//PTHR10997:SF35 - IMPORTIN-7, 8, 11 // SUBFAMILY NOT NAMED |
Chr02 |
- |
View |
Carya illinoinensis |
CiPaw.01G108500 |
PTHR10997//PTHR10997:SF35 - IMPORTIN-7, 8, 11 // SUBFAMILY NOT NAMED |
Chr01 |
- |
View |
Citrullus lanatus |
ClCG08G003770 |
Importin-7, putative |
CG_Chr08 |
+ |
View |
Davidia involucrata |
Dinv22652 |
|
GWHABJS00000016 |
- |
View |
Durio zibethinus |
Duzib268G0977 |
|
NW_019168270.1 |
- |
View |
Durio zibethinus |
Duzib151G0845 |
|
NW_019167904.1 |
- |
View |
Eucalyptus grandis |
Eucgr.H02619 |
|
Chr08 |
- |
View |
Hydrangea macrophylla |
Hma1.2p1_0412F.1_g147160 |
|
Hma1.2p1_0412F.1 |
+ |
View |
Lotus japonicus |
Lj5g0000254 |
PTHR10997//PTHR10997:SF35 - IMPORTIN-7, 8, 11 // SUBFAMILY NOT NAMED |
chr5 |
- |
View |
Malus domestica |
MD04G1028800 |
ARM repeat superfamily protein |
Chr04 |
+ |
View |
Manihot esculenta |
Manes.04G061600 |
|
Chromosome04 |
- |
View |
Pisum sativum |
Psat6g243600 |
Cse1 |
chr6LG2 |
- |
View |
Populus trichocarpa |
Potri.014G149600 |
PTHR10997//PTHR10997:SF35 - IMPORTIN-7, 8, 11 // SUBFAMILY NOT NAMED |
Chr14 |
+ |
View |
Phaseolus vulgaris |
Phvul.007G001700 |
PTHR10997//PTHR10997:SF35 - IMPORTIN-7, 8, 11 // SUBFAMILY NOT NAMED |
Chr07 |
- |
View |
Quercus lobata |
QL10p044188 |
|
10 |
- |
View |
Salix brachista |
Sabra14G0112800 |
|
GWHAAZH00000014 |
+ |
View |
Sechium edule |
Sed0001099 |
|
LG09 |
- |
View |
Solanum lycopersicum |
Solyc09g098240.4 |
Importin beta-like SAD2 (AHRD V3.3 *** A0A1U8GC41_CAPAN) |
SL4.0ch09 |
- |
View |
Solanum pennellii |
Sopen09g036180 |
SAD2 (super sensitive to ABA and drought 2) encodes an importin beta-domain family protein likely to be involved in nuclear transport in ABA signaling. Subcellular localization of GFP-tagged SAD2 showed a predominantly nuclear localization, consistent with a role for SAD2 in nuclear transport. Mutation of SAD2 in Arabidopsis alters abscisic acid sensitivity. SAD2 was ubiquitously expressed at low levels in all tissues except flowers. SAD2 expression was not induced by ABA or stress. Loss of function mutations in SAD2 exhibit increased tolerance for UV stress, increased production of UV protective secondary metabolites and suppression of nuclear localization of MYB4 (a repressor of UV stress response genes). | SUPER SENSITIVE TO ABA AND DROUGHT2 (SAD2) | FUNCTIONS IN: protein transporter activity, binding | INVOLVED IN: protein import into nucleus, docking, protein import into nucleus | LOCATED IN: nucleus, nuclear pore, cytoplasm | EXPRESSED IN: 24 plant structures | EXPRESSED DURING: 13 growth stages | CONTAINS InterPro DOMAIN/s: Importin-beta, N-terminal , Armadillo-like helical , Armadillo-type fold , Exportin/Importin, Cse1-like | BEST Arabidopsis thaliana protein match is: ARM repeat superfamily protein |
Spenn-ch09 |
- |
View |
Tarenaya hassleriana |
THA.LOC104803420 |
importin beta-like SAD2 homolog isoform X1 |
NW_010960188.1 |
+ |
View |
Tripterygium wilfordii |
TWI15G0371 |
|
NC_052247.1 |
+ |
View |
Tripterygium wilfordii |
TWI63G1206 |
|
NC_052240.1 |
+ |
View |
Vaccinium macrocarpon |
vmacro00563 |
Similar to SAD2: Importin beta-like SAD2 (Arabidopsis thaliana OX%3D3702) |
chr1_Vaccinium_macrocarpon_Stevens_v1 |
+ |
View |
Vigna mungo |
VMungo0720G0240 |
|
CM024071.1 |
+ |
View |