| ZmCCT5-NLUC and ZmTFCB-CLUC |
showed strong fluorescence signals in |
tobacco leaf cells in LCI assays |
Nicotiana tabacum |
| His-ZmTFCB |
was not observed in |
panel of (ATGSTU24, GST, GSTU24, AT1G17170) alone |
Zea mays |
| (CAR6, EHB1, AT1G70800) |
interacts with |
(FER, AT3G51550) |
Arabidopsis thaliana |
| (CAR1, AT1G50180) |
interacts with |
(FER, AT3G51550) |
|
| plant SAM domain-containing proteins |
have provided initial insights into |
interaction capabilities of plant SAM domain |
|
| interaction between RAD51D.1 and (ATMSH5, MSH5, AT3G20475) |
is validated through |
bimolecular fluorescence complementation assays in rice protoplasts |
Oryza sativa |
| two out of four genes of S4 and both genes of S5 |
indicate potential interaction with |
(bHLH, AT5G51780) proteins |
Amaranthus hypochondriacus |
| (AtC2, AtGAP1, C2, CAR4, AT3G17980) |
interacts with |
(FER, AT3G51550) |
|
| bimolecular fluorescence complementation |
confirmed |
interaction between EGT2 and three interaction candidates |
Hordeum vulgare |
| GST-tagged (AtC2, AtGAP1, C2, CAR4, AT3G17980) |
interacts with |
His-tagged FER-CD |
|
| (MAC3A, PUB59, AT1G04510) |
is |
potential partner of SKRP |
Arabidopsis thaliana |
| (CAR9, AT1G70790) |
interacts with |
(FER, AT3G51550) |
Arabidopsis thaliana |
| GST-tagged (CAR6, EHB1, AT1G70800) |
interacts with |
His-tagged FER-CD |
|
| EGT2 fused with cYFP at N-terminus (cYFP-EGT2 (+TGA)) |
displayed interaction with |
OMT and GXM |
Hordeum vulgare |
| confined interaction of GXM and HMT with EGT2 in nucleus |
could be explained by |
hypothetical co-factor present only in nucleus but not cytoplasm |
Hordeum vulgare |
| (AGL25, FLC, FLF, RSB6, AT5G10140) EXPRESSOR (FLX, AT2G30120) and -LIKE4 (FLL4, FLX4, AT5G61920) |
contain |
leucine zipper domains |
Arabidopsis thaliana |
| cross between mCherry-CESA6 and μ2-YFP lines |
performed in order to observe |
relationship between (CESA6, E112, IXR2, PRC1, AT5G64740) and μ2 in planta |
Arabidopsis thaliana |
| GST-tagged (CAR10, AT2G01540) |
interacts with |
His-tagged FER-CD |
|
| split-luciferase complementary assay |
confirmed that |
SlERF.C1 and SlMPK8, rather than SlMPK9, showed interaction in vivo |
Solanum lycopersicum |
| μ2-YFP and CLC-mOrange in dark-grown hypocotyls |
exhibited extensive |
colocalization |
Arabidopsis thaliana |
| LepB |
is |
a potential interacting protein of NCR343 |
Medicago truncatula |
| colocalization ratio between μ2-YFP and mCherry-CESA6 particle populations |
not significantly different from |
coincident overlap of randomly distributed particles |
Arabidopsis thaliana |
| (CAR1, AT1G50180) |
directly interacts with |
FER-CD |
|
| SlMPK2 and SlMPK8 |
were found to interplay with |
SlERF.C1 in yeasts |
Solanum lycopersicum |
| absence of FD orthologs in gymnosperms |
suggests that |
interaction with other proteins might be important for PaFTL1 and PaFTL2 function |
Picea abies |
| (CAR10, AT2G01540) |
directly interacts with |
FER-CD |
|
| STRING analysis of BUZZ |
predicts interaction with |
(CYCT1;2, AT4G19560) |
Brachypodium distachyon |
| cytoplasmic part of MoEmc5 |
interacts with |
MoEmc2 |
Magnaporthe oryzae |
| putative NCR343-interacting S. meliloti proteins |
need to be |
confirmed |
Medicago truncatula |
| GmHAD1-2 and GmCHR1 |
interact |
|
Glycine max |
| CRYPTOCHROME 1 (ATCRY1, BLU1, CRY1, HY4, OOP2, AT4G08920) and (EMB1706, MTA, AT4G10760) interaction |
is |
light-independent |
Arabidopsis thaliana |
| two candidates |
were not confirmed |
bimolecular fluorescence complementation |
Hordeum vulgare |
| phenotypic difference in promotion of callus formation in (ATHSFA2, HSFA2, AT2G26150) overexpressing plants in wild-type and QK backgrounds |
suggests |
HSFA1s affect function of (ATHSFA2, HSFA2, AT2G26150) |
Arabidopsis thaliana |
| changes in protein structure caused by inappropriate terminal fusion to fluorescent proteins |
might explain |
lack of confirmation of two candidates |
Hordeum vulgare |
| IP-MS (Mass Spectrometry) assay |
was performed on |
isolated WT symbiosomes treated with synthesized NCR343-FLAG peptides |
Medicago truncatula |
| CaDeSI2 |
interacts with |
CaAITP1 |
Nicotiana benthamiana |
| (CAR3, AT1G73580) |
does not interact with |
(FER, AT3G51550) |
|
| EGT2 |
identified |
79 proteins as putative interaction partners |
Hordeum vulgare |
| BUZZ and AtBUZZ protein sequences |
are predicted to interact with |
10 proteins including four cyclins, three DNA-directed RNA polymerases, and (KTF1, SPT5L, AT5G04290) |
Brachypodium distachyon; Arabidopsis thaliana |
| (PRL1, SCPR44, AT4G15900) |
is |
potential partner of SKRP |
Arabidopsis thaliana |
| (CAR10, AT2G01540) |
interacts with |
(FER, AT3G51550) |
|
| six most abundant NCR343-interacting proteins |
were |
listed |
Medicago truncatula |
| CaDeSI2 |
interacts with |
CaAITP1 |
Nicotiana benthamiana |
| (CAR10, AT2G01540) |
interacts with |
(FER, AT3G51550) |
Arabidopsis thaliana |
| (AtTic62, Tic62, AT3G18890) and AtTROL proteins |
contain |
highly similar Pro-rich FNR-binding domains |
Arabidopsis thaliana |
| conserved EDVID motif (EDMVD in Rx1) |
is required for |
interaction between CC and NB-ARC and LRR domains |
Solanum tuberosum |
| KinG |
did not coprecipitate with |
(EAL1, SGR7, SHR, AT4G37650) T289I-GFP |
Arabidopsis thaliana |
| CVVM motif site |
is important for |
binding to TGB1 |
Nicotiana benthamiana |
| Trp-92 in BrpHL1a |
is |
critical for the interaction with (GL3, MYC6.2, AT5G41315) |
Brassica rapa |
| tetratricopeptide repeat motifs |
mediate |
protein-protein interactions |
|
| KinG |
coprecipitated with |
mobile SHR-GFP |
Arabidopsis thaliana |
| ƊCH KinG |
interacted with |
(DSP3, SIEL, SIEL1, AT3G08800) |
Arabidopsis thaliana |
| (ARAKIN, ATMEKK1, MAPKKK8, MEKK1, AT4G08500) and (ANQ1, ATMKK6, MKK6, SUMM4, AT5G56580) |
associate with each other in |
vivo |
Nicotiana benthamiana |
| kinesin domain of KinG |
is essential for |
interaction with (DSP3, SIEL, SIEL1, AT3G08800) |
Arabidopsis thaliana |
| yeast two-hybrid screening |
was used to screen for |
interacting partners with ETHYLENE RESPONSE1 (AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) and (ETR2, AT3G23150) |
Arabidopsis thaliana |
| interactions between BrpHL1a W92R and (GL3, MYC6.2, AT5G41315) |
were |
hardly detectable in BiFC experiments |
Brassica rapa |
| interactions between BrpHL1a and (GL3, MYC6.2, AT5G41315) |
were |
strong in BiFC experiments |
Brassica rapa |
| pull-down assays |
showed |
relative interaction strengths similar to BiFC |
Brassica rapa |
| (ATCIPK6, CIPK6, SIP3, SNRK3.14, AT4G30960) |
physically interacts with |
(AIP1, AtAIP1, HAI2, HON, AT1G07430) |
|
| (AHG3, ATPP2CA, PP2CA, AT3G11410) |
does not have physical interaction with |
(ATCIPK23, CIPK23, LKS1, PKS17, SnRK3.23, AT1G30270) and (AtCIPK16, CIPK16, SnRK3.18, AT2G25090) |
|
| each FNR-binding domain |
is able to bind |
two FNR molecules |
Arabidopsis thaliana |
| (DSP3, SIEL, SIEL1, AT3G08800) |
directly interacts with |
KinG |
Arabidopsis thaliana |
| RTCS protein |
can heterointeract with |
RTCS-like |
Zea mays |
| critical amino acids in BrpHL1a |
when mutated |
interaction would be disrupted |
Brassica rapa |
| differences in lignification in roots and anthers in OsFBK1 transgenics |
is due to |
protein-protein interaction between OsFBK1 and OsCCR14 |
Oryza sativa |
| OsPP18 |
does not interact with |
rice SAPK family members |
Oryza sativa |
| ZmFNR-ZmFD complex |
was used for studying |
AtFNR-AtFD interaction |
Zea mays; Arabidopsis thaliana |
| C-terminal domain of ZEITLUPE (ADO1, FKL2, LKP1, ZTL, AT5G57360) FLAVIN-BINDING, KELCH REPEAT, F-BOX1 (ADO3, FKF1, AT1G68050) and LOV KELCH PROTEIN2 (ADO2, LKP2, AT2G18915) |
is |
typical protein-protein interaction domain composed of Kelch repeats |
|
| Interaction of FD with FNR |
depends on |
charges, hydrophobic forces, and conformational changes of both proteins |
|
| (PPD2, TIFY4B, AT4G14720) |
interacts with |
other proteins belonging to TIFY class II |
Arabidopsis thaliana |
| (AGL62, AT5G60440) |
directly binds |
four C2 proteins ( (AGL36, AT5G26650) (AGL37, PHE1, AT1G65330) (AGL38, PHE2, AT1G65300) and (AGL90, AT5G27960) ) |
|
| yeast two-hybrid screening |
identified |
many putative nonoverlapping interaction proteins |
Arabidopsis thaliana |
| hydrophobic HLH region of (bHLH, AT5G51780) domain |
functions as |
homo- and heterodimerization domain |
|
| (CIPK1, SnRK3.16, AT3G17510) |
does not physically interact with |
(AKT1, ATAKT1, KT1, AT2G26650) |
|
| (FAS1, FUGU2, NFB2, AT1G65470) (ASF1A, AtSP7, SGA2, SP7, AT1G66740) interaction |
is |
positive control for protein interaction assays |
Arabidopsis thaliana |
| thylakoid-associated fibrillin proteins FBN1a and (FBN1b, AT4G22240) |
have been identified as |
candidate interactors of (ATSS4, SS4, SSIV, AT4G18240) N-terminal region |
|
| GST-tagged (CAR5, AT1G48590) |
interacts with |
His-tagged FER-CD |
|
| (AHG3, ATPP2CA, PP2CA, AT3G11410) |
physically interacts with |
(ATCIPK6, CIPK6, SIP3, SNRK3.14, AT4G30960) |
|
| two amino terminal b-boxes |
are involved in |
protein–protein interaction |
Arabidopsis thaliana |
| (AtTic62, Tic62, AT3G18890) peptide |
holds |
AtFNR1-AtFNR2 heterodimer together in back-to-back conformation |
Arabidopsis thaliana |
| (AtSAM1, MAT1, METK1, SAM-1, SAM1, AT1G02500) (AtSAM2, MAT2, SAM-2, SAM2, AT4G01850) and (MAT3, AT2G36880) proteins |
were identified with |
unique peptides from MAT4-FLAG coimmunoprecipitation |
Arabidopsis thaliana |
| Arabidopsis TZFs |
do not directly interact with |
any PB marker proteins |
Arabidopsis thaliana |
| Rca-α |
makes |
Rca-β |
|
| lack of interaction in Y2H and Co-IP |
suggests |
(GRL, LPL3, NAP1, NAPP, AT2G35110) /H3 interaction might be only transient |
Arabidopsis thaliana |
| yeast two-hybrid experiment |
showed |
CpMYB1 can interact with CpbHLH1 and CpbHLH2 |
Chimonanthus praecox |
| GsCBRLK VD |
is responsible for |
interaction with GsPM30 |
Glycine max |
| (AHG3, ATPP2CA, PP2CA, AT3G11410) |
does not physically interact with |
(ATCIPK23, CIPK23, LKS1, PKS17, SnRK3.23, AT1G30270) |
|
| InLYP1 L9A |
could no longer interact with |
(ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) or (ASK4, SK4, AT1G20140) |
Arabidopsis thaliana |
| (AHG1, AT5G51760) |
physically interacts with |
(ATCIPK6, CIPK6, SIP3, SNRK3.14, AT4G30960) |
|
| (ATFKBP12, FKBP12, FKP12, AT5G64350) in yeast two-hybrid (Y2H) assays |
interacted strongly with |
(CCT, CRP, MED12, AT4G00450) part of CO |
Arabidopsis thaliana |
| regulatory mechanism |
is thought to involve |
disulfide bond structure of oxidized Rca-α docking into the ATP binding site of Rca-β |
|
| protein extracts incubated with a GFP nanobody fused to magnetic beads |
resulted in |
eluting solution included both CO and (ATFKBP12, FKBP12, FKP12, AT5G64350) |
Nicotiana benthamiana |
| cotton GhZFP1 |
interacted with |
(PR-5, PR5, AT1G75040) (pathogenesis-related protein 5) |
Gossypium hirsutum |
| Leu 9 |
is |
critical residue for the F-box domain of InLYP1 to interact with ASK proteins |
Arabidopsis thaliana |
| (ATCIPK6, CIPK6, SIP3, SNRK3.14, AT4G30960) |
physically interacts with |
AIP1H (HAI3, AT2G29380) |
|
| related TZFs |
have been shown to interact with |
numerous proteins |
|
| (BHLH039, bHLH39, ORG3, AT3G56980) |
binds |
LONG HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
|
| (ATCIPK23, CIPK23, LKS1, PKS17, SnRK3.23, AT1G30270) |
physically interacts with |
AIP1H (HAI3, AT2G29380) |
|
| SPINDLY (SPY) |
interacts with |
PSEUDO-RESPONSE REGULATOR 5 (APRR5, PRR5, AT5G24470) |
|
| (GRL, LPL3, NAP1, NAPP, AT2G35110) ;1 homodimer |
is |
positive control for protein interaction assays |
Arabidopsis thaliana |
| regulatory role of (AtUVR8, UVR8, AT5G63860) |
might be influenced by |
MYB13-interacting proteins |
|
| transient bimolecular fluorescence complementation (BiFC) assays in Nicotiana benthamiana |
confirmed |
strong YFP nuclear–cytosolic signal with the (CCT, CRP, MED12, AT4G00450) part of CO |
Nicotiana benthamiana |
| Y2H analysis |
showed |
no interaction of (FAS1, FUGU2, NFB2, AT1G65470) (FAS2, MUB3.9, NFB01, NFB1, AT5G64630) and (ATMSI1, MEE70, MSI1, AT5G58230) with (GRL, LPL3, NAP1, NAPP, AT2G35110) ;1 |
Arabidopsis thaliana |
| S-tagged CO (S·CO) |
was co-expressed with |
His-tagged (ATFKBP12, FKBP12, FKP12, AT5G64350) (H·FK) |
Escherichia coli |
| AIP1H (HAI3, AT2G29380) |
physically interacts with |
(ATCIPK6, CIPK6, SIP3, SNRK3.14, AT4G30960) |
|
| (RUS1, WXR3, AT3G45890) and (RUS2, WXR1, AT2G31190) proteins |
interacted in |
yeast-two-hybrid analysis |
|
| distinct interacting domains of TTP |
determine |
protein interactions |
|
| InLYP1 L9A |
interaction with ASK4 was |
abolished |
Arabidopsis thaliana |
| Y2H screening |
identified |
(CLF, ICU1, SDG1, SET1, AT2G23380) (ACG1, ATMSI4, FVE, MSI4, NFC04, NFC4, AT2G19520) /MULTICOPY SUPPRESSOR OF IRA1 4, and (ATRING1B, RING1B, AT1G03770) as TCP7-interacting proteins |
Arabidopsis thaliana |
| second dsRBD |
primary function is associated with |
protein–protein interactions |
|
| Y2H assay testing the interaction between (ATFKBP12, FKBP12, FKP12, AT5G64350) and the VP-VA mutated form of the (CCT, CRP, MED12, AT4G00450) domain |
showed |
no significant difference from the interaction with the WT domain |
Arabidopsis thaliana |
| InLYP1 L40A |
could still interact with |
at least one ASK protein |
Arabidopsis thaliana |
| (TN13, AT3G04210) |
interacts with |
(EMB3113, PRPS5, RPS5, SCA1, uS5c, AT2G33800) |
Nicotiana benthamiana |
| interaction of (ATCIPK14, ATSR1, CIPK14, PKS24, SnRK3.15, SR1, AT5G01820) /13 with (CIPK5, SnRK3.24, AT5G10930) |
was verified by |
co-immunoprecipitation (Co-IP) |
Cajanus cajan |
| plant-specific protein MACERATOR 4 (CORD4, MACET4, AT1G23790) /CORTICAL MICROTUBULE DISORDERING 4 |
interacts with |
AtAUG7 |
|
| GsBET11a |
could associate with |
all GsCRCK1s and AtCRCK1 |
Glycine max; Arabidopsis thaliana |
| at least some PPR-like domains |
mediate |
protein-protein interactions |
|
| FtsZ protein–protein interactions |
occurs in |
Physcomitrella patens |
Physcomitrella patens |
| (GRL, LPL3, NAP1, NAPP, AT2G35110) and individual H3 histone variants |
were tested for |
interactions |
Arabidopsis thaliana |
| VD22 (N-terminal 56-amino acid region of GsCBRLK) |
is sufficient to interact with |
GsBET11a |
Glycine max |
| six proteins |
were isolated repeatedly |
yeast two-hybrid screening |
Cajanus cajan |
| heterodimers within group S1 or within group C |
were not formed |
within group S1 or within group C |
Malus domestica |
| conserved protein interaction |
is |
strong hint regarding vital regulatory mechanism in plants |
|
| tomato (ATFKBP12, FKBP12, FKP12, AT5G64350) |
had been previously identified as |
putative interactor of a CO homolog (SlCOL1) |
Solanum lycopersicum |
| fluorescence complementation between Chlamydomonas CrCO and Arabidopsis (ATFKBP12, FKBP12, FKP12, AT5G64350) |
reported |
strong signal |
Nicotiana benthamiana |
| co-immunoprecipitation (Co-IP) assay |
showed that TLP precipitates with |
either full-length or N-terminally truncated (SGC, AT4G18530) but not with unrelated Arabidopsis cold-shock protein 3 (ATCSP3, CSP3, AT2G17870) |
Arabidopsis thaliana; Nicotiana benthamiana |
| kelch motif-containing (ACBP4, AtACBP4, AT3G05420) (acyl-CoA-binding protein 4) |
could interact with |
ethylene-responsive element binding protein (ATEBP, EBP, ERF72, RAP2.3, AT3G16770) |
Arabidopsis thaliana |
| Y2H screening of OsMTD2 protein |
did not identify |
ANTH protein |
Oryza sativa |
| K domain |
is sufficient for |
protein–protein interaction |
|
| CcCIPK14 |
was used as bait to screen |
yeast cDNA library prepared from pigeon pea root RNA |
Cajanus cajan |
| GsCBRLK VD |
is responsible for |
interaction with GsMSR5a |
Glycine max |
| GsCBRLK VD |
fulfills a crucial role in |
mediating protein interactions |
Glycine max |
| (AHA2, AtHA2, HA2, PMA2, AT4G30190) |
was found to interact with |
four VAMP7Cs (VAMP711–714) |
Arabidopsis thaliana |
| in vitro pull-down assays |
conducted to confirm |
physical interactions between (AtbZIP, bZIP, AT1G68880) proteins |
|
| electropositive environment of active site of thioredoxin f |
is |
ideal electro-complementary platform for thioredoxin z docking |
Arabidopsis thaliana |
| yeast two-hybrid (Y2H) assays |
investigated |
interactions among six (AtbZIP, bZIP, AT1G68880) members |
Malus domestica |
| cytoplasmic SNARE domain of GsBET11a |
is responsible structure for |
GsBET11a–GsCBRLK interaction |
Glycine max |
| positive clones identified |
corresponded to |
15 different proteins |
Cajanus cajan |
| ID-NLR protein |
self-associates in vivo and in planta through |
CC and (ANK, BDA1, AT5G54610) domains |
|
| P3 and P3IP1 |
interacted with |
each other |
Nicotiana benthamiana |
| non-canonical VP motif of (AT-PHH1, ATCRY2, CRY2, FHA, PHH1, AT1G04400) |
has been recently shown to |
interact with (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) (Constitutive Photomorphogenesis 1) and (SPA1, AT2G46340) |
Arabidopsis thaliana |
| RNA-binding proteins |
are |
AN-interacting proteins |
Arabidopsis thaliana |
| Arabidopsis seed-specific TZF4-6 |
interacted with |
(RD21, RD21A, AT1G47128) (responsive to dehydration 21A) |
Arabidopsis thaliana |
| InLYP1 |
can interact with |
(AtGLDP1, GLDP1, AT4G33010) and (AtGLDP2, GLDP2, AT2G26080) |
Arabidopsis thaliana |
| bHLH6 and (ATSPX4, SPX4, AT5G15330) interaction |
was confirmed by |
BiFC and Co-IP assays |
|
| MdbZIP80 with disrupted α-helical structure |
no longer interacted with |
MdbZIP2 or MdbZIP39 |
Malus domestica |
| interaction between N- and C-terminal domains of γ-gliadin |
was confirmed in planta by |
FRET-FLIM assay |
Nicotiana tabacum |
| polypeptide with the same apparent molecular mass of (BIP, BIP2, AT5G42020) |
is co-selected with |
zein–GFP |
|
| (CN, SPR2, TOR1, AT4G27060) and (AAA1, ATKTN1, BOT1, ERH3, FRA2, FRC2, FRC4, FTR, KATANIN, KTN1, LUE1, AT1G80350) |
interaction dynamics between |
interaction dynamics |
|
| (SPL11, AT1G27360) |
was coimmunoprecipitated with |
OsMTD2 |
Nicotiana tabacum |
| (CES, HAF, AT1G25330) |
binds |
LONG HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
|
| AP21967 |
has no unspecific effects on |
protein dimerization |
|
| An PGII, a PG isoform II from Aspergillus niger |
is required for interaction with |
Pv (ATPGIP2, PGIP2, AT5G06870) |
Aspergillus niger; Phaseolus vulgaris |
| yeast-two-hybrid (Y2H) screening |
identified |
five candidate proteins |
Oryza sativa |
| RXLR31154 and VpPsbP interaction |
takes place in |
chloroplast |
Nicotiana benthamiana |
| both domains of γ-gliadin |
are able to interact in |
in vitro yeast-two hybrid assay |
Saccharomyces cerevisiae |
| AtAPH-1 and presenilin 2 |
showed possible interaction with |
E=20% |
Arabidopsis thaliana |
| p21 peptide |
was analyzed for interactions with |
Pc PCNA proteins |
Phaseolus coccineus |
| ST (truncated version of GsBET11a containing SNARE domain and TMD) |
exhibited interaction with |
GsCBRLK |
Glycine max |
| binding studies with entire FLU protein |
have failed to demonstrate |
trilateral cooperativity for control of ALA synthesis |
|
| BET1s and CRCK1s interaction |
is |
conserved and direct interaction |
Glycine max; Arabidopsis thaliana |
| CcCIPK13 |
interacted with |
CcGRA3, CcCIPK5, CcADF2, CcCYTb, CcAP4L and CcCBL1 |
Cajanus cajan |
| (bHLH106, STC8, AT2G41130) |
binds |
LONG HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
|
| (AtERF98, AtTDR1, ERF98, TDR1, AT3G23230) |
binds |
LONG HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
|
| mass spectrometry of immunoprecipitates |
identified |
WPP domain-interacting tail-anchored protein 2 ( (WIT2, AT1G68910) 72 kDa) |
Arabidopsis thaliana |
| (WIT1, AT5G11390) |
coimmunoprecipitated with |
(WIP1, AT4G28240) |
Arabidopsis thaliana |
| FLAGELLIN SENSING 2 (ATFLS2, FLS2, AT5G63580) -BAK1 interactions |
are likely stabilized by |
protein-protein and protein-lipid interactions |
|
| protein co-precipitated with OsCAS from transgenic Arabidopsis lines |
was not detected |
in transgenic Arabidopsis lines |
Arabidopsis thaliana |
| (ATSNAP33, ATSNAP33B, SNAP33, SNP33, AT5G61210) |
shows weak interaction with |
(ATEXO70B2, EXO70B2, AT1G07000) |
Arabidopsis thaliana; Saccharomyces cerevisiae |
| OsCAS |
could not interact with |
SAT in planta or in yeast |
Oryza sativa |
| Arabidopsis MADS-domain protein AGAMOUS (AG) |
interacts with |
(AGL4, SEP2, AT3G02310) |
Arabidopsis thaliana |
| AtPEN-2 and (APS1, ATPS1, AT3G22890) |
showed significant decreases in donor fluorescence lifetime indicating interactions with |
E=24% |
Arabidopsis thaliana |
| exon D |
is essential for |
Rab10 binding to myosin V tails in vivo |
Homo sapiens |
| (BBX16, COL7, AT1G73870) |
binds |
LONG HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
|
| (ATEOL1, ETO1, AT3G51770) |
specifically interacts with |
Type 2 of ACC synthase (At-ACS5 and Sl-ACS3) |
Arabidopsis thaliana; Solanum lycopersicum |
| GluB subunits |
interact with |
GluA precursor |
Oryza sativa |
| OsSR34 and OsFKBP20-1b |
associate in |
the nucleus |
Oryza sativa |
| glycine to charged residue substitution in BUZZ catalytic domain |
might affect |
protein-protein interactions |
Brachypodium distachyon |
| OsFKBP20-1b and OsSR34 |
physically interact |
|
Oryza sativa |
| (CAR6, EHB1, AT1G70800) |
directly interacts with |
FER-CD |
|
| GST-tagged (CAR9, AT1G70790) |
interacts with |
His-tagged FER-CD |
|
| His-ZmTFCB |
was clearly detected in |
pull-down fraction by GST-ZmCCT5 |
Zea mays |
| PpE18 |
influences |
interaction between NbANKr2 and NbAPX3-1 |
Nicotiana benthamiana |
| CaDeSI2 interaction with CaAITP1 |
occurs within |
cell nucleus |
Nicotiana benthamiana |
| CYCLIN D3;2 ( (CYCD3, CYCD3;1, AT4G34160) ;2) and CYCLIN DEPENDENT KINASE A1 (CDKA;1) proteins |
can interact |
directly |
Arabidopsis thaliana |
| (CMR1, PANS1, AT3G14190) |
likely interacts with the APC/C beyond being |
APC/C target |
Arabidopsis thaliana |
| correlation between content of AtMic60 and (TOM40, AT3G20000) in MTL complex |
highlighted |
specific link between AtMic60 and (TOM40, AT3G20000) |
Arabidopsis thaliana |
| mTfUFO |
interacted with |
(ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) |
|
| Arabidopsis MADS-domain protein AGAMOUS (AG) |
interacts with |
(AGL9, SEP3, AT1G24260) |
Arabidopsis thaliana |
| (CAR9, AT1G70790) |
directly interacts with |
FER-CD |
|
| ZmCCT5 |
was found among |
23 candidate proteins |
Zea mays |
| NbANKr2 |
interacts with |
NbAPX3-1 |
Nicotiana benthamiana |
| (DDP1, PTM, AT5G35210) deletion of OsSYP132 |
did not affect |
interaction with OsVAMP721/722 |
Oryza sativa |
| SUFC |
is |
a potential interacting protein of NCR343 |
Medicago truncatula |
| DIV |
would need to be |
spatially and temporally associated with the DRIFs |
Antirrhinum majus |
| p24δ9 and ERD2a interaction |
much higher at |
pH 6.0 than at pH 7.5 |
Nicotiana tabacum |
| OsFKBP20-1b (FK506-binding protein 20-1b) |
interacts with |
(AtSR45, RNPS1, SR45, AT1G16610) |
Oryza sativa |
| (FER, AT3G51550) phosphorylation activity |
attenuates |
interaction between (CAR9, AT1G70790) and (FER, AT3G51550) |
|
| SlMPK8-FLAG |
co-immunoprecipitated with |
SlERF.C1-HA |
Solanum lycopersicum |
| CaDeSI2 |
interacts with |
CaAITP1 |
Saccharomyces cerevisiae |
| Y2H assay |
was used to identify |
putative ZmTFCB interactors in developing kernels |
Zea mays |
| ovate family proteins (ATOFP1, OFP1, AT5G01840) and (ATOFP5, OFP5, AT4G18830) |
interact with |
BEL proteins |
Arabidopsis thaliana |
| FRET efficiency for AtPEN-2 N74L and (AtPPsPase1, ATPS2, PPsPase1, PS2, AT1G73010) pair |
was very low (E=1%) clearly suggesting |
no interaction occurs between AtPEN-2 N74L and (AtPPsPase1, ATPS2, PPsPase1, PS2, AT1G73010) |
Arabidopsis thaliana |
| (ATSIZ1, SIZ1, AT5G60410) |
inhibits sumoylation of FLC through |
direct interaction with (AGL25, FLC, FLF, RSB6, AT5G10140) |
Arabidopsis thaliana |
| KNATM-B |
selectively interacts with |
BEL proteins |
|
| most of the investigated γ-secretase proteins |
may interact with |
each other |
Arabidopsis thaliana |
| (ATEOL1, ETO1, AT3G51770) |
does not interact with |
Type 1 (Sl-ACS2) or Type 3 (Sl-ACS4) |
Solanum lycopersicum |
| cytokinin |
inhibits |
interaction between Type 2 (ACS, AT5G36880) isozymes and (ATEOL1, ETO1, AT3G51770) protein |
|
| SpOASS |
interacts with |
WtSAT |
Spinacia oleracea; Citrullus lanatus |
| overexpressed mFLC |
could be scavenged by |
endogenous (AGL25, FLC, FLF, RSB6, AT5G10140) |
Arabidopsis thaliana |
| (SPK1, AT4G16340) interaction with inactive form of (ARAC3, ATROP6, RAC3, RHO1PS, ROP6, AT4G35020) |
was confirmed using |
in vivo fluorescence resonance energy transfer (FRET) analysis |
Arabidopsis thaliana |
| western blotting of BN gel with LeCDJ1 antibody |
showed no positive signal |
interaction between LeCDJ1 and protein complexes |
Solanum lycopersicum |
| some other MTL complex components |
not affected by absence of |
AtMic60 |
Arabidopsis thaliana |
| two APC/C degradation motifs (D and DEN boxes) |
are required for |
Y2H interaction with (AtCDC20.1, CDC20.1, AT4G33270) |
Arabidopsis thaliana |
| GmCRY1b-Flag and STF1-GFP |
have in vivo interaction detected by |
co-immunoprecipitation (coIP) assay in Nicotiana benthamiana leaf cells |
Nicotiana benthamiana |
| potato BEL1-like proteins |
have |
binding affinities that vary considerably |
Solanum tuberosum |
| LeCDJ1 |
interacts with |
cpHsp70 |
Solanum lycopersicum |
| yeast two-hybrid screen |
identified |
histone (H1.2, HON2, AT2G30620) (previously called H1-2) as a DME-interacting protein |
Arabidopsis thaliana |
| (AtHsp90-7, AtHsp90.7, HSP90, HSP90.7, SHD, AT4G24190) |
was previously shown to interact directly with |
(ATSAGT1, GT, SAGT1, SGT1, UGT74F2, AT2G43820) (SUPPRESSOR OF G2 ALLELE OF (ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) ) |
Arabidopsis thaliana |
| StBEL13 |
has |
most robust interactions with NTH1 and -15 |
Solanum tuberosum |
| AtAPH-1 and presenilin 1 |
showed possible interaction with |
E=19% |
Arabidopsis thaliana |
| protein interaction network |
based mainly on |
Mα-Mβ and Mα-Mγ interactions |
|
| VESICLE-ASSOCIATED MEMBRANE PROTEIN 711 (ATVAMP711, VAMP711, AT4G32150) and Arabidopsis PM H+-ATPase (AHA1, HA1, OST2, PMA, AT2G18960) interaction |
occurs at |
C-termini |
Arabidopsis thaliana |
| StBEL33 |
has |
strongest interactions with POTH1, NTH22, and NTH20 |
Solanum tuberosum |
| Arabidopsis ortholog of PGSC0003DMP400035788 (AT3G46870) |
was also identified as |
Zn2+-immobilized metal affinity chromatography interaction protein in mitochondria |
Arabidopsis thaliana |
| E. coli FtsZ |
interacts with |
PpFtsZ2-2 |
Physcomitrella patens |
| HSP90.3 and (CPR1, CPR30, AT4G12560) |
may not directly associate |
|
Nicotiana benthamiana |
| pH change |
only affected |
interaction of RFP-p24δ5 with ERD2a-YFP |
Nicotiana tabacum |
| STMADS proteins |
have a capacity to interact with |
other MADS box proteins |
|
| detected modifications of AtFNR |
do not interfere with |
(AtTic62, Tic62, AT3G18890) binding |
Arabidopsis thaliana |
| acidic (N-alpha-acetylated) AtFNR forms |
were bound more by |
both AtFDs compared with basic (nonacetylated) AtFNRs |
Arabidopsis thaliana |
| BBX24IR |
interacts with |
protein encoded by the constitutively spliced transcript |
|
| OMT interaction with EGT2 |
was observed in |
nucleus and cytoplasm |
Hordeum vulgare |
| bimolecular fluorescence complementation (BiFC) assays |
confirmed |
interaction between OsPTD1 and OsSHOC1 |
Nicotiana tabacum |
| Yellow fluorescent protein (YFP) signals |
were detected in |
cells co-expressing N-(HhH) 2 -cYFP + OsPTD1-nYFP |
Nicotiana tabacum |
| yeast two-hybrid (Y2H) |
examined |
potential interaction between (AHL29, SOB3, AT1G76500) and PIFs |
Arabidopsis thaliana |
| Lys-96 in AtFNR2 |
is at |
interface between two monomers in heterodimeric complex |
Arabidopsis thaliana |
| (AtbZIP63, bZIP63, BZO2H3, AT5G28770) |
works through |
protein-protein interactions |
Arabidopsis thaliana |
| 395 non-reciprocal interactions between proteins plus 77 confirmed self-interactions |
could be deduced from |
protein interaction database |
Arabidopsis thaliana |
| StBEL family |
display selective interaction with |
tobacco class I-type KNOX proteins |
Solanum tuberosum |
| StBEL interactions with NTH1 |
exhibit |
some of the lowest levels of β-galactosidase activity |
Solanum tuberosum |
| ΔTP DM3 Col-0 |
was co-expressed with |
(DM2h, AT3G44670) Bla-1 |
Nicotiana benthamiana |
| GEF3 and (ARAC4, ATRAC4, ATROP2, ROP2, AT1G20090) interaction |
occurs via |
(ARAC4, ATRAC4, ATROP2, ROP2, AT1G20090) interaction domain |
Arabidopsis thaliana |
| retention of binding to at least one LEAFY (LFY, LFY3, AT5G61850) -interacting protein |
makes |
loss of binding to important co-factor less likely |
|
| EYFP-DIV and ECFP-RAD |
are able to interact |
in vitro |
Nicotiana benthamiana |
| ribosomal or non-ribosomal RACK1 |
may be important for |
mediating protein–protein interactions |
|
| interaction between p24δ5 and p24β2 |
occurred at both pHs |
although greater at pH 7.5 than at pH 6.0 |
Arabidopsis thaliana |
| PANS1ΔDEN |
showed decreased interaction with |
(AtCDC20.1, CDC20.1, AT4G33270) |
Arabidopsis thaliana |
| (SPK1, AT4G16340) |
interacted with |
(ARAC3, ATROP6, RAC3, RHO1PS, ROP6, AT4G35020) |
Nicotiana benthamiana |
| (AGL30, AT2G03060) and (AGL65, AT1G18750) |
can interact with themselves and with each other in presence of |
(AGL66, AT1G77980) or (AGL104, AT1G22130) |
Arabidopsis thaliana |
| difference in hydrophobic residue cluster |
may affect |
protein-ligand interactions |
|
| mutation of lysine 550 to aspartate in (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
abolishes interaction with |
(HY5, TED 5, AT5G11260) |
|
| MID and (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
demonstrates physical association in |
plant extracts |
Nicotiana benthamiana |
| RFP-p24δ9 |
interacts with |
ERD2a-YFP |
Nicotiana tabacum |
| half of (ATUPF1, LBA1, UPF1, AT5G47010) associated proteins |
co-purified with |
DECAPPING 5 (DCP5, AT1G26110) |
Arabidopsis thaliana |
| pre-mRNA processing 4 kinase C (PRP4Kc, AT3G53640) |
may be partner of |
SERRATE (SE) |
|
| minimal fragment comprising N-terminal 67 amino acids of (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
is sufficient to interact with |
MID protein |
|
| (AtRTE1, RTE1, AT2G26070) |
interacts with |
(ATCB5-C, B5 #1, CB5-C, CYTB5-C, AT2G46650) |
Arabidopsis thaliana |
| propensity for protein–protein interaction |
would be much lower when |
much lower concentrations in diluted leaf extracts at 4 °C |
|
| multiple TPR domains |
mediate |
protein-protein interactions |
|
| (GRL, LPL3, NAP1, NAPP, AT2G35110) associated with induced puncta |
can interact with |
marker for (ARP2, ATARP2, WRM, AT3G27000) /3 complex |
Nicotiana benthamiana |
| DRIF1 sequestered in the cytoplasm |
prevented from |
interacting with DIV in the nucleus |
Nicotiana benthamiana |
| DRIF2 and DIV |
interact in |
nucleus but outside the nucleolus |
Nicotiana benthamiana |
| Pb RxLR24 |
seems likely to interact with |
the majority of RABA proteins |
Arabidopsis thaliana |
| Flag-FZP–GFP complex |
identified |
FZP-associated proteins (FAPs) |
Oryza sativa |
| proline-rich region of Las17 |
interacts with |
Src homology domain 3 of myosin I motor proteins |
|
| RING-finger and acidic domains in (ATPGMP, PGM, PGM1, STF1, AT5G51820) and STF2 |
usually involve |
protein-protein interactions |
Glycine max |
| changes in protein S-acylation state |
are hypothesized to modulate |
protein-protein and protein-membrane interactions |
|
| Bt protein |
are not physiologically related |
(EPSPS, AT1G48860) protein |
|
| Y2H screening |
identified |
26 positive clones |
Oryza sativa |
| (AHL29, SOB3, AT1G76500) and (A-PUT2, bHLHb1, PIF5, PIL6, AT3G59060) |
show no interaction |
in yeast two-hybrid assays |
Arabidopsis thaliana |
| plants excited with specific CFP-exciting lights and detected at the YFP emission window |
showed |
nuclear–cytosolic signal indicating fluorescence resonance energy transfer (FRET) effect |
Nicotiana benthamiana |
| (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) and (AS2, AT1G65620) |
are associated with |
(ATHDA6, AXE1, HDA6, HDAC6, RPD3B, RTS1, SIL1, AT5G63110) |
Arabidopsis thaliana |
| fluorescence complementation between Arabidopsis CO and Chlamydomonas CrFKBP12 |
reported |
strong signal |
Nicotiana benthamiana |
| well-known APC/C targets such as cyclins |
do not recover APC/C subunits when used as bait in |
TAP-TAG experiments |
Arabidopsis thaliana |
| (AP2, AtAP2, FL1, FLO2, AT4G36920) MYB and WRKY protein families |
have been shown to contain |
interacting members |
Arabidopsis thaliana |
| (CAR6, EHB1, AT1G70800) |
interacts with |
(FER, AT3G51550) |
|
| (FER, AT3G51550) |
fine-tunes |
association of (FER, AT3G51550) and CARs |
|
| small subset of plasma membrane-localized μ2-YFP and mCherry-CESA6 particles |
were |
colocalized |
Arabidopsis thaliana |
| (AtSAMS3, MAT4, MTO3, SAMS3, AT3G17390) protein |
can interact with |
(AtSAM1, MAT1, METK1, SAM-1, SAM1, AT1G02500) (AtSAM2, MAT2, SAM-2, SAM2, AT4G01850) (MAT3, AT2G36880) and itself |
Arabidopsis thaliana |
| C2 proteins |
participants of |
Mα-Mγ subnetwork |
|
| TGA transcription factor |
can interact with |
Glutaredoxin (GRX) in the nucleus of plant cells |
Arabidopsis thaliana |
| (AIP1, AtAIP1, HAI2, HON, AT1G07430) |
physically interacts with |
(ATCIPK6, CIPK6, SIP3, SNRK3.14, AT4G30960) |
|
| (ATMEK4, ATMKK4, MKK4, AT1G51660) |
co-immunoprecipitated with |
(RGFR1, RGI1, AT3G24240) receptor |
Arabidopsis thaliana |
| TTP carboxyl terminus |
interacts with |
cytoplasmic hCIN85 (human Cbl-interacting protein85) |
|
| (GRL, LPL3, NAP1, NAPP, AT2G35110) /H3 interaction |
occasionally occurs in |
whole cytoplasm and nucleus |
Arabidopsis thaliana |
| yeast two-hybrid screen |
identified SGC-interacting proteins |
14 N-terminally truncated SGCs and nine thaumatin-like proteins (TLPs) |
Arabidopsis thaliana |
| outcomes of NCR343 interactions with putative partners |
require |
further investigation |
Medicago truncatula |
| SubB, SubL and NdhB in SubM |
are required for |
(Lhca5, AT1G45474) binding to the NDH complex |
|
| PPR motifs of AtPPR4 |
do not interact with |
themselves |
Arabidopsis thaliana |
| MiMSP32 |
interacts in planta with fragments of |
phospholipid-transporting ATPase 1-like (SlALA1), leucine aminopeptidase (SlLAPA2), oxophytodienoate reductase 2 (SlOPR2), and tripeptidyl-peptidase 2 (SlTPPII) |
Solanum lycopersicum |
| SAM domain |
is known as |
protein-protein interaction domain |
|
| SE |
is |
potential partner of SKRP |
Arabidopsis thaliana |
| PpE18 |
interacts with |
NbANKr2 |
Nicotiana benthamiana; Phytophthora parasitica |
| GmCHR1 |
uncovers |
opening part of pocket structure in GmHAD1-2 |
Glycine max |
| GS3-1 and GS3-2 |
interact with |
CLG1 |
Oryza sativa |
| small interfering peptides (siPEP) |
contain |
protein–protein interaction domain |
|
| (ATCB5-A, B5 #6, CB5-A, AT1G26340) isoform |
showed the weakest interaction with |
(AtRTE1, RTE1, AT2G26070) |
Arabidopsis thaliana |
| SubA and SubE |
did not interact with |
SubB in the absence of (PnsL1, PPL2, AT2G39470) (SubL) |
|
| SAM domain in animals |
is known as |
protein-protein interaction domain |
|
| BBX22IR |
interacts with |
protein encoded by the constitutively spliced transcript |
|
| (CAR9, AT1G70790) |
interacts with |
(FER, AT3G51550) |
|
| (CAR7, AT1G70810) |
does not interact with |
(FER, AT3G51550) |
|
| EGT2 fused with cYFP at C-terminus (EGT2 (−TGA)-cYFP) |
displayed interaction with |
HMT |
Hordeum vulgare |
| (ATCDC5, ATMYBCDC5, CDC5, AT1G09770) |
is |
potential partner of SKRP |
Arabidopsis thaliana |
| STRING analysis of BUZZ |
predicts interaction with |
(CYCT1;1, AT1G35440) |
Brachypodium distachyon |
| (CAR9, AT1G70790) |
interacts specifically with |
(BUPS1, PIR1, AT4G39110) |
|
| (CAR9, AT1G70790) 3M |
interaction with FER is not significantly affected by |
(FER, AT3G51550) phosphorylation activity |
|
| GFP-FLAG |
did not co-immunoprecipitate with |
SlERF.C1-HA |
Solanum lycopersicum |
| (ATCPK1, CPK1, AT5G04870) |
known to interact with |
14-3-3 proteins |
Arabidopsis thaliana |
| mTfUFO |
lost ability to interact with |
TfLFY |
|
| (ACBP2, AtACBP2, AT4G27780) |
interacts with |
RELATED TO APETALA2.3 (ATEBP, EBP, ERF72, RAP2.3, AT3G16770) |
Arabidopsis thaliana |
| both AtFNR isoforms |
interact with |
both AtFDs through identical salt bridges |
Arabidopsis thaliana |
| 20 proteins |
were regarded as |
possible interacting proteins of NCR343 |
Medicago truncatula |
| interaction of the two proteins |
was validated in |
planta |
Solanum lycopersicum |
| CaDeSI2 |
is |
bona fide interacting partner of CaAITP1 |
Capsicum annuum |
| Colocalization ratios between μ2-YFP and CLC-mOrange |
significantly higher than |
coincident colocalization between randomly distributed particle populations |
Arabidopsis thaliana |
| (FER, AT3G51550) |
physically interacts with |
subset of CAR proteins |
|
| two proteins |
might be |
false-positive results of yeast-two-hybrid experiment |
Hordeum vulgare |
| NCR peptides |
are presumed to |
interact with S. meliloti proteins directly |
Medicago truncatula |
| (AtC2, AtGAP1, C2, CAR4, AT3G17980) |
interacts with |
(FER, AT3G51550) |
Arabidopsis thaliana |
| (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) |
directly binds to |
(ATMAPK3, ATMPK3, MPK3, AT3G45640) and (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) |
|
| (Nemp_B, PNET2, PNET2_B, AT5G67610) C terminus recruitment by (KAKU4, AT4G31430) |
is independent of |
physical interaction with (KAKU4, AT4G31430) detectable by yeast two-hybrid |
|
| C-terminally truncated CI(1–521 aa) |
could interact with |
Rsc4-3 in yeast |
|
| yeast three-hybrid assay |
showed that |
GS3 can influence the interaction between (DEP1, AT5G53850) /GGC2 and RGB1 |
Oryza sativa |
| (CAR9, AT1G70790) |
interacts specifically with |
(FER, AT3G51550) |
|
| SlAS2 |
can inhibit |
dimerization of SlTCP24 and SlTCP29 proteins |
Solanum lycopersicum |
| dppF1 |
is |
a potential interacting protein of NCR343 |
Medicago truncatula |
| full-length ZmCCT5 and ZmTFCB |
showed only weak interaction on |
TDO medium |
Zea mays |
| PsRGL1 |
identified interaction partner |
PsSOC1 |
Paeonia suffruticosa |
| GST-tagged (CAR1, AT1G50180) |
interacts with |
His-tagged FER-CD |
|
| MiMSP32 -sp |
physically interacts with |
full-length Arabidopsis (ATOPR2, OPR2, AT1G76690) |
Nicotiana benthamiana |
| (CAR5, AT1G48590) |
directly interacts with |
FER-CD |
|
| (CAR1, AT1G50180) |
interacts with |
(FER, AT3G51550) |
Arabidopsis thaliana |
| CaDeSI2 |
interacts with |
CaAITP1 |
Nicotiana benthamiana |
| (CAR5, AT1G48590) |
interacts with |
(FER, AT3G51550) |
Arabidopsis thaliana |
| (AGL25, FLC, FLF, RSB6, AT5G10140) EXPRESSOR (FLX, AT2G30120) and -LIKE4 (FLL4, FLX4, AT5G61920) |
interact with each other |
each other |
Arabidopsis thaliana |
| QdNAC QD08G038820 and QdMYB QD01G020890 gene products |
can specifically interact |
with each other |
Quercus dentata |
| STRING analysis of BUZZ |
predicts interaction with |
(CYCT1;3, AT1G27630) |
Brachypodium distachyon |
| leucine zipper domains |
facilitate |
interaction with (FLA, FRI, RSB7, AT4G00650) |
Arabidopsis thaliana |
| STRING analysis of BUZZ |
predicts interaction with |
(CYCH;1, AT5G27620) |
Brachypodium distachyon |
| (ATCPK5, CPK5, AT4G35310) and (ATCDPK2, ATCPK11, CDPK2, CPK11, AT1G35670) |
do not immunoprecipitate with |
MTP8-C |
Nicotiana benthamiana |
| RAD and DIV |
may compete for |
third protein |
Antirrhinum majus |
| vrn-A1 acts as a protein |
should appear as |
Ta VRN1- Ta HOX1 protein complex |
Triticum aestivum |
| Ta VRN1- Ta HOX1 protein complex |
because of |
direct binding between Ta VRN-A1 and Ta HOX1 |
Triticum aestivum |
| tetratricopeptide repeat (TPR) region |
may act as |
protein–protein interaction domain |
|
| phosphorylation |
might perhaps be relevant for |
interaction with other interactors |
|
| OsPIP2;2 |
probably recruits OsPIP1;3 through |
physical interaction |
Xenopus laevis |
| (RUS1, WXR3, AT3G45890) and (RUS2, WXR1, AT2G31190) proteins |
physically interact with each other in vivo |
each other |
|
| (GRL, LPL3, NAP1, NAPP, AT2G35110) /H3 interaction |
possibly occurs via |
additional protein components |
Arabidopsis thaliana |
| OsSR34-nEYFP and cEYFP-OsFKBP20-1b constructs |
showed reconstitution of |
yellow fluorescent protein (YFP) signal in the nucleus |
Oryza sativa |
| heterodimers containing small interfering peptides (siPEP) with DNA-binding domains |
can compete with |
transcription factor for same DNA-binding domain |
|
| RAD antagonising DIV in the dorsal regions of the flower |
is by |
inhibiting the interaction between the DRIFs and DIV |
Antirrhinum majus |
| MADS and HOX proteins |
have |
direct binding |
Triticum aestivum |
| co-immunoprecipitation of p24δ5 and (ERD2B, AT3G25040) |
only observed when performed at |
pH 6.0 and not at pH 7.5 |
Arabidopsis thaliana |
| (CPR1, CPR30, AT4G12560) associates with |
tested if |
(AtHsp90-7, AtHsp90.7, HSP90, HSP90.7, SHD, AT4G24190) could associate with SCF (CPR1, CPR30, AT4G12560) complex through F-box protein |
Nicotiana benthamiana |
| immunoprecipitation of p24β2 |
did not cause co-immunoprecipitation of |
(ERD2B, AT3G25040) |
Arabidopsis thaliana |
| (ATGPX3, GPX3, GPXL3, AT2G43350) |
participates in |
unbinding state |
Arabidopsis thaliana |
| (AGL66, AT1G77980) and (AGL104, AT1G22130) proteins |
unable to interact directly but can interact with each other in yeast when |
(AGL30, AT2G03060) or (AGL65, AT1G18750) is present as bridge |
Arabidopsis thaliana |
| TfUFO |
interacted with |
(ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) |
|
| this pattern |
suggested that |
these residues may be essential for protein–protein contacts |
|
| deletion mutant lacking the CC domain |
interacted very efficiently with |
ERD2a-YFP |
Nicotiana tabacum |
| (AtRTE1, RTE1, AT2G26070) |
interacts with |
(ATCB5-B, B5 #4, CB5-B, CYTB5-D, AT2G32720) |
Arabidopsis thaliana |
| LisH ( (AtPRP4, AtSAP60, EMB2776, LIS, PRP4, AT2G41500) homology domain) and CtLH (C-terminal to the LisH motif) domains of (TPL, WSIP1, AT1G15750) |
are important for |
transcription factor binding |
Arabidopsis thaliana |
| (WIT2, AT1G68910) |
was found in pull-down fraction from |
transgenic plants expressing YFP-XI-i-Δmotor |
Arabidopsis thaliana |
| effect of p24δ5 on the localization of ERD2a |
mediated by |
direct interaction between both proteins |
Nicotiana tabacum |
| VpGRP2A |
is |
VpRH2-interacting protein |
Vitis vinifera |
| MULTICOPY SUPPRESSOR OF IRA 4 (ACG1, ATMSI4, FVE, MSI4, NFC04, NFC4, AT2G19520) |
co-purified with |
(EBS, AT4G22140) |
Arabidopsis thaliana |
| FRET analysis |
showed |
(ATWNK8, EIP1, WNK8, AT5G41990) association with (ATRGS1, RGS1, AT3G26090) increased upon treatment with 6% D-glucose |
Arabidopsis thaliana |
| (ACBP, ACBP1, AtACBP1, AT5G53470) and (ACBP2, AtACBP2, AT4G27780) |
interact with |
(ERF74, RAP2.12, AT1G53910) |
Arabidopsis thaliana |
| high level of expression of RAD |
is needed to |
completely disrupt the formation of DRIF2–DIV complexes inside the nucleus |
Nicotiana benthamiana |
| potential association of OsCCaMK with sulfhydryl group-containing molecules/proteins through its cysteine residue |
may stem from |
phenotypes of OsCCaMK in legume ccamk mutant |
Oryza sativa; Medicago truncatula; Lotus japonicus |
| new function for (ATDEK1, DEK1, EMB1275, EMB80, AT1G55350) |
is likely to involve |
novel protein–protein interactions |
|
| (AtHsp90-7, AtHsp90.7, HSP90, HSP90.7, SHD, AT4G24190) |
is known to interact with |
(ATSAGT1, GT, SAGT1, SGT1, UGT74F2, AT2G43820) (SUPPRESSOR OF G2 ALLELE OF (ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) ) |
Arabidopsis thaliana |
| immunoprecipitation of p24β2 |
caused co-immunoprecipitation of |
p24δ5 |
Arabidopsis thaliana |
| RAD and DIV |
do not interact directly with one another |
direct interaction |
Antirrhinum majus |
| SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (AGL22, FAQ1, SVP, AT2G22540) and TERMINAL FLOWER 2 (AtLHP1, LHP1, TFL2, AT5G17690) |
interaction requires |
chromoshadow domain of TERMINAL FLOWER 2 (AtLHP1, LHP1, TFL2, AT5G17690) |
Arabidopsis thaliana |
| Pro35S:6Myc-AtANN4 S46A |
reduces |
interaction between (ANNAT4, AtANN4, AT2G38750) and (ATCBL10, CBL10, SCABP8, AT4G33000) |
Arabidopsis thaliana |
| (BRD1, AT1G20670) (BRD2, AT1G76380) and (BRD13, AT5G55040) |
interact with |
(ATBRM, BRM, CHA2, CHR2, FFO3, AT2G46020) (BRAHMA) |
Arabidopsis thaliana |
| protein palmitoylation |
plays essential role in |
protein-protein interactions |
|
| MULTICOPY SUPPRESSOR OF IRA 4 (ACG1, ATMSI4, FVE, MSI4, NFC04, NFC4, AT2G19520) |
is known to interact with |
(CLF, ICU1, SDG1, SET1, AT2G23380) |
Arabidopsis thaliana |
| (ATWNK8, EIP1, WNK8, AT5G41990) phosphorylation preference |
correlated with |
stronger interactions in co-precipitation assays using purified proteins |
Arabidopsis thaliana |
| transgenic mFLC |
may form a complex with |
endogenous (AGL25, FLC, FLF, RSB6, AT5G10140) |
Arabidopsis thaliana |
| (ATSWI3B, CHB2, SWI3B, AT2G33610) |
interact with |
(ATHDA6, AXE1, HDA6, HDAC6, RPD3B, RTS1, SIL1, AT5G63110) histone deacetylase |
Arabidopsis thaliana |
| Ta HOX1 protein |
should have direct interaction with |
Ta VRN-A1 protein |
Triticum aestivum |
| AtGlcAT14A and (AtGALT31A, GALT31A, AT1G32930) proteins |
did not show molecular interactions as indicated by |
acceptor photobleaching FRET technique |
Arabidopsis thaliana |
| RFP-p24δ5 and GFP-p24β2 interaction |
in contrast to |
interaction between RFP-p24δ5 and ERD2a-YFP |
Nicotiana tabacum |
| (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) |
determines specific site of |
COP1–MID interaction |
Allium porrum |
| binding of p24δ5 and ERD2a to COPII subunits |
in contrast to |
binding of (ARF1, AT1G59750) and COPI subunits |
Nicotiana tabacum |
| pSOK1-SOK1-YFP line |
did not retrieve |
(SOK1, AT1G05577) proteins |
Arabidopsis thaliana |
| Rsc4-3-GFP coexpressed with CI-RFP |
showed |
decreased fluorescence lifetime of Rsc4-3-GFP in area where CI-RFP colocalized |
Nicotiana benthamiana |
| 187 S. meliloti proteins |
were |
identified in IP-MS assay |
Medicago truncatula |
| (DEG3, DegP3, AT1G65630) |
is |
a potential interacting protein of NCR343 |
Medicago truncatula |
| hspC2 |
is |
a potential interacting protein of NCR343 |
Medicago truncatula |
| (RISP, AT5G13430) and (PMD2, AT1G06530) |
did not interact with |
AtMic60 or (TOM40, AT3G20000) |
Arabidopsis thaliana |
| clathrin (AtCHC2, CHC2, AT3G08530) |
is |
central node |
Arabidopsis thaliana |
| CC-deficient FLU at membrane |
does not bind sufficient |
(POR, TFC C, AT4G39920) or most probably (AtHEMA1, GluTR, HEMA1, AT1G58290) |
|
| DRIFs |
may be |
important partners for DIV transcriptional activity |
Antirrhinum majus |
| (ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) and (ARR12, AtARR12, RR12, AT2G25180) |
do not interact in planta |
split-YFP assay |
Arabidopsis thaliana |
| InLYP1 L40A |
showed comparable interactions with |
(ASK1, ATSKP1, SKP1, SKP1A, UIP1, AT1G75950) and (ASK4, SK4, AT1G20140) |
Arabidopsis thaliana |
| RXLR31154 and VpPsbP |
interact |
yeast two-hybrid assay |
Plasmopara viticola; Vitis piasezkii |
| DIV |
interacts with |
DRIF1 and DRIF2 |
Antirrhinum majus |
| pull-down assays using transgenic plants expressing tandem-affinity purification (TAP)-tagged (MAG2, AT3G47700) |
resulted in identification of |
MAG2-INTERACTING PROTEINs (MIPs) |
Arabidopsis thaliana |
| (PYG7, AT1G22700) C-terminal domain (amino acids 142–301) |
interacts with |
(PSAC, ATCG01060) |
|
| (GUN1, AT2G31400) PPR tracts |
may represent |
PPR motifs engaging in protein-protein interactions |
Arabidopsis thaliana |
| MKK6-3HA |
coimmunoprecipitates with |
MEKK1-3FLAG |
Nicotiana benthamiana |
| low complexity regions of MSP1 |
may contribute to |
protein-protein or protein-ligand interactions |
Arabidopsis thaliana |
| intrinsic disorder of SKRP |
may contribute to |
transient and weak interactions in vivo |
Arabidopsis thaliana |
| 23 candidate proteins |
were obtained from |
Y2H assay |
Zea mays |
| ZmEB1 |
could physically associate with |
ZmTFCB and ZmTUB3 |
Zea mays |
| Leu zipper motif |
is required for |
protein-protein interactions |
|
| KinG |
did not coprecipitate with |
(EAL1, SGR7, SHR, AT4G37650) ƊLNELDV-GFP |
Arabidopsis thaliana |
| REI1-LIKE1 (REIL1, AT4G31420) and REI1-LIKE2 (FZF, REIL2, STCH4, AT2G24500) |
show |
protein-protein interaction |
Arabidopsis thaliana |
| activation domain |
may mediate interaction with |
WD40 proteins |
Arabidopsis thaliana; Zea mays |
| kelch motif module |
contains |
multiple potential protein–protein contact sites |
|
| yeast two-hybrid (Y2H) screen |
identified |
OsRACK1A |
Oryza sativa; Ustilaginoidea virens |
| high protein expression of (HCR1, PP4-1, PPX-1, PPX1, AT4G26720) in leaves |
despite |
the negative BiFC data |
Nicotiana benthamiana |
| KinG ƊKin |
did not interact with |
(DSP3, SIEL, SIEL1, AT3G08800) |
Arabidopsis thaliana |
| MAT4-FLAG |
was precipitated with |
anti-FLAG beads |
Arabidopsis thaliana |
| GmHAD1-2 |
could interact with GmCHR1 through forming |
10 hydrogen bonds |
Glycine max |
| FZP and NAL1 |
interacted |
each other |
Oryza sativa |
| VESICLE-ASSOCIATED MEMBRANE PROTEIN 711 (ATVAMP711, VAMP711, AT4G32150) and Arabidopsis PM H+-ATPase (AHA2, AtHA2, HA2, PMA2, AT4G30190) interaction |
occurs at |
C-termini |
Arabidopsis thaliana |
| KinG CH domain |
is not required for |
interaction with (DSP3, SIEL, SIEL1, AT3G08800) |
Arabidopsis thaliana |
| (PPD2, TIFY4B, AT4G14720) |
interacts with |
NINJA |
Arabidopsis thaliana |
| MAT4-interacting proteins |
were identified by |
immunoprecipitation followed by mass spectrometry analysis |
Arabidopsis thaliana |
| RTCS protein |
can homointeract with |
rtcs |
Zea mays |
| (DSP3, SIEL, SIEL1, AT3G08800) |
likely serves as a linker between |
KinG and (EAL1, SGR7, SHR, AT4G37650) |
Arabidopsis thaliana |
| E. coli FtsZ |
can substitute |
PpFtsZ3 |
Escherichia coli; Physcomitrella patens |
| (ATHDA6, AXE1, HDA6, HDAC6, RPD3B, RTS1, SIL1, AT5G63110) |
interacts physically and genetically with |
(DDM2, DMT01, DMT1, MET1, MET2, METI, AT5G49160) |
Arabidopsis thaliana |
| co-immunoprecipitation (Co-IP) assay |
detected |
no direct interaction between (H3.1, HTR1, AT5G65360) (H3.3, HTR8, AT5G10980) and (GRL, LPL3, NAP1, NAPP, AT2G35110) |
Arabidopsis thaliana |
| (GRL, LPL3, NAP1, NAPP, AT2G35110) (H3.1, HTR1, AT5G65360) interaction |
occurs in |
cytoplasm |
Arabidopsis thaliana |
| (AtSAMS3, MAT4, MTO3, SAMS3, AT3G17390) protein |
can interact with |
(AtSAM1, MAT1, METK1, SAM-1, SAM1, AT1G02500) (AtSAM2, MAT2, SAM-2, SAM2, AT4G01850) (MAT3, AT2G36880) and itself in vitro |
Escherichia coli |
| candidate functional SNPs |
may be from |
protein-protein interaction domains |
|
| inverse phenotypes of OsCCR14 knockdown and OsFBK1 overexpression |
indicated |
direct interaction between OsCCR14 and OsFBK1 |
Oryza sativa |
| e2fa-2 allele |
is missing |
RBR1-interaction domain |
Arabidopsis thaliana |
| bZIP53-BD co-expressed with bZIP53-AD |
does not induce further |
GUS activation |
Arabidopsis thaliana |
| C-terminal-deleted (AIF2, RITF1, AT3G06590) (AIF2dC-pGADT7) |
abolished |
interaction with (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) |
Arabidopsis thaliana |
| interacting surface |
is within |
TGB1 region spanning amino acid residues 85 to 149 |
Nicotiana benthamiana |
| KinG |
directly interacts with |
(DSP3, SIEL, SIEL1, AT3G08800) |
Arabidopsis thaliana |
| (GUN1, AT2G31400) protein |
is more likely to engage in |
protein-protein interactions |
|
| (DSP3, SIEL, SIEL1, AT3G08800) |
directly interacts with |
(EAL1, SGR7, SHR, AT4G37650) |
Arabidopsis thaliana |
| StTOC1 and StPIF3 |
interact |
|
|
| (MDKIN2, AT2G22610) |
could co-localize or function as heterodimer with |
chromokinesin |
Arabidopsis thaliana |
| affinity purification of SOK2-YFP |
recovered |
SOK2-YFP |
Arabidopsis thaliana |
| MdbZIP80 and MdbZIP91 (group-C members) |
could interact with |
group-S1 members MdbZIP2, MdbZIP39, MdbZIP60 and MdbZIP94 |
Malus domestica |
| N-terminal trimming of AtFNR |
may have effect on |
interaction of AtFNR with (AtTic62, Tic62, AT3G18890) or (TROL, AT4G01050) |
Arabidopsis thaliana |
| luciferase (LUC) complementation imaging (LCI) assay |
was used to verify |
interaction between StbZIP61 and StNPR3L |
Solanum stenotomum |
| PIN1-RFP |
is cotransfected with |
full-length ABP1-GFP |
Nicotiana tabacum |
| affinity purification of SOK2-YFP |
recovered |
ANGUSTIFOLIA (AN) |
Arabidopsis thaliana |
| ankyrin repeats |
mediate |
protein–protein interactions |
Arabidopsis thaliana |
| rice homolog of human ski-interacting protein (SKIP) |
physically interacts with |
(AtSR45, RNPS1, SR45, AT1G16610) |
Oryza sativa |
| acetylated Lys residues (Lys-321 in AtFNR1 and Lys-330 in AtFNR2) |
do not coincide with |
binding sites of (AtTic62, Tic62, AT3G18890) |
Arabidopsis thaliana |
| MAT4-His and (ATGSTU24, GST, GSTU24, AT1G17170) -MAT1, -MAT2, -MAT3, -MAT4, or |
could be purified together |
in protein pull-down assay |
Escherichia coli |
| (AGL62, AT5G60440) |
included in |
Mα-Mγ subnetwork |
|
| yeast two-hybrid (Y2H) assay |
was used to identify |
potential interacting partners of StbZIP61 |
Solanum stenotomum |
| AtPPR4 |
does not interact with |
(ATCAF2, CAF2, AT1G23400) CRS2, (AtRH3, emb1138, RH3, AT5G26742) or (EMB2654, AT2G41720) |
Arabidopsis thaliana |
| (ATWNK8, EIP1, WNK8, AT5G41990) |
directly interacted with |
(AGB1, ATAGB1, ELK4, AT4G34460) (AGG1, ATAGG1, GG1, AT3G63420) |
Arabidopsis thaliana |
| (CAR5, AT1G48590) |
interacts with |
(FER, AT3G51550) |
|
| interaction site of EGT2 with OMT or GXM |
might be different from |
interaction site of EGT2 with HMT |
Hordeum vulgare |
| (AtC2, AtGAP1, C2, CAR4, AT3G17980) |
directly interacts with |
FER-CD |
|
| (MAC3B, PUB60, AT2G33340) |
is |
potential partner of SKRP |
Arabidopsis thaliana |
| interactions between (ATNPR3, NPR3, AT5G45110) (ATNPR4, NPR4, AT4G19660) and (ATNPR1, NIM1, NPR1, SAI1, AT1G64280) |
cannot be independently confirmed |
under experimental conditions |
Arabidopsis thaliana |
| histone deacetylase (HD2C, HDT3, AT5G03740) interactors |
identified |
BRAHMA (ATBRM, BRM, CHA2, CHR2, FFO3, AT2G46020) |
Arabidopsis thaliana |
| CPK5-His and MBP-His-CPK11 |
are not pulled down by |
(ATGSTU24, GST, GSTU24, AT1G17170) -MTP8-C or alone |
|
| (ATRABA1B, BEX5, RAB11, RABA1b, AT1G16920) and (ATRABA4C, RABA4C, SMG1, AT5G47960) |
are included in |
the list of RxLR24 interacting proteins |
|
| (NDC80, AT3G54630) |
underwent homodimerization in |
yeast two-hybrid assay |
Arabidopsis thaliana |
| interaction between ATP6C and (ATP8, ORFB, ATMG00480) or (ATP9, ATMG01080) |
was examined with |
luciferase complementation imaging assay |
Zea mays |
| (ANAC092, ATNAC2, ATNAC6, NAC2, NAC6, ORE1, AT5G39610) transcription factor |
is |
CMV1a interactor |
|
| phosphorylated AtLAZY/LZY |
enhances interaction with |
translocons at the outer envelope membrane of chloroplasts (TOC) proteins on the surface of amyloplasts |
Arabidopsis thaliana |
| bZIP53–bZIP10 dimers |
show higher |
GUS activity than bZIP53–bZIP25 dimers |
Arabidopsis thaliana |
| Albrecht et al. and Kim et al. |
identified |
domain in kinases required for interactions with (CBL, AT3G57050) (ATSOS3, CBL4, SOS3, AT5G24270) |
Arabidopsis thaliana |
| four full-length coding sequence (CDS) clones |
were verified to have actual interactions with |
OsSHOC1 |
Oryza sativa |
| luciferase activity |
was detected after |
co-transfection of ATP6C with (ATP8, ORFB, ATMG00480) or (ATP9, ATMG01080) |
Zea mays |
| (CCT, CRP, MED12, AT4G00450) interactions with PP4c and Tap42 (the yeast homolog of (TAP46, AT5G53000) ) |
have been suggested by |
the yeast interactome study |
Saccharomyces cerevisiae |
| non-DNA-binding proteins |
bind to |
(bHLH, AT5G51780) proteins |
Arabidopsis thaliana |
| LONG HYPOCOTYL 5 (HY5, TED 5, AT5G11260) |
can interact with different target proteins using different motifs |
different target proteins |
|
| strong association of FKBP with FRB |
could fail to mimic |
protein–protein interactions that are weak or transient |
|
| Lys acetylation |
does not appear to sterically hinder |
binding of either AtFD isoform |
Arabidopsis thaliana |
| (AtSAM1, MAT1, METK1, SAM-1, SAM1, AT1G02500) (AtSAM2, MAT2, SAM-2, SAM2, AT4G01850) and (MAT3, AT2G36880) proteins |
were able to interact with |
each other and themselves in both in vivo and in vitro assays |
Arabidopsis thaliana; Escherichia coli |
| dominant negative effect of CC construct coexpression |
depended on |
RanGAP2-binding surface of CC |
Solanum tuberosum |
| (ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) and (ARR1, RR1, AT3G16857) |
do not interact in planta |
split-YFP assay |
Arabidopsis thaliana |
| (TFL-1, TFL1, AT5G03840) |
does not inhibit |
FT movement through direct physical interaction |
|
| ternary interactions |
resulted in |
overlap in domains of Cerulean and mRFP fluorescence |
Nicotiana benthamiana |
| (ATWNK8, EIP1, WNK8, AT5G41990) |
is known to interact with |
β-propeller protein (ATARCA, AtRACK1, RACK1A, RACK1A_AT, RACK1z, SAC53, AT1G18080) |
Arabidopsis thaliana |
| interaction of CO with pseudo response regulators (PRRs) |
has been proposed to involve |
C-terminal domain of CO |
Arabidopsis thaliana |
| cotton GhZFP1 |
interacted with |
(RD21, RD21A, AT1G47128) (responsive to dehydration 21A) |
Gossypium hirsutum |
| interaction of GXM and HMT with EGT2 |
occurred only in |
nucleus |
Hordeum vulgare |
| ATSK32-GFP and OPS-mCherry |
direct interaction revealed by |
Förster resonance energy transfer by fluorescence lifetime imaging (FRET-FLIM) analysis |
Arabidopsis thaliana |
| 14-3-3 |
promotes |
interaction of 14-3-3 and SOS2-like protein kinase 5 (CIPK11, PKS5, SIP4, SNRK3.22, AT2G30360) |
Arabidopsis thaliana |
| SRE3 M1 |
binds to |
(U1-70K, U1SNRNP, AT3G50670) |
Solanum lycopersicum |
| GsBET11a TMD |
is indispensable but not sufficient for |
GsCBRLK interaction |
Glycine max |
| GsCBRLK |
could interact with |
all BET1s in wild soybean and Arabidopsis |
Glycine max; Arabidopsis thaliana |
| MdbZIP80-GST pulled down by MdbZIP2-His and MdbZIP39-His |
suggested |
their interaction in vitro |
|
| CcCIPK14 |
indeed interacted with |
all six proteins |
Cajanus cajan |
| xa25 |
did not interact with |
(COPT1, AT5G59030) or (AtCOPT5, COPT5, AT5G20650) in yeast cells |
Saccharomyces cerevisiae |
| (ATSS4, SS4, SSIV, AT4G18240) N-terminal region |
likely exerts function by |
interacting with other proteins |
|
| interactions between BrcHL1a R92W and (GL3, MYC6.2, AT5G41315) |
were |
strong in BiFC experiments |
Brassica rapa |
| GIGANTEA (GI) |
interacts with |
glycotransferase protein SPINDLY (SPY) |
|
| (XBAT35, AT3G23280) isoform .2 |
can interact with |
(ATELC, ELC, Vps23A, AT3G12400) |
|
| Co-IP analysis |
showed |
no interaction between (FAS1, FUGU2, NFB2, AT1G65470) and (GRL, LPL3, NAP1, NAPP, AT2G35110) ;1 |
Arabidopsis thaliana |
