Arabidopsis thaliana protein interaction network
Laboratório de Biologia Integrativa e Sistêmica (LaBIS)
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AT5G58690 - ( phosphoinositide-specific phospholipase C family protein )

28 Proteins interacs with AT5G58690
LocusMethodFSW Cellular Compartment Classification (C3)Description
AT3G05630

Predicted

Reconstituted Complex

Affinity Capture-Western

FSW = 0.0808

Unknown

PLDP2 PHOSPHOLIPASE D
AT2G42590

Predicted

Phenotypic Enhancement

two hybrid

Affinity Capture-Western

FSW = 0.0141

Unknown

GRF9 (GENERAL REGULATORY FACTOR 9) CALCIUM ION BINDING / PROTEIN BINDING / PROTEIN PHOSPHORYLATED AMINO ACID BINDING
AT5G45970

Predicted

in vivo

in vitro

FSW = 0.1137

Unknown

ARAC2 (ARABIDOPSIS RAC-LIKE 2) GTP BINDING
AT2G26660

Predicted

interologs mapping

Phenotypic Enhancement

FSW = 0.0323

Unknown

SPX2 (SPX DOMAIN GENE 2)
AT3G18130

Predicted

in vivo

in vitro

FSW = 0.0139

Unknown

RACK1C_AT (RECEPTOR FOR ACTIVATED C KINASE 1 C) NUCLEOTIDE BINDING
AT4G34390

Predicted

Affinity Capture-Western

FSW = 0.0865

Unknown

XLG2 (EXTRA-LARGE GTP-BINDING PROTEIN 2) GUANYL NUCLEOTIDE BINDING / SIGNAL TRANSDUCER
AT1G69220

Predicted

in vivo

in vitro

FSW = 0.0441

Unknown

SIK1 ATP BINDING / KINASE/ PROTEIN KINASE/ PROTEIN SERINE/THREONINE KINASE
AT5G03730

Predicted

in vivo

in vivo

in vivo

in vivo

in vivo

in vitro

FSW = 0.0917

Unknown

CTR1 (CONSTITUTIVE TRIPLE RESPONSE 1) KINASE/ PROTEIN BINDING / PROTEIN SERINE/THREONINE KINASE/ PROTEIN SERINE/THREONINE/TYROSINE KINASE
AT3G25980

Predicted

Synthetic Lethality

FSW = 0.0131

Unknown

MITOTIC SPINDLE CHECKPOINT PROTEIN PUTATIVE (MAD2)
AT2G29900

Predicted

Phenotypic Enhancement

FSW = 0.0462

Unknown

PRESENILIN FAMILY PROTEIN
AT3G28030

Predicted

Phenotypic Enhancement

FSW = 0.0321

Unknown

UVH3 (ULTRAVIOLET HYPERSENSITIVE 3) DNA BINDING / CATALYTIC/ ENDONUCLEASE/ NUCLEASE/ SINGLE-STRANDED DNA BINDING
AT3G18430

Predicted

Phenotypic Suppression

FSW = 0.0566

Unknown

CALCIUM-BINDING EF HAND FAMILY PROTEIN
AT5G63770

Predicted

Phenotypic Suppression

Affinity Capture-Western

FSW = 0.1109

Unknown

ATDGK2 (DIACYLGLYCEROL KINASE 2) DIACYLGLYCEROL KINASE
AT3G27530

Predicted

in vivo

in vitro

FSW = 0.0070

Unknown

GC6 (GOLGIN CANDIDATE 6) BINDING / PROTEIN TRANSPORTER
AT5G18680

Predicted

in vivo

in vitro

FSW = 0.1125

Unknown

ATTLP11 (TUBBY LIKE PROTEIN 11) PHOSPHORIC DIESTER HYDROLASE/ TRANSCRIPTION FACTOR
AT5G56580

Predicted

in vitro

in vivo

two hybrid

Affinity Capture-MS

FSW = 0.0717

Unknown

MKK6 (MAP KINASE KINASE 6) MAP KINASE KINASE/ KINASE
AT5G57200

Predicted

in vitro

FSW = 0.0469

Unknown

EPSIN N-TERMINAL HOMOLOGY (ENTH) DOMAIN-CONTAINING PROTEIN / CLATHRIN ASSEMBLY PROTEIN-RELATED
AT3G08960Predicted

two hybrid

FSW = 0.0344

Unknown

BINDING / PROTEIN TRANSPORTER
AT5G59160

Predicted

Affinity Capture-MS

FSW = 0.0221

Unknown

TOPP2 PROTEIN SERINE/THREONINE PHOSPHATASE
AT1G50030

Predicted

two hybrid

Affinity Capture-Western

interologs mapping

interaction prediction

FSW = 0.0216

Unknown

TOR (TARGET OF RAPAMYCIN) 1-PHOSPHATIDYLINOSITOL-3-KINASE/ PROTEIN BINDING
AT2G13680

Predicted

Phenotypic Suppression

FSW = 0.0535

Unknown

CALS5 (CALLOSE SYNTHASE 5) 13-BETA-GLUCAN SYNTHASE
AT2G43790

Predicted

synthetic growth defect

FSW = 0.0359

Unknown

ATMPK6 (ARABIDOPSIS THALIANA MAP KINASE 6) MAP KINASE/ KINASE
AT5G17930

Predicted

Affinity Capture-Western

two hybrid

interologs mapping

synthetic growth defect

interaction prediction

FSW = 0.0804

Unknown

BINDING / PROTEIN BINDING
AT5G42190

Predicted

Synthetic Lethality

FSW = 0.0061

Unknown

ASK2 (ARABIDOPSIS SKP1-LIKE 2) PROTEIN BINDING / UBIQUITIN-PROTEIN LIGASE
AT5G48640

Predicted

Synthetic Rescue

Phenotypic Suppression

FSW = 0.0184

Unknown

CYCLIN FAMILY PROTEIN
AT5G55090

Predicted

interologs mapping

FSW = 0.0191

Unknown

MAPKKK15 ATP BINDING / KINASE/ PROTEIN KINASE/ PROTEIN SERINE/THREONINE KINASE
AT5G63610

Predicted

Phenotypic Suppression

FSW = 0.0220

Unknown

CDKE1 (CYCLIN-DEPENDENT KINASE E1) ATP BINDING / KINASE/ PROTEIN KINASE/ PROTEIN SERINE/THREONINE KINASE
AT1G77740

Predicted

Synthetic Lethality

interologs mapping

FSW = 0.0469

Unknown

1-PHOSPHATIDYLINOSITOL-4-PHOSPHATE 5-KINASE PUTATIVE / PIP KINASE PUTATIVE / PTDINS(4)P-5-KINASE PUTATIVE / DIPHOSPHOINOSITIDE KINASE PUTATIVE

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Fasta sequences:

Proteins

DNA

Quick help

Experimental: This means that the indicated PPI was experimentally demonstrated using Arabidopsis thaliana proteins as model of study. The experiment indicated links to the publication of which this interaction was annotated from
Predicted: The indicated PPI was proposed based on ortholgs studies. The experiment indicated links to the publication of the orthologous PPI was annotated from

FSW

FSW is the Functional Similarity Weight. It represents the proportion of interaction partners that two proteins have in common

Learn more - FSWeight top ranked cut offs

C3

Class A: The PPI is a direct evidence (experimental), the subcellular location was experimentally demonstrated and both, target and source, were indicated as expressed in same cellular compartment
Class B: The PPI is a direct evidence (experimental), the subcellular location was experimentally demonstrated but both, target and source, were indicated as expressed in different cellular compartment
Class C: Same as Class A but the PPI is predicted
Class D: Same as Class A but subcellular location was predicted. P(exp|pred) indicates the probability of this particular predicted location be experimentally demonstrated given all data available on AtPINDB
Unknown: There is no available data to calculate the C3 or the data does not fit onto any class previously described

PEP

PEP is the posterior probability of this particular PPI be experimentally demonstrated once it was predicted. For this release p = 0.0030. If they share same cell compartment p = 0.0029

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How to cite

If you find AtPIN interesting and want to use it in your work please cite us

AtPIN: Arabidopsis thaliana Protein Interaction Network
Marcelo M Brandao, Luiza L Dantas and Marcio C Silva-Filho
BMC Bioinformatics 2009, 10:454

DOI:1471-2105/10/454