Arabidopsis thaliana protein interaction network
Laboratório de Biologia Integrativa e Sistêmica (LaBIS)
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AT1G73690 - ( CDKD11 (CYCLIN-DEPENDENT KINASE D11) ATP binding / kinase/ protein kinase/ protein serine/threonine kinase )

28 Proteins interacs with AT1G73690
LocusMethodFSW Cellular Compartment Classification (C3)Description
AT3G48750

Experimental

protein complementation assay

FSW = 0.1047

Class A:

nucleus

Class B:

plasma membrane

cytosol

Class D:

cytosol (p = 0.67)

CDC2 (CELL DIVISION CONTROL 2) CYCLIN-DEPENDENT PROTEIN KINASE/ KINASE/ PROTEIN BINDING / PROTEIN KINASE
AT1G47210

Experimental

protein complementation assay

FSW = 0.1471

Class A:

nucleus

Class B:

cytosol

Class D:

mitochondrion (p = 0.82)

cytosol (p = 0.67)

CYCLIN FAMILY PROTEIN
AT2G32710

Experimental

protein complementation assay

FSW = 0.3743

Class A:

nucleus

Class D:

mitochondrion (p = 0.82)

KRP4 CYCLIN BINDING / CYCLIN-DEPENDENT PROTEIN KINASE INHIBITOR
AT5G27620

Experimental

two hybrid

protein complementation assay

FSW = 0.0948

Unknown

CYCH1 (CYCLIN H1) CYCLIN-DEPENDENT PROTEIN KINASE/ PROTEIN BINDING / PROTEIN KINASE
AT4G28980

Experimental

protein complementation assay

FSW = 0.2772

Unknown

CYCLIN-DEPENDENT KINASE-ACTIVATING KINASE 1AT / CDK-ACTIVATING KINASE 1AT (CAK1)
AT2G27970

Experimental

protein complementation assay

FSW = 0.1364

Unknown

CKS2 (CDK-SUBUNIT 2) CYCLIN-DEPENDENT PROTEIN KINASE/ CYCLIN-DEPENDENT PROTEIN KINASE REGULATOR
AT5G11300

Experimental

protein complementation assay

two hybrid

FSW = 0.0256

Unknown

CYC3B (MITOTIC-LIKE CYCLIN 3B FROM ARABIDOPSIS) CYCLIN-DEPENDENT PROTEIN KINASE REGULATOR
AT1G15570

Experimental

protein complementation assay

FSW = 0.0750

Unknown

CYCA23 (CYCLIN A23) CYCLIN-DEPENDENT PROTEIN KINASE REGULATOR
AT1G47230

Experimental

protein complementation assay

FSW = 0.1396

Unknown

CYCLIN PUTATIVE
AT1G20610

Experimental

protein complementation assay

FSW = 0.0748

Unknown

CYCB23 (CYCLIN B23) CYCLIN-DEPENDENT PROTEIN KINASE REGULATOR
AT1G70210

Experimental

protein complementation assay

FSW = 0.1021

Unknown

CYCD11 (CYCLIN D11) CYCLIN-DEPENDENT PROTEIN KINASE REGULATOR
AT5G65420

Experimental

protein complementation assay

FSW = 0.1701

Unknown

CYCD41 (CYCLIN D41) CYCLIN-DEPENDENT PROTEIN KINASE REGULATOR
AT5G10440

Experimental

protein complementation assay

FSW = 0.1582

Unknown

CYCD42 (CYCLIN D42) CYCLIN-DEPENDENT PROTEIN KINASE
AT4G37630

Experimental

protein complementation assay

FSW = 0.1922

Unknown

CYCD51 (CYCLIN D51) CYCLIN-DEPENDENT PROTEIN KINASE
AT4G03270

Experimental

protein complementation assay

FSW = 0.1714

Unknown

CYCD61 (CYCLIN D61) CYCLIN-DEPENDENT PROTEIN KINASE
AT1G16330

Experimental

two hybrid

FSW = 0.0693

Unknown

CYCB31 (CYCLIN B31) CYCLIN-DEPENDENT PROTEIN KINASE
AT3G62870

Predicted

Synthetic Lethality

FSW = 0.0073

Unknown

60S RIBOSOMAL PROTEIN L7A (RPL7AB)
AT2G20800

Predicted

Synthetic Rescue

FSW = 0.0949

Unknown

NDB4 (NAD(P)H DEHYDROGENASE B4) NADH DEHYDROGENASE
AT3G54670

Predicted

two hybrid

two hybrid

Affinity Capture-Western

Affinity Capture-Western

FSW = 0.0519

Unknown

TTN8 (TITAN8) ATP BINDING / TRANSPORTER
AT3G19930

Predicted

Synthetic Rescue

FSW = 0.1008

Unknown

STP4 (SUGAR TRANSPORTER 4) CARBOHYDRATE TRANSMEMBRANE TRANSPORTER/ MONOSACCHARIDE TRANSMEMBRANE TRANSPORTER/ SUCROSEHYDROGEN SYMPORTER/ SUGARHYDROGEN SYMPORTER
AT1G79230

Predicted

Synthetic Lethality

FSW = 0.0994

Unknown

MST1 (MERCAPTOPYRUVATE SULFURTRANSFERASE 1) 3-MERCAPTOPYRUVATE SULFURTRANSFERASE/ SULFURTRANSFERASE/ THIOSULFATE SULFURTRANSFERASE
AT1G55890

Predicted

Gene fusion method

FSW = 0.0345

Unknown

PENTATRICOPEPTIDE (PPR) REPEAT-CONTAINING PROTEIN
AT1G07880

Predicted

two hybrid

Affinity Capture-Western

FSW = 0.0188

Unknown

ATMPK13 MAP KINASE/ KINASE
AT1G10810

Predicted

two hybrid

FSW = 0.0450

Unknown

ALDO/KETO REDUCTASE FAMILY PROTEIN
AT1G71530

Predicted

Affinity Capture-Western

two hybrid

Affinity Capture-Western

FSW = 0.1047

Unknown

PROTEIN KINASE FAMILY PROTEIN
AT4G32850

Predicted

Affinity Capture-Western

FSW = 0.0250

Unknown

NPAP (NUCLEAR POLY(A) POLYMERASE) NUCLEOTIDYLTRANSFERASE/ PROTEIN BINDING
AT5G05070

Predicted

Affinity Capture-Western

FSW = 0.0554

Unknown

ZINC ION BINDING
AT5G52200

Predicted

Synthetic Lethality

FSW = 0.0789

Unknown

UNKNOWN PROTEIN

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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