Arabidopsis thaliana protein interaction network
Laboratório de Biologia Integrativa e Sistêmica (LaBIS)
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AT1G07510 - ( ftsh10 (FtsH protease 10) ATP binding / ATPase/ metalloendopeptidase/ nucleoside-triphosphatase/ nucleotide binding / zinc ion binding )

23 Proteins interacs with AT1G07510
LocusMethodFSW Cellular Compartment Classification (C3)Description
AT1G03860

Experimental

Affinity Capture-MS

FSW = 0.2975

Class A:

unclear

plastid

mitochondrion

Class B:

vacuole

Class D:

plastid (p = 0.78)

mitochondrion (p = 0.82)

cytosol (p = 0.67)

ATPHB2 (PROHIBITIN 2)
AT2G29080

Experimental

Affinity Capture-Western

FSW = 0.4808

Class A:

unclear

plastid

mitochondrion

Class D:

plastid (p = 0.78)

mitochondrion (p = 0.82)

cytosol (p = 0.67)

FTSH3 (FTSH PROTEASE 3) ATP-DEPENDENT PEPTIDASE/ ATPASE
AT5G40770

Experimental

Affinity Capture-MS

FSW = 0.2749

Class A:

unclear

mitochondrion

Class B:

vacuole

plastid

plasma membrane

nucleus

cytosol

Class D:

plastid (p = 0.78)

mitochondrion (p = 0.82)

cytosol (p = 0.67)

ATPHB3 (PROHIBITIN 3)
AT4G28510

Experimental

Affinity Capture-MS

FSW = 0.2824

Class A:

unclear

mitochondrion

Class B:

vacuole

plastid

Class D:

plastid (p = 0.78)

mitochondrion (p = 0.82)

cytosol (p = 0.67)

ATPHB1 (PROHIBITIN 1)
AT2G20530

Experimental

Affinity Capture-MS

FSW = 0.2824

Class A:

mitochondrion

Class B:

vacuole

unclear

plastid

Class D:

plastid (p = 0.78)

mitochondrion (p = 0.82)

cytosol (p = 0.67)

ATPHB6 (PROHIBITIN 6)
AT2G26140

Predicted

Synthetic Lethality

Enriched domain pair

Co-expression

FSW = 0.1916

Class C:

unclear

FTSH4 (FTSH PROTEASE 4) ATP-DEPENDENT PEPTIDASE/ ATPASE/ METALLOPEPTIDASE
AT3G27280

Predicted

Affinity Capture-MS

Affinity Capture-Western

FSW = 0.2087

Class C:

plastid

mitochondrion

ATPHB4 (PROHIBITIN 4)
AT1G48030

Predicted

Affinity Capture-MS

FSW = 0.0580

Class C:

plastid

mitochondrion

MTLPD1 (MITOCHONDRIAL LIPOAMIDE DEHYDROGENASE 1) ATP BINDING / DIHYDROLIPOYL DEHYDROGENASE
AT3G10050

Predicted

Phenotypic Suppression

FSW = 0.0544

Class C:

plastid

OMR1 (L-O-METHYLTHREONINE RESISTANT 1) L-THREONINE AMMONIA-LYASE
AT3G05780

Predicted

interologs mapping

Enriched domain pair

Co-expression

FSW = 0.2028

Class C:

mitochondrion

LON3 (LON PROTEASE 3) ATP BINDING / ATP-DEPENDENT PEPTIDASE/ NUCLEOSIDE-TRIPHOSPHATASE/ NUCLEOTIDE BINDING / SERINE-TYPE ENDOPEPTIDASE/ SERINE-TYPE PEPTIDASE
AT5G26860

Predicted

interologs mapping

FSW = 0.0960

Class C:

mitochondrion

LON1 (LON PROTEASE 1) ATP BINDING / ATP-DEPENDENT PEPTIDASE/ SERINE-TYPE PEPTIDASE
AT2G19670

Predicted

two hybrid

FSW = 0.0385

Unknown

PRMT1A (PROTEIN ARGININE METHYLTRANSFERASE 1A) PROTEIN-ARGININE N-METHYLTRANSFERASE
AT2G46470

Predicted

interologs mapping

FSW = 0.1039

Unknown

OXA1L (INNER MEMBRANE PROTEIN OXA1-LIKE)
AT1G64520

Predicted

Affinity Capture-MS

FSW = 0.0096

Unknown

RPN12A (REGULATORY PARTICLE NON-ATPASE 12A) PEPTIDASE
AT1G73570

Predicted

Synthetic Lethality

Synthetic Lethality

FSW = 0.0181

Unknown

SUPPRESSOR OF LIN-12-LIKE PROTEIN-RELATED / SEL-1 PROTEIN-RELATED
AT2G17280

Predicted

Affinity Capture-MS

FSW = 0.0356

Unknown

PHOSPHOGLYCERATE/BISPHOSPHOGLYCERATE MUTASE FAMILY PROTEIN
AT2G43790

Predicted

Synthetic Lethality

FSW = 0.0078

Unknown

ATMPK6 (ARABIDOPSIS THALIANA MAP KINASE 6) MAP KINASE/ KINASE
AT1G78770

Predicted

Synthetic Lethality

FSW = 0.0034

Unknown

CELL DIVISION CYCLE FAMILY PROTEIN
AT1G31660

Predicted

Affinity Capture-MS

FSW = 0.0143

Unknown

FUNCTIONS IN MOLECULAR_FUNCTION UNKNOWN INVOLVED IN BIOLOGICAL_PROCESS UNKNOWN LOCATED IN CELLULAR_COMPONENT UNKNOWN EXPRESSED IN 21 PLANT STRUCTURES EXPRESSED DURING 13 GROWTH STAGES CONTAINS INTERPRO DOMAIN/S BYSTIN (INTERPROIPR007955) HAS 370 BLAST HITS TO 362 PROTEINS IN 156 SPECIES ARCHAE - 0 BACTERIA - 7 METAZOA - 139 FUNGI - 93 PLANTS - 32 VIRUSES - 0 OTHER EUKARYOTES - 99 (SOURCE NCBI BLINK)
AT5G51740

Predicted

Phenotypic Enhancement

FSW = 0.0664

Unknown

PEPTIDASE M48 FAMILY PROTEIN
AT5G13780

Predicted

synthetic growth defect

FSW = 0.0435

Unknown

GCN5-RELATED N-ACETYLTRANSFERASE PUTATIVE
AT1G80410

Predicted

synthetic growth defect

FSW = 0.0473

Unknown

EMB2753 (EMBRYO DEFECTIVE 2753) BINDING
AT1G55255Predicted

synthetic growth defect

FSW = 0.0220

Unknown

EMB2753 (EMBRYO DEFECTIVE 2753) BINDING

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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