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Query: MT-ATP6

RNAi screen result RNAPII IP (PI) CSB IP CSB IP (PI) Chrom. Chrom. (PI) Phosphorylation Ubiquitylation
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[Click on the plots to view the data selection in the respective scatterplot]

Protein Results:

 Results for post-translational modifications: see below | Red/green: hit at lower/upper end of the respective screen
Gene name Point score Z-score sums RNAi high RNAi low RNAPII-IP (PI) CSB-IP CSB-IP (PI) Chrom. Chrom. (PI)
MT-ATP6 0 1.280 0.710 0.570

PTM Sites:

 Back to Protein Results | Red/green: hit at lower/upper end of the respective screen
Gene name PTM type PTM site UV UV (PI) Sequence

Background Information for MT-ATP6:


Pubmed-MT-ATP6 »
Uniprot-MT-ATP6 »
Biogrid-MT-ATP6 »
ProteomicsDB-MT-ATP6 »

Tumorportal-MT-ATP6 »
COSMIC-MT-ATP6 »
GenomeRNAi-MT-ATP6 »
Genecards-MT-ATP6


Protein-protein Interactions for MT-ATP6
Show screen data for Category Name and Description Link to cat description Data Source


Protein Domains in MT-ATP6
Domain name Domain Description TC-NER relevance -log10(p-value)


Protein complexes (CORUM database) featuring MT-ATP6
Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)


Categories featuring MT-ATP6
Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)
Category members GO Category GO:0016021 integral to membrane Database 7.67
Category members GO Category GO:0016887 ATPase activity Database 2.28
Category members GO Category GO:0006200 ATP catabolic process Database 2.13
Category members GO Category GO:0005739 mitochondrion Database 1.67
Category members GO Category GO:0044281 small molecule metabolic process Database 0.35
Category members Disease phenotype Familial_infantile_bilateral_striatal_necrosis Familial infantile bilateral striatal necrosis Database 0.32
Category members GO Category GO:0022904 respiratory electron transport chain Database 0.15
Category members GO Category GO:0005743 mitochondrial inner membrane Database 0.15
Category members Disease phenotype Leber_hereditary_optic_neuropathy Leber hereditary optic neuropathy Database 0.13
Category members Disease phenotype LEBER_OPTIC_ATROPHY LEBER OPTIC ATROPHY Database 0.13
Category members GO Category GO:0044237 cellular metabolic process Database 0.08
Category members Disease phenotype Maternally-inherited_Leigh_syndrome Maternally-inherited Leigh syndrome Database 0.01
Category members GO Category GO:0015986 ATP synthesis coupled proton transport Database 0.01
Category members Disease phenotype Leigh_syndrome Leigh syndrome Database 0
Category members GO Category GO:0000276 mitochondrial proton-transporting ATP synthase complex, coupling factor F(o) Database 0
Category members GO Category GO:0005753 mitochondrial proton-transporting ATP synthase complex Database 0
Category members GO Category GO:0015078 hydrogen ion transmembrane transporter activity Database 0
Category members GO Category GO:0022857 transmembrane transporter activity Database 0
Category members GO Category GO:0042776 mitochondrial ATP synthesis coupled proton transport Database 0
Category members GO Category GO:0045263 proton-transporting ATP synthase complex, coupling factor F(o) Database 0


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