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Query: MT-CO3

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-CO3 0 -0.270 -0.138 -0.132

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-CO3:


Pubmed-MT-CO3 »
Uniprot-MT-CO3 »
Biogrid-MT-CO3 »
ProteomicsDB-MT-CO3 »

Tumorportal-MT-CO3 »
COSMIC-MT-CO3 »
GenomeRNAi-MT-CO3 »
Genecards-MT-CO3


Protein-protein Interactions for MT-CO3
Show screen data for Category Name and Description Link to cat description Data Source


Protein Domains in MT-CO3
Domain name Domain Description TC-NER relevance -log10(p-value)
Category members Cyt_c_oxidase_su3_dom IPR000298 0


Protein complexes (CORUM database) featuring MT-CO3
Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)


Categories featuring MT-CO3
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:0016020 membrane Database 0.52
Category members GO Category GO:0044281 small molecule metabolic process Database 0.35
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 Genetic_recurrent_myoglobinuria Genetic recurrent myoglobinuria Database 0.08
Category members GO Category GO:0045277 respiratory chain complex IV Database 0.08
Category members Disease phenotype Maternally-inherited_Leigh_syndrome Maternally-inherited Leigh syndrome Database 0.01
Category members Disease phenotype Isolated_cytochrome_C_oxidase_deficiency Isolated cytochrome C oxidase deficiency Database 0
Category members Disease phenotype MELAS_SYNDROME MELAS SYNDROME Database 0
Category members Disease phenotype MITOCHONDRIAL_COMPLEX_IV_DEFICIENCY MITOCHONDRIAL COMPLEX IV DEFICIENCY Database 0
Category members GO Category GO:0004129 cytochrome-c oxidase activity Database 0
Category members GO Category GO:0006123 mitochondrial electron transport, cytochrome c to oxygen Database 0
Category members GO Category GO:0008535 respiratory chain complex IV assembly Database 0
Category members GO Category GO:0015002 heme-copper terminal oxidase activity Database 0


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