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Query: SCO1

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)
SCO1 0 -0.304 0.020 0.360 0.240 -0.904

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 SCO1:





Protein-protein Interactions for SCO1

Show screen data for Category Name and Description Link to cat description Data Source
Category members IP bait LRPPRC Cat. description Hein, Mann, Cell 2015
Category members IP bait SYNCRIP Cat. description Hein, Mann, Cell 2015


Protein Domains in SCO1

Domain name Domain Description TC-NER relevance -log10(p-value)
Category members Thioredoxin-like_fold IPR012336 0.16
Category members AhpC/TSA IPR000866 0.13
Category members SCO1/SenC IPR003782 0
Category members Synth_of_cyt-c-oxidase_Sco1/2 IPR017276 0


Protein complexes (CORUM database) featuring SCO1

Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)


Categories featuring SCO1

Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)
Category members GO Category GO:0005739 mitochondrion Database 1.67
Category members GO Category GO:0005743 mitochondrial inner membrane Database 0.15
Category members GO Category GO:0016209 antioxidant activity Database 0.06
Category members GO Category GO:0006878 cellular copper ion homeostasis Database 0.04
Category members Disease phenotype Fatal_infantile_cytochrome_C_oxidase_deficiency Fatal infantile cytochrome C oxidase deficiency Database 0
Category members Disease phenotype MITOCHONDRIAL_COMPLEX_IV_DEFICIENCY MITOCHONDRIAL COMPLEX IV DEFICIENCY Database 0
Category members Disease phenotype mitochondrial_complex_IV_deficiency_(MT-C4D) mitochondrial complex IV deficiency (MT-C4D) Database 0
Category members GO Category GO:0005507 copper ion binding Database 0
Category members GO Category GO:0006091 generation of precursor metabolites and energy Database 0
Category members GO Category GO:0006825 copper ion transport Database 0
Category members GO Category GO:0008535 respiratory chain complex IV assembly Database 0
Category members GO Category GO:0016491 oxidoreductase activity Database 0
Category members GO Category GO:0030016 myofibril Database 0
Category members GO Category GO:0055114 oxidation-reduction process Database 0


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