Organism : Methanococcus maripaludis S2 | Module List :
30S ribosomal protein S24e
Functional Annotations (6)
|Ribosomal protein S24E||cog/ cog|
|nucleotide binding||go/ molecular_function|
|structural constituent of ribosome||go/ molecular_function|
|Ribosome||kegg/ kegg pathway|
Regulation information for MMP0443(Mouseover regulator name to see its description)
Motif information (de novo identified motifs for modules)
There are 8 motifs predicted.
|Motif Id||e-value||Consensus||Motif Logo|
Functional Enrichment for MMP0443
Module neighborhood information for MMP0443
|Gene||Common Name||Description||Module membership|
|MMP0046||hypothetical protein MMP0046||20, 51, 140|
|MMP0060||rplX||50S ribosomal protein LX||61, 96, 138|
|MMP0061||aIF6||translation initiation factor IF-6||8, 61, 96, 138|
|MMP0062||50S ribosomal protein L31e||61, 77, 96, 128, 138|
|MMP0074||hypothetical protein MMP0074||51, 140|
|MMP0075||abortive infection protein||96, 136|
|MMP0091||hypothetical protein MMP0091||51, 106|
|MMP0116||argC||N-acetyl-gamma-glutamyl-phosphate reductase||8, 51|
|MMP0141||hypothetical protein MMP0141||41, 51|
|MMP0142||thiamine pyrophosphate dependent protein||17, 41, 51|
|MMP0163||arsA||arsenite-activated ATPase ArsA||16, 96|
|MMP0242||hypothetical protein MMP0242||8, 39, 96|
|MMP0245||pfdB||prefoldin subunit beta||96, 138|
|MMP0268||truA||tRNA pseudouridine synthase A||49, 51|
|MMP0286||hypothetical protein MMP0286||29, 51|
|MMP0317||hypothetical protein MMP0317||77, 96|
|MMP0350||hexapeptide repeat-containing transferase||80, 96|
|MMP0370||hypothetical protein MMP0370||77, 96|
|MMP0440||DNA-directed RNA polymerase subunit E'||51, 61|
|MMP0441||rpoE2||DNA-directed RNA polymerase subunit E||51, 61|
|MMP0442||hypothetical protein MMP0442||3, 51, 61|
|MMP0443||rps24e||30S ribosomal protein S24e||3, 51, 96, 97|
|MMP0444||30S ribosomal protein S27ae||3, 51, 97|
|MMP0572||slyD||FKBP-type peptidylprolyl isomerase||11, 96|
|MMP0578||aroQ||chorismate mutase||11, 18, 96, 138|
|MMP0657||hypothetical protein MMP0657||8, 29, 96|
|MMP0667||rps2P||30S ribosomal protein S2||3, 105|
|MMP0668||hypothetical protein MMP0668||3, 96, 105|
|MMP0669||30S ribosomal protein S3Ae||3, 105|
|MMP0670||hypothetical protein MMP0670||41, 51|
|MMP0671||ywbE||hypothetical protein MMP0671||51, 87|
|MMP0694||beta-lactamase-like protein||51, 109, 149|
|MMP0695||psmB||proteasome subunit beta||51, 92|
|MMP0884||hypothetical protein MMP0884||39, 51|
|MMP0901||ATP/GTP-binding motif-containing protein||20, 51|
|MMP0946||gatB||aspartyl/glutamyl-tRNA amidotransferase subunit B||8, 81, 96|
|MMP1013||carB||carbamoyl-phosphate synthase large subunit||77, 96|
|MMP1064||adenylate cyclase||4, 51|
|MMP1113||transketoloase, C terminal half||96, 120|
|MMP1147||rpl37e||50S ribosomal protein L37e||18, 96, 138|
|MMP1208||aIF2_gamma||translation initiation factor IF-2 subunit gamma||20, 61, 96|
|MMP1254||purM||phosphoribosylaminoimidazole synthetase||96, 120|
|MMP1260||hypothetical protein MMP1260||40, 96|
|MMP1289||rpl10e||50S ribosomal protein L10e||3, 92, 105|
|MMP1381||beta-lactamase-like protein||51, 92|
|MMP1399||aspartate/glutamate/uridylate kinase||51, 61|
|MMP1400||hypothetical protein MMP1400||61, 92, 97, 105|
|MMP1401||ef1B||elongation factor 1-beta||61, 96, 97, 105|
|MMP1402||hypothetical protein MMP1402||3, 97, 105|
|MMP1403||rpl22p||50S ribosomal protein L22P||3, 61, 92, 96, 97, 105|
|MMP1404||rps3p||30S ribosomal protein S3P||3, 97, 105|
|MMP1405||rpmC||50S ribosomal protein L29P||3, 97|
|MMP1431||2pgk||2-phosphoglycerate kinase||49, 51|
|MMP1432||purA||adenylosuccinate synthetase||29, 51, 130|
|MMP1433||rpl11p||50S ribosomal protein L11P||96, 97, 105|
|MMP1444||methionine aminopeptidase||20, 51, 61, 92|
|MMP1515||hsp60||chaperonin GroEL||77, 96|
|MMP1590||ExsB family protein||24, 51|
|MMP1594||hypothetical protein MMP1594||51, 143|
|MMP1646||hypothetical protein MMP1646||96, 136|
Gene Page Help
If the gene is associated with a module(s), its connection to given modules along with other members of that module are shown as network by using CytoscapeWeb. In this view, each green colored circular nodes represent module member genes, purple colored diamonds represent module motifs and red triangles represent regulators. Each node is connected to module (Bicluster) via edges. This representation provides quick overview of all genes, regulators and motifs for modules. It also allows one to see shared genes/motifs/regulators among diferent modules.
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Regulation tab for each gene includes regulatory influences such as environmental factors or transcription factors or their combinations identified by regulatory network inference algorithms.
If the gene is a member of a module, regulators influencing that module are also considered to regulate the gene. Regulators table list total number of regulatory influences, regulators, modules and type of the influence.
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Network inference algorithm uses de novo motif prediction for assigning genes to modules. If there are any motifs identified in the upstream region of a gene, the motif will be shown here. For each motif sequence logo, consensus and e-value will be shown.
Identification of functional enrichment for the module members is important in associating predicted motifs and regulatory influences with pathways. As described above, the network inference pipeline includes a functional enrichment module by which hypergeometric p-values are used to identify over representation of functional ontology terms among module members.
Network Portal presents functional ontologies from KEGG, GO, TIGRFAM, and COG as separate tables that include function name, type, corrected and uncorrected hypergeometric p-values, and the number of genes assigned to this category out of total number of genes in the module.
Module Members Tab
Identity of gene members in a module may help to identify potential interactions between different functional modules. Therefore, neighbor genes that share the same module(s) with gene under consideration are shown here. For each memebr, gene name, description and modules that contain it are listed.
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CircVisOur circular module explorer is adapted from visquick originally developed by Dick Kreisberg of Ilya Shmulevich lab at ISB for The Cancer Genome Atlas. We use simplified version of visquick to display distribution of module members and their interactions across the genome. This view provides summary of regulation information for a gene. The main components are;
- 1. All genomic elements for the organism are represented as a circle and each element is separated by black tick marks. In this example chromosome and pDV represent main chromosome and plasmid for D. vulgaris Hildenborough, respectively.
- 2. Source gene
- 3. Target genes (other module members)
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