Organism : Bacillus subtilis | Module List :
BSU39930 yxaM

putative efflux transporter (RefSeq)

CircVis
Functional Annotations (3)
Function System
transporter activity go/ molecular_function
transport go/ biological_process
integral to membrane go/ cellular_component
GeneModule member RegulatorRegulator MotifMotif

Cytoscape Web
Regulation information for BSU39930
(Mouseover regulator name to see its description)

BSU39930 is regulated by 18 influences and regulates 0 modules.
Regulators for BSU39930 yxaM (18)
Regulator Module Operator
BSU00470 85 tf
BSU02070 85 tf
BSU15320 85 tf
BSU26870 85 tf
BSU27080 85 tf
BSU27320 85 tf
BSU31530 85 tf
BSU36420 85 tf
BSU37290 85 tf
BSU40410 85 tf
BSU40710 85 tf
BSU00700 141 tf
BSU02220 141 tf
BSU15320 141 tf
BSU15330 141 tf
BSU23450 141 tf
BSU29630 141 tf
BSU36420 141 tf

Warning: BSU39930 Does not regulate any modules!

Motif information (de novo identified motifs for modules)

There are 4 motifs predicted.

Motif Table (4)
Motif Id e-value Consensus Motif Logo
5124 6.20e-04 gAAAgAAAcaGga.t.gagC
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5125 7.40e+01 CagCCaATAGa
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5232 4.20e+00 aGg.GGgAgc
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5233 3.50e+03 aA.atctT.CagGAa
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Motif Help

Transcription factor binding motifs help to elucidate regulatory mechanism. cMonkey integrates powerful de novo motif detection to identify conditionally co-regulated sets of genes. De novo predicted motifs for each module are listed in the module page as motif logo images along with associated prediction statistics (e-values). The main module page also shows the location of these motifs within the upstream sequences of the module member genes.

Motifs of interest can be broadcasted to RegPredict (currently only available for Desulfovibrio vulgaris Hildenborough) in order to compare conservation in similar species. This integrated motif prediction and comparative analysis provides an additional checkpoint for regulatory motif prediction confidence.

Motif e-value: cMonkey tries to identify two motifs per modules in the upstream sequences of the module member genes. Motif e-value is an indicative of the motif co-occurences between the members of the module.Smaller e-values are indicative of significant sequence motifs. Our experience showed that e-values smaller than 10 are generally indicative of significant motifs.

Functional Enrichment for BSU39930

BSU39930 is enriched for 3 functions in 2 categories.
Enrichment Table (3)
Function System
transporter activity go/ molecular_function
transport go/ biological_process
integral to membrane go/ cellular_component
Module neighborhood information for BSU39930

BSU39930 has total of 50 gene neighbors in modules 85, 141
Gene neighbors (50)
Gene Common Name Description Module membership
BSU00640 spoIIE serine phosphatase (RefSeq) 131, 141
BSU00650 yabS hypothetical protein (RefSeq) 131, 141
BSU00660 yabT putative serine/threonine-protein kinase (RefSeq) 137, 141
BSU01910 skfA sporulation killing factor A (RefSeq) 33, 141
BSU01920 skfB synthesis of sporulation killing factor A (RefSeq) 33, 141
BSU01960 skfF sporulation killing factor biosynthesis and export; ABC transporter (permease) (RefSeq) 33, 141
BSU01980 skfH sibling killing effect ; sporulation killing factor biosynthesis and export (RefSeq) 141, 304
BSU02040 ybdN hypothetical protein (RefSeq) 25, 141
BSU02220 ybfI putative transcriptional regulator (AraC/XylS family, cupin family) (RefSeq) 86, 141
BSU10780 yisN hypothetical protein (RefSeq) 85, 127
BSU10790 asnO asparagine synthetase (RefSeq) 85, 127
BSU15330 sigG sporulation sigma factor SigG (RefSeq) 131, 141
BSU17110 pksD enzyme involved in polyketide synthesis (RefSeq) 85, 302
BSU17120 pksE enzyme involved in polyketide synthesis (RefSeq) 85, 306
BSU17130 acpK acyl carrier protein (RefSeq) 85, 306
BSU17140 pksF polyketide beta-ketoacyl:acyl carrier protein synthase (RefSeq) 85, 306
BSU17150 pksG acetyl-S-AcpK beta-ketothioester polyketide intermediate transferase (RefSeq) 85, 306
BSU17160 pksH polyketide biosynthesis enoyl-CoA hydratase (RefSeq) 85, 306
BSU17170 pksI polyketide biosynthesis enoyl-CoA hydratase (RefSeq) 85, 306
BSU17180 pksJ polyketide synthase of type I (RefSeq) 85, 306
BSU17190 pksL polyketide synthase of type I (RefSeq) 85, 306
BSU17200 pksM polyketide synthase (RefSeq) 85, 306
BSU17210 pksN polyketide synthase of type I (RefSeq) 85, 306
BSU17220 pksR polyketide synthase (RefSeq) 85, 306
BSU18330 ppsB plipastatin synthetase (RefSeq) 85, 306
BSU18340 ppsA plipastatin synthetase (RefSeq) 85, 306
BSU19690 kamA lysine 2,3-aminomutase (RefSeq) 141, 399
BSU19720 yodR putative acyloate-acetoacetate CoA-transferase (RefSeq) 141, 399
BSU19730 yodS putative aminoacyloate CoA-transferase (RefSeq) 141, 399
BSU22540 qcrC menaquinol:cytochrome c oxidoreductase (cytochrome cc subunit) (RefSeq) 141, 210
BSU27030 sacC levanase (RefSeq) 85, 329
BSU27040 levG phosphotransferase system (PTS) fructose-specific enzyme IID component (RefSeq) 85, 117
BSU27050 levF phosphotransferase system (PTS) fructose-specific enzyme IIC component (RefSeq) 85, 117
BSU27060 levE phosphotransferase system (PTS) fructose-specific enzyme IIB component (RefSeq) 85, 117
BSU27070 levD phosphotransferase system (PTS) fructose-specific enzyme IIA component (RefSeq) 85, 329
BSU29630 yttP putative transcriptional regulator (RefSeq) 12, 141
BSU30960 glgD glucose-1-phosphate adenylyltransferase (ADP-glucose pyrophosphorylase) beta subunit (RefSeq) 126, 141
BSU30980 glgB glycogen branching enzyme (RefSeq) 141, 304
BSU33140 yvqJ putative efflux protein (RefSeq) 91, 141
BSU39060 citH secondary transporter of divalent metal ions/citrate complexes (RefSeq) 141, 278
BSU39260 bglH aryl-phospho-beta-d-glucosidase (RefSeq) 141, 330
BSU39270 bglP phosphotransferase system (PTS) beta-glucoside-specific enzyme IIBCA component (RefSeq) 141, 330
BSU39350 hutH histidine ammonia-lyase (RefSeq) 85, 326
BSU39360 hutU urocanate hydratase (RefSeq) 85, 326
BSU39370 hutI imidazolonepropionase (RefSeq) 85, 326
BSU39380 hutG formimidoylglutamase (RefSeq) 85, 326
BSU39890 yxbB putative S-adenosylmethionine-dependent methyltransferase (RefSeq) 19, 141
BSU39910 yxnB hypothetical protein (RefSeq) 19, 141
BSU39920 asnH asparagine synthetase (glutamine-hydrolyzing) (RefSeq) 141, 407
BSU39930 yxaM putative efflux transporter (RefSeq) 85, 141
Gene Page Help

Network Tab

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.

Network representation is interactive. You can zoom in/out and move nodes/edges around. Clicking on a node will open up a window to give more details. For genes, Locus tag, organism, genomic coordinates, NCBI gene ID, whether it is transcription factor or not and any associated functional information will be shown. For regulators, number of modules are shown in addition to gene details. For motifs, e-value, consensus sequence and sequence logo will be shown. For modules, expression profile plot, motif information, functional associations and motif locations for each member of the module will be shown.
You can pin information boxes by using button in the box title and open up additional ones on the same screen for comparative analysis.

Regulation Tab

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.

You can see description of the regulator inside the tooltip when you mouseover. In certain cases the regulatory influence is predicted to be the result of the combination of two influences. These are indicated as combiner in the column labeled "Operator".

For transcription factors, an additional table next to regulator table will be show. This table show modules that are influenced by the transcription factor.

Motifs Tab

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.

Functions Tab

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.

Help Tab

This help page. More general help can be accessed by clicking help menu in the main navigation bar.

Social Tab

Network Portal is designed to promote collaboration through social interactions. Therefore interested researchers can share information, questions and updates for a particular gene.

Users can use their Disqus, Facebook, Twitter or Google accounts to connect to this page (We recommend Google). Each module and gene page includes comments tab that lists history of the interactions for that gene. You can browse the history, make updates, raise questions and share these activities with social web.

In the next releases of the network portal, we are planning to create personal space for each user where you can share you space that contains all the analysis steps you did along with relevant information.

CircVis

Our 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)
  • 4. Interactions between source and target genes for a particular module
  • 5. Module(s) that source gene and target genes belong to
  • 6. Visualisation legend
Comments for BSU39930
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Gene Help

Overview

Gene landing pages present genomic, functional, and regulatory information for individual genes. A circular visualization displays connections between the selected gene and genes in the same modules, with as edges drawn between the respective coordinates of the whole genome.

The gene page also lists functional ontology assignments, module membership, and motifs associated with these modules. Genes in the network inherit regulatory influences from the modules to which they belong. Therefore, the regulatory information for each gene is a collection of all regulatory influences on these modules. These are listed as a table that includes influence name, type, and target module. If the gene is a transcription factor, its target modules are also displayed in a table that provides residual values and number of genes.

CircVis

Our 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)
  • 4. Interactions between source and target genes for a particular module
  • 5. Module(s) that source gene and target genes belong to
  • 6. Visualisation legend