Organism : Bacillus subtilis | Module List :
BSU27990 minD

ATPase activator of MinC (RefSeq)

CircVis
Functional Annotations (8)
Function System
Septum formation inhibitor-activating ATPase cog/ cog
barrier septum site selection go/ biological_process
electron transport go/ biological_process
cobalamin biosynthetic process go/ biological_process
oxidoreductase activity go/ molecular_function
ATPase activity go/ molecular_function
cobyrinic acid a,c-diamide synthase activity go/ molecular_function
minD_bact tigr/ tigrfam
GeneModule member RegulatorRegulator MotifMotif

Cytoscape Web
Regulation information for BSU27990
(Mouseover regulator name to see its description)

BSU27990 is regulated by 17 influences and regulates 0 modules.
Regulators for BSU27990 minD (17)
Regulator Module Operator
BSU01010 212 tf
BSU01070 212 tf
BSU04650 212 tf
BSU08990 212 tf
BSU15970 212 tf
BSU16170 212 tf
BSU23210 212 tf
BSU24250 212 tf
BSU25200 212 tf
BSU01010 266 tf
BSU04650 266 tf
BSU09510 266 tf
BSU13210 266 tf
BSU23090 266 tf
BSU28410 266 tf
BSU35840 266 tf
BSU37160 266 tf

Warning: BSU27990 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
5368 4.40e+03 CctAAAgGGA
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5369 1.90e+04 CGGGGA
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5472 2.20e+02 ggaGGAGGtGaaAg
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5473 3.70e+04 AgAaAGGgaGtggCa
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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 BSU27990

BSU27990 is enriched for 8 functions in 3 categories.
Enrichment Table (8)
Function System
Septum formation inhibitor-activating ATPase cog/ cog
barrier septum site selection go/ biological_process
electron transport go/ biological_process
cobalamin biosynthetic process go/ biological_process
oxidoreductase activity go/ molecular_function
ATPase activity go/ molecular_function
cobyrinic acid a,c-diamide synthase activity go/ molecular_function
minD_bact tigr/ tigrfam
Module neighborhood information for BSU27990

BSU27990 has total of 41 gene neighbors in modules 212, 266
Gene neighbors (41)
Gene Common Name Description Module membership
BSU01010 nusG transcription antitermination protein NusG (RefSeq) 212, 397
BSU02270 pssA phosphatidylserine synthase (RefSeq) 66, 212
BSU02280 ybfM putative membrane phosphatase (RefSeq) 69, 212
BSU03370 yckA putative ABC transporter (permease) (RefSeq) 98, 266
BSU03380 yckB putative ABC transporter (binding lipoprotein) (RefSeq) 98, 266
BSU03800 yclN putative iron-siderophore ABC transporter (permease) (RefSeq) 93, 266
BSU03810 yclO putative iron-siderophore ABC transporter (permease) (RefSeq) 93, 266
BSU03820 yclP putative iron-siderophore ABC transporter (ATP-binding protein) (RefSeq) 93, 266
BSU03830 yclQ putative iron-siderophore ABC transporter (binding lipoprotein) (RefSeq) 93, 266
BSU04580 cshA ATP-dependent RNA helicase; cold shock (RefSeq) 266, 322
BSU04650 endB antitoxin MazF (RefSeq) 212, 266
BSU04660 ndoA endoribonuclease toxin (RefSeq) 212, 266
BSU06270 ydjO hypothetical protein (RefSeq) 159, 266
BSU09100 cspB major cold-shock protein, RNA helicase co-factor, RNA co-chaperone (RefSeq) 266, 322
BSU12280 rex transcriptional repressor of the rex ndh operon (RefSeq) 119, 266
BSU12290 ndh NADH dehydrogenase (RefSeq) 119, 266
BSU14770 bipA GTPase (RefSeq) 212, 374
BSU14780 ylaH hypothetical protein (RefSeq) 212, 397
BSU15970 ylxM putative DNA-binding protein (RefSeq) 212, 325
BSU15980 ffh signal recognition particle-like (SRP) GTPase (RefSeq) 212, 325
BSU15990 rpsP 30S ribosomal protein S16 (RefSeq) 212, 374
BSU16000 ylqC putative RNA binding protein (RefSeq) 116, 212
BSU16960 ymdA phosphodiesterase (RefSeq) 107, 266
BSU22780 folE GTP cyclohydrolase I (RefSeq) 228, 266
BSU23370 ypuA hypothetical protein (RefSeq) 7, 266
BSU25160 ispH 4-hydroxy-3-methylbut-2-enyl diphosphate reductase (RefSeq) 226, 266
BSU25400 yqeY hypothetical protein (RefSeq) 7, 266
BSU25410 rpsU 30S ribosomal protein S21 (RefSeq) 7, 266
BSU27580 yrvJ putative N-acetylmuramoyl-L-alanine amidase, family 3 (RefSeq) 266, 322
BSU27990 minD ATPase activator of MinC (RefSeq) 212, 266
BSU28000 minC septum formation inhibitor (RefSeq) 212, 374
BSU28040 radC DNA repair protein RadC (RefSeq) 98, 266
BSU28050 maf Maf-like protein (RefSeq) 98, 266
BSU28470 lysC aspartate kinase (RefSeq) 266, 300
BSU30830 menF menaquinone-specific isochorismate synthase (RefSeq) 212, 272
BSU33870 yvbI putative permease (RefSeq) 197, 266
BSU35730 tagE UDP-glucose:polyglycerol phosphate alpha-glucosyltransferase (RefSeq) 212, 409
BSU35760 tagB teichoic acid primase, CDP-glycerol:N-acetyl-beta-d-mannosaminyl-1, 4-N-acetyl-d-glucosaminyldiphosphoundecaprenyl glycerophosphotransferase (RefSeq) 226, 266
BSU37160 rpoE DNA-directed RNA polymerase subunit delta (RefSeq) 197, 266
BSU40920 yyaF GTP-dependent nucleic acid-binding protein EngD (RefSeq) 98, 266
BSU41060 rpmH 50S ribosomal protein L34 (RefSeq) 119, 266
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 BSU27990
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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