mutS:Quickview: Difference between revisions

From EcoliWiki
Jump to navigation Jump to search
touch
 
(11 intermediate revisions by 2 users not shown)
Line 23: Line 23:
*  ** PLEASE DON'T EDIT THIS TABLE DIRECTLY.  Use the edit table link under the table. **  
*  ** PLEASE DON'T EDIT THIS TABLE DIRECTLY.  Use the edit table link under the table. **  
*  
*  
****************************************************************************************** -->{{Quickview_table_help}}
****************************************************************************************** -->
{|border="2" cellpadding="4" cellspacing="0" style="margin: 1em 1em 1em 0; border: 1px #aaa solid; border-collapse: collapse;"  
{|   id="D49aeed8a5081a" class=" tableEdit New_Quickview_Table"


|-
|-
!align=left {{table_heading_style}} |Standard Name
!align=left {{table_heading_style}} |Standard Name
||
||
''mutS''  
''mutS''
|-
|-
!align=left {{table_heading_style}} |Gene Synonym(s)
!align=left {{table_heading_style}} |Gene Synonym(s)
||
||
''ECK2728, b2733, JW2703, fdv, ant, plm''<ref name='LIB:Riley_2006'/>
''ECK2728, b2733, JW2703, fdv, ant, plm''<ref name='LIB:Riley_2006'/>, plm''
|-
|-
!align=left {{table_heading_style}} |Product Desc.
!align=left {{table_heading_style}} |Product Desc.
Line 45: Line 45:
!align=left {{table_heading_style}} |Product Synonyms(s)
!align=left {{table_heading_style}} |Product Synonyms(s)
||
||
methyl-directed mismatch repair protein<ref name='LIB:Riley_2006'/>, B2733<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>, Plm<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>, Ant<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>, Fdv<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>, MutS<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>  
''methyl-directed mismatch repair protein<ref name='LIB:Riley_2006'/>, B2733<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>, Plm<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>, Ant<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>, Fdv<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/>, MutS<ref name='LIB:EcoCyc10.6'/><ref name='LIB:Riley_2006'/> , ant, ECK2728, fdv, JW2703, plm, b2733''
|-
!align=left {{table_heading_style}} |Function from GO
||
<GO_nr />
|-
|-
!align=left {{table_heading_style}} |Knock-Out Phenotype
!align=left {{table_heading_style}} |Knock-Out Phenotype
Line 58: Line 62:
||
||


|-
!align=left {{table_heading_style}} |Quick Links
||
[[File:porteco.png|link=http://porteco.org/AjaxSearch.jsp?searchString=mutS&s=search]] [[File:EcoCyc.gif|link=http://biocyc.org/ECOLI/NEW-IMAGE?type=NIL&object=EG10625]] [[File:regulondb.jpg|link=http://regulondb.ccg.unam.mx/gene?term=ECK120000618&organism=ECK12&format=jsp&type=gene ]] <br/><br/> [[File:dnadisplay.png|link=http://ecoliwiki.net/tools/display_dna.php?gene=mutS&loc=MG1655%3A2855115..2857676,W3110%3A2855749..2858310,REL606%3A2751953..2754514,DH10B%3A2947657..2950218,BW2952%3A2740927..2743488]] [[File:proteindisplay.png|link=http://ecoliwiki.net/tools/display_protein.php?f=NC_000913&start=2740927&end=2743488&gene=mutS&aa=msaienfdahtpmmqqylrlkaqhpeillfyrmgdfyelfyddakrasqlldisltkrgasagepipmagipyhavenylaklvnqgesvaiceqigdpatskgpverkvvrivtpgtisdeallqerqdnllaaiwqdskgfgyatldissgrfrlsepadretmaaelqrtnpaellyaedfaemsliegrrglrrrplwefeidtarqqlnlqfgtrdlvgfgvenaprglcaagcllqyakdtqrttlphirsitmereqdsiimdaatrrnleitqnlaggaentlasvldctvtpmgsrmlkrwlhmpvrdtrvllerqqtigalqdftaglqpvlrqvgdlerilarlalrtarprdlarmrhafqqlpelraqletvdsapvqalrekmgefaelrdlleraiidtppvlvrdggviasgyneeldewraladgatdylerlevrerertgldtlkvgfnavhgyyiqisrgqshlapinymrrqtlknaeryiipelkeyedkvltskgkalalekqlyeelfdlllphlealqqsasalaeldvlvnlaeraytlnytcptfidkpgiritegrhpvveqvlnepfianplnlspqrrmliitgpnmggkstymrqtalialmayigsyvpaqkveigpidriftrvgaaddlasgrstfmvemtetanilhnateyslvlmdeigrgtstydglslawacaenlankikaltlfathyfeltqlpekmegvanvhldalehgdtiafmhsvqdgaasksyglavaalagvpkevikrarqklrelesispnaaatqvdgtqmsllsvpeetspavealenldpdsltprqalewiyrlkslv]]&nbsp;&nbsp;  [[File:pubmed.jpg|link=http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=Search&Term=mutS+AND+escherichia+coli]]&nbsp;&nbsp;  [[File:textpresso.jpg|link=http://textpresso.tamu.edu/cgi-bin/textpresso/search?q=mutS]]&nbsp;&nbsp;


|-class='sortbottom'
|- class="tableEdit_footer"
|[{{SERVER}}{{SCRIPTPATH}}?title=Special:TableEdit&id=bc145ea147f7e36caf09c1bfeed4ee9d.7218.D49aeed8a5081a&page=7218&pagename={{FULLPAGENAMEE}}&type=1&template=New_Quickview_Table edit table] ||
|<span class="tableEdit_editLink plainlinks">[{{SERVER}}{{SCRIPTPATH}}?title=Special:TableEdit&id=bc145ea147f7e36caf09c1bfeed4ee9d.7218.D49aeed8a5081a&page=7218&pagename={{FULLPAGENAMEE}}&type=1&template=New_Quickview_Table edit table]</span> ||
|}
|}
<!--box uid=bc145ea147f7e36caf09c1bfeed4ee9d.7218.D49aeed8a5081a--></protect>
<!--box uid=bc145ea147f7e36caf09c1bfeed4ee9d.7218.D49aeed8a5081a--></protect>
Line 68: Line 76:
{{BacktoTop}}
{{BacktoTop}}


MutS, also known as the "mismatch recognition" enzyme, is essential for the DNA mismatch repair (MMR) biological pathway. It recognizes base-base mismatches and small nucleotide insertion/deletion mispairs generated during DNA synthesis or damage caused by various agents. After recognizing the mismatches, mutS binds to the mismatch as a homodimer. Although the mutS binding site is sequence-wise identical, the mismatch and mutS are structurally and functionally different, so it is virtually a heterodimer.
MutS, also known as the "mismatch recognition" enzyme, is essential for the DNA mismatch repair (MMR) biological pathway. It recognizes base-base mismatches and small nucleotide insertion/deletion mispairs generated during DNA synthesis or damage caused by various agents. After recognizing the mismatches, MutS binds to the mismatch as a homodimer. Although the MutS binding site is sequence-wise identical, the mismatch and MutS are structurally and functionally different, so it is virtually a heterodimer.


MutS also functions as an ATPase, providing energy for the MMR pathway. After binding to the mismatch, a hemi-methylated dGATC site is located and cleaved by other MMR enzymes. This dGATC binding site is either in the 3' or 5' direction from the mismatch. The entire MMR process is a highly conserved pathway with great similarities between the human pathway and E. coli pathway. The human homolog, MutSα, acts virtually the same as the E. coli form. <ref name='PMID:18157157'/>
MutS also functions as an ATPase, providing energy for the MMR pathway. After binding to the mismatch, a hemi-methylated dGATC site is located and cleaved by other MMR enzymes. This dGATC binding site is either in the 3' or 5' direction from the mismatch. The entire MMR process is a highly conserved pathway with great similarities between the human pathway and ''E. coli'' pathway. The human homolog, MutSα, acts virtually the same as the ''E. coli'' form of the protein.<ref name='PMID:18157157'/>


MutS has weak ATPase activity and may be involved in recognizing the DNA mismatch. MutS C- terminus dimerization, not tetramerization, is required for mismatch repair (Mendillo, 2007).<ref name='LIB:EcoGene'/>
MutS has weak ATPase activity and may be involved in recognizing the DNA mismatch. MutS C-terminus dimerization, not tetramerization, is required for mismatch repair. <ref name='PMID:17426027'/> <ref name='LIB:EcoGene'/>





Latest revision as of 21:47, 27 May 2013

{{#css:Suppresslinks.css}}<css>h1 .editsection { display:none;} h2 .editsection { display:none;}</css>

Quickview   Gene   Gene Product(s)   Expression   Evolution   On One Page    
References Suggestions
Standard Name

mutS

Gene Synonym(s)

ECK2728, b2733, JW2703, fdv, ant, plm[1], plm

Product Desc.

MutS[2][3];

Component of MutHLS complex, methyl-directed mismatch repair[2][3]

Methyl-directed mismatch repair protein; dimeric/tetrameric[4]

Product Synonyms(s)

methyl-directed mismatch repair protein[1], B2733[2][1], Plm[2][1], Ant[2][1], Fdv[2][1], MutS[2][1] , ant, ECK2728, fdv, JW2703, plm, b2733

Function from GO

<GO_nr />

Knock-Out Phenotype
Regulation/Expression

transcription unit(s): mutS[2]

Regulation/Activity
Quick Links



        

See Help:Quickview for help with entering information in the Quickview table.

Notes

[back to top]


MutS, also known as the "mismatch recognition" enzyme, is essential for the DNA mismatch repair (MMR) biological pathway. It recognizes base-base mismatches and small nucleotide insertion/deletion mispairs generated during DNA synthesis or damage caused by various agents. After recognizing the mismatches, MutS binds to the mismatch as a homodimer. Although the MutS binding site is sequence-wise identical, the mismatch and MutS are structurally and functionally different, so it is virtually a heterodimer.

MutS also functions as an ATPase, providing energy for the MMR pathway. After binding to the mismatch, a hemi-methylated dGATC site is located and cleaved by other MMR enzymes. This dGATC binding site is either in the 3' or 5' direction from the mismatch. The entire MMR process is a highly conserved pathway with great similarities between the human pathway and E. coli pathway. The human homolog, MutSα, acts virtually the same as the E. coli form of the protein.[5]

MutS has weak ATPase activity and may be involved in recognizing the DNA mismatch. MutS C-terminus dimerization, not tetramerization, is required for mismatch repair. [6] [4]



References

[back to top]


  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 Riley, M. et al. (2006) Nucleic Acids Res 34:1-6 (corrected supplemental data from B. Wanner)
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 EcoCyc (release 10.6; 2007) Keseler, IM et al. (2005) Nucleic Acids Res. 33(Database issue):D334-7
  3. ↑ 3.0 3.1 EcoCyc (release 11.1; 2007) Keseler, IM et al. (2005) Nucleic Acids Res. 33(Database issue):D334-7
  4. ↑ 4.0 4.1 EcoGene: Rudd, KE (2000) EcoGene: a genome sequence database for Escherichia coli K-12. Nucleic Acids Res 28:60-4.
  5. ↑ Li, GM (2008) Mechanisms and functions of DNA mismatch repair. Cell Res. 18 85-98 PubMed
  6. ↑ Mendillo, ML et al. (2007) Escherichia coli MutS tetramerization domain structure reveals that stable dimers but not tetramers are essential for DNA mismatch repair in vivo. J. Biol. Chem. 282 16345-54 PubMed