Immunotatin of Rv3151

From DrugPedia: A Wikipedia for Drug discovery

(Difference between revisions)
Jump to: navigation, search
(New page: {{immunebox | Name =<b>NADH dehydrogenase subunit G</b> |image= | width=250 |image2= |Swiss Prot = P95175 | Genbank = 887540 | PDB = | DrugBank = ...)
Current revision (08:36, 1 February 2010) (edit) (undo)
(MHC Class-II Binder)
 
(5 intermediate revisions not shown.)
Line 14: Line 14:
}}
}}
=General=
=General=
-
Inhibiion of apoptosis is one important event brought about by Mycobacterium Tuberculosis proteins to conquer the surrounding cells.The survival and persistence of Mycobacterium tuberculosis depends on its ability to actively inhibit the death by apoptosis of infected host cells. The genetic basis for this anti-apoptotic activity and its implication for mycobacterial virulence have not been demonstrated or elucidated. Using a novel gain-of-function genetic screen, we demonstrated that inhibition of infection-induced apoptosis of macrophages is controlled by multiple genetic loci in M. tuberculosis. Characterization of one of these loci in detail revealed that the anti-apoptosis activity was attributable to the type I NADH-dehydrogenase of M. tuberculosis, and was mainly due to the subunit of this multicomponent complex encoded by the nuoG gene. Expression of M. tuberculosis nuoG in nonpathogenic mycobacteria endowed them with the ability to inhibit apoptosis of infected human or mouse macrophages, and increased their virulence in a SCID mouse model. Conversely, deletion of nuoG in M. tuberculosis ablated its ability to inhibit macrophage apoptosis and significantly reduced its virulence in mice. These results identify a key component of the genetic basis for an important virulence trait of M. tuberculosis and support a direct causal relationship between virulence of pathogenic mycobacteria and their ability to inhibit macrophage apoptosis.
+
Inhibiion of apoptosis is an important event brought about by Mycobacterium Tuberculosis proteins to conquer the surrounding cells.The survival and persistence of Mycobacterium tuberculosis depends on its ability to actively inhibit the death by apoptosis of infected host cells. The genetic basis for this anti-apoptotic activity and its implication for mycobacterial virulence have not been demonstrated or elucidated. Using a novel gain-of-function genetic screen, we demonstrated that inhibition of infection-induced apoptosis of macrophages is controlled by multiple genetic loci in M. tuberculosis. Characterization of one of these loci in detail revealed that the anti-apoptosis activity was attributable to the type I NADH-dehydrogenase of M. tuberculosis, and was mainly due to the subunit of this multicomponent complex encoded by the nuoG gene. Expression of M. tuberculosis nuoG in nonpathogenic mycobacteria endowed them with the ability to inhibit apoptosis of infected human or mouse macrophages, and increased their virulence in a SCID mouse model. Conversely, deletion of nuoG in M. tuberculosis ablated its ability to inhibit macrophage apoptosis and significantly reduced its virulence in mice. These results identify a key component of the genetic basis for an important virulence trait of M. tuberculosis and support a direct causal relationship between virulence of pathogenic mycobacteria and their ability to inhibit macrophage apoptosis.
==Protein Sequence==
==Protein Sequence==
Line 30: Line 30:
KIGAGS
KIGAGS
*
*
-
 
=Human Homologue Blast Result=
=Human Homologue Blast Result=
Line 38: Line 37:
<td>subject ids</td><td>% identity</td><td>% positives</td><td>alignment length</td><td> evalue</td></tr>
<td>subject ids</td><td>% identity</td><td>% positives</td><td>alignment length</td><td> evalue</td></tr>
-
<tr><td></td><td> </td><td> </td><td> </td><td> </td></tr>
+
<tr><td>sp|P28331</td><td> 31</td><td> 46</td><td> 683</td><td> 1e-67</td></tr>
-
<tr><td></td><td> </td><td> </td><td> </td><td> </td></tr>
+
<tr><td>sp|Q96RG2</td><td> 27</td><td> 40</td><td> 140</td><td> 1.7</td></tr>
-
<tr><td></td><td> </td><td> </td><td> </td><td> </td></tr>
+
<tr><td>sp|Q9UFP1</td><td> 28</td><td> 43</td><td> 78</td><td> 4.2</td></tr>
-
<tr><td></td><td> </td><td> </td><td> </td><td> </td></tr>
+
<tr><td>sp|Q9UPY6</td><td> 38</td><td> 52</td><td> 36</td><td> 4.9</td></tr>
-
<tr><td></td><td> </td><td> </td><td> </td><td> </td></tr></table>
+
<tr><td>p|Q2M3C7</td><td> 51</td><td> 72</td><td> 29</td><td> 6.2</td></tr></table>
=Alergen Protein=
=Alergen Protein=
Link to [http://www.imtech.res.in/raghava/algpred/ Algpred]<br>
Link to [http://www.imtech.res.in/raghava/algpred/ Algpred]<br>
-
Non Allergen Predicted by AlgPred Server
+
result predicted by[http://crdd.osdd.net/drugpedia/images/Algpred_Out.pdf]
=Bacterial Toxin Prediction=
=Bacterial Toxin Prediction=
Link to [http://www.imtech.res.in/raghava/btxpred/submission.html btxpred]<br>
Link to [http://www.imtech.res.in/raghava/btxpred/submission.html btxpred]<br>
Line 66: Line 65:
Link to [http://www.imtech.res.in/raghava/bcepred/bcepred_submission.html Bcepred]   
Link to [http://www.imtech.res.in/raghava/bcepred/bcepred_submission.html Bcepred]   
<br>
<br>
-
Result Predicited by  []<br>
+
Result Predicited by  [http://crdd.osdd.net/drugpedia/images/B1.pdf]<br>
====ABCpred Analysis====
====ABCpred Analysis====
Link to [http://www.imtech.res.in/raghava/abcpred/ABC_submission.html ABCpred]<br>
Link to [http://www.imtech.res.in/raghava/abcpred/ABC_submission.html ABCpred]<br>
-
Result Predicited by  []<br>
+
Result Predicited by  [http://crdd.osdd.net/drugpedia/images/B2.pdf]<br>
====IEDB Analysis====
====IEDB Analysis====
Link to [http://tools.immuneepitope.org/tools/bcell/iedb_input IEDB]<br>
Link to [http://tools.immuneepitope.org/tools/bcell/iedb_input IEDB]<br>
-
Result Predicited by  []<br>
+
Result Predicited by  [http://crdd.osdd.net/drugpedia/images/B3.pdf]<br>
=MHC Class-I Binder=
=MHC Class-I Binder=
Line 80: Line 79:
Link to [http://www.imtech.res.in/raghava/nhlapred/comp.html nHLApred]
Link to [http://www.imtech.res.in/raghava/nhlapred/comp.html nHLApred]
<br>  
<br>  
-
Result Predicited by  []<br>
+
Result Predicited by  [http://crdd.osdd.net/drugpedia/images/Bbb1.pdf]<br>
==IEDB Analysis==
==IEDB Analysis==
Link to [http://tools.immuneepitope.org/analyze/html/mhc_processing.html IEDB] <br>
Link to [http://tools.immuneepitope.org/analyze/html/mhc_processing.html IEDB] <br>
-
Result Predicted by []
+
Result Predicted by [http://crdd.osdd.net/drugpedia/images/Beta1.txt]
=MHC Class-II Binder=
=MHC Class-II Binder=
==Propred Analysis==
==Propred Analysis==
Link to [http://www.imtech.res.in/raghava/propred/ Propred]<br>
Link to [http://www.imtech.res.in/raghava/propred/ Propred]<br>
-
Result Predicted by []
+
Result Predicted by [http://crdd.osdd.net/drugpedia/images/Beta2.pdf]
==NetMHC-II Analysis==
==NetMHC-II Analysis==
Link to [http://www.cbs.dtu.dk/services/NetMHCII/ NetMHC-II]<br>
Link to [http://www.cbs.dtu.dk/services/NetMHCII/ NetMHC-II]<br>
-
Result Predicted by []
+
Result Predicted by [http://crdd.osdd.net/drugpedia/images/Beta3.txt]
=External Links=
=External Links=

Current revision

Immunotatin of Rv3151
Name
NADH dehydrogenase subunit G
Identifiers
Swiss Prot P95175
Genbank 887540
PDB  ?
Chemical data
Formula  ?
Mol. wt. 85423.2
Pharmacokinetic data
Bioavailability  ?
Solubility  ?
Isoelectric-Point 5.28

Contents

[edit] General

Inhibiion of apoptosis is an important event brought about by Mycobacterium Tuberculosis proteins to conquer the surrounding cells.The survival and persistence of Mycobacterium tuberculosis depends on its ability to actively inhibit the death by apoptosis of infected host cells. The genetic basis for this anti-apoptotic activity and its implication for mycobacterial virulence have not been demonstrated or elucidated. Using a novel gain-of-function genetic screen, we demonstrated that inhibition of infection-induced apoptosis of macrophages is controlled by multiple genetic loci in M. tuberculosis. Characterization of one of these loci in detail revealed that the anti-apoptosis activity was attributable to the type I NADH-dehydrogenase of M. tuberculosis, and was mainly due to the subunit of this multicomponent complex encoded by the nuoG gene. Expression of M. tuberculosis nuoG in nonpathogenic mycobacteria endowed them with the ability to inhibit apoptosis of infected human or mouse macrophages, and increased their virulence in a SCID mouse model. Conversely, deletion of nuoG in M. tuberculosis ablated its ability to inhibit macrophage apoptosis and significantly reduced its virulence in mice. These results identify a key component of the genetic basis for an important virulence trait of M. tuberculosis and support a direct causal relationship between virulence of pathogenic mycobacteria and their ability to inhibit macrophage apoptosis.

[edit] Protein Sequence

>Rv3151, TB.seq 3516743:3519160 MW:85393 VTQAADTDIRVGQPEMVTLTIDGVEISVPKGTLVIRAAELMGIQIPRFCDHPLLEPVGACRQCLVEVEGQRKPLASCTTV ATDDMVVRTQLTSEIADKAQHGVMELLLINHPLDCPMCDKGGECPLQNQAMSNGRTDSRFTEAKRTFAKPINISAQVLLD RERCILCARCTRFSDQIAGDPFIDMQERGALQQVGIYADEPFESYFSGNTVQICPVGALTGTAYRFRARPFDLVSSPSVC EHCASGCAQRTDHRRGKVLRRLAGDDPEVNEEWNCDKGRWAFTYATQPDVITTPLIRDGGDPKGALVPTSWSHAMAVAAQ GLAAARGRTGVLVGGRVTWEDAYAYAKFARITLGTNDIDFRARPHSAEEADFLAARIAGRHMAVSYADLESAPVVLLVGF EPEDESPIVFLRLRKAARRHRVPVYTIAPFATGGLHKMSGRLIKTVPGGEPAALDDLATGAVGDLLATPGAVIIVGERLA TVPGGLSAAARLADTTGARLAWVPRRAGERGALEAGALPTLLPGGRPLADEVARAQVCAAWHIAELPAAAGRDADGILAA AADETLAALLVGGIEPADFADPDAVLAALDATGFVVSLELRHSTVTERADVVFPVAPTTQKAGAFVNWEGRYRTFEPALR GSTLQAGQSDHRVLDALADDMGVHLGVPTVEAAREELAALGIWDGKHAAGPHIAATGPTQPEAGEAILTGWRMLLDEGRL QDGEPYLAGTARTPVVRLSPDTAAEIGAADGEAVTVSTSRGSITLPCSVTDMPDRVVWLPLNSAGSTVHRQLRVTIGSIV KIGAGS

[edit] Human Homologue Blast Result

subject ids% identity% positivesalignment length evalue
sp|P28331 31 46 683 1e-67
sp|Q96RG2 27 40 140 1.7
sp|Q9UFP1 28 43 78 4.2
sp|Q9UPY6 38 52 36 4.9
p|Q2M3C7 51 72 29 6.2

[edit] Alergen Protein

Link to Algpred
result predicted by[1]

[edit] Bacterial Toxin Prediction

Link to btxpred
No Hit Fountd by btxpred server.

[edit] Subcellular Location

Link to TBpred
Cyoplasmic

[edit] Antigens

No Hit Found in AntigenDB
No. Hit Found in IEDB

[edit] B cell Epitopes

[edit] BCEpred Analysis

Link to Bcepred
Result Predicited by [2]

[edit] ABCpred Analysis

Link to ABCpred
Result Predicited by [3]

[edit] IEDB Analysis

Link to IEDB
Result Predicited by [4]

[edit] MHC Class-I Binder

[edit] nHLAPred Analysis

Link to nHLApred
Result Predicited by [5]

[edit] IEDB Analysis

Link to IEDB
Result Predicted by [6]

[edit] MHC Class-II Binder

[edit] Propred Analysis

Link to Propred
Result Predicted by [7]


[edit] NetMHC-II Analysis

Link to NetMHC-II
Result Predicted by [8]

[edit] External Links

  • Database of Mycobacterium tuberculosis genome sequences and related information.