5aay - Revision history

OCA at 04:48, 25 May 2023

OCA — Thu, 25 May 2023 04:48:39 GMT

←Older revision		Revision as of 04:48, 25 May 2023
Line 1:		Line 1:

	==TBK1 recruitment to cytosol-invading Salmonella induces anti- bacterial autophagy==		==TBK1 recruitment to cytosol-invading Salmonella induces anti- bacterial autophagy==
-	<StructureSection load='5aay' size='340' side='right'caption='[[5aay~~]], [[NMR_Ensembles_of_Models \| 20 NMR models~~]]' scene=''>	+	<StructureSection load='5aay' size='340' side='right'caption='[[5aay]]' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5aay]] is a 1 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Human Human~~]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5AAY OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=5AAY FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5aay]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5AAY OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5AAY FirstGlance]. <br>
-	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>~~</td></tr>~~	+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
-	~~<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[5aaq\|5aaq]], [[5aas\|5aas]], [[5aaz\|5aaz]]~~</td></tr>	+	<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5aay FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5aay OCA], [https://pdbe.org/5aay PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5aay RCSB], [https://www.ebi.ac.uk/pdbsum/5aay PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5aay ProSAT]</span></td></tr>
-	<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=5aay FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5aay OCA], [~~http~~://pdbe.org/5aay PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=5aay RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/5aay PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=5aay ProSAT]</span></td></tr>	+
	</table>		</table>
	== Disease ==		== Disease ==
-	[~~[http~~://www.uniprot.org/uniprot/NEMO_HUMAN NEMO_HUMAN]] Defects in IKBKG are the cause of ectodermal dysplasia anhidrotic with immunodeficiency X-linked (EDAID) [MIM:[~~http~~://omim.org/entry/300291 300291]]; also known as hypohidrotic ectodermal dysplasia with immunodeficiency (HED-ID). Is a form of ectoderma dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. Characterized by absence of sweat glands, sparse scalp hair, rare conical teeth and immunological abnormalities resulting in severe infectious diseases.<ref>PMID:14651848</ref> <ref>PMID:16547522</ref> <ref>PMID:21606507</ref> <ref>PMID:19185524</ref> <ref>PMID:11047757</ref> <ref>PMID:11242109</ref> <ref>PMID:11224521</ref> <ref>PMID:12045264</ref> <ref>PMID:15100680</ref> Defects in IKBKG are the cause of ectodermal dysplasia anhidrotic with immunodeficiency-osteopetrosis-lymphedema (OLEDAID) [MIM:[~~http~~://omim.org/entry/300301 300301]]. Defects in IKBKG are a cause of immunodeficiency NEMO-related without anhidrotic ectodermal dysplasia (NEMOID) [MIM:[~~http~~://omim.org/entry/300584 300584]]; also called immunodeficiency without anhidrotic ectodermal dysplasia, isolated immunodeficiency or pure immunodeficiency. Patients manifest immunodeficiency not associated with other abnormalities, and resulting in increased infection susceptibility. Patients suffer from multiple episodes of infectious diseases.<ref>PMID:15100680</ref> <ref>PMID:15356572</ref> Defects in IKBKG are the cause of susceptibility to X-linked familial atypical micobacteriosis type 1 (AMCBX1) [MIM:[~~http~~://omim.org/entry/300636 300636]]; also known as X-linked disseminated atypical mycobacterial infection type 1 or X-linked susceptibility to mycobacterial disease type 1. AMCBX1 is the X-linked recessive form of Mendelian susceptibility to mycobacterial disease (MSMD). MSMD is a congenital syndrome resulting in predisposition to clinical disease caused by weakly virulent mycobacterial species, such as bacillus Calmette-Guerin vaccines and non-tuberculous, environmental mycobacteria. Patients are also susceptible to the more virulent species Mycobacterium tuberculosis.<ref>PMID:19185524</ref> <ref>PMID:16818673</ref> Defects in IKBKG are the cause of recurrent isolated invasive pneumococcal disease type 2 (IPD2) [MIM:[~~http~~://omim.org/entry/300640 300640]]. Recurrent invasive pneumococcal disease (IPD) is defined as two episodes of IPD occurring at least 1 month apart, whether caused by the same or different serotypes or strains. Recurrent IPD occurs in at least 2% of patients in most series, making IPD the most important known risk factor for subsequent IPD.<ref>PMID:16950813</ref> Defects in IKBKG are the cause of incontinentia pigmenti (IP) [MIM:[~~http~~://omim.org/entry/308300 308300]]; formerly designed familial incontinentia pigmenti type II (IP2). IP is a genodermatosis usually prenatally lethal in males. In affected females, it causes abnormalities of the skin, hair, eyes, nails, teeth, skeleton, heart, and central nervous system. The prominent skin signs occur in four classic cutaneous stages: perinatal inflammatory vesicles, verrucous patches, a distinctive pattern of hyperpigmentation and dermal scarring.<ref>PMID:20010814</ref> <ref>PMID:17728323</ref> <ref>PMID:19185524</ref> <ref>PMID:16950813</ref> <ref>PMID:10839543</ref> <ref>PMID:19033441</ref> <ref>PMID:11590134</ref> <ref>PMID:15229184</ref>	+	[https://www.uniprot.org/uniprot/NEMO_HUMAN NEMO_HUMAN] Defects in IKBKG are the cause of ectodermal dysplasia anhidrotic with immunodeficiency X-linked (EDAID) [MIM:[https://omim.org/entry/300291 300291]; also known as hypohidrotic ectodermal dysplasia with immunodeficiency (HED-ID). Is a form of ectoderma dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. Characterized by absence of sweat glands, sparse scalp hair, rare conical teeth and immunological abnormalities resulting in severe infectious diseases.<ref>PMID:14651848</ref> <ref>PMID:16547522</ref> <ref>PMID:21606507</ref> <ref>PMID:19185524</ref> <ref>PMID:11047757</ref> <ref>PMID:11242109</ref> <ref>PMID:11224521</ref> <ref>PMID:12045264</ref> <ref>PMID:15100680</ref> Defects in IKBKG are the cause of ectodermal dysplasia anhidrotic with immunodeficiency-osteopetrosis-lymphedema (OLEDAID) [MIM:[https://omim.org/entry/300301 300301]. Defects in IKBKG are a cause of immunodeficiency NEMO-related without anhidrotic ectodermal dysplasia (NEMOID) [MIM:[https://omim.org/entry/300584 300584]; also called immunodeficiency without anhidrotic ectodermal dysplasia, isolated immunodeficiency or pure immunodeficiency. Patients manifest immunodeficiency not associated with other abnormalities, and resulting in increased infection susceptibility. Patients suffer from multiple episodes of infectious diseases.<ref>PMID:15100680</ref> <ref>PMID:15356572</ref> Defects in IKBKG are the cause of susceptibility to X-linked familial atypical micobacteriosis type 1 (AMCBX1) [MIM:[https://omim.org/entry/300636 300636]; also known as X-linked disseminated atypical mycobacterial infection type 1 or X-linked susceptibility to mycobacterial disease type 1. AMCBX1 is the X-linked recessive form of Mendelian susceptibility to mycobacterial disease (MSMD). MSMD is a congenital syndrome resulting in predisposition to clinical disease caused by weakly virulent mycobacterial species, such as bacillus Calmette-Guerin vaccines and non-tuberculous, environmental mycobacteria. Patients are also susceptible to the more virulent species Mycobacterium tuberculosis.<ref>PMID:19185524</ref> <ref>PMID:16818673</ref> Defects in IKBKG are the cause of recurrent isolated invasive pneumococcal disease type 2 (IPD2) [MIM:[https://omim.org/entry/300640 300640]. Recurrent invasive pneumococcal disease (IPD) is defined as two episodes of IPD occurring at least 1 month apart, whether caused by the same or different serotypes or strains. Recurrent IPD occurs in at least 2% of patients in most series, making IPD the most important known risk factor for subsequent IPD.<ref>PMID:16950813</ref> Defects in IKBKG are the cause of incontinentia pigmenti (IP) [MIM:[https://omim.org/entry/308300 308300]; formerly designed familial incontinentia pigmenti type II (IP2). IP is a genodermatosis usually prenatally lethal in males. In affected females, it causes abnormalities of the skin, hair, eyes, nails, teeth, skeleton, heart, and central nervous system. The prominent skin signs occur in four classic cutaneous stages: perinatal inflammatory vesicles, verrucous patches, a distinctive pattern of hyperpigmentation and dermal scarring.<ref>PMID:20010814</ref> <ref>PMID:17728323</ref> <ref>PMID:19185524</ref> <ref>PMID:16950813</ref> <ref>PMID:10839543</ref> <ref>PMID:19033441</ref> <ref>PMID:11590134</ref> <ref>PMID:15229184</ref>
	== Function ==		== Function ==
-	[~~[http~~://www.uniprot.org/uniprot/NEMO_HUMAN NEMO_HUMAN]] Regulatory subunit of the IKK core complex which phosphorylates inhibitors of NF-kappa-B thus leading to the dissociation of the inhibitor/NF-kappa-B complex and ultimately the degradation of the inhibitor. Its binding to scaffolding polyubiquitin seems to play a role in IKK activation by multiple signaling receptor pathways. However, the specific type of polyubiquitin recognized upon cell stimulation (either 'Lys-63'-linked or linear polyubiquitin) and its functional importance is reported conflictingly. Also considered to be a mediator for TAX activation of NF-kappa-B. Could be implicated in NF-kappa-B-mediated protection from cytokine toxicity (By similarity). Essential for viral activation of IRF3. Involved in TLR3- and IFIH1-mediated antiviral innate response; this function requires 'Lys-27'-linked polyubiquitination.<ref>PMID:14695475</ref> <ref>PMID:19854139</ref> <ref>PMID:20724660</ref>	+	[https://www.uniprot.org/uniprot/NEMO_HUMAN NEMO_HUMAN] Regulatory subunit of the IKK core complex which phosphorylates inhibitors of NF-kappa-B thus leading to the dissociation of the inhibitor/NF-kappa-B complex and ultimately the degradation of the inhibitor. Its binding to scaffolding polyubiquitin seems to play a role in IKK activation by multiple signaling receptor pathways. However, the specific type of polyubiquitin recognized upon cell stimulation (either 'Lys-63'-linked or linear polyubiquitin) and its functional importance is reported conflictingly. Also considered to be a mediator for TAX activation of NF-kappa-B. Could be implicated in NF-kappa-B-mediated protection from cytokine toxicity (By similarity). Essential for viral activation of IRF3. Involved in TLR3- and IFIH1-mediated antiviral innate response; this function requires 'Lys-27'-linked polyubiquitination.<ref>PMID:14695475</ref> <ref>PMID:19854139</ref> <ref>PMID:20724660</ref>
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
Line 25:		Line 24:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Human~~]]	+	[[Category: Homo sapiens]]
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	[[Category: Allen~~, M D~~]]	+	[[Category: Allen MD]]
-	[[Category: Bloor, S]]	+	[[Category: Bloor S]]
-	[[Category: Bycroft, M]]	+	[[Category: Bycroft M]]
-	[[Category: Holden, D]]	+	[[Category: Holden D]]
-	[[Category: Karpiyevitch, M]]	+	[[Category: Karpiyevitch M]]
-	[[Category: Kaul, A]]	+	[[Category: Kaul A]]
-	[[Category: Komander, D]]	+	[[Category: Komander D]]
-	[[Category: Matthews, S]]	+	[[Category: Matthews S]]
-	[[Category: Randow, F]]	+	[[Category: Randow F]]
-	[[Category: Ravenhill, B]]	+	[[Category: Ravenhill B]]
-	[[Category: Thurston~~, T l]]~~	+	[[Category: Thurston Tl]]
-	~~[[Category: Protein binding~~]]	+

OCA at 07:56, 26 June 2019

OCA — Wed, 26 Jun 2019 07:56:16 GMT

←Older revision		Revision as of 07:56, 26 June 2019
Line 1:		Line 1:

	==TBK1 recruitment to cytosol-invading Salmonella induces anti- bacterial autophagy==		==TBK1 recruitment to cytosol-invading Salmonella induces anti- bacterial autophagy==
-	<StructureSection load='5aay' size='340' side='right' caption='[[5aay]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>	+	<StructureSection load='5aay' size='340' side='right'caption='[[5aay]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5aay]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5AAY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5AAY FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5aay]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5AAY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5AAY FirstGlance]. <br>
	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>		</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
	<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[5aaq\|5aaq]], [[5aas\|5aas]], [[5aaz\|5aaz]]</td></tr>		<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[5aaq\|5aaq]], [[5aas\|5aas]], [[5aaz\|5aaz]]</td></tr>
Line 25:		Line 25:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Human]]
		+	[[Category: Large Structures]]
	[[Category: Allen, M D]]		[[Category: Allen, M D]]
	[[Category: Bloor, S]]		[[Category: Bloor, S]]

OCA at 11:40, 14 July 2016

OCA — Thu, 14 Jul 2016 11:40:32 GMT

←Older revision		Revision as of 11:40, 14 July 2016
Line 1:		Line 1:
-	'''Unreleased structure'''

-	~~The entry~~ 5aay is ~~ON HOLD~~ ~~until Paper~~ Publication	+	==TBK1 recruitment to cytosol-invading Salmonella induces anti- bacterial autophagy==
		+	<StructureSection load='5aay' size='340' side='right' caption='[[5aay]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>
		+	== Structural highlights ==
		+	<table><tr><td colspan='2'>[[5aay]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5AAY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5AAY FirstGlance]. <br>
		+	</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand\|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
		+	<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[5aaq\|5aaq]], [[5aas\|5aas]], [[5aaz\|5aaz]]</td></tr>
		+	<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5aay FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5aay OCA], [http://pdbe.org/5aay PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5aay RCSB], [http://www.ebi.ac.uk/pdbsum/5aay PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5aay ProSAT]</span></td></tr>
		+	</table>
		+	== Disease ==
		+	[[http://www.uniprot.org/uniprot/NEMO_HUMAN NEMO_HUMAN]] Defects in IKBKG are the cause of ectodermal dysplasia anhidrotic with immunodeficiency X-linked (EDAID) [MIM:[http://omim.org/entry/300291 300291]]; also known as hypohidrotic ectodermal dysplasia with immunodeficiency (HED-ID). Is a form of ectoderma dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. Characterized by absence of sweat glands, sparse scalp hair, rare conical teeth and immunological abnormalities resulting in severe infectious diseases.<ref>PMID:14651848</ref> <ref>PMID:16547522</ref> <ref>PMID:21606507</ref> <ref>PMID:19185524</ref> <ref>PMID:11047757</ref> <ref>PMID:11242109</ref> <ref>PMID:11224521</ref> <ref>PMID:12045264</ref> <ref>PMID:15100680</ref> Defects in IKBKG are the cause of ectodermal dysplasia anhidrotic with immunodeficiency-osteopetrosis-lymphedema (OLEDAID) [MIM:[http://omim.org/entry/300301 300301]]. Defects in IKBKG are a cause of immunodeficiency NEMO-related without anhidrotic ectodermal dysplasia (NEMOID) [MIM:[http://omim.org/entry/300584 300584]]; also called immunodeficiency without anhidrotic ectodermal dysplasia, isolated immunodeficiency or pure immunodeficiency. Patients manifest immunodeficiency not associated with other abnormalities, and resulting in increased infection susceptibility. Patients suffer from multiple episodes of infectious diseases.<ref>PMID:15100680</ref> <ref>PMID:15356572</ref> Defects in IKBKG are the cause of susceptibility to X-linked familial atypical micobacteriosis type 1 (AMCBX1) [MIM:[http://omim.org/entry/300636 300636]]; also known as X-linked disseminated atypical mycobacterial infection type 1 or X-linked susceptibility to mycobacterial disease type 1. AMCBX1 is the X-linked recessive form of Mendelian susceptibility to mycobacterial disease (MSMD). MSMD is a congenital syndrome resulting in predisposition to clinical disease caused by weakly virulent mycobacterial species, such as bacillus Calmette-Guerin vaccines and non-tuberculous, environmental mycobacteria. Patients are also susceptible to the more virulent species Mycobacterium tuberculosis.<ref>PMID:19185524</ref> <ref>PMID:16818673</ref> Defects in IKBKG are the cause of recurrent isolated invasive pneumococcal disease type 2 (IPD2) [MIM:[http://omim.org/entry/300640 300640]]. Recurrent invasive pneumococcal disease (IPD) is defined as two episodes of IPD occurring at least 1 month apart, whether caused by the same or different serotypes or strains. Recurrent IPD occurs in at least 2% of patients in most series, making IPD the most important known risk factor for subsequent IPD.<ref>PMID:16950813</ref> Defects in IKBKG are the cause of incontinentia pigmenti (IP) [MIM:[http://omim.org/entry/308300 308300]]; formerly designed familial incontinentia pigmenti type II (IP2). IP is a genodermatosis usually prenatally lethal in males. In affected females, it causes abnormalities of the skin, hair, eyes, nails, teeth, skeleton, heart, and central nervous system. The prominent skin signs occur in four classic cutaneous stages: perinatal inflammatory vesicles, verrucous patches, a distinctive pattern of hyperpigmentation and dermal scarring.<ref>PMID:20010814</ref> <ref>PMID:17728323</ref> <ref>PMID:19185524</ref> <ref>PMID:16950813</ref> <ref>PMID:10839543</ref> <ref>PMID:19033441</ref> <ref>PMID:11590134</ref> <ref>PMID:15229184</ref>
		+	== Function ==
		+	[[http://www.uniprot.org/uniprot/NEMO_HUMAN NEMO_HUMAN]] Regulatory subunit of the IKK core complex which phosphorylates inhibitors of NF-kappa-B thus leading to the dissociation of the inhibitor/NF-kappa-B complex and ultimately the degradation of the inhibitor. Its binding to scaffolding polyubiquitin seems to play a role in IKK activation by multiple signaling receptor pathways. However, the specific type of polyubiquitin recognized upon cell stimulation (either 'Lys-63'-linked or linear polyubiquitin) and its functional importance is reported conflictingly. Also considered to be a mediator for TAX activation of NF-kappa-B. Could be implicated in NF-kappa-B-mediated protection from cytokine toxicity (By similarity). Essential for viral activation of IRF3. Involved in TLR3- and IFIH1-mediated antiviral innate response; this function requires 'Lys-27'-linked polyubiquitination.<ref>PMID:14695475</ref> <ref>PMID:19854139</ref> <ref>PMID:20724660</ref>
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	Mammalian cells deploy autophagy to defend their cytosol against bacterial invaders. Anti-bacterial autophagy relies on the core autophagy machinery, cargo receptors, and "eat-me" signals such as galectin-8 and ubiquitin that label bacteria as autophagy cargo. Anti-bacterial autophagy also requires the kinase TBK1, whose role in autophagy has remained enigmatic. Here we show that recruitment of WIPI2, itself essential for anti-bacterial autophagy, is dependent on the localization of catalytically active TBK1 to the vicinity of cytosolic bacteria. Experimental manipulation of TBK1 recruitment revealed that engagement of TBK1 with any of a variety of Salmonella-associated "eat-me" signals, including host-derived glycans and K48- and K63-linked ubiquitin chains, suffices to restrict bacterial proliferation. Promiscuity in recruiting TBK1 via independent signals may buffer TBK1 functionality from potential bacterial antagonism and thus be of evolutionary advantage to the host.

-	~~Authors:~~ Thurston, ~~T.l.~~, Allen, M~~.D.~~, Ravenhill, ~~B., Karpiyevitch,~~ M., Bloor, S., Kaul, A., Matthews~~, S.~~, Komander, D~~., Holden, D.~~, Bycroft, M., Randow, F.	+	Recruitment of TBK1 to cytosol-invading Salmonella induces WIPI2-dependent antibacterial autophagy.,Thurston TL, Boyle KB, Allen M, Ravenhill BJ, Karpiyevich M, Bloor S, Kaul A, Noad J, Foeglein A, Matthews SA, Komander D, Bycroft M, Randow F EMBO J. 2016 Jul 1. pii: e201694491. PMID:27370208<ref>PMID:27370208</ref>

-	~~Description: TBK1 recruitment to cytosol~~-~~invading Salmonella induces anti~~-~~bacterial autophagy~~	+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
-	~~[[Category~~: ~~Unreleased Structures]]~~	+	</div>
-	~~[[Category: Randow, F]]~~	+	<div class="pdbe-citations 5aay" style="background-color:#fffaf0;"></div>
-	~~[[Category: Matthews, S]]~~	+	== References ==
-	~~[[Category: Holden, D]]~~	+	<references/>
-	[[Category: Allen, M.D]]	+	__TOC__
-	~~[[Category: Kaul, A~~]]	+	</StructureSection>
		+	[[Category: Allen, M D]]
	[[Category: Bloor, S]]		[[Category: Bloor, S]]
		+	[[Category: Bycroft, M]]
		+	[[Category: Holden, D]]
	[[Category: Karpiyevitch, M]]		[[Category: Karpiyevitch, M]]
		+	[[Category: Kaul, A]]
	[[Category: Komander, D]]		[[Category: Komander, D]]
		+	[[Category: Matthews, S]]
		+	[[Category: Randow, F]]
	[[Category: Ravenhill, B]]		[[Category: Ravenhill, B]]
-	[[Category: Thurston, T.L]]	+	[[Category: Thurston, T l]]
-	[[Category: ~~Bycroft, M~~]]	+	[[Category: Protein binding]]

OCA at 00:26, 1 December 2015

OCA — Tue, 01 Dec 2015 00:26:21 GMT

←Older revision		Revision as of 00:26, 1 December 2015
Line 11:		Line 11:
	[[Category: Holden, D]]		[[Category: Holden, D]]
	[[Category: Allen, M.D]]		[[Category: Allen, M.D]]
-	[[Category: Bloor, S]]
-	[[Category: Thurston, T.L]]
	[[Category: Kaul, A]]		[[Category: Kaul, A]]
		+	[[Category: Bloor, S]]
	[[Category: Karpiyevitch, M]]		[[Category: Karpiyevitch, M]]
	[[Category: Komander, D]]		[[Category: Komander, D]]
	[[Category: Ravenhill, B]]		[[Category: Ravenhill, B]]
		+	[[Category: Thurston, T.L]]
	[[Category: Bycroft, M]]		[[Category: Bycroft, M]]

OCA: Protected "5aay" [edit=sysop:move=sysop]

OCA — Wed, 12 Aug 2015 12:13:12 GMT

Protected "5aay" [edit=sysop:move=sysop]

←Older revision

Revision as of 12:13, 12 August 2015

OCA: New page: '''Unreleased structure''' The entry 5aay is ON HOLD until Paper Publication Authors: Thurston, T.l., Allen, M.D., Ravenhill, B., Karpiyevitch, M., Bloor, S., Kaul, A., Matthews, S., Ko...

OCA — Wed, 12 Aug 2015 12:13:11 GMT

New page: '''Unreleased structure''' The entry 5aay is ON HOLD until Paper Publication Authors: Thurston, T.l., Allen, M.D., Ravenhill, B., Karpiyevitch, M., Bloor, S., Kaul, A., Matthews, S., Ko...

New page

'''Unreleased structure'''

The entry 5aay is ON HOLD until Paper Publication

Authors: Thurston, T.l., Allen, M.D., Ravenhill, B., Karpiyevitch, M., Bloor, S., Kaul, A., Matthews, S., Komander, D., Holden, D., Bycroft, M., Randow, F.

Description: TBK1 recruitment to cytosol-invading Salmonella induces anti-bacterial autophagy
[[Category: Unreleased Structures]]
[[Category: Randow, F]]
[[Category: Matthews, S]]
[[Category: Holden, D]]
[[Category: Allen, M.D]]
[[Category: Bloor, S]]
[[Category: Thurston, T.L]]
[[Category: Kaul, A]]
[[Category: Karpiyevitch, M]]
[[Category: Komander, D]]
[[Category: Ravenhill, B]]
[[Category: Bycroft, M]]