5d2l - Revision history

OCA at 08:42, 27 September 2023

2023-09-27T08:42:41Z

←Older revision		Revision as of 08:42, 27 September 2023
Line 4:		Line 4:
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure with sequence from [https://en.wikipedia.org/wiki/Cytomegalovirus Cytomegalovirus] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5D2L FirstGlance]. <br>		<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure with sequence from [https://en.wikipedia.org/wiki/Cytomegalovirus Cytomegalovirus] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5D2L FirstGlance]. <br>
-	</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=5d2l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d2l OCA], [https://pdbe.org/5d2l PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5d2l RCSB], [https://www.ebi.ac.uk/pdbsum/5d2l PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5d2l ProSAT]</span></td></tr>	+	</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models\|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution\|Resolution]] 3.511Å</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=5d2l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d2l OCA], [https://pdbe.org/5d2l PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5d2l RCSB], [https://www.ebi.ac.uk/pdbsum/5d2l PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5d2l ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==

OCA at 10:19, 21 June 2023

2023-06-21T10:19:18Z

←Older revision		Revision as of 10:19, 21 June 2023
Line 3:		Line 3:
	<StructureSection load='5d2l' size='340' side='right'caption='[[5d2l]], [[Resolution\|resolution]] 3.51Å' scene=''>		<StructureSection load='5d2l' size='340' side='right'caption='[[5d2l]], [[Resolution\|resolution]] 3.51Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Human Human~~]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=5D2L FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure with sequence from [https://en.wikipedia.org/wiki/Cytomegalovirus Cytomegalovirus] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5D2L FirstGlance]. <br>
-	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">HLA-A, HLAA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN]), B2M, CDABP0092, HDCMA22P ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>	+	</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=5d2l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d2l OCA], [https://pdbe.org/5d2l PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5d2l RCSB], [https://www.ebi.ac.uk/pdbsum/5d2l PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5d2l 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=5d2l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d2l OCA], [~~http~~://pdbe.org/5d2l PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=5d2l RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/5d2l PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=5d2l ProSAT]</span></td></tr>	+
	</table>		</table>
	== Disease ==		== Disease ==
-	[~~[http~~://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN]] Defects in B2M are the cause of hypercatabolic hypoproteinemia (HYCATHYP) [MIM:[~~http~~://omim.org/entry/241600 241600]]. Affected individuals show marked reduction in serum concentrations of immunoglobulin and albumin, probably due to rapid degradation.<ref>PMID:16549777</ref> Note=Beta-2-microglobulin may adopt the fibrillar configuration of amyloid in certain pathologic states. The capacity to assemble into amyloid fibrils is concentration dependent. Persistently high beta(2)-microglobulin serum levels lead to amyloidosis in patients on long-term hemodialysis.<ref>PMID:3532124</ref> <ref>PMID:1336137</ref> <ref>PMID:7554280</ref> <ref>PMID:4586824</ref> <ref>PMID:8084451</ref> <ref>PMID:12119416</ref> <ref>PMID:12796775</ref> <ref>PMID:16901902</ref> <ref>PMID:16491088</ref> <ref>PMID:17646174</ref> <ref>PMID:18835253</ref> <ref>PMID:18395224</ref> <ref>PMID:19284997</ref>	+	[https://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN] Defects in B2M are the cause of hypercatabolic hypoproteinemia (HYCATHYP) [MIM:[https://omim.org/entry/241600 241600]. Affected individuals show marked reduction in serum concentrations of immunoglobulin and albumin, probably due to rapid degradation.<ref>PMID:16549777</ref> Note=Beta-2-microglobulin may adopt the fibrillar configuration of amyloid in certain pathologic states. The capacity to assemble into amyloid fibrils is concentration dependent. Persistently high beta(2)-microglobulin serum levels lead to amyloidosis in patients on long-term hemodialysis.<ref>PMID:3532124</ref> <ref>PMID:1336137</ref> <ref>PMID:7554280</ref> <ref>PMID:4586824</ref> <ref>PMID:8084451</ref> <ref>PMID:12119416</ref> <ref>PMID:12796775</ref> <ref>PMID:16901902</ref> <ref>PMID:16491088</ref> <ref>PMID:17646174</ref> <ref>PMID:18835253</ref> <ref>PMID:18395224</ref> <ref>PMID:19284997</ref>
	== Function ==		== Function ==
-	[~~[http://www.uniprot.org/uniprot/1A02_HUMAN 1A02_HUMAN]] Involved in the presentation of foreign antigens to the immune system. [[http~~://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN]] Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.	+	[https://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN] Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.
	<div style="background-color:#fffaf0;">		<div style="background-color:#fffaf0;">
	== Publication Abstract from PubMed ==		== Publication Abstract from PubMed ==
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	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Human~~]]	+	[[Category: Cytomegalovirus]]
		+	[[Category: Homo sapiens]]
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	[[Category: Gao, M]]	+	[[Category: Gao M]]
-	[[Category: Mariuzza~~, R A]]~~	+	[[Category: Mariuzza RA]]
-	~~[[Category: Complex]]~~	+
-	~~[[Category: Hcmv]]~~	+
-	~~[[Category: Hla-a2]]~~	+
-	~~[[Category: Immune system]]~~	+
-	~~[[Category: Tcr~~]]	+

OCA at 11:18, 25 December 2019

2019-12-25T11:18:55Z

←Older revision		Revision as of 11:18, 25 December 2019
Line 11:		Line 11:
	== Function ==		== Function ==
	[[http://www.uniprot.org/uniprot/1A02_HUMAN 1A02_HUMAN]] Involved in the presentation of foreign antigens to the immune system. [[http://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN]] Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.		[[http://www.uniprot.org/uniprot/1A02_HUMAN 1A02_HUMAN]] Involved in the presentation of foreign antigens to the immune system. [[http://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN]] Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.
		+	<div style="background-color:#fffaf0;">
		+	== Publication Abstract from PubMed ==
		+	Cytomegalovirus (CMV) is a ubiquitous and persistent human pathogen that is kept in check by CD8(+) cytotoxic T lymphocytes. Individuals expressing the major histocompatibility complex (MHC) class I molecule HLA-A2 produce cytotoxic T lymphocytes bearing T cell receptors (TCRs) that recognize the immunodominant CMV epitope NLVPMVATV (NLV). The NLV-specific T cell repertoire is characterized by a high prevalence of TCRs that are frequently observed in multiple unrelated individuals. These public TCRs feature identical, or nearly identical, complementarity-determining region 3alpha (CDR3alpha) and/or CDR3beta sequences. The TCRs may express public CDR3alpha motifs alone, public CDR3beta motifs alone, or dual public CDR3alphabeta motifs. In addition, the same public CDR3alpha motif may pair with different CDR3beta motifs (and the reverse), giving rise to highly diverse NLV-specific TCR repertoires. To investigate the structural underpinnings of this clonal diversity, we determined crystal structures of two public TCRs (C7 and C25) in complex with NLV.HLA-A2. These TCRs utilize completely different CDR3alpha and CDR3beta motifs that, in addition, can associate with multiple variable alpha and variable beta regions in NLV-specific T cell repertoires. The C7.NLV.HLA-A2 and C25.NLV.HLA-A2 complexes exhibit divergent TCR footprints on peptide-MHC such that C25 is more focused on the central portion of the NLV peptide than is C7. These structures combined with molecular modeling show how the public CDR3alpha motif of C25 may associate with different variable alpha regions and how the public CDR3alpha motif of C7 may pair with different CDR3beta motifs. This interchangeability of TCR V regions and CDR3 motifs permits multiple structural solutions to binding an identical peptide-MHC ligand and thereby the generation of a clonally diverse public T cell response to CMV.
		+
		+	Structural Basis for Clonal Diversity of the Public T Cell Response to a Dominant Human Cytomegalovirus Epitope.,Yang X, Gao M, Chen G, Pierce BG, Lu J, Weng NP, Mariuzza RA J Biol Chem. 2015 Nov 27;290(48):29106-19. doi: 10.1074/jbc.M115.691311. Epub, 2015 Oct 1. PMID:26429912<ref>PMID:26429912</ref>
		+
		+	From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br>
		+	</div>
		+	<div class="pdbe-citations 5d2l" style="background-color:#fffaf0;"></div>

	==See Also==		==See Also==

OCA at 16:01, 11 December 2019

2019-12-11T16:01:38Z

←Older revision		Revision as of 16:01, 11 December 2019
Line 1:		Line 1:

	==Crystal structure of TCR C7 in complex with HCMV NLV epitope presented by HLA-A2==		==Crystal structure of TCR C7 in complex with HCMV NLV epitope presented by HLA-A2==
-	<StructureSection load='5d2l' size='340' side='right' caption='[[5d2l]], [[Resolution\|resolution]] 3.51Å' scene=''>	+	<StructureSection load='5d2l' size='340' side='right'caption='[[5d2l]], [[Resolution\|resolution]] 3.51Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5D2L FirstGlance]. <br>		<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5D2L FirstGlance]. <br>
Line 11:		Line 11:
	== Function ==		== Function ==
	[[http://www.uniprot.org/uniprot/1A02_HUMAN 1A02_HUMAN]] Involved in the presentation of foreign antigens to the immune system. [[http://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN]] Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.		[[http://www.uniprot.org/uniprot/1A02_HUMAN 1A02_HUMAN]] Involved in the presentation of foreign antigens to the immune system. [[http://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN]] Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.
		+
		+	==See Also==
		+	*[[Beta-2 microglobulin 3D structures\|Beta-2 microglobulin 3D structures]]
	== References ==		== References ==
	<references/>		<references/>
Line 16:		Line 19:
	</StructureSection>		</StructureSection>
	[[Category: Human]]		[[Category: Human]]
		+	[[Category: Large Structures]]
	[[Category: Gao, M]]		[[Category: Gao, M]]
	[[Category: Mariuzza, R A]]		[[Category: Mariuzza, R A]]

OCA at 12:30, 6 November 2017

2017-11-06T12:30:27Z

←Older revision		Revision as of 12:30, 6 November 2017
Line 1:		Line 1:
		+
	==Crystal structure of TCR C7 in complex with HCMV NLV epitope presented by HLA-A2==		==Crystal structure of TCR C7 in complex with HCMV NLV epitope presented by HLA-A2==
	<StructureSection load='5d2l' size='340' side='right' caption='[[5d2l]], [[Resolution\|resolution]] 3.51Å' scene=''>		<StructureSection load='5d2l' size='340' side='right' caption='[[5d2l]], [[Resolution\|resolution]] 3.51Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5D2L FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5D2L FirstGlance]. <br>
-	</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=5d2l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d2l OCA], [http://pdbe.org/5d2l PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5d2l RCSB], [http://www.ebi.ac.uk/pdbsum/5d2l PDBsum]</span></td></tr>	+	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">HLA-A, HLAA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN]), B2M, CDABP0092, HDCMA22P ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=5d2l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d2l OCA], [http://pdbe.org/5d2l PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5d2l RCSB], [http://www.ebi.ac.uk/pdbsum/5d2l PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5d2l ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
Line 13:		Line 15:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Human]]
	[[Category: Gao, M]]		[[Category: Gao, M]]
	[[Category: Mariuzza, R A]]		[[Category: Mariuzza, R A]]

OCA at 13:53, 7 October 2015

2015-10-07T13:53:10Z

←Older revision		Revision as of 13:53, 7 October 2015
Line 1:		Line 1:
-	'''~~Unreleased structure~~'''	+	==Crystal structure of TCR C7 in complex with HCMV NLV epitope presented by HLA-A2==
-		+	<StructureSection load='5d2l' size='340' side='right' caption='[[5d2l]], [[Resolution\|resolution]] 3.51Å' scene=''>
-	~~The entry~~ 5d2l is ~~ON HOLD until Paper Publication~~	+	== Structural highlights ==
-		+	<table><tr><td colspan='2'>[[5d2l]] is a 20 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D2L OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5D2L FirstGlance]. <br>
-	~~Authors~~: ~~Gao~~, M., ~~Mariuzza~~, R.A.	+	</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=5d2l FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d2l OCA], [http://pdbe.org/5d2l PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5d2l RCSB], [http://www.ebi.ac.uk/pdbsum/5d2l PDBsum]</span></td></tr>
-		+	</table>
-	~~Description~~: ~~Crystal structure~~ of ~~TCR C7~~ in ~~complex with HCMV NLV epitope presented by HLA~~-A2	+	== Disease ==
-	[[~~Category~~: ~~Unreleased Structures~~]]	+	[[http://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN]] Defects in B2M are the cause of hypercatabolic hypoproteinemia (HYCATHYP) [MIM:[http://omim.org/entry/241600 241600]]. Affected individuals show marked reduction in serum concentrations of immunoglobulin and albumin, probably due to rapid degradation.<ref>PMID:16549777</ref> Note=Beta-2-microglobulin may adopt the fibrillar configuration of amyloid in certain pathologic states. The capacity to assemble into amyloid fibrils is concentration dependent. Persistently high beta(2)-microglobulin serum levels lead to amyloidosis in patients on long-term hemodialysis.<ref>PMID:3532124</ref> <ref>PMID:1336137</ref> <ref>PMID:7554280</ref> <ref>PMID:4586824</ref> <ref>PMID:8084451</ref> <ref>PMID:12119416</ref> <ref>PMID:12796775</ref> <ref>PMID:16901902</ref> <ref>PMID:16491088</ref> <ref>PMID:17646174</ref> <ref>PMID:18835253</ref> <ref>PMID:18395224</ref> <ref>PMID:19284997</ref>
-	[[~~Category~~: ~~Mariuzza, R~~.A]]	+	== Function ==
		+	[[http://www.uniprot.org/uniprot/1A02_HUMAN 1A02_HUMAN]] Involved in the presentation of foreign antigens to the immune system. [[http://www.uniprot.org/uniprot/B2MG_HUMAN B2MG_HUMAN]] Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system.
		+	== References ==
		+	<references/>
		+	__TOC__
		+	</StructureSection>
	[[Category: Gao, M]]		[[Category: Gao, M]]
		+	[[Category: Mariuzza, R A]]
		+	[[Category: Complex]]
		+	[[Category: Hcmv]]
		+	[[Category: Hla-a2]]
		+	[[Category: Immune system]]
		+	[[Category: Tcr]]

OCA at 11:18, 20 August 2015

2015-08-20T11:18:00Z

←Older revision		Revision as of 11:18, 20 August 2015
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 5d2l is ON HOLD	+	The entry 5d2l is ON HOLD until Paper Publication

	Authors: Gao, M., Mariuzza, R.A.		Authors: Gao, M., Mariuzza, R.A.

OCA: Protected "5d2l" [edit=sysop:move=sysop]

2015-08-12T13:45:14Z

Protected "5d2l" [edit=sysop:move=sysop]

←Older revision

Revision as of 13:45, 12 August 2015

OCA: New page: '''Unreleased structure''' The entry 5d2l is ON HOLD Authors: Gao, M., Mariuzza, R.A. Description: Crystal structure of TCR C7 in complex with HCMV NLV epitope presented by HLA-A2 [[Ca...

2015-08-12T13:45:13Z

New page: '''Unreleased structure''' The entry 5d2l is ON HOLD Authors: Gao, M., Mariuzza, R.A. Description: Crystal structure of TCR C7 in complex with HCMV NLV epitope presented by HLA-A2 [[Ca...

New page

'''Unreleased structure'''

The entry 5d2l is ON HOLD

Authors: Gao, M., Mariuzza, R.A.

Description: Crystal structure of TCR C7 in complex with HCMV NLV epitope presented by HLA-A2
[[Category: Unreleased Structures]]
[[Category: Mariuzza, R.A]]
[[Category: Gao, M]]