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==NMR structure of 16th module of Immune Adherence Receptor, Cr1 (Cd35)==
==NMR structure of 16th module of Immune Adherence Receptor, Cr1 (Cd35)==
<StructureSection load='1ppq' size='340' side='right'caption='[[1ppq]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
<StructureSection load='1ppq' size='340' side='right'caption='[[1ppq]]' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[1ppq]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PPQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1PPQ FirstGlance]. <br>
<table><tr><td colspan='2'>[[1ppq]] 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=1PPQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1PPQ FirstGlance]. <br>
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[1gkg|1gkg]], [[1gkn|1gkn]]</div></td></tr>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CR1 OR C3BR ([https://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'>[https://proteopedia.org/fgij/fg.htm?mol=1ppq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ppq OCA], [https://pdbe.org/1ppq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1ppq RCSB], [https://www.ebi.ac.uk/pdbsum/1ppq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1ppq ProSAT]</span></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=1ppq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ppq OCA], [https://pdbe.org/1ppq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1ppq RCSB], [https://www.ebi.ac.uk/pdbsum/1ppq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1ppq ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
[[https://www.uniprot.org/uniprot/CR1_HUMAN CR1_HUMAN]] Mediates cellular binding of particles and immune complexes that have activated complement.  
[https://www.uniprot.org/uniprot/CR1_HUMAN CR1_HUMAN] Mediates cellular binding of particles and immune complexes that have activated complement.
== Evolutionary Conservation ==
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
[[Image:Consurf_key_small.gif|200px|right]]
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1ppq ConSurf].
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1ppq ConSurf].
<div style="clear:both"></div>
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The regulators of complement activation (RCA) are critical to health and disease because their role is to ensure that a complement-mediated immune response to infection is proportionate and targeted. Each protein contains an uninterrupted array of from four to 30 examples of the very widely occurring complement control protein (CCP, or sushi) module. The CCP modules mediate specific protein-protein and protein-carbohydrate interactions that are key to the biological function of the RCA and, paradoxically, provide binding sites for numerous pathogens. Although structural and mutagenesis studies of CCP modules have addressed some aspects of molecular recognition, there have been no studies of the role of molecular dynamics in the interaction of CCP modules with their binding partners. NMR has now been used in the first full characterization of the backbone dynamics of CCP modules. The dynamics of two individual modules-the 16th of the 30 modules of complement receptor type 1 (CD35), and the N-terminal module of membrane cofactor protein (CD46)-as well as their solution structures, are compared. Although both examples share broadly similar three-dimensional structures, many structurally equivalent residues exhibit different amplitudes and timescales of local backbone motion. In each case, however, regions of the module-surface implicated by mutagenesis as sites of interactions with other proteins include several mobile residues. This observation suggests further experiments to explore binding mechanisms and identify new binding sites.
Backbone dynamics of complement control protein (CCP) modules reveals mobility in binding surfaces.,O'Leary JM, Bromek K, Black GM, Uhrinova S, Schmitz C, Wang X, Krych M, Atkinson JP, Uhrin D, Barlow PN Protein Sci. 2004 May;13(5):1238-50. PMID:15096630<ref>PMID:15096630</ref>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 1ppq" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Human]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Atkinson, J P]]
[[Category: Atkinson JP]]
[[Category: Barlow, P N]]
[[Category: Barlow PN]]
[[Category: Black, G M]]
[[Category: Black GM]]
[[Category: Bromek, K]]
[[Category: Bromek K]]
[[Category: Krych, M]]
[[Category: Krych M]]
[[Category: Leary, J M.O]]
[[Category: O'Leary JM]]
[[Category: Schmitz, C]]
[[Category: Schmitz C]]
[[Category: Uhrin, D]]
[[Category: Uhrin D]]
[[Category: Uhrinova, S]]
[[Category: Uhrinova S]]
[[Category: Ccp]]
[[Category: Complement]]
[[Category: Immune system]]
[[Category: Module]]
[[Category: Scr]]
[[Category: Sushi]]

Revision as of 08:57, 17 April 2024

NMR structure of 16th module of Immune Adherence Receptor, Cr1 (Cd35)NMR structure of 16th module of Immune Adherence Receptor, Cr1 (Cd35)

Structural highlights

1ppq is a 1 chain structure with sequence from Homo sapiens. Full experimental information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:Solution NMR
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

CR1_HUMAN Mediates cellular binding of particles and immune complexes that have activated complement.

Evolutionary Conservation

Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf.

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA
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