This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


2kyd

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (06:50, 1 May 2024) (edit) (undo)
 
(One intermediate revision not shown.)
Line 1: Line 1:
==RDC and RCSA refinement of an A-form RNA: Improvements in Major Groove Width==
==RDC and RCSA refinement of an A-form RNA: Improvements in Major Groove Width==
-
<StructureSection load='2kyd' size='340' side='right'caption='[[2kyd]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
+
<StructureSection load='2kyd' size='340' side='right'caption='[[2kyd]]' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[2kyd]] is a 2 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KYD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2KYD FirstGlance]. <br>
<table><tr><td colspan='2'>[[2kyd]] is a 2 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KYD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2KYD 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=2kyd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2kyd OCA], [https://pdbe.org/2kyd PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2kyd RCSB], [https://www.ebi.ac.uk/pdbsum/2kyd PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2kyd ProSAT]</span></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='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2kyd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2kyd OCA], [https://pdbe.org/2kyd PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2kyd RCSB], [https://www.ebi.ac.uk/pdbsum/2kyd PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2kyd ProSAT]</span></td></tr>
</table>
</table>
-
<div style="background-color:#fffaf0;">
 
-
== Publication Abstract from PubMed ==
 
-
Ribonucleic acid structure determination by NMR spectroscopy relies primarily on local structural restraints provided by (1)H- (1)H NOEs and J-couplings. When employed loosely, these restraints are broadly compatible with A- and B-like helical geometries and give rise to calculated structures that are highly sensitive to the force fields employed during refinement. A survey of recently reported NMR structures reveals significant variations in helical parameters, particularly the major groove width. Although helical parameters observed in high-resolution X-ray crystal structures of isolated A-form RNA helices are sensitive to crystal packing effects, variations among the published X-ray structures are significantly smaller than those observed in NMR structures. Here we show that restraints derived from aromatic (1)H- (13)C residual dipolar couplings (RDCs) and residual chemical shift anisotropies (RCSAs) can overcome NMR restraint and force field deficiencies and afford structures with helical properties similar to those observed in high-resolution X-ray structures.
 
- 
-
Major groove width variations in RNA structures determined by NMR and impact of 13C residual chemical shift anisotropy and 1H-13C residual dipolar coupling on refinement.,Tolbert BS, Miyazaki Y, Barton S, Kinde B, Starck P, Singh R, Bax A, Case DA, Summers MF J Biomol NMR. 2010 Jul;47(3):205-19. Epub 2010 Jun 15. PMID:20549304<ref>PMID:20549304</ref>
 
- 
-
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
 
-
</div>
 
-
<div class="pdbe-citations 2kyd" style="background-color:#fffaf0;"></div>
 
-
== References ==
 
-
<references/>
 
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
-
[[Category: Barton, S]]
+
[[Category: Barton S]]
-
[[Category: Bax, A]]
+
[[Category: Bax A]]
-
[[Category: Case, D]]
+
[[Category: Case D]]
-
[[Category: Kinde, B]]
+
[[Category: Kinde B]]
-
[[Category: Miyazaki, Y]]
+
[[Category: Miyazaki Y]]
-
[[Category: Singh, R]]
+
[[Category: Singh R]]
-
[[Category: Stark, P]]
+
[[Category: Stark P]]
-
[[Category: Summers, M F]]
+
[[Category: Summers MF]]
-
[[Category: Tolbert, B S]]
+
[[Category: Tolbert BS]]
-
[[Category: A-form rna]]
+
-
[[Category: Moloney murine leukemia virus dimerization signal]]
+
-
[[Category: Rdc and rcsa refinement]]
+
-
[[Category: Rna]]
+
-
[[Category: Slb duplex]]
+

Current revision

RDC and RCSA refinement of an A-form RNA: Improvements in Major Groove Width

PDB ID 2kyd

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools