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.


3bju

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:3bju.jpg|left|200px]]
+
{{Seed}}
 +
[[Image:3bju.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_3bju| PDB=3bju | SCENE= }}
{{STRUCTURE_3bju| PDB=3bju | SCENE= }}
-
'''Crystal Structure of tetrameric form of human lysyl-tRNA synthetase'''
+
===Crystal Structure of tetrameric form of human lysyl-tRNA synthetase===
-
==Overview==
+
<!--
-
In mammals, many aminoacyl-tRNA synthetases are bound together in a multisynthetase complex (MSC) as a reservoir of procytokines and regulation molecules for functions beyond aminoacylation. The alpha(2) homodimeric lysyl-tRNA synthetase (LysRS) is tightly bound in the MSC and, under specific conditions, is secreted to trigger a proinflammatory response. Results by others suggest that alpha(2) LysRS is tightly bound into the core of the MSC with homodimeric beta(2) p38, a scaffolding protein that itself is multifunctional. Not understood is how the two dimeric proteins combine to make a presumptive alpha(2)beta(2) heterotetramer and, in particular, the location of the surfaces on LysRS that would accommodate the p38 interactions. Here we present a 2.3-A crystal structure of a tetrameric form of human LysRS. The relatively loose (as seen in solution) tetramer interface is assembled from two eukaryote-specific sequences, one in the catalytic- and another in the anticodon-binding domain. This same interface is predicted to provide unique determinants for interaction with p38. The analyses suggest how the core of the MSC is assembled and, more generally, that interactions and functions of synthetases can be built and regulated through dynamic protein-protein interfaces. These interfaces are created from small adaptations to what is otherwise a highly conserved (through evolution) polypeptide sequence.
+
The line below this paragraph, {{ABSTRACT_PUBMED_18272479}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 18272479 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_18272479}}
==About this Structure==
==About this Structure==
Line 36: Line 40:
[[Category: Protein biosynthesis]]
[[Category: Protein biosynthesis]]
[[Category: Trna synthetase]]
[[Category: Trna synthetase]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 20:51:49 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 21:05:10 2008''

Revision as of 18:05, 27 July 2008

Image:3bju.png

Template:STRUCTURE 3bju

Crystal Structure of tetrameric form of human lysyl-tRNA synthetase

Template:ABSTRACT PUBMED 18272479

About this Structure

3BJU is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Crystal structure of tetrameric form of human lysyl-tRNA synthetase: Implications for multisynthetase complex formation., Guo M, Ignatov M, Musier-Forsyth K, Schimmel P, Yang XL, Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2331-6. Epub 2008 Feb 13. PMID:18272479

Page seeded by OCA on Sun Jul 27 21:05:10 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/3bju"
Personal tools