We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

1a3r

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1a3r.gif|left|200px]]
+
{{Seed}}
 +
[[Image:1a3r.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1a3r| PDB=1a3r | SCENE= }}
{{STRUCTURE_1a3r| PDB=1a3r | SCENE= }}
-
'''FAB FRAGMENT (ANTIBODY 8F5) COMPLEXED WITH PEPTIDE FROM HUMAN RHINOVIRUS (SEROTYPE 2) VIRAL CAPSID PROTEIN VP2 (RESIDUES 156-170)'''
+
===FAB FRAGMENT (ANTIBODY 8F5) COMPLEXED WITH PEPTIDE FROM HUMAN RHINOVIRUS (SEROTYPE 2) VIRAL CAPSID PROTEIN VP2 (RESIDUES 156-170)===
-
==Overview==
+
<!--
-
The three-dimensional structure of the complex between the Fab fragment of an anti-human rhinovirus neutralizing antibody (8F5) and a cross-reactive synthetic peptide from the viral capsid protein VP2 has been determined at 2.5 A resolution by crystallographic methods. The refinement is presently at an R factor of 0.18 and the antigen-binding site and viral peptide are well defined. The peptide antigen adopts a compact fold by two tight turns and interacts through hydrogen bonds, some with ionic character, and van der Waals contacts with antibody residues from the six hypervariable loops as well as several framework amino acids. The conformation adopted by the peptide is closely related to the corresponding region of the viral protein VP2 on the surface of human rhinovirus 1A whose three-dimensional structure is known. Implications for the cross-reactivity between peptides and the viral capsid are discussed. The peptide-antibody interactions, together with the analysis of mutant viruses that escape neutralization by 8F5 suggest two different mechanisms for viral escape. The comparison between the complexed and uncomplexed antibody structures shows important conformational rearrangements, especially in the hypervariable loops of the heavy chain. Thus, it constitutes a clear example of the 'induced fit' molecular recognition mechanism.
+
The line below this paragraph, {{ABSTRACT_PUBMED_8194515}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 8194515 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_8194515}}
==About this Structure==
==About this Structure==
Line 31: Line 35:
[[Category: Neutralization]]
[[Category: Neutralization]]
[[Category: Rhinovirus]]
[[Category: Rhinovirus]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 09:46:06 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jun 30 15:56:50 2008''

Revision as of 12:56, 30 June 2008

Image:1a3r.png

Template:STRUCTURE 1a3r

FAB FRAGMENT (ANTIBODY 8F5) COMPLEXED WITH PEPTIDE FROM HUMAN RHINOVIRUS (SEROTYPE 2) VIRAL CAPSID PROTEIN VP2 (RESIDUES 156-170)

Template:ABSTRACT PUBMED 8194515

About this Structure

1A3R is a Protein complex structure of sequences from Human rhinovirus 2 and Mus musculus. Full crystallographic information is available from OCA.

Reference

Crystal structure of a human rhinovirus neutralizing antibody complexed with a peptide derived from viral capsid protein VP2., Tormo J, Blaas D, Parry NR, Rowlands D, Stuart D, Fita I, EMBO J. 1994 May 15;13(10):2247-56. PMID:8194515

Page seeded by OCA on Mon Jun 30 15:56:50 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/1a3r"
Personal tools