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.


1ao7

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /> <applet load="1ao7" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ao7, resolution 2.6&Aring;" /> '''COMPLEX BETWEEN HUMA...)
Line 1: Line 1:
-
[[Image:1ao7.gif|left|200px]]<br />
+
[[Image:1ao7.gif|left|200px]]<br /><applet load="1ao7" size="350" color="white" frame="true" align="right" spinBox="true"
-
<applet load="1ao7" size="450" color="white" frame="true" align="right" spinBox="true"
+
caption="1ao7, resolution 2.6&Aring;" />
caption="1ao7, resolution 2.6&Aring;" />
'''COMPLEX BETWEEN HUMAN T-CELL RECEPTOR, VIRAL PEPTIDE (TAX), AND HLA-A 0201'''<br />
'''COMPLEX BETWEEN HUMAN T-CELL RECEPTOR, VIRAL PEPTIDE (TAX), AND HLA-A 0201'''<br />
==Overview==
==Overview==
-
Recognition by a T-cell antigen receptor (TCR) of peptide complexed with a, major histocompatibility complex (MHC) molecule occurs through variable, loops in the TCR structure which bury almost all the available peptide and, a much larger area of the MHC molecule. The TCR fits diagonally across the, MHC peptide-binding site in a surface feature common to all class I and, class II MHC molecules, providing evidence that the nature of binding is, general. A broadly applicable binding mode has implications for the, mechanism of repertoire selection and the magnitude of alloreactions.
+
Recognition by a T-cell antigen receptor (TCR) of peptide complexed with a major histocompatibility complex (MHC) molecule occurs through variable loops in the TCR structure which bury almost all the available peptide and a much larger area of the MHC molecule. The TCR fits diagonally across the MHC peptide-binding site in a surface feature common to all class I and class II MHC molecules, providing evidence that the nature of binding is general. A broadly applicable binding mode has implications for the mechanism of repertoire selection and the magnitude of alloreactions.
==Disease==
==Disease==
Line 11: Line 10:
==About this Structure==
==About this Structure==
-
1AO7 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Human_t-lymphotropic_virus_1 Human t-lymphotropic virus 1] with EMC as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1AO7 OCA].
+
1AO7 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Human_t-lymphotropic_virus_1 Human t-lymphotropic virus 1] with <scene name='pdbligand=EMC:'>EMC</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AO7 OCA].
==Reference==
==Reference==
Line 18: Line 17:
[[Category: Human t-lymphotropic virus 1]]
[[Category: Human t-lymphotropic virus 1]]
[[Category: Protein complex]]
[[Category: Protein complex]]
-
[[Category: Biddison, W.E.]]
+
[[Category: Biddison, W E.]]
-
[[Category: Fan, Q.R.]]
+
[[Category: Fan, Q R.]]
-
[[Category: Garboczi, D.N.]]
+
[[Category: Garboczi, D N.]]
[[Category: Ghosh, P.]]
[[Category: Ghosh, P.]]
[[Category: Utz, U.]]
[[Category: Utz, U.]]
-
[[Category: Wiley, D.C.]]
+
[[Category: Wiley, D C.]]
[[Category: EMC]]
[[Category: EMC]]
[[Category: class i mhc]]
[[Category: class i mhc]]
Line 30: Line 29:
[[Category: viral peptide]]
[[Category: viral peptide]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 16:00:31 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:46:33 2008''

Revision as of 09:46, 21 February 2008


1ao7, resolution 2.6Å

Drag the structure with the mouse to rotate

COMPLEX BETWEEN HUMAN T-CELL RECEPTOR, VIRAL PEPTIDE (TAX), AND HLA-A 0201

Contents

Overview

Recognition by a T-cell antigen receptor (TCR) of peptide complexed with a major histocompatibility complex (MHC) molecule occurs through variable loops in the TCR structure which bury almost all the available peptide and a much larger area of the MHC molecule. The TCR fits diagonally across the MHC peptide-binding site in a surface feature common to all class I and class II MHC molecules, providing evidence that the nature of binding is general. A broadly applicable binding mode has implications for the mechanism of repertoire selection and the magnitude of alloreactions.

Disease

Known diseases associated with this structure: Abacavir hypersensitivity, susceptibility to OMIM:[142800], Ankylosing spondylitis, susceptibility to, 1 OMIM:[142800], Hypoproteinemia, hypercatabolic OMIM:[109700], Stevens-Johnson syndrome, susceptibility to OMIM:[142800]

About this Structure

1AO7 is a Protein complex structure of sequences from Homo sapiens and Human t-lymphotropic virus 1 with as ligand. Full crystallographic information is available from OCA.

Reference

Structure of the complex between human T-cell receptor, viral peptide and HLA-A2., Garboczi DN, Ghosh P, Utz U, Fan QR, Biddison WE, Wiley DC, Nature. 1996 Nov 14;384(6605):134-41. PMID:8906788

Page seeded by OCA on Thu Feb 21 11:46:33 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools