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1p53

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(New page: 200px<br /> <applet load="1p53" size="450" color="white" frame="true" align="right" spinBox="true" caption="1p53, resolution 3.06&Aring;" /> '''The Crystal Structu...)
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<applet load="1p53" size="450" color="white" frame="true" align="right" spinBox="true"
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'''The Crystal Structure of ICAM-1 D3-D5 fragment'''<br />
'''The Crystal Structure of ICAM-1 D3-D5 fragment'''<br />
==Overview==
==Overview==
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We have determined the 3.0 A crystal structure of the three C-terminal, domains 3-5 (D3-D5) of ICAM-1. Combined with the previously known, N-terminal two-domain structure (D1D2), a model of an entire ICAM-1, extracellular fragment has been constructed. This model should represent a, general architecture of other ICAM family members, particularly ICAM-3 and, ICAM-5. The observed intimate dimerization interaction at D4 and a stiff, D4-D5 stem-like architecture provide a good structural explanation for the, existence of preformed ICAM-1 cis dimers on the cell membrane. Together, with another dimerization interface at D1, a band-like one-dimensional, linear cluster of ICAM-1 on an antigen-presenting cell (APC) surface can, be envisioned, which might explain the formation of an immunological, synapse between an activated T cell and APC which is critical for T cell, receptor signaling.
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We have determined the 3.0 A crystal structure of the three C-terminal domains 3-5 (D3-D5) of ICAM-1. Combined with the previously known N-terminal two-domain structure (D1D2), a model of an entire ICAM-1 extracellular fragment has been constructed. This model should represent a general architecture of other ICAM family members, particularly ICAM-3 and ICAM-5. The observed intimate dimerization interaction at D4 and a stiff D4-D5 stem-like architecture provide a good structural explanation for the existence of preformed ICAM-1 cis dimers on the cell membrane. Together with another dimerization interface at D1, a band-like one-dimensional linear cluster of ICAM-1 on an antigen-presenting cell (APC) surface can be envisioned, which might explain the formation of an immunological synapse between an activated T cell and APC which is critical for T cell receptor signaling.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1P53 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with NAG and NDG as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1P53 OCA].
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1P53 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NAG:'>NAG</scene> and <scene name='pdbligand=NDG:'>NDG</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1P53 OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Jochimiak, A.]]
[[Category: Jochimiak, A.]]
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[[Category: Jun, C.D.]]
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[[Category: Jun, C D.]]
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[[Category: Liu, J.H.]]
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[[Category: Liu, J H.]]
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[[Category: Springer, T.A.]]
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[[Category: Springer, T A.]]
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[[Category: Wang, J.H.]]
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[[Category: Wang, J H.]]
[[Category: Yang, Y.]]
[[Category: Yang, Y.]]
[[Category: Zhang, R.]]
[[Category: Zhang, R.]]
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[[Category: igsf domain]]
[[Category: igsf domain]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:40:09 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:25:12 2008''

Revision as of 12:25, 21 February 2008


1p53, resolution 3.06Å

Drag the structure with the mouse to rotate

The Crystal Structure of ICAM-1 D3-D5 fragment

Contents

Overview

We have determined the 3.0 A crystal structure of the three C-terminal domains 3-5 (D3-D5) of ICAM-1. Combined with the previously known N-terminal two-domain structure (D1D2), a model of an entire ICAM-1 extracellular fragment has been constructed. This model should represent a general architecture of other ICAM family members, particularly ICAM-3 and ICAM-5. The observed intimate dimerization interaction at D4 and a stiff D4-D5 stem-like architecture provide a good structural explanation for the existence of preformed ICAM-1 cis dimers on the cell membrane. Together with another dimerization interface at D1, a band-like one-dimensional linear cluster of ICAM-1 on an antigen-presenting cell (APC) surface can be envisioned, which might explain the formation of an immunological synapse between an activated T cell and APC which is critical for T cell receptor signaling.

Disease

Known disease associated with this structure: Malaria, cerebral, susceptibility to OMIM:[147840]

About this Structure

1P53 is a Single protein structure of sequence from Homo sapiens with and as ligands. Full crystallographic information is available from OCA.

Reference

Structural basis for dimerization of ICAM-1 on the cell surface., Yang Y, Jun CD, Liu JH, Zhang R, Joachimiak A, Springer TA, Wang JH, Mol Cell. 2004 Apr 23;14(2):269-76. PMID:15099525

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