1ok2

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==Overview==
==Overview==
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The human complement regulator CD55 is a key molecule protecting, self-cells from complement-mediated lysis. X-ray diffraction and, analytical ultracentrifugation data reveal a rod-like arrangement of four, short consensus repeat (SCR) domains in both the crystal and solution. The, stalk linking the four SCR domains to the glycosylphosphatidylinositol, anchor is extended by the addition of 11 highly charged O-glycans and, positions the domains an estimated 177 A above the membrane. Mutation, mapping and hydrophobic potential analysis suggest that the interaction, with the convertase, and thus complement regulation, depends on the burial, of a hydrophobic patch centered on the linker between SCR domains 2 and 3.
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The human complement regulator CD55 is a key molecule protecting self-cells from complement-mediated lysis. X-ray diffraction and analytical ultracentrifugation data reveal a rod-like arrangement of four short consensus repeat (SCR) domains in both the crystal and solution. The stalk linking the four SCR domains to the glycosylphosphatidylinositol anchor is extended by the addition of 11 highly charged O-glycans and positions the domains an estimated 177 A above the membrane. Mutation mapping and hydrophobic potential analysis suggest that the interaction with the convertase, and thus complement regulation, depends on the burial of a hydrophobic patch centered on the linker between SCR domains 2 and 3.
==Disease==
==Disease==
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[[Category: Billington, J.]]
[[Category: Billington, J.]]
[[Category: Crispin, M.]]
[[Category: Crispin, M.]]
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[[Category: Dwek, R.A.]]
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[[Category: Dwek, R A.]]
[[Category: Esser, D.]]
[[Category: Esser, D.]]
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[[Category: Evans, D.J.]]
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[[Category: Evans, D J.]]
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[[Category: Lea, S.M.]]
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[[Category: Lea, S M.]]
[[Category: Lukacik, P.]]
[[Category: Lukacik, P.]]
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[[Category: Morgan, B.P.]]
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[[Category: Morgan, B P.]]
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[[Category: Radcliffe, C.M.]]
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[[Category: Radcliffe, C M.]]
[[Category: Roversi, P.]]
[[Category: Roversi, P.]]
[[Category: Rudd, P.]]
[[Category: Rudd, P.]]
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[[Category: Smith, G.P.]]
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[[Category: Smith, G P.]]
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[[Category: Smith, R.A.G.]]
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[[Category: Smith, R A.G.]]
[[Category: White, J.]]
[[Category: White, J.]]
[[Category: Williams, P.]]
[[Category: Williams, P.]]
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[[Category: Wormald, M.R.]]
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[[Category: Wormald, M R.]]
[[Category: ACT]]
[[Category: ACT]]
[[Category: GOL]]
[[Category: GOL]]
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[[Category: short consensus repeat domains]]
[[Category: short consensus repeat domains]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 09:59:08 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:18:38 2008''

Revision as of 12:18, 21 February 2008


1ok2, resolution 2.5Å

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DECAY ACCELERATING FACTOR (CD55): THE STRUCTURE OF AN INTACT HUMAN COMPLEMENT REGULATOR.

Contents

Overview

The human complement regulator CD55 is a key molecule protecting self-cells from complement-mediated lysis. X-ray diffraction and analytical ultracentrifugation data reveal a rod-like arrangement of four short consensus repeat (SCR) domains in both the crystal and solution. The stalk linking the four SCR domains to the glycosylphosphatidylinositol anchor is extended by the addition of 11 highly charged O-glycans and positions the domains an estimated 177 A above the membrane. Mutation mapping and hydrophobic potential analysis suggest that the interaction with the convertase, and thus complement regulation, depends on the burial of a hydrophobic patch centered on the linker between SCR domains 2 and 3.

Disease

Known diseases associated with this structure: Blood group Cromer OMIM:[125240], Blood group, Knops system OMIM:[120620], CR1 deficiency OMIM:[120620], Malaria, severe, resistance to OMIM:[120620], SLE susceptibility OMIM:[120620]

About this Structure

1OK2 is a Single protein structure of sequence from Homo sapiens with , and as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

Complement regulation at the molecular level: the structure of decay-accelerating factor., Lukacik P, Roversi P, White J, Esser D, Smith GP, Billington J, Williams PA, Rudd PM, Wormald MR, Harvey DJ, Crispin MD, Radcliffe CM, Dwek RA, Evans DJ, Morgan BP, Smith RA, Lea SM, Proc Natl Acad Sci U S A. 2004 Feb 3;101(5):1279-84. Epub 2004 Jan 20. PMID:14734808

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