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1b09

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{{STRUCTURE_1b09| PDB=1b09 | SCENE= }}
{{STRUCTURE_1b09| PDB=1b09 | SCENE= }}
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'''HUMAN C-REACTIVE PROTEIN COMPLEXED WITH PHOSPHOCHOLINE'''
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===HUMAN C-REACTIVE PROTEIN COMPLEXED WITH PHOSPHOCHOLINE===
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==Overview==
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BACKGROUND: Human C-reactive protein (CRP) is the classical acute phase reactant, the circulating concentration of which rises rapidly and extensively in a cytokine-mediated response to tissue injury, infection and inflammation. Serum CRP values are routinely measured, empirically, to detect and monitor many human diseases. However, CRP is likely to have important host defence, scavenging and metabolic functions through its capacity for calcium-dependent binding to exogenous and autologous molecules containing phosphocholine (PC) and then activating the classical complement pathway. CRP may also have pathogenic effects and the recent discovery of a prognostic association between increased CRP production and coronary atherothrombotic events is of particular interest. RESUTLS: The X-ray structures of fully calcified C-reactive protein, in the presence and absence of bound PC, reveal that although the subunit beta-sheet jellyroll fold is very similar to that of the homologous pentameric protein serum amyloid P component, each subunit is tipped towards the fivefold axis. PC is bound in a shallow surface pocket on each subunit, interacting with the two protein-bound calcium ions via the phosphate group and with Glu81 via the choline moiety. There is also an unexpected hydrophobic pocket adjacent to the ligand. CONCLUSIONS: The structure shows how large ligands containing PC may be bound by CRP via a phosphate oxygen that projects away from the surface of the protein. Multipoint attachment of one planar face of the CRP molecule to a PC-bearing surface would leave available, on the opposite exposed face, the recognition sites for C1q, which have been identified by mutagenesis. This would enable CRP to target physiologically and/or pathologically significant complement activation. The hydrophobic pocket adjacent to bound PC invites the design of inhibitors of CRP binding that may have therapeutic relevance to the possible role of CRP in atherothrombotic events.
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(as it appears on PubMed at http://www.pubmed.gov), where 10368284 is the PubMed ID number.
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{{ABSTRACT_PUBMED_10368284}}
==About this Structure==
==About this Structure==
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[[Category: Pentraxin]]
[[Category: Pentraxin]]
[[Category: Phosphocholine]]
[[Category: Phosphocholine]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 10:54:35 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jun 30 17:58:06 2008''

Revision as of 14:58, 30 June 2008

Image:1b09.png

Template:STRUCTURE 1b09

HUMAN C-REACTIVE PROTEIN COMPLEXED WITH PHOSPHOCHOLINE

Template:ABSTRACT PUBMED 10368284

About this Structure

1B09 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

The physiological structure of human C-reactive protein and its complex with phosphocholine., Thompson D, Pepys MB, Wood SP, Structure. 1999 Feb 15;7(2):169-77. PMID:10368284

Page seeded by OCA on Mon Jun 30 17:58:06 2008

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