1szb

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(New page: 200px<br /> <applet load="1szb" size="450" color="white" frame="true" align="right" spinBox="true" caption="1szb, resolution 2.5&Aring;" /> '''Crystal structure of...)
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[[Image:1szb.gif|left|200px]]<br />
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[[Image:1szb.gif|left|200px]]<br /><applet load="1szb" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="1szb" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1szb, resolution 2.5&Aring;" />
caption="1szb, resolution 2.5&Aring;" />
'''Crystal structure of the human MBL-associated protein 19 (MAp19)'''<br />
'''Crystal structure of the human MBL-associated protein 19 (MAp19)'''<br />
==Overview==
==Overview==
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MAp19 is an alternative splicing product of the MASP-2 gene comprising the, N-terminal CUB1-epidermal growth factor (EGF) segment of MASP-2, plus four, additional residues at its C-terminal end. Like full-length MASP-2, it, forms Ca(2+)-dependent complexes with mannan-binding lectin (MBL) and, L-ficolin. The x-ray structure of human MAp19 was solved to a resolution, of 2.5 A. It shows a head to tail homodimer held together by interactions, between the CUB1 module of one monomer and the EGF module of its, counterpart. A Ca(2+) ion bound to each EGF module stabilizes the dimer, interfaces. A second Ca(2+) ion is bound to the distal end of each CUB1, module, through six ligands contributed by Glu(52), Asp(60), Asp(105), Ser(107), Asn(108), and a water molecule. Compared with its counterpart in, human C1s, the N-terminal end of the MAp19 CUB1 module contains a, 7-residue extension that forms additional inter-monomer contacts. To, identify the residues involved in the interaction of MAp19 with MBL and, L-ficolin, point mutants were generated and their binding ability was, determined using surface plasmon resonance spectroscopy. Six mutations at, Tyr(59), Asp(60), Glu(83), Asp(105), Tyr(106), and Glu(109) either, strongly decreased or abolished interaction with both MBL and L-ficolin., These mutations map a common binding site for these proteins located at, the distal end of each CUB1 module and stabilized by the Ca(2+) ion.
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MAp19 is an alternative splicing product of the MASP-2 gene comprising the N-terminal CUB1-epidermal growth factor (EGF) segment of MASP-2, plus four additional residues at its C-terminal end. Like full-length MASP-2, it forms Ca(2+)-dependent complexes with mannan-binding lectin (MBL) and L-ficolin. The x-ray structure of human MAp19 was solved to a resolution of 2.5 A. It shows a head to tail homodimer held together by interactions between the CUB1 module of one monomer and the EGF module of its counterpart. A Ca(2+) ion bound to each EGF module stabilizes the dimer interfaces. A second Ca(2+) ion is bound to the distal end of each CUB1 module, through six ligands contributed by Glu(52), Asp(60), Asp(105), Ser(107), Asn(108), and a water molecule. Compared with its counterpart in human C1s, the N-terminal end of the MAp19 CUB1 module contains a 7-residue extension that forms additional inter-monomer contacts. To identify the residues involved in the interaction of MAp19 with MBL and L-ficolin, point mutants were generated and their binding ability was determined using surface plasmon resonance spectroscopy. Six mutations at Tyr(59), Asp(60), Glu(83), Asp(105), Tyr(106), and Glu(109) either strongly decreased or abolished interaction with both MBL and L-ficolin. These mutations map a common binding site for these proteins located at the distal end of each CUB1 module and stabilized by the Ca(2+) ion.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1SZB 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 CA as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1SZB OCA].
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1SZB 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=CA:'>CA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SZB OCA].
==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Arlaud, G.J.]]
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[[Category: Arlaud, G J.]]
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[[Category: Fontecilla-Camps, J.C.]]
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[[Category: Fontecilla-Camps, J C.]]
[[Category: Gaboriaud, C.]]
[[Category: Gaboriaud, C.]]
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[[Category: Gregory, L.A.]]
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[[Category: Gregory, L A.]]
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[[Category: Thielens, N.M.]]
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[[Category: Thielens, N M.]]
[[Category: CA]]
[[Category: CA]]
[[Category: calcium]]
[[Category: calcium]]
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[[Category: innate immunity]]
[[Category: innate immunity]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 19:18:31 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:07:45 2008''

Revision as of 13:07, 21 February 2008


1szb, resolution 2.5Å

Drag the structure with the mouse to rotate

Crystal structure of the human MBL-associated protein 19 (MAp19)

Contents

Overview

MAp19 is an alternative splicing product of the MASP-2 gene comprising the N-terminal CUB1-epidermal growth factor (EGF) segment of MASP-2, plus four additional residues at its C-terminal end. Like full-length MASP-2, it forms Ca(2+)-dependent complexes with mannan-binding lectin (MBL) and L-ficolin. The x-ray structure of human MAp19 was solved to a resolution of 2.5 A. It shows a head to tail homodimer held together by interactions between the CUB1 module of one monomer and the EGF module of its counterpart. A Ca(2+) ion bound to each EGF module stabilizes the dimer interfaces. A second Ca(2+) ion is bound to the distal end of each CUB1 module, through six ligands contributed by Glu(52), Asp(60), Asp(105), Ser(107), Asn(108), and a water molecule. Compared with its counterpart in human C1s, the N-terminal end of the MAp19 CUB1 module contains a 7-residue extension that forms additional inter-monomer contacts. To identify the residues involved in the interaction of MAp19 with MBL and L-ficolin, point mutants were generated and their binding ability was determined using surface plasmon resonance spectroscopy. Six mutations at Tyr(59), Asp(60), Glu(83), Asp(105), Tyr(106), and Glu(109) either strongly decreased or abolished interaction with both MBL and L-ficolin. These mutations map a common binding site for these proteins located at the distal end of each CUB1 module and stabilized by the Ca(2+) ion.

Disease

Known disease associated with this structure: MASP2 deficiency OMIM:[605102]

About this Structure

1SZB is a Single protein structure of sequence from Homo sapiens with as ligand. Full crystallographic information is available from OCA.

Reference

The X-ray structure of human mannan-binding lectin-associated protein 19 (MAp19) and its interaction site with mannan-binding lectin and L-ficolin., Gregory LA, Thielens NM, Matsushita M, Sorensen R, Arlaud GJ, Fontecilla-Camps JC, Gaboriaud C, J Biol Chem. 2004 Jul 9;279(28):29391-7. Epub 2004 Apr 26. PMID:15117939

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