1jwi

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(New page: 200px<br /><applet load="1jwi" size="450" color="white" frame="true" align="right" spinBox="true" caption="1jwi, resolution 2.00&Aring;" /> '''Crystal Structure of...)
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[[Image:1jwi.gif|left|200px]]<br /><applet load="1jwi" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1jwi, resolution 2.00&Aring;" />
caption="1jwi, resolution 2.00&Aring;" />
'''Crystal Structure of Bitiscetin, a von Willeband Factor-dependent Platelet Aggregation Inducer.'''<br />
'''Crystal Structure of Bitiscetin, a von Willeband Factor-dependent Platelet Aggregation Inducer.'''<br />
==Overview==
==Overview==
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Bitiscetin, a C-type lectin-like protein isolated from the venom of the, snake Bitis arientans, promotes the interactions between plasma von, Willebrand factor (VWF) and platelet membrane glycoprotein Ib (GPIb) to, induce platelet aggregation. We report here the crystal structure of, bitiscetin at 2.0 A resolution. The overall fold is similar to those of, coagulation factor IX/X-binding protein (IX/X-bp) and flavocetin-A (a, GPIb-binding protein), although these three proteins are functionally, distinct from one another. The characteristic property determining target, recognition is explained mainly by the differences in the surface, potential on the central concave surface. A negatively charged patch on, the surface of bitiscetin is a candidate for the site of binding to the, positively charged surface of the VWF A1 domain, as shown in the case of, another platelet aggregation inducer, botrocetin. However, a positively, charged patch near the central concave surface is unique for bitiscetin, and suggests that it is the binding site for the negatively charged, surface of the VWF A3 domain. Thus, the interactions accounting for VWF, activation by bitiscetin possibly involve both the A1 and A3 domains of, VWF, indicating a specific mechanism of VWF activation by bitiscetin.
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Bitiscetin, a C-type lectin-like protein isolated from the venom of the snake Bitis arientans, promotes the interactions between plasma von Willebrand factor (VWF) and platelet membrane glycoprotein Ib (GPIb) to induce platelet aggregation. We report here the crystal structure of bitiscetin at 2.0 A resolution. The overall fold is similar to those of coagulation factor IX/X-binding protein (IX/X-bp) and flavocetin-A (a GPIb-binding protein), although these three proteins are functionally distinct from one another. The characteristic property determining target recognition is explained mainly by the differences in the surface potential on the central concave surface. A negatively charged patch on the surface of bitiscetin is a candidate for the site of binding to the positively charged surface of the VWF A1 domain, as shown in the case of another platelet aggregation inducer, botrocetin. However, a positively charged patch near the central concave surface is unique for bitiscetin and suggests that it is the binding site for the negatively charged surface of the VWF A3 domain. Thus, the interactions accounting for VWF activation by bitiscetin possibly involve both the A1 and A3 domains of VWF, indicating a specific mechanism of VWF activation by bitiscetin.
==About this Structure==
==About this Structure==
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1JWI is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bitis_arientans Bitis arientans]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1JWI OCA].
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1JWI is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bitis_arientans Bitis arientans]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JWI OCA].
==Reference==
==Reference==
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[[Category: Mizuno, H.]]
[[Category: Mizuno, H.]]
[[Category: Morita, T.]]
[[Category: Morita, T.]]
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[[Category: Qi, M.C.]]
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[[Category: Qi, M C.]]
[[Category: Titani, K.]]
[[Category: Titani, K.]]
[[Category: c-type lectin]]
[[Category: c-type lectin]]
[[Category: domain swapping]]
[[Category: domain swapping]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 00:21:27 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:27:30 2008''

Revision as of 11:27, 21 February 2008


1jwi, resolution 2.00Å

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Crystal Structure of Bitiscetin, a von Willeband Factor-dependent Platelet Aggregation Inducer.

Overview

Bitiscetin, a C-type lectin-like protein isolated from the venom of the snake Bitis arientans, promotes the interactions between plasma von Willebrand factor (VWF) and platelet membrane glycoprotein Ib (GPIb) to induce platelet aggregation. We report here the crystal structure of bitiscetin at 2.0 A resolution. The overall fold is similar to those of coagulation factor IX/X-binding protein (IX/X-bp) and flavocetin-A (a GPIb-binding protein), although these three proteins are functionally distinct from one another. The characteristic property determining target recognition is explained mainly by the differences in the surface potential on the central concave surface. A negatively charged patch on the surface of bitiscetin is a candidate for the site of binding to the positively charged surface of the VWF A1 domain, as shown in the case of another platelet aggregation inducer, botrocetin. However, a positively charged patch near the central concave surface is unique for bitiscetin and suggests that it is the binding site for the negatively charged surface of the VWF A3 domain. Thus, the interactions accounting for VWF activation by bitiscetin possibly involve both the A1 and A3 domains of VWF, indicating a specific mechanism of VWF activation by bitiscetin.

About this Structure

1JWI is a Protein complex structure of sequences from Bitis arientans. Full crystallographic information is available from OCA.

Reference

Crystal structure of bitiscetin, a von Willebrand factor-dependent platelet aggregation inducer., Hirotsu S, Mizuno H, Fukuda K, Qi MC, Matsui T, Hamako J, Morita T, Titani K, Biochemistry. 2001 Nov 13;40(45):13592-7. PMID:11695907

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