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2doi
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(New page: 200px<br /> <applet load="2doi" size="450" color="white" frame="true" align="right" spinBox="true" caption="2doi, resolution 3.100Å" /> '''The X-ray crystall...) |
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caption="2doi, resolution 3.100Å" /> | caption="2doi, resolution 3.100Å" /> | ||
'''The X-ray crystallographic structure of the angiogenesis inhibitor, angiostatin, bound to a peptide from the group A streptococcus protein PAM'''<br /> | '''The X-ray crystallographic structure of the angiogenesis inhibitor, angiostatin, bound to a peptide from the group A streptococcus protein PAM'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
| - | 2DOI is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Plasmin Plasmin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.7 3.4.21.7] Full crystallographic information is available from [http:// | + | 2DOI is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Plasmin Plasmin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.7 3.4.21.7] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2DOI OCA]. |
==Reference== | ==Reference== | ||
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[[Category: pseudo-lysine moiety]] | [[Category: pseudo-lysine moiety]] | ||
| - | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:22:06 2008'' |
Revision as of 15:22, 15 February 2008
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The X-ray crystallographic structure of the angiogenesis inhibitor, angiostatin, bound to a peptide from the group A streptococcus protein PAM
Contents |
Overview
The crystal structure of the human Pg-derived angiogenesis inhibitor, angiostatin, complexed to VEK-30, a peptide from the group A streptococcal, surface protein, PAM, was determined and refined to 2.3 A resolution. This, is the first structure of angiostatin bound to a ligand and provides a, model of the interaction between Pg and streptococcal-derived pathogenic, proteins. VEK-30 contains a "through-space isostere" for C-terminal, lysine, wherein Arg and Glu side chains, separated by one helical turn, bind within the bipolar angiostatin kringle 2 (K2) domain lysine-binding, site. VEK-30 also makes several contacts with K2 residues that exist, outside of the canonical LBS and are not conserved among the other Pg, kringles, thus providing a molecular basis for the selectivity of VEK-30, for K2. The structure also shows that Pg kringle domains undergo, significant structural rearrangement relative to one another and reveals, dimerization between two molecules of angiostatin and VEK-30 related by, crystallographic symmetry. This dimerization, which exists only in the, crystal structure, is consistent with the parallel coiled-coil full-length, PAM dimer expected from sequence similarities and homology modeling.
Disease
Known diseases associated with this structure: Conjunctivitis, ligneous OMIM:[173350], Plasminogen Tochigi disease OMIM:[173350], Plasminogen deficiency, types I and II OMIM:[173350], Thrombophilia, dysplasminogenemic OMIM:[173350]
About this Structure
2DOI is a Protein complex structure of sequences from Homo sapiens. Active as Plasmin, with EC number 3.4.21.7 Full crystallographic information is available from OCA.
Reference
X-ray crystallographic structure of the angiogenesis inhibitor, angiostatin, bound to a peptide from the group A streptococcal surface protein PAM., Cnudde SE, Prorok M, Castellino FJ, Geiger JH, Biochemistry. 2006 Sep 19;45(37):11052-60. PMID:16964966
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