2os5
From Proteopedia
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|PDB= 2os5 |SIZE=350|CAPTION= <scene name='initialview01'>2os5</scene>, resolution 1.60Å | |PDB= 2os5 |SIZE=350|CAPTION= <scene name='initialview01'>2os5</scene>, resolution 1.60Å | ||
|SITE= <scene name='pdbsite=AC1:So4+Binding+Site+For+Residue+D+201'>AC1</scene>, <scene name='pdbsite=AC2:So4+Binding+Site+For+Residue+A+202'>AC2</scene>, <scene name='pdbsite=AC3:So4+Binding+Site+For+Residue+A+203'>AC3</scene> and <scene name='pdbsite=AC4:So4+Binding+Site+For+Residue+B+204'>AC4</scene> | |SITE= <scene name='pdbsite=AC1:So4+Binding+Site+For+Residue+D+201'>AC1</scene>, <scene name='pdbsite=AC2:So4+Binding+Site+For+Residue+A+202'>AC2</scene>, <scene name='pdbsite=AC3:So4+Binding+Site+For+Residue+A+203'>AC3</scene> and <scene name='pdbsite=AC4:So4+Binding+Site+For+Residue+B+204'>AC4</scene> | ||
- | |LIGAND= <scene name='pdbligand=SO4:SULFATE ION'>SO4</scene> | + | |LIGAND= <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene> |
|ACTIVITY= | |ACTIVITY= | ||
|GENE= | |GENE= | ||
+ | |DOMAIN= | ||
+ | |RELATEDENTRY= | ||
+ | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2os5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2os5 OCA], [http://www.ebi.ac.uk/pdbsum/2os5 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2os5 RCSB]</span> | ||
}} | }} | ||
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[[Category: Cho, Y.]] | [[Category: Cho, Y.]] | ||
[[Category: Lolis, E.]] | [[Category: Lolis, E.]] | ||
- | [[Category: SO4]] | ||
[[Category: cytokine]] | [[Category: cytokine]] | ||
[[Category: hookworm]] | [[Category: hookworm]] | ||
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[[Category: nematode]] | [[Category: nematode]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:22:20 2008'' |
Revision as of 01:22, 31 March 2008
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, resolution 1.60Å | |||||||
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Sites: | , , and | ||||||
Ligands: | |||||||
Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Macrophage migration inhibitory factor from Ancylostoma ceylanicum
Overview
Hookworms, parasitic nematodes that infect nearly one billion people worldwide, are a major cause of anemia and malnutrition. We hypothesize that hookworms actively manipulate the host immune response through the production of specific molecules designed to facilitate infection by larval stages and adult worm survival within the intestine. A full-length cDNA encoding a secreted orthologue of the human cytokine, Macrophage Migration Inhibitory Factor (MIF) has been cloned from the hookworm Ancylostoma ceylanicum. Elucidation of the three-dimensional crystal structure of recombinant AceMIF (rAceMIF) revealed an overall structural homology with significant differences in the tautomerase sites of the human and hookworm proteins. The relative bioactivities of human and hookworm MIF proteins were compared using in vitro assays of tautomerase activity, macrophage migration, and binding to MIF receptor CD74. The activity of rAceMIF was not inhibited by the ligand ISO-1, which was previously determined to be an inhibitor of the catalytic site of human MIF. These data define unique immunological, structural, and functional characteristics of AceMIF, thereby establishing the potential for selectively inhibiting the hookworm cytokine as a means of reducing parasite survival and disease pathogenesis.
About this Structure
2OS5 is a Protein complex structure of sequences from Ancylostoma ceylanicum. Full crystallographic information is available from OCA.
Reference
Structural and functional characterization of a secreted hookworm Macrophage Migration Inhibitory Factor (MIF) that interacts with the human MIF receptor CD74., Cho Y, Jones BF, Vermeire JJ, Leng L, DiFedele L, Harrison LM, Xiong H, Kwong YK, Chen Y, Bucala R, Lolis E, Cappello M, J Biol Chem. 2007 Aug 10;282(32):23447-56. Epub 2007 Jun 13. PMID:17567581
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