BSP306 AND INNATE IMMUNITY IN RUMINANTS
BSP306 AND INNATE IMMUNITY IN RUMINANTS
批准号:
8170269
负责人:
GRAEME CARD
金额:
$0.13万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-05-01 至 2011-02-28
关键词:
Binding SitesCattleCommunitiesComplexComputer Retrieval of Information on Scientific Projects DatabaseFamilyFundingGenesGenomeGrantHomologous GeneHost DefenseHumanInstitutionLigandsMammalsMicrobeMusNatural ImmunityOral cavityPlantsPlayProteinsResearchResearch PersonnelResourcesRoleRumenRuminantsSalivaSourceStructureUnited States National Institutes of Healthbactericidal permeability increasing proteindefense responseparotid secretory protein
中文摘要
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英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
In the human, mouse and cattle genomes, there is a contiguous region encoding multiple copies of Bactericidal/Permeability Increasing Protein- like proteins (BPI-like proteins). These proteins are thought to play diverse roles in the innate host-defense response in mammals. In cattle, there are 13 homologues encoded on a 722 kb contiguous region and these represent an expansion of this family compared to humans and mouse (which encode 9 and 11 homologues respectively). We have focused on one of these BPI-like genes, BSP30b, which is the major protein component in the saliva of cattle and is most closely related to the parotid secretory protein (PSP) in mouse and human. It is thought that BSP30b may be responsible for innate protection in the oral cavity of ruminants or, alternatively, may play an important role in the rumen where there exists a very complex anaerobic community of microbes involved in the degradation of plant matter. Elucidation of the structure of BSP30b will show the possible binding site for hydrophobic ligands and give clues to the possible role for this important and abundant protein.
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COMMISSIONING OF BL12-2 ? A NEW HIGH-BRIGHTNESS MACROMOLECULAR CRYSTALLOGRAPHY B
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批准号:7954282
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项目类别:
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资助金额:$11.8万
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财政年份:2009
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负责人:GRAEME CARD
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依托单位:
海外基金