DHRS1 Conclusion: Difference between revisions
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==BALLS== | ==BALLS== | ||
HSDR1 may reduce Glucose by using NADP as an electron donor. Further kinetic studies with other likely substrates (sugars) are needed to confirm this. | Through comparison of HSDR1 against protiens with similar structure it was possible to identify several conserved regions that are important in the folding and function of HSDR1. | ||
HSDR1 may reduce Glucose by using NADP as an electron donor. Further kinetic studies with other likely substrates (sugars) are needed to confirm this. An [G-x(3)-G-x-G] motif that is a Characteristic co-enzyme binding fold may bind a substrate possibly glucose. Site directed mutagenasis and futher Kinietic studies will regveal the role of this motif, if any. | |||
Revision as of 06:40, 9 June 2008
BALLS
Through comparison of HSDR1 against protiens with similar structure it was possible to identify several conserved regions that are important in the folding and function of HSDR1.
HSDR1 may reduce Glucose by using NADP as an electron donor. Further kinetic studies with other likely substrates (sugars) are needed to confirm this. An [G-x(3)-G-x-G] motif that is a Characteristic co-enzyme binding fold may bind a substrate possibly glucose. Site directed mutagenasis and futher Kinietic studies will regveal the role of this motif, if any.
