BASIL2023GVQ8DN35

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== Function ==
== Function ==
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Through computational docking results, the predicted function for the Q8DN35 protein is that of a glucokinase. The use of tools such as NetGO, BLAST, DALI, InterPRO, PyRX and SPRITE allowed for this predicted function. Q8DN35's sequence is related to that of the ROK Kinase family. NetGO predicted that this protein will have glucokinase activity as it's deepest result. PyRX docking data showed us that NAG (2-acetamido-2-deoxy-beta-D-glucopyranose) and F6P (fructose-6-phosphate) had high binding affinity in the potential binding pocket of Q8DN35.
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Through computational docking results, the predicted function for the Q8DN35 protein is that of a glucokinase. The use of tools such as NetGO, BLAST, DALI, InterPRO, PyRX and SPRITE allowed for this predicted function. Q8DN35's sequence is related to that of the ROK Kinase family. NetGO predicted that this protein will have glucokinase activity as it's deepest result. PyRX docking data showed us that NAG (N-acetyl-D-glucosamine) and F6P (fructose-6-phosphate) had high binding affinity in the potential binding pocket of Q8DN35.
== Binding site ==
== Binding site ==

Revision as of 17:42, 10 April 2023

Q8DN35 Protein

The predicted function of the Q8DN35 protein was studied during the spring 2023 semester at Grand View University by Lucas Kramer and Anie Rehbein in CHEM 453 - Biochemical Techniques.

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Contents

Computational Structure

Function

Through computational docking results, the predicted function for the Q8DN35 protein is that of a glucokinase. The use of tools such as NetGO, BLAST, DALI, InterPRO, PyRX and SPRITE allowed for this predicted function. Q8DN35's sequence is related to that of the ROK Kinase family. NetGO predicted that this protein will have glucokinase activity as it's deepest result. PyRX docking data showed us that NAG (N-acetyl-D-glucosamine) and F6P (fructose-6-phosphate) had high binding affinity in the potential binding pocket of Q8DN35.

Binding site

Image:Docking site Q8DN35.png

This image displays potential binding sites to the Q8DN35 protein.

Protein purification analysis

Through the use of a gravity purification column and Ni-NTA resin, Q8DN35 was purified and a Bradford analysis was conducted to determine the amount of protein in the purified sample. This purification resulted in 0.055 mg/mL of protein being purified.

Kinase activity analysis

To observe Q8DN35's activity, a kinase activity was ran with 2 substrates to observe potential substrate usage. The 2 substrates that were tested are NAG and F6P.


References

Proteopedia Page Contributors and Editors (what is this?)

Lucas Kramer, Anie Rehbein, Jaime Prilusky, Bonnie Hall

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