Sandbox Reserved 1321
From Proteopedia
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2r7e is a cool protein. | 2r7e is a cool protein. | ||
== Structural highlights == | == Structural highlights == | ||
- | 2r7e is a 2 chain structure found in humans. It has 5 associated ligands ( <scene name='77/777641/Ca/3'>CA</scene>, <scene name='77/777641/Cu/1'>CU</scene>, BMA, MAN, NAG) and is coded for by 2 different genes, F8 and F8C. 2r7e has | + | 2r7e is a 2 chain structure found in humans. It has 5 associated ligands ( <scene name='77/777641/Ca/3'>CA</scene>, <scene name='77/777641/Cu/1'>CU</scene>, BMA, MAN, NAG) and is coded for by 2 different genes, F8 and F8C. 2r7e has both <scene name='77/777641/Alpha_helix/1'>Alpha Helix</scene> and </StructureSection><scene name='77/777641/Beta_pleated_sheet/1'>Beta Pleated Sheet</scene> secondary structure. Alterations in this structure can lead to improper location of ligands, leading to failed protein function. |
== Ligands == | == Ligands == | ||
2r7e has 5 ligands, which are binding sites for other proteins in Coagulation Factor VIII | 2r7e has 5 ligands, which are binding sites for other proteins in Coagulation Factor VIII | ||
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Mutations in 2r7e can alter the structure of Coagulation Factor VIII, leading to hemophilia a. | Mutations in 2r7e can alter the structure of Coagulation Factor VIII, leading to hemophilia a. | ||
== Relevance == | == Relevance == | ||
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== References == | == References == | ||
h http://www.uniprot.org/uniprot/P00451 | h http://www.uniprot.org/uniprot/P00451 |
Revision as of 21:00, 20 February 2018
This Sandbox is Reserved from January through July 31, 2018 for use in the course HLSC322: Principles of Genetics and Genomics taught by Genevieve Houston-Ludlam at the University of Maryland, College Park, USA. This reservation includes Sandbox Reserved 1311 through Sandbox Reserved 1430. |
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Contents |
2r7e Overview
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Ligands
2r7e has 5 ligands, which are binding sites for other proteins in Coagulation Factor VIII
Function
2r7e is a protein that makes up part of Coagulation Factor VIII, which is a protein complex involved in blood clotting in humans. Coagulation Factor VIII works with calcium and phosholipids to Factor X to its activated form Xa.
Disease
Mutations in 2r7e can alter the structure of Coagulation Factor VIII, leading to hemophilia a.
Relevance
Yay!