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8csw

From Proteopedia

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== Disease ==
== Disease ==
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[[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN]] Hereditary spherocytosis. The disease is caused by variants affecting the gene represented in this entry.
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[[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN]] Hereditary spherocytosis. The disease is caused by variants affecting the gene represented in this entry.
== Function ==
== Function ==
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[[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN]] Probably plays an important role in the regulation of erythrocyte shape and mechanical properties.
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[[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN]] Probably plays an important role in the regulation of erythrocyte shape and mechanical properties.
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Cali, T]]
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[[Category: Cali T]]
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[[Category: Clarke, O B]]
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[[Category: Clarke OB]]
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[[Category: Johnston, J D]]
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[[Category: Johnston JD]]
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[[Category: Kim, K]]
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[[Category: Kim K]]
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[[Category: Noble, A J]]
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[[Category: Noble AJ]]
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[[Category: Vallese, F]]
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[[Category: Vallese F]]
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[[Category: Yen, L Y]]
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[[Category: Yen LY]]
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[[Category: Anion exchange]]
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[[Category: Erythrocyte]]
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[[Category: Glycoprotein]]
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[[Category: Membrane protein]]
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[[Category: Transport protein-structural protein complex]]
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Revision as of 04:50, 8 September 2022

Local refinement of protein 4.2 in Class 2 of erythrocyte ankyrin-1 complex

PDB ID 8csw

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