3oai: Difference between revisions

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== Disease ==
== Disease ==
[https://www.uniprot.org/uniprot/MYP0_HUMAN MYP0_HUMAN] Charcot-Marie-Tooth disease type 1B;Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain;Roussy-Levy syndrome;Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome;Autosomal dominant Charcot-Marie-Tooth disease type 2J;Autosomal dominant Charcot-Marie-Tooth disease type 2I;Autosomal dominant intermediate Charcot-Marie-Tooth disease type D;Dejerine-Sottas syndrome. The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease may be caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
[https://www.uniprot.org/uniprot/MYP0_HUMAN MYP0_HUMAN] Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome;Autosomal dominant intermediate Charcot-Marie-Tooth disease type D;Autosomal dominant Charcot-Marie-Tooth disease type 2I;Roussy-Levy syndrome;Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain;Dejerine-Sottas syndrome;Charcot-Marie-Tooth disease type 1B;Autosomal dominant Charcot-Marie-Tooth disease type 2J. The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease may be caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
== Function ==
== Function ==
[https://www.uniprot.org/uniprot/MALE_ECOLI MALE_ECOLI] Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides.[https://www.uniprot.org/uniprot/MYP0_HUMAN MYP0_HUMAN] Is an adhesion molecule necessary for normal myelination in the peripheral nervous system. It mediates adhesion between adjacent myelin wraps and ultimately drives myelin compaction.<ref>PMID:10545037</ref> <ref>PMID:18337304</ref>  
[https://www.uniprot.org/uniprot/MALE_ECOLI MALE_ECOLI] Involved in the high-affinity maltose membrane transport system MalEFGK. Initial receptor for the active transport of and chemotaxis toward maltooligosaccharides.[https://www.uniprot.org/uniprot/MYP0_HUMAN MYP0_HUMAN] Is an adhesion molecule necessary for normal myelination in the peripheral nervous system. It mediates adhesion between adjacent myelin wraps and ultimately drives myelin compaction.<ref>PMID:10545037</ref> <ref>PMID:18337304</ref>  

Latest revision as of 09:30, 30 October 2024

Crystal structure of the extra-cellular domain of human myelin protein zero

3oai, resolution 2.10Å

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