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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=ANTXR2</id>
	<title>ANTXR2 - История изменений</title>
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	<updated>2026-05-14T09:22:33Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=ANTXR2&amp;diff=5651&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Anthrax toxin receptor 2 precursor (Capillary morphogenesis gene 2 protein) (CMG-2) [CMG2]  ==Publications==  {{medline-entry |title=Anthrax toxin receptor 2-depe...»</title>
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		<updated>2021-05-12T13:53:48Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Anthrax toxin receptor 2 precursor (Capillary morphogenesis gene 2 protein) (CMG-2) [CMG2]  ==Publications==  {{medline-entry |title=Anthrax toxin receptor 2-depe...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Anthrax toxin receptor 2 precursor (Capillary morphogenesis gene 2 protein) (CMG-2) [CMG2]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Anthrax toxin receptor 2-dependent lethal toxin killing in vivo.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/17054395&lt;br /&gt;
|abstract=Anthrax toxin receptors 1 and 2 ([[ANTXR1]] and [[ANTXR2]]) have a related integrin-like inserted (I) domain which interacts with a metal cation that is coordinated by residue D683 of the protective antigen (PA) subunit of anthrax toxin. The receptor-bound metal ion and PA residue D683 are critical for [[ANTXR1]]-PA binding. Since PA can bind to [[ANTXR2]] with reduced affinity in the absence of metal ions, we reasoned that D683 mutant forms of PA might specifically interact with [[ANTXR2]]. We show here that this is the case. The differential ability of [[ANTXR1]] and [[ANTXR2]] to bind D683 mutant PA proteins was mapped to nonconserved receptor residues at the binding interface with PA domain 2. Moreover, a D683K mutant form of PA that bound specifically to human and rat [[ANTXR2]] mediated killing of rats by anthrax lethal toxin, providing strong evidence for the physiological importance of [[ANTXR2]] in anthrax disease pathogenesis.&lt;br /&gt;
|mesh-terms=* Animals&lt;br /&gt;
* Anthrax&lt;br /&gt;
* Antibodies, Bacterial&lt;br /&gt;
* Antigens, Bacterial&lt;br /&gt;
* Bacillus anthracis&lt;br /&gt;
* Bacterial Toxins&lt;br /&gt;
* Base Sequence&lt;br /&gt;
* Humans&lt;br /&gt;
* Longevity&lt;br /&gt;
* Male&lt;br /&gt;
* Membrane Proteins&lt;br /&gt;
* Microfilament Proteins&lt;br /&gt;
* Molecular Sequence Data&lt;br /&gt;
* Neoplasm Proteins&lt;br /&gt;
* Rats&lt;br /&gt;
* Rats, Inbred F344&lt;br /&gt;
* Receptors, Cell Surface&lt;br /&gt;
* Receptors, Peptide&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1617126&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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