1h0c: Difference between revisions

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[[Image:1h0c.png|left|200px]]
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{{STRUCTURE_1h0c|  PDB=1h0c  |  SCENE=  }}  
{{STRUCTURE_1h0c|  PDB=1h0c  |  SCENE=  }}  
===THE CRYSTAL STRUCTURE OF HUMAN ALANINE:GLYOXYLATE AMINOTRANSFERASE===
===THE CRYSTAL STRUCTURE OF HUMAN ALANINE:GLYOXYLATE AMINOTRANSFERASE===
{{ABSTRACT_PUBMED_12899834}}


 
==Disease==
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[[http://www.uniprot.org/uniprot/SPYA_HUMAN SPYA_HUMAN]] Defects in AGXT are the cause of hyperoxaluria primary type 1 (HP1) [MIM:[http://omim.org/entry/259900 259900]]; also known as primary hyperoxaluria type I (PH1) and oxalosis I. HP1 is a rare autosomal recessive inborn error of glyoxylate metabolism characterized by increased excretion of oxalate and glycolate, and the progressive accumulation of insoluble calcium oxalate in the kidney and urinary tract.<ref>PMID:1703535</ref><ref>PMID:2039493</ref><ref>PMID:1349575</ref><ref>PMID:1301173</ref><ref>PMID:8101040</ref><ref>PMID:9192270</ref><ref>PMID:9604803</ref><ref>PMID:10394939</ref><ref>PMID:10453743</ref><ref>PMID:10541294</ref><ref>PMID:10862087</ref><ref>PMID:10960483</ref><ref>PMID:12559847</ref><ref>PMID:12777626</ref><ref>PMID:15253729</ref><ref>PMID:15849466</ref><ref>PMID:15961946</ref><ref>PMID:15963748</ref>  
The line below this paragraph, {{ABSTRACT_PUBMED_12899834}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_12899834}}


==About this Structure==
==About this Structure==
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==Reference==
==Reference==
<ref group="xtra">PMID:012899834</ref><references group="xtra"/>
<ref group="xtra">PMID:012899834</ref><references group="xtra"/><references/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Danpure, C J.]]
[[Category: Danpure, C J.]]
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