1j04: Difference between revisions
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{{STRUCTURE_1j04| PDB=1j04 | SCENE= }} | {{STRUCTURE_1j04| PDB=1j04 | SCENE= }} | ||
===Structural mechanism of enzyme mistargeting in hereditary kidney stone disease in vitro=== | ===Structural mechanism of enzyme mistargeting in hereditary kidney stone disease in vitro=== | ||
{{ABSTRACT_PUBMED_20208150}} | |||
==Disease== | |||
[[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> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:020208150</ref><references group="xtra"/> | <ref group="xtra">PMID:020208150</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Bartlam, M.]] | [[Category: Bartlam, M.]] | ||
