2yob: Difference between revisions

Line 1:

~~'''Unreleased~~ structure~~'''~~

===High resolution AGXT_M structure===

~~The~~ entry ~~2yob~~ is ~~ON HOLD~~ ~~until Paper Publication~~

==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>

~~Authors~~: ~~Fabelo-Rosa, I~~.~~, Mesa-Torres, N~~.~~, Riverol, D~~.~~, Yunta, C~~.~~, Albert, A~~.~~, Salido, E~~.~~, Pey, A.L~~.

==About this Structure==

[[2yob]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2YOB OCA].

~~Description~~: ~~High resolution AGXT_M structure~~

==Reference==

[[Category: Homo sapiens]]

[[Category: Albert, A.]]

[[Category: Fabelo-Rosa, I.]]

[[Category: Mesa-Torres, N.]]

[[Category: Pey, A L.]]

[[Category: Riverol, D.]]

[[Category: Salido, E.]]

[[Category: Yunta, C.]]

[[Category: Agxt folding and stability defect]]

[[Category: Primary hyperoxaluria type i]]

[[Category: Transferase]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+{{STRUCTURE_2yob|  PDB=2yob  |  SCENE=  }}
+===High resolution AGXT_M structure===
-The entry 2yob is ON HOLD  until Paper Publication
+==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>
-Authors: Fabelo-Rosa, I., Mesa-Torres, N., Riverol, D., Yunta, C., Albert, A., Salido, E., Pey, A.L.
+==About this Structure==
+[[2yob]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2YOB OCA].
-Description: High resolution AGXT_M structure
+==Reference==
+<references group="xtra"/><references/>
+[[Category: Homo sapiens]]
+[[Category: Albert, A.]]
+[[Category: Fabelo-Rosa, I.]]
+[[Category: Mesa-Torres, N.]]
+[[Category: Pey, A L.]]
+[[Category: Riverol, D.]]
+[[Category: Salido, E.]]
+[[Category: Yunta, C.]]
+[[Category: Agxt folding and stability defect]]
+[[Category: Primary hyperoxaluria type i]]
+[[Category: Transferase]]