3mjl: Difference between revisions

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===Crystal structure of human arginase I in complex with 2-aminoimidazole. Resolution 1.90 A.===

==Disease==

[[http://www.uniprot.org/uniprot/ARGI1_HUMAN ARGI1_HUMAN]] Defects in ARG1 are the cause of argininemia (ARGIN) [MIM:[http://omim.org/entry/207800 207800]]; also known as hyperargininemia. Argininemia is a rare autosomal recessive disorder of the urea cycle. Arginine is elevated in the blood and cerebrospinal fluid, and periodic hyperammonemia occurs. Clinical manifestations include developmental delay, seizures, mental retardation, hypotonia, ataxia, progressive spastic quadriplegia.<ref>PMID:1463019</ref><ref>PMID:7649538</ref>

==About this Structure==

~~3MJL~~ is a 2 ~~chains~~ structure with ~~sequences~~ 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=3MJL OCA].

[[3mjl]] 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=3MJL OCA].

==Reference==

[[Category: Arginase]]

[[Category: Homo sapiens]]

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[[Category: Manganese cluster]]

[[Category: Metal coordination]]

~~''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed May 5 12:12:31 2010''~~

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@@ Line 1: / Line 1: @@
-{{Seed}}
-[[Image:3mjl.jpg|left|200px]]
-<!--
-The line below this paragraph, containing "STRUCTURE_3mjl", creates the "Structure Box" on the page.
-You may change the PDB parameter (which sets the PDB file loaded into the applet)
-or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
-or leave the SCENE parameter empty for the default display.
--->
 {{STRUCTURE_3mjl|  PDB=3mjl  |  SCENE=  }}
 ===Crystal structure of human arginase I in complex with 2-aminoimidazole. Resolution 1.90 A.===
+==Disease==
+[[http://www.uniprot.org/uniprot/ARGI1_HUMAN ARGI1_HUMAN]] Defects in ARG1 are the cause of argininemia (ARGIN) [MIM:[http://omim.org/entry/207800 207800]]; also known as hyperargininemia. Argininemia is a rare autosomal recessive disorder of the urea cycle. Arginine is elevated in the blood and cerebrospinal fluid, and periodic hyperammonemia occurs. Clinical manifestations include developmental delay, seizures, mental retardation, hypotonia, ataxia, progressive spastic quadriplegia.<ref>PMID:1463019</ref><ref>PMID:7649538</ref>
 ==About this Structure==
-MJL is a 2 chains structure with sequences 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=3MJL OCA].
+[[3mjl]] 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=3MJL OCA].
+==Reference==
+<references group="xtra"/><references/>
 [[Category: Arginase]]
 [[Category: Homo sapiens]]
@@ Line 24: / Line 19: @@
 [[Category: Manganese cluster]]
 [[Category: Metal coordination]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed May  5 12:12:31 2010''