3efh: Difference between revisions

Line 1:

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

[[Image:3efh.jpg|left|200px]]

The ~~entry~~ 3efh ~~is ON HOLD~~

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~~Authors: Peng, X., Li, X.~~

===Crystal structure of human phosphoribosyl pyrophosphate synthetase 1===

~~Description: Solution structure of human phosphoribosyl pyrophosphate synthetase 1~~

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed ~~Sep 17 13~~:41:47 2008''

==Disease==

Known disease associated with this structure: Arts syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850 311850]], Charcot-Marie-Tooth disease, X-linked recessive, 5 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850 311850]], Gout, PRPS-related OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850 311850]], Phosphoribosylpyrophosphate synthetase superactivity OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850 311850]]

==About this Structure==

3EFH is a [[Single protein]] structure of 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=3EFH OCA].

[[Category: Homo sapiens]]

[[Category: Ribose-phosphate diphosphokinase]]

[[Category: Single protein]]

[[Category: Li, X.]]

[[Category: Li, Y.]]

[[Category: Peng, X.]]

[[Category: Charcot-marie-tooth disease]]

[[Category: Deafness]]

[[Category: Disease mutation]]

[[Category: Gout]]

[[Category: Kinase]]

[[Category: Magnesium]]

[[Category: Metal-binding]]

[[Category: Nucleotide biosynthesis]]

[[Category: Polymorphism]]

[[Category: Transferase]]

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 1 22:12:10 2008''

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+{{Seed}}
+[[Image:3efh.jpg|left|200px]]
-The entry 3efh is ON HOLD
+<!--
+The line below this paragraph, containing "STRUCTURE_3efh", 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_3efh|  PDB=3efh  |  SCENE=  }}
-Authors: Peng, X., Li, X.
+===Crystal structure of human phosphoribosyl pyrophosphate synthetase 1===
-Description: Solution structure of human phosphoribosyl pyrophosphate synthetase 1
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 17 13:41:47 2008''
+==Disease==
+Known disease associated with this structure: Arts syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850 311850]], Charcot-Marie-Tooth disease, X-linked recessive, 5 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850 311850]], Gout, PRPS-related OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850 311850]], Phosphoribosylpyrophosphate synthetase superactivity OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850 311850]]
+==About this Structure==
+EFH is a [[Single protein]] structure of 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=3EFH OCA].
+[[Category: Homo sapiens]]
+[[Category: Ribose-phosphate diphosphokinase]]
+[[Category: Single protein]]
+[[Category: Li, X.]]
+[[Category: Li, Y.]]
+[[Category: Peng, X.]]
+[[Category: Charcot-marie-tooth disease]]
+[[Category: Deafness]]
+[[Category: Disease mutation]]
+[[Category: Gout]]
+[[Category: Kinase]]
+[[Category: Magnesium]]
+[[Category: Metal-binding]]
+[[Category: Nucleotide biosynthesis]]
+[[Category: Polymorphism]]
+[[Category: Transferase]]
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct  1 22:12:10 2008''