3hop: Difference between revisions

Line 1:

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

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

The ~~entry~~ 3hop ~~is ON HOLD~~ ~~until Paper Publication~~

<!--

The line below this paragraph, containing "STRUCTURE_3hop", 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.

-->

~~Authors: Clark, A.R., Sawyer, G.M., Robertson, S.P., Sutherland~~-~~Smith,~~ A~~.J.~~

===Structure of the actin-binding domain of human filamin A===

~~Description: Structure of the actin-binding domain of human filamin A~~

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed ~~Jun 17 09~~:47:16 2009''

<!--

The line below this paragraph, {{ABSTRACT_PUBMED_19773341}}, adds the Publication Abstract to the page

(as it appears on PubMed at http://www.pubmed.gov), where 19773341 is the PubMed ID number.

-->

==Disease==

Known disease associated with this structure: Frontometaphyseal dysplasia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Heterotopia, periventricular nodular, with frontometaphyseal dysplasia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Heterotopia, periventricular OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Heterotopia, periventricular, ED variant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Melnick-Needles syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Otopalatodigital syndrome, type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Otopalatodigital syndrome, type II OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]]

==About this Structure==

3HOP is a 2 chains structure of 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=3HOP OCA].

==Reference==

[[Category: Homo sapiens]]

[[Category: Clark, A R.]]

[[Category: Robertson, S P.]]

[[Category: Sawyer, G M.]]

[[Category: Sutherland-Smith, A J.]]

[[Category: Acetylation]]

[[Category: Actin binding domain]]

[[Category: Actin-binding]]

[[Category: Alternative splicing]]

[[Category: Calponin homology domain]]

[[Category: Cytoplasm]]

[[Category: Cytoskeleton]]

[[Category: Disease mutation]]

[[Category: Phosphoprotein]]

[[Category: Polymorphism]]

[[Category: Structural protein]]

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 14 10:24:10 2009''

Navigation menu

Page actions

Page actions

Personal tools

Navigation

Search

Tools

@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+{{Seed}}
+[[Image:3hop.jpg|left|200px]]
-The entry 3hop is ON HOLD  until Paper Publication
+<!--
+The line below this paragraph, containing "STRUCTURE_3hop", 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_3hop|  PDB=3hop  |  SCENE=  }}
-Authors: Clark, A.R., Sawyer, G.M., Robertson, S.P., Sutherland-Smith, A.J.
+===Structure of the actin-binding domain of human filamin A===
-Description: Structure of the actin-binding domain of human filamin A
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 17 09:47:16 2009''
+<!--
+The line below this paragraph, {{ABSTRACT_PUBMED_19773341}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 19773341 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_19773341}}
+==Disease==
+Known disease associated with this structure: Frontometaphyseal dysplasia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Heterotopia, periventricular nodular, with frontometaphyseal dysplasia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Heterotopia, periventricular OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Heterotopia, periventricular, ED variant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Melnick-Needles syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Otopalatodigital syndrome, type I OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]], Otopalatodigital syndrome, type II OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300017 300017]]
+==About this Structure==
+HOP is a 2 chains structure of 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=3HOP OCA].
+==Reference==
+<ref group="xtra">PMID:19773341</ref><references group="xtra"/>
+[[Category: Homo sapiens]]
+[[Category: Clark, A R.]]
+[[Category: Robertson, S P.]]
+[[Category: Sawyer, G M.]]
+[[Category: Sutherland-Smith, A J.]]
+[[Category: Acetylation]]
+[[Category: Actin binding domain]]
+[[Category: Actin-binding]]
+[[Category: Alternative splicing]]
+[[Category: Calponin homology domain]]
+[[Category: Cytoplasm]]
+[[Category: Cytoskeleton]]
+[[Category: Disease mutation]]
+[[Category: Phosphoprotein]]
+[[Category: Polymorphism]]
+[[Category: Structural protein]]
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 14 10:24:10 2009''