2v0f: Difference between revisions

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[[Image:2v0f.~~gif~~|left|200px]]

[[Image:2v0f.png|left|200px]]

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~~'''~~BRK DOMAIN FROM HUMAN CHD7~~'''~~

===BRK DOMAIN FROM HUMAN CHD7===

~~==Overview==~~

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~~CHD7 is a member of the chromodomain helicase DNA binding domain (CHD) family of ATP-dependent chromatin remodelling enzymes. It is mutated in CHARGE syndrome~~, ~~a multiple congenital anomaly condition. CHD7 is one of a subset of CHD proteins~~, ~~unique~~ to ~~metazoans that contain~~ the ~~BRK domain, a protein module also found in the Brahma~~/~~BRG1 family of helicases~~. ~~We describe here~~ the ~~NMR solution structure of the two BRK domains of CHD7~~. ~~Each domain has a compact betabetaalphabeta fold. The second domain has a C~~-~~terminal extension consisting of two additional helices. The structure differs from those of other domains present in chromatin~~-~~associated proteins.~~

The line below this paragraph, {{ABSTRACT_PUBMED_17603073}}, adds the Publication Abstract to the page

(as it appears on PubMed at http://www.pubmed.gov), where 17603073 is the PubMed ID number.

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==About this Structure==

2V0F 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=2V0F OCA].

2V0F is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2V0F OCA].

==Reference==

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[[Category: Transcription]]

[[Category: Transcription regulation]]

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on ~~Sun May 4 17~~:57:30 2008''

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 20:52:42 2008''

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@@ Line 1: / Line 1: @@
-[[Image:2v0f.gif|left|200px]]
+{{Seed}}
+[[Image:2v0f.png|left|200px]]
 <!--
@@ Line 9: / Line 10: @@
 {{STRUCTURE_2v0f|  PDB=2v0f  |  SCENE=  }}
-'''BRK DOMAIN FROM HUMAN CHD7'''
+===BRK DOMAIN FROM HUMAN CHD7===
-==Overview==
+<!--
-CHD7 is a member of the chromodomain helicase DNA binding domain (CHD) family of ATP-dependent chromatin remodelling enzymes. It is mutated in CHARGE syndrome, a multiple congenital anomaly condition. CHD7 is one of a subset of CHD proteins, unique to metazoans that contain the BRK domain, a protein module also found in the Brahma/BRG1 family of helicases. We describe here the NMR solution structure of the two BRK domains of CHD7. Each domain has a compact betabetaalphabeta fold. The second domain has a C-terminal extension consisting of two additional helices. The structure differs from those of other domains present in chromatin-associated proteins.
+The line below this paragraph, {{ABSTRACT_PUBMED_17603073}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 17603073 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_17603073}}
 ==About this Structure==
-V0F 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=2V0F OCA].
+V0F is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2V0F OCA].
 ==Reference==
@@ Line 40: / Line 44: @@
 [[Category: Transcription]]
 [[Category: Transcription regulation]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May  4 17:57:30 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 20:52:42 2008''