1tp4: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
No edit summary
No edit summary
Line 1: Line 1:
[[Image:1tp4.gif|left|200px]]
[[Image:1tp4.gif|left|200px]]


{{Structure
<!--
|PDB= 1tp4 |SIZE=350|CAPTION= <scene name='initialview01'>1tp4</scene>
The line below this paragraph, containing "STRUCTURE_1tp4", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND=
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY=
or leave the SCENE parameter empty for the default display.
|GENE= RAD23A ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
-->
|DOMAIN=
{{STRUCTURE_1tp4| PDB=1tp4 |  SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1tp4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1tp4 OCA], [http://www.ebi.ac.uk/pdbsum/1tp4 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1tp4 RCSB]</span>
}}


'''Solution structure of the XPC binding domain of hHR23A protein'''
'''Solution structure of the XPC binding domain of hHR23A protein'''
Line 27: Line 24:
[[Category: Feigon, J.]]
[[Category: Feigon, J.]]
[[Category: Kamionka, M.]]
[[Category: Kamionka, M.]]
[[Category: dna repair]]
[[Category: Dna repair]]
[[Category: ner]]
[[Category: Ner]]
[[Category: rad23]]
[[Category: Rad23]]
[[Category: xpc]]
[[Category: Xpc]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 10:12:36 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:59:09 2008''

Revision as of 10:12, 3 May 2008

File:1tp4.gif

Template:STRUCTURE 1tp4

Solution structure of the XPC binding domain of hHR23A protein


OverviewOverview

Rad23 proteins are involved both in the ubiquitin-proteasome pathway and in nucleotide excision repair (NER), but the relationship between these two pathways is not yet understood. The two human homologs of Rad23, hHR23A and B, are functionally redundant in NER and interact with xeroderma pigmentosum complementation group C (XPC) protein. The XPC-hHR23 complex is responsible for the specific recognition of damaged DNA, which is an early step in NER. The interaction of the XPC binding domain (XPCB) of hHR23A/B with XPC protein has been shown to be important for its optimal function in NER. We have determined the solution structure of XPCB of hHR23A. The domain consists of five amphipathic helices and reveals hydrophobic patches on the otherwise highly hydrophilic domain surface. The patches are predicted to be involved in interaction with XPC. The XPCB domain has limited sequence homology with any proteins outside of the Rad23 family except for sacsin, a protein involved in spastic ataxia of Charlevoix-Saguenay, which contains a domain with 35% sequence identity.

About this StructureAbout this Structure

1TP4 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Structure of the XPC binding domain of hHR23A reveals hydrophobic patches for protein interaction., Kamionka M, Feigon J, Protein Sci. 2004 Sep;13(9):2370-7. PMID:15322280 Page seeded by OCA on Sat May 3 10:12:36 2008

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA