1wlp

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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1wlp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wlp OCA], [http://www.ebi.ac.uk/pdbsum/1wlp PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1wlp RCSB]</span>
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'''Solution Structure Of The P22Phox-P47Phox Complex'''
'''Solution Structure Of The P22Phox-P47Phox Complex'''
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==Disease==
 
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Known diseases associated with this structure: Chronic granulomatous disease due to deficiency of NCF-1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=608512 608512]], Chronic granulomatous disease, autosomal, due to deficiency of CYBA OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=608508 608508]]
 
==About this Structure==
==About this Structure==
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[[Category: sh3 domain]]
[[Category: sh3 domain]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 14:58:35 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:37:55 2008''

Revision as of 21:37, 30 March 2008


PDB ID 1wlp

Drag the structure with the mouse to rotate
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Solution Structure Of The P22Phox-P47Phox Complex


About this Structure

1WLP is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Mon Mar 31 00:37:55 2008

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