3iu6: Difference between revisions
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{{STRUCTURE_3iu6| PDB=3iu6 | SCENE= }} | {{STRUCTURE_3iu6| PDB=3iu6 | SCENE= }} | ||
===Crystal structure of the sixth bromodomain of human poly-bromodomain containing protein 1 (PB1)=== | ===Crystal structure of the sixth bromodomain of human poly-bromodomain containing protein 1 (PB1)=== | ||
{{ABSTRACT_PUBMED_22464331}} | |||
==Disease== | |||
[[http://www.uniprot.org/uniprot/PB1_HUMAN PB1_HUMAN]] Defects in PBRM1 are a cause of renal cell carcinoma (RCC) [MIM:[http://omim.org/entry/144700 144700]]. It is a heterogeneous group of sporadic or hereditary carcinoma derived from cells of the proximal renal tubular epithelium. It is subclassified into clear cell renal carcinoma (non-papillary carcinoma), papillary renal cell carcinoma, chromophobe renal cell carcinoma, collecting duct carcinoma with medullary carcinoma of the kidney, and unclassified renal cell carcinoma.<ref>PMID:21248752</ref> | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/PB1_HUMAN PB1_HUMAN]] Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Acts as a negative regulator of cell proliferation.<ref>PMID:21248752</ref> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:022464331</ref><references group="xtra"/> | <ref group="xtra">PMID:022464331</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Arrowsmith, C H.]] | [[Category: Arrowsmith, C H.]] |