1dgf: Difference between revisions
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{{STRUCTURE_1dgf| PDB=1dgf | SCENE= }} | {{STRUCTURE_1dgf| PDB=1dgf | SCENE= }} | ||
===HUMAN ERYTHROCYTE CATALASE=== | |||
{{ABSTRACT_PUBMED_10656833}} | |||
== | ==Disease== | ||
[[http://www.uniprot.org/uniprot/CATA_HUMAN CATA_HUMAN]] Defects in CAT are the cause of acatalasemia (ACATLAS) [MIM:[http://omim.org/entry/614097 614097]]. A metabolic disorder characterized by absence of catalase activity in red cells and is often associated with ulcerating oral lesions.<ref>PMID:2308162</ref> | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/CATA_HUMAN CATA_HUMAN]] Occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide. Promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells and normal and transformed fibroblast cells.<ref>PMID:7882369</ref> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:010656833</ref><references group="xtra"/> | <ref group="xtra">PMID:010656833</ref><references group="xtra"/><references/> | ||
[[Category: Catalase]] | [[Category: Catalase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||