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![]() | Full-length human p23 (1-160)
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機能・相同性 | ![]() lung saccule development / prostaglandin-E synthase / prostaglandin-E synthase activity / nuclear receptor-mediated glucocorticoid signaling pathway / prostanoid biosynthetic process / Aryl hydrocarbon receptor signalling / Synthesis of Prostaglandins (PG) and Thromboxanes (TX) / glycogen biosynthetic process / telomerase holoenzyme complex / protein folding chaperone complex ...lung saccule development / prostaglandin-E synthase / prostaglandin-E synthase activity / nuclear receptor-mediated glucocorticoid signaling pathway / prostanoid biosynthetic process / Aryl hydrocarbon receptor signalling / Synthesis of Prostaglandins (PG) and Thromboxanes (TX) / glycogen biosynthetic process / telomerase holoenzyme complex / protein folding chaperone complex / prostaglandin biosynthetic process / skin development / telomerase holoenzyme complex assembly / : / HSF1 activation / telomere maintenance via telomerase / Attenuation phase / chaperone-mediated protein complex assembly / DNA polymerase binding / positive regulation of telomere maintenance via telomerase / telomere maintenance / HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand / ESR-mediated signaling / Hsp90 protein binding / telomerase activity / unfolded protein binding / protein folding / protein-folding chaperone binding / fibroblast proliferation / Estrogen-dependent gene expression / Potential therapeutics for SARS / chromosome, telomeric region / protein stabilization / signal transduction / protein-containing complex / nucleoplasm / nucleus / cytosol 類似検索 - 分子機能 |
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![]() | ![]() タイトル: The C-terminal region of the human p23 chaperone modulates its structure and function. 著者: Thiago V Seraphim / Lisandra M Gava / David Z Mokry / Thiago C Cagliari / Leandro R S Barbosa / Carlos H I Ramos / Júlio C Borges / ![]() 要旨: The p23 protein is a chaperone widely involved in protein homeostasis, well known as an Hsp90 co-chaperone since it also controls the Hsp90 chaperone cycle. Human p23 includes a β-sheet domain, ...The p23 protein is a chaperone widely involved in protein homeostasis, well known as an Hsp90 co-chaperone since it also controls the Hsp90 chaperone cycle. Human p23 includes a β-sheet domain, responsible for interacting with Hsp90; and a charged C-terminal region whose function is not clear, but seems to be natively unfolded. p23 can undergo caspase-dependent proteolytic cleavage to form p19 (p231-142), which is involved in apoptosis, while p23 has anti-apoptotic activity. To better elucidate the function of the human p23 C-terminal region, we studied comparatively the full-length human p23 and three C-terminal truncation mutants: p23₁₋₁₁₇; p23₁₋₁₃₁ and p23₁₋₁₄₂. Our data indicate that p23 and p19 have distinct characteristics, whereas the other two truncations behave similarly, with some differences to p23 and p19. We found that part of the C-terminal region can fold in an α-helix conformation and slightly contributes to p23 thermal-stability, suggesting that the C-terminal interacts with the β-sheet domain. As a whole, our results suggest that the C-terminal region of p23 is critical for its structure-function relationship. A mechanism where the human p23 C-terminal region behaves as an activation/inhibition module for different p23 activities is proposed. |
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試料
![]() | 名称: Full-length human p23 (1-160) / 試料濃度: 1.00-2.00 |
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バッファ | 名称: 25 mM Tris-HCl, 100 mM NaCl, 5 mM B-mercaptoethanol / pH: 7.5 |
要素 #404 | 名称: PTGES, Sba1, p23 / タイプ: protein / 記述: Prostaglandin E synthase 3 / 分子量: 18.841 / 分子数: 1 / 由来: Homo sapiens / 参照: UniProt: Q15185 配列: GSMQPASAKW YDRRDYVFIE FCVEDSKDVN VNFEKSKLTF SCLGGSDNFK HLNEIDLFHC IDPNDSKHKR TDRSILCCLR KGESGQSWPR LTKERAKLNW LSVDFNNWKD WEDDSDEDMS NFDRFSEMMN NMGGDEDVDL PEVDGADDDS QDSDDEKMPD LE |
-実験情報
ビーム | 設備名称: Brazilian Synchrotron Light Laboratory SAXS1 Beamline 地域: Campinas / 国: Brazil ![]() | |||||||||||||||||||||||||||||||||
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検出器 | 名称: Pilatus 300K / タイプ: 20Hz | |||||||||||||||||||||||||||||||||
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距離分布関数 P(R) |
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結果 | コメント: Samples were measured at 1 mg/mL and 2 mg/mL in 1 mm path-length mica cells. All curves were inspected for X-ray damage and aggregation. The experimental molecular weight was determined ...コメント: Samples were measured at 1 mg/mL and 2 mg/mL in 1 mm path-length mica cells. All curves were inspected for X-ray damage and aggregation. The experimental molecular weight was determined by analytical ultracentrifugation.
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