✦ LIBER ✦

Model for stathmin/OP18 binding to tubulin

✍ Scribed by Wallon, Gerlind; Rappsilber, Juri; Mann, Matthias; Serrano, Luis

Book ID: 111746633
Publisher: Nature Publishing Group
Year: 2000
Tongue: English
Weight: 400 KB
Volume: 19
Category: Article
ISSN: 0261-4189
DOI: 10.1093/emboj/19.2.213

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Phosphorylation disrupts the central hel

Phosphorylation disrupts the central helix in Op18/stathmin and suppresses binding to tubulin

✍ Steinmetz, M. O.; Jahnke, W.; Towbin, H.; Garcia-Echeverria, C.; Voshol, H.; Mul 📂 Article 📅 2001 🏛 Nature Publishing Group 🌐 English ⚖ 367 KB

OP18/stathmin binds near the C-terminus

OP18/stathmin binds near the C-terminus of tubulin and facilitates GTP binding

✍ Francisco José Moreno; Michel Bagnat; Filip Lim; Jesús Avila 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 435 KB

Op18/stathmin caps a kinked protofilamen

Op18/stathmin caps a kinked protofilament-like tubulin tetramer

✍ Steinmetz, Michel O.; Kammerer, Richard A.; Jahnke, Wolfgang; Goldie, Kenneth N. 📂 Article 📅 2000 🏛 Nature Publishing Group 🌐 English ⚖ 711 KB

694 The Tubulin-Targeting Agent T0070907

694 The Tubulin-Targeting Agent T0070907 Promotes Tubulin Degradation and Inactivates the Tubulin-Sequestering Protein Stathmin/Op18

✍ Gianni Harris; Katherine L. Schaefer 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 77 KB

Expression of stathmin/op18 as a signifi

Expression of stathmin/op18 as a significant prognostic factor for cervical carcinoma patients

✍ Wang Xi; Wang Rui; Lin Fang; Dong Ke; Gao Ping; Zhang Hui-Zhong 📂 Article 📅 2008 🏛 Springer-Verlag 🌐 English ⚖ 595 KB

Colchicine Models: Synthesis and Binding

Colchicine Models: Synthesis and Binding to Tubulin of Tertamethoxybiphenyls

✍ Yoshikuni Itoh; Arnold Brossi; Ernest Hamel; Chii M. Lin 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 German ⚖ 769 KB

Synthesis of tetramethoxybiphenyl21 was accomplished from 4-phenylcyclohexane-1,3-dione 13 by aromatization to biphenyl 19 and reductive removal of the phenolic OH group as phenyltetrazolyl ether. Tetramethoxybiphenyls 34 and 40 were obtained from 4-phenylcyclohexenone 26 via ester 27. The tetrameth