Kinoshita T - Search Results

1

A crucial role of Cys218 in configuring an unprecedented auto-inhibition form of MAP2K7.

Sogabe Y, Hashimoto T, Matsumoto T, Kirii Y, Sawa M, Kinoshita T. Sogabe Y, et al. Among authors: kinoshita t. Biochem Biophys Res Commun. 2016 Apr 29;473(2):476-81. doi: 10.1016/j.bbrc.2016.03.036. Epub 2016 Mar 15. Biochem Biophys Res Commun. 2016. PMID: 26987717

2

Identification of a selective ERK inhibitor and structural determination of the inhibitor-ERK2 complex.

Ohori M, Kinoshita T, Okubo M, Sato K, Yamazaki A, Arakawa H, Nishimura S, Inamura N, Nakajima H, Neya M, Miyake H, Fujii T. Ohori M, et al. Among authors: kinoshita t. Biochem Biophys Res Commun. 2005 Oct 14;336(1):357-63. doi: 10.1016/j.bbrc.2005.08.082. Biochem Biophys Res Commun. 2005. PMID: 16139248

3

Structure of human Fyn kinase domain complexed with staurosporine.

Kinoshita T, Matsubara M, Ishiguro H, Okita K, Tada T. Kinoshita T, et al. Biochem Biophys Res Commun. 2006 Aug 4;346(3):840-4. doi: 10.1016/j.bbrc.2006.05.212. Epub 2006 Jun 13. Biochem Biophys Res Commun. 2006. PMID: 16782058

4

Role of a cysteine residue in the active site of ERK and the MAPKK family.

Ohori M, Kinoshita T, Yoshimura S, Warizaya M, Nakajima H, Miyake H. Ohori M, et al. Among authors: kinoshita t. Biochem Biophys Res Commun. 2007 Feb 16;353(3):633-7. doi: 10.1016/j.bbrc.2006.12.083. Epub 2006 Dec 20. Biochem Biophys Res Commun. 2007. PMID: 17194451

5

Conformational change of adenosine deaminase during ligand-exchange in a crystal.

Kinoshita T, Tada T, Nakanishi I. Kinoshita T, et al. Biochem Biophys Res Commun. 2008 Aug 15;373(1):53-7. doi: 10.1016/j.bbrc.2008.05.180. Epub 2008 Jun 10. Biochem Biophys Res Commun. 2008. PMID: 18549808

6

Crystal structure of human mono-phosphorylated ERK1 at Tyr204.

Kinoshita T, Yoshida I, Nakae S, Okita K, Gouda M, Matsubara M, Yokota K, Ishiguro H, Tada T. Kinoshita T, et al. Biochem Biophys Res Commun. 2008 Dec 26;377(4):1123-7. doi: 10.1016/j.bbrc.2008.10.127. Epub 2008 Nov 5. Biochem Biophys Res Commun. 2008. PMID: 18983981

7

Structural insight into human CK2alpha in complex with the potent inhibitor ellagic acid.

Sekiguchi Y, Nakaniwa T, Kinoshita T, Nakanishi I, Kitaura K, Hirasawa A, Tsujimoto G, Tada T. Sekiguchi Y, et al. Among authors: kinoshita t. Bioorg Med Chem Lett. 2009 Jun 1;19(11):2920-3. doi: 10.1016/j.bmcl.2009.04.076. Epub 2009 Apr 22. Bioorg Med Chem Lett. 2009. PMID: 19414254

8

Structural basis for the inhibitor recognition of human Lyn kinase domain.

Miyano N, Kinoshita T, Nakai R, Kirii Y, Yokota K, Tada T. Miyano N, et al. Among authors: kinoshita t. Bioorg Med Chem Lett. 2009 Dec 1;19(23):6557-60. doi: 10.1016/j.bmcl.2009.10.038. Epub 2009 Oct 13. Bioorg Med Chem Lett. 2009. PMID: 19857964

9

Crystal structures of MKK4 kinase domain reveal that substrate peptide binds to an allosteric site and induces an auto-inhibition state.

Matsumoto T, Kinoshita T, Kirii Y, Yokota K, Hamada K, Tada T. Matsumoto T, et al. Among authors: kinoshita t. Biochem Biophys Res Commun. 2010 Sep 24;400(3):369-73. doi: 10.1016/j.bbrc.2010.08.071. Epub 2010 Aug 21. Biochem Biophys Res Commun. 2010. PMID: 20732303

10

High-resolution structure of exo-arabinanase from Penicillium chrysogenum.

Sogabe Y, Kitatani T, Yamaguchi A, Kinoshita T, Adachi H, Takano K, Inoue T, Mori Y, Matsumura H, Sakamoto T, Tada T. Sogabe Y, et al. Among authors: kinoshita t. Acta Crystallogr D Biol Crystallogr. 2011 May;67(Pt 5):415-22. doi: 10.1107/S0907444911006299. Epub 2011 Apr 13. Acta Crystallogr D Biol Crystallogr. 2011. PMID: 21543843

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