M. Murata

发表

The structure of phosalacine, a new herbicidal antibiotic containing phosphinothricin.

S. Ōmura, N. Imamura, K. Hinotozawa, 1984, The Journal of antibiotics.

Preliminary crystallographic data for a copper-containing protein, plastocyanin.

J. Ramshaw, P. Colman, J. Guss, 1977, Journal of molecular biology.

Stimulation of Glucose Uptake in Muscle Cells by Prolonged Treatment with Scriptide, a Histone Deacetylase Inhibitor

H. Takigawa-Imamura, K. Nakazawa, M. Murata, 2003, Bioscience, biotechnology, and biochemistry.

Crystallization and preliminary X-ray study of the cathepsin B complexed with CA074, a selective inhibitor.

K. Tomoo, T. Ishida, K. Kitamura, 1992, Journal of molecular biology.

Substrate specificity of bovine cathepsin B and its inhibition by CA074, based on crystal structure refinement of the complex.

K. Tomoo, T. Ishida, K. Kitamura, 2000, Journal of biochemistry.

Phosalacine, a new herbicidal antibiotic containing phosphinothricin. Fermentation, isolation, biological activity and mechanism of action.

S. Ōmura, H. Hanaki, R. Oiwa, 1984, The Journal of antibiotics.

Clarification of substrate specificity of papain by crystal analyses of complexes with covalent-type inhibitors.

T. Ishida, S. Sumiya, K. Kitamura, 1994, Biochimica et biophysica acta.

Novel epoxysuccinyl peptides A selective inhibitor of cathepsin B, in vivo

N. Katunuma, T. Nikawa, T. Towatari, 1991, FEBS letters.

Inhibition of cartilage proteoglycan release by a specific inactivator of cathepsin B and an inhibitor of matrix metalloproteinases. Evidence for two converging pathways of chondrocyte-mediated proteoglycan degradation.

A. Barrett, J. Saklatvala, C. Handley, 1993, Arthritis and rheumatism.

Characterization of CAA0225, a novel inhibitor specific for cathepsin L, as a probe for autophagic proteolysis.

T. Ueno, E. Kominami, I. Tanida, 2009, Biological & pharmaceutical bulletin.

CA074 methyl ester: a proinhibitor for intracellular cathepsin B.

A. Barrett, D. Buttle, M. Murata, 1992, Archives of biochemistry and biophysics.

Low-temperature x-ray absorption spectroscopy of plastocyanin: evidence for copper-site photoreduction at cryogenic temperatures

K. Hodgson, J. Penner‐Hahn, M. Murata, 1989 .

Efficient synthetic method for ethyl (+)-(2S,3S)-3-[(S)-3-methyl- 1-(3-methylbutylcarbamoyl)butylcarbamoyl]-2-oxiranecarb oxylate (EST), a new inhibitor of cysteine proteinases.

M. Murata, Y. Kanaoka, M. Tamai, 1987, Chemical & pharmaceutical bulletin.

X-ray crystal structure analysis of plastocyanin at 2.7 Å resolution

M. Murata, J. Ramshaw, P. Colman, 1978, Nature.

Crystal structure analyses of reduced (CuI) poplar plastocyanin at six pH values.

J. Guss, P. Harrowell, M. Murata, 1987, Journal of molecular biology.

Phase determination by multiple-wavelength x-ray diffraction: crystal structure of a basic "blue" copper protein from cucumbers.

K. Hodgson, R. P. Phizackerley, J. Guss, 1988, Science.

Preliminary crystallographic data for a basic copper-containing protein from cucumber seedlings.

J. Ramshaw, P. Colman, J. Guss, 1977, Journal of molecular biology.

Complete amino acid sequence of plastocyanin from a green alga, Enteromorpha prolifera.

R. Moritz, R. Simpson, E. Nice, 1986, European journal of biochemistry.

Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems II: 2-alkyl and 2-arylthiomethyl derivatives.

M. Murata, T. Kamimura, H. Azami, 1998, The Journal of antibiotics.

Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems--I. 2-Alkoxymethyl derivatives.

M. Murata, T. Kamimura, H. Azami, 1997, Bioorganic & medicinal chemistry.

Synthesis of Isoselenazolo- or Isothiazolo[4, 3-e][1, 4]diazepines

J. Sakakibara, M. Murata, T. Ueda, 1988 .

Oxetin, a new antimetabolite from an actinomycete. Fermentation, isolation, structure and biological activity.

S. Ōmura, A. Furusaki, N. Imamura, 1984, The Journal of antibiotics.

Inhibition of bone resrption by selctive inactivators of cysteine proteinases

Sheila J. Jones, A. Boyde, J. Reynolds, 1994, Journal of cellular biochemistry.

A facile synthesis of [1,2,4]triazino[3,2‐f]purines and [1,2,4]triazepino[3,2‐f]purines

J. Sakakibara, M. Murata, T. Ueda, 1988 .

Screening for new antifolates of microbial origin and a new antifolate AM-8402.

S. Ōmura, H. Tanaka, K. Kimura, 1985, The Journal of antibiotics.

Synthesis and biological activity of analogues of diazaquinomycin A, a new thymidylate synthase inhibitor.

S. Ōmura, H. Tanaka, M. Murata, 1989, The Journal of antibiotics.

7-Hydro-8-methylpteroylglutamylglutamic acid, a new anti-folate from an actinomycete. Fermentation, isolation, structure and biological activity.

S. Ōmura, H. Tanaka, M. Murata, 1987, The Journal of antibiotics.

Diazaquinomycin A, a new antifolate antibiotic, inhibits thymidylate synthase.

S. Ōmura, H. Tanaka, T. Miyasaka, 1985, The Journal of antibiotics.

Maturation and degradation of β‐galactosidase in the post‐Golgi compartment are regulated by cathepsin B and a non‐cysteine protease

Y. Okamura-Oho, S. Zhang, J. Callahan, 1997, FEBS letters.

Amino acid sequence of a basic blue protein from cucumber seedlings.

R. Simpson, M. Murata, F. J. Morgan, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Metabolic fate of loxistatin in rat.

M. Murata, T. Suwa, M. Tamai, 1990, Xenobiotica; the fate of foreign compounds in biological systems.

SYNTHESIS AND CENTRAL NERVOUS SYSTEM STIMULANT ACTIVITY OF CAMPHOR-1,2,4-TRIAZINES FUSED WITH 1,2,4-TRIAZOLE, TETRAZOLE AND 1,2,4-TRIAZINE

N. Murakami, A. Nagatsu, J. Sakakibara, 1997 .

Binding mode of CA074, a specific irreversible inhibitor, to bovine cathepsin B as determined by X-ray crystal analysis of the complex.

Y. Hata, K. Tomoo, T. Ishida, 1997, Journal of biochemistry.

Quantitative evaluation of each catalytic subsite of cathepsin B for inhibitory activity based on inhibitory activity-binding mode relationship of epoxysuccinyl inhibitors by X-ray crystal structure analyses of complexes.

K. Tomoo, T. Ishida, K. Kitamura, 2006, Journal of molecular biology.

Structural basis for development of cathepsin B-specific noncovalent-type inhibitor: crystal structure of cathepsin B-E64c complex.

K. Tomoo, T. Ishida, K. Kitamura, 2002, Biochimica et biophysica acta.

X-ray crystal structure of papain complexed with cathepsin B-specific covalent-type inhibitor: substrate specificity and inhibitory activity.

T. Ishida, S. Sumiya, K. Kitamura, 1998, Biochimica et biophysica acta.

Difference of structural requisite in design of inhibitor of cathepsin B and papain: X-ray crystal structures of complexes

K. Tomoo, T. Ishida, K. Kitamura, 1999 .

Efficient Synthetic Method for Ethyl (+)‐(2S,3S)‐3‐((S)‐3‐Methyl‐1‐(3‐ methylbutylcarbamoyl)butylcarbamoyl)‐2‐oxiranecarboxylate (EST), a New Inhibitor of Cysteine Proteinases.

M. Murata, Y. Kanaoka, M. Tamai, 1987 .

STUDIES ON CEPHALOSPORIN ANTIBIOTICS I. SYNTHESIS, ANTIBACTERIAL ACTIVITY AND ORAL ABSORPTION OF NEW 3-(O-SUBSTITUTED)-7iS-[D-a:-AMINO-«:-(4- HYDROXYPHENYL)ACETAMID O] CEPHALO SPO RINS

Yoshiaki Watanabe, M. Murata, T. Nagate, 2006 .