Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

K Tomoo

Showing results (11-20 of 24) with videos related to

Pageof 3
Sort By:
Journal of Molecular Biology|March 15, 2000
Crystal structure of amylomaltase from thermus aquaticus, a glycosyltransferase catalysing the production of large cyclic glucansI Przylas, K Tomoo, Y Terada, et al.
Journal of Biochemistry|August 1, 1993
Molecular dynamics simulation of 1,2-dilauroyl-L-phosphatidylethanolamine binding to phospholipase A2: an attempt to explain the selective hydrolysis of substrate fatty acid ester at position 2H Ohishi, S Fujii, K Tomoo, et al.
Journal of Molecular Biology|October 5, 1992
Crystallization and preliminary X-ray study of the cathepsin B complexed with CA074, a selective inhibitorA Yamamoto, T Kaji, K Tomoo, et al.
The Journal of Biological Chemistry|February 25, 1989
Revised amino acid sequence, crystallization, and preliminary x-ray diffraction analysis of acidic phospholipase A2 from the venom of Agkistrodon halys blomhoffiiK Tomoo, H Ohishi, T Ishida, et al.
Journal of Biochemistry|May 1, 1997
Binding mode of CA074, a specific irreversible inhibitor, to bovine cathepsin B as determined by X-ray crystal analysis of the complexA Yamamoto, T Hara, K Tomoo, et al.
Biochemical and Biophysical Research Communications|April 15, 1992
Structure of acidic phospholipase A2 for the venom of Agkistrodon halys blomhoffii at 2.8 A resolutionK Tomoo, H Ohishi, M Doi, et al.
Biochemistry|October 3, 1995
Unique binding of a novel synthetic inhibitor, N-[3-[4-[4-(amidinophenoxy)carbonyl]phenyl]-2-methyl-2-propenoyl]- N-allylglycine methanesulfonate, to bovine trypsin, revealed by the crystal structure of the complexY Odagaki, H Nakai, K Senokuchi, et al.
Journal of Biochemistry|April 1, 1993
Crystallization and preliminary X-ray study of Agkistrodon halys blomhoffii phospholipase A2 complexed with a specific inhibitorK Tomoo, S Fujii, T Ishida, et al.
Journal of Biochemistry|February 28, 2001
Binding diversity of a noncovalent-type low-molecular-weight serine protease inhibitor and function of a catalytic water molecule: X-ray crystal structure of PKSI-527--inhibited trypsinK Tomoo, K Satoh, Y Tsuda, et al.
Biochemical and Biophysical Research Communications|August 15, 1995
Design of noncovalent trypsin inhibitor based on the X-ray crystal structure of the complexM Nakamura, K Tomoo, T Ishida, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Journal of Molecular Biology|March 15, 2000
Crystal structure of amylomaltase from thermus aquaticus, a glycosyltransferase catalysing the production of large cyclic glucansI Przylas, K Tomoo, Y Terada, et al.
Journal of Biochemistry|August 1, 1993
Molecular dynamics simulation of 1,2-dilauroyl-L-phosphatidylethanolamine binding to phospholipase A2: an attempt to explain the selective hydrolysis of substrate fatty acid ester at position 2H Ohishi, S Fujii, K Tomoo, et al.
Journal of Molecular Biology|October 5, 1992
Crystallization and preliminary X-ray study of the cathepsin B complexed with CA074, a selective inhibitorA Yamamoto, T Kaji, K Tomoo, et al.
The Journal of Biological Chemistry|February 25, 1989
Revised amino acid sequence, crystallization, and preliminary x-ray diffraction analysis of acidic phospholipase A2 from the venom of Agkistrodon halys blomhoffiiK Tomoo, H Ohishi, T Ishida, et al.
Journal of Biochemistry|May 1, 1997
Binding mode of CA074, a specific irreversible inhibitor, to bovine cathepsin B as determined by X-ray crystal analysis of the complexA Yamamoto, T Hara, K Tomoo, et al.
Biochemical and Biophysical Research Communications|April 15, 1992
Structure of acidic phospholipase A2 for the venom of Agkistrodon halys blomhoffii at 2.8 A resolutionK Tomoo, H Ohishi, M Doi, et al.
Biochemistry|October 3, 1995
Unique binding of a novel synthetic inhibitor, N-[3-[4-[4-(amidinophenoxy)carbonyl]phenyl]-2-methyl-2-propenoyl]- N-allylglycine methanesulfonate, to bovine trypsin, revealed by the crystal structure of the complexY Odagaki, H Nakai, K Senokuchi, et al.
Journal of Biochemistry|April 1, 1993
Crystallization and preliminary X-ray study of Agkistrodon halys blomhoffii phospholipase A2 complexed with a specific inhibitorK Tomoo, S Fujii, T Ishida, et al.
Journal of Biochemistry|February 28, 2001
Binding diversity of a noncovalent-type low-molecular-weight serine protease inhibitor and function of a catalytic water molecule: X-ray crystal structure of PKSI-527--inhibited trypsinK Tomoo, K Satoh, Y Tsuda, et al.
Biochemical and Biophysical Research Communications|August 15, 1995
Design of noncovalent trypsin inhibitor based on the X-ray crystal structure of the complexM Nakamura, K Tomoo, T Ishida, et al.
Pageof 3