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

Wolfram Bode

Showing results (11-20 of 64) with videos related to

Pageof 7
Sort By:
Journal of Molecular Biology|March 9, 2002
The methyl group of N(alpha)(Me)Arg-containing peptides disturbs the active-site geometry of thrombin, impairing efficient cleavageRainer Friedrich, Torsten Steinmetzer, Robert Huber, et al.
Journal of Molecular Biology|August 7, 2002
The crystal structure of human alpha1-tryptase reveals a blocked substrate-binding regionUlf Marquardt, Frank Zettl, Robert Huber, et al.
Journal of Molecular Biology|August 30, 2003
X-ray structure of isoaspartyl dipeptidase from E.coli: a dinuclear zinc peptidase evolved from amidohydrolasesDaniela Jozic, Jens T Kaiser, Robert Huber, et al.
Journal of Molecular Biology|April 7, 2004
Crystal structure of human carboxypeptidase M, a membrane-bound enzyme that regulates peptide hormone activityDavid Reverter, Klaus Maskos, Fulong Tan, et al.
Biological Chemistry|November 20, 2002
(R)-3-Amidinophenylalanine-derived inhibitors of factor Xa with a novel active-site binding modeMarkus Michael Mueller, Stefan Sperl, Jörg Stürzebecher, et al.
Biological Chemistry|October 6, 2005
The NC1 dimer of human placental basement membrane collagen IV: does a covalent crosslink exist?Manuel E Than, Gleb P Bourenkov, Stefan Henrich, et al.
Journal of Molecular Biology|April 10, 2003
Crystals of urokinase type plasminogen activator complexes reveal the binding mode of peptidomimetic inhibitorsEwa Zeslawska, Uwe Jacob, Andrea Schweinitz, et al.
European Journal of Medicinal Chemistry|October 24, 2007
Structure of a novel thrombin inhibitor with an uncharged D-amino acid as P1 residueRainer Friedrich, Daniel Riester, Peter Göttig, et al.
FEBS Letters|October 22, 2002
The influence of residue 190 in the S1 site of trypsin-like serine proteases on substrate selectivity is universally conservedKatrin Sichler, Karl Peter Hopfner, Erhard Kopetzki, et al.
Biochemistry|February 20, 2002
Characterization of the residues involved in the human alpha-thrombin-haemadin complex: an exosite II-binding inhibitorJohn L Richardson, Pablo Fuentes-Prior, J Evan Sadler, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
Journal of Molecular Biology|March 9, 2002
The methyl group of N(alpha)(Me)Arg-containing peptides disturbs the active-site geometry of thrombin, impairing efficient cleavageRainer Friedrich, Torsten Steinmetzer, Robert Huber, et al.
Journal of Molecular Biology|August 7, 2002
The crystal structure of human alpha1-tryptase reveals a blocked substrate-binding regionUlf Marquardt, Frank Zettl, Robert Huber, et al.
Journal of Molecular Biology|August 30, 2003
X-ray structure of isoaspartyl dipeptidase from E.coli: a dinuclear zinc peptidase evolved from amidohydrolasesDaniela Jozic, Jens T Kaiser, Robert Huber, et al.
Journal of Molecular Biology|April 7, 2004
Crystal structure of human carboxypeptidase M, a membrane-bound enzyme that regulates peptide hormone activityDavid Reverter, Klaus Maskos, Fulong Tan, et al.
Biological Chemistry|November 20, 2002
(R)-3-Amidinophenylalanine-derived inhibitors of factor Xa with a novel active-site binding modeMarkus Michael Mueller, Stefan Sperl, Jörg Stürzebecher, et al.
Biological Chemistry|October 6, 2005
The NC1 dimer of human placental basement membrane collagen IV: does a covalent crosslink exist?Manuel E Than, Gleb P Bourenkov, Stefan Henrich, et al.
Journal of Molecular Biology|April 10, 2003
Crystals of urokinase type plasminogen activator complexes reveal the binding mode of peptidomimetic inhibitorsEwa Zeslawska, Uwe Jacob, Andrea Schweinitz, et al.
European Journal of Medicinal Chemistry|October 24, 2007
Structure of a novel thrombin inhibitor with an uncharged D-amino acid as P1 residueRainer Friedrich, Daniel Riester, Peter Göttig, et al.
FEBS Letters|October 22, 2002
The influence of residue 190 in the S1 site of trypsin-like serine proteases on substrate selectivity is universally conservedKatrin Sichler, Karl Peter Hopfner, Erhard Kopetzki, et al.
Biochemistry|February 20, 2002
Characterization of the residues involved in the human alpha-thrombin-haemadin complex: an exosite II-binding inhibitorJohn L Richardson, Pablo Fuentes-Prior, J Evan Sadler, et al.
Pageof 7