The Crystal Structure of Thrombin-activable Fibrinolysis Inhibitor (TAFI) Provides the Structural Basis for Its Intrinsic Activity and the Short Half-life of TAFIa by Anand, Kanchan, Pallares, Irantzu, Valnickova, Zuzana, Christensen, Trine, Vendrell, Josep, Wendt, K. Ulrich, Schreuder, Herman A., Enghild, Jan J., Avilés, Francesc X.

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Sodium‐site in serine protease domain of human coagulation factor IXa: evidence from the crystal structure and molecular dynamics simulations study by Vadivel, Kanagasabai, Schreuder, Herman A., Liesum, Alexander, Schmidt, Amy E., Goldsmith, Gunaseelan, Bajaj, S. Paul

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Novel Small Molecule Inhibitors of Activated Thrombin Activatable Fibrinolysis Inhibitor (TAFIa) from Natural Product Anabaenopeptin by Halland, Nis, Brönstrup, Mark, Czech, Jörg, Czechtizky, Werngard, Evers, Andreas, Follmann, Markus, Kohlmann, Markus, Schiell, Matthias, Kurz, Michael, Schreuder, Herman A, Kallus, Christopher

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Sulfamide as Zinc Binding Motif in Small Molecule Inhibitors of Activated Thrombin Activatable Fibrinolysis Inhibitor (TAFIa) by Halland, Nis, Czech, Jörg, Czechtizky, Werngard, Evers, Andreas, Follmann, Markus, Kohlmann, Markus, Schreuder, Herman A, Kallus, Christopher

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Crystal structure of cathepsin A, a novel target for the treatment of cardiovascular diseases by Schreuder, Herman A., Liesum, Alexander, Kroll, Katja, Böhnisch, Britta, Buning, Christian, Ruf, Sven, Sadowski, Thorsten

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Inhibition of Human Neutrophil Elastase. 4. Design, Synthesis, X-ray Crystallographic Analysis, and Structure−Activity Relationships for a Series of P2-Modified, Orally Active Pept... by Cregge, Robert J, Durham, Sherrie L, Farr, Robert A, Gallion, Steven L, Hare, C. Michelle, Hoffman, Robert V, Janusz, Michael J, Kim, Hwa-Ok, Koehl, Jack R, Mehdi, Shujaath, Metz, William A, Peet, Norton P, Pelton, John T, Schreuder, Herman A, Sunder, Shyam, Tardif, Chantal

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Crystal Structures of Wild-Type p-Hydroxybenzoate Hydroxylase Complexed with 4-Aminobenzoate, 2,4-Dihydroxybenzoate, and 2-Hydroxy-4-aminobenzoate and of the Tyr222Ala Mutant Compl... by Schreuder, Herman A, Mattevi, Andrea, Obmolova, Galina, Kalk, Kor H, Hol, Wim G. J, van der Bolt, Frank J. T, van Berkel, Willem J. H

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X-ray structure of antistasin at 1.9 Å resolution and its modelled complex with blood coagulation factor Xa by Lapatto, Risto, Krengel, Ute, Schreuder, Herman A., Arkema, Anita, de Boer, Bijtske, Kalk, Kor H., Hol, Wim G.J., Grootenhuis, Peter D.J., Mulders, John W.M., Dijkema, Rein, Theunissen, Henri J.M., Dijkstra, Bauke W.

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Formation of the active site of ribulose-1,5-bisphosphate carboxylase/oxygenase by a disorder-order transition from the unactivated to the activated form by Schreuder, H.A, Knight, S, Curmi, P.M.G, Andersson, I, Cascio, D, Branden, C.I, Eisenberg, D

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Interdomain binding of NADPH in p-Hydroxybenzoate Hydroxylase as Suggested by Kinetic, Crystallographic and Modeling Studies of Histidine 162 and Arginine 269 Variants by Eppink, Michel H.M., Schreuder, Herman A., van Berkel, Willem J.H.

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Molecular Design and Characterization of an α-Thrombin Inhibitor Containing a Novel P1 Moiety by Malikayil, J. A, Burkhart, Joseph P, Schreuder, Herman A, Broersma, Robert J, Tardif, Chantal, Kutcher, Louis W, Mehdi, Shujaath, Schatzman, Gerald L, Neises, Bernhard, Peet, Norton P

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Crystal Structures of Mutant Pseudomonas aeruginosa p-Hydroxybenzoate Hydroxylases: The Tyr201Phe, Tyr385Phe, and Asn300Asp Variants by Lah, Myoung Soo, Palfey, Bruce A, Schreuder, Herman A, Ludwig, Martha L

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Switch of coenzyme specificity of p -hydroxybenzoate hydroxylase 1 1Edited by A. R. Fersht by Eppink, Michel H.M, Overkamp, Karin M, Schreuder, Herman A, Van Berkel, Willem J.H

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Phe161 and Arg166 variants of p‐hydroxybenzoate hydroxylase by Eppink, Michel H.M., Bunthof, Christine, Schreuder, Herman A., van Berkel, Willem J.H.

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Identification of a novel conserved sequence motif in flavoprotein hydroxylases with a putative dual function in FAD/NAD(P)H binding by Eppink, Michel H. M., Berkel, Willem J. H. Van, Schreuder, Herman A.

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The coenzyme analog adenosine 5-diphosphoribose displaces FAD in the active site of p-hydroxybenzoate hydroxylase. An x-ray crystallographic investigation by Van der Laan, Jan M, Schreuder, Herman A, Swarte, Myra B. A, Wierenga, Rik K, Kalk, Kor H, Hol, Wim G. J, Drenth, Jan

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Switch of coenzyme specificity of p-hydroxybenzoate hydroxylase by Eppink, M H, Overkamp, K M, Schreuder, H A, Van Berkel, W J

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Analysis of the active site of the flavoprotein p-hydroxybenzoate hydroxylase and some ideas with respect to its reaction mechanism by Schreuder, Herman A, Hol, Wim G. J, Drenth, Jan

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Inhibition of Human Neutrophil Elastase. 4. Design, Synthesis, X-ray Crystallographic Analysis, and Structure−Activity Relationships for a Series of P 2 -Modified, Orally Active Pe... by Cregge, Robert J., Durham, Sherrie L., Farr, Robert A., Gallion, Steven L., Hare, C. Michelle, Hoffman, Robert V., Janusz, Michael J., Kim, Hwa-Ok, Koehl, Jack R., Mehdi, Shujaath, Metz, William A., Peet, Norton P., Pelton, John T., Schreuder, Herman A., Sunder, Shyam, Tardif, Chantal

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Chitinase and β-1,3-glucanase in the lutoid-body fraction of Hevea latex by Subroto, Toto, van Koningsveld, Gerrit A., Schreuder, Herman A., Soedjanaatmadja, Ukun M.S., Beintema, Jaap J.

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