Research of our group mainly relies on third-party funding. Over the last 17 years in
total 9.745 million Euros have been spent. The table and diagram below show the annually
spent funds, subdivided into funding sources.
Funding agency |
Title |
Funding in Euro |
DFG |
Structural studies of Shigella-specific Pathogenicity Factors as a
Prerequisite for Rational Drug Design
|
189,750 |
DFG |
Understanding the Binding Characteristics of Aldose Reductase
|
113,250 |
DFG |
Structure-based Design, Synthesis and Crystallographic
Characterisation of Aspartyl protease Inhibitors: Target proteins
for HIV- and Malaria-infection
|
132,550 |
DFG - FO 806 |
Cross-correlation of Protein Binding Pockets to detect related
Binding Epitopes, unexpected Cross-reactivity and Functional
Relationships
|
216,000 |
DFG |
Interfering with Intracellular Protein-protein Interactions -
Probing Protein Functions with Small Molecules, Perturbance of
Enzyme Function by Blocking Dimer Interface Formation: Novel Route
to Specific Antibiotics
|
289,100 |
CCDC |
Development of a Scoring Function |
28,402 |
CCDC |
Studentship on Cambridge Structural Database – Knowledge-based Hot
Spot Analysis
|
106,812 |
Bayer Schering |
From Targets to Novel Drugs |
50,000 |
Sanofi |
Comparison of Binding Pocket using Cavbase to Analyse and Correlate
Proteins across Protein Families and Design of Focused Libraries for
de novo Design
|
111,000 |
Beiersdorf |
Design of Inhibitors for humane Tyrosinase by Molecular Modeling
and Crystallography
|
126,000 |
BMBF |
Fragmentscreening "FragScreen" BioChance Plus, New methods
for Experimental and Computational Fragment-based Drug Design
|
910,876 |
BMBF Zedira |
Development of Factor XIIIa - Inhibitors to Prevent Thrombosis
|
100,000 |
LOEWE Synmikro |
Data Mining Methoden zur graphbasierten Analyse von Proteinstrukturdaten,
Protein-Ligand & Protein-Protein Interaktionen
|
132,300 |
LOEWE Synmikro |
Development of novel bioinformatics methods for the prediction of
protein function and interactions. Experimental validation
|
168,000 |
ERC AG |
Chemogenomic profiling of drug-protein binding by shape,
enthalpy/entropy and interaction kinetics
|
1,754,615 |
BMBF FKZ |
Aufbau einer "Beamline zum direkten Fragmentscreening" an
Proteinkristallen zur Leitstrukturentwicklung
|
640,609 |
DFG |
17beta-Hydroxysteroid Dehydrogenase Typ 14: Enzymstruktur-basierte
Entwicklung von potenten und selektiven Inhibitoren mit Hilfe von
Kristallisation und Enzymcharakterisierung
|
156,500 |
LOEWE SynChemBio |
Innovative Synthesechemie für die selektive Modulation
biologischer Prozesse - Schwerpunkt S-07
|
140,000 |
DFG |
Durchführung einer Tagung FiMC
|
25,000 |
BMBF Zedira |
Entwicklung von Faktor XIIIa - Inhibitoren zur Thromboprophylaxe
- Stufe 2
|
59,901 |
GA-Nr. 675555 |
EU-Projekt AEGIS (Accelerated Early staGe dIScovery – EU-Horizon 2020 “Marie Skłodowska-Curie Innovative Training Networks”-Maßnahme
|
498,432 |
BMBF Frag4Lead FKZ 05K16RM1 |
Hochdurchsatz-Kristallographie am Synchrotron: von Fragmenten zu Leitstrukturen Förderzeitraum: 01.07.2016 – 30.06.2019
|
925,158 |
DFG KL 1204/23-1 |
Entwicklung niedermolekularer Inhibitoren und Stabilisatoren der Dimerisierung von tRNA-Guanin Transglykosylase
|
325,950 |
BMBF 03EGSHE147 |
EXIST-Gründerstipendium: smart-soak – Dienstleistungen in der Wirkstoffentwicklung
|
156,600 |
LOEWE DRUID |
Wirkstoffentwicklungen zum Bekämpfen der Virulenzentwicklung des Ruhr-Erregers Shigella
|
230,400 |
Total |
|
7,587,205 |