Hochschulschrift
Structure-based drug design on the enoyl-ACP reductases of Yersinia pestis and Burkholderia pseudomallei
- Weitere Titel
-
Struktur-basiertes Wirkstoffdesign an Enoyl-ACP Reductase von Yersinia pestis und Burkholderia pseudomallei
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
Würzburg, Universität Würzburg, Dissertation, 2012
- Schlagwort
-
Yersinia
Burkholderia
Arzneimitteldesign
Fettsäurestoffwechsel
Arzneimittelentwicklung
Arzneimitteldesign
- Ereignis
-
Veröffentlichung
- (wo)
-
Würzburg
- (wer)
-
Universität Würzburg
- (wann)
-
2012
- Urheber
- Beteiligte Personen und Organisationen
-
Kisker, Caroline
- URN
-
urn:nbn:de:bvb:20-opus-70869
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:57 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Objekttyp
- Hochschulschrift
Beteiligte
- Hirschbeck, Maria
- Kisker, Caroline
- Universität Würzburg
Entstanden
- 2012
Ähnliche Objekte (12)
Structure-based drug design on the enoyl-ACP reductases of Yersinia pestis and Burkholderia pseudomallei : = Struktur-basiertes Wirkstoffdesign an Enoyl-ACP Reductase von Yersinia pestis und Burkholderia pseudomallei
In silico structure-based optimisation of pyrrolidine carboxamides as Mycobacterium tuberculosis enoyl-ACP reductase inhibitors
Structural and Functional Characterization of the Enzymes Involved in the Menaquinone Biosynthesis and Benzoate Degradation
The Intricate Network of Replication-dependent Interstrand Crosslink DNA Repair
Structure-Based Drug Design on Enzymes of the Fatty Acid Biosynthesis Pathway
Structural basis of ubiquitin recognition and rational design of novel covalent inhibitors targeting Cdu1 from \(Chlamydia\) \(Trachomatis\)
Structural and functional characterization of nucleotide excision repair proteins
Structural and functional characterization of TFIIH from Chaetomium thermophilum
A RecQ helicase in disguise: Characterization of the unconventional Structure and Function of the human Genome Caretaker RecQ4
Nucleotide Excision Repair : From Recognition to Incision of damaged DNA
Investigations on the nucleotide excision repair protein XPD as a target for synthetic lethality
Targeting the Bacterial Fatty-Acid Synthesis Pathway: Towards the Development of Slow-Onset Inhibitors and the Characterisation of Protein-Protein Interactions
Structure-based drug design on the enoyl-ACP reductases of Yersinia pestis and Burkholderia pseudomallei : = Struktur-basiertes Wirkstoffdesign an Enoyl-ACP Reductase von Yersinia pestis und Burkholderia pseudomallei
In silico structure-based optimisation of pyrrolidine carboxamides as Mycobacterium tuberculosis enoyl-ACP reductase inhibitors
Structural and Functional Characterization of the Enzymes Involved in the Menaquinone Biosynthesis and Benzoate Degradation
The Intricate Network of Replication-dependent Interstrand Crosslink DNA Repair
Structure-Based Drug Design on Enzymes of the Fatty Acid Biosynthesis Pathway
Structural basis of ubiquitin recognition and rational design of novel covalent inhibitors targeting Cdu1 from \(Chlamydia\) \(Trachomatis\)
Structural and functional characterization of nucleotide excision repair proteins
Structural and functional characterization of TFIIH from Chaetomium thermophilum
A RecQ helicase in disguise: Characterization of the unconventional Structure and Function of the human Genome Caretaker RecQ4
Nucleotide Excision Repair : From Recognition to Incision of damaged DNA
Investigations on the nucleotide excision repair protein XPD as a target for synthetic lethality
Targeting the Bacterial Fatty-Acid Synthesis Pathway: Towards the Development of Slow-Onset Inhibitors and the Characterisation of Protein-Protein Interactions
Structure-based drug design on the enoyl-ACP reductases of Yersinia pestis and Burkholderia pseudomallei : = Struktur-basiertes Wirkstoffdesign an Enoyl-ACP Reductase von Yersinia pestis und Burkholderia pseudomallei
In silico structure-based optimisation of pyrrolidine carboxamides as Mycobacterium tuberculosis enoyl-ACP reductase inhibitors
Structural and Functional Characterization of the Enzymes Involved in the Menaquinone Biosynthesis and Benzoate Degradation
The Intricate Network of Replication-dependent Interstrand Crosslink DNA Repair
Structure-Based Drug Design on Enzymes of the Fatty Acid Biosynthesis Pathway
Structural basis of ubiquitin recognition and rational design of novel covalent inhibitors targeting Cdu1 from \(Chlamydia\) \(Trachomatis\)
Structural and functional characterization of nucleotide excision repair proteins
Structural and functional characterization of TFIIH from Chaetomium thermophilum
A RecQ helicase in disguise: Characterization of the unconventional Structure and Function of the human Genome Caretaker RecQ4
Nucleotide Excision Repair : From Recognition to Incision of damaged DNA
Investigations on the nucleotide excision repair protein XPD as a target for synthetic lethality