UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 169

Sortiert nach

LRRK2 kinase activity is dependent on LRRK2 GTP binding capacity but independent of LRRK2 GTP binding

PloS one, 2011-08, Vol.6 (8), p.e23207

2011

Link zum Volltext

Verfügbarkeit prüfen

A educação na prisão não é uma mera atividade

Educação & Realidade, 2013-03, Vol.38 (1), p.33-49

Maeyer, Marc De

2013

Link zum Volltext

Verfügbarkeit prüfen

Structural elucidation of a novel mechanism for the bacteriophage-based inhibition of the RNA degradosome

eLife, 2016-07, Vol.5

2016

Link zum Volltext

Verfügbarkeit prüfen

Virus evolution reveals an exclusive role for LEDGF/p75 in chromosomal tethering of HIV

PLoS pathogens, 2007-03, Vol.3 (3), p.e47

2007

Link zum Volltext

Verfügbarkeit prüfen

L’éducation en prison à la périphérie de l’éducation pour tous

International review of education, 2019-10, Vol.65 (5), p.811-832

De Maeyer, Marc

2019

Link zum Volltext

Verfügbarkeit prüfen

Tuning the Size and Properties of ClyA Nanopores Assisted by Directed Evolution

Journal of the American Chemical Society, 2013-09, Vol.135 (36), p.13456-13463

2013

Link zum Volltext

Verfügbarkeit prüfen

Kinases as targets for Parkinson's disease: from genetics to therapy

CNS & neurological disorders drug targets, 2011-09, Vol.10 (6), p.724

2011

Link zum Volltext

Verfügbarkeit prüfen

Rational design of small-molecule inhibitors of the LEDGF/p75-integrase interaction and HIV replication

Nature chemical biology, 2010-06, Vol.6 (6), p.442

2010

Link zum Volltext

Verfügbarkeit prüfen

'Drc', a structurally novel ssDNA-binding transcription regulator of N4-related bacterial viruses

Nucleic acids research, 2020-01, Vol.48 (1), p.445

2020

Link zum Volltext

Verfügbarkeit prüfen

HIV-1 Integrase Variants Retarget Viral Integration and Are Associated with Disease Progression in a Chronic Infection Cohort

Cell host & microbe, 2014-11, Vol.16 (5), p.651-662

2014

Link zum Volltext

Verfügbarkeit prüfen

LEDGINs, non-catalytic site inhibitors of HIV-1 integrase: a patent review (2006 - 2014)

Expert opinion on therapeutic patents, 2014-06, Vol.24 (6), p.609-632

2014

Link zum Volltext

Verfügbarkeit prüfen

Biochemical characterization of highly purified leucine-rich repeat kinases 1 and 2 demonstrates formation of homodimers

PloS one, 2012-08, Vol.7 (8), p.e43472-e43472

2012

Link zum Volltext

Verfügbarkeit prüfen

The dead-end elimination theorem and its use in protein side-chain positioning

Nature (London), 1992-04, Vol.356 (6369), p.539-542

1992

Link zum Volltext

Verfügbarkeit prüfen

Evidence for DNA-Binding Domain–Ligand-Binding Domain Communications in the Androgen Receptor

Molecular and Cellular Biology, 2012-08, Vol.32 (15), p.3033-3043

2012

Link zum Volltext

Verfügbarkeit prüfen

The Dead-End Elimination Method, Tryptophan Rotamers, and Fluorescence Lifetimes

Biophysical journal, 2003-09, Vol.85 (3), p.1894-1902

2003

Link zum Volltext

Verfügbarkeit prüfen

Identification of the LEDGF/p75 Binding Site in HIV-1 Integrase

Journal of molecular biology, 2007-02, Vol.365 (5), p.1480-1492

2007

Link zum Volltext

Verfügbarkeit prüfen

Pharmacophore modeling: advances, limitations, and current utility in drug discovery

Journal of receptor, ligand and channel research, 2014-01, Vol.7, p.81

2014

Link zum Volltext

Verfügbarkeit prüfen

Structural basis for the high Ca²⁺ affinity of the ubiquitous SERCA2b Ca²⁺ pump

Proceedings of the National Academy of Sciences - PNAS, 2009-11, Vol.106 (44), p.18533-18538

2009

Link zum Volltext

Verfügbarkeit prüfen

Computational Studies of the Active and Inactive Regulatory Domains of Response Regulator PhoP Using Molecular Dynamics Simulations

Molecular informatics, 2017-11, Vol.36 (11), p.n/a

2017

Link zum Volltext

Verfügbarkeit prüfen

Mapping the binding interface between an HIV-1 inhibiting intrabody and the viral protein Rev

PloS one, 2013-04, Vol.8 (4), p.e60259

2013

Link zum Volltext

Verfügbarkeit prüfen

pKa modulation of the acid/base catalyst within GH32 and GH68: a role in substrate/inhibitor specificity?

PloS one, 2012-05, Vol.7 (5), p.e37453-e37453

2012

Link zum Volltext

Verfügbarkeit prüfen

Mutations in Human Immunodeficiency Virus Type 1 Integrase Confer Resistance to the Naphthyridine L-870,810 and Cross-Resistance to the Clinical Trial Drug GS-9137

Antimicrobial Agents and Chemotherapy, 2008-06, Vol.52 (6), p.2069-2078

2008

Link zum Volltext

Verfügbarkeit prüfen

Mechanism of Nonpolar Model Substances to Inhibit Primary Gushing Induced by Hydrophobin HFBI

Journal of agricultural and food chemistry, 2015-05, Vol.63 (18), p.4673-4682

2015

Link zum Volltext

Verfügbarkeit prüfen

Expression, purification and preliminary biochemical and structural characterization of the leucine rich repeat namesake domain of leucine rich repeat kinase 2

Biochimica et biophysica acta, 2012-03, Vol.1824 (3), p.450-460

2012

Link zum Volltext

Verfügbarkeit prüfen

Structure based discovery of small molecule suppressors targeting bacterial lysozyme inhibitors

Biochemical and biophysical research communications, 2011-02, Vol.405 (4), p.527-532

2011

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 169

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(159)
Mit Volltextzugriff
(158)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(116)
Life Sciences & Biomedicine
(93)
Biochemistry & Molecular Biology
(50)
Humans
(41)
Models, Molecular
(36)
Amino Acid Sequence
(26)
Protein Conformation
(25)
Binding Sites
(24)
Physical Sciences
(23)
Molecular Sequence Data
(22)
Mutation
(22)
Protein Binding
(22)
Biological And Medical Sciences
(21)
Proteins
(21)
Biophysics
(19)
Chemistry
(17)
Kinetics
(17)
Animals
(16)
Fundamental And Applied Biological Sciences. Psychology
(14)
Protein Structure, Tertiary
(14)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

LRRK2 kinase activity is dependent on LRRK2 GTP binding capacity but independent of LRRK2 GTP binding

A educação na prisão não é uma mera atividade

Structural elucidation of a novel mechanism for the bacteriophage-based inhibition of the RNA degradosome

Virus evolution reveals an exclusive role for LEDGF/p75 in chromosomal tethering of HIV

L’éducation en prison à la périphérie de l’éducation pour tous

Tuning the Size and Properties of ClyA Nanopores Assisted by Directed Evolution

Kinases as targets for Parkinson's disease: from genetics to therapy

Rational design of small-molecule inhibitors of the LEDGF/p75-integrase interaction and HIV replication

'Drc', a structurally novel ssDNA-binding transcription regulator of N4-related bacterial viruses

HIV-1 Integrase Variants Retarget Viral Integration and Are Associated with Disease Progression in a Chronic Infection Cohort

LEDGINs, non-catalytic site inhibitors of HIV-1 integrase: a patent review (2006 - 2014)

Biochemical characterization of highly purified leucine-rich repeat kinases 1 and 2 demonstrates formation of homodimers

The dead-end elimination theorem and its use in protein side-chain positioning

Evidence for DNA-Binding Domain–Ligand-Binding Domain Communications in the Androgen Receptor

The Dead-End Elimination Method, Tryptophan Rotamers, and Fluorescence Lifetimes

Identification of the LEDGF/p75 Binding Site in HIV-1 Integrase

Pharmacophore modeling: advances, limitations, and current utility in drug discovery

Structural basis for the high Ca²⁺ affinity of the ubiquitous SERCA2b Ca²⁺ pump

Computational Studies of the Active and Inactive Regulatory Domains of Response Regulator PhoP Using Molecular Dynamics Simulations

Mapping the binding interface between an HIV-1 inhibiting intrabody and the viral protein Rev

pKa modulation of the acid/base catalyst within GH32 and GH68: a role in substrate/inhibitor specificity?

Mutations in Human Immunodeficiency Virus Type 1 Integrase Confer Resistance to the Naphthyridine L-870,810 and Cross-Resistance to the Clinical Trial Drug GS-9137

Mechanism of Nonpolar Model Substances to Inhibit Primary Gushing Induced by Hydrophobin HFBI

Expression, purification and preliminary biochemical and structural characterization of the leucine rich repeat namesake domain of leucine rich repeat kinase 2

Structure based discovery of small molecule suppressors targeting bacterial lysozyme inhibitors

Suchergebnisse filtern