Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Rational design of small-molecule inhibitors of the LEDGF/p75-integrase interaction and HIV replication.
|
Nat Chem Biol
|
2010
|
2.48
|
2
|
A structural basis for the unique binding features of the human vitamin D-binding protein.
|
Nat Struct Biol
|
2002
|
1.78
|
3
|
Development of resistance against diketo derivatives of human immunodeficiency virus type 1 by progressive accumulation of integrase mutations.
|
J Virol
|
2003
|
1.54
|
4
|
Virus evolution reveals an exclusive role for LEDGF/p75 in chromosomal tethering of HIV.
|
PLoS Pathog
|
2007
|
1.41
|
5
|
Insight into the mode of action of the LRRK2 Y1699C pathogenic mutant.
|
J Neurochem
|
2011
|
1.33
|
6
|
Multiple mutations in human immunodeficiency virus-1 integrase confer resistance to the clinical trial drug S-1360.
|
AIDS
|
2004
|
1.28
|
7
|
Identification of the LEDGF/p75 binding site in HIV-1 integrase.
|
J Mol Biol
|
2006
|
1.24
|
8
|
LRRK2 kinase activity is dependent on LRRK2 GTP binding capacity but independent of LRRK2 GTP binding.
|
PLoS One
|
2011
|
1.19
|
9
|
Binding of the concave surface of the Sds22 superhelix to the alpha 4/alpha 5/alpha 6-triangle of protein phosphatase-1.
|
J Biol Chem
|
2002
|
1.11
|
10
|
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.
|
Antimicrob Agents Chemother
|
2008
|
1.10
|
11
|
Biochemical characterization of highly purified leucine-rich repeat kinases 1 and 2 demonstrates formation of homodimers.
|
PLoS One
|
2012
|
1.09
|
12
|
Evidence for DNA-binding domain--ligand-binding domain communications in the androgen receptor.
|
Mol Cell Biol
|
2012
|
1.03
|
13
|
Elimination of a human T-cell region in staphylokinase by T-cell screening and computer modeling.
|
Thromb Haemost
|
2002
|
1.03
|
14
|
Structural basis for the high Ca2+ affinity of the ubiquitous SERCA2b Ca2+ pump.
|
Proc Natl Acad Sci U S A
|
2009
|
0.99
|
15
|
Tuning the size and properties of ClyA nanopores assisted by directed evolution.
|
J Am Chem Soc
|
2013
|
0.95
|
16
|
The dead-end elimination method, tryptophan rotamers, and fluorescence lifetimes.
|
Biophys J
|
2003
|
0.93
|
17
|
Impact on replicative fitness of the G48E substitution in the protease of HIV-1: an in vitro and in silico evaluation.
|
J Acquir Immune Defic Syndr
|
2008
|
0.89
|
18
|
An alternate sucrose binding mode in the E203Q Arabidopsis invertase mutant: an X-ray crystallography and docking study.
|
Proteins
|
2008
|
0.87
|
19
|
A consensus tetrapeptide selected by phage display adopts the conformation of a dominant discontinuous epitope of a monoclonal anti-VWF antibody that inhibits the von Willebrand factor-collagen interaction.
|
J Biol Chem
|
2003
|
0.86
|
20
|
LEDGINs, non-catalytic site inhibitors of HIV-1 integrase: a patent review (2006 - 2014).
|
Expert Opin Ther Pat
|
2014
|
0.86
|
21
|
Experimental indication for the existence of multiple Trp rotamers in von Willebrand Factor A3 domain.
|
Proteins
|
2004
|
0.84
|
22
|
Staphylokinase-specific cell-mediated immunity in humans.
|
J Immunol
|
2002
|
0.83
|
23
|
Paratope and epitope mapping of the antithrombotic antibody 6B4 in complex with platelet glycoprotein Ibalpha.
|
J Biol Chem
|
2007
|
0.82
|
24
|
Tryptophan rotamers as evidenced by X-ray, fluorescence lifetimes, and molecular dynamics modeling.
|
Biophys J
|
2006
|
0.82
|
25
|
Biochemical and structural characterization of TLXI, the Triticum aestivum L. thaumatin-like xylanase inhibitor.
|
J Enzyme Inhib Med Chem
|
2009
|
0.81
|
26
|
Paratope determination of the antithrombotic antibody 82D6A3 based on the crystal structure of its complex with the von Willebrand factor A3-domain.
|
J Biol Chem
|
2005
|
0.81
|
27
|
Expression, purification and preliminary biochemical and structural characterization of the leucine rich repeat namesake domain of leucine rich repeat kinase 2.
|
Biochim Biophys Acta
|
2012
|
0.81
|
28
|
Structure based discovery of small molecule suppressors targeting bacterial lysozyme inhibitors.
|
Biochem Biophys Res Commun
|
2011
|
0.81
|
29
|
Understanding the role of defective invertases in plants: tobacco Nin88 fails to degrade sucrose.
|
Plant Physiol
|
2013
|
0.81
|
30
|
In vivo neutralization of a C2 domain-specific human anti-Factor VIII inhibitor by an anti-idiotypic antibody.
|
Blood
|
2003
|
0.80
|
31
|
An optimized MM/PBSA virtual screening approach applied to an HIV-1 gp41 fusion peptide inhibitor.
|
Proteins
|
2011
|
0.79
|
32
|
Mutation of the H-bond acceptor S119 in the ADAMTS13 metalloprotease domain reduces secretion and substrate turnover in a patient with congenital thrombotic thrombocytopenic purpura.
|
Blood
|
2009
|
0.79
|
33
|
Computational investigation of the HIV-1 Rev multimerization using molecular dynamics simulations and binding free energy calculations.
|
Proteins
|
2012
|
0.78
|
34
|
Mapping the binding interface between an HIV-1 inhibiting intrabody and the viral protein Rev.
|
PLoS One
|
2013
|
0.78
|
35
|
How do rotameric conformations influence the time-resolved fluorescence of tryptophan in proteins? A perspective based on molecular modeling and quantum chemistry.
|
Curr Protein Pept Sci
|
2008
|
0.78
|
36
|
pKa modulation of the acid/base catalyst within GH32 and GH68: a role in substrate/inhibitor specificity?
|
PLoS One
|
2012
|
0.78
|
37
|
Identification of small peptides inhibiting the integrase-LEDGF/p75 interaction through targeting the cellular co-factor.
|
J Pept Sci
|
2013
|
0.77
|
38
|
An unusual red-edge excitation and time-dependent Stokes shift in the single tryptophan mutant protein DD-carboxypeptidase from Streptomyces: the role of dynamics and tryptophan rotamers.
|
Protein Sci
|
2007
|
0.77
|
39
|
Exploration of the activation pathway of Deltaalpha-Chymotrypsin with molecular dynamics simulations and correlation with kinetic experiments.
|
Eur Biophys J
|
2008
|
0.77
|
40
|
Study of recombinant antibody fragments and PAI-1 complexes combining protein-protein docking and results from site-directed mutagenesis.
|
Structure
|
2007
|
0.77
|
41
|
Identification of a small molecule that modulates platelet glycoprotein Ib-von Willebrand factor interaction.
|
J Biol Chem
|
2012
|
0.76
|
42
|
Protein simulations: the absorption spectrum of barnase point mutants.
|
Protein Sci
|
2004
|
0.76
|
43
|
Validation of APRI and FIB-4 score in an Antwerp cohort of chronic hepatitis C patients.
|
Acta Gastroenterol Belg
|
2015
|
0.76
|
44
|
Tryptophan conformations associated with partial unfolding in ribonuclease T1.
|
Biophys J
|
2009
|
0.76
|
45
|
An integrated fragment based screening approach for the discovery of small molecule modulators of the VWF-GPIbα interaction.
|
Chem Commun (Camb)
|
2012
|
0.76
|
46
|
Influence of limited proteolysis, detergent treatment and lyophilization on the phenoloxidase activity of Rapana thomasiana hemocyanin.
|
Int J Biol Macromol
|
2009
|
0.76
|
47
|
Conformational stabilization at the active site of molluskan (Rapana thomasiana) hemocyanin by a cysteine-histidine thioether bridge A study by mass spectrometry and molecular modeling.
|
Peptides
|
2006
|
0.75
|
48
|
Genome wide analysis and comparative docking studies of new diaryl furan derivatives against human cyclooxygenase-2, lipoxygenase, thromboxane synthase and prostacyclin synthase enzymes involved in inflammatory pathway.
|
J Mol Graph Model
|
2009
|
0.75
|
49
|
Combined molecular and supramolecular bottom-up nanoengineering for enhanced nonlinear optical response: experiments, modeling, and approaching the fundamental limit.
|
J Chem Phys
|
2007
|
0.75
|