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About
Mischa Machius
Author PubWeight™ 73.01
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Three-dimensional structure of the complexin/SNARE complex.
Neuron
2002
3.69
2
Structural basis of actin filament nucleation and processive capping by a formin homology 2 domain.
Nature
2005
3.31
3
Structure of the photolyase-like domain of cryptochrome 1 from Arabidopsis thaliana.
Proc Natl Acad Sci U S A
2004
2.48
4
Side chain and backbone contributions of Phe508 to CFTR folding.
Nat Struct Mol Biol
2004
2.43
5
Structural basis for CoREST-dependent demethylation of nucleosomes by the human LSD1 histone demethylase.
Mol Cell
2006
2.32
6
Crystal structure of a 12 ANK repeat stack from human ankyrinR.
EMBO J
2002
2.27
7
p31comet blocks Mad2 activation through structural mimicry.
Cell
2007
2.26
8
Structural basis of Rho GTPase-mediated activation of the formin mDia1.
Mol Cell
2005
2.16
9
Artificial ligand binding within the HIF2alpha PAS-B domain of the HIF2 transcription factor.
Proc Natl Acad Sci U S A
2009
2.02
10
Structural basis for a Munc13-1 homodimer to Munc13-1/RIM heterodimer switch.
PLoS Biol
2006
1.88
11
Structural basis of histone demethylation by LSD1 revealed by suicide inactivation.
Nat Struct Mol Biol
2007
1.59
12
Munc13 C2B domain is an activity-dependent Ca2+ regulator of synaptic exocytosis.
Nat Struct Mol Biol
2010
1.58
13
Structural and energetic mechanisms of cooperative autoinhibition and activation of Vav1.
Cell
2010
1.51
14
Structural basis for the inhibition of the LSD1 histone demethylase by the antidepressant trans-2-phenylcyclopropylamine.
Biochemistry
2007
1.44
15
Changes at the KinA PAS-A dimerization interface influence histidine kinase function.
Biochemistry
2008
1.43
16
Insights into mad2 regulation in the spindle checkpoint revealed by the crystal structure of the symmetric mad2 dimer.
PLoS Biol
2008
1.41
17
The crystal structure of a self-activating G protein alpha subunit reveals its distinct mechanism of signal initiation.
Sci Signal
2011
1.40
18
Crystal structure of human dihydrolipoamide dehydrogenase: NAD+/NADH binding and the structural basis of disease-causing mutations.
J Mol Biol
2005
1.37
19
Structure and substrate recruitment of the human spindle checkpoint kinase Bub1.
Mol Cell
2008
1.32
20
Diffraction data analysis in the presence of radiation damage.
Acta Crystallogr D Biol Crystallogr
2010
1.27
21
Structural basis for the evolutionary inactivation of Ca2+ binding to synaptotagmin 4.
Nat Struct Mol Biol
2004
1.26
22
Discovery of Novel Small Molecule Mer Kinase Inhibitors for the Treatment of Pediatric Acute Lymphoblastic Leukemia.
ACS Med Chem Lett
2012
1.22
23
Crystal structure of the TAO2 kinase domain: activation and specificity of a Ste20p MAP3K.
Structure
2004
1.21
24
Localization and structure of the ankyrin-binding site on beta2-spectrin.
J Biol Chem
2008
1.21
25
Structural insight into interactions between dihydrolipoamide dehydrogenase (E3) and E3 binding protein of human pyruvate dehydrogenase complex.
Structure
2006
1.19
26
Metal-mediated affinity and orientation specificity in a computationally designed protein homodimer.
J Am Chem Soc
2011
1.19
27
Structural basis for inactivation of the human pyruvate dehydrogenase complex by phosphorylation: role of disordered phosphorylation loops.
Structure
2008
1.12
28
Computational design of a symmetric homodimer using β-strand assembly.
Proc Natl Acad Sci U S A
2011
1.12
29
Crystal structure of the Tp34 (TP0971) lipoprotein of treponema pallidum: implications of its metal-bound state and affinity for human lactoferrin.
J Biol Chem
2006
1.10
30
The PnrA (Tp0319; TmpC) lipoprotein represents a new family of bacterial purine nucleoside receptor encoded within an ATP-binding cassette (ABC)-like operon in Treponema pallidum.
J Biol Chem
2006
1.09
31
Structural analysis of Xanthomonas XopD provides insights into substrate specificity of ubiquitin-like protein proteases.
J Biol Chem
2007
1.08
32
Molecular mechanism for regulation of the human mitochondrial branched-chain alpha-ketoacid dehydrogenase complex by phosphorylation.
Structure
2004
0.99
33
Crystal structure of the 47-kDa lipoprotein of Treponema pallidum reveals a novel penicillin-binding protein.
J Biol Chem
2002
0.98
34
Crystal structure of the Formin mDia1 in autoinhibited conformation.
PLoS One
2010
0.96
35
Pseudo-cyclization through intramolecular hydrogen bond enables discovery of pyridine substituted pyrimidines as new Mer kinase inhibitors.
J Med Chem
2013
0.96
36
Computational design of the sequence and structure of a protein-binding peptide.
J Am Chem Soc
2011
0.95
37
Hyperthermostabilization of Bacillus licheniformis alpha-amylase and modulation of its stability over a 50 degrees C temperature range.
Protein Eng
2003
0.94
38
Structure and mechanism of a eukaryotic FMN adenylyltransferase.
J Mol Biol
2009
0.93
39
Monovalent cation dependence and preference of GHKL ATPases and kinases.
FEBS Lett
2003
0.92
40
Cross-talk between thiamin diphosphate binding and phosphorylation loop conformation in human branched-chain alpha-keto acid decarboxylase/dehydrogenase.
J Biol Chem
2004
0.91
41
Discovery of Mer specific tyrosine kinase inhibitors for the treatment and prevention of thrombosis.
J Med Chem
2013
0.91
42
Structural evidence that the 32-kilodalton lipoprotein (Tp32) of Treponema pallidum is an L-methionine-binding protein.
J Biol Chem
2004
0.90
43
Crystal structure of the RIM2 C2A-domain at 1.4 A resolution.
Biochemistry
2005
0.89
44
Crystal structures of the effector-binding domain of repressor Central glycolytic gene Regulator from Bacillus subtilis reveal ligand-induced structural changes upon binding of several glycolytic intermediates.
Mol Microbiol
2008
0.87
45
Increasing sequence diversity with flexible backbone protein design: the complete redesign of a protein hydrophobic core.
Structure
2012
0.87
46
A proximal arginine R206 participates in switching of the Bradyrhizobium japonicum FixL oxygen sensor.
J Mol Biol
2006
0.87
47
Crystal structure of inhibitor-bound P450BM-3 reveals open conformation of substrate access channel.
Biochemistry
2008
0.86
48
Structural determinants of affinity enhancement between GoLoco motifs and G-protein alpha subunit mutants.
J Biol Chem
2010
0.86
49
The two active sites in human branched-chain alpha-keto acid dehydrogenase operate independently without an obligatory alternating-site mechanism.
J Biol Chem
2007
0.85
50
Biophysical and bioinformatic analyses implicate the Treponema pallidum Tp34 lipoprotein (Tp0971) in transition metal homeostasis.
J Bacteriol
2012
0.83
51
Heterotrimeric G-protein signaling is critical to pathogenic processes in Entamoeba histolytica.
PLoS Pathog
2012
0.83
52
Crystal structure of the RIM1alpha C2B domain at 1.7 A resolution.
Biochemistry
2007
0.83
53
Structural determinants of RGS-RhoGEF signaling critical to Entamoeba histolytica pathogenesis.
Structure
2012
0.79
54
Roles of His291-alpha and His146-beta' in the reductive acylation reaction catalyzed by human branched-chain alpha-ketoacid dehydrogenase: refined phosphorylation loop structure in the active site.
J Biol Chem
2003
0.79
55
Interactions of substrates at the surface of P450s can greatly enhance substrate potency.
Biochemistry
2007
0.79
56
A single active-site mutation of P450BM-3 dramatically enhances substrate binding and rate of product formation.
Biochemistry
2011
0.77