-
1
-
-
84875138812
-
Getting in shape: Controlling peptide bioactivity and bioavailability using conformational constraints
-
Bock, J. E., Gavenonis, J. & Kritzer, J. A. Getting in shape: controlling peptide bioactivity and bioavailability using conformational constraints. ACS Chem. Biol. 8, 488-499 (2013).
-
(2013)
ACS Chem. Biol.
, vol.8
, pp. 488-499
-
-
Bock, J.E.1
Gavenonis, J.2
Kritzer, J.A.3
-
2
-
-
84937518958
-
Structure-based design of inhibitors of protein-protein interactions: Mimicking peptide binding epitopes
-
Pelay-Gimeno, M., Glas, A., Koch, O. & Grossmann, T. N. Structure-based design of inhibitors of protein-protein interactions: mimicking peptide binding epitopes. Angew. Chem. Int. Ed. 54, 8896-8927 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 8896-8927
-
-
Pelay-Gimeno, M.1
Glas, A.2
Koch, O.3
Grossmann, T.N.4
-
3
-
-
84915748758
-
Constraining cyclic peptides to mimic protein structure motifs
-
Hill, T. A., Shepherd, N. E., Diness, F. & Fairlie, D. P. Constraining cyclic peptides to mimic protein structure motifs. Angew. Chem. Int. Ed. 53, 13020-13041 (2014).
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 13020-13041
-
-
Hill, T.A.1
Shepherd, N.E.2
Diness, F.3
Fairlie, D.P.4
-
4
-
-
79952741178
-
Cilengitide: The first anti-angiogenic small molecule drug candidate. Design, synthesis and clinical evaluation
-
Mas-Moruno, C., Rechenmacher, F. & Kessler, H. Cilengitide: the first anti-angiogenic small molecule drug candidate. design, synthesis and clinical evaluation. Anticancer Agents Med. Chem. 10, 753-768 (2010).
-
(2010)
Anticancer Agents Med. Chem.
, vol.10
, pp. 753-768
-
-
Mas-Moruno, C.1
Rechenmacher, F.2
Kessler, H.3
-
5
-
-
77149159117
-
Peptidomimetic antibiotics target outer-membrane biogenesis in Pseudomonas aeruginosa
-
Srinivas, N. et al. Peptidomimetic antibiotics target outer-membrane biogenesis in Pseudomonas aeruginosa. Science 327, 1010-1013 (2010).
-
(2010)
Science
, vol.327
, pp. 1010-1013
-
-
Srinivas, N.1
-
6
-
-
84922619874
-
Direct inhibition of oncogenic KRAS by hydrocarbonstapled SOS1 helices
-
Leshchiner, E. S. et al. Direct inhibition of oncogenic KRAS by hydrocarbonstapled SOS1 helices. Proc. Natl Acad. Sci. USA 112, 1761-1766 (2015).
-
(2015)
Proc. Natl Acad. Sci. USA
, vol.112
, pp. 1761-1766
-
-
Leshchiner, E.S.1
-
7
-
-
70449671729
-
Direct inhibition of the NOTCH transcription factor complex
-
Moellering, R. E. et al. Direct inhibition of the NOTCH transcription factor complex. Nature 462, 182-188 (2009).
-
(2009)
Nature
, vol.462
, pp. 182-188
-
-
Moellering, R.E.1
-
8
-
-
84860390239
-
An orthosteric inhibitor of the Ras-Sos interaction
-
Patgiri, A., Yadav, K. K., Arora, P. S. & Bar-Sagi, D. An orthosteric inhibitor of the Ras-Sos interaction. Nat. Chem. Biol. 7, 585-587 (2011).
-
(2011)
Nat. Chem. Biol.
, vol.7
, pp. 585-587
-
-
Patgiri, A.1
Yadav, K.K.2
Arora, P.S.3
Bar-Sagi, D.4
-
9
-
-
84868145117
-
Inhibition of oncogenic Wnt signaling through direct targeting of β-catenin
-
Grossmann, T. N. et al. Inhibition of oncogenic Wnt signaling through direct targeting of β-catenin. Proc. Natl Acad. Sci. USA 109, 17942-17947 (2012).
-
(2012)
Proc. Natl Acad. Sci. USA
, vol.109
, pp. 17942-17947
-
-
Grossmann, T.N.1
-
10
-
-
84928957792
-
Inhibition of Ras signaling by blocking Ras-effector interactions with cyclic peptides
-
Upadhyaya, P. et al. Inhibition of Ras signaling by blocking Ras-effector interactions with cyclic peptides. Angew. Chem. Int. Ed. 54, 7602-7606 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 7602-7606
-
-
Upadhyaya, P.1
-
11
-
-
84892163643
-
Macrocyclic drugs and clinical candidates: What can medicinal chemists learn from their properties?
-
Giordanetto, F. & Kihlberg, J. Macrocyclic drugs and clinical candidates: what can medicinal chemists learn from their properties? J. Med. Chem. 57, 278-295 (2014).
-
(2014)
J. Med. Chem.
, vol.57
, pp. 278-295
-
-
Giordanetto, F.1
Kihlberg, J.2
-
12
-
-
84894430612
-
Direct targeting of Rab-GTPase-effector interactions
-
Spiegel, J. et al. Direct targeting of Rab-GTPase-effector interactions. Angew. Chem. Int. Ed. 53, 2498-2503 (2014).
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 2498-2503
-
-
Spiegel, J.1
-
13
-
-
84896512272
-
Disulfide-rich macrocyclic peptides as templates in drug design
-
Northfield, S. E. et al. Disulfide-rich macrocyclic peptides as templates in drug design. Eur. J. Med. Chem. 77, 248-257 (2014).
-
(2014)
Eur. J. Med. Chem.
, vol.77
, pp. 248-257
-
-
Northfield, S.E.1
-
14
-
-
84879017232
-
Cyclotides as grafting frameworks for protein engineering and drug design applications
-
Poth, A. G., Chan, L. Y. & Craik, D. J. Cyclotides as grafting frameworks for protein engineering and drug design applications. Biopolymers 100, 480-491 (2013).
-
(2013)
Biopolymers
, vol.100
, pp. 480-491
-
-
Poth, A.G.1
Chan, L.Y.2
Craik, D.J.3
-
15
-
-
67650305952
-
Phage-encoded combinatorial chemical libraries based on bicyclic peptides
-
Heinis, C., Rutherford, T., Freund, S. & Winter, G. Phage-encoded combinatorial chemical libraries based on bicyclic peptides. Nat. Chem. Biol. 5, 502-507 (2009).
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 502-507
-
-
Heinis, C.1
Rutherford, T.2
Freund, S.3
Winter, G.4
-
16
-
-
84874296906
-
Polycyclic peptide therapeutics
-
Baeriswyl, V. & Heinis, C. Polycyclic peptide therapeutics. Chem. Med. Chem. 8, 377-384 (2013).
-
(2013)
Chem. Med. Chem.
, vol.8
, pp. 377-384
-
-
Baeriswyl, V.1
Heinis, C.2
-
17
-
-
79959580534
-
Contemporary strategies for peptide macrocyclization
-
White, C. J. & Yudin, A. K. Contemporary strategies for peptide macrocyclization. Nat. Chem. 3, 509-524 (2011).
-
(2011)
Nat. Chem.
, vol.3
, pp. 509-524
-
-
White, C.J.1
Yudin, A.K.2
-
18
-
-
26844576835
-
Amide bond formation and peptide coupling
-
Montalbetti, C. A. & Falque, V. Amide bond formation and peptide coupling. Tetrahedron 61, 10827-10852 (2005).
-
(2005)
Tetrahedron
, vol.61
, pp. 10827-10852
-
-
Montalbetti, C.A.1
Falque, V.2
-
19
-
-
84893119472
-
Multifaceted roles of disulfide bonds. Peptides as therapeutics
-
Góngora-Benítez, M., Tulla-Puche, J. & Albericio, F. Multifaceted roles of disulfide bonds. peptides as therapeutics. Chem. Rev. 114, 901-926 (2014).
-
(2014)
Chem. Rev.
, vol.114
, pp. 901-926
-
-
Góngora-Benítez, M.1
Tulla-Puche, J.2
Albericio, F.3
-
20
-
-
84945301819
-
Acetone-linked peptides: A convergent approach for peptide macrocyclization and labeling
-
Assem, N., Ferreira, D. J., Wolan, D. W. & Dawson, P. E. Acetone-linked peptides: a convergent approach for peptide macrocyclization and labeling. Angew. Chem. Int. Ed. 54, 8665-8668 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 8665-8668
-
-
Assem, N.1
Ferreira, D.J.2
Wolan, D.W.3
Dawson, P.E.4
-
21
-
-
84940723071
-
A thiol-ene coupling approach to native peptide stapling and macrocyclization
-
Wang, Y. & Chou, D. H.-C. A thiol-ene coupling approach to native peptide stapling and macrocyclization. Angew. Chem. Int. Ed. 54, 10931-10934 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 10931-10934
-
-
Wang, Y.1
Chou, D.H.-C.2
-
22
-
-
84915756301
-
Linear aliphatic dialkynes as alternative linkers for double-click stapling of p53-derived peptides
-
Lau, Y. H., Andrade, P., de McKenzie, G. J., Venkitaraman, A. R. & Spring, D. R. Linear aliphatic dialkynes as alternative linkers for double-click stapling of p53-derived peptides. ChemBioChem. 15, 2680-2683 (2014).
-
(2014)
ChemBioChem
, vol.15
, pp. 2680-2683
-
-
Lau, Y.H.1
Andrade, P.2
De McKenzie, G.J.3
Venkitaraman, A.R.4
Spring, D.R.5
-
23
-
-
84955191585
-
Double strain-promoted macrocyclization for the rapid selection of cell-active stapled peptides
-
Lau, Y. H. et al. Double strain-promoted macrocyclization for the rapid selection of cell-active stapled peptides. Angew. Chem. Int. Ed. 54, 15410-15413 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 15410-15413
-
-
Lau, Y.H.1
-
24
-
-
84930226972
-
New peptide architectures through C-H activation stapling between tryptophan-phenylalanine/tyrosine residues
-
Mendive-Tapia, L. et al. New peptide architectures through C-H activation stapling between tryptophan-phenylalanine/tyrosine residues. Nat. Commun. 6, 7160 (2015).
-
(2015)
Nat. Commun.
, vol.6
, pp. 7160
-
-
Mendive-Tapia, L.1
-
25
-
-
84916912015
-
Peptide stapling techniques based on different macrocyclisation chemistries
-
Lau, Y. H., Andrade, P., de Wu, Y. & Spring, D. R. Peptide stapling techniques based on different macrocyclisation chemistries. Chem. Soc. Rev. 44, 91-102 (2015).
-
(2015)
Chem. Soc. Rev.
, vol.44
, pp. 91-102
-
-
Lau, Y.H.1
Andrade, P.2
De Wu, Y.3
Spring, D.R.4
-
26
-
-
84862908454
-
Structure of the stapled p53 peptide bound to Mdm2
-
Baek, S. et al. Structure of the stapled p53 peptide bound to Mdm2. J. Am. Chem. Soc. 134, 103-106 (2012).
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 103-106
-
-
Baek, S.1
-
27
-
-
79959492294
-
Design and structure of stapled peptides binding to estrogen receptors
-
Phillips, C. et al. Design and structure of stapled peptides binding to estrogen receptors. J. Am. Chem. Soc. 133, 9696-9699 (2011).
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 9696-9699
-
-
Phillips, C.1
-
28
-
-
84894431432
-
Constrained peptides with target-adapted cross-links as inhibitors of a pathogenic protein-protein interaction
-
Glas, A. et al. Constrained peptides with target-adapted cross-links as inhibitors of a pathogenic protein-protein interaction. Angew. Chem. Int. Ed. 53, 2489-2493 (2014).
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 2489-2493
-
-
Glas, A.1
-
29
-
-
79960169768
-
A role for ring-closing metathesis in medicinal chemistry: Mimicking secondary architectures in bioactive peptides
-
Pérez de Vega, M. J., García-Aranda, M. I. & González-Muñiz, R. A role for ring-closing metathesis in medicinal chemistry: mimicking secondary architectures in bioactive peptides. Med. Res. Rev. 31, 677-715 (2011).
-
(2011)
Med. Res. Rev.
, vol.31
, pp. 677-715
-
-
Pérez De-Vega, M.J.1
García-Aranda, M.I.2
González-Muñiz, R.3
-
30
-
-
33746052447
-
Evaluation of biologically relevant short alpha-helices stabilized by a main-chain hydrogen-bond surrogate
-
Wang, D., Chen, K., Kulp, J. L. & Arora, P. S. Evaluation of biologically relevant short alpha-helices stabilized by a main-chain hydrogen-bond surrogate. J. Am. Chem. Soc. 128, 9248-9256 (2006).
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 9248-9256
-
-
Wang, D.1
Chen, K.2
Kulp, J.L.3
Arora, P.S.4
-
31
-
-
84865689618
-
End-capped α-helices as modulators of protein function
-
Mahon, A. B. & Arora, P. S. End-capped α-helices as modulators of protein function. Drug Discov. Today Technol. 9, e57-e62 (2012).
-
(2012)
Drug Discov. Today Technol.
, vol.9
, pp. e57-e62
-
-
Mahon, A.B.1
Arora, P.S.2
-
32
-
-
84934996624
-
Hydrocarbon stapled peptides as modulators of biological function
-
Cromm, P. M., Spiegel, J. & Grossmann, T. N. Hydrocarbon stapled peptides as modulators of biological function. ACS Chem. Biol. 10, 1362-1375 (2015).
-
(2015)
ACS Chem. Biol.
, vol.10
, pp. 1362-1375
-
-
Cromm, P.M.1
Spiegel, J.2
Grossmann, T.N.3
-
33
-
-
79958086652
-
Synthesis of all-hydrocarbon Stapled α-helical peptides by ring-closing olefin metathesis
-
Kim, Y.-W., Grossmann, T. N. & Verdine, G. L. Synthesis of all-hydrocarbon Stapled α-helical peptides by ring-closing olefin metathesis. Nat. Protoc. 6, 761-771 (2011).
-
(2011)
Nat. Protoc.
, vol.6
, pp. 761-771
-
-
Kim, Y.-W.1
Grossmann, T.N.2
Verdine, G.L.3
-
34
-
-
0032542374
-
Highly efficient synthesis of covalently crosslinked peptide helices by ring-closing metathesis
-
Blackwell, H. E. & Grubbs, R. H. Highly efficient synthesis of covalently crosslinked peptide helices by ring-closing metathesis. Angew. Chem. Int. Ed. 37, 3281-3284 (1998).
-
(1998)
Angew. Chem. Int. Ed.
, vol.37
, pp. 3281-3284
-
-
Blackwell, H.E.1
Grubbs, R.H.2
-
35
-
-
0034697649
-
An all-hydrocarbon cross-linking system for enhancing the helicity and metabolic stability of peptides
-
Schafmeister, C. E., Po, J. & Verdine, G. L. An all-hydrocarbon cross-linking system for enhancing the helicity and metabolic stability of peptides. J. Am. Chem. Soc. 122, 5891-5892 (2000).
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 5891-5892
-
-
Schafmeister, C.E.1
Po, J.2
Verdine, G.L.3
-
36
-
-
12744277997
-
Preorganization induced synthesis of a crossed alkene-bridged nisin Z DE-ring mimic by ring-closing metathesis
-
Ghalit, N., Rijkers, D. T. S., Kemmink, J., Versluis, C. & Liskamp, R. M. J. Preorganization induced synthesis of a crossed alkene-bridged nisin Z DE-ring mimic by ring-closing metathesis. Chem. Commun. 192-194 (2005).
-
(2005)
Chem. Commun.
, pp. 192-194
-
-
Ghalit, N.1
Rijkers, D.T.S.2
Kemmink, J.3
Versluis, C.4
Liskamp, R.M.J.5
-
37
-
-
84886913894
-
Synthesis and structural characterization of the individual diastereoisomers of a cross-stapled alkene-bridged nisin DE-ring mimic
-
Slootweg, J. C., Kemmink, J., Liskamp, R. M. J. & Rijkers, D. T. Synthesis and structural characterization of the individual diastereoisomers of a cross-stapled alkene-bridged nisin DE-ring mimic. Org. Biomol. Chem. 11, 7486-7496 (2013).
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 7486-7496
-
-
Slootweg, J.C.1
Kemmink, J.2
Liskamp, R.M.J.3
Rijkers, D.T.4
-
38
-
-
77956294635
-
Hydrocarbon double-stapling remedies the proteolytic instability of a lengthy peptide therapeutic
-
Bird, G. H. et al. Hydrocarbon double-stapling remedies the proteolytic instability of a lengthy peptide therapeutic. Proc. Natl Acad. Sci. USA 107, 14093-14098 (2010).
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 14093-14098
-
-
Bird, G.H.1
-
39
-
-
67650448251
-
Regioselective formation of interlocked dicarba bridges in naturally occurring cyclic peptide toxins using olefin metathesis
-
Robinson, A. J. et al. Regioselective formation of interlocked dicarba bridges in naturally occurring cyclic peptide toxins using olefin metathesis. Chem. Commun. 28, 4293-4295 (2009).
-
(2009)
Chem. Commun.
, vol.28
, pp. 4293-4295
-
-
Robinson, A.J.1
-
40
-
-
84906872219
-
Stitched α-helical peptides via bis ring-closing metathesis
-
Hilinski, G. J. et al. Stitched α-helical peptides via bis ring-closing metathesis. J. Am. Chem. Soc. 136, 12314-12322 (2014).
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 12314-12322
-
-
Hilinski, G.J.1
-
41
-
-
84874639402
-
Alkyne metathesis on the rise
-
Fürstner, A. Alkyne metathesis on the rise. Angew. Chem. Int. Ed. 52, 2794-2819 (2013).
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 2794-2819
-
-
Fürstner, A.1
-
42
-
-
0035906505
-
Synthesis of diaminosuberic acid derivatives via ring-closing alkyne metathesis
-
Aguilera, B. et al. Synthesis of diaminosuberic acid derivatives via ring-closing alkyne metathesis. J. Org. Chem. 66, 3584-3589 (2001).
-
(2001)
J. Org. Chem.
, vol.66
, pp. 3584-3589
-
-
Aguilera, B.1
-
43
-
-
2342557082
-
Ring-closing alkyne metathesis mediated synthesis of cyclic β-turn mimetics
-
Ijsselstijn, M. et al. Ring-closing alkyne metathesis mediated synthesis of cyclic β-turn mimetics. Tetrahedron Lett. 45, 4379-4382 (2004).
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4379-4382
-
-
Ijsselstijn, M.1
-
44
-
-
22244435602
-
Ringclosing alkyne metathesis approach toward the synthesis of alkyne mimics of thioether A-, B-, C-, and DE-ring systems of the lantibiotic nisin Z
-
Ghalit, N., Poot, A. J., Fürstner, A., Rijkers, D. T. S. & Liskamp, R. M. J. Ringclosing alkyne metathesis approach toward the synthesis of alkyne mimics of thioether A-, B-, C-, and DE-ring systems of the lantibiotic nisin Z. Org. Lett. 7, 2961-2964 (2005).
-
(2005)
Org. Lett.
, vol.7
, pp. 2961-2964
-
-
Ghalit, N.1
Poot, A.J.2
Fürstner, A.3
Rijkers, D.T.S.4
Liskamp, R.M.J.5
-
45
-
-
84864606288
-
Optimized synthesis, structural investigations, ligand tuning and synthetic evaluation of silyloxy-based alkyne metathesis catalysts
-
Heppekausen, J. et al. Optimized synthesis, structural investigations, ligand tuning and synthetic evaluation of silyloxy-based alkyne metathesis catalysts. Chem. Eur. J. 18, 10281-10299 (2012).
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 10281-10299
-
-
Heppekausen, J.1
-
46
-
-
77955563276
-
Practical new silyloxybased alkyne metathesis catalysts with optimized activity and selectivity profiles
-
Heppekausen, J., Stade, R., Goddard, R. & Fürstner, A. Practical new silyloxybased alkyne metathesis catalysts with optimized activity and selectivity profiles. J. Am. Chem. Soc. 132, 11045-11057 (2010).
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 11045-11057
-
-
Heppekausen, J.1
Stade, R.2
Goddard, R.3
Fürstner, A.4
-
47
-
-
84941909045
-
One-pot selective homodimerization/hydrogenation strategy for sequential dicarba bridge formation
-
Burnley, J., Jackson, W. R. & Robinson, A. J. One-pot selective homodimerization/hydrogenation strategy for sequential dicarba bridge formation. J. Org. Chem. 80, 9057-9063 (2015).
-
(2015)
J. Org. Chem.
, vol.80
, pp. 9057-9063
-
-
Burnley, J.1
Jackson, W.R.2
Robinson, A.J.3
-
48
-
-
16844387479
-
The Ras superfamily at a glance
-
Wennerberg, K., Rossman, K. L. & Der, C. J. The Ras superfamily at a glance. J. Cell Sci. 118, 843-846 (2005).
-
(2005)
J. Cell Sci.
, vol.118
, pp. 843-846
-
-
Wennerberg, K.1
Rossman, K.L.2
Der, C.J.3
-
49
-
-
84927600481
-
KRAS as a therapeutic target
-
McCormick, F. KRAS as a therapeutic target. Clin. Cancer Res. 21, 1797-1801 (2015).
-
(2015)
Clin. Cancer Res.
, vol.21
, pp. 1797-1801
-
-
McCormick, F.1
-
50
-
-
84904721890
-
Small-molecule modulation of Ras signaling
-
Spiegel, J., Cromm, P. M., Zimmermann, G., Grossmann, T. N. & Waldmann, H. Small-molecule modulation of Ras signaling. Nat. Chem. Biol. 10, 613-622 (2014).
-
(2014)
Nat. Chem. Biol.
, vol.10
, pp. 613-622
-
-
Spiegel, J.1
Cromm, P.M.2
Zimmermann, G.3
Grossmann, T.N.4
Waldmann, H.5
-
51
-
-
84946045247
-
Direct modulation of small GTPase activity and function
-
Cromm, P. M., Spiegel, J., Grossmann, T. N. & Waldmann, H. Direct modulation of small GTPase activity and function. Angew. Chem. Int. Ed. 54, 13516-13537 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 13516-13537
-
-
Cromm, P.M.1
Spiegel, J.2
Grossmann, T.N.3
Waldmann, H.4
-
52
-
-
84896090174
-
Dragging ras back in the ring
-
Stephen, A. G., Esposito, D., Bagni, R. K. & McCormick, F. Dragging ras back in the ring. Cancer Cell 25, 272-281 (2014).
-
(2014)
Cancer Cell
, vol.25
, pp. 272-281
-
-
Stephen, A.G.1
Esposito, D.2
Bagni, R.K.3
McCormick, F.4
-
53
-
-
84888639050
-
K-Ras(G12C) inhibitors allosterically control GTP affinity and effector interactions
-
Ostrem, J. M., Peters, U., Sos, M. L., Wells, J. A. & Shokat, K. M. K-Ras(G12C) inhibitors allosterically control GTP affinity and effector interactions. Nature 503, 548-551 (2013).
-
(2013)
Nature
, vol.503
, pp. 548-551
-
-
Ostrem, J.M.1
Peters, U.2
Sos, M.L.3
Wells, J.A.4
Shokat, K.M.5
-
54
-
-
84862549205
-
A competitive nucleotide binding inhibitor: In vitro characterization of Rab7 GTPase inhibition
-
Agola, J. O. et al. A competitive nucleotide binding inhibitor: in vitro characterization of Rab7 GTPase inhibition. ACS Chem. Biol. 7, 1095-1108 (2012).
-
(2012)
ACS Chem. Biol.
, vol.7
, pp. 1095-1108
-
-
Agola, J.O.1
-
55
-
-
84908053767
-
Rab proteins: The key regulators of intracellular vesicle transport
-
Bhuin, T. & Roy, J. K. Rab proteins: the key regulators of intracellular vesicle transport. Exp. Cell Res. 328, 1-19 (2014).
-
(2014)
Exp. Cell Res.
, vol.328
, pp. 1-19
-
-
Bhuin, T.1
Roy, J.K.2
-
56
-
-
78751656754
-
Role of Rab GTPases in membrane traffic and cell physiology
-
Hutagalung, A. H. & Novick, P. J. Role of Rab GTPases in membrane traffic and cell physiology. Physiol. Rev. 91, 119-149 (2011).
-
(2011)
Physiol. Rev.
, vol.91
, pp. 119-149
-
-
Hutagalung, A.H.1
Novick, P.J.2
-
57
-
-
58149181482
-
Structural basis for recruitment of Rab6-interacting protein 1 to Golgi via a RUN domain
-
Recacha, R. et al. Structural basis for recruitment of Rab6-interacting protein 1 to Golgi via a RUN domain. Structure 17, 21-30 (2009).
-
(2009)
Structure
, vol.17
, pp. 21-30
-
-
Recacha, R.1
-
58
-
-
0032509547
-
Improved procedures for the synthesis of (S)-2-[N-(N′-benzylprolyl)amino] benzophenone (BPB) and Ni(II) complexes of Schiff's bases derived from BPB and amino acids
-
Belokon', Y. N., Tararov, V. I., Maleev, V. I., Savel'eva, T. F. & Ryzhov, M. G. Improved procedures for the synthesis of (S)-2-[N-(N′-benzylprolyl)amino] benzophenone (BPB) and Ni(II) complexes of Schiff's bases derived from BPB and amino acids. Tetrahedron 9, 4249-4252 (1998).
-
(1998)
Tetrahedron
, vol.9
, pp. 4249-4252
-
-
Belokon, Y.N.1
Tararov, V.I.2
Maleev, V.I.3
Savel'Eva, T.F.4
Ryzhov, M.G.5
-
59
-
-
84865324626
-
Chemical synthesis of hydrocarbon-stapled peptides for protein interaction research and therapeutic targeting
-
Bird, G. H., Crannell, W. C. & Walensky, L. D. Chemical synthesis of hydrocarbon-stapled peptides for protein interaction research and therapeutic targeting. Curr. Protoc. Chem. Biol. 3, 99-117 (2011).
-
(2011)
Curr. Protoc. Chem. Biol.
, vol.3
, pp. 99-117
-
-
Bird, G.H.1
Crannell, W.C.2
Walensky, L.D.3
-
60
-
-
79955000748
-
A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1
-
Hou, X. et al. A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1. EMBO J. 30, 1659-1670 (2011).
-
(2011)
EMBO J.
, vol.30
, pp. 1659-1670
-
-
Hou, X.1
-
61
-
-
61749097741
-
Chaperone-assisted production of active human Rab8A GTPase in Escherichia coli
-
Bleimling, N., Alexandrov, K., Goody, R. & Itzen, A. Chaperone-assisted production of active human Rab8A GTPase in Escherichia coli. Protein Expr. Purif. 65, 190-195 (2009).
-
(2009)
Protein Expr. Purif.
, vol.65
, pp. 190-195
-
-
Bleimling, N.1
Alexandrov, K.2
Goody, R.3
Itzen, A.4
-
62
-
-
0029831063
-
Kinetics of interaction of Rab5 and Rab7 with nucleotides and magnesium ions
-
Simon, I., Zerial, M. & Goody, R. S. Kinetics of interaction of Rab5 and Rab7 with nucleotides and magnesium ions. J. Biol. Chem. 271, 20470-20478 (1996).
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 20470-20478
-
-
Simon, I.1
Zerial, M.2
Goody, R.S.3
-
63
-
-
70349306558
-
Application of fluorescence polarization in HTS assays
-
Huang, X. & Aulabaugh, A. Application of fluorescence polarization in HTS assays. Methods Mol. Biol. 565, 127-143 (2009).
-
(2009)
Methods Mol. Biol.
, vol.565
, pp. 127-143
-
-
Huang, X.1
Aulabaugh, A.2
|