Year |
Citation |
Score |
2023 |
Pandey AK, Ganguly HK, Sinha SK, Daniels KE, Yap GPA, Patel S, Zondlo NJ. An Inherent Difference between Serine and Threonine Phosphorylation: Phosphothreonine Strongly Prefers a Highly Ordered, Compact, Cyclic Conformation. Acs Chemical Biology. PMID 37595155 DOI: 10.1021/acschembio.3c00068 |
0.372 |
|
2023 |
Bhatt MR, Zondlo NJ. Synthesis and conformational preferences of peptides and proteins with cysteine sulfonic acid. Organic & Biomolecular Chemistry. 21: 2779-2800. PMID 36920119 DOI: 10.1039/d3ob00179b |
0.34 |
|
2020 |
Tressler CM, Zondlo NJ. Perfluoro--Butyl Hydroxyprolines as Sensitive, Conformationally Responsive Molecular Probes: Detection of Protein Kinase Activity by F NMR. Acs Chemical Biology. PMID 32125821 DOI: 10.1021/Acschembio.0C00131 |
0.464 |
|
2020 |
Urmey AR, Zondlo NJ. Cysteine oxidation to the sulfinic acid induces oxoform-specific lanthanide binding and fluorescence in a designed peptide. Free Radical Biology & Medicine. PMID 32097680 DOI: 10.1016/J.Freeradbiomed.2020.02.020 |
0.407 |
|
2020 |
Urmey AR, Zondlo NJ. Synthesis of peptides with cysteine sulfinic acid via the cysteine methoxybenzyl sulfone Peptide Science. 112. DOI: 10.1002/Pep2.24137 |
0.405 |
|
2019 |
Urmey AR, Zondlo NJ. Structural preferences of cysteine sulfinic acid: The sulfinate engages in multiple local interactions with the peptide backbone. Free Radical Biology & Medicine. PMID 31883974 DOI: 10.1016/J.Freeradbiomed.2019.12.030 |
0.42 |
|
2019 |
Costantini NV, Ganguly HK, Martin MI, Wenzell NA, Yap GPA, Zondlo NJ. The distinct conformational landscapes of 4S-substituted prolines that promote an endo ring pucker. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31237705 DOI: 10.1002/Chem.201902382 |
0.365 |
|
2019 |
Urmey AR, Zondlo NJ. Design of a Protein Motif Responsive to Tyrosine Nitration and an Encoded Turn-Off Sensor of Tyrosine Nitration. Biochemistry. PMID 31140788 DOI: 10.1021/Acs.Biochem.9B00334 |
0.446 |
|
2019 |
Gao F, Thornley BS, Tressler CM, Naduthambi D, Zondlo NJ. Phosphorylation-dependent protein design: design of a minimal protein kinase-inducible domain. Organic & Biomolecular Chemistry. PMID 30942803 DOI: 10.1039/C9Ob00502A |
0.481 |
|
2018 |
Wenzell NA, Ganguly HK, Pandey AK, Bhatt MR, Yap GPA, Zondlo NJ. Electronic and steric control of n→π* interactions: stabilization of the α-helix conformation without a hydrogen bond. Chembiochem : a European Journal of Chemical Biology. PMID 30548564 DOI: 10.1002/Cbic.201800785 |
0.365 |
|
2018 |
Scheuermann MJ, Forbes CR, Zondlo NJ. Redox-Responsive Protein Design: Design of a Small Protein Motif Dependent on Glutathionylation. Biochemistry. PMID 30511831 DOI: 10.1021/Acs.Biochem.8B00973 |
0.408 |
|
2017 |
Tressler CM, Zondlo NJ. Perfluoro-tert-butyl Homoserine is a Helix-Promoting, Highly Fluorinated, NMR-Sensitive Aliphatic Amino Acid: Detection of the Estrogen Receptor•Coactivator Protein-Protein Interaction by 19F NMR. Biochemistry. PMID 28165218 DOI: 10.1021/Acs.Biochem.6B01020 |
0.416 |
|
2016 |
Tressler CM, Zondlo NJ. Synthesis of Perfluoro-tert-butyl Tyrosine, for Application in (19)F NMR, via a Diazonium-Coupling Reaction. Organic Letters. 18: 6240-6243. PMID 27978684 DOI: 10.1021/Acs.Orglett.6B02858 |
0.382 |
|
2016 |
Forbes CR, Pandey AK, Ganguly HK, Yap GP, Zondlo NJ. 4R- and 4S-iodophenyl hydroxyproline, 4R-pentynoyl hydroxyproline, and S-propargyl-4-thiolphenylalanine: conformationally biased and tunable amino acids for bioorthogonal reactions. Organic & Biomolecular Chemistry. PMID 26806113 DOI: 10.1039/C5Ob02473K |
0.401 |
|
2014 |
Pandey AK, Thomas KM, Forbes CR, Zondlo NJ. Tunable control of polyproline helix (PPII) structure via aromatic electronic effects: an electronic switch of polyproline helix. Biochemistry. 53: 5307-14. PMID 25075447 DOI: 10.1021/Bi500696K |
0.369 |
|
2014 |
Tressler CM, Zondlo NJ. (2 S,4 R)- and (2 S,4 S)-Perfluoro- tert -butyl 4-hydroxyproline: Two conformationally distinct proline amino acids for sensitive application in 19F NMR Journal of Organic Chemistry. 79: 5880-5886. PMID 24870929 DOI: 10.1021/Jo5008674 |
0.406 |
|
2014 |
Elbaum MB, Zondlo NJ. OGlcNAcylation and phosphorylation have similar structural effects in α-helices: Post-translational modifications as inducible start and stop signals in α-helices, with greater structural effects on threonine modification Biochemistry. 53: 2242-2260. PMID 24641765 DOI: 10.1021/Bi500117C |
0.397 |
|
2014 |
Brister MA, Pandey AK, Bielska AA, Zondlo NJ. OGlcNAcylation and phosphorylation have opposing structural effects in tau: phosphothreonine induces particular conformational order. Journal of the American Chemical Society. 136: 3803-16. PMID 24559475 DOI: 10.1021/Ja407156M |
0.417 |
|
2014 |
Zondlo NJ, Pandey A, Ganguly H, Elbaum M, Brister M. P4-258: ON THE NATURE OF THE TAU R406W MUTATION: INCREASED CIS PSER404-PRO405 AMIDE BOND IN TAU R406W DUE TO A PHOSPHORYLATION-SENSITIVE CIS-PROLINE-AROMATIC INTERACTION Alzheimer's & Dementia. 10: P879-P880. DOI: 10.1016/J.Jalz.2014.07.029 |
0.325 |
|
2013 |
Naduthambi D, Bhor S, Elbaum MB, Zondlo NJ. Synthesis of a tetrasubstituted tetrahydronaphthalene scaffold for α-helix mimicry via a MgBr2-catalyzed Friedel-Crafts epoxide cycloalkylation. Organic Letters. 15: 4892-5. PMID 24016333 DOI: 10.1021/Ol402334J |
0.333 |
|
2013 |
Pandey AK, Naduthambi D, Thomas KM, Zondlo NJ. Proline editing: A general and practical approach to the synthesis of functionally and structurally diverse peptides. Analysis of steric versus stereoelectronic effects of 4-substituted prolines on conformation within peptides Journal of the American Chemical Society. 135: 4333-4363. PMID 23402492 DOI: 10.1021/Ja3109664 |
0.443 |
|
2013 |
Zondlo NJ. Aromatic-proline interactions: Electronically tunable CH/π interactions Accounts of Chemical Research. 46: 1039-1049. PMID 23148796 DOI: 10.1021/Ar300087Y |
0.384 |
|
2012 |
Brown AM, Zondlo NJ. A propensity scale for type II polyproline helices (PPII): aromatic amino acids in proline-rich sequences strongly disfavor PPII due to proline-aromatic interactions. Biochemistry. 51: 5041-51. PMID 22667692 DOI: 10.1021/Bi3002924 |
0.42 |
|
2012 |
Forbes CR, Zondlo NJ. Synthesis of thiophenylalanine-containing peptides via Cu(I)-mediated cross-coupling Organic Letters. 14: 464-467. PMID 22224916 DOI: 10.1021/Ol202947F |
0.374 |
|
2012 |
Balakrishnan S, Scheuermann MJ, Zondlo NJ. Arginine mimetics using α-guanidino acids: introduction of functional groups and stereochemistry adjacent to recognition guanidiniums in peptides. Chembiochem : a European Journal of Chemical Biology. 13: 259-70. PMID 22213184 DOI: 10.1002/Cbic.201100638 |
0.612 |
|
2011 |
Zondlo N, Gao F. P4-330: Fluorescence imaging of cdk5, GSK-3b, MARK, and Fyn kinase activities in solution and in cells via novel encodable sensors Alzheimer's & Dementia. 7: e25-e26. DOI: 10.1016/J.Jalz.2011.09.075 |
0.355 |
|
2011 |
Zondlo N, Brister M, Bielska A. P4-329: Opposing structural effects of glycosylation and phosphorylation on tau Alzheimer's & Dementia. 7: e25-e25. DOI: 10.1016/J.Jalz.2011.09.074 |
0.308 |
|
2010 |
Zondlo NJ. Non-covalent interactions: Fold globally, bond locally Nature Chemical Biology. 6: 567-568. PMID 20644541 DOI: 10.1038/Nchembio.413 |
0.306 |
|
2010 |
Am Ende CW, Meng HY, Ye M, Pandey AK, Zondlo NJ. Design of lanthanide fingers: Compact lanthanide-binding metalloproteins Chembiochem. 11: 1738-1747. PMID 20623571 DOI: 10.1002/Cbic.201000056 |
0.39 |
|
2010 |
Zondlo SC, Gao F, Zondlo NJ. Design of an encodable tyrosine kinase-inducible domain: Detection of tyrosine kinase activity by terbium luminescence Journal of the American Chemical Society. 132: 5619-5621. PMID 20361796 DOI: 10.1021/Ja100862U |
0.432 |
|
2010 |
Zondlo NJ, Gao F, White S. O4-04-06: Imaging cdk5, GSK-3, and MARK kinase activities with a small, genetically encoded fluorescent sensor Alzheimer's & Dementia. 6: S156-S156. DOI: 10.1016/J.Jalz.2010.05.486 |
0.355 |
|
2009 |
Zondlo NJ, Gao F. P4-152: Imaging CDK5 kinase activity with a small, genetically encodable fluorescent sensor Alzheimer's & Dementia. 5: P476-P476. DOI: 10.1016/J.Jalz.2009.04.719 |
0.358 |
|
2008 |
Balakrishnan S, Zhao C, Zondlo NJ. ChemInform Abstract: Convergent and Stereospecific Synthesis of Molecules Containing α-Functionalized Guanidiniums via α-Guanidino Acids. Cheminform. 39. DOI: 10.1002/chin.200817052 |
0.484 |
|
2007 |
Balakrishnan S, Zhao C, Zondlo NJ. Convergent and stereospecific synthesis of molecules containing alpha-functionalized guanidiniums via alpha-guanidino acids. The Journal of Organic Chemistry. 72: 9834-7. PMID 17979289 DOI: 10.1021/Jo701766C |
0.526 |
|
2006 |
Zondlo SC, Lee AE, Zondlo NJ. Determinants of specificity of MDM2 for the activation domains of p53 and p65: Proline27 disrupts the MDM2-binding motif of p53 Biochemistry. 45: 11945-11957. PMID 17002294 DOI: 10.1021/Bi060309G |
0.305 |
|
2006 |
Naduthambi D, Zondlo NJ. Stereoelectronic tuning of the structure and stability of the Trp cage miniprotein Journal of the American Chemical Society. 128: 12430-12431. PMID 16984189 DOI: 10.1021/Ja0648458 |
0.42 |
|
2006 |
Balakrishnan S, Zondlo NJ. Design of a protein kinase-inducible domain. Journal of the American Chemical Society. 128: 5590-1. PMID 16637598 DOI: 10.1021/Ja057692H |
0.585 |
|
2006 |
Bielska AA, Zondlo NJ. Hyperphosphorylation of tau induces local polyproline II helix Biochemistry. 45: 5527-5537. PMID 16634634 DOI: 10.1021/Bi052662C |
0.426 |
|
2006 |
Thomas KM, Naduthambi D, Zondlo NJ. Electronic control of amide cis-trans isomerism via the aromatic-prolyl interaction Journal of the American Chemical Society. 128: 2216-2217. PMID 16478167 DOI: 10.1021/Ja057901Y |
0.345 |
|
2006 |
Meng HY, Thomas KM, Lee AE, Zondlo NJ. Effects of i and i+3 residue identity on cis-trans isomerism of the aromatici+1-prolyli+2 amide bond: Implications for type VI β-turn formation Biopolymers - Peptide Science Section. 84: 192-204. PMID 16208767 DOI: 10.1002/Bip.20382 |
0.378 |
|
2005 |
Thomas KM, Naduthambi D, Tririya G, Zondlo NJ. Proline editing: A divergent strategy for the synthesis of conformationally diverse peptides Organic Letters. 7: 2397-2400. PMID 15932207 DOI: 10.1021/Ol0506720 |
0.405 |
|
1999 |
Zondlo NJ, Schepartz A. Highly specific DNA recognition by a designed miniature protein [2] Journal of the American Chemical Society. 121: 6938-6939. DOI: 10.1021/Ja990968Z |
0.532 |
|
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