Frederick C. Streich

713 total citations
10 papers, 380 citations indexed

About

Frederick C. Streich is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Frederick C. Streich has authored 10 papers receiving a total of 380 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Oncology and 2 papers in Cell Biology. Recurrent topics in Frederick C. Streich's work include Ubiquitin and proteasome pathways (6 papers), Peptidase Inhibition and Analysis (4 papers) and Cancer-related Molecular Pathways (3 papers). Frederick C. Streich is often cited by papers focused on Ubiquitin and proteasome pathways (6 papers), Peptidase Inhibition and Analysis (4 papers) and Cancer-related Molecular Pathways (3 papers). Frederick C. Streich collaborates with scholars based in United States. Frederick C. Streich's co-authors include Christopher D. Lima, Arthur L. Haas, Virginia P. Ronchi, Brajesh Kumar, Jennifer M. Klein, Thomas J. Siepmann, James B. Delehanty, Eddie L. Chang, Ellen R. Goldman and D. Andrew Knight and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Dalton Transactions.

In The Last Decade

Frederick C. Streich

10 papers receiving 376 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Frederick C. Streich United States	8	329	138	55	47	39	10	380
Peter Littlefield United States	5	465 1.4×	174 1.3×	51 0.9×	34 0.7×	64 1.6×	5	525
Wassim Abdulrahman France	7	666 2.0×	183 1.3×	35 0.6×	30 0.6×	37 0.9×	9	722
Francis P. McManus Canada	14	459 1.4×	108 0.8×	27 0.5×	87 1.9×	34 0.9×	24	537
Mark A. Nakasone United States	13	516 1.6×	223 1.6×	110 2.0×	38 0.8×	68 1.7×	18	574
Nathalie Eisenhardt Germany	8	655 2.0×	122 0.9×	33 0.6×	47 1.0×	83 2.1×	11	676
Xavier H. Mascle Canada	9	378 1.1×	94 0.7×	45 0.8×	101 2.1×	23 0.6×	11	439
Patrick Schreiner Germany	6	337 1.0×	106 0.8×	86 1.6×	23 0.5×	103 2.6×	6	381
Mathew Stanley United Kingdom	9	386 1.2×	135 1.0×	110 2.0×	39 0.8×	28 0.7×	12	460
Wolfgang Uerkvitz Denmark	10	331 1.0×	116 0.8×	44 0.8×	66 1.4×	82 2.1×	11	374
H. Aitkenhead United Kingdom	9	487 1.5×	136 1.0×	31 0.6×	39 0.8×	64 1.6×	13	534

Countries citing papers authored by Frederick C. Streich

Since Specialization

Citations

This map shows the geographic impact of Frederick C. Streich's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Frederick C. Streich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Frederick C. Streich more than expected).

Fields of papers citing papers by Frederick C. Streich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Frederick C. Streich. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Frederick C. Streich. The network helps show where Frederick C. Streich may publish in the future.

Co-authorship network of co-authors of Frederick C. Streich

This figure shows the co-authorship network connecting the top 25 collaborators of Frederick C. Streich. A scholar is included among the top collaborators of Frederick C. Streich based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Frederick C. Streich. Frederick C. Streich is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

Dagbay, Kevin B., Frederick C. Streich, Justin Jackson, et al.. (2020). Structural basis of specific inhibition of extracellular activation of pro- or latent myostatin by the monoclonal antibody SRK-015. Journal of Biological Chemistry. 295(16). 5404–5418. 17 indexed citations

Streich, Frederick C. & Christopher D. Lima. (2018). Strategies to Trap Enzyme-Substrate Complexes that Mimic Michaelis Intermediates During E3-Mediated Ubiquitin-Like Protein Ligation. Methods in molecular biology. 1844. 169–196. 6 indexed citations

Streich, Frederick C. & Christopher D. Lima. (2016). Capturing a substrate in an activated RING E3/E2–SUMO complex. Nature. 536(7616). 304–308. 83 indexed citations

Edwards, Daniel, et al.. (2014). Convergent Evolution in the Assembly of Polyubiquitin Degradation Signals by the Shigella flexneri IpaH9.8 Ligase. Journal of Biological Chemistry. 289(49). 34114–34128. 13 indexed citations

Streich, Frederick C. & Christopher D. Lima. (2014). Structural and Functional Insights to Ubiquitin-Like Protein Conjugation. Annual Review of Biophysics. 43(1). 357–379. 128 indexed citations

Streich, Frederick C., et al.. (2013). Tripartite Motif Ligases Catalyze Polyubiquitin Chain Formation through a Cooperative Allosteric Mechanism. Journal of Biological Chemistry. 288(12). 8209–8221. 39 indexed citations

Siepmann, Thomas J., et al.. (2011). E1-E2 Interactions in Ubiquitin and Nedd8 Ligation Pathways. Journal of Biological Chemistry. 287(1). 311–321. 48 indexed citations

Streich, Frederick C. & Arthur L. Haas. (2010). Activation of Ubiquitin and Ubiquitin-Like Proteins. Sub-cellular biochemistry. 54. 1–16. 20 indexed citations

Hartsock, Robert W., et al.. (2005). Monofunctionalized Tetraazacrowns for Use in Bioconjugation and Catalysis. Synthesis and Reactivity in Inorganic Metal-Organic and Nano-Metal Chemistry. 35(9). 727–731. 1 indexed citations

10.

Knight, D. Andrew, et al.. (2004). Carboxylic acid functionalized cobalt(iii) cyclen complexes for catalytic hydrolysis of phosphodiester bonds. Dalton Transactions. 2006–2006. 25 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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