Preparation of active Cdc7/Dbf4 kinase from yeast cells
Methods in Enzymology, ISSN: 0076-6879, Vol: 283, Page: 390-398
1997
- 6Citations
- 11Captures
Metric Options: Counts1 Year3 YearSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations6
- Citation Indexes6
- CrossRef4
- Captures11
- Readers11
- 11
Article Description
This chapter discusses the preparation of active cdc7/Dbf4 kinase from yeast cells. Saccharomyces cerevisiae cdc7 mutants are blocked in the cell cycle at the G1/S boundary at the restrictive temperature. Biochemical studies have shown that Cdc7 is a serine/threonine protein kinase that phosphorylates histone H1. It has been proposed that Cdc7 kinase is a component, along with Clb5,6/Cdc28 kinase, of S phase-promoting factor (SPF). Thus, there is great interest in determining what activates Cdc7 kinase at G1/S 5 and in defining its in vivo substrates. Progress in characterizing the kinase in these respects has been limited, however, not only because it is active only transiently during the cell cycle and is present only at low levels in the cell, but also because it has been unexpectedly difficult to express active Cdc7 in available expression systems and because the only test substrate, histone H1, is not an efficient substrate.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0076687997830327; http://dx.doi.org/10.1016/s0076-6879(97)83032-7; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0030811586&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/9251036; http://linkinghub.elsevier.com/retrieve/pii/S0076687997830327; https://linkinghub.elsevier.com/retrieve/pii/S0076687997830327; http://dx.doi.org/10.1016/s0076-6879%2897%2983032-7; https://dx.doi.org/10.1016/s0076-6879%2897%2983032-7
Elsevier BV
Provide Feedback
Have ideas for a new metric? Would you like to see something else here?Let us know