(Q27748804)

1

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R A Engh

2

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A Girod

3

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V Kinzel

4

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R Huber

5

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D Bossemeyer

A new alkaloid AM-2282 OF Streptomyces origin. Taxonomy, fermentation, isolation and preliminary characterization

6

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publication date

15 December 1997

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published in

Structure

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volume

5

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issue

12

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page(s)

1627-37

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2897%2900310-9

7 January 2021

28 Use and specificity of staurosporine, UCN-O1, and calphostin C as protein kinase inhibitors

1 reference

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7 January 2021

Staurosporine is a potent inhibitor of p34cdc2 and p34cdc2-like kinases

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2897%2900310-9

7 January 2021

Staurosporine, a potent inhibitor of phospholipid/Ca++dependent protein kinase

1 reference

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7 January 2021

Characterization of specific binding sites for [3H]-staurosporine on various protein kinases

1 reference

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7 January 2021

Characterization of receptor tyrosine-specific protein kinases by the use of inhibitors. Staurosporine is a 100-times more potent inhibitor of insulin receptor than IGF-I receptor.

1 reference

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7 January 2021

Staurosporine causes epidermal growth factor to induce differentiation in PC12 cells via receptor up-regulation

1 reference

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7 January 2021

Staurosporine induces a complete program of terminal differentiation in neoplastic mouse keratinocytes via activation of protein kinase C.

1 reference

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7 January 2021

Staurosporine induces programmed cell death in embryonic neurons and activation of the ceramide pathway.

1 reference

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7 January 2021

Programmed cell death and the control of cell survival: lessons from the nervous system

1 reference

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7 January 2021

A derivative of staurosporine (CGP 41 251) shows selectivity for protein kinase C inhibition and in vitro anti-proliferative as well as in vivo anti-tumor activity

1 reference

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7 January 2021

Staurosporine: An Effective Inhibitor for Ca2+/Calmodulin-Dependent Protein Kinase II

1 reference

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7 January 2021

Different susceptibility of protein kinases to staurosporine inhibition. Kinetic studies and molecular bases for the resistance of protein kinase CK2

1 reference

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7 January 2021

Inhibitors of protein kinase C. 2. Substituted bisindolylmaleimides with improved potency and selectivity

1 reference

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7 January 2021

Crystal structures of catalytic subunit of cAMP-dependent protein kinase in complex with isoquinolinesulfonyl protein kinase inhibitors H7, H8, and H89. Structural implications for selectivity

1 reference

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7 January 2021

High-resolution crystal structures of human cyclin-dependent kinase 2 with and without ATP: bound waters and natural ligand as guides for inhibitor design

1 reference

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7 January 2021

Structural basis for specificity and potency of a flavonoid inhibitor of human CDK2, a cell cycle kinase.

1 reference

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7 January 2021

Structural basis for selectivity of the isoquinoline sulfonamide family of protein kinase inhibitors

1 reference

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7 January 2021

Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors

1 reference

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7 January 2021

A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocket

1 reference

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7 January 2021

Modelling study of protein kinase inhibitors: binding mode of staurosporine and origin of the selectivity of CGP 52411

1 reference

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7 January 2021

Inhibition mechanisms of staurosporine and H7 to cAMP-dependent protein kinase through docking study

1 reference

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7 January 2021

Cloning of the C alpha catalytic subunit of the bovine cAMP-dependent protein kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2897%2900310-9

7 January 2021

Crystal Structure of the Catalytic Subunit of Cyclic Adenosine Monophosphate-Dependent Protein Kinase

1 reference

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7 January 2021

Crystal structure of a polyhistidine-tagged recombinant catalytic subunit of cAMP-dependent protein kinase complexed with the peptide inhibitor PKI(5-24) and adenosine

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2897%2900310-9

7 January 2021

Crystal structure of the catalytic subunit of cAMP-dependent protein kinase complexed with MgATP and peptide inhibitor

1 reference

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7 January 2021

Structure of the mammalian catalytic subunit of cAMP-dependent protein kinase and an inhibitor peptide displays an open conformation

1 reference

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7 January 2021

A binary complex of the catalytic subunit of cAMP-dependent protein kinase and adenosine further defines conformational flexibility

1 reference

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7 January 2021

Crystal structures of the myristylated catalytic subunit of cAMP-dependent protein kinase reveal open and closed conformations

1 reference

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7 January 2021

Protein kinase catalytic domain sequence database: identification of conserved features of primary structure and classification of family members

1 reference

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7 January 2021

2.0 A refined crystal structure of the catalytic subunit of cAMP-dependent protein kinase complexed with a peptide inhibitor and detergent

1 reference

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7 January 2021

Synergistic binding of nucleotides and inhibitors to cAMP-dependent protein kinase examined by acrylodan fluorescence spectroscopy

1 reference

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7 January 2021

Adenosine cyclic 3',5'-monophosphate-dependent protein kinase: Interaction of the catalytic subunit and holoenzyme with lin-benzoadenine nucleotides

1 reference

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7 January 2021

Multiple modes of ligand recognition: crystal structures of cyclin-dependent protein kinase 2 in complex with ATP and two inhibitors, olomoucine and isopentenyladenine

1 reference

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7 January 2021

The glycine-rich sequence of protein kinases: a multifunctional element

1 reference

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7 January 2021

Three-dimensional structure of mammalian casein kinase I: molecular basis for phosphate recognition

1 reference

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7 January 2021

Expression of the catalytic subunit of cAMP-dependent protein kinase in Escherichia coli: multiple isozymes reflect different phosphorylation states.

1 reference

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7 January 2021

In vivo activation of recombinant cAPK catalytic subunit active site mutants by coexpression of the wild-type enzyme, evidence for intermolecular cotranslational phosphorylation

1 reference

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7 January 2021

The CCP4 suite: programs for protein crystallography

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7 January 2021

AMoRe: an automated package for molecular replacement

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7 January 2021

Free R value: a novel statistical quantity for assessing the accuracy of crystal structures

1 reference

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7 January 2021

Accurate bond and angle parameters for X-ray protein structure refinement

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2897%2900310-9

7 January 2021

Improved methods for building protein models in electron density maps and the location of errors in these models

1 reference

https://api.crossref.org/works/10.1016%2FS0969-2126%2897%2900310-9

7 January 2021

X-Ray crystal structure of staurosporine: a new alkaloid from a Streptomyces strain

1 reference

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7 January 2021

Absolute Configuration of Staurosporine By X-Ray Analysis

1 reference

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7 January 2021

10.1016/S0969-2126(97)00310-9

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

9438863

1 reference

Consolidated OpenCitations Corpus – April 2017