246 results on '"Ding, Huangen"'
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2. Iron–sulfur cluster assembly scaffold protein IscU is required for activation of ferric uptake regulator (Fur) in Escherichiacoli
3. Ferric uptake regulator (Fur) binds a [2Fe-2S] cluster to regulate intracellular iron homeostasis in Escherichia coli
4. Ferric uptake regulators (Fur) from Vibriocholerae and Helicobacterpylori bind a [2Fe–2S] cluster in response to elevation of intracellular free iron content
5. Electron transfer activity of the nanodisc-bound mitochondrial outer membrane protein mitoNEET
6. Ferric uptake regulator (Fur) reversibly binds a [2Fe-2S] cluster to sense intracellular iron homeostasis in Escherichia coli
7. Exploring the FMN binding site in the mitochondrial outer membrane protein mitoNEET
8. Light-induced release of nitric oxide from the nitric oxide-bound CDGSH-type [2Fe–2S] clusters in mitochondrial protein Miner2
9. Electron transfer kinetics of the mitochondrial outer membrane protein mitoNEET
10. The mitochondrial outer membrane protein mitoNEET is a redox enzyme catalyzing electron transfer from FMNH2 to oxygen or ubiquinone
11. Direct Nitric Oxide Signal Transduction via Nitrosylation of Iron-Sulfur Centers in the SoxR Transcription Activator
12. Binding of Nitric Oxide in CDGSH-type [2Fe-2S] Clusters of the Human Mitochondrial Protein Miner2
13. Flavin nucleotides act as electron shuttles mediating reduction of the [2Fe-2S] clusters in mitochondrial outer membrane protein mitoNEET
14. In vivo Kinetics of a Redox-Regulated Transcriptional Switch
15. Glutathione-Mediated Destabilization in vitro of [2Fe-2S] Centers in the SoxR Regulatory Protein
16. Deletion of the Proposed Iron Chaperones IscA/SufA Results in Accumulation of a Red Intermediate Cysteine Desulfurase IscS in Escherichia coli
17. Reduction of mitochondrial protein mitoNEET [2Fe–2S] clusters by human glutathione reductase
18. Redox Control of Human Mitochondrial Outer Membrane Protein MitoNEET [2Fe-2S] Clusters by Biological Thiols and Hydrogen Peroxide
19. Nitric Oxide reversibly inhibits the redox transition of the [2Fe-2S] cluster in the mitochondrial outer membrane protein mitoNEET
20. Nitric oxide reversibly binds the reduced [2Fe-2S] cluster in mitochondrial outer membrane protein mitoNEET and inhibits its electron transfer activity
21. Iron-Sulfur Clusters and Proteins
22. Iron–sulfur proteins are the major source of protein-bound dinitrosyl iron complexes formed in Escherichia coli cells under nitric oxide stress
23. Ferric Uptake Regulator (Fur) Regulates Intracellular Iron Homeostasis via reversible binding of a [2Fe‐2S] cluster in Escherichia coli
24. Ferric uptake regulators (Fur) from Vibrio cholerae and Helicobacter pylori bind a [2Fe–2S] cluster in response to elevation of intracellular free iron content
25. Iron and zinc binding activity of Escherichia coli topoisomerase I homolog YrdD
26. Oxygen is required for the l-cysteine-mediated decomposition of protein-bound dinitrosyl–iron complexes
27. Redox Control of the DNA Damage-inducible Protein DinG Helicase Activity via Its Iron-Sulfur Cluster
28. Competition of zinc ion for the [2Fe–2S] cluster binding site in the diabetes drug target protein mitoNEET
29. Escherichia coli topoisomerase I is an iron and zinc binding protein
30. Redox Control of Mitochondrial Outer Membrane Protein MitoNEET Iron-Sulfur Clusters: 341
31. Dynamic Metabolism of Iron-Sulfur Proteins in Response to Nitric Oxide in Rat Heart Muscle Cells: 2
32. Copper binding in IscA inhibits iron-sulphur cluster assembly in Escherichia coli
33. Escherichia coli FtnA acts as an iron buffer for re-assembly of iron–sulfur clusters in response to hydrogen peroxide stress
34. Distinct Iron Binding Property of Two Putative Iron Donors for the Iron-Sulfur Cluster Assembly: IscA AND THE BACTERIAL FRATAXIN ORTHOLOG CyaY UNDER PHYSIOLOGICAL AND OXIDATIVE STRESS CONDITIONS
35. Regulation of the Mitochondrial Protein mitoNEET [2Fe-2S] Cluster by Nitric Oxide: 211
36. Interplay of IscA and IscU in Biogenesis of Iron-Sulfur Clusters
37. Harnessing toxic reactions to signal stress: reactions of nitric oxide with iron–sulfur centers and the informative case of SoxR protein
38. Iron-sulfur Proteins Comprise the Major Source of Protein-bound Dinitrosyl Iron Complexes Formed in Escherichia coli Cells under Nitric Oxide Stress: 306
39. Cellular Repair Mechanism for Protein-Bound Dinitrosyl Iron Complexes: 296
40. Thioredoxin Reductase System Mediates Iron Binding in IscA and Iron Delivery for the Iron-Sulfur Cluster Assembly in IscU*
41. Nitric oxide-induced bacteriostasis and modification of iron-sulphur proteins in Escherichia coli
42. Specifically Inactivation of Aconitase B by NO and Cellular Repair in E.coli: 66
43. Escherichia coli Ferritin A Functions in Both Oxidative Stress Response and Re-Assembly of Iron-Sulfur Clusters: 29
44. Thiol-mediated disassembly and reassembly of (2Fe-2S) clusters in the redox-regulated transcription factor SoxR
45. [35] Escherichia coli SoxR protein: Sensor/transducer of oxidative stress and nitric oxide
46. Redox signal transduction via iron-sulfur clusters in the SoxR transcription activator
47. Redox signal transduction: mutations shifting [2Fe-2S] centers of the SoxR sensor-regulator to the oxidized form
48. CELLULAR REPAIR ACTIVITY FOR THE PROTEIN-BOUND DINITROSYL IRON COMPLEXES: 286
49. IscA Mediates Iron Delivery for Assembly of Iron-Sulfur Clusters in IscU under the Limited Accessible Free Iron Conditions
50. 9. Transcriptional regulation via redox-sensitive iron-sulphur centres in an oxidative stress response
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