150 results on '"Dmitriev, Oleg Y."'
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2. At sixes and sevens: cryptic domain in the metal binding chain of the human copper transporter ATP7A
3. The KH domain facilitates the substrate specificity and unwinding processivity of DDX43 helicase
4. Author response: MEMO1 binds iron and modulates iron homeostasis in cancer cells
5. The metal chaperone Atox1 regulates the activity of the human copper transporter ATP7B by modulating domain dynamics
6. Structure of the Subunit c Oligomer in the F1F0 ATP Synthase: Model Derived from Solution Structure of the Monomer and Cross-Linking in the Native Enzyme
7. Nanobodies as Probes for Protein Dynamics in Vitro and in Cells
8. Molecular Architecture of the Copper-Transporting ATPase ATP7B
9. List of Contributors
10. MEMO1 is a Metal Containing Regulator of Iron Homeostasis in Cancer Cells
11. Interactions between Metal-binding Domains Modulate Intracellular Targeting of Cu(I)-ATPase ATP7B, as Revealed by Nanobody Binding
12. Engineered Protein Model of the ATP synthase H+- Channel Shows No Salt Bridge at the Rotor-Stator Interface
13. Molecular Events Initiating Exit of a Copper-transporting ATPase ATP7B from the Trans-Golgi Network
14. Cellular copper levels determine the phenotype of the Arg⁸⁷⁵ variant of ATP7B/Wilson disease protein
15. Interaction with Monomeric Subunit c Drives Insertion of ATP Synthase Subunit a into the Membrane and Primes a-c Complex Formation
16. Difference in Stability of the N-domain Underlies Distinct Intracellular Properties of the E1064A and H1069Q Mutants of Copper-transporting ATPase ATP7B
17. MEMO1 Is a Metal Containing Regulator of Iron Homeostasis in the Cell
18. Mechanism of tumor resistance to cisplatin mediated by the copper transporter ATP7B1
19. Interaction of transmembrane helices in ATP synthase subunit a in solution as revealed by spin label difference NMR
20. Cu(II) and dopamine bind to α-synuclein and cause large conformational changes
21. The Oligomeric Subunit c Rotor in the Fo Sector of ATP Synthase: Unresolved Questions in Our Understanding of Function
22. Structure of Ala24/Asp61 (results in) Asp24/Asn61 substituted subunit c of Escherichia coli ATP synthase: implications for the mechanism of proton transport and rotary movement in the F (sub)o complex
23. Cell-free synthesis of membrane subunits of ATP synthase in phospholipid bicelles: NMR shows subunit a fold similar to the protein in the cell membrane
24. The rigid connecting loop stabilizes hairpin folding of the two helices of the ATP synthase subunit c
25. Chapter 5 - Molecular Architecture of the Copper-Transporting ATPase ATP7B
26. NMR assignment of the Wilson disease associated protein N-domain
27. Subunit a of the E. coli ATP synthase: reconstitution and high resolution NMR with protein purified in a mixed polarity solvent
28. Backbone 1H, 15N and 13C assignments for the subunit a of the E. Coli ATP synthase
29. Mechanics of coupling proton movements to c-ring rotation in ATP synthase
30. Nanobodies against the metal binding domains of ATP7B as tools to study copper transport in the cell
31. Structural model of the transmembrane F o rotary sector of H +-transporting ATP synthase derived by solution NMR and intersubunit cross-linking in situ
32. Coupling proton movements to c-ring rotation in F 1F o ATP synthase: aqueous access channels and helix rotations at the a– c interface
33. Structure of Ala20 → Pro/Pro64 → Ala Substituted Subunit c ofEscherichia coli ATP Synthase in Which the Essential Proline Is Switched between Transmembrane Helices
34. Letter to the Editor: Backbone 1H, 15N and 13C Assignments for the Subunit a of the E. Coli ATP Synthase
35. Defining the Domain of Binding of F1 Subunit ε with the Polar Loop of F0 Subunit c in theEscherichia coli ATP Synthase
36. Function and regulation of human copper-transporting ATPases
37. The Structure of Metal Binding Domain 1 of the Copper Transporter ATP7B Reveals Mechanism of a Singular Wilson Disease Mutation
38. Binding of Copper and Cisplatin to Atox1 Is Mediated by Glutathione through the Formation of Metal–Sulfur Clusters
39. Dynamics of the metal binding domains and regulation of the human copper transporters ATP7B and ATP7A
40. Engineered Protein Model of the ATP synthase H+- Channel Shows No Salt Bridge at the Rotor-Stator Interface.
41. One-step amino acid selective isotope labeling of proteins in prototrophic Escherichia coli strains
42. Copper chaperone Atox1 interacts with the metal-binding domain of Wilson's disease protein in cisplatin detoxification
43. Cell-free synthesis of membrane subunits of ATP synthase in phospholipid bicelles: NMR shows subunitafold similar to the protein in the cell membrane
44. Cellular copper levels determine the phenotype of the Arg 875 variant of ATP7B/Wilson disease protein
45. Crystallization and preliminary X-ray studies of the N-domain of the Wilson disease associated protein
46. The soluble metal-binding domain of the copper transporter ATP7B binds and detoxifies cisplatin
47. Subunitaof theE. coliATP synthase: reconstitution and high resolution NMR with protein purified in a mixed polarity solvent
48. Mechanics of coupling proton movements toc-ring rotation in ATP synthase
49. Structural model of the transmembrane Fo rotary sector of H+-transporting ATP synthase derived by solution NMR and intersubunit cross-linking in situ
50. Coupling proton movements to c-ring rotation in F1Fo ATP synthase: aqueous access channels and helix rotations at the a–c interface
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