| scholarly article | Q13442814 |
| P50 | author | Xiaodong Zhang | Q21264874 |
| Hajime Niwa | Q117221960 | ||
| P2093 | author name string | Kosuke Morikawa | |
| Masasuke Yoshida | |||
| Daisuke Tsuchiya | |||
| Ryoji Suno | |||
| P2860 | cites work | The complete genome of the hyperthermophilic bacterium Aquifex aeolicus | Q22122406 |
| Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination | Q26778405 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 575-585 | |
| P577 | publication date | 2006-06-01 | |
| P1433 | published in | Molecular Cell | Q3319468 |
| P1476 | title | Structure of the whole cytosolic region of ATP-dependent protease FtsH. | |
| P478 | volume | 22 |
| Q27678477 | A Novel Family of Soluble Minimal Scaffolds Provides Structural Insight into the Catalytic Domains of Integral Membrane Metallopeptidases |
| Q47324929 | ATP is a driving force in the repair of photosystem II during photoinhibition. |
| Q37687114 | ATP-bound form of the D1 AAA domain inhibits an essential function of Cdc48p/p97. |
| Q27306879 | An FtsH protease is recruited to the mitochondrion of Plasmodium falciparum |
| Q27940248 | An intersubunit signaling network coordinates ATP hydrolysis by m-AAA proteases |
| Q37776304 | Arabidopsis Chloroplast FtsH, var2 and Suppressors of var2 Leaf Variegation: a Review |
| Q34483930 | Architectural switch in plant photosynthetic membranes induced by light stress. |
| Q38193464 | Architecture and function of metallopeptidase catalytic domains |
| Q38120240 | Big steps toward understanding dynein. |
| Q27652542 | Biochemical and Structural Studies of Yeast Vps4 Oligomerization |
| Q91720574 | Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation |
| Q82619781 | Cooperative three-step motions in catalytic subunits of F(1)-ATPase correlate with 80 degrees and 40 degrees substep rotations |
| Q27664441 | Crystal structure of Lon protease: molecular architecture of gated entry to a sequestered degradation chamber |
| Q21142751 | Crystal structure of the ATPase domain of the human AAA+ protein paraplegin/SPG7 |
| Q89186855 | Dissecting Substrate Specificities of the Mitochondrial AFG3L2 Protease |
| Q33581498 | Dissecting the N-ethylmaleimide-sensitive factor: required elements of the N and D1 domains |
| Q27678263 | Dual functions of the Hsm3 protein in chaperoning and scaffolding regulatory particle subunits during the proteasome assembly |
| Q34575754 | Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease |
| Q37166178 | Electron microscopic evidence in support of alpha-solenoid models of proteasomal subunits Rpn1 and Rpn2. |
| Q37961719 | FtsH proteases located in the plant chloroplast |
| Q35310299 | FtsH-dependent processing of RNase colicins D and E3 means that only the cytotoxic domains are imported into the cytoplasm |
| Q54322871 | Hijacking cellular functions for processing and delivery of colicins E3 and D into the cytoplasm. |
| Q36023269 | Membrane proteases in the bacterial protein secretion and quality control pathway |
| Q51018275 | Molecular Mechanism of Substrate Processing by the Cdc48 ATPase Complex. |
| Q33710845 | Multifunctional Mitochondrial AAA Proteases |
| Q34102568 | Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. |
| Q37783446 | New insights into the types and function of proteases in plastids. |
| Q34636507 | Protein degradation within mitochondria: versatile activities of AAA proteases and other peptidases |
| Q90124570 | Proteolysis mediated by the membrane-integrated ATP-dependent protease FtsH has a unique nonlinear dependence on ATP hydrolysis rates |
| Q37956411 | Proteolytic system of plant mitochondria |
| Q37489256 | Quality control of cytoplasmic membrane proteins in Escherichia coli |
| Q38340360 | Quality control of photosystem II: FtsH hexamers are localized near photosystem II at grana for the swift repair of damage |
| Q44788945 | Quality control of photosystem II: direct imaging of the changes in the thylakoid structure and distribution of FtsH proteases in spinach chloroplasts under light stress. |
| Q37948597 | Regulated proteolysis in Gram-negative bacteria--how and when? |
| Q41456400 | Regulation of ribulose-1,5-bisphosphate carboxylase/oxygenase (rubisco) activase: product inhibition, cooperativity, and magnesium activation |
| Q37892093 | Requirements for the catalytic cycle of the N-ethylmaleimide-Sensitive Factor (NSF). |
| Q37231823 | Salt stress inhibits photosystems II and I in cyanobacteria |
| Q54448078 | Sensor I threonine of the AAA+ ATPase transcriptional activator PspF is involved in coupling nucleotide triphosphate hydrolysis to the restructuring of sigma 54-RNA polymerase. |
| Q30377186 | Sequential processing of the Toxoplasma apicoplast membrane protein FtsH1 in topologically distinct domains during intracellular trafficking |
| Q88645890 | Structural basis for disassembly of katanin heterododecamers |
| Q37629892 | Structural changes of the thylakoid membrane network induced by high light stress in plant chloroplasts |
| Q41791766 | Structural characterization of full-length NSF and 20S particles |
| Q45262190 | Structural constraints for protein repair in plant photosynthetic membranes |
| Q37223884 | Structural frameworks for considering microbial protein- and nucleic acid-dependent motor ATPases |
| Q93013129 | Structural insights into ATP hydrolysis by the MoxR ATPase RavA and the LdcI-RavA cage-like complex |
| Q27650383 | Structural studies on Helicobacter pylori ATP-dependent protease, FtsH |
| Q48373223 | Structure of the mitochondrial inner membrane AAA+ protease YME1 gives insight into substrate processing. |
| Q27685291 | Structures of an ATP-independent Lon-like protease and its complexes with covalent inhibitors |
| Q42738109 | Substrate recognition by AAA+ ATPases: distinct substrate binding modes in ATP-dependent protease Yme1 of the mitochondrial intermembrane space |
| Q27677933 | The 2.8 Å crystal structure of the dynein motor domain |
| Q21128663 | The AAA+ superfamily of functionally diverse proteins |
| Q64072136 | The Chloroplast Envelope Protease FTSH11 - Interaction With CPN60 and Identification of Potential Substrates |
| Q42825745 | The FtsH protease heterocomplex in Arabidopsis: dispensability of type-B protease activity for proper chloroplast development |
| Q27658411 | The crystal structure of apo-FtsH reveals domain movements necessary for substrate unfolding and translocation |
| Q28482991 | The hetero-hexameric nature of a chloroplast AAA+ FtsH protease contributes to its thermodynamic stability |
| Q37833811 | The nuts and bolts of ring-translocase structure and mechanism |
| Q27700985 | The structure of Aquifex aeolicus FtsH in the ADP-bound state reveals a C2-symmetric hexamer |
| Q50450330 | The variegated mutants lacking chloroplastic FtsHs are defective in D1 degradation and accumulate reactive oxygen species |
| Q87141513 | Thylakoid FtsH protease contributes to photosystem II and cytochrome b6f remodeling in Chlamydomonas reinhardtii under stress conditions |
| Q42036779 | Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia |
| Q50505494 | Variegated tobacco leaves generated by chloroplast FtsH suppression: implication of FtsH function in the maintenance of thylakoid membranes. |
| Q42976619 | m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria |
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