review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0968-0004(00)01589-9 |
P698 | PubMed publication ID | 10916152 |
P2093 | author name string | Kispal G | |
Lill R | |||
P2860 | cites work | Targeting of a human iron-sulfur cluster assembly enzyme, nifs, to different subcellular compartments is regulated through alternative AUG utilization | Q22008653 |
The genome sequence of Rickettsia prowazekii and the origin of mitochondria | Q22122428 | ||
Cysteine desulfurase activity indicates a role for NIFS in metallocluster biosynthesis | Q24563237 | ||
Molecular control of vertebrate iron metabolism: mRNA-based regulatory circuits operated by iron, nitric oxide, and oxidative stress | Q24630216 | ||
Structure of a NifS homologue: X-ray structure analysis of CsdB, an Escherichia coli counterpart of mammalian selenocysteine lyase | Q27621507 | ||
Crystal structure of a NifS-like protein from Thermotoga maritima: implications for iron sulphur cluster assembly | Q27621752 | ||
Crystal structure of the cystine C-S lyase from Synechocystis: stabilization of cysteine persulfide for FeS cluster biosynthesis | Q27622181 | ||
The ABC transporter Atm1p is required for mitochondrial iron homeostasis | Q27930511 | ||
The mitochondrial proteins Atm1p and Nfs1p are essential for biogenesis of cytosolic Fe/S proteins | Q27930939 | ||
YAH1 of Saccharomyces cerevisiae: a new essential gene that codes for a protein homologous to human adrenodoxin. | Q27931131 | ||
Characterization of recombinant adrenodoxin reductase homologue (Arh1p) from yeast. Implication in in vitro cytochrome p45011beta monooxygenase system | Q27931350 | ||
Isa1p is a component of the mitochondrial machinery for maturation of cellular iron-sulfur proteins and requires conserved cysteine residues for function | Q27932548 | ||
Role of Saccharomyces cerevisiae ISA1 and ISA2 in iron homeostasis | Q27932926 | ||
Mitochondrial Isa2p plays a crucial role in the maturation of cellular iron-sulfur proteins | Q27933489 | ||
A mitochondrial ferredoxin is essential for biogenesis of cellular iron-sulfur proteins | Q27934289 | ||
The cold sensitivity of a mutant of Saccharomyces cerevisiae lacking a mitochondrial heat shock protein 70 is suppressed by loss of mitochondrial DNA. | Q27935128 | ||
Suppressors of superoxide dismutase (SOD1) deficiency in Saccharomyces cerevisiae. Identification of proteins predicted to mediate iron-sulfur cluster assembly | Q27935180 | ||
Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin | Q27935734 | ||
Yeast mitochondrial protein, Nfs1p, coordinately regulates iron-sulfur cluster proteins, cellular iron uptake, and iron distribution | Q27935828 | ||
Saccharomyces cerevisiae ISU1 and ISU2: members of a well-conserved gene family for iron-sulfur cluster assembly | Q27936186 | ||
Mt-Hsp70 homolog, Ssc2p, required for maturation of yeast frataxin and mitochondrial iron homeostasis | Q27936400 | ||
Evidence for a conserved system for iron metabolism in the mitochondria of Saccharomyces cerevisiae | Q27936874 | ||
Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A) | Q28117190 | ||
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia | Q28250989 | ||
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion | Q28275699 | ||
cDNA cloning and characterization of mouse nifS-like protein, m-Nfs1: mitochondrial localization of eukaryotic NifS-like proteins | Q28584700 | ||
Identification of a human mitochondrial ABC transporter, the functional orthologue of yeast Atm1p | Q28609294 | ||
NifS-directed assembly of a transient [2Fe-2S] cluster within the NifU protein | Q28646400 | ||
The essential role of mitochondria in the biogenesis of cellular iron-sulfur proteins | Q33793010 | ||
Mitochondrial iron metabolism in the yeast Saccharomyces cerevisiae | Q33793016 | ||
Nitrogenase metalloclusters: structures, organization, and synthesis | Q36123210 | ||
Steroidogenic electron transport in adrenal cortex mitochondria | Q40336827 | ||
Nitrogenase structure and function: a biochemical-genetic perspective | Q40945164 | ||
Functional assignment of the ORF2-iscS-iscU-iscA-hscB-hscA-fdx-ORF3 gene cluster involved in the assembly of Fe-S clusters in Escherichia coli | Q42612860 | ||
Assembly of iron-sulfur clusters. Identification of an iscSUA-hscBA-fdx gene cluster from Azotobacter vinelandii | Q42677490 | ||
Evidence for cysteine persulfide as reaction product of L-Cyst(e)ine C-S-lyase (C-DES) from Synechocystis. Analyses using cystine analogues and recombinant C-DES. | Q42688762 | ||
Mechanism for the desulfurization of L-cysteine catalyzed by the nifS gene product | Q45089404 | ||
POSTTRANSLATIONAL ASSEMBLY OF PHOTOSYNTHETIC METALLOPROTEINS. | Q46777561 | ||
Deletion of the yeast homologue of the human gene associated with Friedreich's ataxia elicits iron accumulation in mitochondria | Q48047307 | ||
A novel L-cysteine/cystine C-S-lyase directing [2Fe-2S] cluster formation of Synechocystis ferredoxin | Q48050983 | ||
Role of a NifS-like protein from the cyanobacterium Synechocystis PCC 6803 in the maturation of FeS proteins. | Q53915304 | ||
nifU gene product from Azotobacter vinelandii is a homodimer that contains two identical [2Fe-2S] clusters. | Q54623946 | ||
Modular organization and identification of a mononuclear iron-binding site within the NifU protein | Q73810537 | ||
ARH1 of Saccharomyces cerevisiae: a new essential gene that codes for a protein homologous to the human adrenodoxin reductase | Q77567864 | ||
Low iron concentration and aconitase deficiency in a yeast frataxin homologue deficient strain | Q78155068 | ||
P433 | issue | 8 | |
P921 | main subject | mitochondrion | Q39572 |
P1104 | number of pages | 5 | |
P304 | page(s) | 352-356 | |
P577 | publication date | 2000-08-01 | |
P1433 | published in | Trends in Biochemical Sciences | Q1565711 |
P1476 | title | Maturation of cellular Fe-S proteins: an essential function of mitochondria | |
P478 | volume | 25 |
Q57246532 | 19 Analysis of Gene Function of Mitochondria |
Q58697245 | A Cultural Algorithm for the Representation of Mitochondrial Population |
Q28828950 | A New Tessera into the Interactome of the isc Operon: A Novel Interaction between HscB and IscS |
Q40455795 | A Northwestern blotting approach for studying iron regulatory element-binding proteins. |
Q42597188 | A dimer of the FeS cluster biosynthesis protein IscA from cyanobacteria binds a [2Fe2S] cluster between two protomers and transfers it to [2Fe2S] and [4Fe4S] apo proteins |
Q28218819 | A mitochondrial remnant in the microsporidian Trachipleistophora hominis |
Q49168459 | A mutation of the mitochondrial ABC transporter Sta1 leads to dwarfism and chlorosis in the Arabidopsis mutant starik. |
Q24685689 | A novel eukaryotic factor for cytosolic Fe-S cluster assembly |
Q27932490 | A specific role of the yeast mitochondrial carriers MRS3/4p in mitochondrial iron acquisition under iron-limiting conditions |
Q34022567 | A tribute to sulfur |
Q48167404 | ACCUMULATION OF PHOTOSYSTEM ONE1, a member of a novel gene family, is required for accumulation of [4Fe-4S] cluster-containing chloroplast complexes and antenna proteins. |
Q36476001 | ALR and liver regeneration |
Q36703656 | Acknowledging selection at sub-organismal levels resolves controversy on pro-cooperation mechanisms |
Q64917807 | An Entamoeba-Specific Mitosomal Membrane Protein with Potential Association to the Golgi Apparatus. |
Q28554805 | An Interactome-Centered Protein Discovery Approach Reveals Novel Components Involved in Mitosome Function and Homeostasis in Giardia lamblia |
Q27938563 | An essential function of the mitochondrial sulfhydryl oxidase Erv1p/ALR in the maturation of cytosolic Fe/S proteins |
Q27939048 | An interaction between frataxin and Isu1/Nfs1 that is crucial for Fe/S cluster synthesis on Isu1. |
Q46454744 | Analysis of Paracoccidioides lutzii mitochondria: a proteomic approach. |
Q35937989 | Assembling the mitochondrial outer membrane |
Q41885896 | AtNAP1 represents an atypical SufB protein in Arabidopsis plastids |
Q34837031 | AtNAP7 is a plastidic SufC-like ATP-binding cassette/ATPase essential for Arabidopsis embryogenesis. |
Q42971518 | AtSufE is an essential activator of plastidic and mitochondrial desulfurases in Arabidopsis |
Q27933759 | Biochemical characterization of yeast mitochondrial Grx5 monothiol glutaredoxin. |
Q27939225 | Biogenesis of cytosolic ribosomes requires the essential iron-sulphur protein Rli1p and mitochondria |
Q36239823 | Biogenesis of iron-sulfur proteins in eukaryotes: components, mechanism and pathology |
Q34804474 | Biogenesis of iron-sulphur clusters in amitochondriate and apicomplexan protists |
Q51733067 | Chapter 15 Isolation of Saccharomyces cerevisiae mitochondria for Mössbauer, EPR, and electronic absorption spectroscopic analyses. |
Q38302461 | Characterization of Arabidopsis thaliana SufE2 and SufE3: functions in chloroplast iron-sulfur cluster assembly and Nad synthesis. |
Q44213653 | Characterization of a NifS-like chloroplast protein from Arabidopsis. Implications for its role in sulfur and selenium metabolism |
Q24529525 | Characterization of human glutaredoxin 2 as iron-sulfur protein: a possible role as redox sensor |
Q41839849 | Characterization of iron binding in IscA, an ancient iron-sulphur cluster assembly protein |
Q27936228 | Characterization of iron-sulfur protein assembly in isolated mitochondria. A requirement for ATP, NADH, and reduced iron |
Q44599887 | Characterization of the Soluble Domain of the ABC7 Type Transporter Atm1 |
Q35720434 | Chloroplast iron-sulfur cluster protein maturation requires the essential cysteine desulfurase CpNifS |
Q46548895 | Compensation for a defective interaction of the hsp70 ssq1 with the mitochondrial Fe-S cluster scaffold isu. |
Q27931231 | Components involved in assembly and dislocation of iron-sulfur clusters on the scaffold protein Isu1p |
Q46925586 | CpSufE activates the cysteine desulfurase CpNifS for chloroplastic Fe-S cluster formation. |
Q31154352 | Cryptosporidium parvum Cpn60 targets a relict organelle |
Q34444269 | Deficiency of glutaredoxin 5 reveals Fe-S clusters are required for vertebrate haem synthesis |
Q36154260 | Degenerate mitochondria |
Q36119106 | Dynamic subcompartmentalization of the mitochondrial inner membrane |
Q28191465 | Electrochemical behaviour of human adrenodoxin on a pyrolytic graphite electrode |
Q27008081 | Erythroid heme biosynthesis and its disorders |
Q34989379 | Eukaryotic genomes contain a [2Fez.sbnd;2S] ferredoxin isoform with a conserved C-terminal sequence motif |
Q36748734 | Evolution and cellular function of monothiol glutaredoxins: involvement in iron-sulphur cluster assembly. |
Q34646440 | Evolution of intracellular compartmentalization. |
Q44653693 | Evolutionary biology: essence of mitochondria. |
Q33301160 | Expression, purification, and characterization of a [Fe2S2] cluster containing ferredoxin from Acidithiobacillus ferrooxidans |
Q55408572 | Fe-S cluster assembly in the supergroup Excavata. |
Q33952565 | Feedback regulation of iron-sulfur cluster biosynthesis |
Q30556364 | Female and male gamete mitochondria are distinct and complementary in transcription, structure, and genome function |
Q28361124 | Ferredoxin reductase affects p53-dependent, 5-fluorouracil-induced apoptosis in colorectal cancer cells |
Q28216801 | Ferritin, iron homeostasis, and oxidative damage |
Q35526990 | Formation of hydrogen sulfide from cysteine in Saccharomyces cerevisiae BY4742: genome wide screen reveals a central role of the vacuole |
Q42263212 | Frataxin, a conserved mitochondrial protein, in the hydrogenosome of Trichomonas vaginalis |
Q35613137 | Friedreich ataxia-update on pathogenesis and possible therapies |
Q78747075 | Friedreich's ataxia |
Q30620822 | From data towards knowledge: revealing the architecture of signaling systems by unifying knowledge mining and data mining of systematic perturbation data |
Q47914805 | Functional and molecular characterization of the frataxin homolog from Arabidopsis thaliana. |
Q24556663 | Functional link between ribosome formation and biogenesis of iron-sulfur proteins |
Q33617940 | Functions and cellular localization of cysteine desulfurase and selenocysteine lyase in Trypanosoma brucei |
Q28264035 | Genetic instability in budding and fission yeast-sources and mechanisms |
Q22122366 | Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi |
Q24534322 | Giardia mitosomes and trichomonad hydrogenosomes share a common mode of protein targeting |
Q64057955 | Glia maturation factor-γ regulates murine macrophage iron metabolism and M2 polarization through mitochondrial ROS |
Q35216696 | Glutathione reductase and a mitochondrial thioredoxin play overlapping roles in maintaining iron-sulfur enzymes in fission yeast |
Q35910500 | Glutathione-coordinated [2Fe-2S] cluster: a viable physiological substrate for mitochondrial ABCB7 transport |
Q59262067 | GroEL-assisted refolding of adrenodoxin during chemical cluster insertion |
Q27934525 | Grx5 is a mitochondrial glutaredoxin required for the activity of iron/sulfur enzymes |
Q35817466 | HSC20 interacts with frataxin and is involved in iron-sulfur cluster biogenesis and iron homeostasis |
Q42724594 | High-level mitochondriology at high altitude. Workshop on mitochondrial (dys-)function |
Q42123490 | Homology of SMP domains to the TULIP superfamily of lipid-binding proteins provides a structural basis for lipid exchange between ER and mitochondria |
Q36284729 | How Escherichia coli and Saccharomyces cerevisiae build Fe/S proteins. |
Q37698326 | How do yeast sense mitochondrial dysfunction? |
Q40738268 | Human mitochondrial ferritin expressed in HeLa cells incorporates iron and affects cellular iron metabolism |
Q34991115 | Hydrogenosomes in the diplomonad Spironucleus salmonicida |
Q40634129 | Identification and molecular characterization of mitochondrial ferredoxins and ferredoxin reductase from Arabidopsis |
Q46230543 | Impact of season on liver mitochondrial oxidative stress and the expression of HSP70 in grey mullets from contaminated estuary |
Q34278670 | Interaction between Nbp35 and Cfd1 proteins of cytosolic Fe-S cluster assembly reveals a stable complex formation in Entamoeba histolytica |
Q35543759 | Iron Transport and Signaling in Plants |
Q47923323 | Iron-Sulfur Protein Assembly in Human Cells |
Q37795588 | Iron-Sulfur World in Aerobic and Hyperthermoacidophilic ArchaeaSulfolobus |
Q48138152 | Iron-sulfur cluster biogenesis in chloroplasts. Involvement of the scaffold protein CpIscA. |
Q36331495 | Iron-sulfur cluster biosynthesis in photosynthetic organisms |
Q36488119 | Iron-sulfur cluster synthesis, iron homeostasis and oxidative stress in Friedreich ataxia |
Q24309526 | Iron-sulfur protein maturation in human cells: evidence for a function of frataxin |
Q34407914 | Iron-sulphur cluster biogenesis and mitochondrial iron homeostasis |
Q37201453 | Is cancer a severe delayed hypersensitivity reaction and histamine a blueprint? |
Q34084359 | Jac1, a mitochondrial J-type chaperone, is involved in the biogenesis of Fe/S clusters in Saccharomyces cerevisiae |
Q58032914 | Knock-downs of Iron-Sulfur Cluster Assembly Proteins IscS and IscU Down-regulate the Active Mitochondrion of ProcyclicTrypanosoma brucei |
Q39703195 | Lack of the ApbC or ApbE protein results in a defect in Fe-S cluster metabolism in Salmonella enterica serovar Typhimurium |
Q28611246 | Leucine biosynthesis in fungi: entering metabolism through the back door |
Q28270882 | Localization and functionality of microsporidian iron-sulphur cluster assembly proteins |
Q73699104 | MDL1 is a high copy suppressor of ATM1: evidence for a role in resistance to oxidative stress |
Q27937151 | Maintenance of structure and function of mitochondrial Hsp70 chaperones requires the chaperone Hep1. |
Q43993760 | Maturation of cytosolic iron-sulfur proteins requires glutathione |
Q27933308 | Mdm31 and Mdm32 are inner membrane proteins required for maintenance of mitochondrial shape and stability of mitochondrial DNA nucleoids in yeast |
Q34701880 | Metallochaperones: bind and deliver |
Q37122625 | Methionine sulphoxide reductases protect iron-sulphur clusters from oxidative inactivation in yeast. |
Q30887580 | Mitochondria and hydrogenosomes are two forms of the same fundamental organelle |
Q36558011 | Mitochondria in hematopoiesis and hematological diseases. |
Q34290821 | Mitochondrial ABC transporters |
Q45305353 | Mitochondrial HSP70 cognate-mediated differential expression of JNK1/2 in the pollution stressed grey mullets, Mugil cephalus |
Q44117703 | Mitochondrial Hsp60, resistance to oxidative stress, and the labile iron pool are closely connected in Saccharomyces cerevisiae |
Q34210566 | Mitochondrial complex I from Arabidopsis and rice: orthologs of mammalian and fungal components coupled with plant-specific subunits |
Q27935174 | Mitochondrial ferredoxin is required for heme A synthesis in Saccharomyces cerevisiae |
Q27015737 | Mitochondrial iron-sulfur cluster dysfunction in neurodegenerative disease |
Q38121943 | Mitochondrial pathophysiology in Friedreich's ataxia |
Q28183972 | Mitochondrial remnant organelles of Giardia function in iron-sulphur protein maturation |
Q48342811 | Mitochondrial type iron-sulfur cluster assembly in the amitochondriate eukaryotes Trichomonas vaginalis and Giardia intestinalis, as indicated by the phylogeny of IscS. |
Q36671888 | Mitochondrial-type assembly of FeS centers in the hydrogenosomes of the amitochondriate eukaryote Trichomonas vaginalis |
Q33989995 | Mitochondrion-derived organelles in protists and fungi |
Q37763217 | Mitochondrion-related organelles in eukaryotic protists |
Q51670074 | Mnsod overexpression extends the yeast chronological (G(0)) life span but acts independently of Sir2p histone deacetylase to shorten the replicative life span of dividing cells. |
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Q28676963 | Molecular paleontology and complexity in the last eukaryotic common ancestor |
Q28486420 | Mycobacterium tuberculosis FprA, a novel bacterial NADPH-ferredoxin reductase |
Q35113597 | Niche metabolism in parasitic protozoa |
Q34368406 | Nifs and Sufs in malaria |
Q36557698 | Novel TPR-containing subunit of TOM complex functions as cytosolic receptor for Entamoeba mitosomal transport |
Q27930254 | Nuclear monothiol glutaredoxins of Saccharomyces cerevisiae can function as mitochondrial glutaredoxins |
Q36143730 | One ring to rule them all: trafficking of heme and heme synthesis intermediates in the metazoans |
Q36052586 | Parasite plastids: approaching the endgame |
Q37268020 | Phenotypic characterization and comparative transcriptomics of evolved Saccharomyces cerevisiae strains with improved tolerance to lignocellulosic derived inhibitors |
Q44270146 | Phycocyanobilin:ferredoxin oxidoreductase of Anabaena sp. PCC 7120. Biochemical and spectroscopic. |
Q47447832 | Phylogenetic affinity of aGiardia lambliacysteine desulfurase conforms to canonical pattern of mitochondrial ancestry |
Q51982383 | Phylogenetic analysis of the complete genome sequence of Encephalitozoon cuniculi supports the fungal origin of microsporidia and reveals a high frequency of fast-evolving genes. |
Q34672818 | Progress with parasite plastids |
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Q27658128 | Protein recognition in ferredoxin-P450 electron transfer in the class I CYP199A2 system from Rhodopseudomonas palustris |
Q40728294 | Recycling of RNA binding iron regulatory protein 1 into an aconitase after nitric oxide removal depends on mitochondrial ATP. |
Q38822948 | Redox Modulation Matters: Emerging Functions for Glutaredoxins in Plant Development and Stress Responses |
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Q43875428 | Repair of nitric oxide-modified ferredoxin [2Fe-2S] cluster by cysteine desulfurase (IscS). |
Q27937472 | Role of YHM1, encoding a mitochondrial carrier protein, in iron distribution of yeast |
Q24297460 | Role of human mitochondrial Nfs1 in cytosolic iron-sulfur protein biogenesis and iron regulation |
Q44727107 | Saccharomyces cerevisiae glutaredoxin 5-deficient cells subjected to continuous oxidizing conditions are affected in the expression of specific sets of genes |
Q47657508 | Sequence-specific interaction between mitochondrial Fe-S scaffold protein Isu and Hsp70 Ssq1 is essential for their in vivo function |
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Q40715849 | Structure-function analysis of yeast Grx5 monothiol glutaredoxin defines essential amino acids for the function of the protein. |
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Q27937118 | The Cfd1-Nbp35 complex acts as a scaffold for iron-sulfur protein assembly in the yeast cytosol |
Q27938366 | The Nfs1 interacting protein Isd11 has an essential role in Fe/S cluster biogenesis in mitochondria |
Q53943133 | The PmSOD1 gene of the protistan parasite Perkinsus marinus complements the sod2Delta mutant of Saccharomyces cerevisiae, and directs an iron superoxide dismutase to mitochondria. |
Q34501867 | The Saccharomyces cerevisiae mitochondrial succinate:ubiquinone oxidoreductase |
Q35623933 | The Trichomonas vaginalis hydrogenosome proteome is highly reduced relative to mitochondria, yet complex compared with mitosomes |
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Q45103948 | The chloroplast NifS-like protein of Arabidopsis thaliana is required for iron-sulfur cluster formation in ferredoxin |
Q48101907 | The complete DNA sequence of the mitochondrial genome of the dermatophyte fungus Epidermophyton floccosum |
Q42109299 | The effects of mitochondrial iron homeostasis on cofactor specificity of superoxide dismutase 2. |
Q24556514 | The eukaryotic P loop NTPase Nbp35: an essential component of the cytosolic and nuclear iron-sulfur protein assembly machinery |
Q89930944 | The evolution history of Fe-S cluster A-type assembly protein reveals multiple gene duplication events and essential protein motifs |
Q47644981 | The heme synthesis defect of mutants impaired in mitochondrial iron-sulfur protein biogenesis is caused by reversible inhibition of ferrochelatase |
Q27937584 | The hydrogenase-like Nar1p is essential for maturation of cytosolic and nuclear iron-sulphur proteins |
Q24801265 | The iron-sulfur cluster assembly genes iscS and iscU of Entamoeba histolytica were acquired by horizontal gene transfer |
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