scholarly article | Q13442814 |
P2093 | author name string | W Zhu | |
I Stojiljkovic | |||
D J Hunt | |||
A R Richardson | |||
P2860 | cites work | Sequence Analysis of the Genome of the Unicellular Cyanobacterium Synechocystis sp. Strain PCC6803. II. Sequence Determination of the Entire Genome and Assignment of Potential Protein-coding Regions | Q21994433 |
High resolution two-dimensional electrophoresis of proteins | Q24608190 | ||
Use of T7 RNA polymerase to direct expression of cloned genes | Q27860692 | ||
Non-iron metalloporphyrins: potent antibacterial compounds that exploit haem/Hb uptake systems of pathogenic bacteria | Q28370006 | ||
A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive expression of specific genes | Q29547324 | ||
Iron acquisition systems in the pathogenic Neisseria | Q33670869 | ||
Transport of intact porphyrin by HpuAB, the hemoglobin-haptoglobin utilization system of Neisseria meningitidis. | Q33742126 | ||
Hemin uptake system of Yersinia enterocolitica: similarities with other TonB-dependent systems in gram-negative bacteria | Q33938714 | ||
Carbon Monoxide: a Putative Neural Messenger | Q34305648 | ||
Cobalt Induction of Hepatic Heme Oxygenase; with Evidence That Cytochrome P -450 Is Not Essential for This Enzyme Activity | Q35114818 | ||
Identification and purification of a conserved heme-regulated hemoglobin-binding outer membrane protein from Haemophilus ducreyi | Q35398650 | ||
Cloning of a DNA fragment encoding a heme-repressible hemoglobin-binding outer membrane protein from Haemophilus influenzae. | Q35511173 | ||
Ferrochelatase activity and protoporphyrin IX utilization in Haemophilus influenzae | Q35588728 | ||
Iron in Neisseria meningitidis: minimum requirements, effects of limitation, and characteristics of uptake | Q36345057 | ||
Ability of Neisseria gonorrhoeae, Neisseria meningitidis, and commensal Neisseria species to obtain iron from transferrin and iron compounds. | Q36426082 | ||
The enzymatic conversion of heme to bilirubin by microsomal heme oxygenase | Q36475899 | ||
Heme oxygenase 1 is required for mammalian iron reutilization | Q36601831 | ||
Reduced stress defense in heme oxygenase 1-deficient cells. | Q36601994 | ||
The heme oxygenase gene (pbsA) in the red alga Rhodella violacea is discontinuous and transcriptionally activated during iron limitation | Q36617065 | ||
Fur regulon in gram-negative bacteria. Identification and characterization of new iron-regulated Escherichia coli genes by a fur titration assay. | Q36742176 | ||
Carbon monoxide production from heme compounds by bacteria | Q36836326 | ||
Neisseria meningitidis tonB, exbB, and exbD genes: Ton-dependent utilization of protein-bound iron in Neisseriae | Q36843545 | ||
Utilization of host iron sources by Corynebacterium diphtheriae: identification of a gene whose product is homologous to eukaryotic heme oxygenases and is required for acquisition of iron from heme and hemoglobin | Q36843552 | ||
Isolation and characterization of a cDNA from the rat brain that encodes hemoprotein heme oxygenase-3. | Q36878111 | ||
The occurrence of chlamydial and gonococcal salpingitis during the menstrual cycle | Q37903105 | ||
A novel mechanism for upregulation of the Escherichia coli K-12 hmp (flavohaemoglobin) gene by the 'NO releaser', S-nitrosoglutathione: nitrosation of homocysteine and modulation of MetR binding to the glyA-hmp intergenic region. | Q38332558 | ||
Molecular characterization of hpuAB, the haemoglobin-haptoglobin-utilization operon of Neisseria meningitidis | Q38348677 | ||
HmbR outer membrane receptors of pathogenic Neisseria spp.: iron-regulated, hemoglobin-binding proteins with a high level of primary structure conservation | Q38354804 | ||
HmbR, a hemoglobin-binding outer membrane protein of Neisseria meningitidis, undergoes phase variation | Q39494891 | ||
Heme oxygenase: function, multiplicity, regulatory mechanisms, and clinical applications | Q39648092 | ||
Transcription of the Corynebacterium diphtheriae hmuO gene is regulated by iron and heme | Q39831444 | ||
Properties of nonheme iron in a cell envelope fraction from Escherichia coli | Q40096428 | ||
NEISSERIA GONORRHOEAE. I. VIRULENCE GENETICALLY LINKED TO CLONAL VARIATION. | Q40254776 | ||
Pharmaceutics and drug delivery aspects of heme and porphyrin therapy | Q40840313 | ||
Pathogenesis of acute pelvic inflammatory disease: Role of contraception and other risk factors | Q40881100 | ||
Transport of haemin across the cytoplasmic membrane through a haemin-specific periplasmic binding-protein-dependent transport system in Yersinia enterocolitica | Q41498750 | ||
Heme oxygenase (HO-1): His-132 stabilizes a distal water ligand and assists catalysis | Q46078167 | ||
Expression and characterization of a heme oxygenase (Hmu O) from Corynebacterium diphtheriae. Iron acquisition requires oxidative cleavage of the heme macrocycle | Q46466951 | ||
Heme oxygenase active-site residues identified by heme-protein cross-linking during reduction of CBrCl3. | Q46516499 | ||
Metal ion regulation of gene expression. Fur repressor-operator interaction at the promoter region of the aerobactin system of pColV-K30. | Q46857170 | ||
Heme degradation as catalyzed by a recombinant bacterial heme oxygenase (Hmu O) from Corynebacterium diphtheriae | Q47946397 | ||
Phase variation of HpuAB and HmbR, two distinct haemoglobin receptors of Neisseria meningitidis DNM2. | Q47957751 | ||
Differential roles of homologous recombination pathways in Neisseria gonorrhoeae pilin antigenic variation, DNA transformation and DNA repair | Q47977090 | ||
The Neisseria meningitidis haemoglobin receptor: its role in iron utilization and virulence | Q48075145 | ||
A family of small repeated elements with some transposon-like properties in the genome of Neisseria gonorrhoeae | Q48315962 | ||
In vitro insertional mutagenesis with a selectable DNA fragment | Q48387759 | ||
Algal heme oxygenase from Cyanidium caldarium. Partial purification and fractionation into three required protein components. | Q50894735 | ||
Histidine-132 does not stabilize a distal water ligand and is not an important residue for the enzyme activity in heme oxygenase-1. | Q54567522 | ||
Partial purification and reconstitution of the heme oxygenase system from pig spleen microsomes. | Q55061447 | ||
Effect of porphyrins and host iron transport proteins on outer membrane protein expression in Porphyromonas (Bacteroides) gingivalis: identification of a novel 26 kDa hemin-repressible surface protein | Q67506493 | ||
The antibacterial activity of haemin compared with cobalt, zinc and magnesium protoporphyrin and its effect on potassium loss and ultrastructure of Staphylococcus aureus | Q70495872 | ||
Heme-heme oxygenase complex: structure and properties of the catalytic site from resonance Raman scattering | Q72413293 | ||
Insertionally inactivated and inducible recA alleles for use in Neisseria | Q73303146 | ||
Identification of histidine 45 as the axial heme iron ligand of heme oxygenase-2 | Q74192331 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 439-447 | |
P577 | publication date | 2000-01-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Use of heme compounds as iron sources by pathogenic neisseriae requires the product of the hemO gene | |
P478 | volume | 182 |
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Q38823562 | Heme Oxygenases in Cardiovascular Health and Disease |
Q38791019 | Heme Synthesis and Acquisition in Bacterial Pathogens. |
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Q28306266 | Heme oxygenase-1/carbon monoxide: from basic science to therapeutic applications |
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