Flavorubredoxin, an inducible catalyst for nitric oxide reduction and detoxification in Escherichia coli.
about
Imidazole antibiotics inhibit the nitric oxide dioxygenase function of microbial flavohemoglobin.Bacterial flavohemoglobin: a molecular tool to probe mammalian nitric oxide biologyWidespread distribution in pathogenic bacteria of di-iron proteins that repair oxidative and nitrosative damage to iron-sulfur centersThe O2-scavenging flavodiiron protein in the human parasite Giardia intestinalisHistidine ligand variants of a flavo-diiron protein: effects on structure and activitiesTranscriptional regulation of bacterial virulence gene expression by molecular oxygen and nitric oxideReductive dioxygen scavenging by flavo-diiron proteins of Clostridium acetobutylicumNitric oxide scavenging and detoxification by the Mycobacterium tuberculosis haemoglobin, HbN in Escherichia coliA kinetic platform to determine the fate of nitric oxide in Escherichia coliHemoglobin: a nitric-oxide dioxygenaseThe yjeB (nsrR) gene of Escherichia coli encodes a nitric oxide-sensitive transcriptional regulator.Identification of Histoplasma capsulatum transcripts induced in response to reactive nitrogen species.Two-pronged survival strategy for the major cystic fibrosis pathogen, Pseudomonas aeruginosa, lacking the capacity to degrade nitric oxide during anaerobic respiration.Essential roles of three enhancer sites in sigma54-dependent transcription by the nitric oxide sensing regulatory protein NorR.Nitric oxide and nitrous oxide turnover in natural and engineered microbial communities: biological pathways, chemical reactions, and novel technologies.The transcriptional repressor protein NsrR senses nitric oxide directly via a [2Fe-2S] cluster.Analysis of the genome of the Escherichia coli O157:H7 2006 spinach-associated outbreak isolate indicates candidate genes that may enhance virulence.Global analysis of extracytoplasmic stress signaling in Escherichia coli.In vitro reconstitution of an NADPH-dependent superoxide reduction pathway from Pyrococcus furiosus.Iron-based redox switches in biology.Neuroglobin, nitric oxide, and oxygen: functional pathways and conformational changesHeme-biosynthetic porphobilinogen deaminase protects Aspergillus nidulans from nitrosative stressBioinspired heme, heme/nonheme diiron, heme/copper, and inorganic NOx chemistry: *NO((g)) oxidation, peroxynitrite-metal chemistry, and *NO((g)) reductive coupling.Insights into the nitric oxide reductase mechanism of flavodiiron proteins from a flavin-free enzymeLight-induced N₂O production from a non-heme iron-nitrosyl dimer.Vibrio fischeri flavohaemoglobin protects against nitric oxide during initiation of the squid-Vibrio symbiosis.Direct inhibition by nitric oxide of the transcriptional ferric uptake regulation protein via nitrosylation of the ironSpectroscopic characterization of heme iron-nitrosyl species and their role in NO reductase mechanisms in diiron proteins.Domain architectures of sigma54-dependent transcriptional activatorsNO-inducible nitrosothionein mediates NO removal in tandem with thioredoxin.Prominent roles of the NorR and Fur regulators in the Escherichia coli transcriptional response to reactive nitrogen species.Bacterial hemoglobins and flavohemoglobins: versatile proteins and their impact on microbiology and biotechnology.Peroxidase activity and involvement in the oxidative stress response of roseobacter denitrificans truncated hemoglobin.Nitric oxide in chemostat-cultured Escherichia coli is sensed by Fnr and other global regulators: unaltered methionine biosynthesis indicates lack of S nitrosation.Thiols in nitric oxide synthase-containing Nocardia sp. strain NRRL 5646.Integrated network analysis identifies nitric oxide response networks and dihydroxyacid dehydratase as a crucial target in Escherichia coli.Mechanisms of resistance to oxidative and nitrosative stress: implications for fungal survival in mammalian hostsVibrational analysis of mononitrosyl complexes in hemerythrin and flavodiiron proteins: relevance to detoxifying NO reductase.Inactivation of a single gene enables microaerobic growth of the obligate anaerobe Bacteroides fragilis.The NsrR regulon in nitrosative stress resistance of Salmonella enterica serovar Typhimurium
P2860
Q24523649-DF9D7D3E-F14D-41B2-8EAE-19F15608B06AQ24633608-99ADBAEE-241E-4692-8CCE-4754AD54A6DEQ24657985-4902CD56-5834-42E3-BB02-C4FF60ACB769Q27649309-0AEBAA5B-C8F8-4560-A60F-B249ABCB502AQ27673398-1CDC89BA-A625-4840-A41E-F94D33F1876CQ28083166-C02C486D-3B0E-41B5-B74A-85448DCD4E9BQ28485888-2FCBB17D-2DB3-4F4C-8779-E4E5DC26AF4BQ28486473-2883874D-EBCE-4044-A4CE-FD3C9B08E73EQ28487462-3686F204-6F13-44F6-9B4C-CFB17BBAD5C0Q28661723-4082D124-641E-49CA-9FEE-7A32AD6106A0Q28768625-01EBC874-D5CF-4BE1-BF8A-1A6F9DBA16B7Q28769317-8C035D1A-12E7-4A5F-B7EA-8AEE22EB72EBQ30441279-879F2316-C8F6-4277-B721-BC71420D790BQ30493456-08BF4DFF-4F45-4DAA-8501-01245C94A01AQ31105894-A6ACABFC-E535-46C0-93CC-3C15B279A9B9Q33383198-F617905A-71F3-4F09-A453-823D5C0BA5BCQ33385189-320D6C8B-2241-4AD1-AF4B-15E00EFCB38FQ33504535-DD92A7C9-FB0A-4B4A-AC56-4DB7315BE1FFQ33716403-50D09E77-F85A-4761-9CFE-87936E5AAE7EQ33741265-C50857DE-210D-4DD0-8614-4D55C59B277DQ33853801-DF682B1D-83E5-4738-A61C-00DB24DF0D62Q34061870-05534D29-0A67-41D0-8AEB-9E5C97AFA817Q34062209-AC3F020D-F704-4719-820D-B331D60D9CB1Q34071881-456112AB-4F1A-427D-98E0-CED9972BE716Q34160488-9A6466DC-F23A-4610-9582-663A12540BA2Q34297716-A4B496F7-349C-440D-8072-A60073A566E2Q34429282-45C357A1-3FDD-498A-A6A9-83CEBB149B50Q34528275-A00F0F6B-3AC1-4CBB-A34E-E2EA032EDB4EQ34768956-C23ED092-1EF1-4043-A0AB-B0A0CEEF3AFCQ34954350-A44C169E-D807-4115-9975-C6F5CC02CB16Q35554051-4126B9DD-AC52-4CB0-B2A4-9FD9D6F20BCEQ35556410-9F63B6C3-B4DD-4461-8F0D-F8CA076C9F15Q35556614-5E4E5329-81C8-418D-BE75-3BF4282CA4D1Q35759462-E17045A1-671A-45F3-A80F-F3D8DAC1DD4AQ35844339-59A020C9-B52E-4ED0-9FAA-2A0A6ED47B33Q35850236-63E396FD-576E-451B-A161-C1FEA7A05697Q35859750-D6F19723-518C-4371-8142-9999A68D55ADQ35911051-AF6CBF7E-F622-4655-BEE2-B5AD1364A1B4Q36132768-12DDE69E-D9E4-4975-AEBF-7D1B55312457Q36223343-1BE33007-6E68-446E-9ADC-954DBD0853E7
P2860
Flavorubredoxin, an inducible catalyst for nitric oxide reduction and detoxification in Escherichia coli.
description
2001 nî lūn-bûn
@nan
2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@ast
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@en
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@nl
type
label
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@ast
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@en
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@nl
prefLabel
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@ast
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@en
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@nl
P2093
P2860
P356
P1476
Flavorubredoxin, an inducible ...... ification in Escherichia coli.
@en
P2093
Anne M Gardner
Paul R Gardner
Ryan A Helmick
P2860
P304
P356
10.1074/JBC.M110471200
P407
P577
2001-12-18T00:00:00Z