How Biology Handles Nitrite

The isolation of a hexaheme cytochrome from Desulfovibrio desulfuricans and its identification as a new type of nitrite reductase.

Liu, M. C., & Peck, H. D. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)43021-9 · Cited by 157

Expression and evolution of functionally distinct haemoglobin genes in plants

Hunt, P. W., Watts, R. A., Trevaskis, B., Llewellyn, D. J., Burnell, J. N., Dennis, E. S., & Peacock, W. J. (2001) · Plant Molecular Biology · doi:10.1023/a:1012440926982 · Cited by 156

Nitric Oxide and Nitrous Oxide Production by Soybean and Winged Bean during the in Vivo Nitrate Reductase Assay

Dean, J. V., & Harper, J. E. (1986) · PLANT PHYSIOLOGY · doi:10.1104/pp.82.3.718 · Cited by 156

Neuroglobin and cytoglobin overexpression protects human SH-SY5Y neuroblastoma cells against oxidative stress-induced cell death

Fordel, E., Thijs, L., Martinet, W., Lenjou, M., Laufs, T., Bockstaele, D. R. V., Moens, L. J., & Dewilde, S. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.09.027 · Cited by 156

Hunting for Plant Nitric Oxide Synthase Provides New Evidence of a Central Role for Plastids in Nitric Oxide Metabolism

Gas‐Pascual, E., Flores-Pérez, Ú., Sauret-Gueto, S., & Rodrı́guez-Concepción, M. (2009) · The Plant Cell · doi:10.1105/tpc.108.065243 · Cited by 156

Role of myoglobin in the antioxidant defense of the heart

Flögel, U., Gödecke, A., Klotz, L., & Schrader, J. (2004) · The FASEB Journal · doi:10.1096/fj.03-1382fje · Cited by 156

Rapid increase of NO release in plant cell cultures induced by cytokinin

Tun, N. N., Holk, A., & Scherer, G. F. E. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)03164-7 · Cited by 155

The Haemoglobin/Nitric Oxide Cycle: Involvement in Flooding Stress and Effects on Hormone Signalling

Igamberdiev, A. U., Baron, K. N., Manac'h, N., STOIMENOVA, M., & Hill, R. D. (2005) · Annals of Botany · doi:10.1093/aob/mci210 · Cited by 155

A NapC/NirT‐type cytochrome c (NrfH) is the mediator between the quinone pool and the cytochrome c nitrite reductase of Wolinella succinogenes

Simon, J., Groß, R., Einsle, O., Kroneck, P. M. H., Kröger, A., & Klimmek, O. (2000) · Molecular Microbiology · doi:10.1046/j.1365-2958.2000.01742.x · Cited by 155

Tandem Orientation of Duplicated Xanthine Dehydrogenase Genes from Arabidopsis thaliana

Hesberg, C., Hänsch, R., Mendel, R. R., & Bittner, F. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312929200 · Cited by 155

Glucose-6-Phosphate Dehydrogenase Plays a Pivotal Role in Nitric Oxide-Involved Defense Against Oxidative Stress Under Salt Stress in Red Kidney Bean Roots

Liu, Y., Wu, R., Wan, Q., Xie, G., & Bi, Y. (2007) · Plant and Cell Physiology · doi:10.1093/pcp/pcm020 · Cited by 155

Evolution of an octahaem cytochrome c protein family that is key to aerobic and anaerobic ammonia oxidation by bacteria

Klotz, M. G., Schmid, M. C., Strous, M., den Camp, H. J. M. O., Jetten, M. S. M., & Hooper, A. B. (2008) · Environmental Microbiology · doi:10.1111/j.1462-2920.2008.01733.x · Cited by 154

Electronic Structure of Six-Coordinate Iron(III)−Porphyrin NO Adducts: The Elusive Iron(III)−NO(radical) State and Its Influence on the Properties of These Complexes

Praneeth, V. K. K., Paulat, F., Berto, T. C., DeBeer, S., Näther, C., Sulok, C. D., & Lehnert, N. (2008) · Journal of the American Chemical Society · doi:10.1021/ja801860u · Cited by 154

Experiments on muscle haemoglobin in vivo ; the instantaneous measurement of muscle metabolism

Millikan, G. A. (1937) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1937.0052 · Cited by 154

NADH-dependent metabolism of nitric oxide in alfalfa root cultures expressing barley hemoglobin

Igamberdiev, A. U., Sereg�lyes, C., Manac'h, N., & Hill, R. D. (2004) · Planta · doi:10.1007/s00425-003-1192-3 · Cited by 154

Nitric oxide production occurs downstream of reactive oxygen species in guard cells during stomatal closure induced by chitosan in abaxial epidermis of Pisum sativum

Srivastava, N., Gonugunta, V. K., Puli, M. R., & Raghavendra, A. S. (2008) · Planta · doi:10.1007/s00425-008-0855-5 · Cited by 154

Effects of Neuroglobin Overexpression on Acute Brain Injury and Long-Term Outcomes After Focal Cerebral Ischemia

Wang, X., Liu, J., Zhu, H., Tejima, E., Tsuji, K., Murata, Y., Atochin, D. N., Huang, P. L., Zhang, C., & Lo, E. H. (2008) · Stroke · doi:10.1161/strokeaha.107.506022 · Cited by 154

Globins in nonvertebrate species: dispersal by horizontal gene transfer and evolution of the structure-function relationships

Moens, L. J., Vanfleteren, J. R., de Peer, Y. V., Peeters, K., Kapp, O. H., Czeluzniak, J., Goodman, M., Blaxter, M., & Vinogradov, S. N. (1996) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a025592 · Cited by 153

A Structure of the Human Apoptosome at 12.8 Å Resolution Provides Insights into This Cell Death Platform

Yu, X., Acehan, D., Ménétret, J., Booth, C. R., Ludtke, S. J., Riedl, S. J., Shi, Y., Wang, X., & Akey, C. W. (2005) · Structure · doi:10.1016/j.str.2005.09.006 · Cited by 153

Alkane degradation under anoxic conditions by a nitrate‐reducing bacterium with possible involvement of the electron acceptor in substrate activation

Zedelius, J., Rabus, R., Grundmann, O., Werner, I., Brodkorb, D., Schreiber, F., Ehrenreich, P., Behrends, A., Wilkes, H., Kube, M., et al. (2010) · Environmental Microbiology Reports · doi:10.1111/j.1758-2229.2010.00198.x · Cited by 152

Post-translational regulation of nitrate reductase activity: a role for Ca2+ and 14-3-3 proteins

Huber, S. C., Bachmann, M., & Huber, J. L. A. (1996) · Trends in Plant Science · doi:10.1016/s1360-1385(96)10046-7 · Cited by 152

The structure of iron–sulfur proteins

Sticht, H., & ROSCH, P. J. (1998) · Progress in Biophysics and Molecular Biology · doi:10.1016/s0079-6107(98)00027-3 · Cited by 152

Molecular diversity of nitrite reductase genes ( nirK ) in nitrifying bacteria

Cantera, J. L., & Stein, L. Y. (2006) · Environmental Microbiology · doi:10.1111/j.1462-2920.2006.01198.x · Cited by 152

Nitric oxide synthase reduces nitrite to NO under anoxia

Vanin, A. F., Bevers, L. M., Slama-Schwok, A., & van Faassen, E. E. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-006-6374-2 · Cited by 151

An overview of the biological significance of endogenous gases: new roles for old molecules

Li, L., & Moore, P. K. (2007) · Biochemical Society Transactions · doi:10.1042/bst0351138 · Cited by 151

Formation of S-Nitrosothiols via Direct Nucleophilic Nitrosation of Thiols by Peroxynitrite with Elimination of Hydrogen Peroxide

van der Vliet, A., Hoen, P. A. C. ’., Wong, P., Bast, A., & Cross, C. E. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.46.30255 · Cited by 151

Cytochrome c, an ideal antioxidant

Pereverzev, M. O., Vygodina, T. V., Konstantinov, A. A., & Skulachev, V. P. (2003) · Biochemical Society Transactions · doi:10.1042/bst0311312 · Cited by 150

NO Dioxygenase Activity in Hemoglobins Is Ubiquitous In Vitro, but Limited by Reduction In Vivo

Smagghe, B. J., Trent, J. T., & Hargrove, M. S. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002039 · Cited by 150

Apoptosis: checkpoint at the mitochondrial frontier

Bossy‐Wetzel, E., & Green, D. R. (1999) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(99)00032-4 · Cited by 150

Nia1 and Nia2 are Involved in Exogenous Salicylic Acid‐induced Nitric Oxide Generation and Stomatal Closure in Arabidopsis

Hao, F., Shi-Ling, Z. H. A. O., Dong, H., Zhang, H., Sun, L., & Miao, C. (2010) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2010.00920.x · Cited by 149

Peroxisomes as a cellular source of reactive nitrogen species signal molecules

del Río, L. A. (2010) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2010.10.022 · Cited by 149

Control of the redox state of the nicotinamide–adenine dinucleotide couple in rat liver cytoplasm

Stubbs, M., Veech, R. L., & Krebs, H. A. (1972) · Biochemical Journal · doi:10.1042/bj1260059 · Cited by 149

Structural and redox plasticity in the heterodimeric periplasmic nitrate reductase

Arnoux, P., Sabaty, M., Alric, J., Frangioni, B., Guigliarelli, B., Adriano, J.-M., & Pignol, D. (2003) · Nature Structural & Molecular Biology · doi:10.1038/nsb994 · Cited by 149

Growth ofNitrobacterby dissimilatoric nitrate reduction

Freitag, A., Rudert, M., & Bock, E. (1987) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1987.tb02524.x · Cited by 149

Further Evidence that Cytoplasmic Acidosis Is a Determinant of Flooding Intolerance in Plants

Roberts, J. K. M., Andrade, F. H., & Anderson, I. C. (1985) · PLANT PHYSIOLOGY · doi:10.1104/pp.77.2.492 · Cited by 148

Binding and activation of nitrite and nitric oxide by copper nitrite reductase and corresponding model complexes

Merkle, A. C., & Lehnert, N. (2011) · Dalton Transactions · doi:10.1039/c1dt11049g · Cited by 148

Cytochrome c-catalyzed oxidation of organic molecules by hydrogen peroxide

Radí, R., Thomson, L., Rubbo, H., & Prodanov, E. (1991) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(91)90171-e · Cited by 148

Nitrification rates and 15N abundances of N2O and NO3− in the western North Pacific

Yoshida, N., Morimoto, H., Hirano, M., Koike, I., Matsuo, S., Wada, E., Saino, T., & Hattori, A. (1989) · Nature · doi:10.1038/342895a0 · Cited by 148

Ligand binding and protein dynamics in neuroglobin

Kriegl, J. M., Bhattacharyya, A. J., Nienhaus, K., Deng, P., Minkow, O., & Nienhaus, G. U. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.082244399 · Cited by 148

Membrane-bound nitrite oxidoreductase of Nitrobacter: evidence for a nitrate reductase system

Sundermeyer, H., Meyer, W., Warninghoff, B., & Bock, E. (1984) · Archives of Microbiology · doi:10.1007/bf00454918 · Cited by 147

Decreased arginine and nitrite levels in nitrate reductase-deficient Arabidopsis thaliana plants impair nitric oxide synthesis and the hypersensitive response to Pseudomonas syringae

Modolo, L. V., Augusto, O., Almeida, I. M. G., Pinto-Maglio, C. A. F., Oliveira, H. C., Seligman, K., & Salgado, I. (2006) · Plant Science · doi:10.1016/j.plantsci.2006.02.010 · Cited by 147

Concerted Nitric Oxide Formation and Release from the Simultaneous Reactions of Nitrite with Deoxy- and Oxyhemoglobin

Grubina, R., Huang, Z., Shiva, S., Joshi, M. S., Azarov, I., Basu, S., Ringwood, L. A., Jiang, A., Hogg, N., Kim‐Shapiro, D. B., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700546200 · Cited by 147

Cytochrome oxidase as a redox-linked proton pump.

Bg, M. (1992) · PubMed · Cited by 147

Inhibitory Effects of Nitric Oxide on Oxidative Phosphorylation in Plant Mitochondria

Yamasaki, H., Shimoji, H., Ohshiro, Y., & Sakihama, Y. (2001) · Nitric Oxide · doi:10.1006/niox.2001.0353 · Cited by 147

Anammox organism KSU‐1 expresses a NirK‐type copper‐containing nitrite reductase instead of a NirS‐type with cytochrome cd1

Hira, D., Toh, H., Migita, C. T., Okubo, H., Nishiyama, T., Hattori, M., Furukawa, K., & Fujii, T. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.04.041 · Cited by 147

Characterization of the effects of oxygen on xanthine oxidase-mediated nitric oxide formation

Li, H., Samouilov, A., Liu, X., & Zweier, J. L. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m314336200 · Cited by 146

Dietary nitrite and nitrate: a review of potential mechanisms of cardiovascular benefits

Machha, A., & Schechter, A. N. (2011) · European Journal of Nutrition · doi:10.1007/s00394-011-0192-5 · Cited by 146

Nitrate-Nitrite-Nitric Oxide Pathway: Implications for Anesthesiology and Intensive Care

Weitzberg, E., Hezel, M., Lundberg, J. O., & Warner, D. S. (2010) · Anesthesiology · doi:10.1097/aln.0b013e3181fcf3cc · Cited by 145

Ischemia-reperfusion in humans. Appearance of xanthine oxidase activity.

Friedl, H. P., Smith, D. J., Till, G. O., Thomson, P. D., Louis, D. S., & Ward, P. A. (1990) · Europe PMC (PubMed Central) · Cited by 145

Amino acids and gaseous signaling

Li, X., Bazer, F. W., Gao, H., Jobgen, W. S., Johnson, G. A., Li, P., McKnight, J. R., Satterfield, M. C., Spencer, T. E., & Wu, G. (2009) · Amino Acids · doi:10.1007/s00726-009-0264-5 · Cited by 144

Nitrite–nitric oxide control of mitochondrial respiration at the frontier of anoxia

Benamar, A., Rolletschek, H., Borisjuk, L., Avelange‐Macherel, M., Curien, G., Mostefai, H. A., Andriantsitohaina, R., & Macherel, D. (2008) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2008.06.002 · Cited by 144

Reactions of ferrous neuroglobin and cytoglobin with nitrite under anaerobic conditions

Petersen, M. G., Dewilde, S., & Fago, A. (2008) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2008.05.008 · Cited by 144

Endothelial nitric oxide synthase reduces nitrite anions to NO under anoxia

Gautier, C., van Faassen, E., Mikula, I., Martasek, P., & Slama-Schwok, A. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.01.031 · Cited by 143

The reaction of neuroglobin with potential redox protein partners cytochrome b5 and cytochrome c

Fago, A., Mathews, A. J., Moens, L. J., Dewilde, S., & Brittain, T. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.08.003 · Cited by 142

Dietary polyphenols generate nitric oxide from nitrite in the stomach and induce smooth muscle relaxation

Rocha, B. S., Gago, B., Barbosa, R. M., & Laranjinha, J. (2009) · Toxicology · doi:10.1016/j.tox.2009.09.008 · Cited by 142

Cardioprotection and mitochondrial S-nitrosation: Effects of S-nitroso-2-mercaptopropionyl glycine (SNO-MPG) in cardiac ischemia–reperfusion injury

Nadtochiy, S. M., Burwell, L. S., & Brookes, P. S. (2007) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2007.01.010 · Cited by 142

Milk xanthine oxidase type D (dehydrogenase) and type O (oxidase). Purification, interconversion and some properties

Battelli, M. G., Lorenzoni, E., & Stirpe, F. (1973) · Biochemical Journal · doi:10.1042/bj1310191 · Cited by 141

The Kinetics of the Reactions of Leghemoglobin with Oxygen and Carbon Monoxide

Wittenberg, J. B., Appleby, C. A., & Wittenberg, B. A. (1972) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)45734-7 · Cited by 141

Nitrate reductase activation state in barley roots in relation to the energy and carbohydrate status

Botrel, A., & Kaiser, W. M. (1997) · Planta · doi:10.1007/s004250050094 · Cited by 141

Is nitrate reductase a major player in the plant NO (nitric oxide) game?

Meyer, C., Lea, U. S., Provan, F., Kaiser, W. M., & Lillo, C. (2005) · Photosynthesis Research · doi:10.1007/s11120-004-3548-3 · Cited by 141

Functional Coupling of Oxygen Binding and Vasoactivity inS-Nitrosohemoglobin

McMahon, T., Stone, A. E., Bonaventura, J., Singel, D. J., & Stamler, J. S. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m000532200 · Cited by 140

On the virtual existence of superoxide anions in mitochondria: thoughts regarding its role in pathophysiology

Forman, H. J., & Azzi, A. (1997) · The FASEB Journal · doi:10.1096/fasebj.11.5.9141504 · Cited by 139

Acetate Assimilation by Nitrobacter agilis in Relation to Its “Obligate Autotrophy”

Smith, A. J., & Hoare, D. S. (1968) · Journal of Bacteriology · doi:10.1128/jb.95.3.844-855.1968 · Cited by 139

Reactions of Nitric Oxide with Metalloproteins

Radí, R. (1996) · Chemical Research in Toxicology · doi:10.1021/tx950176s · Cited by 139

Stoichiometry of the reaction of oxyhemoglobin with nitrite

Kosaka, H., Imaizumi, K., Imai, K., & Tyuma, I. (1979) · Biochimica et Biophysica Acta (BBA) - Protein Structure · doi:10.1016/0005-2795(79)90235-6 · Cited by 139

Nitrite as a Substrate and Inhibitor of Myeloperoxidase

van Dalen, C. J., Winterbourn, C. C., Senthilmohan, R., & Kettle, A. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.16.11638 · Cited by 139

Characterization of recombinant soybean leghemoglobin a and apolar distal histidine mutants

Hargrove, M. S., Barry, J. K., Brucker, E. A., Berry, M. B., Phillips, G. N., Olson, J. S., Arredondo‐Peter, R., Dean, J., Klucas, R. V., & Sarath, G. (1997) · Journal of Molecular Biology · doi:10.1006/jmbi.1996.0833 · Cited by 139

Coordination structure of the ferric heme iron in engineered distal histidine myoglobin mutants

Ikeda‐Saito, M., Hori, H., Andersson, L. A., Prince, R. C., Pickering, I. J., George, G. N., Sanders, C. R., Lutz, R., McKelvey, E. J., & Mattera, R. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)50024-7 · Cited by 138

Neuronal and endothelium‐derived mediators in the modulation of the gastric microcirculation: integrity in the balance

Whittle, B. J. R. (1993) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1993.tb13763.x · Cited by 138

Functional Analysis of Conserved Aspartate and Histidine Residues Located Around the Type 2 Copper Site of Copper-Containing Nitri Reductase

Kataoka, K., Furusawa, H., Takagi, K., Yamaguchi, K., & Suzuki, S. (2000) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a022613 · Cited by 138

Review: Correlations between oxygen affinity and sequence classifications of plant hemoglobins

Smagghe, B. J., Hoy, J. A., Percifield, R. J., Kundu, S., Hargrove, M. S., Sarath, G., Hilbert, J., Watts, R. A., Dennis, E. S., Peacock, W. J., et al. (2009) · Biopolymers · doi:10.1002/bip.21256 · Cited by 138

Reactions of NO and nitrite with heme models and proteins

Ford, P. C. (2010) · Inorganic Chemistry · doi:10.1021/ic902073z · Cited by 138

A new facultatively nitrite oxidizing bacterium, Nitrobacter vulgaris sp. nov.

Bock, E., Koops, H., M�ller, U. C., & Rudert, M. (1990) · Archives of Microbiology · doi:10.1007/bf00247805 · Cited by 138

Cytoglobin/STAP, its unique localization in splanchnic fibroblast-like cells and function in organ fibrogenesis

Nakatani, K., Okuyama, H., Shimahara, Y., Saeki, S., Kim, D.-H., Nakajima, Y., Seki, S., Kawada, N., & Yoshizato, K. (2004) · Laboratory Investigation · doi:10.1038/labinvest.3700013 · Cited by 137

Nitrite confers protection against myocardial infarction: Role of xanthine oxidoreductase, NADPH oxidase and KATP channels

Baker, J. E., Su, J., Fu, X., Hsu, A., Gross, G. J., Tweddell, J. S., & Hogg, N. (2007) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2007.07.057 · Cited by 137

Alcohol-induced breast cancer: a proposed mechanism

Wright, R. M., McManaman, J. L., & Repine, J. E. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00204-4 · Cited by 137

Small mouse cholangiocytes proliferate in response to H1 histamine receptor stimulation by activation of the IP 3 /CaMK I/CREB pathway

Francis, H., Glaser, S. S., DeMorrow, S., Gaudio, E., Ueno, Y., Venter, J. K., Dostal, D. E., Onori, P., Franchitto, A., Marzioni, M., et al. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00369.2007 · Cited by 136

Floral Transition and Nitric Oxide Emission During Flower Development in Arabidopsis thaliana is Affected in Nitrate Reductase-Deficient Plants

Seligman, K., Saviani, E. E., Oliveira, H. C., Pinto-Maglio, C. A. F., & Salgado, I. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn089 · Cited by 136

PYRIDINE COENZYMES OF SUBCELLULAR TISSUE FRACTIONS

Jacobson, K. B., & Kaplan, N. O. (1957) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)70843-0 · Cited by 135

Structure of a Nitric Oxide Synthase Heme Protein from Bacillus subtilis,

Pant, K., Bilwes, A. M., Adak, S., Stuehr, D. J., & Crane, B. R. (2002) · Biochemistry · doi:10.1021/bi0263715 · Cited by 135

Direct Detection of Radicals in Intact Soybean Nodules: Presence of Nitric Oxide-Leghemoglobin Complexes

Mathieu, C., Moreau, S., Frendo, P., Puppo, A., & Davies, M. J. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00440-1 · Cited by 135

NMR and ESR studies of the interactions of cytochrome c with mixed cardiolipin-phosphatidylcholine vesicles

Brown, L. R., & Wüthrich, K. (1977) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(77)90290-5 · Cited by 134

Xanthine oxidase activity in the circulation of rats following hemorrhagic shock

Tan, S., Yokoyama, Y., Dickens, E., Cash, T., Freeman, B. Α., & Parks, D. A. (1993) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(93)90040-2 · Cited by 134

Nitrite oxidoreductase from Nitrobacter hamburgensis: redox centers and their catalytic role

Meincke, M., Eberhard Bock, C., Kastrau, D. H. W., & Kroneck, P. M. H. (1992) · Archives of Microbiology · doi:10.1007/bf00245215 · Cited by 134

Symbiotic Rhizobium and Nitric Oxide Induce Gene Expression of Non-symbiotic Hemoglobin in Lotus japonicus

Shimoda, Y., Nagata, M., Suzuki, A., Abe, M., Sato, S., Kato, T., Tabata, S., Higashi, S., & Uchiumi, T. (2005) · Plant and Cell Physiology · doi:10.1093/pci/pci001 · Cited by 134

Low-temperature magnetic circular dichroism studies of native laccase: confirmation of a trinuclear copper active site

Spira, D. J., Allendorf, M. D., & Solomon, E. I. (1986) · Journal of the American Chemical Society · doi:10.1021/ja00277a043 · Cited by 133

The molybdenum oxotransferases and related enzymes

Hille, R. (2013) · Dalton Transactions · doi:10.1039/c2dt32376a · Cited by 133

A Comparison of the Inner-Sphere Reorganization Energies of Cytochromes, Iron−Sulfur Clusters, and Blue Copper Proteins

Sigfridsson, E., Olsson, M. H. M., & Ryde, U. (2001) · The Journal of Physical Chemistry B · doi:10.1021/jp0037403 · Cited by 133

ESR Spin-trapping of a Protein-derived Tyrosyl Radical from the Reaction of Cytochrome with Hydrogen Peroxide

Barr, D. P., Gunther, M. R., Deterding, L. J., Tomer, K. B., & Mason, R. P. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.26.15498 · Cited by 132

Structure and Function of Xanthine Oxidoreductase

Hille, R. (2006) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.200600087 · Cited by 132

Characterization of the Mechanism and Magnitude of Cytoglobin-mediated Nitrite Reduction and Nitric Oxide Generation under Anaerobic Conditions

Li, H., Hemann, C., Abdelghany, T. M., El-Mahdy, M. A., & Zweier, J. L. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.342378 · Cited by 132

Cloning, expression, and characterization of a nitric oxide synthase protein from Deinococcus radiodurans

Adak, S., Bilwes, A. M., Panda, K., Hosfield, D. J., Aulak, K. S., McDonald, J. F., Tainer, J. A., Getzoff, E. D., Crane, B. R., & Stuehr, D. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.012470099 · Cited by 132

Synthetic Modeling of Nitrite Binding and Activation by Reduced Copper Proteins. Characterization of Copper(I)−Nitrite Complexes That Evolve Nitric Oxide

Halfen, J. A., Mahapatra, S., Wilkinson, E. C., Gengenbach, A. J., Young, V. G., QUE, L. J., & Tolman, W. B. (1996) · Journal of the American Chemical Society · doi:10.1021/ja952691i · Cited by 132

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