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4HM3

Naphthalene 1,2-Dioxygenase bound to ethylbenzene

Summary for 4HM3
Entry DOI10.2210/pdb4hm3/pdb
Related4HM0 4HM1 4HM2 4HM4 4HM5 4HM6 4HM7 4HM8
DescriptorNaphthalene 1,2-dioxygenase subunit alpha, Naphthalene 1,2-dioxygenase subunit beta, 1,2-ETHANEDIOL, ... (8 entities in total)
Functional Keywordsoxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor
Biological sourcePseudomonas sp. C18
More
Total number of polymer chains2
Total formula weight73852.07
Authors
Ferraro, D.J.,Ramaswamy, S. (deposition date: 2012-10-17, release date: 2013-10-30, Last modification date: 2024-09-18)
Primary citationFerraro, D.J.,Okerlund, A.,Brown, E.,Ramaswamy, S.
One enzyme, many reactions: structural basis for the various reactions catalyzed by naphthalene 1,2-dioxygenase.
Iucrj, 4:648-656, 2017
Cited by
PubMed Abstract: Rieske nonheme iron oxygenases (ROs) are a well studied class of enzymes. Naphthalene 1,2-dioxygenase (NDO) is used as a model to study ROs. Previous work has shown how side-on binding of oxygen to the mononuclear iron provides this enzyme with the ability to catalyze stereospecific and regiospecific -dihydroxylation reactions. It has been well documented that ROs catalyze a variety of other reactions, including mono-oxygenation, desaturation, O- and N-dealkylation, sulfoxidation . NDO itself catalyzes a variety of these reactions. Structures of NDO in complex with a number of different substrates show that the orientation of the substrate in the active site controls not only the regiospecificity and stereospecificity, but also the type of reaction catalyzed. It is proposed that the mononuclear iron-activated dioxygen attacks the atoms of the substrate that are most proximal to it. The promiscuity of delivering two products (apparently by two different reactions) from the same substrate can be explained by the possible binding of the substrate in slightly different orientations aided by the observed flexibility of residues in the binding pocket.
PubMed: 28989720
DOI: 10.1107/S2052252517008223
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5 Å)
Structure validation

226707

數據於2024-10-30公開中

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