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4B1A

Crystal structure of lysozyme with Keggin molecule

Summary for 4B1A
Entry DOI10.2210/pdb4b1a/pdb
DescriptorLYSOZYME C, Phosphomolybdate keggin, SODIUM ION, ... (5 entities in total)
Functional Keywordshydrolase, corm
Biological sourceGALLUS GALLUS (CHICKEN)
Total number of polymer chains1
Total formula weight16211.83
Authors
Mukhopadhyay, A.,Silva, T.S.,Romao, M.J.,Romao, C.C. (deposition date: 2012-07-09, release date: 2013-02-06, Last modification date: 2024-11-06)
Primary citationSeixas, J.D.,Mukhopadhyay, A.,Santos-Silva, T.,Otterbein, L.E.,Gallo, D.J.,Rodrigues, S.S.,Guerreiro, B.H.,Goncalves, A.M.,Penacho, N.,Marques, A.R.,Coelho, A.C.,Reis, P.M.,Romao, M.J.,Romao, C.C.
Characterization of a Versatile Organometallic Pro-Drug (Corm) for Experimental Co Based Therapeutics.
Dalton Trans, 42:5985-, 2013
Cited by
PubMed Abstract: The complex fac-[Mo(CO)(3)(histidinate)]Na has been reported to be an effective CO-Releasing Molecule in vivo, eliciting therapeutic effects in several animal models of disease. The CO releasing profile of this complex in different settings both in vitro and in vivo reveals that the compound can readily liberate all of its three CO equivalents under biological conditions. The compound has low toxicity and cytotoxicity and is not hemolytic. CO release is accompanied by a decrease in arterial blood pressure following administration in vivo. We studied its behavior in solution and upon the interaction with proteins. Reactive oxygen species (ROS) generation upon exposure to air and polyoxomolybdate formation in soaks with lysozyme crystals were observed as processes ensuing from the decomposition of the complex and the release of CO.
PubMed: 23223860
DOI: 10.1039/C2DT32174B
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.67 Å)
Structure validation

237992

數據於2025-06-25公開中

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