F75A4939C1C9E06838A1C1C4C58DF4370D4C6C1C7FEAD0BE5D03B4915F40A58FF10D6404AF7FBDABFD3EF93D612AEFE2

Inactivates the type B streptogramin antibiotics by linearizing the lactone ring at the ester linkage, generating a free phenylglycine carboxylate and converting the threonyl moiety into 2-amino-butenoic acid.

Source:http://purl.uniprot.org/SHA-384/F75A4939C1C9E06838A1C1C4C58DF4370D4C6C1C7FEAD0BE5D03B4915F40A58FF10D6404AF7FBDABFD3EF93D612AEFE2

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Inactivates the type B streptogramin antibiotics by linearizing the lactone ring at the ester linkage, generating a free phenylglycine carboxylate and converting the threonyl moiety into 2-amino-butenoic acid.