oleandomycin

oleandomycin is a lipid of Polyketides (PK) class. The involved functions are known as 5-(carboxyamino)imidazole ribonucleotide mutase activity, Methylation, enzyme activity, Anabolism and Biosynthetic Pathways. Oleandomycin often locates in Chromosomes and Protoplasm. The associated genes with oleandomycin are resistance genes, Open Reading Frames, CTTNBP2 gene, Gene Feature and Gene Clusters.

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Introduction

To understand associated biological information of oleandomycin, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with oleandomycin?

There are no associated biomedical information in the current reference collection.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with oleandomycin

MeSH term MeSH ID Detail
Bacterial Infections D001424 21 associated lipids
Body Weight D001835 333 associated lipids
Drug Hypersensitivity D004342 20 associated lipids
Total 3

PubChem Associated disorders and diseases

What pathways are associated with oleandomycin

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with oleandomycin?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with oleandomycin?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with oleandomycin?

There are no associated biomedical information in the current reference collection.

What genes are associated with oleandomycin?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with oleandomycin?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with oleandomycin

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Authors Title Published Journal PubMed Link
Williams GJ et al. Optimizing glycosyltransferase specificity via "hot spot" saturation mutagenesis presents a catalyst for novobiocin glycorandomization. 2008 Chem. Biol. pmid:18420146
Weidlich M et al. Differential activity profiles of translation inhibitors in whole-cell and cell-free approaches. 2008 Lett. Appl. Microbiol. pmid:18028330
Ferreira AL et al. Doxorubicin as an antioxidant: maintenance of myocardial levels of lycopene under doxorubicin treatment. 2007 Free Radic. Biol. Med. pmid:17664138
Williams GJ et al. Expanding the promiscuity of a natural-product glycosyltransferase by directed evolution. 2007 Nat. Chem. Biol. pmid:17828251
González de la Huebra MJ et al. Sample preparation strategy for the simultaneous determination of macrolide antibiotics in animal feedingstuffs by liquid chromatography with electrochemical detection (HPLC-ECD). 2007 J Pharm Biomed Anal pmid:17257795
Parker KA and Wang P Deconstruction-reconstruction strategy for accessing valuable polyketides. Preparation of the C15-C24 stereopentad of discodermolide. 2007 Org. Lett. pmid:17924640
Novak P et al. Systematic approach to understanding macrolide-ribosome interactions: NMR and modeling studies of oleandomycin and its derivatives. 2006 J Phys Chem A pmid:16405329
García-Mayor MA et al. Liquid chromatography-UV diode-array detection method for multi-residue determination of macrolide antibiotics in sheep's milk. 2006 J Chromatogr A pmid:16682049
Wang J et al. Determination of five macrolide antibiotic residues in eggs using liquid chromatography/electrospray ionization tandem mass spectrometry. 2005 J. Agric. Food Chem. pmid:15769104
Yang M et al. Probing the breadth of macrolide glycosyltransferases: in vitro remodeling of a polyketide antibiotic creates active bacterial uptake and enhances potency. 2005 J. Am. Chem. Soc. pmid:15984838