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4UFC

Crystal structure of the GH95 enzyme BACOVA_03438

Summary for 4UFC
Entry DOI10.2210/pdb4ufc/pdb
DescriptorGH95, CALCIUM ION, beta-L-galactopyranose, ... (4 entities in total)
Functional Keywordshydrolase, glycoside hydrolase, xylan, alpha-l-galactosidase, gut microbiota
Biological sourceBACTEROIDES OVATUS
Total number of polymer chains2
Total formula weight183845.09
Authors
Primary citationRogowski, A.,Briggs, J.A.,Mortimer, J.C.,Tryfona, T.,Terrapon, N.,Lowe, E.C.,Basle, A.,Morland, C.,Day, A.M.,Zheng, H.,Rogers, T.E.,Thompson, P.,Hawkins, A.R.,Yadav, M.P.,Henrissat, B.,Martens, E.C.,Dupree, P.,Gilbert, H.J.,Bolam, D.N.
Glycan Complexity Dictates Microbial Resource Allocation in the Large Intestine.
Nat.Commun., 6:7481-, 2015
Cited by
PubMed Abstract: The structure of the human gut microbiota is controlled primarily through the degradation of complex dietary carbohydrates, but the extent to which carbohydrate breakdown products are shared between members of the microbiota is unclear. We show here, using xylan as a model, that sharing the breakdown products of complex carbohydrates by key members of the microbiota, such as Bacteroides ovatus, is dependent on the complexity of the target glycan. Characterization of the extensive xylan degrading apparatus expressed by B. ovatus reveals that the breakdown of the polysaccharide by the human gut microbiota is significantly more complex than previous models suggested, which were based on the deconstruction of xylans containing limited monosaccharide side chains. Our report presents a highly complex and dynamic xylan degrading apparatus that is fine-tuned to recognize the different forms of the polysaccharide presented to the human gut microbiota.
PubMed: 26112186
DOI: 10.1038/NCOMMS8481
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.81 Å)
Structure validation

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