7W18
Complex structure of alginate lyase PyAly with M5
Summary for 7W18
| Entry DOI | 10.2210/pdb7w18/pdb |
| Descriptor | Alginate lyase, beta-D-mannopyranuronic acid-(1-4)-beta-D-mannopyranuronic acid-(1-4)-beta-D-mannopyranuronic acid-(1-4)-beta-D-mannopyranuronic acid-(1-4)-beta-D-mannopyranuronic acid (3 entities in total) |
| Functional Keywords | pl7 family, alginate lyase, complex, lyase |
| Biological source | Neopyropia yezoensis (susabi-nori) |
| Total number of polymer chains | 1 |
| Total formula weight | 27861.76 |
| Authors | Liu, W.Z.,Lyu, Q.Q.,Zhang, K.K. (deposition date: 2021-11-19, release date: 2022-08-17, Last modification date: 2024-05-29) |
| Primary citation | Zhang, K.,Li, Z.,Zhu, Q.,Cao, H.,He, X.,Zhang, X.H.,Liu, W.,Lyu, Q. Determination of oligosaccharide product distributions of PL7 alginate lyases by their structural elements. Commun Biol, 5:782-782, 2022 Cited by PubMed Abstract: Alginate lyases can be used to produce well-defined alginate oligosaccharides (AOSs) because of their specificities for AOS products. A large number of alginate lyases have been recorded in the CAZy database; however, the majority are annotated-only alginate lyases that include little information on their products, thus limiting their applications. Here, we establish a simple and experiment-saving approach to predict product distributions for PL7 alginate lyases through extensive structural biology, bioinformatics and biochemical studies. Structural study on several PL7 alginate lyases reveals that two loops around the substrate binding cleft determine product distribution. Furthermore, a database containing the loop information of all annotated-only single-domain PL7 alginate lyases is constructed, enabling systematic exploration of the association between loop and product distribution. Based on these results, a simplified loop/product distribution relationship is proposed, giving us information on product distribution directly from the amino acid sequence. PubMed: 35918517DOI: 10.1038/s42003-022-03721-1 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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