7ec9: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
No edit summary
No edit summary
Line 8: Line 8:
</table>
</table>
== Function ==
== Function ==
[[https://www.uniprot.org/uniprot/Q9X274_THEMA Q9X274_THEMA]]  
[https://www.uniprot.org/uniprot/Q9X274_THEMA Q9X274_THEMA]  
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==

Revision as of 09:53, 25 January 2023

Structure of the Thermotoga maritima Family 5 endo-glucanase in complex with 1-deoxynojiromycinStructure of the Thermotoga maritima Family 5 endo-glucanase in complex with 1-deoxynojiromycin

Structural highlights

7ec9 is a 2 chain structure with sequence from Thermotoga maritima MSB8. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Ligands:,
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

Q9X274_THEMA

Publication Abstract from PubMed

TmCel5B is a lichenase belonging to glycoside hydrolase family 5 subfamily 36 (GH5_36). To gain insights into the active site of this subfamily which contains multifunctional endoglycanases, we determined the crystal structure of TmCel5B in complex with an iminosugar, 1-deoxynojiromycin (DNJ). DNJ is bound to the -1 subsite, making a network of non-covalent interactions with the acid/base residue Glu139, the nucleophile Glu259, and with other residues that are conserved across the GH5 family. The catalytic site displayed a Glu-Arg-Glu triad of the catalytic glutamates that is unique to the GH5_36 subfamily. Structural comparison of active sites of GH5_36 homologs revealed divergent residues and loop regions that are likely molecular determinants of homolog-specific properties. Furthermore, a comparative analysis of the binding modes of iminocyclitol complexes of GH5 homologs revealed the structural basis of their binding to GH5 glycosidases, in which the subsite binding location, the interactions of the ligand with specific conserved residues, and the electrostatic interactions of the catalytic glutamates with the ring nitrogen, are crucial.

Structure of an iminosugar complex of a glycoside hydrolase family 5 lichenase provides insights into the active site.,Garg P, Manoj N Biochimie. 2022 Sep 6. pii: S0300-9084(22)00226-7. doi:, 10.1016/j.biochi.2022.09.001. PMID:36084911[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

  1. Garg P, Manoj N. Structure of an iminosugar complex of a glycoside hydrolase family 5 lichenase provides insights into the active site. Biochimie. 2022 Sep 6. pii: S0300-9084(22)00226-7. doi:, 10.1016/j.biochi.2022.09.001. PMID:36084911 doi:http://dx.doi.org/10.1016/j.biochi.2022.09.001

7ec9, resolution 1.80Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA