9X86 image
Deposition Date 2025-10-18
Release Date 2026-04-08
Last Version Date 2026-05-13
Entry Detail
PDB ID:
9X86
Keywords:
Title:
Crystal Structure of dehydratase ApmL in Amipurimycin biosynthesis
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
3.50 Å
R-Value Free:
0.32
R-Value Work:
0.26
R-Value Observed:
0.26
Space Group:
P 61 2 2
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Amc20
Gene (Uniprot):amc20
Chain IDs:A
Chain Length:297
Number of Molecules:1
Biological Source:Streptomyces novoguineensis
Primary Citation
Deoxysugar Formation via 4',5'-Dehydration on PKS Assembly Line in Nucleoside Antibiotic Biosynthesis.
Angew.Chem.Int.Ed.Engl. 65 ? ? (2026)
PMID: 41902592 DOI: 10.1002/anie.6927983

Abstact

Amipurimycin is a peptidyl nucleoside antibiotic characterized by a C(9) high-carbon sugar, with potent activity against the rice blast pathogen Pyricularia oryzae. The biosynthetic machinery of the C-4' methylene group in its deoxy sugar has remained unknown. This study reveals that ApmL, a hypothetical protein in the DUF3500 family, functions as a 4',5'-dehydratase whose activity is strictly dependent on the PKS assembly line. Together with its partner reductase ApmM, they complete a two-step C-4' deoxygenation process via dehydration-reduction. We achieve the first in vitro reconstitution of this unique PKS-coupled dehydration process and show direct interaction between ApmL and PKS proteins. Our findings establish ApmL as a new family of dehydratase and uncover a noncanonical deoxygenation strategy in nucleoside antibiotic biosynthesis.

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