8SL7
Butyricicoccus sp. BIOML-A1 tryptophanase complex with (3S) ALG-05
Summary for 8SL7
| Entry DOI | 10.2210/pdb8sl7/pdb |
| Descriptor | Tryptophanase, (E)-3-[(3S)-3-chloro-2-oxo-2,3-dihydro-1H-indol-3-yl]-N-({3-hydroxy-2-methyl-5-[(phosphonooxy)methyl]pyridin-4-yl}methylidene)-L-alanine (3 entities in total) |
| Functional Keywords | tryptophan-indole lyase, tryptophananse, plp-dependent enzyme, inhibitor-bound complex, lyase |
| Biological source | Butyricicoccus sp. BIOML-A1 |
| Total number of polymer chains | 4 |
| Total formula weight | 260638.62 |
| Authors | Graboski, A.L.,Redinbo, M.R. (deposition date: 2023-04-21, release date: 2023-08-23, Last modification date: 2023-11-29) |
| Primary citation | Graboski, A.L.,Kowalewski, M.E.,Simpson, J.B.,Cao, X.,Ha, M.,Zhang, J.,Walton, W.G.,Flaherty, D.P.,Redinbo, M.R. Mechanism-based inhibition of gut microbial tryptophanases reduces serum indoxyl sulfate. Cell Chem Biol, 30:1402-1413.e7, 2023 Cited by PubMed Abstract: Indoxyl sulfate is a microbially derived uremic toxin that accumulates in late-stage chronic kidney disease and contributes to both renal and cardiovascular toxicity. Indoxyl sulfate is generated by the metabolism of indole, a compound created solely by gut microbial tryptophanases. Here, we characterize the landscape of tryptophanase enzymes in the human gut microbiome and find remarkable structural and functional similarities across diverse taxa. We leverage this homology through a medicinal chemistry campaign to create a potent pan-inhibitor, (3S) ALG-05, and validate its action as a transition-state analog. (3S) ALG-05 successfully reduces indole production in microbial culture and displays minimal toxicity against microbial and mammalian cells. Mice treated with (3S) ALG-05 show reduced cecal indole and serum indoxyl sulfate levels with minimal changes in other tryptophan-metabolizing pathways. These studies present a non-bactericidal pan-inhibitor of gut microbial tryptophanases with potential promise for reducing indoxyl sulfate in chronic kidney disease. PubMed: 37633277DOI: 10.1016/j.chembiol.2023.07.015 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.07 Å) |
Structure validation
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