9NQL
Cryo electron microscopic analysis of the adduct of syringolin analog with the Mtb 20S proteasome
This is a non-PDB format compatible entry.
Summary for 9NQL
| Entry DOI | 10.2210/pdb9nql/pdb |
| EMDB information | 49668 |
| Descriptor | Proteasome subunit beta, Proteasome subunit alpha, methyl N-{[2-({(3Z,5R,8R)-5-[(1H-indol-3-yl)methyl]-2,7-dioxo-1,6-diazacyclododec-3-en-8-yl}amino)-2-oxoethyl]carbamoyl}-L-valinate (3 entities in total) |
| Functional Keywords | proteasome inhibitor, mycobacterium tuberculosis, hydrolase-antibiotic complex, hydrolase/antibiotic |
| Biological source | Mycobacterium tuberculosis More |
| Total number of polymer chains | 28 |
| Total formula weight | 725212.28 |
| Authors | |
| Primary citation | Gu, X.,Rowheder, P.J.,Yu, Z.,Mohapatra, A.,Lun, S.,Jiang, X.,Li, D.,Yan, N.L.,Detomasi, T.C.,Pomares, D.F.T.,Chen, Y.,Gestwicki, J.E.,Lin, G.,Bishai, W.R.,Ernst, J.D.,Cheng, Y.,Craik, C.S.,Sello, J.K. Substrate Mimicry by Inhibitors of the Mycobacterium tuberculosis 20S Proteasome and Their Activity against Mycobacteria In Vitro and in Macrophages Acs Chem.Biol., 2026 Cited by DOI: 10.1021/acschembio.6c00448PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (2.16 Å) |
Structure validation
Download full validation report






