5WGB

Crystal Structure of the Human mitochondrial Cysteine Desulfurase in complex with ISD11 and E. coli ACP1 protein at 2.75A

Summary for 5WGB

• Entry DOI: 10.2210/pdb5wgb/pdb
• Descriptor: Cysteine desulfurase, mitochondrial, LYR motif-containing protein 4, Acyl carrier protein, ... (5 entities in total)
• Functional Keywords: human mitochondrial cysteine desulfurse lyr motif containing protein 4 acyl carrier protein 1 (e.coli), transferase
• Biological source: Homo sapiens (Human); More
• Cellular location: Isoform Mitochondrial: Mitochondrion. Isoform Cytoplasmic: Cytoplasm: Q9Y697; Mitochondrion: Q9HD34; Cytoplasm : B7MJ81
• Total number of polymer chains: 3
• Total formula weight: 67460.73

Authors

Boniecki, M.T.,Cygler, M. (deposition date: 2017-07-13, release date: 2017-07-26, Last modification date: 2023-10-04)

Primary citation

Boniecki, M.T.,Freibert, S.A.,Muhlenhoff, U.,Lill, R.,Cygler, M.
Structure and functional dynamics of the mitochondrial Fe/S cluster synthesis complex.
Nat Commun, 8:1287-1287, 2017

PubMed Abstract: Iron-sulfur (Fe/S) clusters are essential protein cofactors crucial for many cellular functions including DNA maintenance, protein translation, and energy conversion. De novo Fe/S cluster synthesis occurs on the mitochondrial scaffold protein ISCU and requires cysteine desulfurase NFS1, ferredoxin, frataxin, and the small factors ISD11 and ACP (acyl carrier protein). Both the mechanism of Fe/S cluster synthesis and function of ISD11-ACP are poorly understood. Here, we present crystal structures of three different NFS1-ISD11-ACP complexes with and without ISCU, and we use SAXS analyses to define the 3D architecture of the complete mitochondrial Fe/S cluster biosynthetic complex. Our structural and biochemical studies provide mechanistic insights into Fe/S cluster synthesis at the catalytic center defined by the active-site Cys of NFS1 and conserved Cys, Asp, and His residues of ISCU. We assign specific regulatory rather than catalytic roles to ISD11-ACP that link Fe/S cluster synthesis with mitochondrial lipid synthesis and cellular energy status.

PubMed: 29097656
DOI: 10.1038/s41467-017-01497-1

Experimental method

X-RAY DIFFRACTION (2.75 Å)