9q6g
PYCR2 complexed with NAD+ and (2S)-2-hydroxy-3,3-dimethylbutanoic acid
Structural highlights
DiseaseP5CR2_HUMAN PYCR2-related microcephaly-progressive leukoencephalopathy;Autosomal recessive primary microcephaly. The disease is caused by variants affecting the gene represented in this entry. FunctionP5CR2_HUMAN Oxidoreductase that catalyzes the last step in proline biosynthesis, which corresponds to the reduction of pyrroline-5-carboxylate to L-proline using NAD(P)H (PubMed:23024808, PubMed:2722838, PubMed:6894153). At physiologic concentrations, has higher specific activity in the presence of NADH (PubMed:23024808, PubMed:2722838, PubMed:6894153). Involved in cellular response to oxidative stress (PubMed:25865492). In some cell types, such as erythrocytes, its primary function may be the generation of NADP(+) (PubMed:2722838, PubMed:6894153).[1] [2] [3] [4] Publication Abstract from PubMedProline metabolism is selectively altered in cancer cells, providing ATP, redox balance, and proline for cell growth. The final enzyme of proline biosynthesis is Delta(1)-pyrroline-5-carboxylate (P5C) reductase (PYCR), which catalyzes the NAD(P)H-dependent reduction of P5C to proline. Humans have three PYCR isoforms, PYCR1 and PYCR2 in the mitochondrion and PYCR3 in the cytosol. Interest in developing selective inhibitors of PYCR enzymes has significantly increased over the past decade. Orthosteric inhibitors of PYCR1 have been developed, but they may lack specificity given the near identity of the active sites of PYCR1 and PYCR2. Here, we explored a new strategy of targeting noncatalytic cysteines to gain isoform selectivity. Initial results with iodoacetamide showed higher inhibition of PYCR2 relative to PYCR1, a result that was further explored with the thiol-reactive compound ebselen. Ebselen treatment resulted in a complete loss of PYCR2 activity with an IC(50) value of 22 nM, which is 10-fold more sensitive than with PYCR1. Results from protection assays with dithiothreitol, site-directed mutagenesis, and mass spectrometry implicate Cys232 in PYCR2 as the target of ebselen. A new crystal structure of PYCR2 shows that Cys232 is in the P5C-binding loop, whereas PYCR1 contains a serine at this position. Our study provides new insight into the structural and functional roles of unique cysteine residues in PYCR2. Further, our results demonstrate proof-of-concept for targeting a noncatalytic cysteine as a new approach for selectively inhibiting PYCR2 over PYCR1. Targeting a Unique Cysteine Residue to Achieve Isoform-Selective Inhibition of the Proline Biosynthetic Enzyme Pyrroline-5-Carboxylate Reductase 2.,Rossman TC, Meeks KR, Purohit G, Naldrett MJ, Tanner JJ, Becker DF ACS Chem Biol. 2026 May 15;21(5):1063-1072. doi: 10.1021/acschembio.6c00060. Epub , 2026 Apr 21. PMID:42014936[5] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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