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2OG4

Structure of an expanded Jab1-MPN-like domain of splicing factor Prp8p from yeast

Summary for 2OG4
Entry DOI10.2210/pdb2og4/pdb
DescriptorPre-mRNA-splicing factor 8 (2 entities in total)
Functional Keywordsisopeptidase, jab1/mpn domain, pre-mrna splicing, protein-protein interaction, prp8p, pseudoenzyme, spliceosome activation, u5-200k protein, protein binding
Biological sourceSaccharomyces cerevisiae
Cellular locationNucleus : P33334
Total number of polymer chains1
Total formula weight28743.52
Authors
Pena, V.,Liu, S.,Luehrmann, R.,Wahl, M.C. (deposition date: 2007-01-05, release date: 2007-03-13, Last modification date: 2023-12-27)
Primary citationPena, V.,Liu, S.,Bujnicki, J.M.,Luhrmann, R.,Wahl, M.C.
Structure of a multipartite protein-protein interaction domain in splicing factor prp8 and its link to retinitis pigmentosa.
Mol.Cell, 25:615-624, 2007
Cited by
PubMed Abstract: Protein Prp8 interacts with several other spliceosomal proteins, snRNAs, and the pre-mRNA and thereby organizes the active site(s) of the spliceosome. The DEAD-box protein Brr2 and the GTPase Snu114 bind to the Prp8 C terminus, a region where mutations in human Prp8 are linked to the RP13 form of Retinitis pigmentosa. We show crystallographically that the C-terminal domain of yeast Prp8p exhibits a Jab1/MPN-like core known from deubiquitinating enzymes. Insertions and terminal appendices are grafted onto this core, covering a putative isopeptidase center whose metal binding site is additionally impaired. Targeted yeast-two-hybrid analyses show that the RP13-linked region in the C-terminal appendix of human Prp8 is essential for binding of human Brr2 and Snu114, and that RP13 point mutations in this fragment weaken these interactions. We conclude that the expanded Prp8 Jab1/MPN domain represents a pseudoenzyme converted into a protein-protein interaction platform and that dysfunction of this platform underlies Retinitis pigmentosa.
PubMed: 17317632
DOI: 10.1016/j.molcel.2007.01.023
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

238895

數據於2025-07-16公開中

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