2BKR

NEDD8 NEDP1 complex

Summary for 2BKR

• Entry DOI: 10.2210/pdb2bkr/pdb
• Related: 1NDD 1R4M 1R4N 1XT9 2BKQ
• Descriptor: SENTRIN-SPECIFIC PROTEASE 8, NEDDYLIN (3 entities in total)
• Functional Keywords: protein-binding-hydrolase complex, ubiquitin, hydrolase, protease, thiol protease, ubl conjugation pathway, ubiquitin-hydrolase complex, protein-binding/hydrolase
• Biological source: HOMO SAPIENS (HUMAN); More
• Cellular location: Nucleus: Q15843
• Total number of polymer chains: 2
• Total formula weight: 32734.22

Authors

Shen, L.N.,Liu, H.,Dong, C.,Xirodimas, D.,Naismith, J.H.,Hay, R.T. (deposition date: 2005-02-18, release date: 2005-09-15, Last modification date: 2024-05-08)

Primary citation

Shen, L.N.,Liu, H.,Dong, C.,Xirodimas, D.,Naismith, J.H.,Hay, R.T.
Structural Basis of Nedd8 Ubiquitin Discrimination by the Deneddylating Enzyme Nedp1
Embo J., 24:1341-, 2005

PubMed Abstract: NEDD8 (neural precursor cell expressed developmentally downregulated gene 8)-specific protease NEDP1 processes preNEDD8 to its mature form and deconjugates NEDD8 from substrates such as p53 and cullins. Although NEDD8 and ubiquitin are highly related in sequence and structure, their attachment to a protein leads to different biological effects. It is therefore critical that NEDP1 discriminates between NEDD8 and ubiquitin, and this requires remarkable precision in molecular recognition. To determine the basis of this specificity, we have determined the crystal structure of NEDP1 in isolation and in a transition state complex with NEDD8. This reveals that NEDP1 is a cysteine protease of the Ulp family. Binding of NEDD8 induces a dramatic conformational change in a flexible loop that swings over the C-terminus of NEDD8 locking it into an extended beta-structure optimal for catalysis. Structural, mutational and biochemical studies have identified key residues involved in molecular recognition. A single-residue difference in the C-terminus of NEDD8 and ubiquitin contributes significantly to the ability of NEDP1 to discriminate between them. In vivo analysis indicates that NEDP1 mutants perturb deNEDDylation of the tumour suppressor p53.

PubMed: 15775960
DOI: 10.1038/SJ.EMBOJ.7600628

Experimental method

X-RAY DIFFRACTION (1.9 Å)