3ID7

Crystal structure of renal dipeptidase from Streptomyces coelicolor A3(2)

Summary for 3ID7

• Entry DOI: 10.2210/pdb3id7/pdb
• Descriptor: Dipeptidase, ZINC ION, CHLORIDE ION, ... (4 entities in total)
• Functional Keywords: dipeptidase, streptomyces coelicolor a3(2), hydrolase
• Biological source: Streptomyces coelicolor
• Total number of polymer chains: 1
• Total formula weight: 43472.41

Authors

Fedorov, A.A.,Fedorov, E.V.,Cummings, J.,Raushel, F.M.,Almo, S.C. (deposition date: 2009-07-20, release date: 2010-01-12, Last modification date: 2024-02-21)

Primary citation

Cummings, J.A.,Nguyen, T.T.,Fedorov, A.A.,Kolb, P.,Xu, C.,Fedorov, E.V.,Shoichet, B.K.,Barondeau, D.P.,Almo, S.C.,Raushel, F.M.
Structure, mechanism, and substrate profile for Sco3058: the closest bacterial homologue to human renal dipeptidase .
Biochemistry, 49:611-622, 2010

PubMed Abstract: Human renal dipeptidase, an enzyme associated with glutathione metabolism and the hydrolysis of beta-lactams, is similar in sequence to a cluster of approximately 400 microbial proteins currently annotated as nonspecific dipeptidases within the amidohydrolase superfamily. The closest homologue to the human renal dipeptidase from a fully sequenced microbe is Sco3058 from Streptomyces coelicolor. Dipeptide substrates of Sco3058 were identified by screening a comprehensive series of l-Xaa-l-Xaa, l-Xaa-d-Xaa, and d-Xaa-l-Xaa dipeptide libraries. The substrate specificity profile shows that Sco3058 hydrolyzes a broad range of dipeptides with a marked preference for an l-amino acid at the N-terminus and a d-amino acid at the C-terminus. The best substrate identified was l-Arg-d-Asp (k(cat)/K(m) = 7.6 x 10(5) M(-1) s(-1)). The three-dimensional structure of Sco3058 was determined in the absence and presence of the inhibitors citrate and a phosphinate mimic of l-Ala-d-Asp. The enzyme folds as a (beta/alpha)(8) barrel, and two zinc ions are bound in the active site. Site-directed mutagenesis was used to probe the importance of specific residues that have direct interactions with the substrate analogues in the active site (Asp-22, His-150, Arg-223, and Asp-320). The solvent viscosity and kinetic effects of D(2)O indicate that substrate binding is relatively sticky and that proton transfers do not occurr during the rate-limiting step. A bell-shaped pH-rate profile for k(cat) and k(cat)/K(m) indicated that one group needs to be deprotonated and a second group must be protonated for optimal turnover. Computational docking of high-energy intermediate forms of l/d-Ala-l/d-Ala to the three-dimensional structure of Sco3058 identified the structural determinants for the stereochemical preferences for substrate binding and turnover.

PubMed: 20000809
DOI: 10.1021/bi901935y

Experimental method

X-RAY DIFFRACTION (1.3 Å)