2fr6
Crystal Structure of Mouse Cytidine Deaminase Complexed with Cytidine
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OverviewOverview
Cytidine deaminase (CDA) is a zinc-dependent enzyme that catalyzes the, deamination of cytidine or deoxycytidine to form uridine or deoxyuridine., Here we present the crystal structure of mouse CDA (MmCDA), complexed with, either tetrahydrouridine (THU), 3-deazauridine (DAU), or cytidine. In the, MmCDA-DAU complex, it clearly demonstrates that cytidine is distinguished, from uridine by its 4-NH(2) group that acts as a hydrogen bond donor. In, the MmCDA-cytidine complex, cytidine, unexpectedly, binds as the substrate, instead of the deaminated product in three of the four subunits, and in, the remaining subunit it binds as the product uridine. Furthermore, the, charge-neutralizing Arg68 of MmCDA has also exhibited two alternate, conformations, I and II. In conformation I, the only conformation observed, in the other structurally known homotetrameric CDAs, Arg68 hydrogen bonds, Cys65 and Cys102 to modulate part of their negative charges. However, in, conformation II the side chain of Arg68 rotates about 130 degrees around, the Cgamma-Cdelta bond and abolishes these hydrogen bonds. The lack of, hydrogen bonding may indirectly weaken the zinc-product interaction by, increased electron donation from cysteine to the zinc ion, suggesting a, novel product-expelling mechanism. On the basis of known structures, structural analysis further reveals two subclasses of homotetrameric CDAs, that can be identified according to the position of the, charge-neutralizing arginine residue. Implications for CDA-RNA interaction, have also been considered.
About this StructureAbout this Structure
2FR6 is a Single protein structure of sequence from Mus musculus with ZN, SO4, CTN, URI and NH3 as ligands. Active as Cytidine deaminase, with EC number 3.5.4.5 Full crystallographic information is available from OCA.
ReferenceReference
The 1.48 A resolution crystal structure of the homotetrameric cytidine deaminase from mouse., Teh AH, Kimura M, Yamamoto M, Tanaka N, Yamaguchi I, Kumasaka T, Biochemistry. 2006 Jun 27;45(25):7825-33. PMID:16784234
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