Phosphatases structure

Burke, T. R. and Zhang, Z. Y. (1998) Protein-tyrosine phosphatases Structure, mechanism, and inhibitor discovery. Biopolymers 47, 225-241. 

Protein lyrosine Phosphatases Structure, Function, and impiication in Human Disease... 

Zhang ZY (2002) Protein tyrosine phosphatases, structure and function, substrate specificity, and inhibitor development. Annu Rev Pharmacol Toxicol 42 209-234... 

Rudolph J (2007) Cdc25 phosphatases structure, specificity, and mechanism. Biochemistry 46 3595-3604... 

Table 2. Predicted intrinsic and apparent pKa values for the Cys403 residue in Yersinia phosphatase for different models of the structure the data refer to a temperature of 293 K and an ionic strength corresponding to 150 mM of monovalent salt. See the text for the detailed description of the conditions under which each pK estimation was made. The experimentally determined value is 4.67 [39]...

Alkaline phosphatase, 2,774 mechanism, 6,612 metal substitution, 6,611 structure, 6,611 zinc, 5.1006 6,610 Alkanes... 

Phosphonate analogs to phosphate esters, in which the P—0 bond is formally replaced by a P—C bond, have attracted attention due to their stability toward the hydrolytic action of phosphatases, which renders them potential inhibitors or regulators of metabolic processes. Two alternative pathways, in fact, may achieve introduction of the phosphonate moiety by enzyme catalysis. The first employs the bioisosteric methylene phosphonate analog (39), which yields products related to sugar 1-phosphates such as (71)/(72) (Figure 10.28) [102,107]. This strategy is rather effective because of the inherent stability of (39) as a replacement for (25), but depends on the individual tolerance of the aldolase for structural modification close... 

Primary structure analysis of phenylphosphate carboxylase of T. aromatica is performed in detail, to clarify the reaction mechanism involving four kinds of subunits. The a, (3, y, 8 subunits have molecular masses of 54, 53, 18, and lOkDa, respectively, which make up the active phenylphosphate carboxylase. The primary structures of a and (3 subunits show homology with 3-octaprenyl-4-hydroxybenzoate decarboxylase, 4-hydroxybenzoate decarboxylase, and vanil-late decarboxylase, whereas y subunit is unique and not characterized. The 18kDa 8 subunit belongs to a hydratase/phosphatase protein family. Taking 4-hydroxybenzoate decarboxylase into consideration, Schiihle and Fuchs postulate that the a(3y core enzyme catalyzes the reversible carboxylation. ... 

Bennett MS, Z Guan, M Laurberg, X-D Su (2001) Bacillus subtilis arsenate reductase is structurally and functionally similar to low molecular weight protein tyrosine phosphatases. Proc Natl Acad Sci USA 98 13577-13582. 

Some haloperoxidases contain vanadium and a review of vanadium peroxidases has been given (Butler 1998). The structure of the vanadium enzyme in the terrestrial fungus Cur-vularia inaequalis has been determined by x-ray analysis (Messerschmidt et al. 1997), and the apochloroperoxidase possesses, in addition, phosphatase activity that can be rationalized on the basis of the isomorphism of phosphate and vanadate (Renirie et al. 2000). 

Two dinuclear complexes, with five-coordinate zinc centers, derived from tris((2-pyridyl)-methyl) amine were synthesized and bridging phosphate or phosphate ester groups. The X-ray structure of the phosphate monoester complex shows a syn-anti bridging mode in contrast to alkaline phosphatase in which it is syn-syn 448 Fenton and co-workers have also studied other related dizinc species of compartmental ligands 449... 

Corrano and co-workers have characterized phosphate ester species with a mixed donor heteroscorpionate tripod zinc species 452 Krebs and co-workers synthesized purple acid phosphatase mimics including a structurally characterized FemZnn phosphate bridged dimeric species.453... 

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