|
54
|
157
|
3gxgA |
Crystal structure of putative phosphatase (duf442) (yp_001181608.1) from shewanella putrefaciens cn-32 at 1.60 a resolution |
|
66
|
179
|
3f81A |
Interaction of vhr with sa3 |
|
203
|
590
|
3f41A |
Structure of the tandemly repeated protein tyrosine phosphatase like phytase from mitsuokella multacida |
|
111
|
282
|
3f9aA |
W354f yersinia enterocolitica ptpase complexed with tungstate |
|
111
|
282
|
3f9bA |
W354f yersinia enterocolitica ptpase complexed with divanadate |
|
110
|
282
|
3f99A |
W354f yersinia enterocolitica ptpase apo form |
|
53
|
144
|
3ezzA |
Crystal structure of human mkp-2 |
|
97
|
281
|
3eu0A |
Crystal structure of the s-nitrosylated cys215 of ptp1b |
|
51
|
151
|
3emuA |
Crystal structure of a leucine rich repeat and phosphatase domain containing protein from entamoeba histolytica |
|
89
|
283
|
3eb1A |
Crystal structure ptp1b complex with small molecule inhibitor lzp-25 |
|
95
|
282
|
3eaxA |
Crystal structure ptp1b complex with small molecule compound lzp-6 |
|
108
|
313
|
3d1qA |
Structure of the ptp-like phytase expressed by selenomonas ruminantium at an ionic strength of 400 mm |
|
93
|
282
|
3d9cA |
Crystal structure ptp1b complex with aryl seleninic acid |
|
110
|
313
|
3d1oA |
Structure of the ptp-like phytase expressed by selenomonas ruminantium at an ionic strength of 300 mm |
|
95
|
292
|
3d44A |
Crystal structure of heptp in complex with a dually phosphorylated erk2 peptide mimetic |
|
91
|
292
|
3d42A |
Crystal structure of heptp in complex with a monophosphorylated erk2 peptide |
|
108
|
313
|
3d1hA |
Structure of the ptp-like phytase expressed by selenomonas ruminantium at an ionic strength of 500 mm |
|
63
|
164
|
3cm3A |
High resolution crystal structure of the vaccinia virus dual-specificity phosphatase vh1 |
|
105
|
290
|
3cweA |
Ptp1b in complex with a phosphonic acid inhibitor |
|
104
|
282
|
3bluA |
Crystal structure yoph complexed with inhibitor pvs |
|
102
|
282
|
3bm8A |
Crystal structure of yoph mutant d356a complexed with irreversible inhibitor pvsn |
|
95
|
282
|
3bltA |
Crystal structures of yoph complexed with pvsn and pvs, inhibitors of yoph which co-valent bind to cys of active site |
|
97
|
296
|
3brhA |
Protein tyrosine phosphatase ptpn-22 (lyp) bound to the mono-phosphorylated lck active site peptide |
|
96
|
283
|
3b7oA |
Crystal structure of the human tyrosine phosphatase shp2 (ptpn11) with an accessible active site |
|
103
|
315
|
3awfA |
Crystal structure of pten-like domain of ci-vsp (236-576) |
|
108
|
318
|
3awgA |
Crystal structure of pten-like domain of ci-vsp g356a mutant (248-576) |
|
101
|
316
|
3aweA |
Crystal structure of pten-like domain of ci-vsp (248-576) |
|
96
|
282
|
3a5jA |
Crystal structure of protein-tyrosine phosphatase 1b |
|
91
|
281
|
3a5kA |
Crystal structure of protein-tyrosine phosphatase 1b |
|
108
|
297
|
2zmmA |
Crystal structure of ptp1b-inhibitor complex |
|
106
|
297
|
2zn7A |
Crystal structures of ptp1b-inhibitor complexes |
|
108
|
282
|
2yduA |
Crystal structure of yoph in complex with 3-(1,1-dioxido-3- oxoisothiazolidin-5-yl)benzaldeyde |
|
154
|
439
|
2y66A |
New 5-benzylidenethiazolidine-4-one inhibitors of bacterial murd ligase: design, synthesis, crystal structures, and biological evaluation |
|
152
|
439
|
2y1oA |
Dual-target inhibitor of murd and mure ligases: design, synthesis and binding mode studies |
|
154
|
439
|
2y68A |
Structure-based design of a new series of d-glutamic acid-based inhibitors of bacterial murd ligase |
|
115
|
282
|
2y2fA |
Crystal structure of yersinia pestis yoph in complex with an aminooxy- containing platform compound for inhibitor design |
|
152
|
439
|
2y67A |
New 5-benzylidenethiazolidine-4-one inhibitors of bacterial murd ligase: design, synthesis, crystal structures, and biological evaluation |
|
62
|
175
|
2y96A |
Structure of human dual-specificity phosphatase 27 |
|
150
|
507
|
2xjaA |
Structure of mure from m.tuberculosis with dipeptide and adp |
|
156
|
439
|
2xpcA |
Second-generation sulfonamide inhibitors of murd: activity optimisation with conformationally rigid analogues of d-glutamic acid |
|
155
|
439
|
2x5oA |
Discovery of novel 5-benzylidenerhodanine- and 5-benzylidene- thiazolidine-2,4-dione inhibitors of murd ligase |
|
163
|
508
|
2wtzA |
Mure ligase of mycobacterium tuberculosis |
|
62
|
168
|
2wgpA |
Crystal structure of human dual specificity phosphatase 14 |
|
153
|
439
|
2wjpA |
Crystal structure of murd ligase in complex with d-glu containing rhodanine inhibitor |
|
151
|
438
|
2vteA |
Crystal structure of murd ligase in complex with d-glu containing sulfonamide inhibitor |
|
155
|
439
|
2vtdA |
Crystal structure of murd ligase in complex with d-glu containing sulfonamide inhibitor |
|
157
|
466
|
2vorA |
Crystal structures of mycobacterium tuberculosis folylpolyglutamate synthase complexed with adp and amppcp |
|
163
|
466
|
2vosA |
Mycobacterium tuberculosis folylpolyglutamate synthase complexed with adp |
|
100
|
297
|
2vexA |
Crystal strucutre of protein tyrosine phosphatase 1b in complex with an isothiazolidinone-containing inhibitor |
|
99
|
296
|
2veuA |
Crystal structure of protein tyrosine phosphatase 1b in complex with an isothiazolidinone-containing inhibitor |
