|
96
|
282
|
1t49A |
Allosteric inhibition of protein tyrosine phosphatase 1b |
|
96
|
298
|
1t48A |
Allosteric inhibition of protein tyrosine phosphatase 1b |
|
93
|
282
|
1t4jA |
Allosteric inhibition of protein tyrosine phosphatase 1b |
|
42
|
152
|
1rxdA |
Crystal structure of human protein tyrosine phosphatase 4a1 |
|
33
|
172
|
1r6hA |
Solution structure of human prl-3 |
|
107
|
282
|
1qz0A |
Crystal structure of the yersinia pestis phosphatase yoph in complex with a phosphotyrosyl mimetic-containing hexapeptide |
|
90
|
278
|
1rpmA |
Human receptor protein tyrosine phosphatase mu, domain 1 |
|
98
|
282
|
1qxkA |
Monoacid-based, cell permeable, selective inhibitors of protein tyrosine phosphatase 1b |
|
61
|
177
|
1qb0A |
Human cdc25b catalytic domain |
|
100
|
282
|
1pynA |
Dual-site potent, selective protein tyrosine phosphatase 1b inhibitor using a linked fragment strategy and a malonate head on the first site |
|
107
|
297
|
1ptuA |
Crystal structure of protein tyrosine phosphatase 1b complexed with phosphotyrosine-containing hexa-peptide (dadepyl-nh2) |
|
107
|
298
|
1ptyA |
Crystal structure of protein tyrosine phosphatase 1b complexed with two phosphotyrosine molecules |
|
104
|
297
|
1pxhA |
Crystal structure of protein tyrosine phosphatase 1b with potent and selective bidentate inhibitor compound 2 |
|
10
|
108
|
1q7xA |
Solution structure of the alternatively spliced pdz2 domain (pdz2b) of ptp-bas (hptp1e) |
|
107
|
298
|
1q1mA |
A highly efficient approach to a selective and cell active ptp1b inhibitors |
|
96
|
289
|
1q6tA |
The structure of phosphotyrosine phosphatase 1b in complex with compound 11 |
|
105
|
297
|
1pttA |
Crystal structure of protein tyrosine phosphatase 1b complexed with phosphotyrosine-containing tetra-peptide (ac-depyl-nh2) |
|
61
|
154
|
1phrA |
The crystal structure of a low molecular phosphotyrosine protein phosphatase |
|
98
|
289
|
1q6nA |
The structure of phosphotyrosine phosphatase 1b in complex with compound 4 |
|
102
|
289
|
1q6mA |
The structure of phosphotyrosine phosphatase 1b in complex with compound 3 |
|
100
|
289
|
1q6jA |
The structure of phosphotyrosine phosphatase 1b in complex with compound 2 |
|
99
|
289
|
1q6sA |
The structure of phosphotyrosine phosphatase 1b in complex with compound 9 |
|
63
|
157
|
1pntA |
Crystal structure of bovine heart phosphotyrosyl phosphatase at 2.2 angstroms resolution |
|
109
|
297
|
1ptvA |
Crystal structure of protein tyrosine phosphatase 1b complexed with phosphotyrosine |
|
100
|
287
|
1q6pA |
The structure of phosphotyrosine phosphatase 1b in complex with compound 6 |
|
106
|
283
|
1pa9A |
Yersinia protein-tyrosine phosphatase complexed with pncs (yop51,pasteurella x,ptpase,yop51delta162) (catalytic domain, residues 163-468) mutant with cys 235 replaced by arg (c235r) |
|
99
|
282
|
1onyA |
Oxalyl-aryl-amino benzoic acid inhibitors of ptp1b, compound 17 |
|
22
|
146
|
1p8aA |
Solution structure of the low molecular weight protein tyrosine phosphatase from tritrichomonas foetus |
|
113
|
302
|
1pa1A |
Crystal structure of the c215d mutant of protein tyrosine phosphatase 1b |
|
97
|
282
|
1ph0A |
Non-carboxylic acid-containing inhibitor of ptp1b targeting the second phosphotyrosine site |
|
16
|
99
|
1oziA |
The alternatively spliced pdz2 domain of ptp-bl |
|
96
|
282
|
1onzA |
Oxalyl-aryl-amino benzoic acid inhibitors of ptp1b, compound 8b |
|
66
|
245
|
1p15A |
Crystal structure of the d2 domain of rptpa |
|
116
|
338
|
1ohdA |
Structure of cdc14 in complex with tungstate |
|
113
|
338
|
1ohcA |
Structure of the proline directed phosphatase cdc14 |
|
92
|
281
|
1oesA |
Oxidation state of protein tyrosine phosphatase 1b |
|
99
|
280
|
1oevA |
Oxidation state of protein tyrosine phosphatase 1b |
|
93
|
280
|
1oemX |
Ptp1b with the catalytic cysteine oxidized to a sulfenyl-amide bond |
|
96
|
280
|
1oeuA |
Oxidation state of protein tyrosine phosphatase 1b |
|
98
|
280
|
1oeoX |
Ptp1b with the catalytic cysteine oxidized to sulfonic acid |
|
113
|
338
|
1oheA |
Structure of cdc14b phosphatase with a peptide ligand |
|
99
|
280
|
1oetA |
Oxidation state of protein tyrosine phosphatase 1b |
|
99
|
296
|
1nweA |
Ptp1b r47c modified at c47 with n-[4-(2-{2-[3-(2-bromo-acetylamino)-propionylamino]-3-hydroxy-propionylamino}-ethyl)-phenyl]-oxalamic acid |
|
97
|
282
|
1no6A |
Potent, selective protein tyrosine phosphatase 1b inhibitor compound 5 using a linked-fragment strategy |
|
99
|
282
|
1nz7A |
Potent, selective inhibitors of protein tyrosine phosphatase 1b using a second phosphotyrosine binding site, complexed with compound 19. |
|
29
|
98
|
1nz6A |
Crystal structure of auxilin j-domain |
|
96
|
283
|
1nwlA |
Crystal structure of the ptp1b complexed with sp7343-sp7964, a ptyr mimetic |
|
94
|
282
|
1nl9A |
Potent, selective protein tyrosine phosphatase 1b inhibitor compound 12 using a linked-fragment strategy |
|
92
|
282
|
1nnyA |
Potent, selective protein tyrosine phosphatase 1b inhibitor compound 23 using a linked-fragment strategy |
|
27
|
182
|
1n4cA |
Nmr structure of the j-domain and clathrin substrate binding domain of bovine auxilin |
