|
99
|
282
|
1onyA |
Oxalyl-aryl-amino benzoic acid inhibitors of ptp1b, compound 17 |
|
66
|
245
|
1p15A |
Crystal structure of the d2 domain of rptpa |
|
96
|
282
|
1onzA |
Oxalyl-aryl-amino benzoic acid inhibitors of ptp1b, compound 8b |
|
97
|
282
|
1ph0A |
Non-carboxylic acid-containing inhibitor of ptp1b targeting the second phosphotyrosine site |
|
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 |
|
99
|
280
|
1oetA |
Oxidation state of protein tyrosine phosphatase 1b |
|
96
|
280
|
1oeuA |
Oxidation state of protein tyrosine phosphatase 1b |
|
98
|
280
|
1oeoX |
Ptp1b with the catalytic cysteine oxidized to sulfonic acid |
|
97
|
282
|
1no6A |
Potent, selective protein tyrosine phosphatase 1b inhibitor compound 5 using a linked-fragment strategy |
|
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 |
|
92
|
282
|
1nnyA |
Potent, selective protein tyrosine phosphatase 1b inhibitor compound 23 using a linked-fragment strategy |
|
96
|
283
|
1nwlA |
Crystal structure of the ptp1b complexed with sp7343-sp7964, a ptyr mimetic |
|
99
|
282
|
1nz7A |
Potent, selective inhibitors of protein tyrosine phosphatase 1b using a second phosphotyrosine binding site, complexed with compound 19. |
|
94
|
282
|
1nl9A |
Potent, selective protein tyrosine phosphatase 1b inhibitor compound 12 using a linked-fragment strategy |
|
99
|
287
|
1lqfA |
Structure of ptp1b in complex with a peptidic bisphosphonate inhibitor |
|
110
|
283
|
1lyvA |
High-resolution structure of the catalytically inactive yersinia tyrosine phosphatase c403a mutant in complex with phosphate. |
|
78
|
273
|
1l8kA |
T cell protein-tyrosine phosphatase structure |
|
106
|
297
|
1l8gA |
Crystal structure of ptp1b complexed with 7-(1,1-dioxo-1h-benzo[d]isothiazol-3-yloxymethyl)-2-(oxalyl-amino)-4,7-dihydro-5h-thieno[2,3-c]pyran-3-carboxylic acid |
|
188
|
570
|
1larA |
Crystal structure of the tandem phosphatase domains of rptp lar |
|
99
|
297
|
1kakA |
Human tyrosine phosphatase 1b complexed with an inhibitor |
|
106
|
297
|
1kavA |
Human tyrosine phosphatase 1b complexed with an inhibitor |
|
97
|
284
|
1i57A |
Crystal structure of apo human ptp1b (c215s) mutant |
|
69
|
283
|
1gwzA |
Crystal structure of the catalytic domain of the protein tyrosine phosphatase shp-1 |
|
111
|
296
|
1gfyA |
Residue 259 is a key determinant of substrate specificity of protein-tyrosine phosphatase 1b and alpha |
|
122
|
373
|
1g4uS |
Crystal structure of the salmonella tyrosine phosphatase and gtpase activating protein sptp bound to rac1 |
|
81
|
284
|
1fprA |
Crystal structure of the complex formed between the catalytic domain of shp-1 and an in vitro peptide substrate py469 derived from shps-1. |
|
105
|
369
|
1g4wR |
Crystal structure of the salmonella tyrosine phosphatase and gtpase activating protein sptp |
|
103
|
297
|
1g7fA |
Human ptp1b catalytic domain complexed with pnu177496 |
|
106
|
297
|
1g7gA |
Human ptp1b catalytic domain complexes with pnu179326 |
|
98
|
297
|
1g1fA |
Crystal structure of protein tyrosine phosphatase 1b complexed with a tri-phosphorylated peptide (rdi(ptr)etd(ptr)(ptr)rk) from the insulin receptor kinase |
|
99
|
297
|
1jlnA |
Crystal structure of the catalytic domain of protein tyrosine phosphatase ptp-sl/br7 |
|
92
|
298
|
1g1hA |
Crystal structure of protein tyrosine phosphatase 1b complexed with a bis-phosphorylated peptide (etd(ptr)(ptr)rkggkgll) from the insulin receptor kinase |
|
97
|
298
|
1g1gA |
Crystal structure of protein tyrosine phosphatase 1b complexed with a mono-phosphorylated peptide (etdy(ptr)rkggkgll) from the insulin receptor kinase |
|
106
|
297
|
1ecvA |
Crystal structure of protein tyrosine phosphatase 1b complexed with 5-iodo-2-(oxalyl-amino)-benzoic acid |
|
107
|
299
|
1eenA |
Crystal structure of protein tyrosine phosphatase 1b complexed with acetyl-d-a-d-bpa-ptyr-l-i-p-q-q-g |
|
108
|
297
|
1eeoA |
Crystal structure of protein tyrosine phosphatase 1b complexed with acetyl-e-l-e-f-ptyr-m-d-y-e-nh2 |
|
94
|
281
|
1jf7A |
Human ptp1b catalytic domain complexed with pnu177836 |
|
107
|
297
|
1c84A |
Crystal structure of protein tyrosine phosphatase 1b complexed with 3-(oxalyl-amino)-naphthalene-2-carboxlic acid |
|
107
|
297
|
1c87A |
Crystal structure of protein tyrosine phosphatase 1b complexed with 2-(oxalyl-amino-4,7-dihydro-5h-thieno[2,3-c]pyran-3-carboxylic acid |
|
94
|
297
|
1bzhA |
Cyclic peptide inhibitor of human ptp1b |
|
106
|
296
|
1c86A |
Crystal structure of protein tyrosine phosphatase 1b (r47v,d48n) complexed with 2-(oxalyl-amino-4,7-dihydro-5h-thieno[2,3-c]pyran-3-carboxylic acid |
|
103
|
297
|
1c83A |
Crystal structure of protein tyrosine phosphatase 1b complexed with 6-(oxalyl-amino)-1h-indole-5-carboxylic acid |
|
102
|
297
|
1bzcA |
Human ptp1b catalytic domain complexed with tpi |
|
102
|
297
|
1bzjA |
Human ptp1b complexed with tpicooh |
|
104
|
297
|
1c88A |
Crystal structure of protein tyrosine phosphatase 1b complexed with 2-(oxalyl-amino)-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine-3-carboxylic acid |
|
108
|
297
|
1c85A |
Crystal structure of protein tyrosine phosphatase 1b complexed with 2-(oxalyl-amino)-benzoic acid |
|
110
|
297
|
1aaxA |
Crystal structure of protein tyrosine phosphatase 1b complexed with two bis(para-phosphophenyl)methane (bppm) molecules |
|
93
|
284
|
1a5yA |
Protein tyrosine phosphatase 1b cysteinyl-phosphate intermediate |
