|
172
|
455
|
7yjgA |
Crystal structure of the p450 bm3 heme domain mutant f87a/t268v/a82c/l181m in complex with n-imidazolyl-pentanoyl-l-phenylalanine and hydroxylamine |
|
177
|
454
|
7ydaA |
Crystal structure of the p450 bm3 heme domain mutant f87v/t268v/a184v in complex with n-imidazolyl-pentanoyl-l-phenylalanine and hydroxylamine |
|
174
|
451
|
7yjhA |
Crystal structure of the p450 bm3 heme domain mutant f87v/t268i in complex with n-imidazolyl-pentanoyl-l-phenylalanine and hydroxylamine |
|
176
|
454
|
7ydeA |
Crystal structure of the p450 bm3 heme domain mutant f87t/t268v/i263v in complex with n-imidazolyl-hexanoyl-l-phenylalanine and hydroxylamine |
|
180
|
454
|
7ydcA |
Crystal structure of the p450 bm3 heme domain mutant f87l/t268v/v78c in complex with n-imidazolyl-pentanoyl-l-phenylalanine and hydroxylamine |
|
160
|
451
|
7yftA |
Crystal structure of the p450 bm3 heme domain mutant f87a/t268v/a82c/l181m in complex with n-imidazolyl-pentanoyl-l-phenylalanine, indane and hydroxylamine |
|
151
|
450
|
8hkjA |
Crystal structure of the cyp102a5 haem domain isolated from bacillus cereus |
|
175
|
454
|
8dsgA |
P411-pfa carbene transferase |
|
145
|
471
|
8ewmA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
148
|
471
|
8ewqA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
144
|
468
|
8exbA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
150
|
468
|
8ewrA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
151
|
471
|
8eweA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
144
|
471
|
8ewsA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
148
|
470
|
8ewpA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
150
|
469
|
8ewnA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
148
|
468
|
8ewdA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
157
|
470
|
8ewlA |
Crystal structure of cyp3a4 bound to an inhibitor |
|
175
|
454
|
7wg0A |
Structure of the manganese protoporphyrin ix-reconstituted cyp102a1 heme domain with n-palmitoyl-l-phenylalanine |
|
165
|
453
|
7wdhA |
Crystal structure of the p450 bm3 heme domain mutant f87a in complex with n-imidazolyl-hexanoyl-l-phenylalanine, phenol and hydroxylamine |
|
171
|
454
|
7wy1A |
Structure of the oxomolybdenum mesoporphyrin ix-reconstituted cyp102a1 haem domain with n-enanthyl-l-prolyl-l-phenylalanine in complex with styerene |
|
164
|
454
|
7wdeA |
Crystal structure of the p450 bm3 heme domain mutant f87l in complex with n-imidazolyl-hexanoyl-l-phenylalanine, styrene and hydroxylamine |
|
185
|
454
|
7wy4A |
Structure of the cyp102a1 f87a haem domain with n-enanthyl-l-prolyl-l-phenylalanine in complex with styrene |
|
180
|
454
|
7wy3A |
Structure of the oxomolybdenum mesoporphyrin ix-reconstituted cyp102a1 f87v mutant haem domain with n-(5-cyclohexyl)valeroyl-l-phenylalanine in complex with styrene |
|
177
|
454
|
7wy2A |
Structure of the oxomolybdenum mesoporphyrin ix-reconstituted cyp102a1 f87a mutant haem domain with n-enanthyl-l-prolyl-l-phenylalanine in complex with styrene |
|
165
|
454
|
7wdiA |
Crystal structure of the p450 bm3 heme domain mutant f87k in complex with n-imidazolyl-hexanoyl-l-phenylalanine and hydroxylamine |
|
162
|
454
|
7wddA |
Crystal structure of the p450 bm3 heme domain mutant f87k in complex with n-imidazolyl-hexanoyl-l-phenylalanine, styrene and hydroxylamine |
|
158
|
454
|
7wdgA |
Crystal structure of the p450 bm3 heme domain mutant f87l in complex with n-imidazolyl-hexanoyl-l-phenylalanine, phenol and hydroxylamine |
|
174
|
454
|
7w9dA |
Crystal structure of the oxomolybdenum mesoporphyrin ix-reconstituted cyp102a1 (p450bm3) heme domain with n-hexadecanoyl-l-homoserine |
|
167
|
452
|
7w97A |
Crystal structure of the cyp102a1 (p450bm3) heme domain with n-hexadecanoyl-l-homoserine |
|
172
|
454
|
7w9jA |
Crystal structure of the oxomolybdenum mesoporphyrin ix-reconstituted cyp102a1 (p450bm3) heme domain with n-dodecanoyl-l-homoserine lactone |
|
161
|
472
|
8dycA |
Human cyp3a4 bound to a substrate |
|
140
|
469
|
7uazA |
Crystal structure of human cyp3a4 with the caged inhibitor |
|
131
|
468
|
7uayA |
Crystal structure of human cyp3a4 with the caged inhibitor |
|
153
|
470
|
7ufdA |
Human cyp3a4 bound to an inhibitor |
|
146
|
471
|
7ufeA |
Human cyp3a4 bound to an inhibitor |
|
142
|
468
|
7uffA |
Human cyp3a4 bound to an inhibitor |
|
164
|
471
|
7ufbA |
Cyp3a4 bound to an inhibitor |
|
147
|
470
|
7uf9A |
Cyp3a4 bound to an inhibitor |
|
147
|
470
|
7ufaA |
Cyp3a4 bound to an inhibitor |
|
152
|
470
|
7ufcA |
Human cyp3a4 bound to an inhibitor |
|
168
|
473
|
7sv2A |
Human cytochrome p450 (cyp) 3a5 ternary complex with azamulin |
|
144
|
470
|
7ladA |
Clobetasol propionate bound to cyp3a5 |
|
169
|
463
|
7rl2A |
Crystal structure of the human cytochrome p450 2c9*8 (cyp2c9*8) genetic variant in complex with the drug losartan |
|
177
|
454
|
7d0tA |
Structure of the cyp102a1 haem domain with n-carboxybenzyl-l-prolyl-l-phenylalanine in complex with (s)-1-indanylamine |
|
178
|
454
|
7d0uA |
Structure of the cyp102a1 haem domain with n-enanthyl-l-prolyl-l-phenylalanine in complex with ethylamine |
|
176
|
454
|
7d1fA |
Structure of the cyp102a1 haem domain with n-enanthyl-l-prolyl-l-phenylalanine in complex with methylamine |
|
179
|
455
|
7cx8A |
Structure of the cyp102a1 haem domain with n-(5-cyclohexyl)valeroyl-l-phenylalanine in complex with (r)-1-tetralylamine |
|
176
|
454
|
7conA |
Structure of the cyp102a1 haem domain with n-{2-[4-(trifluoromethoxy)phenoxy]}acetoyl-l-phenylalanine in complex with n-propylamine |
|
169
|
453
|
7cvrA |
Structure of the cyp102a1 haem domain with n-carboxybenzyl-l-prolyl-l-phenylalanine in complex with (s)-1-tetralylamine |