|
175
|
454
|
7cp8A |
Structure of the cyp102a1 haem domain with n-(5-cyclohexyl)valeroyl-l-phenylalanine in complex with (r)-1-indanylamine |
|
181
|
454
|
7cknA |
Structure of the cyp102a1 haem domain with n-{2-[4-(trifluoromethoxy)phenoxy]}acetoyl-l-phenylalanine in complex with isopropylamine |
|
178
|
454
|
7cooA |
Structure of the cyp102a1 haem domain with n-carboxybenzyl-l-prolyl-l-phenylalanine in complex with cyclohexylamine |
|
179
|
455
|
7cx6A |
Structure of the cyp102a1 haem domain with n-(5-cyclohexyl)valeroyl-l-phenylalanine in complex with (r)-(+)-1-phenylethylamine |
|
181
|
454
|
7cziA |
Structure of the cyp102a1 haem domain with n-{2-[4-(trifluoromethoxy)phenoxy]}acetoyl-l-phenylalanine |
|
162
|
473
|
7mk8A |
Crystal structure of a surface mutant of human fetal-specific cyp3a7 bound to dithiothreitol |
|
155
|
470
|
7ks8A |
Crystal structure of human cyp3a4 with the caged inhibitor |
|
137
|
469
|
7ksaA |
Crystal structure of human cyp3a4 with the caged inhibitor |
|
126
|
469
|
7kvjA |
Human cyp3a4 bound to an inhibitor |
|
149
|
469
|
7kvsA |
Human cyp3a4 bound to an inhibitor |
|
142
|
468
|
7kvoA |
Human cyp3a4 bound to an inhibitor |
|
145
|
470
|
7kvkA |
Human cyp3a4 bound to an inhibitor |
|
144
|
469
|
7kviA |
Human cyp3a4 bound to an inhibitor |
|
130
|
468
|
7kvhA |
Human cyp3a4 bound to an inhibitor |
|
137
|
468
|
7kvqA |
Human cyp3a4 bound to an inhibitor |
|
153
|
469
|
7kvpA |
Human cyp3a4 bound to an inhibitor |
|
140
|
468
|
7kvnA |
Human cyp3a4 bound to an inhibitor |
|
140
|
469
|
7kvmA |
Human cyp3a4 bound to an inhibitor |
|
178
|
453
|
6k3qA |
Crystal structure of p450bm3 with n-(3-cyclohexylpropanoyl)-l-prolyl-l-phenylalanine |
|
170
|
456
|
6h1oA |
Structure of the bm3 heme domain in complex with voriconazole |
|
172
|
453
|
6h1sA |
Structure of the bm3 heme domain in complex with fluconazole |
|
172
|
456
|
6h1tA |
Structure of the bm3 heme domain in complex with clotrimazole |
|
166
|
455
|
6h1lA |
Structure of the bm3 heme domain in complex with tioconazole |
|
168
|
464
|
6bwwA |
Crystal structure of an acetate and cymal-5 bound cytochrome p450 2b4 f429h mutant |
|
158
|
469
|
6csdA |
V308e mutant of cytochrome p450 2d6 complexed with prinomastat |
|
156
|
471
|
6mjmA |
Substrate free cytochrome p450 3a5 (cyp3a5) |
|
159
|
467
|
6csbA |
V308e mutant of cytochrome p450 2d6 complexed with thioridazine |
|
140
|
395
|
5it1A |
Streptomyces peucetius cyp105p2 complex with biphenyl compound |
|
152
|
455
|
5jquA |
Crystal structure of cytochrome p450 bm3 heme domain g265f/t269v/l272w/l322i/f405m/a406s (wivs-fm) variant with iron(iii) deuteroporphyrin ix bound |
|
171
|
457
|
5jq2A |
Crystal structure of the ru(bpy)2phena functionalized p450 bm3 l407c heme domain mutant in complex with n-palmitoylglycine |
|
172
|
458
|
5jtdA |
Crystal structure of the ru(bpy)2phena functionalized p450 bm3 l407c heme domain mutant in complex with dmso. |
|
137
|
463
|
6iq5A |
Crystal structure of cyp1b1 and inhibitor having azide group |
|
169
|
464
|
5iuzA |
Structure of p450 2b4 f202w mutant (cymal-5) |
|
156
|
464
|
5iutA |
Structure of p450 2b4 f202w mutant |
|
153
|
476
|
6dwnA |
Structure of human cytochrome p450 1a1 with erlotinib |
|
169
|
478
|
6dwmA |
Structure of human cytochrome p450 1a1 with bergamottin |
|
186
|
480
|
6c93A |
Effects of the e310a mutation of cytochrome p450 4b1 (cyp4b1) on n-octane binding and heme ruffling |
|
181
|
482
|
6c94A |
Structure of cytochrome p450 4b1 (cyp4b1) complexed with the inhibitor het0016 |
|
126
|
452
|
5zisA |
Crystal structure of mn-protoporphyrinix-reconstituted p450bm3 |
|
124
|
452
|
5zlhA |
Crystal structure of mn-protoporphyrinix-reconstituted p450bm3 |
|
157
|
469
|
5veuA |
Human cytochrome p450 3a5 (cyp3a5) |
|
158
|
464
|
5em4A |
Structure of cyp2b4 f244w in a ligand free conformation |
|
158
|
453
|
5b2vA |
Crystal structure of p450bm3 with n-perfluorohexanoyl-l-tryptophan |
|
171
|
453
|
5b2xA |
Crystal structure of p450bm3 mutant with n-perfluoroheptanoyl-l-tryptophan |
|
170
|
452
|
5b2wA |
Crystal structure of p450bm3 with n-perfluorododecanoyl-l-tryptophan |
|
173
|
453
|
5b2uA |
Crystal structure of p450bm3 with n-perfluorohexanoyl -l-tryptophan |
|
157
|
460
|
4zfbA |
Cytochrome p450 pentamutant from bm3 bound to palmitic acid |
|
153
|
460
|
4zfaA |
Cytochrome p450 wild type from bm3 with bound peg |
|
176
|
457
|
4duaA |
Cytochrome p450 bm3h-9d7 mri sensor, no ligand |
|
123
|
390
|
4dqkA |
Crystal structure of the fad binding domain of cytochrome p450 bm3 |
