|
140
|
395
|
5it1A |
Streptomyces peucetius cyp105p2 complex with biphenyl compound |
|
162
|
473
|
5irqA |
Human cytochrome p450 17a1 bound to inhibitors (r)- and (s)- orteronel |
|
134
|
405
|
3w9cA |
Crystal structure of the electron transfer complex of cytochrome p450cam with putidaredoxin |
|
127
|
406
|
5ikiA |
Cyp106a2 with substrate abietic acid |
|
136
|
398
|
5livA |
Crystal structure of myxobacterial cyp260a1 |
|
130
|
406
|
5li7A |
Crystal structure of mycobacterium tuberculosis cyp126a1 in complex with 1-(3-(1h-imidazol-1-yl)propyl)-3-((3s,5s,7s)-adamantan-1-yl)urea |
|
146
|
391
|
5l91A |
The 2.2 a crystal structure of cyp109e1 from bacillus megaterium bound with four corticosterone molecules |
|
140
|
409
|
5li8A |
Crystal structure of mycobacterium tuberculosis cyp126a1 in complex with ketoconazole |
|
161
|
424
|
5m0oC |
Crystal structure of cytochrome p450 olet h85q in complex with arachidonic acid |
|
162
|
424
|
5m0pA |
Crystal structure of cytochrome p450 olet f79a in complex with arachidonic acid |
|
163
|
423
|
5m0nA |
Crystal structure of cytochrome p450 olet in complex with formate |
|
132
|
406
|
5li6A |
Crystal structure of mycobacterium tuberculosis cyp126a1 in complex with n-isopropyl-n-((3-(4-methoxyphenyl)-1,2,4-oxadiazol-5-yl)methyl)-2-(4-nitrophenyl)acetamide |
|
140
|
388
|
5l94A |
The 2.25 a crystal structure of cyp109e1 from bacillus megaterium in complex with testosterone |
|
138
|
397
|
5l1wA |
X-ray structure of 2-mercaptoethanol modified m81c mutant of cytochrome p450 pntm with pentalenolactone f |
|
140
|
397
|
5l1uA |
X-ray structure of m81a mutant of cytochrome p450 pntm with pentalenolactone f |
|
144
|
397
|
5l1rA |
X-ray structure of the substrate-free cytochrome p450 pntm |
|
143
|
397
|
5l1tA |
X-ray structure of m77s mutant of cytochrome p450 pntm with pentalenolactone f |
|
144
|
397
|
5l1sA |
X-ray structure of f232l mutant of cytochrome p450 pntm with pentalenolactone f |
|
142
|
397
|
5l1pA |
X-ray structure of cytochrome p450 pntm with pentalenolactone |
|
141
|
397
|
5l1vA |
X-ray structure of m81c mutant of cytochrome p450 pntm with pentalenolactone f |
|
141
|
397
|
5l1qA |
X-ray structure of cytochrome p450 pntm with dihydropentalenolactone f |
|
162
|
452
|
5jl9A |
Human placental aromatase cytochrome p450 (cyp19a1): androstenedione complex #4 |
|
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 |
|
163
|
452
|
5jl6A |
Human placental aromatase cytochrome p450 (cyp19a1): androstenedione complex #2 |
|
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. |
|
169
|
464
|
5iuzA |
Structure of p450 2b4 f202w mutant (cymal-5) |
|
154
|
474
|
5irvA |
Human cytochrome p450 17a1 bound to inhibitor vt-464 |
|
145
|
406
|
5ik1A |
Open state of p450cam after soaking in camphor |
|
156
|
464
|
5iutA |
Structure of p450 2b4 f202w mutant |
|
130
|
393
|
5ibhA |
Crystal structure mycobacterium tuberculosis cyp121 in complex with inhibitor fragment 26h |
|
134
|
394
|
5ibdA |
Crystal structure mycobacterium tuberculosis cyp121 in complex with inhibitor fragment 24a |
|
129
|
393
|
5ibiA |
Crystal structure mycobacterium tuberculosis cyp121 in complex with inhibitor fragment 26a |
|
134
|
394
|
5ibeA |
Crystal structure mycobacterium tuberculosis cyp121 in complex with inhibitor fragment 25a |
|
141
|
393
|
5hiwA |
Sorangium cellulosum so ce56 cytochrome p450 260b1 |
|
147
|
405
|
5gxgA |
High-resolution crystal structure of the electron transfer complex of cytochrome p450cam with putidaredoxin |
|
133
|
389
|
5foiA |
Crystal structure of mycinamicin viii c21 methyl hydroxylase mycci from micromonospora griseorubida bound to mycinamicin viii |
|
145
|
450
|
4ck8A |
Sterol 14-alpha demethylase (cyp51)from trypanosoma cruzi in complex with (r)-1-(2,4-dichlorophenyl)-2-(1h-imidazol-1-yl)ethyl 4-(4-(3,4- dichlorophenyl)piperazin-1-yl)phenylcarbamate (lfd) |
|
145
|
405
|
7cppA |
The structural basis for substrate-induced changes in redox potential and spin equilibrium in cytochrome p450(cam) |
|
143
|
405
|
8cppA |
Crystal structures of cytochrome p450-cam complexed with camphane, thiocamphor, and adamantane: factors controlling p450 substrate hydroxylation |
|
141
|
405
|
6cp4A |
P450cam d251n mutant |
|
143
|
405
|
6cppA |
Crystal structures of cytochrome p450-cam complexed with camphane, thiocamphor, and adamantane: factors controlling p450 substrate hydroxylation |
|
158
|
464
|
5em4A |
Structure of cyp2b4 f244w in a ligand free conformation |
|
93
|
365
|
5bv5A |
Structure of cyp119 with t213a and c317h mutations |
|
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 |
|
155
|
472
|
5a1rA |
Crystal structure of cytochrome p450 3a4 bound to progesterone |
|
145
|
467
|
5a5jA |
Cytochrome 2c9 p450 inhibitor complex |
