|
12
|
107
|
7cf9B |
Structure of ryr1 (ca2+/chl) |
|
12
|
75
|
6m4vB |
Crystal structure of mbp fused split fkbp in complex with rapamycin |
|
23
|
108
|
6m4uA |
Crystal structure of fkbp-frb t2098l mutant in complex with rapamycin |
|
11
|
75
|
6m4wD |
Crystal structure of mbp fused split fkbp-frb t2098l mutant in complex with rapamycin |
|
113
|
403
|
6m4wA |
Crystal structure of mbp fused split fkbp-frb t2098l mutant in complex with rapamycin |
|
98
|
400
|
6m4vA |
Crystal structure of mbp fused split fkbp in complex with rapamycin |
|
13
|
107
|
7jmgA |
Functional pathways of biomolecules retrieved from single-particle snapshots - frame 22 - state 2 (s2) |
|
13
|
107
|
7jmiA |
Functional pathways of biomolecules retrieved from single-particle snapshots - frame 29 - state 3 (s3) |
|
15
|
107
|
7jmfA |
Functional pathways of biomolecules retrieved from single-particle snapshots - frame 42 - state 6 (s6) |
|
13
|
107
|
7jmhA |
Functional pathways of biomolecules retrieved from single-particle snapshots - frame 35 - state 4 (s4) |
|
12
|
107
|
7jmjA |
Functional pathways of biomolecules retrieved from single-particle snapshots - frame 37 - state 5 (s5) |
|
15
|
107
|
6pv6A |
Functional pathways of biomolecules retrieved from single-particle snapshots |
|
24
|
94
|
6xd8A |
Crystal structure of peptidylprolyl isomerase (prsa) fragment from bacillus anthracis |
|
51
|
165
|
6x4qA |
Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors: (2r,5s,11s,14s,18e)-14-cyclobutyl-2,11,17,17-tetramethyl-15-oxa-3,9,12,26,29-pentaazatetracyclo[18.5.3.1~5,9~.0~23,27~]nonacosa-1(25),18,20(28),21,23,26-hexaene-4,10,13,16-tetrone (compound 33) |
|
55
|
165
|
6x4pA |
Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors: (2r,5s,11s,14s,18e)-2,11,17,17-tetramethyl-14-(propan-2-yl)-15-oxa-3,9,12,26,29-pentaazatetracyclo[18.5.3.1~5,9~.0~23,27~]nonacosa-1(25),18,20(28),21,23,26-hexaene-4,10,13,16-tetrone (compound 28) |
|
52
|
167
|
6x4mA |
Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors: tert-butyl [(2s)-1-{[(3s,17s)-2,16-dioxo-10,15-dioxa-1,21-diazatricyclo[15.3.1.1~5,9~]docosa-5(22),6,8-trien-3-yl]amino}-3-methyl-1-oxobutan-2-yl]carbamate (compound 3) |
|
51
|
163
|
6x4oA |
Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors: (2r,5s,11s,14s,18e)-2,11-dimethyl-14-(propan-2-yl)-3-oxa-9,12,15,21,29-pentaazatetracyclo[18.5.3.1~5,9~.0~23,27~]nonacosa-1(26),18,20,22,24,27-hexaene-4,10,13,16-tetrone (compound 21) |
|
49
|
165
|
6x4nA |
Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors: (2r,5s,11s,14s,18e)-2,11,17,17-tetramethyl-14-(propan-2-yl)-3-oxa-9,12,15,26,29-pentaazatetracyclo[18.5.3.1~5,9~.0~23,27~]nonacosa-1(25),18,20(28),21,23,26-hexaene-4,10,13,16-tetrone (compound 24) |
|
54
|
163
|
6x3rA |
Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors |
|
51
|
166
|
6x3yA |
Human cyclophilin a bound to a series of acylcic and macrocyclic inhibitors |
|
33
|
128
|
6tx4A |
Crystal structure of human fkbp51 fk1 domain a19t mutant in complex with 2-pyridone |
|
32
|
128
|
6tx6A |
Crystal structure of human fkbp51 fk1 domain a19t mutant in complex with nicotinamide |
|
32
|
128
|
6tx8A |
Crystal structure of human fkbp51 fk1 domain a19t mutant in complex with imidazole |
|
33
|
128
|
6tx5A |
Crystal structure of human fkbp51 fk1 domain a19t mutant in complex with 4-methylimidazole |
|
35
|
128
|
6txxA |
Crystal structure of human fkbp51 fk1 domain a19t mutant in complex with safit2 |
|
34
|
128
|
6tx9A |
Crystal structure of human fkbp51 fk1 domain a19t mutant in complex with hydantoin |
|
30
|
128
|
6tx7A |
Crystal structure of human fkbp51 fk1 domain a19t mutant in complex with 2-piperidone |
|
31
|
131
|
6rcyA |
Crystal structure of fk1 domain of fkbp52 in complex with a bio-inspired hybrid fluorescent ligand |
|
17
|
151
|
1ix5A |
Solution structure of the methanococcus thermolithotrophicus fkbp |
|
4
|
39
|
1i6cA |
Solution structure of pin1 ww domain |
|
17
|
120
|
1j6yA |
Solution structure of pin1at from arabidopsis thaliana |
|
14
|
96
|
1eq3A |
Nmr structure of human parvulin hpar14 |
|
8
|
85
|
1hxvA |
Ppiase domain of the mycoplasma genitalium trigger factor |
|
28
|
107
|
1f40A |
Solution structure of fkbp12 complexed with gpi-1046, a neurotrophic ligand |
|
6
|
39
|
1i8gB |
Solution structure of pin1 ww domain complexed with cdc25 phosphothreonine peptide |
|
13
|
107
|
1fkrA |
Solution structure of fkbp, a rotamase enzyme and receptor for fk506 and rapamycin |
|
8
|
106
|
1l1pA |
Solution structure of the ppiase domain from e. coli trigger factor |
|
4
|
39
|
1i8hB |
Solution structure of pin1 ww domain complexed with human tau phosphothreonine peptide |
|
16
|
92
|
1jnsA |
Nmr structure of the e. coli peptidyl-prolyl cis/trans-isomerase parvulin 10 |
|
19
|
166
|
1clhA |
Three-dimensional solution structure of escherichia coli periplasmic cyclophilin |
|
12
|
104
|
1fjdA |
Human parvulin-like peptidyl prolyl cis/trans isomerase, hpar14 |
|
29
|
164
|
6qdvi |
Human post-catalytic p complex spliceosome |
|
41
|
216
|
6hixBQ |
Cryo-em structure of the trypanosoma brucei mitochondrial ribosome - this entry contains the large mitoribosomal subunit |
|
38
|
190
|
6hixBZ |
Cryo-em structure of the trypanosoma brucei mitochondrial ribosome - this entry contains the large mitoribosomal subunit |
|
3
|
35
|
1w2b5 |
Trigger factor ribosome binding domain in complex with 50s |
|
13
|
100
|
2d3o1 |
Structure of ribosome binding domain of the trigger factor on the 50s ribosomal subunit from d. radiodurans |
|
46
|
216
|
6hivBQ |
Cryo-em structure of the trypanosoma brucei mitochondrial ribosome - this entry contains the complete mitoribosome |
|
39
|
190
|
6hivBZ |
Cryo-em structure of the trypanosoma brucei mitochondrial ribosome - this entry contains the complete mitoribosome |
|
28
|
159
|
6ff4V |
Human bact spliceosome core structure |
|
38
|
159
|
5xjcS |
Cryo-em structure of the human spliceosome just prior to exon ligation at 3.6 angstrom |
