| 8pqh |
PDGFRA T674I mutant kinase domain in complex with avapritinib |
21.2 |
67.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8pqi |
PDGFRA T674I mutant kinase domain in complex with avapritinib derivative 9 |
20.8 |
68.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8pqj |
PDGFRA wild-type kinase domain |
20.6 |
64.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8pqk |
APO crystal structure of PDGFRA-T674I kinase domain |
20.4 |
62.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8pql |
;K48-linked ubiquitin chain formation with a cullin-RING E3 ligase and Cdc34: NEDD8-CUL2-RBX1-ELOB/C-FEM1C with trapped UBE2R2-donor UB-acceptor UB-SIL1 peptide
; |
54.3 |
168.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pqm |
The DNA-binding domain of L-lactate utilization repressor (LutR-DBD) from Bacillus subtilis |
14.5 |
58.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pqn |
NQO1 bound to RBS-10 |
33.9 |
111.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8pqo |
PITP in complex with the inhibitor VT01545 |
20.2 |
49.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pqp |
;Nucleoside 2'deoxyribosyltransferase from Chroococcidiopsis thermalis PCC 7203 D62N Mutant bound to ImmH-Forodesine
; |
22.3 |
70.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8pqq |
;Nucleoside 2'deoxyribosyltransferase from Chroococcidiopsis thermalis PCC 7203 E88Q Mutant bound to Clofarabine
; |
25.4 |
81.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8pqr |
;Nucleoside 2'deoxyribosyltransferase from Chroococcidiopsis thermalis PCC 7203 WT bound to DAD_Immucillin-H
; |
25.3 |
78.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8pqs |
;Nucleoside 2'deoxyribosyltransferase from Chroococcidiopsis thermalis PCC 7203 E88A Mutant
; |
25.3 |
81.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8pqt |
;Nucleoside 2'deoxyribosyltransferase from Chroococcidiopsis thermalis PCC 7203 WT bound to Bis-Tris
; |
20.4 |
65.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8pqu |
NMR structure of the Thermus thermophilus PilF-GSPIIB domain in the apo state |
17.6 |
61.1 |
SOLUTION NMR |
GOOD
|
| 8pqv |
Cytoplasmic dynein-1 motor domain in post-powerstroke state |
49.8 |
162.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8pqw |
Cytoplasmic dynein-1 motor domain bound to dynactin-p150glued and LIS1 |
59.0 |
207.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pqx |
p97 (VCP) mutant - F539A state III |
52.2 |
165.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pqy |
Cytoplasmic dynein-1 motor domain bound to LIS1 |
54.0 |
186.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pqz |
Cytoplasmic dynein-1 A1/A2 motor domains bound to LIS1 |
71.8 |
264.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pr0 |
Cytoplasmic dynein-A heavy chain bound to dynactin-p150glued and IC-LC tower |
62.4 |
214.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pr1 |
Cytoplasmic dynein-B heavy chain bound to IC-LC tower |
76.8 |
216.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pr2 |
Cytoplasmic dynein-1 heavy chain bound to JIP3-LZI |
49.7 |
196.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8pr3 |
Cytoplasmic dynein-1 heavy chain bound to JIP3-RH1 |
50.1 |
172.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pr4 |
Dynactin pointed end bound to JIP3 |
35.7 |
112.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pr5 |
Structure of the autoinhibited dynactin p150glued projection |
81.3 |
233.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8pr6 |
Crystal structure of Corynebacterium glutamicum mycoredoxin-3 at 1.7 A resolution. |
17.3 |
56.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8pr7 |
Aurora-A in complex with CEP192 and an inhibitory monobody |
30.7 |
107.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8pr9 |
The structure of v13Bagel2 |
24.5 |
74.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8pra |
The structure of v13Bagel4 |
24.5 |
72.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8prb |
The structure of v13Bagel6 |
14.0 |
50.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8prc |
The structure of v13Bagel8 |
14.0 |
51.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8prd |
The structure of nvBagel2 |
12.9 |
43.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8pre |
The structure of nvBagel2 in the presence of Zn(II) |
13.1 |
42.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8prf |
The structure of nvBagel5 |
13.3 |
44.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8prg |
The structure of nvBagel6 |
13.0 |
44.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8prh |
The structure of nvBagel7 |
13.1 |
31.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pri |
The structure of nvBagel9 |
13.0 |
43.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8prj |
The structure of v31Bagel8 |
19.5 |
59.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8prk |
;THE R78K AND D117E ACTIVE SITE VARIANTS OF SACCHAROMYCES CEREVISIAE SOLUBLE INORGANIC PYROPHOSPHATASE: STRUCTURAL STUDIES AND MECHANISTIC IMPLICATIONS
; |
27.3 |
90.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8prl |
The structure of v22Bagel8 |
19.6 |
71.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8prm |
The structure of nvBagel2 binding the P8W48O184 polyoxometalate |
17.9 |
55.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8prn |
E1M, K50A, R52A, D97A, E99A MUTANT OF RH. BLASTICA PORIN |
20.8 |
67.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8pro |
The structure of nvBagel2 binding the P8W48O184 polyoxometalate |
13.7 |
49.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8prp |
The structure of nvBagel2 in the presence of Cd(II) |
13.2 |
41.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8prq |
The structure of nvBagel2 in the presence of Cu(II) |
13.2 |
43.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8prr |
The structure of nvBagel4 in the presence of Co(II) |
13.1 |
43.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8prs |
The structure of nvBagel4 |
24.4 |
73.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8prt |
The structure of nvBagel8 in the presence of Co(II) |
13.1 |
45.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8pru |
Engineered form of T thermophiles AHIR |
43.8 |
133.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8prv |
Asymmetric unit of the yeast fatty acid synthase in the non-rotated state with ACP at the ketosreductase domain (FASamn sample) |
63.6 |
210.2 |
ELECTRON MICROSCOPY |
GOOD
|