| 8u5t |
Structure of Mango II variant aptamer bound to T01-6A-B |
22.6 |
77.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8u5v |
The mTORC1 cholesterol sensor LYCHOS (GPR155) - auxin bound, closed state |
26.3 |
85.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8u5w |
De novo designed pentameric helical bundle protein |
34.1 |
107.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8u5x |
The mTORC1 cholesterol sensor LYCHOS (GPR155) - auxin bound, open state |
27.2 |
91.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u5y |
human RADX trimer bound to ssDNA |
46.4 |
152.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u5z |
Structure of Mango II variant aptamer bound to T01-7M-B |
22.7 |
81.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8u60 |
Structure of Mango II variant2 aptamer bound to T01-6A |
22.7 |
79.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8u61 |
Human RADX tetramer bound to ssDNA |
51.6 |
175.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u62 |
Cryo-EM structure of PsBphP in Pfr state, Dimer of Dimers FL |
35.6 |
118.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u63 |
Cryo-EM structure of PsBphP in Pfr state, Dimer of Dimers PSM only |
35.0 |
105.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8u64 |
Cryo-EM structure of PsBphP in Pfr state, medial PSM only |
35.0 |
107.6 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8u65 |
Cryo-EM structure of PsBphP in Pfr state, splayed PSM only |
34.9 |
104.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8u66 |
Firmicutes Rubisco |
44.9 |
135.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u69 |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 3-chloro-5-(4-chloro-2-(2-(5-chloro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)ethoxy)phenoxy)benzonitrile (JLJ334), a non-nucleoside inhibitor
; |
35.0 |
114.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6a |
Crystal Structure of HIV-1 Reverse Transcriptase in Complex with (JLJ729), a non-nucleoside inhibitor |
35.2 |
116.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6b |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(4-chloro-3-(3-chloro-5-cyanophenoxy)phenethyl)acrylamide (JLJ731), a non-nucleoside inhibitor
; |
35.2 |
116.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6c |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 2-chloro-N-(4-chloro-3-(3-chloro-5-cyanophenoxy)phenethyl)acetamide (JLJ732), a non-nucleoside inhibitor
; |
35.2 |
115.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6d |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(2-(4-chloro-3-(3-chloro-5-cyanophenoxy)phenoxy)ethyl)-N-methylacrylamide (JLJ736), a non-nucleoside inhibitor
; |
35.2 |
116.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6e |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(4-chloro-3-(3-chloro-5-cyanophenoxy)phenethyl)-N-methylacrylamide (JLJ738), a non-nucleoside inhibitor
; |
35.2 |
115.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6f |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(2-(5-chloro-2-(3-chloro-5-cyanophenoxy)phenoxy)ethyl)-N-methylacrylamide (JLJ742), a non-nucleoside inhibitor
; |
35.3 |
115.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6g |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 3-(2-(2-(3-acryloyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)ethoxy)-4-chlorophenoxy)-5-chlorobenzonitrile (JLJ744), a non-nucleoside inhibitor
; |
35.0 |
114.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6h |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 3-(2-(2-(3-acryloyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)ethoxy)-4-chlorophenoxy)-5-chlorobenzonitrile (JLJ744), a non-nucleoside inhibitor
; |
50.9 |
167.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6i |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(2-(2-((2-cyanoindolizin-8-yl)oxy)phenoxy)ethyl)-N-methylacrylamide (JLJ745), a non-nucleoside inhibitor
; |
35.1 |
115.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8u6j |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(2-(5-chloro-2-((2-cyanoindolizin-8-yl)oxy)phenoxy)ethyl)-N-methylacrylamide (JLJ746), a non-nucleoside inhibitor
; |
35.0 |
114.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8u6k |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(2-(2-((6-cyanonaphthalen-1-yl)oxy)phenoxy)ethyl)-N-methylacrylamide (JLJ747), a non-nucleoside inhibitor
; |
35.0 |
114.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6l |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(2-(5-chloro-2-((6-cyanonaphthalen-1-yl)oxy)phenoxy)ethyl)-N-methylacrylamide (JLJ748), a non-nucleoside inhibitor
; |
35.1 |
115.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6m |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with N-(2-(2-((6-chloro-2-cyanoindolizin-8-yl)oxy)phenoxy)ethyl)-N-methylacrylamide (JLJ751), a non-nucleoside inhibitor
; |
35.3 |
112.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6n |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 3-(2-((6-cyanonaphthalen-1-yl)oxy)phenoxy)-N,N-dimethylpropanamide (JLJ752), a non-nucleoside inhibitor
; |
34.2 |
111.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6o |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with5-(2-(3-oxo-3-(pyrrolidin-1-yl)propoxy)phenoxy)-2-naphthonitrile (JLJ753), a non-nucleoside inhibitor
; |
35.1 |
115.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6p |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 3-(2-((2-cyanoindolizin-8-yl)oxy)phenoxy)-N,N-dimethylpropanamide (JLJ754), a non-nucleoside inhibitor
; |
34.9 |
114.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6q |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 8-(2-(3-oxo-3-(pyrrolidin-1-yl)propoxy)phenoxy)indolizine-2-carbonitrile (JLJ755), a non-nucleoside inhibitor
; |
35.2 |
114.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8u6r |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 3-(2-((2-cyanoindolizin-8-yl)oxy)phenoxy)-N-(2,2-difluoroethyl)propanamide (JLJ756), a non-nucleoside inhibitor
; |
35.2 |
113.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8u6s |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 8-(2-(3-morpholino-3-oxopropoxy)phenoxy)indolizine-2-carbonitrile (JLJ757), a non-nucleoside inhibitor
; |
34.6 |
113.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6t |
;Crystal Structure of HIV-1 Reverse Transcriptase in Complex with 5-(2-(2-(3-acryloyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)ethoxy)phenoxy)-2-naphthonitrile (JLJ758), a non-nucleoside inhibitor
; |
34.9 |
114.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6x |
ATP-dependent DNA ligase Lig E from Neisseria gonorrhoeae |
23.2 |
77.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8u6y |
Preholo-Proteasome from Beta 3 D205 deletion |
65.7 |
249.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u6z |
SLC9C1 at pH 8 in presence of K+ |
43.0 |
132.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u70 |
Crystal structure of malaria transmission-blocking anti-Pfs48/45 antibody RUPA-58. |
49.5 |
155.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8u71 |
Structure of sea urchin SLC9C1 at pH 8 in Na+ |
42.3 |
128.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u72 |
Cryo-EM structure of the SPARTA oligomer with guide RNA and target DNA |
71.8 |
253.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u73 |
R399A sea urchin SLC9C1 pH 8 in Na+ |
42.2 |
131.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8u75 |
R399A mutant of sea urchin SLC9C1 at pH 6 in Na+ - Compressed state |
40.5 |
124.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8u77 |
Crystal structure of Taf14 in complex with Yng1 |
23.1 |
73.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8u78 |
Structure of a N-Me-D-Gln4,Lys10-teixobactin analogue |
15.7 |
54.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8u79 |
Crystal Structure of Substrate Binding Protein of Thermus thermophilus TAXI-TRAP protein with L-glutamate |
20.0 |
62.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8u7b |
Crystal structure of Apo form of Short Prokaryotic Argonaute TIR-APAZ (SPARTA) heterodimer |
33.5 |
113.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8u7c |
Engineered NEMO minimal IKK-binding domain |
29.4 |
111.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8u7d |
R399A mutant of sea urchin SLC9C1 at pH 6 in Na+ - Relaxed state |
40.8 |
127.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8u7e |
Structure of Sts-1 HP domain with rebamipide derivative |
43.3 |
149.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8u7f |
Crystal structure of CIB_12 beta-galactosidase from Cuniculiplasma divulgatum |
34.9 |
115.7 |
X-RAY DIFFRACTION |
GOOD
|