| 8vzo |
Cryo-EM structure of FLVCR2 in the outward-facing state with choline bound |
28.4 |
99.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8vzp |
Crystal Structure of the ER-alpha Ligand-binding Domain (L372S, L536S) in complex with k-403 |
33.1 |
104.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8vzq |
Crystal Structure of the ER-alpha Ligand-binding Domain (L372S, L536S) in complex with k-406 |
34.1 |
111.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8vzr |
Crystal structure of dehaloperoxidase A in complex with substrate 4-bromo-o-cresol |
24.2 |
88.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8vzv |
Human TDO (hTDO) in complex with LM10 |
33.9 |
102.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8vzw |
Structure of humanized MS-Hu6 Fab fragment |
25.1 |
79.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8vzx |
Q108K:K40L:T53A:R58F mutant of hCRBPII bound to synthetic fluorophore TD-1V |
27.6 |
88.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8vzy |
Q108K:K40L:T51V:T53S:R58Y mutant of hCRBPII bound to synthetic fluorophore TD-1V |
22.3 |
75.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8vzz |
Q108K:K40L:T51V:T53S:Y19W:R58W mutant of hCRBPII bound to synthetic fluorophore TD-1V |
21.8 |
72.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8w00 |
Q108K:K40L:T51V:T53S:Y19W:R58W:L117E mutant of hCRBPII bound to synthetic fluorophore TD-1V |
21.9 |
72.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w01 |
Crystal structure of DUF1735 domain-containing protein (GH18-like) from Bacteroides faecium at 2.7 A resolution (Space group C2) |
26.6 |
92.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8w02 |
Q108K:K40L:T51V:T53S:R58W mutant of hCRBPII bound to synthetic fluorophore TD-1V |
21.8 |
71.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8w03 |
Crystal Structure of the ER-alpha Ligand-binding Domain (L372S, L536S) in complex with k-1154 |
34.5 |
118.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8w04 |
Crystal structure of DUF1735-domain containing protein (GH18-like) from Bacteroides faecium at 2.9 A resolution (Space group P21) |
41.5 |
148.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8w05 |
;Crystal Structure of the reconstruction of the ancestral triosephosphate isomerase of the last opisthokont common ancestor obtained by maximum likelihood
; |
43.4 |
141.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8w06 |
;Crystal Structure of the reconstruction of the ancestral triosephosphate isomerase of the last opisthokont common ancestor obtained by maximum likelihood with PGH
; |
41.4 |
130.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8w07 |
Crystal Structure of the ER-alpha Ligand-binding Domain (L372S, L536S) in complex with k-402 |
33.2 |
106.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w08 |
;Crystal Structure of the worst case reconstruction of the ancestral triosephosphate isomerase of the last opisthokont common ancestor obtained by maximum likelihood
; |
25.3 |
78.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w09 |
HIV-1 wild-type intasome core |
37.4 |
124.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w0a |
Human DNA polymerase theta helicase domain in complex with ssDNA, dimer form |
44.2 |
151.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w0b |
Crystal structure of Acetyl-CoA synthetase 2 from Candida albicans in complex with a cyclopropyl AMP ester inhibitor |
40.2 |
127.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0c |
Crystal structure of Acetyl-CoA synthetase 2 from Candida albicans in complex with a cyclopentyl ester AMP inhibitor |
40.2 |
121.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0d |
Crystal structure of Acetyl-CoA synthetase 2 from Candida albicans in complex with an isopropyl AMP ester inhibitor |
40.2 |
127.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0e |
Cryo-EM structure of a human MCM2-7 single hexamer on dsDNA |
47.5 |
139.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w0f |
Cryo-EM structure of a human MCM2-7 double hexamer on dsDNA |
67.8 |
238.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w0g |
Cryo-EM structure of a human MCM2-7 dimer |
75.8 |
222.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w0h |
Crystal structure of Acetyl-CoA synthetase 2 from Candida albicans in complex with an isopropyl AMP ester inhibitor (trigonal form) |
41.2 |
129.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0i |
Cryo-EM structure of the human MCM2-7 heterohexamer |
50.4 |
152.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w0j |
Crystal structure of Acetyl-CoA synthetase 2 from Candida albicans in complex with a propyne AMP ester inhibitor |
39.7 |
125.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0k |
Minimal PutA proline dehydrogenase domain (design #2) complexed with 1-hydroxyethane-1-sulfonate |
28.9 |
88.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0l |
Crystal structure of Acetyl-CoA synthetase 2 from Candida albicans in complex with a propyne AMP ester inhibitor and CoA |
40.2 |
126.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0m |
Crystal structure of Acetyl-CoA synthetase 2 from Candida albicans in complex with a Acetyl Sulfamate AMP ester inhibitor |
38.3 |
120.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w0n |
IRED crystal structure |
24.7 |
80.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0o |
GDH-105 crystal structure |
46.8 |
160.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0p |
BsaXI -- Type IIB R-M system |
55.0 |
190.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w0q |
Pembrolizumab CDR-H3 Loop Mimic |
9.2 |
33.3 |
SOLUTION NMR |
GOOD
|
| 8w0r |
Human EBP complexed with compound 1 |
25.1 |
77.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8w0s |
Human EBP complexed with compound 3a |
25.2 |
78.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8w0t |
Human LCAD |
35.4 |
108.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w0u |
Human LCAD complexed with Acetoacetyl Coenzyme A |
35.4 |
108.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w0v |
Crystal structure of broadly neutralizing antibody hcab55 in complex with Hepatitis C virus envelope glycoprotein E2 ectodomain |
34.1 |
118.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0w |
Crystal structure of broadly neutralizing antibody hcab64 in complex with Hepatitis C virus envelope glycoprotein E2 ectodomain |
34.0 |
113.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0x |
Crystal structure of broadly neutralizing antibody hcab40 in complex with Hepatitis C virus envelope glycoprotein E2 ectodomain |
32.9 |
115.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8w0y |
Crystal structure of broadly neutralizing antibody hcab17 in complex with Hepatitis C virus envelope glycoprotein E2 ectodomain |
45.7 |
168.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w0z |
Human LCAD complexed with Lauric Acid |
52.0 |
178.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w10 |
Plasmodium vivax PMX-MK7602 inhibitor complex |
30.7 |
101.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8w11 |
Structure of human PIN1 covalently derivatized with SuFEx compound |
21.6 |
72.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8w12 |
Cryo-EM structure of VP3-VP6 heterohexamer |
62.1 |
192.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w13 |
;Crystal structure of MYST acetyltransferase domain in complex with N-(1-(5-bromo-2-methoxyphenyl)-1H-1,2,3-triazol-4-yl)-2-methoxybenzenesulfonamide
; |
21.3 |
79.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w14 |
Rhodanese-like domain from Acinetobacter baumannii 118362 |
21.4 |
71.0 |
X-RAY DIFFRACTION |
GOOD
|