| 2bfl |
;Bacillus cereus metallo-beta-lactamase (BcII) Arg (121) Cys mutant. Solved at pH5 using 20mM ZnSO4 in buffer. 1mM DTT was used as a reducing agent.
; |
26.1 |
84.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2bfm |
Leishmania major pteridine reductase 1 in complex with NADP and trimethoprim |
30.0 |
93.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bfn |
;The crystal structure of the complex of the haloalkane dehalogenase LinB with the product of dehalogenation reaction 1,2-dichloropropane.
; |
18.8 |
63.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2bfo |
Leishmania major pteridine reductase 1 in complex with NADPH |
29.9 |
92.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2bfp |
Leishmania major pteridine reductase 1 in complex with NADP and tetrahydrobiopterin |
29.9 |
91.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2bfq |
MACRO DOMAINS ARE ADP-RIBOSE BINDING MOLECULES |
16.8 |
53.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2bfr |
The Macro domain is an ADP-ribose binding module |
16.8 |
52.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2bfu |
X-ray structure of CPMV top component |
27.6 |
95.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bfv |
MONOCLONAL ANTIBODY FRAGMENT FV4155 FROM E. COLI |
18.6 |
57.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bfw |
Structure of the C domain of glycogen synthase from Pyrococcus abyssi |
17.2 |
51.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2bfx |
Mechanism of Aurora-B activation by INCENP and inhibition by Hesperadin. |
41.3 |
126.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2bfy |
Complex of Aurora-B with INCENP and Hesperadin. |
41.2 |
127.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2bfz |
;Bacillus cereus metallo-beta-lactamase (BcII) Arg (121) Cys mutant. Solved at pH4.5 using 20mM ZnSO4 in buffer. 1mM DTT was used as a reducing agent. Cys221 is oxidized.
; |
26.1 |
84.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2bg1 |
Active site restructuring regulates ligand recognition in classA Penicillin-binding proteins (PBPs) |
24.6 |
87.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2bg2 |
;Bacillus cereus metallo-beta-lactamase (BcII) Arg (121) Cys mutant. Solved at pH4.5 using 20mM ZnSO4 in the buffer. 1mM DTT and 1mM TCEP- HCl were used as reducing agents. Cys221 is reduced.
; |
26.1 |
85.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2bg5 |
;Crystal Structure of the Phosphoenolpyruvate-binding Enzyme I-Domain from the Thermoanaerobacter tengcongensis PEP: Sugar Phosphotransferase System (PTS)
; |
35.5 |
111.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bg6 |
;Bacillus cereus metallo-beta-lactamase (BcII) Arg (121) Cys mutant. Solved at pH5 using 20 Micromolar ZnSO4 in the buffer. 1mM DTT was used as a reducing agent. Cys221 is oxidized.
; |
26.4 |
84.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2bg7 |
;Bacillus cereus metallo-beta-lactamase (BcII) Arg (121) Cys mutant. Solved at pH4.5 using 20 Micromolar ZnSO4 in the buffer. 1mM DTT was used as a reducing agent. Cys221 is oxidized.
; |
26.2 |
85.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2bg8 |
;Bacillus cereus metallo-beta-lactamase (BcII) Arg (121) Cys mutant. Solved at pH4.5 using 20 Micromolar ZnSO4 in the buffer. 1mM DTT and 1mM TCEP-HCl were used as reducing agents.
; |
26.1 |
84.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bg9 |
REFINED STRUCTURE OF THE NICOTINIC ACETYLCHOLINE RECEPTOR AT 4A RESOLUTION. |
43.9 |
153.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 2bga |
;Bacillus cereus metallo-beta-lactamase (BcII) Arg (121) Cys mutant. Solved at pH7 using 20 Micromolar ZnSO4 in the buffer. 1mM DTT was used as a reducing agent. Cys221 is oxidized.
; |
26.2 |
84.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgc |
PrfA-G145S, a constitutive active mutant of the Transcriptional Regulator In L.monocytogenes |
41.2 |
133.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgd |
Structure-based design of Protein Tyrosine Phosphatase-1B Inhibitors |
20.0 |
66.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bge |
Structure-based design of Protein Tyrosine Phosphatase-1B Inhibitors |
20.0 |
67.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgf |
NMR structure of Lys48-linked di-ubiquitin using chemical shift perturbation data together with RDCs and 15N-relaxation data |
16.5 |
53.1 |
SOLUTION NMR |
REASONABLE
|
| 2bgg |
The structure of a Piwi protein from Archaeoglobus fulgidus complexed with a 16nt siRNA duplex. |
34.6 |
111.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgh |
Crystal structure of Vinorine Synthase |
34.1 |
117.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgi |
;X-Ray Structure of the Ferredoxin-NADP(H) Reductase from Rhodobacter capsulatus complexed with three molecules of the detergent n-heptyl- beta-D-thioglucoside at 1.7 Angstroms
; |
19.1 |
61.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgj |
X-Ray Structure of the Ferredoxin-NADP(H) Reductase from Rhodobacter capsulatus at 2.1 Angstroms |
33.2 |
102.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bgk |
X-Ray structure of apo-Secoisolariciresinol Dehydrogenase |
25.6 |
81.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bgl |
X-Ray structure of binary-Secoisolariciresinol Dehydrogenase |
19.8 |
70.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgm |
X-Ray structure of ternary-Secoisolariciresinol Dehydrogenase |
19.8 |
74.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgn |
HIV-1 Tat protein derived N-terminal nonapeptide Trp2-Tat(1-9) bound to the active site of Dipeptidyl peptidase IV (CD26) |
75.4 |
224.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgo |
Mannan Binding Module from Man5C |
13.4 |
41.7 |
SOLUTION NMR |
GOOD
|
| 2bgp |
Mannan Binding Module from Man5C in bound conformation |
13.3 |
42.0 |
SOLUTION NMR |
GOOD
|
| 2bgq |
apo aldose reductase from barley |
20.1 |
61.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bgr |
Crystal structure of HIV-1 Tat derived nonapeptides Tat(1-9) bound to the active site of Dipeptidyl peptidase IV (CD26) |
39.5 |
128.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgs |
HOLO ALDOSE REDUCTASE FROM BARLEY |
19.9 |
60.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bgt |
;CRYSTAL STRUCTURE OF THE DNA MODIFYING ENZYME BETA-GLUCOSYLTRANSFERASE IN THE PRESENCE AND ABSENCE OF THE SUBSTRATE URIDINE DIPHOSPHOGLUCOSE
; |
22.1 |
72.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgu |
;CRYSTAL STRUCTURE OF THE DNA MODIFYING ENZYME BETA-GLUCOSYLTRANSFERASE IN THE PRESENCE AND ABSENCE OF THE SUBSTRATE URIDINE DIPHOSPHOGLUCOSE
; |
21.6 |
75.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgv |
X-ray structure of ferric cytochrome c-550 from Paracoccus versutus |
14.9 |
47.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bgw |
XPF from Aeropyrum pernix, complex with DNA |
26.4 |
82.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bgy |
Fit of the x-ray structure of the baterial flagellar hook fragment flge31 into an EM map from the hook of Caulobacter crescentus. |
29.5 |
96.5 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 2bgz |
ATOMIC MODEL OF THE BACTERIAL FLAGELLAR BASED ON DOCKING AN X-RAY DERIVED HOOK STRUCTURE INTO AN EM MAP. |
29.2 |
95.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 2bh0 |
Crystal structure of a SeMet derivative of EXPA from Bacillus subtilis at 2.5 angstrom |
18.4 |
64.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2bh1 |
;X-ray structure of the general secretion pathway complex of the N- terminal domain of EpsE and the cytosolic domain of EpsL of Vibrio cholerae
; |
31.8 |
107.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bh2 |
;Crystal Structure of E. coli 5-methyluridine methyltransferase RumA in complex with ribosomal RNA substrate and S-adenosylhomocysteine.
; |
33.9 |
112.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2bh3 |
Zn substituted E. coli Aminopeptidase P in complex with product |
25.8 |
88.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2bh4 |
X-ray structure of the M100K variant of ferric cyt c-550 from Paracoccus versutus determined at 100 K. |
15.0 |
47.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2bh5 |
X-ray structure of the M100K variant of ferric cyt c-550 from Paracoccus versutus determined at 295 K. |
15.1 |
46.7 |
X-RAY DIFFRACTION |
GOOD
|