| 2g14 |
Photolyzed CO L29F Myoglobin: 3.16us |
16.6 |
50.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2g15 |
Structural Characterization of autoinhibited c-Met kinase |
21.2 |
69.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2g16 |
Structure of S65A Y66S GFP variant after backbone fragmentation |
18.3 |
57.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2g17 |
The structure of N-acetyl-gamma-glutamyl-phosphate reductase from Salmonella typhimurium. |
20.9 |
67.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2g18 |
Crystal Structure of Nostoc sp. 7120 phycocyanobilin:ferredoxin oxidoreductase (PcyA) Apoprotein |
46.5 |
145.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2g19 |
Cellular Oxygen Sensing: Crystal Structure of Hypoxia-Inducible Factor Prolyl Hydroxylase (PHD2) |
18.2 |
63.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1a |
Crystal structure of the complex between Apha class B acid phosphatase/phosphotransferase |
23.8 |
73.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2g1d |
Solution Structure of Ribosomal Protein S24E from Thermoplasma acidophilum |
16.9 |
67.9 |
SOLUTION NMR |
REASONABLE
|
| 2g1e |
Solution Structure of TA0895 |
13.1 |
39.3 |
SOLUTION NMR |
EXCELLENT
|
| 2g1g |
Solution structure of the anticodon loop of S. Pombe tRNAi including the naturally occurring N6-threonyl adenine |
10.8 |
36.0 |
SOLUTION NMR |
GOOD
|
| 2g1h |
Structure of E.coli FabD complexed with glycerol |
19.6 |
62.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1j |
Crystal structure of Mycobacterium tuberculosis Shikimate Kinase at 2.0 angstrom resolution |
20.9 |
61.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2g1k |
Crystal structure of Mycobacterium tuberculosis shikimate kinase in complex with shikimate at 1.75 angstrom resolution |
16.7 |
52.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1l |
Crystal structure of the FHA domain of human kinesin family member C |
— |
— |
X-RAY DIFFRACTION |
—
|
| 2g1m |
Cellular Oxygen Sensing: Crystal Structure of Hypoxia-Inducible Factor Prolyl Hydroxylase (PHD2) |
17.6 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1n |
;Ketopiperazine-based renin inhibitors: Optimization of the "C" ring
; |
35.8 |
110.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g1o |
;Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring
; |
36.0 |
110.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g1p |
Structure of E. coli DNA adenine methyltransferase (DAM) |
28.4 |
95.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g1q |
crystal structure of KSP in complex with inhibitor 9h |
31.3 |
109.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1r |
Ketopiperazine-Based Renin Inhibitors: Optimization of the C Ring |
35.9 |
110.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1s |
Ketopiperazine-Based Renin Inhibitors: Optimization of the C Ring |
35.9 |
107.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1t |
A Src-like Inactive Conformation in the Abl Tyrosine Kinase Domain |
41.5 |
142.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1u |
CRYSTAL STRUCTURE OF A PUTATIVE TRANSPORT PROTEIN (TM1088A) FROM THERMOTOGA MARITIMA AT 1.50 A RESOLUTION |
16.2 |
54.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1w |
NMR structure of the Aquifex aeolicus tmRNA pseudoknot PK1 |
11.5 |
38.9 |
SOLUTION NMR |
GOOD
|
| 2g1y |
;Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring
; |
35.9 |
106.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2g1z |
X-ray structure of the oligonucleotide sequence d(AAATTT) |
12.7 |
44.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g20 |
Ketopiperazine-Based Renin Inhibitors: Optimization of the C Ring |
35.8 |
111.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g21 |
;Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring
; |
36.0 |
108.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2g22 |
;Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring
; |
36.0 |
110.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2g24 |
;Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring
; |
36.1 |
109.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2g25 |
E. Coli Pyruvate Dehydrogenase Phosphonolactylthiamin Diphosphate Complex |
34.2 |
105.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2g26 |
;Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring
; |
36.2 |
110.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g27 |
;Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring
; |
36.5 |
111.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g28 |
E. Coli Pyruvate Dehydrogenase H407A variant Phosphonolactylthiamin Diphosphate Complex |
34.3 |
106.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2g29 |
crystal structure of the periplasmic nitrate-binding protein NrtA from Synechocystis PCC 6803 |
20.8 |
71.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2g2b |
NMR structure of the human allograft inflammatory factor 1 |
17.0 |
42.9 |
SOLUTION NMR |
REASONABLE
|
| 2g2c |
Putative molybdenum cofactor biosynthesis protein from Corynebacterium diphtheriae. |
15.9 |
50.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2g2d |
Crystal structure of a putative pduO-type ATP:cobalamin adenosyltransferase from Mycobacterium tuberculosis |
17.5 |
69.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2g2f |
A Src-like Inactive Conformation in the Abl Tyrosine Kinase Domain |
56.7 |
170.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g2h |
A Src-like Inactive Conformation in the Abl Tyrosine Kinase Domain |
28.1 |
94.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2g2i |
A Src-like Inactive Conformation in the Abl Tyrosine Kinase Domain |
27.9 |
87.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2g2k |
NMR structure of an N-terminal fragment of the eukaryotic initiation factor 5 (eIF5) |
21.1 |
89.3 |
SOLUTION NMR |
REASONABLE
|
| 2g2l |
Crystal Structure of the Second PDZ Domain of SAP97 in Complex with a GluR-A C-terminal Peptide |
20.3 |
63.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2g2n |
Crystal Structure of E.coli transthyretin-related protein with bound Zn |
22.8 |
71.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2g2o |
Structure of E.coli FabD complexed with sulfate |
19.6 |
63.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2g2p |
Crystal Structure of E.coli transthyretin-related protein with bound Zn and Br |
22.6 |
71.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2g2q |
The crystal structure of G4, the poxviral disulfide oxidoreductase essential for cytoplasmic disulfide bond formation |
26.4 |
73.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2g2r |
Green-fluorescent antibody 11G10 in complex with its hapten (nitro-stilbene derivative) |
30.9 |
89.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2g2s |
Structure of S65G Y66S GFP variant after spontaneous peptide hydrolysis |
18.2 |
58.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2g2u |
Crystal Structure of the SHV-1 Beta-lactamase/Beta-lactamase inhibitor protein (BLIP) complex |
22.8 |
75.1 |
X-RAY DIFFRACTION |
GOOD
|