| 1s6i |
;Ca2+-regulatory region (CLD) from soybean calcium-dependent protein kinase-alpha (CDPK) in the presence of Ca2+ and the junction domain (JD)
; |
23.1 |
60.6 |
SOLUTION NMR |
REASONABLE
|
| 1s6j |
N-terminal Region of the Ca2+-saturated calcium regulatory domain (CLD) from Soybean Calcium-dependent Protein Kinase-alpha (CDPK) |
16.5 |
44.5 |
SOLUTION NMR |
REASONABLE
|
| 1s6l |
Solution structure of MerB, the Organomercurial Lyase involved in the bacterial mercury resistance system |
19.5 |
63.3 |
SOLUTION NMR |
REASONABLE
|
| 1s6m |
Conjugative Relaxase Trwc In Complex With Orit DNA. Metal-Bound Structure |
22.9 |
76.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1s6n |
NMR Structure of Domain III of the West Nile Virus Envelope Protein, Strain 385-99 |
13.9 |
43.2 |
SOLUTION NMR |
GOOD
|
| 1s6o |
Solution structure and backbone dynamics of the apo-form of the second metal-binding domain of the Menkes protein ATP7A |
12.2 |
43.3 |
SOLUTION NMR |
GOOD
|
| 1s6p |
CRYSTAL STRUCTURE OF HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R100943 |
35.1 |
113.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1s6q |
CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R147681 |
35.6 |
116.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1s6r |
908R class c beta-lactamase bound to iodo-acetamido-phenyl boronic acid |
20.7 |
68.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1s6u |
Solution structure and backbone dynamics of the Cu(I) form of the second metal-binding domain of the Menkes protein ATP7A |
12.0 |
40.2 |
SOLUTION NMR |
GOOD
|
| 1s6v |
Structure of a cytochrome c peroxidase-cytochrome c site specific cross-link |
30.7 |
99.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1s6w |
Solution Structure of hybrid white striped bass hepcidin |
7.9 |
27.6 |
SOLUTION NMR |
GOOD
|
| 1s6x |
Solution structure of VSTx |
8.4 |
30.9 |
SOLUTION NMR |
REASONABLE
|
| 1s6y |
2.3A crystal structure of phospho-beta-glucosidase |
22.0 |
65.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1s6z |
Enhanced Green Fluorescent Protein Containing the Y66L Substitution |
18.2 |
56.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1s70 |
Complex between protein ser/thr phosphatase-1 (delta) and the myosin phosphatase targeting subunit 1 (MYPT1) |
28.3 |
88.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1s72 |
REFINED CRYSTAL STRUCTURE OF THE HALOARCULA MARISMORTUI LARGE RIBOSOMAL SUBUNIT AT 2.4 ANGSTROM RESOLUTION |
68.7 |
263.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1s73 |
Crystal Structure of Mesopone Cytochrome c Peroxidase (R-isomer) [MpCcP-R] |
19.6 |
63.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1s74 |
SOLUTION STRUCTURE OF A DNA DUPLEX CONTAINING AN ALPHA-ANOMERIC ADENOSINE: INSIGHTS INTO SUBSTRATE RECOGNITION BY ENDONUCLEASE IV |
12.1 |
39.5 |
SOLUTION NMR |
REASONABLE
|
| 1s75 |
SOLUTION STRUCTURE OF A DNA DUPLEX CONTAINING AN ALPHA-ANOMERIC ADENOSINE: INSIGHTS INTO SUBSTRATE RECOGNITION BY ENDONUCLEASE IV |
12.0 |
42.6 |
SOLUTION NMR |
GOOD
|
| 1s76 |
T7 RNA polymerase alpha beta methylene ATP elongation complex |
30.5 |
99.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1s77 |
T7 RNAP product pyrophosphate elongation complex |
30.5 |
100.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1s78 |
Insights into ErbB signaling from the structure of the ErbB2-pertuzumab complex |
51.1 |
168.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1s79 |
Solution structure of the central RRM of human La protein |
16.1 |
58.8 |
SOLUTION NMR |
REASONABLE
|
| 1s7a |
NMR structure of the La motif of human La protein |
15.2 |
40.7 |
SOLUTION NMR |
REASONABLE
|
| 1s7c |
Crystal structure of MES buffer bound form of glyceraldehyde 3-phosphate dehydrogenase from Escherichia coli |
21.1 |
69.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7d |
Crystal structure of refined tetragonal crystal of YodA from Escherichia coli |
17.7 |
50.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1s7e |
Solution structure of HNF-6 |
33.1 |
115.6 |
SOLUTION NMR |
GOOD
|
| 1s7f |
RimL- Ribosomal L7/L12 alpha-N-protein acetyltransferase crystal form I (apo) |
17.2 |
55.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1s7g |
Structural Basis for the Mechanism and Regulation of Sir2 Enzymes |
36.2 |
113.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1s7h |
Structural Genomics, 2.2A crystal structure of protein YKOF from Bacillus subtilis |
36.1 |
111.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7i |
1.8 A Crystal Structure of a Protein of Unknown Function PA1349 from Pseudomonas aeruginosa |
18.2 |
60.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7j |
Crystal structure of phenazine biosynthesis protein PhzF family (Enterococcus faecalis) |
25.4 |
75.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1s7k |
RimL- Ribosomal L7/L12 alpha-N-protein acetyltransferase crystal form 2 (apo) |
17.1 |
55.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7l |
RimL- Ribosomal L7/L12 alpha-N-protein acetyltransferase in complex with Coenzyme A (CoA-Cys134 Disulfide) |
17.1 |
51.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7m |
Crystal Structure of HiaBD1 |
33.0 |
103.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1s7n |
Ribosomal L7/L12 alpha-N-protein acetyltransferase in complex with Coenzyme A (CoA free sulfhydryl) |
35.3 |
114.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7o |
Crystal structure of putative DNA binding protein SP_1288 from Streptococcus pygenes |
27.0 |
93.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7p |
Solution structure of thermolysin digested microcin J25 |
7.5 |
31.3 |
SOLUTION NMR |
REASONABLE
|
| 1s7q |
;Crystal structures of the murine class I major histocompatibility complex H-2Kb in complex with LCMV-derived gp33 index peptide and three of its escape variants
; |
23.6 |
76.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1s7r |
;Crystal structures of the murine class I major histocompatibility complex H-2Kb in complex with LCMV-derived gp33 index peptide and three of its escape variants
; |
32.1 |
98.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1s7s |
;Crystal structures of the murine class I major histocompatibility complex H-2Kb in complex with LCMV-derived gp33 index peptide and three of its escape variants
; |
23.6 |
75.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1s7t |
;Crystal structures of the murine class I major histocompatibility complex H-2Kb in complex with LCMV-derived gp33 index peptide and three of its escape variants
; |
33.0 |
106.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1s7u |
;Crystal structures of the murine class I major histocompatibility complex H-2Db in complex with LCMV-derived gp33 index peptide and three of its escape variants
; |
50.6 |
146.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7v |
;Crystal structures of the murine class I major histocompatibility complex H-2Db in complex with LCMV-derived gp33 index peptide and three of its escape variants
; |
39.6 |
123.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7w |
;Crystal structures of the murine class I major histocompatibility complex H-2Db in complex with LCMV-derived gp33 index peptide and three of its escape variants
; |
53.9 |
162.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7x |
;Crystal structures of the murine class I major histocompatibility complex H-2Db in complex with LCMV-derived gp33 index peptide and three of its escape variants
; |
54.0 |
165.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7y |
Crystal structure of the GluR6 ligand binding core in complex with glutamate at 1.75 A resolution orthorhombic form |
25.6 |
83.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1s7z |
Structure of Ocr from Bacteriophage T7 |
16.1 |
41.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1s80 |
Structure of Serine Acetyltransferase from Haemophilis influenzae Rd |
33.8 |
104.9 |
X-RAY DIFFRACTION |
GOOD
|