| 1fol |
REDUCED BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH L-ARG(H4B-FREE) |
30.0 |
94.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1fon |
CRYSTAL STRUCTURE OF BOVINE PROCARBOXYPEPTIDASE A-S6 SUBUNIT III, A HIGHLY STRUCTURED TRUNCATED ZYMOGEN E |
22.9 |
73.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1foo |
BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH L-ARG AND NO(H4B-FREE) |
30.0 |
95.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1fop |
BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH L-ARG AND NO(H4B-BOUND) |
29.9 |
93.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1foq |
PENTAMERIC MODEL OF THE BACTERIOPHAGE PHI29 PROHEAD RNA |
67.6 |
173.8 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 1for |
STRUCTURE DETERMINATION OF AN FAB FRAGMENT THAT NEUTRALIZES HUMAN RHINOVIRUS AND ANALYSIS OF THE FAB-VIRUS COMPLEX |
25.8 |
79.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1fos |
TWO HUMAN C-FOS:C-JUN:DNA COMPLEXES |
28.6 |
90.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1fot |
STRUCTURE OF THE UNLIGANDED CAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT FROM SACCHAROMYCES CEREVISIAE |
21.7 |
67.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1fou |
CONNECTOR PROTEIN FROM BACTERIOPHAGE PHI29 |
51.2 |
142.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1fov |
GLUTAREDOXIN 3 FROM ESCHERICHIA COLI IN THE FULLY OXIDIZED FORM |
12.3 |
38.3 |
SOLUTION NMR |
GOOD
|
| 1fow |
NMR STRUCTURE OF L11-C76, THE C-TERMINAL DOMAIN OF 50S RIBOSOMAL PROTEIN L11, MINIMIZED AVERAGE STRUCTURE |
14.9 |
56.3 |
SOLUTION NMR |
GOOD
|
| 1fox |
NMR STRUCTURE OF L11-C76, THE C-TERMINAL DOMAIN OF 50S RIBOSOMAL PROTEIN L11, 33 STRUCTURES |
14.0 |
38.1 |
SOLUTION NMR |
REASONABLE
|
| 1foy |
;THE RNA BINDING DOMAIN OF RIBOSOMAL PROTEIN L11: THREE-DIMENSIONAL STRUCTURE OF THE RNA-BOUND FORM OF THE PROTEIN, NMR, MINIMIZED AVERAGE STRUCTURE
; |
14.2 |
46.9 |
SOLUTION NMR |
GOOD
|
| 1foz |
STRUCTURE OF CYCLIC PEPTIDE INHIBITORS OF MAMMALIAN RIBONUCLEOTIDE REDUCTASE |
6.4 |
23.6 |
SOLUTION NMR |
GOOD
|
| 1fp0 |
SOLUTION STRUCTURE OF THE PHD DOMAIN FROM THE KAP-1 COREPRESSOR |
21.2 |
82.3 |
SOLUTION NMR |
REASONABLE
|
| 1fp1 |
CRYSTAL STRUCTURE ANALYSIS OF CHALCONE O-METHYLTRANSFERASE |
23.9 |
80.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1fp2 |
CRYSTAL STRUCTURE ANALYSIS OF ISOFLAVONE O-METHYLTRANSFERASE |
24.0 |
79.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1fp3 |
CRYSTAL STRUCTURE OF N-ACYL-D-GLUCOSAMINE 2-EPIMERASE FROM PORCINE KIDNEY |
29.4 |
96.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1fp4 |
CRYSTAL STRUCTURE OF THE ALPHA-H195Q MUTANT OF NITROGENASE |
38.1 |
116.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1fp5 |
CRYSTAL STRUCTURE ANALYSIS OF THE HUMAN IGE-FC CEPSILON3-CEPSILON4 FRAGMENT. |
21.1 |
69.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1fp6 |
THE NITROGENASE FE PROTEIN FROM AZOTOBACTER VINELANDII COMPLEXED WITH MGADP |
35.7 |
118.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1fp7 |
MONOVALENT CATION BINDING SITES IN N10-FORMYLTETRAHYDROFOLATE SYNTHETASE FROM MOORELLA THERMOACETICA |
36.7 |
123.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1fp8 |
STRUCTURE OF THE AMYLOMALTASE FROM THERMUS THERMOPHILUS HB8 IN SPACE GROUP P21212 |
24.3 |
78.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1fp9 |
STRUCTURE OF AMYLOMALTASE FROM THERMUS THERMOPHILUS HB8 IN SPACE GROUP C2 |
24.2 |
76.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpb |
;CRYSTAL STRUCTURE OF THE NEUTRAL FORM OF FRUCTOSE 1,6-BISPHOSPHATASE COMPLEXED WITH REGULATORY INHIBITOR FRUCTOSE 2,6-BISPHOSPHATE AT 2.6-ANGSTROMS RESOLUTION
; |
26.7 |
86.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpc |
ACTIVE SITE MIMETIC INHIBITION OF THROMBIN |
18.9 |
57.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1fpd |
;STRUCTURAL ASPECTS OF THE ALLOSTERIC INHIBITION OF FRUCTOSE-1,6-BISPHOSPHATASE BY AMP: THE BINDING OF BOTH THE SUBSTRATE ANALOGUE 2,5-ANHYDRO-D-GLUCITOL-1,6-BISPHOSPHATE AND CATALYTIC METAL IONS MONITORED BY X-RAY CRYSTALLOGRAPHY
; |
26.7 |
88.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpe |
;STRUCTURAL ASPECTS OF THE ALLOSTERIC INHIBITION OF FRUCTOSE-1,6-BISPHOSPHATASE BY AMP: THE BINDING OF BOTH THE SUBSTRATE ANALOGUE 2,5-ANHYDRO-D-GLUCITOL-1,6-BISPHOSPHATE AND CATALYTIC METAL IONS MONITORED BY X-RAY CRYSTALLOGRAPHY
; |
26.7 |
88.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpf |
;STRUCTURAL ASPECTS OF THE ALLOSTERIC INHIBITION OF FRUCTOSE-1,6-BISPHOSPHATASE BY AMP: THE BINDING OF BOTH THE SUBSTRATE ANALOGUE 2,5-ANHYDRO-D-GLUCITOL-1,6-BISPHOSPHATE AND CATALYTIC METAL IONS MONITORED BY X-RAY CRYSTALLOGRAPHY
; |
26.7 |
88.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpg |
;STRUCTURAL ASPECTS OF THE ALLOSTERIC INHIBITION OF FRUCTOSE-1,6-BISPHOSPHATASE BY AMP: THE BINDING OF BOTH THE SUBSTRATE ANALOGUE 2,5-ANHYDRO-D-GLUCITOL-1,6-BISPHOSPHATE AND CATALYTIC METAL IONS MONITORED BY X-RAY CRYSTALLOGRAPHY
; |
26.7 |
87.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1fph |
THE INTERACTION OF THROMBIN WITH FIBRINOGEN: A STRUCTURAL BASIS FOR ITS SPECIFICITY |
19.6 |
60.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpi |
;FRUCTOSE-1,6-BISPHOSPHATASE (D-FRUCTOSE-1,6-BISPHOSPHATE 1-PHOSPHOHYDROLASE) COMPLEXED WITH AMP, 2,5-ANHYDRO-D-GLUCITOL-1,6-BISPHOSPHATE AND POTASSIUM IONS (100 MM)
; |
26.8 |
87.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpj |
;FRUCTOSE-1,6-BISPHOSPHATASE (D-FRUCTOSE-1,6-BISPHOSPHATE 1-PHOSPHOHYDROLASE) COMPLEXED WITH AMP, 2,5-ANHYDRO-D-GLUCITOL-1,6-BISPHOSPHATE, THALLIUM (10 MM) AND LITHIUM IONS (10 MM)
; |
26.5 |
87.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpk |
FRUCTOSE-1,6-BISPHOSPHATASE (D-FRUCTOSE-1,6-BISPHOSPHATE 1-PHOSPHOHYDROLASE) COMPLEXED WITH THALLIUM IONS (10 MM) |
26.4 |
87.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpl |
;FRUCTOSE-1,6-BISPHOSPHATASE (D-FRUCTOSE-1,6-BISPHOSPHATE 1-PHOSPHOHYDROLASE) COMPLEXED WITH AMP, 2,5-ANHYDRO-D-GLUCITOL-1,6-BISPHOSPHATE AND THALLIUM IONS (10 MM)
; |
26.4 |
88.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpm |
MONOVALENT CATION BINDING SITES IN N10-FORMYLTETRAHYDROFOLATE SYNTHETASE FROM MOORELLA THERMOACETICA |
36.5 |
123.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpn |
HUMAN RHINOVIRUS SEROTYPE 2 (HRV2) |
29.4 |
93.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpo |
HSC20 (HSCB), A J-TYPE CO-CHAPERONE FROM E. COLI |
30.7 |
95.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1fpp |
PROTEIN FARNESYLTRANSFERASE COMPLEX WITH FARNESYL DIPHOSPHATE |
27.2 |
91.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpq |
CRYSTAL STRUCTURE ANALYSIS OF SELENOMETHIONINE SUBSTITUTED CHALCONE O-METHYLTRANSFERASE |
22.9 |
76.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpr |
;CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN THE CATALYTIC DOMAIN OF SHP-1 AND AN IN VITRO PEPTIDE SUBSTRATE PY469 DERIVED FROM SHPS-1.
; |
20.2 |
70.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1fps |
CRYSTAL STRUCTURE OF RECOMBINANT FARNESYL DIPHOSPHATE SYNTHASE AT 2.6 ANGSTROMS RESOLUTION |
22.6 |
72.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1fpt |
;THREE-DIMENSIONAL STRUCTURE OF THE COMPLEX BETWEEN THE FAB FRAGMENT OF AN NEUTRALIZING ANTIBODY FOR TYPE 1 POLIOVIRUS AND ITS VIRAL EPITOPE
; |
25.8 |
86.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpu |
CRYSTAL STRUCTURE OF ABL KINASE DOMAIN IN COMPLEX WITH A SMALL MOLECULE INHIBITOR |
31.7 |
119.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpv |
STRUCTURE DETERMINATION OF FELINE PANLEUKOPENIA VIRUS EMPTY PARTICLES |
29.4 |
103.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpw |
STRUCTURE OF YEAST FREQUENIN |
18.8 |
67.1 |
SOLUTION NMR |
REASONABLE
|
| 1fpy |
CRYSTAL STRUCTURE OF GLUTAMINE SYNTHETASE FROM SALMONELLA TYPHIMURIUM WITH INHIBITOR PHOSPHINOTHRICIN |
54.4 |
163.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1fpz |
;CRYSTAL STRUCTURE ANALYSIS OF KINASE ASSOCIATED PHOSPHATASE (KAP) WITH A SUBSTITUTION OF THE CATALYTIC SITE CYSTEINE (CYS140) TO A SERINE
; |
52.3 |
140.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1fq0 |
KDPG ALDOLASE FROM ESCHERICHIA COLI |
27.6 |
82.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1fq1 |
CRYSTAL STRUCTURE OF KINASE ASSOCIATED PHOSPHATASE (KAP) IN COMPLEX WITH PHOSPHO-CDK2 |
25.8 |
82.6 |
X-RAY DIFFRACTION |
EXCELLENT
|