| 1sre |
CRYSTALLOGRAPHIC AND THERMODYNAMIC COMPARISON OF NATURAL AND SYNTHETIC LIGANDS BOUND TO STREPTAVIDIN |
17.9 |
59.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1srf |
STRUCTURE-BASED DESIGN OF SYNTHETIC AZOBENZENE LIGANDS FOR STREPTAVIDIN |
17.6 |
54.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1srg |
STRUCTURE-BASED DESIGN OF SYNTHETIC AZOBENZENE LIGANDS FOR STREPTAVIDIN |
17.8 |
58.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1srh |
STRUCTURE-BASED DESIGN OF SYNTHETIC AZOBENZENE LIGANDS FOR STREPTAVIDIN |
17.6 |
58.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1sri |
STRUCTURE-BASED DESIGN OF SYNTHETIC AZOBENZENE LIGANDS FOR STREPTAVIDIN |
18.0 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1srj |
STRUCTURE-BASED DESIGN OF SYNTHETIC AZOBENZENE LIGANDS FOR STREPTAVIDIN |
17.8 |
57.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1srk |
Solution structure of the third zinc finger domain of FOG-1 |
9.7 |
41.2 |
SOLUTION NMR |
REASONABLE
|
| 1srl |
1H AND 15N ASSIGNMENTS AND SECONDARY STRUCTURE OF THE SRC SH3 DOMAIN |
12.1 |
37.5 |
SOLUTION NMR |
GOOD
|
| 1srm |
1H AND 15N ASSIGNMENTS AND SECONDARY STRUCTURE OF THE SRC SH3 DOMAIN |
10.7 |
35.2 |
SOLUTION NMR |
GOOD
|
| 1srn |
THE REFINED CRYSTAL STRUCTURE OF A FULLY ACTIVE SEMISYNTHETIC RIBONUCLEASE AT 1.8 ANGSTROMS RESOLUTION |
15.1 |
50.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1sro |
S1 RNA BINDING DOMAIN, NMR, 20 STRUCTURES |
12.6 |
44.3 |
SOLUTION NMR |
GOOD
|
| 1srp |
STRUCTURAL ANALYSIS OF SERRATIA PROTEASE |
26.5 |
94.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1srq |
Crystal Structure of the Rap1GAP catalytic domain |
42.1 |
141.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1srr |
CRYSTAL STRUCTURE OF A PHOSPHATASE RESISTANT MUTANT OF SPORULATION RESPONSE REGULATOR SPO0F FROM BACILLUS SUBTILIS |
26.1 |
81.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1srs |
SERUM RESPONSE FACTOR (SRF) CORE COMPLEXED WITH SPECIFIC SRE DNA |
20.4 |
61.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1sru |
Crystal structure of full length E. coli SSB protein |
23.1 |
83.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1srv |
THERMUS THERMOPHILUS GROEL (HSP60 CLASS) FRAGMENT (APICAL DOMAIN) COMPRISING RESIDUES 192-336 |
15.9 |
50.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1srx |
THREE-DIMENSIONAL STRUCTURE OF ESCHERICHIA COLI THIOREDOXIN-S2 TO 2.8 ANGSTROMS RESOLUTION |
13.5 |
47.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1sry |
REFINED CRYSTAL STRUCTURE OF THE SERYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS AT 2.5 ANGSTROMS RESOLUTION |
33.8 |
117.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1srz |
Solution structure of the second complement control protein (CCP) module of the GABA(B)R1a receptor, Pro-119 trans conformer |
13.2 |
36.0 |
SOLUTION NMR |
REASONABLE
|
| 1ss1 |
STAPHYLOCOCCAL PROTEIN A, B-DOMAIN, Y15W MUTANT, NMR, 25 STRUCTURES |
12.1 |
31.4 |
SOLUTION NMR |
REASONABLE
|
| 1ss2 |
Solution structure of the second complement control protein (CCP) module of the GABA(B)R1a receptor, Pro-119 cis conformer |
13.4 |
36.6 |
SOLUTION NMR |
REASONABLE
|
| 1ss3 |
Solution structure of Ole e 6, an allergen from olive tree pollen |
23.8 |
64.2 |
SOLUTION NMR |
REASONABLE
|
| 1ss4 |
Crystal Structure of the Glyoxalase Family Protein APC24694 from Bacillus cereus |
19.6 |
59.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ss6 |
Solution structure of SEP domain from human p47 |
16.1 |
43.8 |
SOLUTION NMR |
REASONABLE
|
| 1ss7 |
Compensating bends in a 16 base-pair DNA oligomer containing a T3A3 segment |
18.1 |
47.5 |
SOLUTION NMR |
REASONABLE
|
| 1ss8 |
GroEL |
54.4 |
146.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ss9 |
Crystal Structural Analysis of Active Site Mutant Q189E of LgtC |
19.2 |
57.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ssa |
A STRUCTURAL INVESTIGATION OF CATALYTICALLY MODIFIED F12OL AND F12OY SEMISYNTHETIC RIBONUCLEASES |
15.2 |
51.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ssb |
A STRUCTURAL INVESTIGATION OF CATALYTICALLY MODIFIED F12OL AND F12OY SEMISYNTHETIC RIBONUCLEASES |
15.1 |
48.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1ssc |
;THE 1.6 ANGSTROMS STRUCTURE OF A SEMISYNTHETIC RIBONUCLEASE CRYSTALLIZED FROM AQUEOUS ETHANOL. COMPARISON WITH CRYSTALS FROM SALT SOLUTIONS AND WITH RNASE A FROM AQUEOUS ALCOHOL SOLUTIONS
; |
15.1 |
51.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ssd |
Understanding protein lids: Structural analysis of active hinge mutants in triosephosphate isomerase |
25.4 |
80.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1sse |
Solution structure of the oxidized form of the Yap1 redox domain |
22.5 |
61.3 |
SOLUTION NMR |
REASONABLE
|
| 1ssf |
Solution structure of the mouse 53BP1 fragment (residues 1463-1617) |
14.5 |
46.5 |
SOLUTION NMR |
GOOD
|
| 1ssg |
Understanding protein lids: Structural analysis of active hinge mutants in triosephosphate isomerase |
25.3 |
80.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ssh |
Crystal structure of the SH3 domain from a S. cerevisiae hypothetical 40.4 kDa protein in complex with a peptide |
12.6 |
39.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1ssj |
A DNA DUPLEX CONTAINING A CHOLESTEROL ADDUCT (BETA-ANOMER) |
12.2 |
37.5 |
SOLUTION NMR |
EXCELLENT
|
| 1ssk |
Structure of the N-terminal RNA-binding Domain of the SARS CoV Nucleocapsid Protein |
21.0 |
79.1 |
SOLUTION NMR |
GOOD
|
| 1ssl |
Solution structure of the PSI domain from the Met receptor |
9.5 |
34.0 |
SOLUTION NMR |
GOOD
|
| 1ssm |
Serine Acetyltransferase- Apoenzyme (truncated) |
33.5 |
105.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ssn |
STAPHYLOKINASE, SAKSTAR VARIANT, NMR, 20 STRUCTURES |
15.8 |
50.6 |
SOLUTION NMR |
GOOD
|
| 1sso |
SOLUTION STRUCTURE AND DNA-BINDING PROPERTIES OF A THERMOSTABLE PROTEIN FROM THE ARCHAEON SULFOLOBUS SOLFATARICUS |
13.6 |
49.4 |
SOLUTION NMR |
GOOD
|
| 1ssp |
WILD-TYPE URACIL-DNA GLYCOSYLASE BOUND TO URACIL-CONTAINING DNA |
19.6 |
59.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ssq |
Serine Acetyltransferase- Complex with Cysteine |
29.5 |
107.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1sst |
Serine Acetyltransferase- Complex with CoA |
25.5 |
72.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1ssu |
;Structural and biochemical evidence for disulfide bond heterogeneity in active forms of the somatomedin B domain of human vitronectin
; |
11.5 |
30.9 |
SOLUTION NMR |
REASONABLE
|
| 1ssv |
Compensating bends in a 16 base-pair DNA oligomer containing a T3A3 segment |
17.9 |
46.5 |
SOLUTION NMR |
REASONABLE
|
| 1ssw |
Crystal structure of phage T4 lysozyme mutant Y24A/Y25A/T26A/I27A/C54T/C97A |
17.4 |
57.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ssx |
0.83A resolution crystal structure of alpha-lytic protease at pH 8 |
16.4 |
52.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1ssy |
Crystal structure of phage T4 lysozyme mutant G28A/I29A/G30A/C54T/C97A |
47.9 |
152.1 |
X-RAY DIFFRACTION |
REASONABLE
|