| 1lu1 |
THE STRUCTURE OF THE DOLICHOS BIFLORUS SEED LECTIN IN COMPLEX WITH THE FORSSMAN DISACCHARIDE |
18.5 |
59.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1lu2 |
DOLICHOS BIFLORUS SEED LECTIN IN COMPLEX WITH THE BLOOD GROUP A TRISACCHARIDE |
26.0 |
83.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1lu3 |
;Separate Fitting of the Anticodon Loop Region of tRNA (nucleotide 26-42) in the Low Resolution Cryo-EM Map of an EF-Tu Ternary Complex (GDP and Kirromycin) Bound to E. coli 70S Ribosome
; |
11.1 |
36.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 1lu4 |
;1.1 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF A SECRETED MYCOBACTERIUM TUBERCULOSIS DISULFIDE OXIDOREDUCTASE HOMOLOGOUS TO E. COLI DSBE: IMPLICATIONS FOR FUNCTIONS
; |
14.9 |
43.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1lu5 |
2.4 Angstrom Crystal Structure of the Asymmetric Platinum Complex {Pt(ammine)(cyclohexylamine)}2+ Bound to a Dodecamer DNA Duplex |
17.3 |
60.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1lu8 |
Solution structure of GsMTx-4 |
8.1 |
32.2 |
SOLUTION NMR |
GOOD
|
| 1lu9 |
Structure of methylene-tetrahydromethanopterin dehydrogenase from Methylobacterium extorquens AM1 |
33.0 |
102.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1lua |
Structure of methylene-tetrahydromethanopterin dehydrogenase from Methylobacterium extorquens AM1 complexed with NADP |
33.6 |
102.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1luc |
BACTERIAL LUCIFERASE |
27.0 |
85.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1lud |
SOLUTION STRUCTURE OF DIHYDROFOLATE REDUCTASE COMPLEXED WITH TRIMETHOPRIM AND NADPH, 24 STRUCTURES |
15.9 |
49.8 |
SOLUTION NMR |
GOOD
|
| 1lue |
RECOMBINANT SPERM WHALE MYOGLOBIN H64D/V68A/D122N MUTANT (MET) |
16.6 |
52.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1luf |
Crystal Structure of the MuSK Tyrosine Kinase: Insights into Receptor Autoregulation |
20.0 |
61.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1lug |
Full Matrix Error Analysis of Carbonic Anhydrase |
18.5 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1luh |
;SOLUTION NMR STRUCTURE OF SELF-COMPLIMENTARY DUPLEX 5'-D(TCCG*CGGA)2 CONTAINING A TRIMETHYLENE CROSSLINK AT THE N2 POSITION OF G*
; |
12.4 |
43.6 |
SOLUTION NMR |
GOOD
|
| 1lui |
NMR Structures of Itk SH2 domain, Pro287cis isoform, ensemble of 20 low energy structures |
13.2 |
40.5 |
SOLUTION NMR |
GOOD
|
| 1luj |
Crystal Structure of the Beta-catenin/ICAT Complex |
34.5 |
123.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1luk |
NMR Structure of the Itk SH2 domain, Pro287cis, Energy minimized average structure |
14.3 |
48.8 |
SOLUTION NMR |
GOOD
|
| 1lul |
DB58, A LEGUME LECTIN FROM DOLICHOS BIFLORUS |
38.7 |
123.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1lum |
NMR Structure of the Itk SH2 domain, Pro287trans, 20 low energy structures |
13.2 |
42.0 |
SOLUTION NMR |
GOOD
|
| 1lun |
NMR Structure of the Itk SH2 domain, Pro287trans, energy minimized average structure |
14.5 |
51.0 |
SOLUTION NMR |
GOOD
|
| 1lup |
Solution structure of a toxin (GsMTx2) from the tarantula, Grammostola spatulata, which inhibits mechanosensitive ion channels |
9.3 |
39.5 |
SOLUTION NMR |
REASONABLE
|
| 1luq |
Full Matrix Error Analysis of Streptavidin |
17.9 |
57.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1lur |
Crystal Structure of the GalM/aldose Epimerase Homologue from C. elegans, Northeast Structural Genomics Target WR66 |
32.4 |
108.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1luu |
NMR SOLUTION STRUCTURE OF THE ANTICODON OF YEAST TRNA-PHE WITH 4 MODIFICATIONS (OMC32 OMG34 1MG37 5MC40) |
11.8 |
39.7 |
SOLUTION NMR |
REASONABLE
|
| 1luv |
;CATALYTIC AND STRUCTURAL EFFECTS OF AMINO-ACID SUBSTITUTION AT HIS 30 IN HUMAN MANGANESE SUPEROXIDE DISMUTASE: INSERTION OF VAL CGAMMA INTO THE SUBSTRATE ACCESS CHANNEL
; |
26.7 |
82.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1luw |
;CATALYTIC AND STRUCTURAL EFFECTS OF AMINO-ACID SUBSTITUTION AT HIS 30 IN HUMAN MANGANESE SUPEROXIDE DISMUTASE: INSERTION OF VAL CGAMMA INTO THE SUBSTRATE ACCESS CHANNEL
; |
26.7 |
83.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1lux |
NMR SOLUTION STRUCTURE OF THE ANTICODON OF YEAST TRNA-PHE WITH 3 MODIFICATIONS (OMC32 OMG34 M5C40) |
10.8 |
36.8 |
SOLUTION NMR |
GOOD
|
| 1luz |
Crystal Structure of the K3L Protein From Vaccinia Virus (Wisconsin Strain) |
21.6 |
72.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1lv0 |
Crystal structure of the Rab effector guanine nucleotide dissociation inhibitor (GDI) in complex with a geranylgeranyl (GG) peptide |
23.7 |
78.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1lv1 |
Crystal Structure Analysis of the non-active site mutant of tethered HIV-1 protease to 2.1A resolution |
18.4 |
61.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1lv2 |
Hepatocyte Nuclear Factor 4 is a Transcription Factor that Constitutively Binds Fatty Acids |
19.0 |
61.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1lv3 |
Solution NMR Structure of Zinc Finger Protein yacG from Escherichia coli. Northeast Structural Genomics Consortium Target ET92. |
19.2 |
86.6 |
SOLUTION NMR |
REASONABLE
|
| 1lv4 |
Human catestatin 21-mer |
6.8 |
23.9 |
SOLUTION NMR |
GOOD
|
| 1lv5 |
Crystal Structure of the Closed Conformation of Bacillus DNA Polymerase I Fragment Bound to DNA and dCTP |
38.2 |
136.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1lv7 |
Crystal Structure of the AAA domain of FtsH |
21.8 |
71.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1lv8 |
Crystal structure of calf spleen purine nucleoside phosphorylase in a new space group with full trimer in the asymmetric unit |
36.5 |
112.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1lv9 |
CXCR3 Binding Chemokine IP-10/CXCL10 |
11.0 |
39.7 |
SOLUTION NMR |
GOOD
|
| 1lva |
Crystal structure of a C-terminal fragment of Moorella thermoacetica elongation factor SelB |
27.1 |
87.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1lvb |
CATALYTICALLY INACTIVE TOBACCO ETCH VIRUS PROTEASE COMPLEXED WITH SUBSTRATE |
25.5 |
78.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1lvc |
;Crystal structure of the adenylyl cyclase domain of anthrax edema factor (EF) in complex with calmodulin and 2' deoxy, 3' anthraniloyl ATP
; |
41.2 |
125.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1lve |
STRUCTURE OF THE VARIABLE DOMAIN OF HUMAN IMMUNOGLOBULIN K-4 LIGHT CHAIN LEN |
14.9 |
56.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1lvf |
syntaxin 6 |
21.6 |
80.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1lvg |
Crystal structure of mouse guanylate kinase in complex with GMP and ADP |
17.1 |
52.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1lvh |
The Structure of Phosphorylated beta-phosphoglucomutase from Lactoccocus lactis to 2.3 angstrom resolution |
30.8 |
97.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1lvj |
STRUCTURE OF TAR RNA COMPLEXED WITH A TAT-TAR INTERACTION NANOMOLAR INHIBITOR THAT WAS IDENTIFIED BY COMPUTATIONAL SCREENING |
17.4 |
63.4 |
SOLUTION NMR |
GOOD
|
| 1lvk |
;X-RAY CRYSTAL STRUCTURE OF THE MG (DOT) 2'(3')-O-(N-METHYLANTHRANILOYL) NUCLEOTIDE BOUND TO DICTYOSTELIUM DISCOIDEUM MYOSIN MOTOR DOMAIN
; |
29.9 |
101.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1lvl |
THE REFINED STRUCTURE OF PSEUDOMONAS PUTIDA LIPOAMIDE DEHYDROGENASE COMPLEXED WITH NAD+ AT 2.45 ANGSTROMS RESOLUTION |
24.9 |
76.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1lvm |
CATALYTICALLY ACTIVE TOBACCO ETCH VIRUS PROTEASE COMPLEXED WITH PRODUCT |
25.9 |
81.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1lvn |
CRYSTAL STRUCTURE OF E. COLI AMINE OXIDASE COMPLEXED WITH TRANYLCYPROMINE |
33.9 |
105.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1lvo |
Structure of coronavirus main proteinase reveals combination of a chymotrypsin fold with an extra alpha-helical domain |
48.9 |
162.5 |
X-RAY DIFFRACTION |
GOOD
|