| 1a0e |
XYLOSE ISOMERASE FROM THERMOTOGA NEAPOLITANA |
31.8 |
101.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a0f |
CRYSTAL STRUCTURE OF GLUTATHIONE S-TRANSFERASE FROM ESCHERICHIA COLI COMPLEXED WITH GLUTATHIONESULFONIC ACID |
21.9 |
65.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a0g |
;L201A MUTANT OF D-AMINO ACID AMINOTRANSFERASE COMPLEXED WITH PYRIDOXAMINE-5'-PHOSPHATE
; |
26.3 |
90.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0h |
;THE X-RAY CRYSTAL STRUCTURE OF PPACK-MEIZOTHROMBIN DESF1: KRINGLE/THROMBIN AND CARBOHYDRATE/KRINGLE/THROMBIN INTERACTIONS AND LOCATION OF THE LINKER CHAIN
; |
30.8 |
98.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0i |
ATP-DEPENDENT DNA LIGASE FROM BACTERIOPHAGE T7 COMPLEX WITH ATP |
23.7 |
85.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a0j |
CRYSTAL STRUCTURE OF A NON-PSYCHROPHILIC TRYPSIN FROM A COLD-ADAPTED FISH SPECIES. |
31.6 |
106.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0k |
PROFILIN I FROM ARABIDOPSIS THALIANA |
15.1 |
45.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0l |
HUMAN BETA-TRYPTASE: A RING-LIKE TETRAMER WITH ACTIVE SITES FACING A CENTRAL PORE |
33.6 |
103.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a0m |
1.1 ANGSTROM CRYSTAL STRUCTURE OF A-CONOTOXIN [TYR15]-EPI |
9.8 |
32.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0n |
;NMR STUDY OF THE SH3 DOMAIN FROM FYN PROTO-ONCOGENE TYROSINE KINASE COMPLEXED WITH THE SYNTHETIC PEPTIDE P2L CORRESPONDING TO RESIDUES 91-104 OF THE P85 SUBUNIT OF PI3-KINASE, FAMILY OF 25 STRUCTURES
; |
12.1 |
45.5 |
SOLUTION NMR |
GOOD
|
| 1a0o |
CHEY-BINDING DOMAIN OF CHEA IN COMPLEX WITH CHEY |
56.8 |
171.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a0p |
SITE-SPECIFIC RECOMBINASE, XERD |
21.1 |
68.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0q |
29G11 COMPLEXED WITH PHENYL [1-(1-N-SUCCINYLAMINO)PENTYL] PHOSPHONATE |
24.8 |
77.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a0r |
HETEROTRIMERIC COMPLEX OF PHOSDUCIN/TRANSDUCIN BETA-GAMMA |
26.1 |
88.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0s |
SUCROSE-SPECIFIC PORIN |
32.9 |
96.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0t |
SUCROSE-SPECIFIC PORIN, WITH BOUND SUCROSE MOLECULES |
32.6 |
93.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0u |
HEMOGLOBIN (VAL BETA1 MET) MUTANT |
24.8 |
70.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a0z |
HEMOGLOBIN (VAL BETA1 MET) MUTANT |
24.8 |
70.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a11 |
NMR STRUCTURE OF MEMBRANE SPANNING SEGMENT 2 OF THE ACETYLCHOLINE RECEPTOR IN DPC MICELLES, 10 STRUCTURES |
12.0 |
43.8 |
SOLUTION NMR |
REASONABLE
|
| 1a12 |
REGULATOR OF CHROMOSOME CONDENSATION (RCC1) OF HUMAN |
32.3 |
92.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a13 |
G PROTEIN-BOUND CONFORMATION OF MASTOPARAN-X, NMR, 14 STRUCTURES |
5.7 |
15.8 |
SOLUTION NMR |
REASONABLE
|
| 1a14 |
;COMPLEX BETWEEN NC10 ANTI-INFLUENZA VIRUS NEURAMINIDASE SINGLE CHAIN ANTIBODY WITH A 5 RESIDUE LINKER AND INFLUENZA VIRUS NEURAMINIDASE
; |
27.3 |
95.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1a15 |
SDF-1ALPHA |
16.0 |
54.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1a16 |
AMINOPEPTIDASE P FROM E. COLI WITH THE INHIBITOR PRO-LEU |
25.9 |
88.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1a17 |
TETRATRICOPEPTIDE REPEATS OF PROTEIN PHOSPHATASE 5 |
24.4 |
103.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a18 |
PHENANTHROLINE MODIFIED MURINE ADIPOCYTE LIPID BINDING PROTEIN |
15.1 |
47.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1a19 |
BARSTAR (FREE), C82A MUTANT |
18.3 |
64.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1a |
C-SRC (SH2 DOMAIN WITH C188A MUTATION) COMPLEXED WITH ACE-FORMYL PHOSPHOTYR-GLU-(N,N-DIPENTYL AMINE) |
19.6 |
65.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1b |
C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-PHOSPHOTYR-GLU-(N,N-DIPENTYL AMINE) |
19.7 |
69.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1c |
C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-PHOSPHOTYR-GLU-(N-ME(-(CH2)3-CYCLOPENTYL)) |
19.7 |
63.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1d |
YEAST RNA POLYMERASE SUBUNIT RPB8, NMR, MINIMIZED AVERAGE STRUCTURE, ALPHA CARBONS ONLY |
17.1 |
59.2 |
SOLUTION NMR |
GOOD
|
| 1a1e |
C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-PHOSPHOTYR-GLU-(3-BUTYLPIPERIDINE) |
19.6 |
63.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1f |
DSNR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GACC SITE) |
15.8 |
41.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a1g |
DSNR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GCGT SITE) |
15.9 |
54.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1h |
QGSR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GCAC SITE) |
16.2 |
56.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a1i |
RADR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GCAC SITE) |
16.1 |
55.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1j |
RADR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GCGT SITE) |
16.0 |
41.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a1k |
RADR (ZIF268 VARIANT) ZINC FINGER-DNA COMPLEX (GACC SITE) |
16.1 |
56.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1l |
ZIF268 ZINC FINGER-DNA COMPLEX (GCAC SITE) |
16.1 |
55.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1m |
MHC CLASS I MOLECULE B*5301 COMPLEXED WITH PEPTIDE TPYDINQML FROM GAG PROTEIN OF HIV2 |
24.3 |
76.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a1n |
MHC CLASS I MOLECULE B*3501 COMPLEXED WITH PEPTIDE VPLRPMTY FROM THE NEF PROTEIN (75-82) OF HIV1 |
24.2 |
75.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a1o |
MHC CLASS I MOLECULE B*5301 COMPLEXED WITH PEPTIDE LS6 (KPIVQYDNF) FROM THE MALARIA PARASITE P. FALCIPARUM |
24.3 |
75.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a1p |
COMPSTATIN, NMR, 21 STRUCTURES |
6.5 |
23.2 |
SOLUTION NMR |
REASONABLE
|
| 1a1q |
HEPATITIS C VIRUS NS3 PROTEINASE |
29.6 |
97.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1r |
HCV NS3 PROTEASE DOMAIN:NS4A PEPTIDE COMPLEX |
23.0 |
74.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a1s |
ORNITHINE CARBAMOYLTRANSFERASE FROM PYROCOCCUS FURIOSUS |
20.4 |
63.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1a1t |
STRUCTURE OF THE HIV-1 NUCLEOCAPSID PROTEIN BOUND TO THE SL3 PSI-RNA RECOGNITION ELEMENT, NMR, 25 STRUCTURES |
16.0 |
66.0 |
SOLUTION NMR |
REASONABLE
|
| 1a1u |
SOLUTION STRUCTURE DETERMINATION OF A P53 MUTANT DIMERIZATION DOMAIN, NMR, MINIMIZED AVERAGE STRUCTURE |
13.9 |
42.1 |
SOLUTION NMR |
GOOD
|
| 1a1v |
HEPATITIS C VIRUS NS3 HELICASE DOMAIN COMPLEXED WITH SINGLE STRANDED SDNA |
23.6 |
71.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a1w |
FADD DEATH EFFECTOR DOMAIN, F25Y MUTANT, NMR MINIMIZED AVERAGE STRUCTURE |
14.0 |
44.6 |
SOLUTION NMR |
GOOD
|