| 1he1 |
Crystal structure of the complex between the GAP domain of the Pseudomonas aeruginosa ExoS toxin and human Rac |
29.4 |
99.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1he2 |
Human biliverdin IX beta reductase: NADP/biliverdin IX alpha ternary complex |
17.0 |
51.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1he3 |
Human biliverdin IX beta reductase: NADP/mesobiliverdin IV alpha ternary complex |
16.8 |
53.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1he4 |
Human biliverdin IX beta reductase: NADP/FMN ternary complex |
16.9 |
51.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1he5 |
Human biliverdin IX beta reductase: NADP/Lumichrome ternary complex |
16.8 |
53.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1he7 |
Human Nerve growth factor receptor TrkA |
19.1 |
73.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1he8 |
Ras G12V - PI 3-kinase gamma complex |
34.0 |
120.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1he9 |
Crystal structure of the GAP domain of the Pseudomonas aeruginosa ExoS toxin |
16.5 |
59.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hea |
CARBONIC ANHYDRASE II (CARBONATE DEHYDRATASE) (HCA II) (E.C.4.2.1.1) MUTANT WITH LEU 198 REPLACED BY ARG (L198R) |
18.6 |
59.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1heb |
STRUCTURAL CONSEQUENCES OF HYDROPHILIC AMINO-ACID SUBSTITUTIONS IN THE HYDROPHOBIC POCKET OF HUMAN CARBONIC ANHYDRASE II |
18.6 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1hec |
STRUCTURAL CONSEQUENCES OF HYDROPHILIC AMINO-ACID SUBSTITUTIONS IN THE HYDROPHOBIC POCKET OF HUMAN CARBONIC ANHYDRASE II |
18.7 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1hed |
STRUCTURAL CONSEQUENCES OF HYDROPHILIC AMINO-ACID SUBSTITUTIONS IN THE HYDROPHOBIC POCKET OF HUMAN CARBONIC ANHYDRASE II |
18.6 |
56.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1hee |
Crystal structure of bovine pancreatic carboxypeptidase A complexed with L-N-hydroxyaminocarbonyl phenylalanine at 2.3 A |
35.9 |
120.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1hef |
;The crystal structures at 2.2 angstroms resolution of hydroxyethylene-based inhibitors bound to human immunodeficiency virus type 1 protease show that the inhibitors are present in two distinct orientations
; |
14.8 |
50.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1heg |
;The crystal structures at 2.2 angstroms resolution of hydroxyethylene-based inhibitors bound to human immunodeficiency virus type 1 protease show that the inhibitors are present in two distinct orientations
; |
15.0 |
53.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1heh |
C-terminal xylan binding domain from Cellulomonas fimi xylanase 11A |
13.8 |
48.5 |
SOLUTION NMR |
GOOD
|
| 1hei |
STRUCTURE OF THE HEPATITIS C VIRUS RNA HELICASE DOMAIN |
29.4 |
89.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1hej |
C-terminal xylan binding domain from Cellulomonas fimi xylanase 11A |
13.0 |
45.7 |
SOLUTION NMR |
GOOD
|
| 1hek |
Crystal structure of equine infectious anaemia virus matrix antigen (EIAV MA) |
20.3 |
66.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1hel |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF COMPENSATING MUTATIONS WITHIN THE CORE OF CHICKEN EGG WHITE LYSOZYME |
15.3 |
52.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1hem |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF COMPENSATING MUTATIONS WITHIN THE CORE OF CHICKEN EGG WHITE LYSOZYME |
15.2 |
50.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hen |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF COMPENSATING MUTATIONS WITHIN THE CORE OF CHICKEN EGG WHITE LYSOZYME |
15.2 |
50.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1heo |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF COMPENSATING MUTATIONS WITHIN THE CORE OF CHICKEN EGG WHITE LYSOZYME |
15.2 |
51.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1hep |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF COMPENSATING MUTATIONS WITHIN THE CORE OF CHICKEN EGG WHITE LYSOZYME |
15.2 |
51.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1heq |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF COMPENSATING MUTATIONS WITHIN THE CORE OF CHICKEN EGG WHITE LYSOZYME |
15.3 |
51.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1her |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF COMPENSATING MUTATIONS WITHIN THE CORE OF CHICKEN EGG WHITE LYSOZYME |
15.3 |
52.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1hes |
MU2 ADAPTIN SUBUNIT (AP50) OF AP2 ADAPTOR (SECOND DOMAIN), COMPLEXED WITH P-selectin INTERNALIZATION PEPTIDE SHLGTYGVFTNAA |
24.1 |
87.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1het |
atomic X-ray structure of liver alcohol dehydrogenase containing a hydroxide adduct to NADH |
30.0 |
103.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1heu |
ATOMIC X-RAY STRUCTURE OF LIVER ALCOHOL DEHYDROGENASE CONTAINING Cadmium and a hydroxide adduct to NADH |
30.0 |
103.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1hev |
HEVEIN: THE NMR ASSIGNMENT AND AN ASSESSMENT OF SOLUTION-STATE FOLDING FOR THE AGGLUTININ-TOXIN MOTIF |
9.2 |
34.3 |
SOLUTION NMR |
GOOD
|
| 1hew |
;REFINEMENT OF AN ENZYME COMPLEX WITH INHIBITOR BOUND AT PARTIAL OCCUPANCY. HEN EGG-WHITE LYSOZYME AND TRI-N-ACETYLCHITOTRIOSE AT 1.75 ANGSTROMS RESOLUTION
; |
15.4 |
51.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1hex |
;STRUCTURE OF 3-ISOPROPYLMALATE DEHYDROGENASE IN COMPLEX WITH NAD+: LIGAND-INDUCED LOOP-CLOSING AND MECHANISM FOR COFACTOR SPECIFICITY
; |
21.4 |
69.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1hey |
INVESTIGATING THE STRUCTURAL DETERMINANTS OF THE P21-LIKE TRIPHOSPHATE AND MG2+ BINDING SITE |
15.2 |
46.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hez |
Structure of P. magnus protein L bound to a human IgM Fab. |
36.0 |
116.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1hf0 |
Crystal structure of the DNA-binding domain of Oct-1 bound to DNA as a dimer |
23.7 |
80.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1hf2 |
Crystal structure of the bacterial cell-division inhibitor MinC from T. maritima |
32.1 |
101.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hf3 |
ATOMIC X-RAY STRUCTURE OF LIVER ALCOHOL DEHYDROGENASE CONTAINING Cadmium and a hydroxide adduct to NADH |
29.6 |
102.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1hf4 |
STRUCTURAL EFFECTS OF MONOVALENT ANIONS ON POLYMORPHIC LYSOZYME CRYSTALS |
22.3 |
73.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1hf6 |
ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHAERENS IN THE ORTHORHOMBIC CRYSTAL FORM IN COMPLEX WITH CELLOTRIOSE |
19.0 |
55.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hf8 |
CALM-N N-terminal domain of clathrin assembly lymphoid myeloid leukaemia protein |
21.0 |
71.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hf9 |
C-Terminal Coiled-Coil Domain from Bovine IF1 |
18.3 |
72.0 |
SOLUTION NMR |
REASONABLE
|
| 1hfa |
CALM-N N-terminal domain of clathrin assembly lymphoid myeloid leukaemia protein, PI(4,5)P2 complex |
21.4 |
79.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hfb |
;Crystal structure of the tyrosine-regulated 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase from Saccharomyces cerevisiae complexed with phosphoenolpyruvate
; |
51.1 |
167.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1hfc |
1.56 ANGSTROM STRUCTURE OF MATURE TRUNCATED HUMAN FIBROBLAST COLLAGENASE |
16.0 |
50.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1hfd |
HUMAN COMPLEMENT FACTOR D IN A P21 CRYSTAL FORM |
17.7 |
56.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hfe |
1.6 A RESOLUTION STRUCTURE OF THE FE-ONLY HYDROGENASE FROM DESULFOVIBRIO DESULFURICANS |
33.1 |
106.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1hff |
;NMR solution structures of the vMIP-II 1-10 peptide from Kaposi's sarcoma-associated herpesvirus.
; |
7.3 |
20.0 |
SOLUTION NMR |
REASONABLE
|
| 1hfg |
;NMR solution structure of vMIP-II 1-71 from Kaposi's sarcoma-associated herpesvirus (minimized average structure).
; |
14.1 |
47.9 |
SOLUTION NMR |
GOOD
|
| 1hfh |
SOLUTION STRUCTURE OF A PAIR OF COMPLEMENT MODULES BY NUCLEAR MAGNETIC RESONANCE |
18.9 |
66.2 |
SOLUTION NMR |
GOOD
|
| 1hfi |
SOLUTION STRUCTURE OF A PAIR OF COMPLEMENT MODULES BY NUCLEAR MAGNETIC RESONANCE |
13.4 |
48.5 |
SOLUTION NMR |
GOOD
|