| 1gfg |
CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME SUBSTITUTED AT THE SURFACE POSITIONS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfh |
CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME SUBSTITUTED AT THE SURFACE POSITIONS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfi |
STRUCTURES OF ACTIVE CONFORMATIONS OF GI ALPHA 1 AND THE MECHANISM OF GTP HYDROLYSIS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfj |
CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME SUBSTITUTED AT THE SURFACE POSITIONS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfk |
CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME SUBSTITUTED AT THE SURFACE POSITIONS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfl |
STRUCTURE OF GREEN FLUORESCENT PROTEIN |
2 |
2 |
X-RAY DIFFRACTION |
| 1gfm |
OMPF PORIN (MUTANT D113G) |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfn |
OMPF PORIN DELETION (MUTANT DELTA 109-114) |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfo |
OMPF PORIN (MUTANT R132P) |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfp |
OMPF PORIN (MUTANT R42C) |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfq |
OMPF PORIN (MUTANT R82C) |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfr |
CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME SUBSTITUTED AT THE SURFACE POSITIONS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfs |
GDP-FUCOSE SYNTHETASE FROM E. COLI |
1 |
1 |
X-RAY DIFFRACTION |
| 1gft |
CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME SUBSTITUTED AT THE SURFACE POSITIONS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfu |
CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME SUBSTITUTED AT THE SURFACE POSITIONS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfv |
CRYSTAL STRUCTURE OF MUTANT HUMAN LYSOZYME SUBSTITUTED AT THE SURFACE POSITIONS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfw |
THE 2.8 ANGSTROM CRYSTAL STRUCTURE OF CASPASE-3 (APOPAIN OR CPP32)IN COMPLEX WITH AN ISATIN SULFONAMIDE INHIBITOR. |
5 |
5 |
X-RAY DIFFRACTION |
| 1gfy |
RESIDUE 259 IS A KEY DETERMINANT OF SUBSTRATE SPECIFICITY OF PROTEIN-TYROSINE PHOSPHATASE 1B AND ALPHA |
1 |
1 |
X-RAY DIFFRACTION |
| 1gfz |
FLAVOPIRIDOL INHIBITS GLYCOGEN PHOSPHORYLASE BY BINDING AT THE INHIBITOR SITE |
1 |
1 |
X-RAY DIFFRACTION |
| 1gg0 |
CRYSTAL STRUCTURE ANALYSIS OF KDOP SYNTHASE AT 3.0 A |
2 |
2 |
X-RAY DIFFRACTION |
| 1gg1 |
CRYSTAL STRUCTURE ANALYSIS OF DAHP SYNTHASE IN COMPLEX WITH MN2+ AND 2-PHOSPHOGLYCOLATE |
1 |
1 |
X-RAY DIFFRACTION |
| 1gg2 |
G PROTEIN HETEROTRIMER MUTANT GI_ALPHA_1(G203A) BETA_1 GAMMA_2 WITH GDP BOUND |
1 |
1 |
X-RAY DIFFRACTION |
| 1gg3 |
CRYSTAL STRUCTURE OF THE PROTEIN 4.1R MEMBRANE BINDING DOMAIN |
3 |
3 |
X-RAY DIFFRACTION |
| 1gg4 |
CRYSTAL STRUCTURE OF ESCHERICHIA COLI UDPMURNAC-TRIPEPTIDE D-ALANYL-D-ALANINE-ADDING ENZYME (MURF) AT 2.3 ANGSTROM RESOLUTION |
2 |
2 |
X-RAY DIFFRACTION |
| 1gg5 |
CRYSTAL STRUCTURE OF A COMPLEX OF HUMAN NAD[P]H-QUINONE OXIDOREDUCTASE AND A CHEMOTHERAPEUTIC DRUG (E09) AT 2.5 A RESOLUTION |
2 |
2 |
X-RAY DIFFRACTION |
| 1gg6 |
CRYSTAL STRUCTURE OF GAMMA CHYMOTRYPSIN WITH N-ACETYL-PHENYLALANINE TRIFLUOROMETHYL KETONE BOUND AT THE ACTIVE SITE |
1 |
1 |
X-RAY DIFFRACTION |
| 1gg8 |
DESIGN OF INHIBITORS OF GLYCOGEN PHOSPHORYLASE: A STUDY OF ALPHA-AND BETA-C-GLUCOSIDES AND 1-THIO-BETA-D-GLUCOSE COMPOUNDS |
1 |
1 |
X-RAY DIFFRACTION |
| 1gg9 |
CRYSTAL STRUCTURE OF CATALASE HPII FROM ESCHERICHIA COLI, HIS128ASN VARIANT. |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggb |
MAJOR ANTIGEN-INDUCED DOMAIN REARRANGEMENTS IN AN ANTIBODY |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggc |
MAJOR ANTIGEN-INDUCED DOMAIN REARRANGEMENTS IN AN ANTIBODY |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggd |
CRYSTAL STRUCTURE OF GAMMA CHYMOTRYPSIN WITH N-ACETYL-LEUCIL-PHENYLALANINE ALDEHYDE BOUND AT THE ACTIVE SITE |
3 |
3 |
X-RAY DIFFRACTION |
| 1gge |
CRYSTAL STRUCTURE OF CATALASE HPII FROM ESCHERICHIA COLI, NATIVE STRUCTURE AT 1.9 A RESOLUTION. |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggf |
CRYSTAL STRUCTURE OF CATALASE HPII FROM ESCHERICHIA COLI, VARIANT HIS128ASN, COMPLEX WITH HYDROGEN PEROXIDE. |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggg |
GLUTAMINE BINDING PROTEIN OPEN LIGAND-FREE STRUCTURE |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggh |
CRYSTAL STRUCTURE OF CATALASE HPII FROM ESCHERICHIA COLI, HIS128ALA VARIANT. |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggi |
CRYSTAL STRUCTURE OF AN HIV-1 NEUTRALIZING ANTIBODY 50.1 IN COMPLEX WITH ITS V3 LOOP PEPTIDE ANTIGEN |
2 |
2 |
X-RAY DIFFRACTION |
| 1ggj |
CRYSTAL STRUCTURE OF CATALASE HPII FROM ESCHERICHIA COLI, ASN201ALA VARIANT. |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggk |
CRYSTAL STRUCTURE OF CATALASE HPII FROM ESCHERICHIA COLI, ASN201HIS VARIANT. |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggl |
HUMAN CELLULAR RETINOL BINDING PROTEIN III |
2 |
2 |
X-RAY DIFFRACTION |
| 1ggm |
GLYCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS COMPLEXED WITH GLYCYL-ADENYLATE |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggn |
Structures of glycogen phosphorylase-inhibitor complexes and the implications for structure-based drug design |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggo |
T453A MUTANT OF PYRUVATE, PHOSPHATE DIKINASE |
2 |
2 |
X-RAY DIFFRACTION |
| 1ggp |
CRYSTAL STRUCTURE OF TRICHOSANTHES KIRILOWII LECTIN-1 AND ITS RELATION TO THE TYPE 2 RIBOSOME INACTIVATING PROTEINS |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggq |
OUTER SURFACE PROTEIN C (OSPC) OF BORRELIA BURGDORFERI STRAIN B31 |
3 |
3 |
X-RAY DIFFRACTION |
| 1ggr |
COMPLEX OF ENZYME IIAGLC AND THE HISTIDINE-CONTAINING PHOSPHOCARRIER PROTEIN HPR FROM ESCHERICHIA COLI NMR, RESTRAINED REGULARIZED MEAN STRUCTURE |
3 |
3 |
SOLUTION NMR |
| 1ggt |
THREE-DIMENSIONAL STRUCTURE OF A TRANSGLUTAMINASE: HUMAN BLOOD COAGULATION FACTOR XIII |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggu |
HUMAN FACTOR XIII WITH CALCIUM BOUND IN THE ION SITE |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggv |
CRYSTAL STRUCTURE OF THE C123S MUTANT OF DIENELACTONE HYDROLASE (DLH) BOUND WITH THE PMS MOIETY OF THE PROTEASE INHIBITOR, PHENYLMETHYLSULFONYL FLUORIDE (PMSF) |
1 |
1 |
X-RAY DIFFRACTION |
| 1ggw |
CDC4P FROM SCHIZOSACCHAROMYCES POMBE |
26 |
26 |
SOLUTION NMR |
| 1ggx |
RED FLUORESCENT PROTEIN (FP583 OR DSRED(CLONTECH)) FROM DISCOSOMA SP. |
1 |
1 |
X-RAY DIFFRACTION |