| 2y1f |
X-ray structure of 1-deoxy-D-xylulose 5-phosphate reductoisomerase, DXR, Rv2870c, from Mycobacterium tuberculosis, in complex with a 3,4- dichlorophenyl-substituted fosmidomycin analogue, manganese and NADPH. |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1g |
X-ray structure of 1-deoxy-D-xylulose 5-phosphate reductoisomerase, DXR, Rv2870c, from Mycobacterium tuberculosis, in complex with a 3,4- dichlorophenyl-substituted FR900098 analogue and manganese. |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1h |
Crystal structure of the human TatD-domain protein 3 (TATDN3) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1i |
Crystal structure of a S-diastereomer analogue of the spore photoproduct in complex with fragment DNA polymerase I from Bacillus stearothermophilus |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1j |
CRYSTAL STRUCTURE OF A R-DIASTEREOMER ANALOGUE OF THE SPORE PHOTOPRODUCT IN COMPLEX WITH FRAGMENT DNA POLYMERASE I FROM BACILLUS STEAROTHERMOPHILUS |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1k |
STRUCTURE OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY CBDP (12H SOAK): PHOSPHOSERINE ADDUCT |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1l |
Caspase-8 in Complex with DARPin-8.4 |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1m |
Structure of native c-Cbl |
6 |
6 |
X-RAY DIFFRACTION |
| 2y1n |
Structure of c-Cbl-ZAP-70 peptide complex |
2 |
2 |
X-RAY DIFFRACTION |
| 2y1o |
Dual-target Inhibitor of MurD and MurE Ligases: Design, Synthesis and Binding Mode Studies |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1p |
Catalytic domain of mouse 2',3'-cyclic nucleotide 3'- phosphodiesterase, complexed with citrate |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1q |
Crystal Structure of ClpC N-terminal Domain |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1r |
Structure of MecA121 & ClpC N-domain complex |
16 |
16 |
X-RAY DIFFRACTION |
| 2y1s |
Microvirin lectin |
40 |
40 |
SOLUTION NMR |
| 2y1t |
Bacillus subtilis prophage dUTPase in complex with dUDP |
2 |
2 |
X-RAY DIFFRACTION |
| 2y1v |
Full length structure of RrgB Pilus protein from Streptococcus pneumoniae |
3 |
3 |
X-RAY DIFFRACTION |
| 2y1w |
CRYSTAL STRUCTURE OF COACTIVATOR ASSOCIATED ARGININE METHYLTRANSFERASE 1 (CARM1) IN COMPLEX WITH SINEFUNGIN AND INDOLE INHIBITOR |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1x |
CRYSTAL STRUCTURE OF COACTIVATOR ASSOCIATED ARGININE METHYLTRANSFERASE 1 (CARM1) IN COMPLEX WITH SINEFUNGIN AND INDOLE INHIBITOR |
2 |
2 |
X-RAY DIFFRACTION |
| 2y1y |
Human alphaB crystallin ACD(residues 71-157) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y1z |
Human alphaB Crystallin ACD R120G |
1 |
1 |
X-RAY DIFFRACTION |
| 2y20 |
The mechanisms of HAMP-mediated signaling in transmembrane receptors - the A291I mutant |
3 |
3 |
X-RAY DIFFRACTION |
| 2y21 |
The mechanisms of HAMP-mediated signaling in transmembrane receptors - the A291V mutant |
6 |
6 |
X-RAY DIFFRACTION |
| 2y22 |
Human AlphaB-crystallin Domain (residues 67-157) |
6 |
6 |
X-RAY DIFFRACTION |
| 2y23 |
CRYSTAL STRUCTURE OF THE MYOMESIN DOMAINS MY9-MY11 |
1 |
1 |
X-RAY DIFFRACTION |
| 2y24 |
STRUCTURAL BASIS FOR SUBSTRATE RECOGNITION BY ERWINIA CHRYSANTHEMI GH5 GLUCURONOXYLANASE |
1 |
1 |
X-RAY DIFFRACTION |
| 2y25 |
Crystal structure of the myomesin domains My11-My13 |
2 |
2 |
X-RAY DIFFRACTION |
| 2y26 |
Transmission defective mutant of Grapevine Fanleaf virus |
1 |
3 |
X-RAY DIFFRACTION |
| 2y27 |
crystal structure of PaaK1 in complex with ATP from Burkholderia cenocepacia |
1 |
1 |
X-RAY DIFFRACTION |
| 2y28 |
crystal structure of Se-Met AmpD derivative |
3 |
3 |
X-RAY DIFFRACTION |
| 2y29 |
Structure of segment KLVFFA from the amyloid-beta peptide (Ab, residues 16-21), alternate polymorph III |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2a |
Structure of segment KLVFFA from the amyloid-beta peptide (Ab, residues 16-21), alternate polymorph I |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2b |
crystal structure of AmpD in complex with reaction products |
3 |
3 |
X-RAY DIFFRACTION |
| 2y2c |
crystal structure of AmpD Apoenzyme |
3 |
3 |
X-RAY DIFFRACTION |
| 2y2d |
crystal structure of AmpD holoenzyme |
3 |
3 |
X-RAY DIFFRACTION |
| 2y2e |
crystal structure of AmpD grown at pH 5.5 |
3 |
3 |
X-RAY DIFFRACTION |
| 2y2f |
Crystal structure of Yersinia pestis YopH in complex with an aminooxy- containing platform compound for inhibitor design |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2g |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (A01) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2h |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (ZA2) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2i |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (ZA3) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2j |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (ZA4) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2k |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (ZA5) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2l |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (E06) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2m |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (E08) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2n |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (E07) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2o |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (EO9) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2p |
Penicillin-binding protein 1b (pbp-1b) in complex with an alkyl boronate (z10) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2q |
PENICILLIN-BINDING PROTEIN 1B (PBP-1B) IN COMPLEX WITH AN ALKYL BORONATE (Z06) |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2t |
E. coli CsgC in reduced form |
1 |
1 |
X-RAY DIFFRACTION |
| 2y2u |
Nonaged form of Mouse Acetylcholinesterase inhibited by VX-Update |
2 |
2 |
X-RAY DIFFRACTION |
| 2y2v |
Nonaged form of Mouse Acetylcholinesterase inhibited by sarin-Update |
2 |
2 |
X-RAY DIFFRACTION |