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Page 1126 of 5099 · 254917 entries
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| PDB ID | Title | official curves | Structure unit | Experimental Method |
|---|---|---|---|---|
| 2ycf | Crystal Structure of Checkpoint Kinase 2 in complex with Inhibitor PV1531 | 1 | 1 | X-RAY DIFFRACTION |
| 2ycg | Structure of unreduced ferric cytochrome c peroxidase obtained by multicrystal method | 1 | 1 | X-RAY DIFFRACTION |
| 2ych | PilM-PilN type IV pilus biogenesis complex | 1 | 1 | X-RAY DIFFRACTION |
| 2yci | methyltransferase native | 1 | 1 | X-RAY DIFFRACTION |
| 2ycj | methyltransferase bound with methyltetrahydrofolate | 1 | 1 | X-RAY DIFFRACTION |
| 2yck | methyltransferase bound with tetrahydrofolate | 1 | 1 | X-RAY DIFFRACTION |
| 2ycl | complete structure of the corrinoid,iron-sulfur protein including the N-terminal domain with a 4Fe-4S cluster | 1 | 1 | X-RAY DIFFRACTION |
| 2ycm | Inhibitors of herbicidal target IspD | 1 | 1 | X-RAY DIFFRACTION |
| 2ycn | Y71F mutant of tyrosine phenol-lyase from Citrobacter freundii in complex with quinonoid intermediate formed with 3-fluoro-L-tyrosine | 1 | 1 | X-RAY DIFFRACTION |
| 2ycp | F448H mutant of tyrosine phenol-lyase from Citrobacter freundii in complex with quinonoid intermediate formed with 3-fluoro-L-tyrosine | 1 | 1 | X-RAY DIFFRACTION |
| 2ycq | Crystal structure of checkpoint kinase 2 in complex with inhibitor PV1115 | 1 | 1 | X-RAY DIFFRACTION |
| 2ycr | Crystal structure of checkpoint kinase 2 in complex with inhibitor PV976 | 1 | 1 | X-RAY DIFFRACTION |
| 2ycs | Crystal structure of checkpoint kinase 2 in complex with PV788 | 1 | 1 | X-RAY DIFFRACTION |
| 2yct | Tyrosine phenol-lyase from Citrobacter freundii in complex with pyridine N-oxide and the quinonoid intermediate formed with L-alanine | 1 | 1 | X-RAY DIFFRACTION |
| 2ycw | TURKEY BETA1 ADRENERGIC RECEPTOR WITH STABILISING MUTATIONS AND BOUND ANTAGONIST CARAZOLOL | 2 | 2 | X-RAY DIFFRACTION |
| 2ycx | TURKEY BETA1 ADRENERGIC RECEPTOR WITH STABILISING MUTATIONS AND BOUND ANTAGONIST CYANOPINDOLOL | 2 | 2 | X-RAY DIFFRACTION |
| 2ycy | TURKEY BETA1 ADRENERGIC RECEPTOR WITH STABILISING MUTATIONS AND BOUND ANTAGONIST CYANOPINDOLOL | 2 | 2 | X-RAY DIFFRACTION |
| 2ycz | TURKEY BETA1 ADRENERGIC RECEPTOR WITH STABILISING MUTATIONS AND BOUND ANTAGONIST IODOCYANOPINDOLOL | 2 | 2 | X-RAY DIFFRACTION |
| 2yd0 | Crystal structure of the soluble domain of human endoplasmic reticulum aminopeptidase 1 ERAP1 | 1 | 1 | X-RAY DIFFRACTION |
| 2yd1 | Crystal structure of the N-terminal Ig1-2 module of Drosophila Receptor Protein Tyrosine Phosphatase DLAR | 1 | 1 | X-RAY DIFFRACTION |
| 2yd2 | Crystal structure of the N-terminal Ig1-2 module of Human Receptor Protein Tyrosine Phosphatase Sigma | 1 | 1 | X-RAY DIFFRACTION |
| 2yd3 | Crystal structure of the N-terminal Ig1-2 module of Human Receptor Protein Tyrosine Phosphatase Sigma | 1 | 1 | X-RAY DIFFRACTION |
| 2yd4 | Crystal structure of the N-terminal Ig1-2 module of Chicken Receptor Protein Tyrosine Phosphatase Sigma | 1 | 1 | X-RAY DIFFRACTION |
| 2yd5 | Crystal structure of the N-terminal Ig1-2 module of Human Receptor Protein Tyrosine Phosphatase LAR | 1 | 1 | X-RAY DIFFRACTION |
| 2yd6 | Crystal structure of the N-terminal Ig1-2 module of Human Receptor Protein Tyrosine Phosphatase Delta | 1 | 1 | X-RAY DIFFRACTION |
| 2yd7 | Crystal structure of the N-terminal Ig1-2 module of Human Receptor Protein Tyrosine Phosphatase Delta | 2 | 2 | X-RAY DIFFRACTION |
| 2yd8 | Crystal structure of the N-terminal Ig1-2 module of Human Receptor Protein Tyrosine Phosphatase LAR in complex with sucrose octasulphate | 1 | 1 | X-RAY DIFFRACTION |
| 2yd9 | Crystal structure of the N-terminal Ig1-3 module of Human Receptor Protein Tyrosine Phosphatase Sigma | 1 | 1 | X-RAY DIFFRACTION |
| 2yda | Sulfolobus sulfataricus 2-keto-3-deoxygluconate aldolase Y103F,Y130F, A198F variant | 1 | 1 | X-RAY DIFFRACTION |
| 2ydb | Catalytic domain of mouse 2',3'-cyclic nucleotide 3'- phosphodiesterase, soaked with 2',3'-cyclic NADP | 1 | 1 | X-RAY DIFFRACTION |
| 2ydc | Catalytic domain of mouse 2',3'-cyclic nucleotide 3'- phosphodiesterase, soaked with GTP | 1 | 1 | X-RAY DIFFRACTION |
| 2ydd | Catalytic domain of mouse 2',3'-cyclic nucleotide 3'- phosphodiesterase, soaked with 2',3'-cyclic AMP | 1 | 1 | X-RAY DIFFRACTION |
| 2yde | FACTOR INHIBITING HIF-1 ALPHA IN COMPLEX WITH S-2-HYDROXYGLUTARATE | 1 | 1 | X-RAY DIFFRACTION |
| 2ydf | HUMAN SERUM ALBUMIN COMPLEXED WITH IOPHENOXIC ACID | 2 | 2 | X-RAY DIFFRACTION |
| 2ydg | Ascorbate co-crystallized HEWL. | 1 | 1 | X-RAY DIFFRACTION |
| 2ydh | Crystal structure of the SAM-I riboswitch A94G U34 G18U G19U variant in complex with SAM | 1 | 1 | X-RAY DIFFRACTION |
| 2ydi | Discovery of Checkpoint Kinase Inhibitor AZD7762 by Structure Based Design and Optimization of Thiophene Carboxamide Ureas | 1 | 1 | X-RAY DIFFRACTION |
| 2ydj | Discovery of Checkpoint Kinase Inhibitor AZD7762 by Structure Based Design and Optimization of Thiophene Carboxamide Ureas | 2 | 2 | X-RAY DIFFRACTION |
| 2ydk | Discovery of Checkpoint Kinase Inhibitor AZD7762 by Structure Based Design and Optimization of Thiophene Carboxamide Ureas | 1 | 1 | X-RAY DIFFRACTION |
| 2ydl | Crystal structure of SH3C from CIN85 | 1 | 1 | X-RAY DIFFRACTION |
| 2ydm | Structural characterization of angiotensin-I converting enzyme in complex with a selenium analogue of captopril | 1 | 1 | X-RAY DIFFRACTION |
| 2ydo | Thermostabilised HUMAN A2a Receptor with adenosine bound | 1 | 1 | X-RAY DIFFRACTION |
| 2ydp | Structure of the E242A mutant of the alpha-l-arabinofuranosidase arb93a from fusarium graminearum in complex with an iminosugar inhibitor | 3 | 3 | X-RAY DIFFRACTION |
| 2ydq | CpOGA D298N in complex with hOGA-derived O-GlcNAc peptide | 1 | 1 | X-RAY DIFFRACTION |
| 2ydr | CpOGA D298N in complex with p53-derived O-GlcNAc peptide | 1 | 1 | X-RAY DIFFRACTION |
| 2yds | CpOGA D298N in complex with TAB1-derived O-GlcNAc peptide | 1 | 1 | X-RAY DIFFRACTION |
| 2ydt | STRUCTURE OF THE ALPHA-L-ARABINOFURANOSIDASE ARB93A from FUSARIUM Graminearum in complexe with an iminosugar inhibitor | 1 | 1 | X-RAY DIFFRACTION |
| 2ydu | Crystal structure of YopH in complex with 3-(1,1-dioxido-3- oxoisothiazolidin-5-yl)benzaldeyde | 1 | 1 | X-RAY DIFFRACTION |
| 2ydv | Thermostabilised HUMAN A2a Receptor with NECA bound | 1 | 1 | X-RAY DIFFRACTION |
| 2ydw | Crystal Structure of the First Bromodomain of Human Brd2 with the inhibitor GW841819X | 2 | 2 | X-RAY DIFFRACTION |