Search Count: 12
 |
Crystal Structure Of Lysine Specific Demethylase 1 (Lsd1) With Tak-418, Fad-Adduct
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2021-03-24 Classification: OXIDOREDUCTASE Ligands: HUF, GOL, IMD, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-03-24
Ligands: HUF, GOL, IMD, MG
 |
Cryo-Em Structure Of K+-Bound Herg Channel
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2021-01-20 Classification: TRANSPORT PROTEIN Ligands: K |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2021-01-20
Ligands: K
 |
Cryo-Em Structure Of K+-Bound Herg Channel In The Presence Of Astemizole
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2021-01-20 Classification: TRANSPORT PROTEIN Ligands: K |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2021-01-20
Ligands: K
 |
Crystal Structure Of Mcl-1 In Complex With Compound 4
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-11-27 Classification: APOPTOSIS Ligands: LC3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-27
Ligands: LC3
 |
Crystal Structure Of Mcl-1 In Complex With Compound 10
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2013-11-27 Classification: APOPTOSIS Ligands: LC6 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-27
Ligands: LC6
 |
Crystal Structure Of Bcl-Xl In Complex With Compound 10
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.45 Å Release Date: 2013-11-27 Classification: APOPTOSIS Ligands: LC6, PO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-27
Ligands: LC6, PO4
 |
Crystal Structure Of Faah In Complex With Inhibitor
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.91 Å Release Date: 2013-02-06 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 17J |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2013-02-06
Ligands: 17J
 |
Egfr Kinase Domain T790M/L858R Mutant With Tak-285
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.35 Å Release Date: 2013-01-16 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 03P |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: 03P
 |
Egfr Kinase Domain T790M/L858R Mutant With Compound 2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2013-01-16 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: W2P |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: W2P
 |
Egfr Kinase Domain T790M/L858R Mutant With Hki-272
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2013-01-16 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: HKI, MES |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: HKI, MES
 |
Egfr Kinase Domain T790M/L858R Mutant With Compound 4
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2013-01-16 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: W2R, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: W2R, EDO
 |
Egfr Kinase Domain With Compound4
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-01-16 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: W2R, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: W2R, SO4