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Search Count: 13

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9DZN image
Kat6A Myst Domain Complexed With A H3K14-Coa Bisubstrate Inhibitor

8DD5 image
Crystal Structure Of Kat6A In Complex With Inhibitor Ctx-648 (Pf-9363)

6WF3 image
Crystal Structure Of Human Naa50 In Complex With A Cofactor Derived Inhibitor (Compound 1)

6WF5 image
Crystal Structure Of Human Naa50 In Complex With A Truncated Cofactor Derived Inhibitor (Compound 2)

6WFG image
Crystal Structure Of Human Naa50 In Complex With An Inhibitor (Compound 3) Identified Using Dna Encoded Library Technology

6WFK image
Crystal Structure Of Human Naa50 In Complex With Coa And An Inhibitor (Compound 4A) Identified Using Dna Encoded Library Technology
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.87 Å Release Date: 2020-07-01
Classification: TRANSFERASE
Ligands: COA, U2J

6WFN image
Crystal Structure Of Human Naa50 In Complex With Accoa And An Inhibitor (Compound 4A) Identified Using Dna Encoded Library Technology

6WFO image
Crystal Structure Of Human Naa50 In Complex With Accoa And An Inhibitor (Compound 4B) Identified Using Dna Encoded Library Technology

4W2R image
Structure Of Hs/Acprc2 In Complex With 5,8-Dichloro-2-[(4-Methoxy-6-Methyl-2-Oxo-1,2-Dihydropyridin-3-Yl)Methyl]-7-[(R)-Methoxy(Oxetan-3-Yl)Methyl]-3,4-Dihydroisoquinolin-1(2H)-One

5WHR image
Discovery Of A Novel And Selective Ido-1 Inhibitor Pf-06840003 And Its Characterization As A Potential Clinical Candidate.

6B3W image
Structure Of Hs/Acprc2 In Complex With 5,8-Dichloro-7-(3,5-Dimethyl-1,2-Oxazol-4-Yl)-2-[(4,6-Dimethyl-2-Oxo-1,2-Dihydropyridin-3-Yl)Methyl]-3,4-Dihydroisoquinolin-1(2H)-One

5IJ7 image
Structure Of Hs/Acprc2 In Complex With A Pyridone Inhibitor

5IJ8 image
Structure Of The Primary Oncogenic Mutant Y641N Hs/Acprc2 In Complex With A Pyridone Inhibitor
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