Search Count: 42
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Crystal Structure Of Human Chd1 Tandem Chromodomain In Complex With The Ethoxyquinoline-Based Inhibitor 2B
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2026-05-20 Classification: PEPTIDE BINDING PROTEIN Ligands: A1JUQ, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-05-20
Ligands: A1JUQ, DMS
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Crystal Structure Of Human Chd1 Tandem Chromodomain In Complex With The Ethoxyquinoline-Based Inhibitor 2L
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.35 Å Release Date: 2026-05-20 Classification: PEPTIDE BINDING PROTEIN Ligands: EDO, A1JUR, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-05-20
Ligands: EDO, A1JUR, DMS
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Crystal Structure Of Human Chd1 Tandem Chromodomain In Complex With The Ethoxyquinazoline-Based Inhibitor 1Q
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2026-05-20 Classification: PEPTIDE BINDING PROTEIN Ligands: A1JUO, DMS, EDO, BU3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-05-20
Ligands: A1JUO, DMS, EDO, BU3
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Crystal Structure Of Human Chd1 Tandem Chromodomain In Complex With The Ethoxyquinoline-Based Inhibitor 2N
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2026-05-20 Classification: PEPTIDE BINDING PROTEIN Ligands: A1JUP, EDO, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-05-20
Ligands: A1JUP, EDO, DMS
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Crystal Structure Of Human Chd1 Tandem Chromodomain In Complex With The Ethoxyquinoline-Based Inhibitor 2S
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2026-05-20 Classification: PEPTIDE BINDING PROTEIN Ligands: A1JUS, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-05-20
Ligands: A1JUS, EDO
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Crystal Structure Of Human Sirt2 In Complex With The Covalent Adduct Of Sirreal-Triazole Inhibitor Mz242 And Adp-Ribose
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.10 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: A1JK7, BU3, ZN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: A1JK7, BU3, ZN
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Crystal Structure Of Human Sirt2 In Complex With Sirreal-Triazole Inhibitor Sh10
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: ZN, BU3, EDO, A1JK0 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: ZN, BU3, EDO, A1JK0
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Crystal Structure Of Human Sirt2 In Complex With Sirreal-Triazole Inhibitor Lg023
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: ZN, A1JK1, BU3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: ZN, A1JK1, BU3
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Crystal Structure Of Human Sirt2 In Complex With The Covalent Adduct Of Sirreal-Triazole Inhibitor Lg023 And Adp-Ribose
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: ZN, A1JK2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: ZN, A1JK2
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Crystal Structure Of Human Sirt2 In Complex With Peptide Triazole Inhibitor Otdi1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: ZN, EDO, A1JK5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: ZN, EDO, A1JK5
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Crystal Structure Of Human Sirt2 In Complex With The Covalent Adduct Of Peptide Triazole Inhibitor Otdi1 And Adp-Ribose
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: ZN, A1JK4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: ZN, A1JK4
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Crystal Structure Of Human Sirt2 In Complex With Peptide Triazole Inhibitor Ltdi1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: ZN, A1JK3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: ZN, A1JK3
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Crystal Structure Of Human Sirt2 In Complex With The Covalent Adduct Of Peptide Triazole Inhibitor Ltdi1 And Adp-Ribose
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: ZN, A1JK8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: ZN, A1JK8
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Crystal Structure Of Human Sirt3 In Complex With The Covalent Adduct Of Peptide Triazole Inhibitor Ltdi1 And Adp-Ribose
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2025-11-12 Classification: HYDROLASE Ligands: ZN, BU3, A1JK8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: ZN, BU3, A1JK8
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Human Histone Deacetylase Sirt2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2025-08-20 Classification: HYDROLASE Ligands: ZN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-08-20
Ligands: ZN
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Human Sirt2 In Complex With Rw-78
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2025-08-20 Classification: HYDROLASE Ligands: A1JLK, ZN, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-08-20
Ligands: A1JLK, ZN, EDO
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Human Sirt2 In Complex With Rw-80
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2025-08-20 Classification: HYDROLASE Ligands: ZN, A1JLL, EDO, ACT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-08-20
Ligands: ZN, A1JLL, EDO, ACT
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Crystal Structure Of Polyphosphate Kinase 2-Ii (Ppk2-Ii) From Lysinibacillus Fusiformis Bound To Adp (Form I)
Organism: Lysinibacillus fusiformis
Method: X-RAY DIFFRACTION Resolution:2.88 Å Release Date: 2025-07-16 Classification: TRANSFERASE Ligands: ADP, PO4 |
Organism: Lysinibacillus fusiformis
Method: X-RAY DIFFRACTION
Release Date: 2025-07-16
Ligands: ADP, PO4
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Crystal Structure Of Human Sirt2 In Complex With A Pyrazole-Based Fragment Inhibitor And Nad+
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2025-06-04 Classification: HYDROLASE Ligands: ZN, EDO, DMS, NAD, A1IBW |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-06-04
Ligands: ZN, EDO, DMS, NAD, A1IBW
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Crystal Structure Of Human Sirt2 In Apo Form With Opened Selectivity Pocket
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.25 Å Release Date: 2025-05-28 Classification: HYDROLASE Ligands: ZN, DMS, PG4, EDO, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-05-28
Ligands: ZN, DMS, PG4, EDO, PEG