Search Count: 25
 |
The Rigid Portion Of Cryo-Em Structure Of Herpesvirus Helicase-Primase Complex Prepared With Forked Dna And Atp-Gamma-S
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY Release Date: 2025-08-13 Classification: REPLICATION, TRANSFERASE |
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY
Release Date: 2025-08-13
 |
The Flexible Portion Of Cryo-Em Structure Of Herpesvirus Helicase-Primase Complex Prepared With Forked Dna And Atp-Gamma-S
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY Release Date: 2025-08-13 Classification: REPLICATION, TRANSFERASE |
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY
Release Date: 2025-08-13
 |
The Rigid Portion Of Cryo-Em Structure Of Herpesvirus Helicase-Primase Complex Prepared With Forked Dna, Atp-Gamma-S And Pritelivir
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY Release Date: 2025-08-13 Classification: REPLICATION, TRANSFERASE |
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY
Release Date: 2025-08-13
 |
The Flexible Portion Of Cryo-Em Structure Of Herpesvirus Helicase-Primase Complex Prepared With Forked Dna, Atp-Gamma-S And Pritelivir
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY Resolution:3.40 Å Release Date: 2025-08-13 Classification: REPLICATION, TRANSFERASE/INHIBITOR Ligands: A1BXB |
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY
Release Date: 2025-08-13
Ligands: A1BXB
 |
The Rigid Portion Of Cryo-Em Structure Of Herpesvirus Helicase-Primase Complex With Pritelivir
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY Release Date: 2025-08-13 Classification: REPLICATION, TRANSFERASE/INHIBITOR |
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY
Release Date: 2025-08-13
 |
The Flexible Portion Of Cryo-Em Structure Of Herpesvirus Helicase-Primase Complex With Pritelivir
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY Release Date: 2025-08-13 Classification: REPLICATION, TRANSFERASE/INHIBITOR Ligands: A1BXB |
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY
Release Date: 2025-08-13
Ligands: A1BXB
 |
The Flexible Portion Of Cryo-Em Structure Of Herpesvirus Helicase-Primase Complex With Amenamevir
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY Release Date: 2025-08-13 Classification: REPLICATION, TRANSFERASE/INHIBITOR Ligands: A1BXD |
Organism: Herpesviridae
Method: ELECTRON MICROSCOPY
Release Date: 2025-08-13
Ligands: A1BXD
 |
Cryo-Em Structure Of Human Enterovirus D68 Usa/Il/14-18952
Organism: Enterovirus d68
Method: ELECTRON MICROSCOPY Release Date: 2025-03-26 Classification: VIRUS |
Organism: Enterovirus d68
Method: ELECTRON MICROSCOPY
Release Date: 2025-03-26
 |
Cryo-Em Structure Of Human Enterovirus D68 Usa/Il/14-18952 In Complex With Fc-Mfsd6(L3)
Organism: Homo sapiens, Enterovirus d68
Method: ELECTRON MICROSCOPY Release Date: 2025-03-26 Classification: VIRUS |
Organism: Homo sapiens, Enterovirus d68
Method: ELECTRON MICROSCOPY
Release Date: 2025-03-26
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:2.39 Å Release Date: 2022-11-23 Classification: HYDROLASE Ligands: ZN, 8IY |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:2.45 Å Release Date: 2022-11-02 Classification: HYDROLASE Ligands: ZN, 98O |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2022-11-02 Classification: HYDROLASE Ligands: ZN, 99I |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:1.92 Å Release Date: 2022-11-02 Classification: HYDROLASE Ligands: ZN, 9DO |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2022-11-02 Classification: HYDROLASE Ligands: ZN, 9A1 |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:2.01 Å Release Date: 2022-11-02 Classification: HYDROLASE Ligands: ZN, 9B9 |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Escherichia coli (strain k12)
Method: X-RAY DIFFRACTION Resolution:2.45 Å Release Date: 2022-09-07 Classification: HYDROLASE Ligands: ZN, 7PX |
Organism: Escherichia coli (strain k12)
Method: X-RAY DIFFRACTION
Release Date: 2022-09-07
Ligands: ZN, 7PX
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2022-09-07 Classification: HYDROLASE Ligands: ZN, 7PX |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2022-09-07 Classification: HYDROLASE Ligands: ZN, 7S6 |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:2.04 Å Release Date: 2022-09-07 Classification: HYDROLASE Ligands: ZN, 7S2 |
 |
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
Organism: Pseudomonas aeruginosa (strain atcc 15692 / dsm 22644 / cip 104116 / jcm 14847 / lmg 12228 / 1c / prs 101 / pao1)
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2022-09-07 Classification: HYDROLASE Ligands: ZN, 7T5, EDO |