Chlorine in PDB, part 409 (files: 16321-16360),
PDB 6g8m-6ggn
Experimental structures of coordination spheres of Chlorine (Cl) in bioorganic
molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius
around Chlorine atoms. PDB files: 16321-16360 (PDB 6g8m-6ggn).
-
6g8m (Cl: 2) - Yeast 20S Proteasome in Complex with Cystargolide B Derivative 1
Other atoms:
Mg (8);
-
6g8n (Cl: 2) - Yeast 20S Proteasome in Complex with Cystargolide B Derivative 2
Other atoms:
Mg (8);
-
6g8p (Cl: 1) - 14-3-3SIGMA in Complex with A P129BETA3P and L132BETA3L Mutated Yap PS127 Phosphopeptide
Other atoms:
Ca (2);
-
6g8q (Cl: 2) - 14-3-3SIGMA in Complex with A A130BETA3A and Q133BETA3Q Mutated Yap PS127 Phosphopeptide
Other atoms:
Ca (1);
Na (3);
-
6g8x (Cl: 2) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g8y (Cl: 1) - Crystal Structures of the Single Pdz Domains From GRASP65 and Their Interaction with the Golgin GM130
-
6g91 (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g93 (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g94 (Cl: 4) - Structure of E. Coli Hydrogenase-1 C19G Variant in Complex with Cytochrome B
Other atoms:
Ni (4);
Mg (4);
Fe (50);
-
6g97 (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g9a (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g9d (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g9h (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g9i (Cl: 1) - Crystal Structure of Ebolavirus Glycoprotein in Complex with Clomipramine
-
6g9j (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g9k (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g9m (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6g9n (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6gaj (Cl: 4) - Crystal Structure of the T1L Reovirus SIGMA1 Coiled Coil Tail (Iodide)
Other atoms:
I (3);
-
6gak (Cl: 2) - Crystal Structure of the T1L Reovirus SIGMA1 Coiled Coil Tail (Chloride)
-
6gal (Cl: 2) - Structure of Fully Reduced Hydrogenase (Hyd-1) Variant E28Q Collected at pH 10
Other atoms:
Ni (2);
Mg (2);
Fe (24);
-
6gao (Cl: 3) - Crystal Structure of the T1L Reovirus SIGMA1 Coiled Coil Tail and Body
-
6gb0 (Cl: 2) - The Structure of Variant K294A of the Mo-Insertase Domain CNX1E From Arabidopsis Thaliana in Complex with Amp
Other atoms:
Mg (1);
-
6gb9 (Cl: 1) - The Structure of Variant S328A of the Mo-Insertase Domain CNX1E From Arabidopsis Thaliana in Complex with Amp
Other atoms:
Mg (1);
-
6gbw (Cl: 1) - Thrombin in Complex with MI2100 ((S)-N-(2-(Aminomethyl)-5- Chlorobenzyl)-1-((Benzylsulfonyl)-L-Arginyl)Pyrrolidine-2- Carboxamide)
Other atoms:
Na (2);
-
6gcp (Cl: 14) - Trypanosoma Brucei PTR1 in Complex with Inhibitor 2D (F186)
-
6gcr (Cl: 1) - Focal Adhesion Kinase Catalytic Domain in Complex with Irreversible Inhibitor
-
6gcw (Cl: 2) - Focal Adhesion Kinase Catalytic Domain in Complex with Irreversible Inhibitor
-
6gcx (Cl: 1) - Focal Adhesion Kinase Catalytic Domain in Complex with Irreversible Inhibitor
-
6gdq (Cl: 2) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6ge0 (Cl: 1) - Fragment-Based Discovery of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2
-
6geo (Cl: 1) - Crystal Structure of Mycobacterium Tuberculosis Cytochrome P450 CYP121A1 in Complex with Triazole Pyrazole Inhibitor 10J
Other atoms:
Fe (1);
-
6ges (Cl: 3) - Crystal Structure of ERK1 Covalently Bound to SM1-71
-
6gey (Cl: 8) - Trypanosoma Brucei PTR1 in Complex with Inhibitor 4G (F125)
-
6gfs (Cl: 1) - Thermodynamic, Crystallographic and Computational Studies of Non Mammalian Fatty Acid Binding to Bovine B-Lactoglobulin
-
6ggg (Cl: 1) - Mineralocorticoid Receptor in Complex with (S)-13
Other atoms:
F (1);
-
6ggi (Cl: 3) - Crystal Structure of COTB2 in Complex with 2-Fluoro-3,7,18- Dolabellatriene
Other atoms:
F (2);
Mg (9);
K (2);
-
6ggk (Cl: 1) - Crystal Structure of COTB2 C-Terminal Truncation
Other atoms:
Mg (3);
-
6ggl (Cl: 1) - Crystal Structure of COTB2 Variant F107A
Other atoms:
Mg (2);
-
6ggn (Cl: 3) - In Vitro and in Vivo Characterization of A Novel, Highly Potent P53- MDM2 Inhibitor
Page generated: Tue Feb 25 08:59:48 2025
|
