Chlorine in PDB, part 550 (files: 21961-22000),
PDB 7ruz-7s2k
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: 21961-22000 (PDB 7ruz-7s2k).
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7ruz (Cl: 3) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-8445
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7rv0 (Cl: 2) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-8446
Other atoms:
F (1);
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7rv1 (Cl: 1) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-8826
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7rv2 (Cl: 2) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-8828
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7rv3 (Cl: 2) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-9124
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7rv4 (Cl: 3) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-9153
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7rv5 (Cl: 1) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-9287
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7rv6 (Cl: 1) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-9288
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7rv7 (Cl: 1) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-9322
Other atoms:
Ca (1);
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7rv8 (Cl: 1) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-10268
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7rv9 (Cl: 1) - Crystal Structure of the BCL6 Btb Domain in Complex with Oicr-10269
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7rvy (Cl: 1) - Structure of the Sars-Cov-2 Main Protease in Complex with Inhibitor MPI25
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7rvz (Cl: 1) - Structure of the Sars-Cov-2 Main Protease in Complex with Inhibitor MPI26
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7rw0 (Cl: 1) - Structure of the Sars-Cov-2 Main Protease in Complex with Inhibitor MPI27
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7rw7 (Cl: 2) - Crystal Structure of Human Methionine Adenosyltransferase 2A (MAT2A) in Complex with Sam and Allosteric Inhibitor Compound 9
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7rwg (Cl: 2) - "Crystal Structure of Human Methionine Adenosyltransferase 2A (MAT2A) in Complex with Sam and Allosteric Inhibitor Agi-43192
Other atoms:
F (3);
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7rwh (Cl: 1) - Crystal Structure of Human Methionine Adenosyltransferase 2A (MAT2A) in Complex with Sam and Allosteric Inhibitor Agi-41998
Other atoms:
Mg (3);
F (3);
Br (1);
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7rwn (Cl: 1) - Crystal Structure of Bptf Bromodomain in Complex with 4-Chloro-5-{4- [(Dimethylamino)Methyl]Anilino}-2-Methylpyridazin-3(2H)-One
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7rwo (Cl: 1) - Crystal Structure of Bptf Bromodomain in Complex with 4-Chloro-2- Methyl-5-[(1,2,3,4-Tetrahydroisoquinolin-7-Yl)Amino]Pyridazin-3(2H)- One
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7rwp (Cl: 1) - Crystal Structure of Bptf Bromodomain in Complex with 5-[4- (Aminomethyl)Anilino]-4-Chloro-2-Methylpyridazin-3(2H)-One
Other atoms:
Ca (1);
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7rwq (Cl: 1) - Crystal Structure of Bptf Bromodomain in Complex with 4-Chloro-2- Methyl-5-[(1,2,3,4-Tetrahydroisoquinolin-6-Yl)Amino]Pyridazin-3(2H)- One
Other atoms:
Ca (1);
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7rwu (Cl: 1) - Crystal Structure of Ni-Bound RIDC1 Variant in the Presence of Reductant
Other atoms:
Fe (1);
Ni (3);
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7rxf (Cl: 2) - Multi-Conformer Model of Apo Ketosteroid Isomerase Y57F Mutant From Pseudomonas Putida (Pksi) at 250 K
Other atoms:
Mg (2);
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7rxk (Cl: 4) - Multi-Conformer Model of Apo Ketosteroid Isomerase Y32F/Y57F Mutant From Pseudomonas Putida (Pksi) at 250 K
Other atoms:
Mg (2);
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7ry4 (Cl: 4) - Multi-Conformer Model of Ketosteroid Isomerase Y57F/D40N Mutant From Pseudomonas Putida (Pksi) Bound to A Transition State Analog at 250 K
Other atoms:
Mg (6);
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7rya (Cl: 2) - S. Cerevisiae CYP51 I471T Mutant Complexed with Itraconazole
Other atoms:
Fe (1);
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7rzc (Cl: 4) - Papain-Like Protease of Sars Cov-2 in Complex with JUN9-84-3 Inhibitor
Other atoms:
Zn (3);
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7rzd (Cl: 1) - Crystal Structure of Hla-B*07:02 in Complex with Mll(747-755) Peptide
Other atoms:
Na (1);
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7rzo (Cl: 1) - Crystal Structure of A Dihydrofolate Reductase (Fola) From Stenotrophomonas Maltophilia
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7s0u (Cl: 1) - PRMT5/MEP50 Crystal Structure with Mta and Phthalazinone Fragment Bound
Other atoms:
Na (1);
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7s14 (Cl: 3) - Crystal Structure of Putative Nad(P)H-Flavin Oxidoreductase From Haemophilus Influenzae 86-028NP
Other atoms:
K (2);
Ca (2);
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7s1a (Cl: 3) - Crystal Structure of Putative Nad(P)H-Flavin Oxidoreductase From Haemophilus Influenzae Rd KW20
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7s1n (Cl: 1) - N-Aromatic-Substituted Indazole Derivatives As Brain Penetrant and Orally Bioavailable JNK3 Inhibitors
Other atoms:
F (1);
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7s1s (Cl: 1) - PRMT5/MEP50 Crystal Structure with Mta and Mrtx-1719 Bound
Other atoms:
F (1);
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7s1x (Cl: 2) - Cryo-Em Structure of Human NKCC1 K289NA492EL671C Bound with Bumetanide
Other atoms:
K (2);
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7s1y (Cl: 2) - Cryo-Em Structure of Human NKCC1 K289NA492E Bound with Bumetanide
Other atoms:
K (2);
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7s25 (Cl: 3) - ROCK1 in Complex with Ligand G4998
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7s2i (Cl: 5) - Crystal Structure of Sulfonamide Resistance Enzyme SUL1 in Complex with 6-Hydroxymethylpterin
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7s2j (Cl: 7) - Crystal Structure of Sulfonamide Resistance Enzyme SUL2 Apoenzyme
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7s2k (Cl: 1) - Crystal Structure of Sulfonamide Resistance Enzyme SUL2 in Complex with 7,8-Dihydropteroate, Magnesium, and Pyrophosphate
Other atoms:
Mg (1);
Page generated: Tue Feb 25 09:05:10 2025
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