Chlorine in PDB, part 218 (files: 8681-8720),
PDB 4hw2-4i1u
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: 8681-8720 (PDB 4hw2-4i1u).
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4hw2 (Cl: 12) - Discovery of Potent Mcl-1 Inhibitors Using Fragment-Based Methods and Structure-Based Design
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4hw3 (Cl: 12) - Discovery of Potent Mcl-1 Inhibitors Using Fragment-Based Methods and Structure-Based Design
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4hw6 (Cl: 10) - Crystal Structure of A Hypothetical Protein (BACOVA_00264) From Bacteroides Ovatus Atcc 8483 at 1.70 A Resolution
Other atoms:
I (12);
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4hw8 (Cl: 3) - 2.25 Angstrom Structure of the Extracellular Solute-Binding Protein From Staphylococcus Aureus in Complex with Maltose.
Other atoms:
K (4);
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4hwc (Cl: 2) - Structure of ATBAG1
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4hws (Cl: 2) - Crystal Structure of E. Coli Threonyl-Trna Synthetase Bound to A Novel Inhibitor
Other atoms:
Zn (2);
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4hx2 (Cl: 1) - Crystal Structure of Streptomyces Caespitosus Sermetstatin in Complex with Bacillus Licheniformis Subtilisin
Other atoms:
K (2);
Zn (2);
As (1);
Ca (4);
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4hxf (Cl: 1) - Acylaminoacyl Peptidase in Complex with Z-Gly-Gly-Phe-Chloromethyl Ketone
Other atoms:
Mg (5);
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4hxg (Cl: 2) - Pyrococcus Horikoshii Acylaminoacyl Peptidase (Orthorhombic Crystal Form)
Other atoms:
Mg (21);
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4hxw (Cl: 1) - Pyrrolopyrimidine Inhibitors of Dna Gyrase B and Topoisomerase IV, Part I: Structure Guided Discovery and Optimization of Dual Targeting Agents with Potent, Broad-Spectrum Enzymatic Activity.
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4hxx (Cl: 2) - Pyridinylpyrimidines Selectively Inhibit Human Methionine Aminopeptidase-1
Other atoms:
Co (3);
K (1);
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4hy1 (Cl: 2) - Pyrrolopyrimidine Inhibitors of Dna Gyrase B and Topoisomerase IV, Part I: Structure Guided Discovery and Optimization of Dual Targeting Agents with Potent, Broad-Spectrum Enzymatic Activity.
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4hyf (Cl: 3) - Structural Basis and Sar For Od 270, A Lead Stage 1,2,4-Triazole Based Specific TANKYRASE1/2 Inhibitor
Other atoms:
Zn (3);
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4hym (Cl: 1) - Pyrrolopyrimidine Inhibitors of Dna Gyrase B and Topoisomerase IV, Part I: Structure Guided Discovery and Optimization of Dual Targeting Agents with Potent, Broad-Spectrum Enzymatic Activity.
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4hyr (Cl: 3) - Structure of Putative Glucarate Dehydratase From Acidaminococcus Sp. D21 with Unusual Static Disorder
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4hyv (Cl: 1) - Pyruvate Kinase (Pyk) From Trypanosoma Brucei in the Presence of Magnesium, Pep and F26BP
Other atoms:
Mg (2);
K (2);
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4hyw (Cl: 1) - Pyruvate Kinase (Pyk) From Trypanosoma Brucei in the Presence of Magnesium and F26BP
Other atoms:
Mg (2);
K (2);
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4hyz (Cl: 6) - Crystal Structure of A Hypothetical Protein (RUMGNA_01855) From Ruminococcus Gnavus Atcc 29149 at 2.25 A Resolution
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4hzc (Cl: 1) - Crystal Structure of Serine Acetyltransferase From Brucella Abortus Strain S19
Other atoms:
Mg (9);
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4hzg (Cl: 1) - Structure of Haloalkane Dehalogenase Dhaa From Rhodococcus Rhodochrous
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4hzo (Cl: 1) - The Structure of the Bifunctional Acetyltransferase/Decarboxylase Lnmk From the Leinamycin Biosynthetic Pathway Revealing Novel Activity For A Double Hot Dog Fold
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4hzp (Cl: 1) - The Structure of the Bifunctional Acetyltransferase/Decarboxylase Lnmk From the Leinamycin Biosynthetic Pathway Revealing Novel Activity For A Double Hot Dog Fold
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4hzr (Cl: 1) - Crystal Structure of ACK1 Kinase Domain
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4hzt (Cl: 1) - Structure-Based Design of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage the Catalytic Aspartates
Other atoms:
Zn (3);
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4i07 (Cl: 1) - Structure of Mature Form of Cathepsin B1 From Schistosoma Mansoni
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4i0c (Cl: 7) - The Structure of the Camelid Antibody CABHUL5 in Complex with Human Lysozyme
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4i0d (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
Other atoms:
Zn (3);
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4i0e (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
Other atoms:
Br (1);
Zn (3);
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4i0f (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
Other atoms:
Zn (3);
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4i0g (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
Other atoms:
Br (1);
Zn (3);
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4i0s (Cl: 1) - Crystal Structure of Spleen Tyrosine Kinase Complexed with 2-(6- Chloro-1-Methyl-1H-Indazol-3-Yl)-5H-Pyrrolo[2,3-B]Pyrazine-7- Carboxylic Acid Isopropylamide
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4i0u (Cl: 13) - Improved Structure of Thermotoga Maritima Cora at 2.7 A Resolution
Other atoms:
Mg (24);
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4i0w (Cl: 3) - Structure of the Clostridium Perfringens Cspb Protease
Other atoms:
Na (2);
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4i0z (Cl: 1) - Structure-Based Design of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage the Catalytic Aspartates
Other atoms:
Zn (4);
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4i10 (Cl: 1) - Structure-Based Design of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage the Catalytic Aspartates
Other atoms:
Zn (3);
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4i12 (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
Other atoms:
Zn (3);
Na (2);
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4i1a (Cl: 2) - Crystal Structure of the Apo Form of Rapi
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4i1c (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
Other atoms:
Zn (3);
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4i1k (Cl: 4) - Crystal Structure of VRN1 (Residues 208-341)
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4i1u (Cl: 1) - Apo Crystal Structure of A Dephospho-Coa Kinase From Burkholderia Vietnamiensis
Page generated: Sun Dec 15 09:59:07 2024
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