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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).
  1. 4hw2 (Cl: 12) - Discovery of Potent Mcl-1 Inhibitors Using Fragment-Based Methods and Structure-Based Design
  2. 4hw3 (Cl: 12) - Discovery of Potent Mcl-1 Inhibitors Using Fragment-Based Methods and Structure-Based Design
  3. 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);
  4. 4hw8 (Cl: 3) - 2.25 Angstrom Structure of the Extracellular Solute-Binding Protein From Staphylococcus Aureus in Complex with Maltose.
    Other atoms: K (4);
  5. 4hwc (Cl: 2) - Structure of ATBAG1
  6. 4hws (Cl: 2) - Crystal Structure of E. Coli Threonyl-Trna Synthetase Bound to A Novel Inhibitor
    Other atoms: Zn (2);
  7. 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);
  8. 4hxf (Cl: 1) - Acylaminoacyl Peptidase in Complex with Z-Gly-Gly-Phe-Chloromethyl Ketone
    Other atoms: Mg (5);
  9. 4hxg (Cl: 2) - Pyrococcus Horikoshii Acylaminoacyl Peptidase (Orthorhombic Crystal Form)
    Other atoms: Mg (21);
  10. 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.
  11. 4hxx (Cl: 2) - Pyridinylpyrimidines Selectively Inhibit Human Methionine Aminopeptidase-1
    Other atoms: Co (3); K (1);
  12. 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.
  13. 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);
  14. 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.
  15. 4hyr (Cl: 3) - Structure of Putative Glucarate Dehydratase From Acidaminococcus Sp. D21 with Unusual Static Disorder
  16. 4hyv (Cl: 1) - Pyruvate Kinase (Pyk) From Trypanosoma Brucei in the Presence of Magnesium, Pep and F26BP
    Other atoms: Mg (2); K (2);
  17. 4hyw (Cl: 1) - Pyruvate Kinase (Pyk) From Trypanosoma Brucei in the Presence of Magnesium and F26BP
    Other atoms: Mg (2); K (2);
  18. 4hyz (Cl: 6) - Crystal Structure of A Hypothetical Protein (RUMGNA_01855) From Ruminococcus Gnavus Atcc 29149 at 2.25 A Resolution
  19. 4hzc (Cl: 1) - Crystal Structure of Serine Acetyltransferase From Brucella Abortus Strain S19
    Other atoms: Mg (9);
  20. 4hzg (Cl: 1) - Structure of Haloalkane Dehalogenase Dhaa From Rhodococcus Rhodochrous
  21. 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
  22. 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
  23. 4hzr (Cl: 1) - Crystal Structure of ACK1 Kinase Domain
  24. 4hzt (Cl: 1) - Structure-Based Design of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage the Catalytic Aspartates
    Other atoms: Zn (3);
  25. 4i07 (Cl: 1) - Structure of Mature Form of Cathepsin B1 From Schistosoma Mansoni
  26. 4i0c (Cl: 7) - The Structure of the Camelid Antibody CABHUL5 in Complex with Human Lysozyme
  27. 4i0d (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
    Other atoms: Zn (3);
  28. 4i0e (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
    Other atoms: Br (1); Zn (3);
  29. 4i0f (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
    Other atoms: Zn (3);
  30. 4i0g (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
    Other atoms: Br (1); Zn (3);
  31. 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
  32. 4i0u (Cl: 13) - Improved Structure of Thermotoga Maritima Cora at 2.7 A Resolution
    Other atoms: Mg (24);
  33. 4i0w (Cl: 3) - Structure of the Clostridium Perfringens Cspb Protease
    Other atoms: Na (2);
  34. 4i0z (Cl: 1) - Structure-Based Design of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage the Catalytic Aspartates
    Other atoms: Zn (4);
  35. 4i10 (Cl: 1) - Structure-Based Design of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage the Catalytic Aspartates
    Other atoms: Zn (3);
  36. 4i12 (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
    Other atoms: Zn (3); Na (2);
  37. 4i1a (Cl: 2) - Crystal Structure of the Apo Form of Rapi
  38. 4i1c (Cl: 1) - Design and Synthesis of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors
    Other atoms: Zn (3);
  39. 4i1k (Cl: 4) - Crystal Structure of VRN1 (Residues 208-341)
  40. 4i1u (Cl: 1) - Apo Crystal Structure of A Dephospho-Coa Kinase From Burkholderia Vietnamiensis
Page generated: Thu Dec 28 02:13:54 2023

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