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Chlorine in PDB, part 329 (files: 13121-13160), PDB 5lz2-5m5a

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: 13121-13160 (PDB 5lz2-5m5a).
  1. 5lz2 (Cl: 1) - Fragment-Based Inhibitors of Lipoprotein Associated Phospholipase A2
    Other atoms: Na (1);
  2. 5lz4 (Cl: 2) - Fragment-Based Inhibitors of Lipoprotein Associated Phospholipase A2
    Other atoms: F (1);
  3. 5lz5 (Cl: 2) - Fragment-Based Inhibitors of Lipoprotein Associated Phospholipase A2
    Other atoms: F (1);
  4. 5lz7 (Cl: 1) - Fragment-Based Inhibitors of Lipoprotein Associated Phospholipase A2
    Other atoms: F (1);
  5. 5lz8 (Cl: 2) - Fragment-Based Inhibitors of Lipoprotein Associated Phospholipase A2
    Other atoms: F (1);
  6. 5lz9 (Cl: 1) - Fragment-Based Inhibitors of Lipoprotein Associated Phospholipase A2
    Other atoms: F (1); Na (1);
  7. 5lzm (Cl: 2) - Comparison of the Crystal Structure of Bacteriophage T4 Lysozyme at Low, Medium, and High Ionic Strengths
  8. 5m05 (Cl: 1) - Chicken Smooth Muscle Myosin Motor Domain Co-Crystallized with the Specific Ck-571 Inhibitor, Mgadp Form
    Other atoms: F (1); Mg (1);
  9. 5m0d (Cl: 2) - Structure-Based Evolution of A Hybrid Steroid Series of Autotaxin Inhibitors
    Other atoms: Zn (2); I (9); Ca (1); Na (1);
  10. 5m0e (Cl: 2) - Structure-Based Evolution of A Hybrid Steroid Series of Autotaxin Inhibitors
    Other atoms: Zn (2); I (14); Ca (1); Na (2);
  11. 5m0m (Cl: 2) - Structure-Based Evolution of A Hybrid Steroid Series of Autotaxin Inhibitors
    Other atoms: Zn (2); I (12); Ca (1); Na (2);
  12. 5m0s (Cl: 2) - Structure-Based Evolution of A Hybrid Steroid Series of Autotaxin Inhibitors
    Other atoms: Zn (2); I (13); Ca (1); Na (1);
  13. 5m11 (Cl: 1) - Structural and Functional Probing of Porz, An Essential Bacterial Surface Component of the Type-IX Secretion System of Human Oral- Microbiomic Porphyromonas Gingivalis.
    Other atoms: Zn (8); As (1); Ca (4);
  14. 5m1y (Cl: 3) - The Case of 1LKR Held at the Pdb and Its Variable Amino Acid Occupancies; Re Refinement of 4OW9 to Correct This
    Other atoms: I (26); Pt (3); Na (1);
  15. 5m24 (Cl: 1) - Rarg Mutant-S371E
  16. 5m27 (Cl: 6) - Structure of A Bacterial Light-Regulated Adenylyl Cylcase
    Other atoms: Ca (2);
  17. 5m28 (Cl: 2) - Maltodextrin Binding Protein MALE1 From L. Casei BL23 Bound to Maltotriose
  18. 5m2a (Cl: 6) - Structure of A Bacterial Light-Regulated Adenylyl Cylcase
    Other atoms: Mg (1);
  19. 5m2b (Cl: 4) - Yeast 20S Proteasome with Human BETA5I (1-138) and Human BETA6 (97- 111; 118-133) in Complex with Thiazole Based Inhibitor RO19
    Other atoms: Mg (7);
  20. 5m2h (Cl: 4) - Crystal Structure of Vancomycin-Zn(II)-Citrate Complex
    Other atoms: Zn (1);
  21. 5m2k (Cl: 4) - Crystal Structure of Vancomycin-Zn(II) Complex
    Other atoms: Zn (1);
  22. 5m2t (Cl: 6) - X-Ray Structure of Uridine Phosphorylase From Vibrio Cholerae in Complex with Uridine at 1.03 A Resolution
    Other atoms: Mg (1); Na (3);
  23. 5m2v (Cl: 2) - Structure of GLUK1 Ligand-Binding Domain (S1S2) in Complex with (2S, 4R)-4-(2-Carboxyphenoxy)Pyrrolidine-2-Carboxylic Acid at 3.18 A Resolution
  24. 5m31 (Cl: 3) - Macrodomain of Thermus Aquaticus Darg
  25. 5m3e (Cl: 1) - Macrodomain of Thermus Aquaticus Darg in Complex with Adp-Ribose
  26. 5m3i (Cl: 3) - Macrodomain of Mycobacterium Tuberculosis Darg
  27. 5m3t (Cl: 3) - Structural Tuning of CD81LEL (Space Group P64)
  28. 5m44 (Cl: 5) - Complex Structure of Human Protein Kinase CK2 Catalytic Subunit with A Thieno[2,3-D]Pyrimidin Inhibitor Crystallized Under High-Salt Conditions
  29. 5m4c (Cl: 1) - Complex Structure of Human Protein Kinase CK2 Catalytic Subunit with A Thieno[2,3-D]Pyrimidin Inhibitor Crystallized Under Low-Salt Conditions
  30. 5m4f (Cl: 4) - Complex Structure of Human Protein Kinase CK2 Catalytic Subunit with the Inhibitor 4'-Carboxy-6,8-Chloro-Flavonol (FLC21) Crystallized Under Low-Salt Conditions
  31. 5m4i (Cl: 7) - Complex Structure of Human Protein Kinase CK2 Catalytic Subunit with the Inhibitor 4'-Carboxy-6,8-Chloro-Flavonol (FLC21) Crystallized Under High-Salt Conditions
  32. 5m4k (Cl: 1) - Application of Off-Rate Screening in the Identification of Novel Pan- Isoform Inhibitors of Pyruvate Dehydrogenase Kinase
    Other atoms: Mg (1);
  33. 5m4m (Cl: 4) - Application of Off-Rate Screening in the Identification of Novel Pan- Isoform Inhibitors of Pyruvate Dehydrogenase Kinase
  34. 5m4n (Cl: 5) - Application of Off-Rate Screening in the Identification of Novel Pan- Isoform Inhibitors of Pyruvate Dehydrogenase Kinase
  35. 5m4p (Cl: 4) - Application of Off-Rate Screening in the Identification of Novel Pan- Isoform Inhibitors of Pyruvate Dehydrogenase Kinase
  36. 5m4u (Cl: 3) - Orthorhombic Complex Structure of Human Protein Kinase CK2 Catalytic Subunit (Isoform CK2ALPHA') with the Inhibitor 4'-Carboxy-6,8-Chloro- Flavonol (FLC21)
  37. 5m4v (Cl: 3) - X-Ray Structure of the Mambaquaretin-1, A Selective Antagonist of the Vasopressin Type 2 Receptor
  38. 5m55 (Cl: 1) - NEK2 Bound to Arylaminopurine 71
  39. 5m56 (Cl: 6) - Monoclinic Complex Structure of Human Protein Kinase CK2 Catalytic Subunit (Isoform CK2ALPHA') with the Inhibitor 4'-Carboxy-6,8-Chloro- Flavonol (FLC21)
  40. 5m5a (Cl: 1) - Crystal Structure of Melk in Complex with An Inhibitor
    Other atoms: Na (2);
Page generated: Wed Nov 4 03:59:18 2020

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