Fluorine in PDB, part 77 (files: 3041-3080),
PDB 4olm-4pa0
Experimental structures of coordination spheres of Fluorine (F) in bioorganic
molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius
around Fluorine atoms. PDB files: 3041-3080 (PDB 4olm-4pa0).
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4olm (F: 4) - Crystal Structure of W741L-Ar-Lbd Bound with Co-Regulator Peptide
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4op1 (F: 6) - Gkrp Bound to AMG0556 and Sorbitol-6-Phosphate
Other atoms:
I (28);
Cl (2);
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4op2 (F: 6) - Gkrp Bound to Amg-0471 and Sorbitol-6-Phosphate
Other atoms:
I (26);
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4op3 (F: 6) - Human Gkrp Bound to Amg-5112 and Sorbitol-6-Phosphate
Other atoms:
I (25);
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4opx (F: 1) - Structure of Human Parp-1 Bound to A Dna Double Strand Break in Complex with (2R)-5-Fluoro-2-Methyl-2,3-Dihydro-1-Benzofuran-7- Carboxamide
Other atoms:
Zn (4);
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4oql (F: 4) - Crystal Structure of Thymidine Kinase From Herpes Simplex Virus Type 1 in Complex with Df-Edu
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4oqm (F: 2) - Crystal Structure of Thymidine Kinase From Herpes Simplex Virus Type 1 in Complex with F-Ara-Edu
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4oqv (F: 8) - High Resolution Crystal Structure of Human Dihydroorotate Dehydrogenase Bound with DSM338 (N-[3,5-Difluoro-4-(Trifluoromethyl) Phenyl]-5-Methyl-2-(Trifluoromethyl)[1,2,4]Triazolo[1,5-A]Pyrimidin- 7-Amine)
Other atoms:
Na (2);
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4or2 (F: 2) - Human Class C G Protein-Coupled Metabotropic Glutamate Receptor 1 in Complex with A Negative Allosteric Modulator
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4ori (F: 8) - Rat Dihydroorotate Dehydrogenase Bound with DSM338 (N-[3,5-Difluoro-4- (Trifluoromethyl)Phenyl]-5-Methyl-2-(Trifluoromethyl)[1,2, 4]Triazolo[1,5-A]Pyrimidin-7-Amine)
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4orm (F: 8) - Crystal Structure of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound with Inhibitor DSM338 (N-[3,5-Difluoro-4- (Trifluoromethyl)Phenyl]-5-Methyl-2-(Trifluoromethyl)[1,2, 4]Triazolo[1,5-A]Pyrimidin-7-Amine)
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4otr (F: 1) - Crystal Structure of Btk Kinase Domain Complexed with 6-Cyclopropyl-2- [3-[5-[[5-(4-Ethylpiperazin-1-Yl)-2-Pyridyl]Amino]-1-Methyl-6-Oxo-3- Pyridyl]-2-(Hydroxymethyl)Phenyl]-8-Fluoro-Isoquinolin-1-One
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4oty (F: 2) - Crystal Structure of Lumiracoxib Bound to the Apo-Mouse- Cyclooxygenase-2
Other atoms:
Cl (2);
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4ovz (F: 2) - X-Ray Structural and Biological Evaluation of A Series of Potent and Highly Selective Inhibitors of Human Coronavirus Papain-Like Proteases
Other atoms:
Zn (2);
Na (1);
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4ow0 (F: 2) - X-Ray Structural and Biological Evaluation of A Series of Potent and Highly Selective Inhibitors of Human Coronavirus Papain-Like Proteases
Other atoms:
Zn (2);
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4owm (F: 2) - Anthranilate Phosphoribosyl Transferase From Mycobacterium Tuberculosis in Complex with 3-Fluoroanthranilate, Prpp and Magnesium
Other atoms:
Mg (4);
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4own (F: 4) - Anthranilate Phosphoribosyl Transferase From Mycobacterium Tuberculosis in Complex with 5-Fluoroanthranilate, Prpp and Magnesium
Other atoms:
Mg (4);
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4owo (F: 4) - Anthranilate Phosphoribosyl Transferase From Mycobacterium Tuberculosis in Complex with 6-Fluoroanthranilate, Prpp and Magnesium
Other atoms:
Mg (4);
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4oys (F: 3) - Crystal Structure of VPS34 in Complex with SAR405.
Other atoms:
Cl (1);
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4oyt (F: 3) - Crystal Structure of Ternary Complex of Plasmodium Vivax Shmt with D- Serine and Folinic Acid
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4oz2 (F: 1) - Human Solac Complexed with 4-(4-Fluorophenyl)-3-Methyl-1H-Pyrazole
Other atoms:
Cl (1);
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4oz3 (F: 3) - Human Solac Complexed with 4-Phenyl-3-(Trifluoromethyl)-1H-Pyrazole
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4p1u (F: 2) - Influenza A (Flu) Virus Polymerase Basic Protein 2 (PB2) Bound to VX787, An Azaindole Inhibitor
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4p2h (F: 1) - Structure of Human Dna Polymerase Complexed with N7MG in the Template Opposite to Incoming Non-Hydrolyzable Ttp with Manganese in the Active Site
Other atoms:
Mn (2);
Na (2);
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4p44 (F: 1) - X-Ray Structure of Human Glutamate Carboxypeptidase II (Gcpii) in Complex with A Phosphoramidate Inhibitor Jrb-4-81
Other atoms:
Zn (2);
Ca (1);
Cl (1);
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4p45 (F: 1) - X-Ray Structure of Human Glutamate Carboxypeptidase II (Gcpii) in Complex with A Phosphoramidate Inhibitor Jrb-4-73
Other atoms:
Zn (2);
Ca (1);
Cl (1);
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4p5z (F: 3) - Human EPHA3 Kinase Domain in Complex with Quinoxaline Derivatives
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4p6g (F: 4) - Crystal Structure of Human Cathepsin S Bound to A Non-Covalent Inhibitor.
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4p75 (F: 6) - Phers in Complex with Compound 4A
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4p8c (F: 12) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Non- Covalent Inhibitor QN127
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4p8h (F: 6) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Nitro- Benzothiazole 6A
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4p8k (F: 6) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Non- Covalent Inhibitor TY38C
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4p8l (F: 8) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Non- Covalent Inhibitor TY36C
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4p8m (F: 6) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Non- Covalent Inhibitor QN114
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4p8n (F: 12) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Non- Covalent Inhibitor QN118
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4p8o (F: 2) - S. Aureus Gyrase Bound to An Aminobenzimidazole Urea Inhibitor
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4p8p (F: 6) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Non- Covalent Inhibitor QN127
Other atoms:
Cl (2);
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4p8t (F: 6) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Non- Covalent Inhibitor QN129
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4p8y (F: 3) - Crystal Structure of M. Tuberculosis DPRE1 in Complex with the Non- Covalent Inhibitor TY21C
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4pa0 (F: 2) - Omecamtiv Mercarbil Binding Site on the Human Beta-Cardiac Myosin Motor Domain
Page generated: Sun Dec 15 10:23:28 2024
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