Fluorine in PDB, part 69 (files: 2721-2760),
PDB 4j0v-4jps
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: 2721-2760 (PDB 4j0v-4jps).
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4j0v (F: 2) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((4R,5R)-2-Amino-5-Fluoro-4-Methyl-5,6-Dihydro-4H- [1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]-Amide
Other atoms:
Na (2);
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4j0y (F: 2) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((4R,5S)-2-Amino-5-Fluoro-4-Methyl-5,6-Dihydro-4H- [1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]-Amide
Other atoms:
Na (2);
-
4j0z (F: 3) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((4S,5R)-2-Amino-5-Fluoro-4-Fluoromethyl-5,6- Dihydro-4H-[1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]-Amide
Other atoms:
Na (2);
-
4j14 (F: 2) - Crystal Structure of Human Cytochrome P450 CYP46A1 with Posaconazole Bound
Other atoms:
Fe (1);
-
4j17 (F: 3) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((S)-2-Amino-4-Difluoromethyl-5,6-Dihydro-4H-[1, 3]Oxazin-4-Yl)-4-Fluoro-Phenyl]-Amide
Other atoms:
Na (2);
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4j1c (F: 4) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((S)-2-Amino-5,5-Difluoro-4-Fluoromethyl-5,6- Dihydro-4H-[1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]-Amide
Other atoms:
Na (2);
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4j1e (F: 5) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((4S,6S)-2-Amino-4-Fluoromethyl-6-Trifluoromethyl- 5,6-Dihydro-4H-[1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]-Amide
Other atoms:
Na (2);
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4j1f (F: 4) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((4S,6S)-2-Amino-4-Methyl-6-Trifluoromethyl-5,6- Dihydro-4H-[1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]-Amide
Other atoms:
Na (2);
-
4j1h (F: 4) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((4S,6R)-2-Amino-4-Methyl-6-Trifluoromethyl-5,6- Dihydro-4H-[1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]-Amide
Other atoms:
Na (2);
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4j1i (F: 5) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((4R,5R,6R)-2-Amino-5-Fluoro-4-Methyl-6- Trifluoromethyl-5,6-Dihydro-4H-[1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]- Amide
Other atoms:
Na (2);
-
4j1k (F: 5) - Crystal Structure of Bace-1 in Complex with 5-Cyano-Pyridine-2- Carboxylic Acid [3-((4R,5R,6S)-2-Amino-5-Fluoro-4-Methyl-6- Trifluoromethyl-5,6-Dihydro-4H-[1,3]Oxazin-4-Yl)-4-Fluoro-Phenyl]- Amide
Other atoms:
Na (2);
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4j3j (F: 12) - Crystal Structure of Dpp-IV with Compound C3
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4j52 (F: 1) - Crystal Structure of PLK1 in Complex with A Pyrimidodiazepinone Inhibitor
Other atoms:
Zn (1);
-
4j53 (F: 3) - Crystal Structure of PLK1 in Complex with Tak-960
Other atoms:
Zn (1);
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4j6a (F: 6) - Crystal Structure of Ribonuclease A Soaked in 40% 2,2,2- Trifluoroethanol: One of Twelve in Mscs Set
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4j6i (F: 3) - Discovery of Thiazolobenzoxepin PI3-Kinase Inhibitors That Spare the PI3-Kinase Beta Isoform
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4j8m (F: 3) - Aurora A in Complex with CD532
Other atoms:
Mg (1);
As (1);
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4j8w (F: 3) - X-Ray Structure of NCP145 with Chlorido(Eta-6-P-Cymene)(N- Fluorophenyl-2-Pyridinecarbothioamide)Osmium(II)
Other atoms:
Mg (1);
Os (3);
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4ja2 (F: 3) - Structural Basis of A Rationally Rewired Protein-Protein Interface (RR468MUTANT V13P, L14I, I17M and N21V)
Other atoms:
Mg (1);
-
4ja8 (F: 6) - Complex of Mitochondrial Isocitrate Dehydrogenase R140Q Mutant with Agi-6780 Inhibitor
Other atoms:
Ca (2);
-
4jas (F: 3) - Structural Basis of A Rationally Rewired Protein-Protein Interface (HK853MUTANT A268V, A271G, T275M, V294T and D297E and RR468MUTANT V13P, L14I, I17M and N21V)
Other atoms:
Mg (2);
-
4jav (F: 6) - Structural Basis of A Rationally Rewired Protein-Protein Interface (HK853WT and RR468MUTANT V13P, L14I, I17M and N21V)
Other atoms:
Mg (4);
Cl (1);
-
4jb4 (F: 2) - Expression, Purification, Characterization, and Solution uc(Nmr) Study of Highly Deuterated Yeast Cytochrome C Peroxidase with Enhanced Solubility
Other atoms:
Fe (2);
-
4jby (F: 2) - Crystal Structure of Thymidine Kinase From Herpes Simplex Virus Type 1 in Complex with F-SK78
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4jds (F: 4) - SETD7 in Complex with Inhibitor Pf-5426 and S-Adenosyl-Methionine
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4jii (F: 3) - Crystal Structure of AKR1B10 Complexed with Nadp+ and Zopolrestat
Other atoms:
Na (1);
-
4jjs (F: 3) - Crystal Structure of Hcv NS5B Polymerase in Complex with Compound 2
Other atoms:
Mg (2);
-
4jju (F: 10) - Crystal Structure of Hcv NS5B Polymerase in Complex with Compound 29
Other atoms:
Mg (4);
-
4jkv (F: 8) - Structure of the Human Smoothened 7TM Receptor in Complex with An Antitumor Agent
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4jlg (F: 8) - SETD7 in Complex with Inhibitor (R)-Pfi-2 and S-Adenosyl-Homocysteine
-
4jlj (F: 4) - Human Dck C4S-S74E Mutant in Complex with Udp and the F2.1.1 Inhibitor (2-[({2-[3-(2-Fluoroethoxy)-4-Methoxyphenyl]-1,3-Thiazol-4- Yl}Methyl)Sulfanyl]Pyrimidine-4,6-Diamine)
-
4jlk (F: 4) - Human Dck C4S-S74E Mutant in Complex with Udp and the F2.2.1 Inhibitor (2-[({2-[3-(2-Fluoroethoxy)-4-Methoxyphenyl]-5-Methyl-1,3-Thiazol-4- Yl}Methyl)Sulfanyl]Pyrimidine-4,6-Diamine)
-
4jlm (F: 3) - Human Dck C4S-S74E Mutant in Complex with Udp and the F2.3.1 Inhibitor (2-[({5-Ethyl-2-[3-(2-Fluoroethoxy)-4-Methoxyphenyl]-1,3-Thiazol-4- Yl}Methyl)Sulfanyl]Pyrimidine-4,6-Diamine)
-
4jln (F: 2) - Human Dck C4S-S74E Mutant in Complex with Udp and the F2.4.1 Inhibitor (2-[({2-[3-(2-Fluoroethoxy)-4-Methoxyphenyl]-5-Propyl-1,3-Thiazol-4- Yl}Methyl)Sulfanyl]Pyrimidine-4,6-Diamine)
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4jlt (F: 1) - Crystal Structure of P450 2B4(H226Y) in Complex with Paroxetine
Other atoms:
Fe (1);
-
4jma (F: 3) - Crystal Structure of Cytochrome C Peroxidase W191G-Gateless in Complex with 3-Fluorocatechol
Other atoms:
Fe (1);
-
4jnc (F: 3) - Soluble Epoxide Hydrolase Complexed with A Carboxamide Inhibitor
-
4joa (F: 2) - Crystal Structure of Human Anaplastic Lymphoma Kinase in Complex with 7-Azaindole Based Inhibitor
-
4jp4 (F: 8) - MMP13 in Complex with A Reverse Hydroxamate Zn-Binder
Other atoms:
Zn (4);
Ca (4);
Na (2);
-
4jps (F: 3) - Co-Crystal Structures of the Lipid Kinase PI3K Alpha with Pan and Isoform Selective Inhibitors
Page generated: Sun Dec 15 10:23:10 2024
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