Fluorine in PDB, part 25 (files: 961-1000),
PDB 2vh0-2wbk
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: 961-1000 (PDB 2vh0-2wbk).
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2vh0 (F: 1) - Structure and Property Based Design of Factor Xa Inhibitors: Biaryl Pyrrolidin-2-Ones Incorporating Basic Heterocyclic Motifs
Other atoms:
Mg (1);
Ca (1);
Cl (1);
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2vh6 (F: 1) - Structure and Property Based Design of Factor Xa Inhibitors: Pyrrolidin-2-Ones with Biaryl P4 Motifs
Other atoms:
Cl (1);
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2vj7 (F: 3) - Human Bace-1 in Complex with 3-(Ethylamino)-N-((1S,2R)-2- Hydroxy-1-(Phenylmethyl)-3-(((3-(Trifluoromethyl)Phenyl) Methyl)Amino)Propyl)-5-(2-Oxo-1-Pyrrolidinyl)Benzamide
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2vk7 (F: 2) - The Structure of Clostridium Perfringens Nani Sialidase and Its Catalytic Intermediates
Other atoms:
Ca (4);
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2vkq (F: 3) - Crystal Structure of Human Cytosolic 5'-Nucleotidase III ( Cn-III, NT5C3) in Complex with Beryllium Trifluoride
Other atoms:
Mg (1);
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2vnm (F: 6) - Human Bace-1 in Complex with 3-(1,1-Dioxidotetrahydro-2H-1, 2-Thiazin-2-Yl)-5-(Ethylamino)-N-((1S,2R)-2-Hydroxy-1-( Phenylmethyl)-3-(((3-(Trifluoromethyl)Phenyl)Methyl)Amino) Propyl)Benzamide
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2vnn (F: 3) - Human Bace-1 in Complex with 7-Ethyl-N-((1S,2R)-2-Hydroxy-1- (Phenylmethyl)-3-(((3-(Trifluoromethyl)Phenyl)Methyl)Amino) Propyl)-1-Methyl-3,4-Dihydro-1H-(1,2,5)Thiadiazepino(3,4,5- Hi)Indole-9-Carboxamide 2,2-Dioxide
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2vp6 (F: 8) - Structural Studies of Nucleoside Analog and Feedback Inhibitor Binding to Drosophila Melanogaster Multisubstrate Deoxyribonucleoside Kinase
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2vpp (F: 4) - Drosophila Melanogaster Deoxyribonucleoside Kinase Successfully Activates Gemcitabine in Transduced Cancer Cell Lines
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2vqj (F: 3) - Structure of HDAC4 Catalytic Domain Bound to A Trifluoromethylketone Inhbitor
Other atoms:
K (2);
Zn (2);
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2vqo (F: 6) - Structure of HDAC4 Catalytic Domain with A Gain-of-Function Muation Bound to A Trifluoromethylketone Inhbitor
Other atoms:
K (4);
Zn (2);
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2vqq (F: 6) - Structure of HDAC4 Catalytic Domain (A Double Cysteine-to- Alanine Mutant) Bound to A Trifluoromethylketone Inhbitor
Other atoms:
K (4);
Zn (2);
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2vr1 (F: 2) - Crystal Structure of Biotin Carboxylase From E. Coli in Complex with Atp Analog, ADPCF2P.
Other atoms:
Cl (2);
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2vs2 (F: 2) - Neutron Diffraction Structure of Endothiapepsin in Complex with A Gem-Diol Inhibitor.
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2vtd (F: 1) - Crystal Structure of Murd Ligase in Complex with D-Glu Containing Sulfonamide Inhibitor
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2vtn (F: 1) - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
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2vto (F: 1) - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
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2vtp (F: 3) - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
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2vtq (F: 2) - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
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2vtt (F: 2) - Identification of N-(4-Piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (AT7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-Ray Crystallography and Structure Based Drug Design.
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2vui (F: 3) - Crystal Structure of the Hupr Receiver Domain in Inhibitory Phospho-State
Other atoms:
Mg (2);
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2vvc (F: 2) - Aminopyrrolidine Factor Xa Inhibitor
Other atoms:
Ca (1);
Cl (2);
Na (2);
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2vvt (F: 4) - Glutamate Racemase (Muri) From E. Faecalis in Complex with A 9-Benzyl Purine Inhibitor
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2vvu (F: 1) - Aminopyrrolidine Factor Xa Inhibitor
Other atoms:
Ca (1);
Cl (1);
Na (1);
-
2vvv (F: 1) - Aminopyrrolidine-Related Triazole Factor Xa Inhibitor
Other atoms:
Ca (1);
Cl (1);
Na (1);
-
2vwl (F: 1) - Aminopyrrolidine Factor Xa Inhibitor
Other atoms:
Ca (1);
Cl (2);
Na (1);
-
2vwm (F: 2) - Aminopyrrolidine Factor Xa Inhibitor
Other atoms:
Cl (2);
Na (2);
-
2vwn (F: 1) - Aminopyrrolidine Factor Xa Inhibitor
Other atoms:
Ca (1);
Cl (3);
Na (2);
-
2vwo (F: 2) - Aminopyrrolidine Factor Xa Inhibitor
Other atoms:
Ca (1);
Cl (3);
Na (3);
-
2vz2 (F: 2) - Human Mao B in Complex with Mofegiline
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2w0w (F: 3) - Crystal Structure of Glmu From Haemophilus Influenzae in Complex with Quinazoline Inhibitor 2
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2w17 (F: 1) - CDK2 in Complex with the Imidazole Pyrimidine Amide, Compound (S)-8B
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2w1c (F: 1) - Structure Determination of Aurora Kinase in Complex with Inhibitor
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2w3i (F: 2) - Crystal Structure of Fxa in Complex with 4,4-Disubstituted Pyrrolidine-1,2-Dicarboxamide Inhibitor 2
Other atoms:
Cl (1);
Ca (1);
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2w3k (F: 1) - Crystal Structure of Fxa in Complex with 4,4-Disubstituted Pyrrolidine-1,2-Dicarboxamide Inhibitor 1
Other atoms:
Cl (1);
Ca (1);
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2w4o (F: 2) - Crystal Structure of Human CAMK4 in Complex with 4-Amino( Sulfamoyl-Phenylamino)-Triazole-Carbothioic Acid (2,6- Difluoro-Phenyl)-Amide)
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2w5u (F: 3) - Flavodoxin From Helicobacter Pylori in Complex with the C3 Inhibitor
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2wap (F: 6) - 3D-Crystal Structure of Humanized-Rat Fatty Acid Amide Hydrolase (Faah) Conjugated with the Drug-Like Urea Inhibitor Pf-3845
Other atoms:
Cl (1);
Na (3);
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2wb4 (F: 6) - Activated Diguanylate Cyclase Pled in Complex with C-Di-Gmp
Other atoms:
Mg (3);
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2wbk (F: 2) - Structure of the Michaelis Complex of Beta-Mannosidase, MAN2A, Provides Insight Into the Conformational Itinerary of Mannoside Hydrolysis
Other atoms:
Br (12);
Cl (7);
Page generated: Sun Dec 15 10:21:32 2024
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