Fluorine in PDB, part 139 (files: 5521-5560),
PDB 6dkw-6e5g
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: 5521-5560 (PDB 6dkw-6e5g).
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6dkw (F: 6) - Crystal Structure of Trk-A in Complex with the Pan-Trk Kinase Inhibitor, Compound 3.
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6dmg (F: 2) - A Multiconformer Ligand Model of EK6 Bound to ERK2
Other atoms:
Cl (4);
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6dmi (F: 6) - A Multiconformer Ligand Model of 5T5 Bound to Bace-1
Other atoms:
Cl (3);
Na (2);
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6dnp (F: 2) - Crystal Structure of Mycobacterium Tuberculosis Malate Synthase in Complex with 2-F-3-Methyl-6-F-Phenyldiketoacid
Other atoms:
Mg (2);
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6dpq (F: 1) - Mapping the Binding Trajectory of A Suicide Inhibitor in Human Indoleamine 2,3-Dioxygenase 1
Other atoms:
Fe (1);
Cl (1);
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6dpr (F: 2) - Mapping the Binding Trajectory of A Suicide Inhibitor in Human Indoleamine 2,3-Dioxygenase 1
Other atoms:
Fe (1);
Cl (2);
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6dpy (F: 2) - X-Ray Crystal Structure of Ampc Beta-Lactamase with Inhibitor
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6drw (F: 2) - JAK2 JH1 in Complex with Jnj-7706621 (Crystal Form 2)
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6dte (F: 6) - Glcnac-Inspired Cyclophellitol Bound to Nagz
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6dtw (F: 2) - Hiv-1 Reverse Transcriptase Y181C Mutant in Complex with Jlj 578
Other atoms:
Mg (1);
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6dtx (F: 2) - Wildtype Hiv-1 Reverse Transcriptase in Complex with Jlj 578
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6duc (F: 3) - Crystal Structure of Mutant Beta-K167T Tryptophan Synthase in Complex with Inhibitor N-(4'-Trifluoromethoxybenzenesulfonyl)-2-Amino-1- Ethylphosphate (F9F) at the Alpha-Site, Cesium Ion at the Metal Coordination Site, and 2-Aminophenol Quinonoid (1D0) at the Beta-Site
Other atoms:
Cs (4);
Cl (11);
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6due (F: 4) - Toxoplasma Gondii Myoa, A Class-Xiv Myosin, in the Pre-Powerstroke State
Other atoms:
Mg (1);
Al (1);
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6duk (F: 6) - Egfr with An Allosteric Inhibitor
Other atoms:
Mg (6);
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6dum (F: 1) - ALDH1A1 N121S in Complex with 6-{[(3-Fluorophenyl)Methyl]Sulfanyl}-2- (Oxetan-3-Yl)-5-Phenyl-2,5-Dihydro-4H-Pyrazolo[3,4-D]Pyrimidin-4-One (Compound 13G)
Other atoms:
Yb (2);
Cl (7);
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6dup (F: 3) - Crystal Structure of Pxr in Complex with Compound 7
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6duq (F: 36) - Structure of A Rho-Nusg Kow Domain Complex
Other atoms:
Mg (12);
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6dvo (F: 1) - Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Bavarostat
Other atoms:
K (2);
Zn (1);
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6dw5 (F: 8) - SAMHD1 Bound to Gemcitabine-Tp in the Catalytic Pocket
Other atoms:
Ni (1);
Mg (10);
Na (4);
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6dwd (F: 8) - SAMHD1 Bound to Clofarabine-Tp in the Catalytic Pocket and Allosteric Pocket
Other atoms:
Mg (10);
Na (23);
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6dwe (F: 12) - Crystal Structure of Tryptophan Synthase From M. Tuberculosis - Aminoacrylate- and BRD0059-Bound Form
Other atoms:
Cs (9);
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6dwk (F: 4) - SAMHD1 Bound to Fludarabine-Tp in the Catalytic Pocket
Other atoms:
Mg (9);
Na (23);
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6dxx (F: 3) - Human N-Acylethanolamine-Hydrolyzing Acid Amidase (Naaa) in Complex with Non-Covalent Benzothiazole-Piperazine Inhibitor ARN19702, in Presence of Triton X-100
Other atoms:
Cl (12);
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6dxz (F: 1) - Rabbit N-Acylethanolamine-Hydrolyzing Acid Amidase (Naaa) in Complex with Non-Covalent Benzothiazole-Piperazine Inhibitor ARN19702, in Presence of Triton X-100
Other atoms:
K (1);
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6dz5 (F: 2) - Citrobacter Freundii Tyrosine Phenol-Lyase F448A Mutant Complexed with L-Alanine
Other atoms:
K (2);
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6dzo (F: 3) - Crystal Structure of Salmonella Typhimurium Tryptophan Synthase Mutant Beta-Q114A with 2-({[4-(Trifluoromethoxy)Phenyl]Sulfonyl}Amino)Ethyl Dihydrogen Phosphate (F9F) at the Alpha-Site, Cesium Ion at the Metal Coordination Site, and [3-Hydroxy-2-Methyl-5-Phosphonooxymethyl- Pyridin-4-Ylmethyl]-Serine (Pls) at the Beta-Site.
Other atoms:
Cs (4);
Cl (13);
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6dzw (F: 1) - Cryo-Em Structure of the TS2-Inactive Human Serotonin Transporter in Complex with Paroxetine and 15B8 Fab and 8B6 Scfv
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6e0r (F: 1) - Halk in Complex with Compound 7 N-((1S)-1-(5-Fluoropyridin-2-Yl) Ethyl)-1-(5-Methyl-1H-Pyrazol-3-Yl)-3-(Oxetan-3-Ylsulfonyl)-1H- Pyrrolo[2,3-B]Pyridin-6-Amine
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6e22 (F: 2) - Displacement of WDR5 From Chromatin By A Pharmacological Win Site Inhibitor with Picomolar Affinity
-
6e23 (F: 2) - Displacement of WDR5 From Chromatin By A Pharmacological Win Site Inhibitor with Picomolar Affinity
Other atoms:
Cl (4);
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6e2v (F: 3) - Mddef in Complex with Mvapp, ADPBEF3 and Magnesium
Other atoms:
Mg (2);
-
6e3e (F: 2) - Structure of Rorgt in Complex with A Novel Inverse Agonist.
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6e3s (F: 3) - Crystal Structure of the Heterodimeric Hif-2 Complex with Antagonist PT2385
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6e3z (F: 16) - Structure of Bace-1 in Complex with Ligand 8
Other atoms:
Cl (8);
-
6e40 (F: 3) - Crystal Structure of the Indoleamine 2,3-Dioxygenase 1 (IDO1) in Complexed with Ferric Heme and Epacadostat
Other atoms:
Br (3);
Fe (4);
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6e41 (F: 6) - Crystal Structure of Human Indoleamine 2,3-Dioxygenase 1 (IDO1) in Complex with Ferric Heme and An Epacadostat Analog
Other atoms:
Br (6);
Fe (4);
-
6e4w (F: 2) - Structure of Ampk Bound to Activator
Other atoms:
Cl (3);
-
6e54 (F: 2) - Crystal Structure of Lpxc From Pseudomonas Aeruginosa in Complex with Ligand PT802
Other atoms:
Zn (1);
Ca (2);
Cl (2);
-
6e59 (F: 7) - Crystal Structure of the Human NK1 Tachykinin Receptor
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6e5g (F: 6) - Crystal Structure of Human TEAD2-Yap Binding Domain Covalently Bound to An Allosteric Regulator
Page generated: Wed Nov 13 08:09:43 2024
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