Fluorine in PDB, part 21 (files: 801-840),
PDB 2oh4-2pdk
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: 801-840 (PDB 2oh4-2pdk).
-
2oh4 (F: 4) - Crystal Structure of VEGFR2 with A Benzimidazole-Urea Inhibitor
-
2ohn (F: 1) - X-Ray Crystal Structure of Beta Secretase Complexed with 4- (4-Fluorobenzyl)Piperidine
Other atoms:
I (3);
-
2oi4 (F: 1) - Crystal Structure of Human PIM1 in Complex with Fluorinated Ruthenium Pyridocarbazole
Other atoms:
Ru (1);
Cl (1);
-
2ojj (F: 1) - Crystal Structure of ERK2 in Complex with (S)-N-(1-(3- Chloro-4-Fluorophenyl)-2-Hydroxyethyl)-4-(4-(3- Chlorophenyl)-1H-Pyrazol-3-Yl)-1H-Pyrrole-2-Carboxamide
Other atoms:
Cl (2);
-
2ole (F: 6) - Crystal Structure of Human Dipeptidyl Peptidase IV (Dppiv) Complex with Cyclic Hydrazine Derivatives
-
2ong (F: 2) - Crystal Structure of of Limonene Synthase with 2- Fluorogeranyl Diphosphate (Fgpp).
Other atoms:
Mn (6);
-
2onh (F: 2) - Crystal Structure of of Limonene Synthase with 2- Fluorolinalyl Diphosphate(Flpp)
Other atoms:
Mn (6);
-
2oo8 (F: 3) - Synthesis, Structural Analysis, and Sar Studies of Triazine Derivatives As Potent, Selective Tie-2 Inhibitors
-
2oow (F: 2) - Mif Bound to A Fluorinated Oxim Derivative
-
2op3 (F: 6) - The Structure of Cathepsin S with A Novel 2- Arylphenoxyacetaldehyde Inhibitor Derived By the Substrate Activity Screening (Sas) Method
-
2opa (F: 1) - Ywhb Binary Complex with 2-Fluoro-P-Hydroxycinnamate
-
2opb (F: 2) - Structure of K57A Hpnmt with Inhibitor 3-Fluoromethyl-7- Thiomorpholinosulfonamide-Thiq and Adohcy
-
2oph (F: 2) - Human Dipeptidyl Peptidase IV in Complex with An Alpha Amino Acid Inhibitor
Other atoms:
Na (1);
-
2opm (F: 1) - Human Farnesyl Diphosphate Synthase Complexed with Bisphosphonate Bph-461
Other atoms:
Mg (3);
-
2opp (F: 1) - Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with GW420867X.
Other atoms:
Mg (1);
-
2opq (F: 1) - Crystal Structure of L100I Mutant Hiv-1 Reverse Transcriptase in Complex with GW420867X.
-
2opr (F: 1) - Crystal Structure of K101E Mutant Hiv-1 Reverse Transcriptase in Complex with GW420867X.
-
2ops (F: 1) - Crystal Structure of Y188C Mutant Hiv-1 Reverse Transcriptase in Complex with GW420867X.
-
2oqi (F: 3) - Human Dipeptidyl Peptidase IV (DPP4) with Piperidinone- Constrained Phenethylamine
-
2oqv (F: 3) - Human Dipeptidyl Peptidase IV (DPP4) with Piperidine- Constrained Phenethylamine
-
2osc (F: 3) - Synthesis, Structural Analysis, and Sar Studies of Triazine Derivatives As Potent, Selective Tie-2 Inhibitors
-
2ow1 (F: 6) - Mmp-9 Active Site Mutant with Trifluoromethyl Hydroxamate Inhibitor
Other atoms:
Cl (3);
Ca (8);
Zn (4);
-
2ow2 (F: 4) - Mmp-9 Active Site Mutant with Difluoro Butanoic Acid Inhibitor
Other atoms:
Cl (2);
Ca (6);
Zn (4);
-
2p15 (F: 6) - Crystal Structure of the Er Alpha Ligand Binding Domain with the Agonist Ortho-Trifluoromethylphenylvinyl Estradiol
-
2p2v (F: 1) - Crystal Structure Analysis of Monofunctional Alpha-2,3- Sialyltransferase Cst-I From Campylobacter Jejuni
Other atoms:
Cl (1);
-
2p3g (F: 1) - Crystal Structure of A Pyrrolopyridine Inhibitor Bound to Mapkap Kinase-2
-
2p4i (F: 6) - Evolution of A Highly Selective and Potent 2-(Pyridin-2-Yl)- 1,3,5-Triazine Tie-2 Kinase Inhibitor
-
2p4y (F: 6) - Crystal Structure of Human Ppar-Gamma-Ligand Binding Domain Complexed with An Indole-Based Modulator
Other atoms:
Cl (2);
-
2p54 (F: 3) - A Crystal Structure of Ppar Alpha Bound with SRC1 Peptide and GW735
-
2p55 (F: 3) - X-Ray Structure of the Human Mitogen-Activated Protein Kinase Kinase 1 (MEK1) in A Complex with Ligand and Mgatp
Other atoms:
Mg (1);
-
2p83 (F: 6) - Potent and Selective Isophthalamide S2 Hydroxyethylamine Inhibitor of BACE1
-
2p8h (F: 1) - Crystal Structure of Human Beta Secretase Complexed with Inhibitor
-
2p8s (F: 24) - Human Dipeptidyl Peptidase IV/CD26 in Complex with A Cyclohexalamine Inhibitor
Other atoms:
Na (1);
-
2pb1 (F: 2) - Exo-B-(1,3)-Glucanase From Candida Albicans in Complex with Unhydrolysed and Covalently Linked 2,4-Dinitrophenyl-2- Deoxy-2-Fluoro-B-D-Glucopyranoside at 1.9 A
-
2pd5 (F: 3) - Human Aldose Reductase Mutant V47I Complexed with Zopolrestat
-
2pd9 (F: 1) - Human Aldose Reductase Mutant V47I Complexed with Fidarestat.
-
2pdb (F: 3) - Human Aldose Reductase Mutant F121P Complexed with Zopolrestat.
-
2pdf (F: 3) - Human Aldose Reductase Mutant L300P Complexed with Zopolrestat.
-
2pdi (F: 3) - Human Aldose Reductase Mutant L300A Complexed with Zopolrestat at 1.55 A.
-
2pdk (F: 1) - Human Aldose Reductase Mutant L301M Complexed with Sorbinil.
Page generated: Thu Dec 28 03:59:50 2023
|
