Manganese in PDB, part 69 (files: 2721-2760),
PDB 5hzz-5jpf
Experimental structures of coordination spheres of Manganese (Mn) in bioorganic
molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius
around Manganese atoms. PDB files: 2721-2760 (PDB 5hzz-5jpf).
-
5hzz (Mn: 6) - Crystal Structure of DR2231_E47A Mutant in Complex with Dump and Manganese
-
5i13 (Mn: 2) - Endonuclease Inhibitor 2 Bound to Influenza Strain H1N1 Polymerase Acidic Subunit N-Terminal Region at pH 7.0
Other atoms:
Cl (2);
-
5i4k (Mn: 2) - Metal Abc Transporter From Listeria Monocytogenes with Manganese
Other atoms:
Cl (1);
-
5i67 (Mn: 2) - Crystal Structure Analysis of Mtb Pepck Mutant C273S
-
5ie9 (Mn: 4) - Crystal Structure of the Bacillus-Conserved Mazg Protein, A Nucleotide Pyrophosphohydrolase
-
5inp (Mn: 2) - Mouse TDP2 Reaction Product (5'-Phosphorylated Dna)-MN2+ Complex
-
5isl (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor C49 (2-{[(2-{[(E)-2- (Dimethylamino)Ethenyl](Ethyl)Amino}-2-Oxoethyl) Amino]Methyl}Pyridine-4-Carboxylic Acid)
-
5ivb (Mn: 1) - A High Resolution Structure of A Linked KDM5A Jmj Domain with Alpha- Ketoglutarate
-
5ivc (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor N3 (4'-[(2- Phenylethyl)Carbamoyl][2,2'-Bipyridine]-4-Carboxylic Acid)
-
5ive (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor N8 ( 5-Methyl-7-Oxo-6- (Propan-2-Yl)-4,7-Dihydropyrazolo[1,5-A]Pyrimidine-3-Carbonitrile)
-
5ivf (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor N10 8-(1-Methyl-1H- Imidazol-4-Yl)-2-(4,4,4-Trifluorobutoxy)Pyrido[3,4-D]Pyrimidin-4-Ol
Other atoms:
F (3);
-
5ivj (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor N11 [3-({1-[2-(4,4- Difluoropiperidin-1-Yl)Ethyl]-5-Fluoro-1H-Indazol-3-Yl}Amino) Pyridine-4-Carboxylic Acid]
Other atoms:
F (5);
-
5ivv (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor N12 [3-((1-Methyl-1H- Pyrrolo[2,3-B]Pyridin-3-Yl)Amino)Isonicotinic Acid]
-
5ivy (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor N16 [3-(2-(4- Chlorophenyl)Acetamido)Isonicotinic Acid]
Other atoms:
Cl (1);
-
5iw0 (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor N19 [2-(5-((4-Chloro-2- Methylbenzyl)Oxy)-1H-Pyrazol-1-Yl)Isonicotinic Acid]
Other atoms:
Cl (1);
-
5iwf (Mn: 1) - Linked KDM5A Jmj Domain Bound to the Inhibitor 2-(((2-((2- (Dimethylamino)Ethyl)(Ethyl)Amino)-2-Oxoethyl)Amino)Methyl) Isonicotinamid
-
5iwi (Mn: 5) - 1.98A Structure of GSK945237 with S.Aureus Dna Gyrase and Singly Nicked Dna
Other atoms:
F (2);
Cl (1);
-
5iwm (Mn: 2) - 2.5A Structure of GSK945237 with S.Aureus Dna Gyrase and Dna.
Other atoms:
F (2);
-
5ize (Mn: 6) - Hantaan Virus L Protein Cap-Snatching Endonuclease
-
5izm (Mn: 2) - The Crystal Structure of Human Eefsec in Complex with Gdpnp
-
5izo (Mn: 8) - Bacillus Nanornase A (H103A) + 2 Divalent Cations + PO4 at the Active Site
-
5j1n (Mn: 1) - Lassa Virus L Protein Cap-Snatching Endonuclease. Bound to One Manganese Ion
-
5j1p (Mn: 3) - Lassa Virus L Protein Cap-Snatching Endonuclease. Bound to Two Manganese Ions
-
5j42 (Mn: 2) - Crystal Structure of M2HTDP2-Cat in Complex with A Small Molecule Inhibitor
-
5j6f (Mn: 2) - Crystal Structure of DAH7PS-Cm Complex From Geobacillus Sp. with Prephenate
-
5j8l (Mn: 4) - Crystal Structure of D-Tagatose 3-Epimerase C66S From Pseudomonas Cichorii in Complex with 1-Deoxy L-Tagatose, Using A Crystal Grown in Microgravity
-
5jaz (Mn: 2) - Structure of Plasmodium Falciparum Dxr in Complex with A Beta- Substituted Fosmidomycin Analogue, LC51 and Manganese
-
5jbi (Mn: 2) - Structure of Plasmodium Falciparum Dxr in Complex with A Beta- Substituted Fosmidomycin Analogue, LC52 and Manganese
-
5jc1 (Mn: 2) - Structure of Plasmodium Falciparum Dxr in Complex with A Beta- Substituted Fosmidomycin Analogue, LC55 and Manganese
-
5jfr (Mn: 2) - Potent, Reversible METAP2 Inhibitors Via Fragment Based Drug Discovery
Other atoms:
F (1);
-
5jht (Mn: 2) - Apo Form of Influenza Strain H1N1 Polymerase Acidic Subunit N-Terminal Region Crystallized with Potassium Sodium Tartrate
-
5jhu (Mn: 2) - Potent, Reversible METAP2 Inhibitors Via Fbdd
-
5jhv (Mn: 4) - Apo Form of Influenza Strain H1N1 Polymerase Acidic Subunit N-Terminal Region Crystallized with Polyethylene Glycol 8000
-
5ji6 (Mn: 2) - Potent, Reversible METAP2 Inhibitors Via Fbdd
Other atoms:
F (3);
-
5jju (Mn: 4) - Crystal Structure of RV2837C Complexed with 5'-Papa and 5'-Amp
-
5jmp (Mn: 2) - Structure of Plasmodium Falciparum Dxr in Complex with A Beta- Substituted Fosmidomycin Analogue, LC57 and Manganese
Other atoms:
F (2);
-
5jmw (Mn: 2) - Structure of Plasmodium Falciparum Dxr in Complex with A Beta- Substituted Fosmidomycin Analogue, LC50 and Manganese
-
5jnl (Mn: 2) - Structure of Plasmodium Falciparum Dxr in Complex with A Beta- Substituted Fosmidomycin Analogue, LC54 and Manganese
Other atoms:
F (6);
-
5jo0 (Mn: 2) - Structure of Plasmodium Falciparum Dxr in Complex with A Beta- Substituted Fosmidomycin Analogue, LC56 and Manganese
-
5jpf (Mn: 2) - Serine/Threonine Phosphatase Z1 (Candida Albicans) Binds to Inhibitor Microcystin-Lr
Page generated: Tue Dec 10 21:04:31 2024
|
