Bromine in PDB, part 52 (files: 2041-2080),
PDB 6yod-7akh
Experimental structures of coordination spheres of Bromine (Br) in bioorganic
molecules from X-Ray and NMR experiments. Coordination spheres were calculated with 5.0 Angstroms radius
around Bromine atoms. PDB files: 2041-2080 (PDB 6yod-7akh).
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6yod (Br: 7) - Structure of Lysozyme From Sin Imisx Setup Collected By Rotation Serial Crystallography on Crystals Prelocated By 2D X-Ray Phase- Contrast Imaging
Other atoms:
Na (1);
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6yoe (Br: 7) - Structure of Lysozyme From Sin Imisx Setup Collected By Still Serial Crystallography on Crystals Prelocated By 2D X-Ray Phase-Contrast Imaging
Other atoms:
Na (1);
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6ysj (Br: 2) - Thrombin in Complex with 2-Amino-1-(4-Bromophenyl)Ethan-1-One (J10)
Other atoms:
Na (2);
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6yvw (Br: 1) - Hif Prolyl Hydroxylase 2 (PHD2/ EGLN1) in Complex with Monocyclic Bb- 328
Other atoms:
Fe (1);
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6yvz (Br: 1) - Hif Prolyl Hydroxylase 2 (PHD2/ EGLN1) in Complex with Bicyclic Jls- 367
Other atoms:
Mn (1);
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6z0q (Br: 1) - Crystal Structure of Saicar Synthetase (Purc) From Mycobacterium Abscessus in Complex with Fragment 2
Other atoms:
F (1);
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6z2s (Br: 2) - Crystal Structure of Adhibin Analogue-Bound Myosin-2
Other atoms:
V (1);
Mg (1);
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6z6d (Br: 18) - Crystal Structure of the HK97 Bacteriophage Large Terminase
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6z6r (Br: 1) - Aspartyl/Asparaginyl Beta-Hydroxylase (Asph) Oxygenase and Tpr Domains in Complex with Manganese, N-Oxalyl-Alpha-Methylalanine, and Factor X Substrate Peptide Fragment(39MER-4SER)
Other atoms:
Mn (1);
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6z8g (Br: 23) - Crystal Structure of VSG13 Soaked in 0.5 M Used to Phase VSG13 to Solve the Structure.
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6zc4 (Br: 3) - Small-Molecule Inhibitors of the Pdz Domain of Dishevelled Proteins Interrupt Wnt Signalling
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6zc6 (Br: 2) - Small-Molecule Inhibitors of the Pdz Domain of Dishevelled Proteins Interrupt Wnt Signalling
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6zc7 (Br: 3) - Small-Molecule Inhibitors of the Pdz Domain of Dishevelled Proteins Interrupt Wnt Signalling
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6zis (Br: 2) - Crystal Structure of A Cgrp Receptor Ectodomain Heterodimer with Bound High Affinity Inhibitor
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6zt1 (Br: 13) - Two States of A De Novo Hexameric Coiled Coil Assembly Cc-TYPE2- (Laidge)4
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6zvo (Br: 1) - Crystal Structure of Unliganded Mlkl Executioner Domain
Other atoms:
Cl (3);
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6zwe (Br: 2) - Crystal Structure of Human Acetylcholinesterase in Complex with ((6- ((2E,4E)-5-(Benzo[D][1,3]Dioxol-5-Yl)Penta-2,4-Dienamido)Hexyl) Triphenylphosphonium Bromide)
Other atoms:
Cl (23);
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6zwi (Br: 3) - Human Butyrylcholinesterase in Complex with ((6-((2E,4E)-5- (Benzo[D][1,3]Dioxol-5-Yl)Penta-2,4-Dienamido)Hexyl) Triphenylphosphonium Bromide)
Other atoms:
Cl (4);
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6zxx (Br: 12) - Catabolic Reductive Dehalogenase Nprdha, N-Terminally Tagged.
Other atoms:
Co (3);
Fe (24);
Na (3);
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6zy1 (Br: 9) - Catabolic Reductive Dehalogenase Nprdha, N-Terminally Tagged in Complex with 3-Bromo-4-Hydroxybenzoic Acid
Other atoms:
Co (3);
Fe (24);
Na (3);
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7a0h (Br: 25) - Structure of Homodimeric Actin Capping Protein Alpha Subunit From Plasmodium Berghei
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7a1b (Br: 2) - Crystal Structure of Human Protein Kinase CK2ALPHA' (CSNK2A2 Gene Product) in Complex with the Atp-Competitive Inhibitor 5,6-Dibromo- 1H-Triazolo[4,5-B]Pyridine
Other atoms:
Cl (2);
Na (1);
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7a1t (Br: 7) - A Collapsed Hexameric State of A De Novo Coiled-Coil Assembly: Cc- TYPE2-(Gglaid)4-W19BRPHE.
Other atoms:
Cd (1);
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7a1y (Br: 1) - KRASG12C Gdp Form in Complex with CPD2
Other atoms:
Mg (1);
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7a1z (Br: 1) - Crystal Structure of Human Protein Kinase CK2ALPHA' (CSNK2A2 Gene Product) in Complex with the Atp-Competitive Inhibitor 6-Bromo-5- Chloro-1H-Triazolo[4,5-B]Pyridine
Other atoms:
Cl (2);
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7a22 (Br: 6) - Crystal Structure of Human Protein Kinase CK2ALPHA' (CSNK2A2 Gene Product) in Complex with the Atp-Competitive Inhibitor 5,6,7- Tribromo-1H-Triazolo[4,5-B]Pyridine
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7a2h (Br: 3) - Crystal Structure of Human Protein Kinase CK2ALPHA' (CSNK2A2 Gene Product) in Complex with the Atp-Competitive Inhibitor 5,6,7- Tribromo-1H-Imidazo[4,5-B]Pyridine
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7a3i (Br: 6) - Crystal Structure of DPP8 in Complex with A 4-Oxo-B-Lactam Based Inhibitor, LMC375
Other atoms:
Na (3);
Cl (3);
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7a3k (Br: 3) - Crystal Structure of DPP8 in Complex with A B-Lactam Based Inhibitor, A296.1
Other atoms:
Cl (8);
Na (3);
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7a47 (Br: 6) - KRASG12C Gdp Form in Complex with CPD4
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7a49 (Br: 2) - Crystal Structure of Human Protein Kinase CK2ALPHA (CSNK2A1 Gene Product) in Complex with the Atp-Competitive Inhibitor 6-Bromo-5- Chloro-1H-Triazolo[4,5-B]Pyridine
Other atoms:
Cl (2);
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7a4b (Br: 4) - Crystal Structure of Human Protein Kinase CK2ALPHA (CSNK2A1 Gene Product) in Complex with the Atp-Competitive Inhibitor 5,6-Dibromo- 1H-Triazolo[4,5-B]Pyridine
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7a4c (Br: 6) - Crystal Structure of Human Protein Kinase CK2ALPHA (CSNK2A1 Gene Product) in Complex with the Atp-Competitive Inhibitor 5,6,7- Tribromo-1H-Triazolo[4,5-B]Pyridine
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7a51 (Br: 1) - Structure of DYRK1A in Complex with Compound 5
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7acu (Br: 4) - Crystal Structure of Human Transthyretin in Complex with Benzbromarone
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7ah6 (Br: 4) - Crystal Structure of Indoleamine 2,3-Dioxygenase 1 (IDO1) in Complex with Ferric Heme and Mmg-0752
Other atoms:
Fe (2);
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7ak0 (Br: 2) - Human MALT1(329-729) in Complex with A Chromane Urea Containing Inhibitor
Other atoms:
Cl (2);
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7akb (Br: 2) - Structure of DYRK1A in Complex with Compound 56
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7ake (Br: 2) - Structure of DYRK1A in Complex with Compound 58
Other atoms:
Cl (1);
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7akh (Br: 1) - Structure of DYRK2 in Complex with Compound 58
Other atoms:
Cl (1);
Page generated: Wed Nov 13 07:06:41 2024
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