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Displaying 20 of 44 results for "FA2H"
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Dataset Title Dataset ID Primary Publications Keywords
Hydroxylase domain of scs7p PDB:4ZR1 The Crystal Structure of an Integral Membrane Fatty Acid alpha-Hydroxylase.
T
fatty acid hydroxylase fa2h homolog
Full length scs7p (only hydroxylase domain visible) PDB:4ZR0 The Crystal Structure of an Integral Membrane Fatty Acid alpha-Hydroxylase.
T
fatty acid hydroxylase fa2h
Cytochrome P450SP alpha (CYP152B1) mutant F288G PDB:3AWP Crystal structure of H2O2-dependent cytochrome P450SPalpha with its bound fatty acid substrate: insight into the regioselective hydroxylation of fatty acids at the alpha position.
C
OXIDOREDUCTASE
Cytochrome P450
Peroxygenase
Oxidoreductase
Cytochrome P450SP alpha (CYP152B1) wild-type with palmitic acid PDB:3AWM Crystal structure of H2O2-dependent cytochrome P450SPalpha with its bound fatty acid substrate: insight into the regioselective hydroxylation of fatty acids at the alpha position
C
OXIDOREDUCTASE
Cytochrome P450
Peroxygenase
Oxidoreductase
Cytochrome P450SP alpha (CYP152B1) in complex with (R)-ibuprophen PDB:3VM4 Chiral-substrate-assisted stereoselective epoxidation catalyzed by H2O2-dependent cytochrome P450SP alpha
OXIDOREDUCTASE
Cytochrome P450
OXIDOREDUCTASE
Cytochrome P450SP alpha (CYP152B1) mutant R241E PDB:3VNO A substrate-binding-state mimic of H2O2-dependent cytochrome P450 produced by one-point mutagenesis and peroxygenation of non-native substrates
OXIDOREDUCTASE
Cytochrome P450
OXIDOREDUCTASE
Crystal Structure of FAAH in complex with inhibitor PDB:4HBP Synthesis, SAR study, and biological evaluation of a series of piperazine ureas as fatty acid amide hydrolase (FAAH) inhibitors.
S
Fatty Acid Amide Hydrolase
3D-crystal structure of humanized-rat fatty acid amide hydrolase (FAAH) conjugated with Carbamate inhibitor URB597 PDB:3LJ7 Crystal structure of fatty acid amide hydrolase bound to the carbamate inhibitor URB597: discovery of a deacylating water molecule and insight into enzyme inactivation
C
FAAH fatty acid amide hydrolase
3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH THE DRUG-LIKE UREA INHIBITOR PF-3845 PDB:2WAP Discovery and Characterization of a Highly Selective Faah Inhibitor that Reduces Inflammatory Pain.
D
FATTY ACID AMIDE HYDROLASE FAAH
Cytochrome P450SP alpha (CYP152B1) mutant L78F PDB:3AWQ Crystal structure of H2O2-dependent cytochrome P450SPalpha with its bound fatty acid substrate: insight into the regioselective hydroxylation of fatty acids at the alpha position.
C
OXIDOREDUCTASE
Cytochrome P450
Peroxygenase
Oxidoreductase
3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH THE DRUG-LIKE UREA INHIBITOR PF-3845 at 2.42A RESOLUTION PDB:3LJ6 Crystal structure of fatty acid amide hydrolase bound to the carbamate inhibitor URB597: discovery of a deacylating water molecule and insight into enzyme inactivation
C
FAAH fatty acid amide hydrolase
Cytochrome P450SP alpha (CYP152B1) mutant A245H PDB:3VTJ A substrate-binding-state mimic of H2O2-dependent cytochrome P450 produced by one-point mutagenesis and peroxygenation of non-native substrates
OXIDOREDUCTASE
Cytochrome P450
Peroxygenase
Oxidoreductase
Structure of FAAH with a non-steroidal anti-inflammatory drug PDB:4DO3 A Binding Site for Nonsteroidal Anti-inflammatory Drugs in Fatty Acid Amide Hydrolase.
A
HYDROLASE/HYDROLASE INHIBITOR
AMIDASE
HYDROLASE
ANANDAMIDE
NSAID
DRUG
COX
INHIBITOR
INFLAMMATION
PAIN
HYDROLASE-HYDROLASE INHIBITOR complex
Cytochrome P450SP alpha (CYP152B1) mutant A245E PDB:3VOO A substrate-binding-state mimic of H2O2-dependent cytochrome P450 produced by one-point mutagenesis and peroxygenation of non-native substrates
OXIDOREDUCTASE
Cytochrome P450
Oxidoreductase
3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH 7-PHENYL-1-(5-(PYRIDIN-2-YL)OXAZOL-2-YL)HEPTAN-1-ONE, AN ALPHA-KETOOXAZOLE PDB:2WJ2 Binding and Inactivation Mechanism of a Humanized Fatty Acid Amide Hydrolase by Alpha-Ketoheterocycle Inhibitors Revealed from Cocrystal Structures.
B
FATTY ACID AMIDE HYDROLASE
3D-CRYSTAL STRUCTURE OF HUMANIZED-RAT FATTY ACID AMIDE HYDROLASE (FAAH) CONJUGATED WITH 7-PHENYL-1-(4-(PYRIDIN-2-YL)OXAZOL-2-YL)HEPTAN-1-ONE, AN ALPHA-KETOOXAZOLE PDB:2WJ1 Binding and Inactivation Mechanism of a Humanized Fatty Acid Amide Hydrolase by Alpha-Ketoheterocycle Inhibitors Revealed from Cocrystal Structures.
B
FATTY ACID AMIDE HYDROLASE
X-RAY STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS CYTOCHROME P450 CYP124 IN COMPLEX WITH PHYTANIC ACID PDB:2WM4 Biochemical and Structural Characterization of Cyp124: A Methyl-Branched Lipid {Omega}-Hydroxylase from Mycobacterium Tuberculosis.
B
FATTY ACID
Structure of cytochrome P450 4B1 (CYP4B1) complexed with octane: An n-Alkane and fatty acid omega-hydroxylase with a covalently bound heme PDB:5T6Q The Crystal Structure of Cytochrome P450 4B1 (CYP4B1) Monooxygenase Complexed with Octane Discloses Several Structural Adaptations for omega-Hydroxylation.
fatty acid omega-hydroxylase
Crystal structure of fatty acid amide hydrolase with small molecule inhibitor PDB:3QK5 Identification of potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitors.
I
FAAH Fatty-acid amide hydrolase
Human fatty acid synthase: Structure and substrate selectivity of the thioesterase domain PDB:1XKT Human fatty acid synthase: structure and substrate selectivity of the thioesterase domain.
H
hydroxylase Human fatty acid synthase hydroxylase