Reaction Details |
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Target | (S)-6-hydroxynicotine oxidase |
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Ligand | BDBM181056 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Steady-State Kinetics |
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pH | 8±n/a |
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Kd | 2.000e+6± 1.200e+6 nM |
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Comments | extracted |
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Citation | Fitzpatrick, PF; Chadegani, F; Zhang, S; Roberts, KM; Hinck, CS Mechanism of the Flavoprotein l-Hydroxynicotine Oxidase: Kinetic Mechanism, Substrate Specificity, Reaction Product, and Roles of Active-Site Residues. Biochemistry55:697-703 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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(S)-6-hydroxynicotine oxidase |
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Name: | (S)-6-hydroxynicotine oxidase |
Synonyms: | L‐Hydroxynicotine oxidase (LHNO) |
Type: | Protein |
Mol. Mass.: | 46260.18 |
Organism: | Arthrobacter nicotinovorans |
Description: | O86101 |
Residue: | 425 |
Sequence: | MYDAIVVGGGFSGLKAARDLTNAGKKVLLLEGGERLGGRAYSRESRNVPGLRVEIGGAYL
HRKHHPRLAAELDRYGIPTAAASEFTSFRHRLGPTAVDQAFPIPGSEAVAVEAATYTLLR
DAHRIDLEKGLENQDLEDLDIPLNEYVDKLDLPPVSRQFLLAWAWNMLGQPADQASALWM
LQLVAAHHYSILGVVLSLDEVFSNGSADLVDAMSQEIPEIRLQTVVTGIDQSGDVVNVTV
KDGHAFQAHSVIVATPMNTWRRIVFTPALPERRRSVIEEGHGGQGLKILIHVRGAEAGIE
CVGGGIFPTLYDYCEVSESERLLVAFTDSGSFDPTDIGAVKDAVLYYLPEVEVLGIDYHD
WIADPLFEGPWVAPRVGQFSRVHKELGEPAGRIHFVGSDVSLEFPGYIEGALETAECAVN
AILHS
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BDBM181056 |
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n/a |
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Name | BDBM181056 |
Synonyms: | (S)-4-(1-methylpyrrolidine-2-yl)phenol |
Type | Small organic molecule |
Emp. Form. | C11H16NO |
Mol. Mass. | 178.2503 |
SMILES | C[NH+]1CCC[C@H]1c1ccc(O)cc1 |r| |
Structure |
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