Structure of PDB 6fw9 Chain B Binding Site BS02
Receptor Information
>6fw9 Chain B (length=415) Species:
243365
(Chromobacterium violaceum ATCC 12472) [
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KHSSDICIVGAGISGLTCASHLLDSPACRGLSLRIFDMQQEAGGRIRSKM
LDGKASIELGAGRYSPQLHPHFQSAMQHYSQKSEVYPFTQLKFKSHVQQK
LKRAMNELSPRLKEHGKESFLQFVSRYQGHDSAVGMIRSMGYDALFLPDI
SAEMAYDIVGKHPEIQSVTDNDANQWFAAETGFAGLIQGIKAKVKAAGAR
FSLGYRLLSVRTDGDGYLLQLAGDDGWKLEHRTRHLILAIPPSAMAGLNV
DFPEAWSGARYGSLPLFKGFLTYGEPWWLDYKLDDQVLIVDNPLRKIYFK
GDKYLFFYTDSEMANYWRGCVAEGEDGYLEQIRTHLASALGIVRERIPQP
LAHVHKYWAHGVEFCRDIDHPSALSHRDSGIIACSDAYTEHCGWMEGGLL
SAREASRLLLQRIAA
Ligand information
Ligand ID
FT6
InChI
InChI=1S/C11H11FN2O2/c12-7-1-2-8-6(3-9(13)11(15)16)5-14-10(8)4-7/h1-2,4-5,9,14H,3,13H2,(H,15,16)/t9-/m0/s1
InChIKey
YMEXGEAJNZRQEH-VIFPVBQESA-N
SMILES
Software
SMILES
CACTVS 3.341
N[C@@H](Cc1c[nH]c2cc(F)ccc12)C(O)=O
ACDLabs 10.04
O=C(O)C(N)Cc2c1ccc(F)cc1nc2
OpenEye OEToolkits 1.5.0
c1cc2c(cc1F)[nH]cc2CC(C(=O)O)N
CACTVS 3.341
N[CH](Cc1c[nH]c2cc(F)ccc12)C(O)=O
OpenEye OEToolkits 1.5.0
c1cc2c(cc1F)[nH]cc2C[C@@H](C(=O)O)N
Formula
C11 H11 F N2 O2
Name
6-FLUORO-L-TRYPTOPHAN;
(S)-2-AMINO-3-(6-FLUORO-1H-INDOL-3-YL)PROPANOIC ACID
ChEMBL
DrugBank
ZINC
ZINC000000056393
PDB chain
6fw9 Chain B Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
6fw9
A GenoChemetic strategy for derivatization of the violacein natural product scaffold
Resolution
2.739 Å
Binding residue
(original residue number in PDB)
R64 H163 Y309 V363 W397
Binding residue
(residue number reindexed from 1)
R63 H162 Y308 V362 W394
Annotation score
3
Enzymatic activity
Enzyme Commision number
1.4.3.23
: 7-chloro-L-tryptophan oxidase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
Biological Process
GO:0017000
antibiotic biosynthetic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:6fw9
,
PDBe:6fw9
,
PDBj:6fw9
PDBsum
6fw9
PubMed
UniProt
Q9S3V1
|VIOA_CHRVO Flavin-dependent L-tryptophan oxidase VioA (Gene Name=vioA)
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