Structure of PDB 7d4k Chain B Binding Site BS02
Receptor Information
>7d4k Chain B (length=440) Species:
439493
(Candidatus Pelagibacter sp. HTCC7211) [
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SKVAIIGAGPCGLSILRAFEHLEKKGEKIPEIVCFEKQESWGGLWNYNWR
TGSDQYGDPVPNSMYRYLWSNGPKECLEFADYSFDQHFGKSIPSFPPREV
LQDYILGRVSKGNIKNKIKFNTRVINTVYRNDKFEINYQDKVNDKTLSDT
FDYLVVSTGHFSVPFIPEYEGMSSFPGRIMHSHDFRDAEEFRGKNVIVLG
SSYSAEDVALQCNKYGAKSVTIGYRHNPMGFKWPKGMKEVHYLDKLDGKK
AIFKDGTEQDADVVILCTGYLHHFPFLDESLKLKTHNRLYPPKLYKGVVW
QDNHKLLYLGMQDQFHTFNMFDCQAWFARDVIMDKIKMPSDDEIDKDINK
WVSMEEKLENPDQMIDFQTEYTKELHNISDYPKIDFELIRKHFKEWEHHK
VEDILTYRNKSFSSPVTGSVAPVHHTPWEKAMDDSMKTFL
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
7d4k Chain B Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
7d4k
Structural and Mechanistic Insights Into Dimethylsulfoxide Formation Through Dimethylsulfide Oxidation.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
I7 G8 G10 P11 C12 E37 K38 Q39 G44 L45 W46 S71 N72 R124 V125 T159 F162 F277 Q315 T318
Binding residue
(residue number reindexed from 1)
I6 G7 G9 P10 C11 E36 K37 Q38 G43 L44 W45 S70 N71 R123 V124 T158 F161 F276 Q314 T317
Annotation score
2
Enzymatic activity
Enzyme Commision number
1.14.13.148
: trimethylamine monooxygenase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0004499
N,N-dimethylaniline monooxygenase activity
GO:0050660
flavin adenine dinucleotide binding
GO:0050661
NADP binding
View graph for
Molecular Function
External links
PDB
RCSB:7d4k
,
PDBe:7d4k
,
PDBj:7d4k
PDBsum
7d4k
PubMed
34630359
UniProt
B6BQB2
|TMM_PELS7 Trimethylamine monooxygenase (Gene Name=tmm)
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