Structure of PDB 7w2j Chain D Binding Site BS01
Receptor Information
>7w2j Chain D (length=537) Species:
376620
(Gluconobacter japonicus) [
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LSADVVIIGAGICGSLLAHKLVRNGLSVLLLDAGPRRDRSQIVENWRNMP
PDNKSQYDYATPYPSVPWAPHTNYFPDNNYLIVKGPDRTAYKQGIIKGVG
GTTWHWAASSWRYLPNDFKLHSTYGVGRDYAMSYDELEPYYYEAECEMGV
MGPNGEEITPSAPRQNPWPMTSMPYGYGDRTFTEIVSKLGFSNTPVPQAR
NSRPYDGRPQCCGNNNCMPICPIGAMYNGVYAAIKAEKLGAKIIPNAVVY
AMETDAKNRITAISFYDPDKQSHRVVAKTFVIAANGIETPKLLLLAANDR
NPHGIANSSDLVGRNMMDHPGIGMSFQSAEPIWAGGGSVQMSSITNFRDG
DFRSEYAATQIGYNNTAQNSRAGMKALSMGLVGKKLDEEIRRRTAHGVDI
YANHEVLPDPNNRLVLSKDYKDALGIPHPEVTYDVGEYVRKSAAISRQRL
MDIAKAMGGTEIEMTPYFTPNNHITGGTIMGHDPRDSVVDKWLRTHDHSN
LFLATGATMAASGTVNSTLTMAALSLRAADAILNDLK
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
7w2j Chain D Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
7w2j
Structural and Bioelectrochemical Elucidation of Direct Electron Transfer-type Membrane-bound Fructose Dehydrogenase
Resolution
3.6 Å
Binding residue
(original residue number in PDB)
G14 G16 D37 A38 Y64 K102 G106 T107 T108 H110 W111 S114 V254 A289 N290 E293 K296 L297 N477 N521 S522 T523
Binding residue
(residue number reindexed from 1)
G9 G11 D32 A33 Y59 K97 G101 T102 T103 H105 W106 S109 V249 A284 N285 E288 K291 L292 N472 N516 S517 T518
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.1.5.14
: fructose 5-dehydrogenase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0016614
oxidoreductase activity, acting on CH-OH group of donors
GO:0047904
fructose 5-dehydrogenase activity
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0006000
fructose metabolic process
Cellular Component
GO:0005886
plasma membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7w2j
,
PDBe:7w2j
,
PDBj:7w2j
PDBsum
7w2j
PubMed
UniProt
M1VMF7
|FDHL_GLUJA Fructose dehydrogenase large subunit (Gene Name=fdhL)
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