Structure of PDB 5lnx Chain D Binding Site BS02
Receptor Information
>5lnx Chain D (length=374) Species:
224308
(Bacillus subtilis subsp. subtilis str. 168) [
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MHVQEQVMMRKMVRDFARKEIAPAAEIMEKTDEFPFQLIKKMGKHGLMGI
PVPEQYGGAGADVVSYILAIHEISRISAAVGVILSVHTSVGTNPILYFGN
EEQKMKYIPNLASGDHLGAFALTEPHSGSDAGSLRTTAIKKNGKYLLNGS
KIFITNGGAADIYITFALTAPDQGRHGISAFIVEKNTPGFTVGKKERKLG
LYGSNTTELIFDNAEVPEANLLGKEGDGFHIAMANLNVGRIGIAAQALGI
AEAALEHAVDYAKQRVQFGRPIAANQGISFKLADMATRAEAARHLVYHAA
DLHNRLNCGKEASMAKQFASDAAVKALDAVQIYGGYGYMKDYPVERLLRD
AKVTQIYEGTNEIQRLIISKYLLG
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
5lnx Chain D Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5lnx
Crystal structure of acyl-CoA dehydrogenase (MmgC) from bacillus subtilis.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
L123 T124 G129 S130 F154 T156 Y359 T362 E364
Binding residue
(residue number reindexed from 1)
L122 T123 G128 S129 F153 T155 Y357 T360 E362
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L123 T124 G240 E360 K372
Catalytic site (residue number reindexed from 1)
L122 T123 G239 E358 K370
Enzyme Commision number
1.3.99.-
Gene Ontology
Molecular Function
GO:0003995
acyl-CoA dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016627
oxidoreductase activity, acting on the CH-CH group of donors
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0030435
sporulation resulting in formation of a cellular spore
GO:0033539
fatty acid beta-oxidation using acyl-CoA dehydrogenase
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5lnx
,
PDBe:5lnx
,
PDBj:5lnx
PDBsum
5lnx
PubMed
UniProt
P45857
|ACDB_BACSU Acyl-CoA dehydrogenase (Gene Name=mmgC)
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