Structure of PDB 1knp Chain A Binding Site BS01
Receptor Information
>1knp Chain A (length=529) Species:
562
(Escherichia coli) [
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PEHSCDVLIIGSGAAGLSLALRLADQHQVIVLSKGPVTEGSTFYAQGGIA
AVFDETDSIDSHVEDTLIAGAGICDRHAVEFVASNARSCVQWLIDQGVLF
DTHIQPNGEESYHLTREGGHSHRRILHAADATGREVETTLVSKALNHPNI
RVLERTNAVDLIVSDKIGLPGTRRVVGAWVWNRNKETVETCHAKAVVLAT
GGASKVYQYTTNPDISSGDGIAMAWRAGCRVANLEFNQFHPTALYHPQAR
NFLLTEALRGEGAYLKRPDGTRFMPDFDERGELAPRDIVARAIDHEMKRL
GADCMFLDISHKPADFIRQHFPMIYEKLLGLGIDLTQEPVPIVPAAHYTC
GGVMVDDHGRTDVEGLYAIGEVSYTGLHGANLMASNSLLECLVYGWSAAE
DITRRMPYAHDISTLPPWDESRVENPDERVVIQHNWHELRLFMWDYVGIV
RTTKRLERALRRITMLQQEIDEYYAHFRVSNNLLELRNLVQVAELIVRCA
MMRKESRGLHFTLDYPELLTHSGPSILSP
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
1knp Chain A Residue 800 [
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Receptor-Ligand Complex Structure
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PDB
1knp
Structure of FAD-bound L-aspartate oxidase: insight into substrate specificity and catalysis.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
G15 S16 A19 S37 K38 S45 T46 Y48 A49 G51 G52 A162 A203 T204 G205 D223 L257 H351 Y352 E375 S391 L392 C395
Binding residue
(residue number reindexed from 1)
G11 S12 A15 S33 K34 S41 T42 Y44 A45 G47 G48 A158 A199 T200 G201 D219 L253 H347 Y348 E371 S387 L388 C391
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E121 Q242 H244 L257 E260 R263 R290 H351 Y352 L386
Catalytic site (residue number reindexed from 1)
E117 Q238 H240 L253 E256 R259 R286 H347 Y348 L382
Enzyme Commision number
1.4.3.16
: L-aspartate oxidase.
1.5.99.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008734
L-aspartate oxidase activity
GO:0016491
oxidoreductase activity
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0009435
NAD biosynthetic process
GO:0019363
pyridine nucleotide biosynthetic process
GO:0034628
'de novo' NAD biosynthetic process from aspartate
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1knp
,
PDBe:1knp
,
PDBj:1knp
PDBsum
1knp
PubMed
11863440
UniProt
P10902
|NADB_ECOLI L-aspartate oxidase (Gene Name=nadB)
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