Structure of PDB 4i3x Chain E Binding Site BS01
Receptor Information
>4i3x Chain E (length=476) Species:
266834
(Sinorhizobium meliloti 1021) [
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VRHEPMRIAGRLVDTDDRVEVRYPWNDTVVGTVPAGRAEHAREAFAIAAA
YQPKLTRYERQKILLATAEALAARKEEISDVITLELGISKADSLYEVGRA
FDVFTLAGQMCIRDDGEIFSCDLTPHGKARKIFTMREPLTAISAITPFNH
PLNMVAHKVAPAIATNNCVVVKPTELTPMTALLLADILYEAGLPPEMLSV
VTGWPADIGMEMITNPHVDLVTFTGSVPVGKLIAANAHYKRQVLELGGND
PLIILNDLSDDDLARAADLAVAGATKNSGQRCTAVKRILCQESVADRFVP
LVLERAKRLRFGDPMDRSTDLGTVIHEKAAALFEERVMRAAEEGADILYH
PGRSGALLPPIVVDRVPHQSDLVLEETFGPIIPIVRVPDDDDATITLSNS
TAFGLSSGVCTNDYRRMQKYIAGLKVGTVNIWEVPGYRIEMSPFGGIKDS
GNGYKEGVIEAMKSFTNVKTFSLPWP
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
4i3x Chain E Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
4i3x
Structure and function of phosphonoacetaldehyde dehydrogenase: the missing link in phosphonoacetate formation.
Resolution
2.07 Å
Binding residue
(original residue number in PDB)
I154 T155 P156 F157 N158 K181 T183 G218 T233 G234 S235 V238 E254 L255 G256 C291 E385 F387 F453
Binding residue
(residue number reindexed from 1)
I145 T146 P147 F148 N149 K172 T174 G209 T224 G225 S226 V229 E245 L246 G247 C282 E376 F378 F444
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N158 K181 E254 C291 E385 E465
Catalytic site (residue number reindexed from 1)
N149 K172 E245 C282 E376 E456
Enzyme Commision number
1.2.1.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008911
lactaldehyde dehydrogenase (NAD+) activity
GO:0016491
oxidoreductase activity
GO:0016620
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
View graph for
Molecular Function
External links
PDB
RCSB:4i3x
,
PDBe:4i3x
,
PDBj:4i3x
PDBsum
4i3x
PubMed
24361046
UniProt
Q92UV7
|PHNY_RHIME Phosphonoacetaldehyde dehydrogenase (Gene Name=phnY)
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