Structure of PDB 4dmm Chain D Binding Site BS01
Receptor Information
>4dmm Chain D (length=237) Species:
1140
(Synechococcus elongatus PCC 7942 = FACHB-805) [
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LPLTDRIALVTGASRGIGRAIALELAAAGAKVAVNYASSAGAADEVVAAI
AAAGGEAFAVKADVSQESEVEALFAAVIERWGRLDVLVNNAGITRDTLLL
RMKRDDWQSVLDLNLGGVFLCSRAAAKIMLKQRSGRIINIASVVGEMGNP
GQANYSAAKAGVIGLTKTVAKELASRGITVNAVAPGFIATKLLEVIPLGR
YGEAAEVAGVVRFLAADPAAAYITGQVINIDGGLVMA
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)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[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
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[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]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)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
4dmm Chain D Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4dmm
3-oxoacyl-[acyl-carrier-protein] reductase from Synechococcus elongatus PCC 7942 in complex with NADP
Resolution
2.38 Å
Binding residue
(original residue number in PDB)
G15 S17 R18 G19 I20 A40 S41 S42 D66 V67 N93 A94 L116 I143 S145 Y158 K162 P188 G189 I191 T193
Binding residue
(residue number reindexed from 1)
G12 S14 R15 G16 I17 A37 S38 S39 D63 V64 N90 A91 L113 I140 S142 Y155 K159 P185 G186 I188 T190
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G19 S145 Q155 Y158 K162
Catalytic site (residue number reindexed from 1)
G16 S142 Q152 Y155 K159
Enzyme Commision number
1.1.1.100
: 3-oxoacyl-[acyl-carrier-protein] reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004316
3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0051287
NAD binding
Biological Process
GO:0006633
fatty acid biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4dmm
,
PDBe:4dmm
,
PDBj:4dmm
PDBsum
4dmm
PubMed
UniProt
Q31QF3
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