Structure of PDB 4qed Chain A Binding Site BS01
Receptor Information
>4qed Chain A (length=248) Species:
1282
(Staphylococcus epidermidis) [
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MKKNVLITGGFKGIGKQVALEFLKNDYHVCITSRYFEKEKRIPHLFSSYE
ENISFYQLDVTDEEQVNEIINKIVKKFGRLDVLVNNAGISLSDGLLTETK
TTDFNKMINTNILGTYFCMKYALKHMQKVSCGAIVNISSITGLSGFPYSI
LFGSTKHAVIGLTKGAAVEFADKGIKINAVAPGIIKTETLQKEIDSGEFS
EDSISSIHPMQKLGTTLDVAKGIYFLANEDNNFITGHVLSIDGGYLSQ
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
4qed Chain A Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
4qed
Substrate Specificity of the Lanthipeptide Peptidase ElxP and the Oxidoreductase ElxO.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
K13 G14 I15 S34 R35 K39 D60 V61 N87 A88 G89 I138 F153 K157 I186
Binding residue
(residue number reindexed from 1)
K12 G13 I14 S33 R34 K38 D59 V60 N86 A87 G88 I137 F152 K156 I185
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G14 N112 S140 F153 K157
Catalytic site (residue number reindexed from 1)
G13 N111 S139 F152 K156
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
View graph for
Molecular Function
External links
PDB
RCSB:4qed
,
PDBe:4qed
,
PDBj:4qed
PDBsum
4qed
PubMed
24866416
UniProt
I6ZQW6
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