Structure of PDB 5t2u Chain A Binding Site BS01
Receptor Information
>5t2u Chain A (length=241) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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HMELEGLTALVTGGTSGIGLESARLMAAEGADVVITGRDAQRGEQAAADI
GHGARFVQADLGDLDSVADLAAQAPDVDILVNNAGIYPQASTFDQDVAGF
QQLFDTNVRGTYFLVAAAAKGMVARGHGSIVNITTLAAHKGFPGTSVYGA
TKAALESLTRTWAAEFGANGVRVNSVSPGPTRTPTTLEQLGDFIDDVAAG
LPLRRTAAPEEIAQAVLFLASPRASFVTGSTLYVDGGGYAV
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
5t2u Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5t2u
Binding of NADP(+) triggers an open-to-closed transition in a mycobacterial FabG beta-ketoacyl-ACP reductase.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
G12 G16 R37 D38 R41 D59 L60 N82 A83 Y86 I132 T134 Y147 K151 P177 P179 T180 T182 T184 T185
Binding residue
(residue number reindexed from 1)
G13 G17 R38 D39 R42 D60 L61 N83 A84 Y87 I133 T135 Y148 K152 P178 P180 T181 T183 T185 T186
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G16 T134 T144 Y147 K151
Catalytic site (residue number reindexed from 1)
G17 T135 T145 Y148 K152
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
View graph for
Molecular Function
External links
PDB
RCSB:5t2u
,
PDBe:5t2u
,
PDBj:5t2u
PDBsum
5t2u
PubMed
28126742
UniProt
A0R723
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