Structure of PDB 4wuo Chain A Binding Site BS02
Receptor Information
>4wuo Chain A (length=349) Species:
300852
(Thermus thermophilus HB8) [
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ASMKVAVLPGDGIGPEVTEAALKVLRALDEAEGLGLAYEVFPFGGAAIDA
FGEPFPEPTRKGVEEAEAVLLGSVGGPKWDGLPRKIRPETGLLSLRKSQD
LFANLRPAKVFPGLERLSPLKEEIARGVDVLIVRELTGGIYFGEPRGMSE
AEAWNTERYSKPEVERVARVAFEAARKRRKHVVSVDKANVLEVGEFWRKT
VEEVGRGYPDVALEHQYVDAMAMHLVRSPARFDVVVTGNIFGDILSDLAS
VLPGSLGLLPSASLGRGTPVFAPVHGSAPDIAGKGIANPTAAILSAAMML
EHAFGLVELARKVEDAVAKALLETPPPDLGGSAGTEAFTATVLRHLAAA
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
4wuo Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4wuo
Glutamate 270 plays an essential role in K(+)-activation and domain closure of Thermus thermophilus isopropylmalate dehydrogenase.
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
I11 S71 V72 G73 E87 L90 G255 H273 G274 S275 A276 D278 I279 N286
Binding residue
(residue number reindexed from 1)
I13 S73 V74 G75 E89 L92 G257 H275 G276 S277 A278 D280 I281 N288
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
Y139 K185 D217 D241 D245
Catalytic site (residue number reindexed from 1)
Y141 K187 D219 D243 D247
Enzyme Commision number
1.1.1.85
: 3-isopropylmalate dehydrogenase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003862
3-isopropylmalate dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:0051287
NAD binding
Biological Process
GO:0009098
L-leucine biosynthetic process
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:4wuo
,
PDBe:4wuo
,
PDBj:4wuo
PDBsum
4wuo
PubMed
25497013
UniProt
Q5SIY4
|LEU3_THET8 3-isopropylmalate dehydrogenase (Gene Name=leuB)
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