Structure of PDB 4tsk Chain A Binding Site BS04
Receptor Information
>4tsk Chain A (length=333) Species:
521098
(Alicyclobacillus acidocaldarius subsp. acidocaldarius DSM 446) [
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EKIYYDADISIQPLADKRIAVIGYGSQGHAHAQNLRDSGFDVVIGLRPGS
SWAKAEADGFRVMAVGEAVEESDVIMILLPDERQPAVYEREIRPYLTAGK
ALAFAHGFNIHFSQIQPPKDVDVFMVAPKGPGHLVRRVYEAGGGVPALIA
VHQDASGQAKDLALAYARGIGAGRAGILTTTFREETETDLFGEQAVLCGG
LSALIKAGFETLVEAGYQPEIAYFECLHEMKLIVDLIYEGGLEYMRYSIS
DTAQWGDFTSGPRIINEETKKEMRRILADIQSGAFAKSWILENQANRPMF
NAINRRELEHPIEVVGRKLRSMMPFIKAKRPGD
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/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/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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)C1=CN(C=CC1)[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
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
4tsk Chain A Residue 405 [
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Receptor-Ligand Complex Structure
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PDB
4tsk
Uncovering rare NADH-preferring ketol-acid reductoisomerases.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
Y25 G26 S27 Q28 L47 R48 S52 L79 L80 P81 D82 H107 P132
Binding residue
(residue number reindexed from 1)
Y24 G25 S26 Q27 L46 R47 S51 L78 L79 P80 D81 H106 P131
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
K130 D190 E194
Catalytic site (residue number reindexed from 1)
K129 D189 E193
Enzyme Commision number
1.1.1.86
: ketol-acid reductoisomerase (NADP(+)).
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004455
ketol-acid reductoisomerase activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0050661
NADP binding
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009082
branched-chain amino acid biosynthetic process
GO:0009097
isoleucine biosynthetic process
GO:0009099
L-valine biosynthetic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4tsk
,
PDBe:4tsk
,
PDBj:4tsk
PDBsum
4tsk
PubMed
25172159
UniProt
C8WR67
|ILVC_ALIAD Ketol-acid reductoisomerase (NADP(+)) (Gene Name=ilvC)
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