Structure of PDB 3rku Chain C Binding Site BS01
Receptor Information
>3rku Chain C (length=268) Species:
4932
(Saccharomyces cerevisiae) [
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HMSQGRKAAERLAKKTVLITGASAGIGKATALEYLEASNGDMKLILAARR
LEKLEELKKTIDQEFPNAKVHVAQLDITQAEKIKPFIENLPQEFKDIDIL
VNNAGKALGSDRVGQIATEDIQDVFDTNVTALINITQAVLPIFQAKNSGD
IVNLGSIAGRDAYPTGSIYCASKFAVGAFTDSLRKELINTKIRVILIAPG
LVETEFSLVRYRGNEEQAKNVYKDTTPLMADDVADLIVYATSRKQNTVIA
DTLIFPTNQASPHHIFRG
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
3rku Chain C Residue 268 [
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Receptor-Ligand Complex Structure
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PDB
3rku
Substrate Fingerprint and the Structure of NADP+ Dependent Serine Dehydrogenase from Saccharomyces cerevisiae complexed with NADP+
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
G20 S22 G24 I25 A47 R48 R49 L74 D75 I76 N102 A103 G104 K105 S155 Y168 K172 P198 G199 V201 T203 E204 F205
Binding residue
(residue number reindexed from 1)
G21 S23 G25 I26 A48 R49 R50 L75 D76 I77 N103 A104 G105 K106 S156 Y169 K173 P199 G200 V202 T204 E205 F206
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
A106 N127 S155 Y168 K172 N213
Catalytic site (residue number reindexed from 1)
A107 N128 S156 Y169 K173 N214
Enzyme Commision number
1.1.1.-
1.1.1.381
: 3-hydroxy acid dehydrogenase.
Gene Ontology
Molecular Function
GO:0004090
carbonyl reductase (NADPH) activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016614
oxidoreductase activity, acting on CH-OH group of donors
GO:0031132
serine 3-dehydrogenase activity
GO:0052588
diacetyl reductase ((S)-acetoin forming) (NAD+) activity
Biological Process
GO:0045149
acetoin metabolic process
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3rku
,
PDBe:3rku
,
PDBj:3rku
PDBsum
3rku
PubMed
UniProt
Q05016
|YM71_YEAST NADP-dependent 3-hydroxy acid dehydrogenase (Gene Name=YMR226C)
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