Structure of PDB 2dfv Chain B Binding Site BS02
Receptor Information
>2dfv Chain B (length=346) Species:
70601
(Pyrococcus horikoshii OT3) [
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EKMVAIMKTKPGYGAELVEVDVPKPGPGEVLIKVLATSICGTDLHIYEWN
EWAQSRIKPPQIMGHEVAGEVVEIGPGVEGIEVGDYVSVETHIVCGKCYA
CRRGQYHVCQNTKIFGVDTDGVFAEYAVVPAQNIWKNPKSIPPEYATLQE
PLGNAVDTVLAGPISGKSVLITGAGPLGLLGIAVAKASGAYPVIVSEPSD
FRRELAKKVGADYVINPFEEDVVKEVMDITDGNGVDVFLEFSGAPKALEQ
GLQAVTPAGRVSLLGLYPGKVTIDFNNLIIFKALTIYGITGRHLWETWYT
VSRLLQSGKLNLDPIITHKYKGFDKYEEAFELMRAGKTGKVVFMLK
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
2dfv Chain B Residue 2401 [
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Receptor-Ligand Complex Structure
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PDB
2dfv
The first crystal structure of L-threonine dehydrogenase.
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
N156 G175 G177 P178 L179 S198 E199 P200 R204 F243 S244 A246 L266 G267 L268 I291 T292
Binding residue
(residue number reindexed from 1)
N154 G173 G175 P176 L177 S196 E197 P198 R202 F241 S242 A244 L264 G265 L266 I289 T290
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
C42 G43 T44 H47 H67 E68 C97 C100 C103 C111 K115 P153 A157 K342
Catalytic site (residue number reindexed from 1)
C40 G41 T42 H45 H65 E66 C95 C98 C101 C109 K113 P151 A155 K340
Enzyme Commision number
1.1.1.103
: L-threonine 3-dehydrogenase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0008743
L-threonine 3-dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016597
amino acid binding
GO:0030554
adenyl nucleotide binding
GO:0043168
anion binding
GO:0046872
metal ion binding
GO:0070401
NADP+ binding
GO:0070403
NAD+ binding
Biological Process
GO:0006566
threonine metabolic process
GO:0006567
threonine catabolic process
GO:0019518
L-threonine catabolic process to glycine
GO:0051262
protein tetramerization
GO:0051289
protein homotetramerization
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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External links
PDB
RCSB:2dfv
,
PDBe:2dfv
,
PDBj:2dfv
PDBsum
2dfv
PubMed
17188300
UniProt
O58389
|TDH_PYRHO L-threonine 3-dehydrogenase (Gene Name=tdh)
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