Structure of PDB 2p9e Chain D Binding Site BS01
Receptor Information
>2p9e Chain D (length=403) Species:
562
(Escherichia coli) [
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KDKIKFLLVEGVHQKALESLRAAGYTNIEFHKGALDDEQLKESIRDAHFI
GLRSRTHLTEDVINAAEKLVAIGAFAIGTNQVDLDAAAKRGIPVFNAPFS
NTRSVAELVIGELLLLLRGVPEANAKAHRGVWNKLAAGSFEARGKKLGII
GYGHIGTQLGILAESLGMYVYFYDIENKLPLGNATQVQHLSDLLNMSDVV
SLHVPENPSTKNMMGAKEISLMKPGSLLINASRGTVVDIPALADALASKH
LAGAAIDVFPTEPATNSDPFTSPLAEFDNVLLTPHIGGSTQEAQENIGLE
VAGKLIKYSDNGSTLSAVNFPEVSLPLHVGRRLMHIHENRPGVLTALNKI
FAEQGVNIAAQYLQTSAQMGYVVIDIEADEDVAEKALQAMKAIPGTIRAR
LLY
Ligand information
Ligand ID
NAI
InChI
InChI=1S/C21H29N7O14P2/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/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BOPGDPNILDQYTO-NNYOXOHSSA-N
SMILES
Software
SMILES
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)O)N
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)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
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)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)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
Formula
C21 H29 N7 O14 P2
Name
1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE;
NADH
ChEMBL
CHEMBL1234616
DrugBank
DB00157
ZINC
ZINC000008215403
PDB chain
2p9e Chain D Residue 511 [
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Receptor-Ligand Complex Structure
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PDB
2p9e
The Effect of Hinge Mutations on Effector Binding and Domain Rotation in Escherichia coli D-3-Phosphoglycerate Dehydrogenase
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
V112 G160 H161 I162 Y180 D181 I182 K185 H210 V211 P212 A238 S239 R240 H292 G294 G295
Binding residue
(residue number reindexed from 1)
V105 G153 H154 I155 Y173 D174 I175 K178 H203 V204 P205 A231 S232 R233 H285 G287 G288
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N108 R240 D264 E269 H292
Catalytic site (residue number reindexed from 1)
N101 R233 D257 E262 H285
Enzyme Commision number
1.1.1.399
: 2-oxoglutarate reductase.
1.1.1.95
: phosphoglycerate dehydrogenase.
Gene Ontology
Molecular Function
GO:0004617
phosphoglycerate 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:0047545
2-hydroxyglutarate dehydrogenase activity
GO:0051287
NAD binding
GO:0070403
NAD+ binding
GO:0070404
NADH binding
GO:0070905
serine binding
Biological Process
GO:0006564
L-serine 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:2p9e
,
PDBe:2p9e
,
PDBj:2p9e
PDBsum
2p9e
PubMed
17459882
UniProt
P0A9T0
|SERA_ECOLI D-3-phosphoglycerate dehydrogenase (Gene Name=serA)
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