Structure of PDB 5n6c Chain A Binding Site BS01
Receptor Information
>5n6c Chain A (length=300) Species:
9606
(Homo sapiens) [
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AKVLISDSLDPCCRKILQDGGLQVVEKQNLSKEELIAELQDCEGLIVRSA
TKVTADVINAAEKLQVVGRAGTGVDNVDLEAATRKGILVMNTPNGNSLSA
AELTCGMIMCLARQIPQATASMKDGKWERKKFMGTELNGKTLGILGLGRI
GREVATRMQSFGMKTIGYDPIISPEVSASFGVQQLPLEEIWPLCDFITVH
TPLLPSTTGLLNDNTFAQCKKGVRVVNCARGGIVDEGALLRALQSGQCAG
AALDVFTEEPPRDRALVDHENVISCPHLGASTKEAQSRCGEEIAVQFVDM
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
5n6c Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5n6c
Structural insights into the enzymatic activity and potential substrate promiscuity of human 3-phosphoglycerate dehydrogenase (PHGDH).
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
T78 G152 R155 I156 Y174 D175 P176 H206 T207 P208 T213 C234 A235 R236 H283 G285
Binding residue
(residue number reindexed from 1)
T72 G146 R149 I150 Y168 D169 P170 H200 T201 P202 T207 C228 A229 R230 H277 G279
Annotation score
4
Binding affinity
MOAD
: Ka=22500M^-1
Enzymatic activity
Catalytic site (original residue number in PDB)
N102 R236 D260 E265 H283
Catalytic site (residue number reindexed from 1)
N96 R230 D254 E259 H277
Enzyme Commision number
1.1.1.37
: malate dehydrogenase.
1.1.1.399
: 2-oxoglutarate reductase.
1.1.1.95
: phosphoglycerate dehydrogenase.
Gene Ontology
Molecular Function
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0051287
NAD binding
View graph for
Molecular Function
External links
PDB
RCSB:5n6c
,
PDBe:5n6c
,
PDBj:5n6c
PDBsum
5n6c
PubMed
29262655
UniProt
O43175
|SERA_HUMAN D-3-phosphoglycerate dehydrogenase (Gene Name=PHGDH)
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