Structure of PDB 3ing Chain A Binding Site BS01
Receptor Information
>3ing Chain A (length=319) Species:
2303
(Thermoplasma acidophilum) [
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KEIRIILMGTGNVGLNVLRIIDASNRRRFSIKVVGVSDSRSYASGRNLDI
SSIISNKEKTGRISDRAFSGPEDLMGEAADLLVDCTPASRDGVREYSLYR
MAFESGMNVVTANKSGLANKWHDIMDSANQNSKYIRYEATVAGGVPLFSV
LDYSILPSKVKRFRGIVSSTINYVIRNMANGRSLRDVVDDAIKKGIAESN
PQDDLNGLDAARKSVILVNHIFGTEYTLNDVEYSGVDERSYNANDRLVTE
VYVDDRRPVAVSRIISLNKDDFLMSIGMDGLGYQIETDSNGTVNVSDIYD
GPYETAGAVVNDILLLSKV
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
3ing Chain A Residue 326 [
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Receptor-Ligand Complex Structure
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PDB
3ing
Crystal structure of Homoserine dehydrogenase (NP_394635.1) from THERMOPLASMA ACIDOPHILUM at 1.95 A resolution
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
G10 T11 G12 N13 V14 D41 S42 K60 C88 T89 P90 A115 N116 K117 A142 E201 S202 P305 T308
Binding residue
(residue number reindexed from 1)
G9 T10 G11 N12 V13 D38 S39 K57 C85 T86 P87 A112 N113 K114 A139 E198 S199 P302 T305
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D212 K216
Catalytic site (residue number reindexed from 1)
D209 K213
Enzyme Commision number
1.1.1.3
: homoserine dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004412
homoserine dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0050661
NADP binding
Biological Process
GO:0006520
amino acid metabolic process
GO:0009088
threonine biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3ing
,
PDBe:3ing
,
PDBj:3ing
PDBsum
3ing
PubMed
UniProt
Q9HIZ7
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