Structure of PDB 5bsf Chain E Binding Site BS01
Receptor Information
>5bsf Chain E (length=272) Species:
3880
(Medicago truncatula) [
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IIPIPADSYTLGFIGAGKMAESIAKGAVRSGVLSPSRIKTAIHSNPARRT
AFESIGITVLSSNDDVVRDSNVVVFSVKPQLLKDVVLKLKPLLTKDKLLV
SVAAGIKMKDLQEWAGHERFIRVMPNTAATVGEAASVMSLGGAATEEDAN
LISQLFGSIGKIWKADDKYFDAITGLSGSGPAYIYLAIEALADGGVAAGL
PRDLALSLASQTVLGAASMATQSGKHPGQLKDDVTSPGGTTIAGVHELEK
AGFRGILMNAVVAAAKRSQELS
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
5bsf Chain E Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5bsf
The structure of Medicago truncatula delta (1)-pyrroline-5-carboxylate reductase provides new insights into regulation of proline biosynthesis in plants.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
G17 G19 K20 M21 H45 N65 S78 V79 K80 L83 V104 A106 P127
Binding residue
(residue number reindexed from 1)
G15 G17 K18 M19 H43 N63 S76 V77 K78 L81 V102 A104 P125
Annotation score
3
Enzymatic activity
Enzyme Commision number
1.5.1.2
: pyrroline-5-carboxylate reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004735
pyrroline-5-carboxylate reductase activity
GO:0016491
oxidoreductase activity
Biological Process
GO:0006561
proline biosynthetic process
GO:0055129
L-proline biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5bsf
,
PDBe:5bsf
,
PDBj:5bsf
PDBsum
5bsf
PubMed
26579138
UniProt
G7KRM5
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