Structure of PDB 2cwh Chain A Binding Site BS03
Receptor Information
>2cwh Chain A (length=332) Species:
323
(Pseudomonas syringae pv. tomato) [
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TQTVSYPQLIDLLRRIFVVHGTSPEVADVLAENCASAQRDGSHSHGIFRI
PGYLSSLASGWVDGKAVPVVEDVGAAFVRVDACNGFAQPALAAARSLLID
KARSAGVAILAIRGSHHFAALWPDVEPFAEQGLVALSMVNSMTCVVPHGA
RQPLFGTNPIAFGAPRAGGEPIVFDLATSAIAHGDVQIAAREGRLLPAGM
GVDRDGLPTQEPRAILDGGALLPFGGHKGSALSMMVELLAAGLTGGNFSF
EFDWSKHPGAQTPWTGQLLIVIDPDKGAGQHFAQRSEELVRQLHGVGQER
LPGDRRYLERARSMAHGIVIAQADLERLQELA
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
2cwh Chain B Residue 1510 [
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Receptor-Ligand Complex Structure
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PDB
2cwh
Crystal structures of Delta1-piperideine-2-carboxylate/Delta1-pyrroline-2-carboxylate reductase belonging to a new family of NAD(P)H-dependent oxidoreductases: conformational change, substrate recognition, and stereochemistry of the reaction
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
H157 H236 K237
Binding residue
(residue number reindexed from 1)
H148 H227 K228
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H54
Catalytic site (residue number reindexed from 1)
H45
Enzyme Commision number
1.4.1.17
: N-methylalanine dehydrogenase.
1.5.1.21
: 1-piperideine-2-carboxylate/1-pyrroline-2-carboxylate reductase (NADPH).
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
GO:0047125
delta1-piperideine-2-carboxylate reductase activity
GO:0050132
N-methylalanine dehydrogenase activity
GO:0050241
pyrroline-2-carboxylate reductase activity
GO:0070401
NADP+ binding
Biological Process
GO:0006560
proline metabolic process
GO:0030416
methylamine metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2cwh
,
PDBe:2cwh
,
PDBj:2cwh
PDBsum
2cwh
PubMed
16192274
UniProt
Q4U331
|PY2CR_PSEUB Delta(1)-pyrroline-2-carboxylate/Delta(1)-piperideine-2-carboxylate reductase (Gene Name=dpkA)
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