Structure of PDB 1n7g Chain B Binding Site BS03
Receptor Information
>1n7g Chain B (length=336) Species:
3702
(Arabidopsis thaliana) [
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RKIALITGITGQDGSYLTEFLLGKGYEVHGLIRRSSNFNTQRINHIYIDK
ALMKLHYADLTDASSLRRWIDVIKPDEVYNLAAQSHVAVSFEIPDYTADV
VATGALRLLEAVRSHTIDSGRTVKYYQAGSSEMFGSTPPPQSETTPFHPR
SPYAASKCAAHWYTVNYREAYGLFACNGILFNHESPRRGENFVTRKITRA
LGRIKVGLQTKLFLGNLQASRDWGFAGDYVEAMWLMLQQEKPDDYVVATE
EGHTVEEFLDVSFGYLGLNWKDYVEIDQRYFRPAEVDNLQGDASKAKEVL
GWKPQVGFEKLVKMMVDEDLELAKREKVLVDAGYMD
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
1n7g Chain D Residue 704 [
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Receptor-Ligand Complex Structure
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PDB
1n7g
The structure of the MUR1 GDP-mannose 4,6-dehydratase from A. thaliana: Implications for ligand binding and specificity.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
R61 S62 S63
Binding residue
(residue number reindexed from 1)
R34 S35 S36
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S162 S163 E164 Y185 K189
Catalytic site (residue number reindexed from 1)
S130 S131 E132 Y153 K157
Enzyme Commision number
4.2.1.47
: GDP-mannose 4,6-dehydratase.
Gene Ontology
Molecular Function
GO:0005525
GTP binding
GO:0008446
GDP-mannose 4,6-dehydratase activity
GO:0016829
lyase activity
Biological Process
GO:0009826
unidimensional cell growth
GO:0019673
GDP-mannose metabolic process
GO:0042350
GDP-L-fucose biosynthetic process
GO:0042351
'de novo' GDP-L-fucose biosynthetic process
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1n7g
,
PDBe:1n7g
,
PDBj:1n7g
PDBsum
1n7g
PubMed
12501186
UniProt
P93031
|GMD2_ARATH GDP-mannose 4,6 dehydratase 2 (Gene Name=MUR1)
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