Structure of PDB 1n7g Chain A Binding Site BS02
Receptor Information
>1n7g Chain A (length=333) Species:
3702
(Arabidopsis thaliana) [
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RKIALITGITGQDGSYLTEFLLGKGYEVHGLIRRSSNFNTQRINHIYKAL
MKLHYADLTDASSLRRWIDVIKPDEVYNLAAQSHVAVSFEIPDYTADVVA
TGALRLLEAVRSHTIDSGRTVKYYQAGSSEMFGSTPPPQSETTPFHPRSP
YAASKCAAHWYTVNYREAYGLFACNGILFNHESPRRGENFVTRKITRALG
RIKVGLQTKLFLGNLQASRDWGFAGDYVEAMWLMLQQEKPDDYVVATEEG
HTVEEFLDVSFGYLGLNWKDYVEIDQRYFRPAEVDNLQGDASKAKEVLGW
KPQVGFEKLVKMMVDEDLELAKREKVLVDAGYM
Ligand information
Ligand ID
GDR
InChI
InChI=1S/C16H25N5O15P2/c1-4-7(22)9(24)11(26)15(33-4)35-38(30,31)36-37(28,29)32-2-5-8(23)10(25)14(34-5)21-3-18-6-12(21)19-16(17)20-13(6)27/h3-5,7-11,14-15,22-26H,2H2,1H3,(H,28,29)(H,30,31)(H3,17,19,20,27)/t4-,5-,7-,8-,9+,10-,11+,14-,15-/m1/s1
InChIKey
LQEBEXMHBLQMDB-GDJBGNAASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC1C(C(C(C(O1)OP(=O)(O)OP(=O)(O)OCC2C(C(C(O2)n3cnc4c3N=C(NC4=O)N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
C[C@@H]1[C@H]([C@@H]([C@@H]([C@H](O1)O[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]2[C@H]([C@H]([C@@H](O2)n3cnc4c3N=C(NC4=O)N)O)O)O)O)O
CACTVS 3.341
C[CH]1O[CH](O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)n3cnc4C(=O)NC(=Nc34)N)[CH](O)[CH](O)[CH]1O
CACTVS 3.341
C[C@H]1O[C@H](O[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)n3cnc4C(=O)NC(=Nc34)N)[C@@H](O)[C@@H](O)[C@@H]1O
ACDLabs 10.04
O=P(OC1OC(C(O)C(O)C1O)C)(O)OP(=O)(O)OCC4OC(n2c3N=C(N)NC(=O)c3nc2)C(O)C4O
Formula
C16 H25 N5 O15 P2
Name
GUANOSINE-5'-DIPHOSPHATE-RHAMNOSE
ChEMBL
CHEMBL1233001
DrugBank
DB02547
ZINC
ZINC000008218184
PDB chain
1n7g Chain A Residue 801 [
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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)
S117 S162 Y185 N214 R220 F224 V225 K228 G247 R253 R314 E317
Binding residue
(residue number reindexed from 1)
S83 S128 Y151 N180 R186 F190 V191 K194 G213 R219 R280 E283
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S162 S163 E164 Y185 K189
Catalytic site (residue number reindexed from 1)
S128 S129 E130 Y151 K155
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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