Structure of PDB 4e5y Chain A Binding Site BS01
Receptor Information
>4e5y Chain A (length=307) Species:
9606
(Homo sapiens) [
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SMRILVTGGSGLVGKAIQKVVADGAGEDWVFVSSKDADLTDTAQTRALFE
KVQPTHVIHLAAMVGGLFRNIKYNLDFWRKNVHMNDNVLHSAFEVGARKV
VSCLSTCIFPDKTTYPIDETMIHNGPPHNSNFGYSYAKRMIDVQNRAYFQ
QYGCTFTAVIPTNVFGPHDNFNIEDGHVLPGLIHKVHLAKSSGSALTVWG
TGNPRRQFIYSLDLAQLFIWVLREYNEVEPIILSVGEEDEVSIKEAAEAV
VEAMDFHGEVTFDGQFKKTASNSKLRTYLPDFRFTPFKQAVKETCAWFTD
NYEQARK
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
4e5y Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4e5y
Structure of human FX protein, the key enzyme in the biosynthesis of GDP-L-fucose
Resolution
2.37 Å
Binding residue
(original residue number in PDB)
G14 S16 G17 L18 V19 S42 S43 L48 L69 A71 C112 L113 S114 K147 P170 V173 R320
Binding residue
(residue number reindexed from 1)
G8 S10 G11 L12 V13 S33 S34 L39 L60 A62 C103 L104 S105 K138 P161 V164 R306
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S114 T115 C116 Y143 K147 H186
Catalytic site (residue number reindexed from 1)
S105 T106 C107 Y134 K138 H177
Enzyme Commision number
1.1.1.271
: GDP-L-fucose synthase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0016853
isomerase activity
GO:0042356
GDP-4-dehydro-D-rhamnose reductase activity
GO:0042802
identical protein binding
GO:0047918
GDP-mannose 3,5-epimerase activity
GO:0050577
GDP-L-fucose synthase activity
Biological Process
GO:0007159
leukocyte cell-cell adhesion
GO:0009226
nucleotide-sugar biosynthetic process
GO:0010595
positive regulation of endothelial cell migration
GO:0019673
GDP-mannose metabolic process
GO:0042351
'de novo' GDP-L-fucose biosynthetic process
GO:1904906
positive regulation of endothelial cell-matrix adhesion via fibronectin
Cellular Component
GO:0005829
cytosol
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4e5y
,
PDBe:4e5y
,
PDBj:4e5y
PDBsum
4e5y
PubMed
UniProt
Q13630
|FCL_HUMAN GDP-L-fucose synthase (Gene Name=GFUS)
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