Structure of PDB 4b8w Chain B Binding Site BS01
Receptor Information
>4b8w Chain B (length=300) Species:
9606
(Homo sapiens) [
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YFQSMRILVTGGSGLVGKAIQKVVAPGEDWVFVSSKDADLTDTAQTRALF
EKVQPTHVIHLAAMVNLDFWRKNVHMNDNVLHSAFEVGARKVVSCLSTCI
FPDKTTYPIDETMIHNGPPHNSNFGYSYAKRMIDVQNRAYFQQYGCTFTA
VIPTNVFGPHDNFNIEDGHVLPGLIHKVHLAKSSGSALTVWGTGNPRRQF
IYSLDLAQLFIWVLREYNEVEPIILSVGEEDEVSIKEAAEAVVEAMDFHG
EVTFDTTKSDGQFKKTASNSKLRTYLPDFRFTPFKQAVKETCAWFTDNYE
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/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/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)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[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
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[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]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)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
4b8w Chain B Residue 900 [
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Receptor-Ligand Complex Structure
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PDB
4b8w
Crystal Structure of Human Gdp-L-Fucose Synthase with Bound Nadp and Gdp, Tetragonal Crystal Form
Resolution
2.75 Å
Binding residue
(original residue number in PDB)
G14 S16 G17 L18 V19 S43 L48 L69 A70 A71 C112 L113 Y143 K147 T171 V173 H186
Binding residue
(residue number reindexed from 1)
G11 S13 G14 L15 V16 S35 L40 L61 A62 A63 C95 L96 Y126 K130 T154 V156 H169
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)
S97 T98 C99 Y126 K130 H169
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
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4b8w
,
PDBe:4b8w
,
PDBj:4b8w
PDBsum
4b8w
PubMed
UniProt
Q13630
|FCL_HUMAN GDP-L-fucose synthase (Gene Name=GFUS)
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