Structure of PDB 2fnu Chain A Binding Site BS02
Receptor Information
>2fnu Chain A (length=373) Species:
85962
(Helicobacter pylori 26695) [
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MKEFAYSEPCLDKEDKKAVLEVLNSKQLTQGKRSLLFEEALCEFLGVKHA
LVFNSATSALLTLYRNFSEFSADRNEIITTPISFVATANMLLESGYTPVF
AGIKNDGNIDELALEKLINERTKAIVSVDYAGKSVEVESVQKLCKKHSLS
FLSDSSHALGSEYQNKKVGGFALASVFSFHAIKPITTAEGGAVVTNDSEL
HEKMKLFRSHGMLKKDFFEGEVKSIGHNFRLNEIQSALGLSQLKKAPFLM
QKREEAALTYDRIFKDNPYFTPLHPLLKDKSSNHLYPILMHQKFFTCKKL
ILESLHKRGILAQVHYKPIYQYQLYQQLFNTAPLKSAEDFYHAEISLPCH
ANLNLESVQNIAHSVLKTFESFK
Ligand information
Ligand ID
UD1
InChI
InChI=1S/C17H27N3O17P2/c1-6(22)18-10-13(26)11(24)7(4-21)35-16(10)36-39(31,32)37-38(29,30)33-5-8-12(25)14(27)15(34-8)20-3-2-9(23)19-17(20)28/h2-3,7-8,10-16,21,24-27H,4-5H2,1H3,(H,18,22)(H,29,30)(H,31,32)(H,19,23,28)/t7-,8-,10-,11-,12-,13-,14-,15-,16-/m1/s1
InChIKey
LFTYTUAZOPRMMI-CFRASDGPSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(=O)NC1C(C(C(OC1OP(=O)(O)OP(=O)(O)OCC2C(C(C(O2)N3C=CC(=O)NC3=O)O)O)CO)O)O
CACTVS 3.341
CC(=O)N[CH]1[CH](O)[CH](O)[CH](CO)O[CH]1O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)N3C=CC(=O)NC3=O
ACDLabs 10.04
O=P(OC1OC(C(O)C(O)C1NC(=O)C)CO)(O)OP(=O)(O)OCC3OC(N2C=CC(=O)NC2=O)C(O)C3O
CACTVS 3.341
CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N3C=CC(=O)NC3=O
OpenEye OEToolkits 1.5.0
CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@@H]1O[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=CC(=O)NC3=O)O)O)CO)O)O
Formula
C17 H27 N3 O17 P2
Name
URIDINE-DIPHOSPHATE-N-ACETYLGLUCOSAMINE
ChEMBL
CHEMBL388154
DrugBank
DB03397
ZINC
ZINC000008551100
PDB chain
2fnu Chain A Residue 902 [
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Receptor-Ligand Complex Structure
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PDB
2fnu
Structural and Functional Characterization of PseC, an Aminotransferase Involved in the Biosynthesis of Pseudaminic Acid, an Essential Flagellar Modification in Helicobacter pylori
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
Y6 E8 P9 F84 H180 A181 I182 Q313 H315 Y316
Binding residue
(residue number reindexed from 1)
Y6 E8 P9 F84 H180 A181 I182 Q313 H315 Y316
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
F84 D154 H157 H180 K183 K214 G220 R230
Catalytic site (residue number reindexed from 1)
F84 D154 H157 H180 K183 K214 G220 R230
Enzyme Commision number
2.6.1.92
: UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine transaminase.
Gene Ontology
Molecular Function
GO:0008483
transaminase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0000271
polysaccharide biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2fnu
,
PDBe:2fnu
,
PDBj:2fnu
PDBsum
2fnu
PubMed
16421095
UniProt
O25130
|PSEC_HELPY UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine transaminase (Gene Name=pseC)
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