Structure of PDB 2cnb Chain A Binding Site BS01
Receptor Information
>2cnb Chain A (length=366) Species:
5691
(Trypanosoma brucei) [
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SHMRVLVCGGAGYIGSHFVRALLRDTNHSVVIVDSLVGTHGKSDHVETRE
NVARKLQQSDGPKPPWADRYAALEVGDVRNEDFLNGVFTRHGPIDAVVHM
CAFLAVGESVRDPLKYYDNNVVGILRLLQAMLLHKCDKIIFSSSAAIFGN
PTNAEPIDINAKKSPESPYGESKLIAERMIRDCAEAYGIKGICLRYFNAC
GAHEDGDIGEHYQGSTHLIPIILGRVMSDIAPDDKRMPIFGTDYPTPDGT
CVRDYVHVCDLASAHILALDYVEKLGPNDKSKYFSVFNLGTSRGYSVREV
IEVARKTTGHPIPVRECGRREGDPAYLVAASDKAREVLGWKPKYDTLEAI
METSWKFQRTHPNGYA
Ligand information
Ligand ID
UFG
InChI
InChI=1S/C15H23FN2O16P2/c16-8-5(3-19)32-14(12(24)10(8)22)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)18-2-1-7(20)17-15(18)25/h1-2,5-6,8-14,19,21-24H,3-4H2,(H,26,27)(H,28,29)(H,17,20,25)/t5-,6-,8-,9-,10+,11-,12-,13-,14-/m1/s1
InChIKey
OAPPZHVTNHJVAL-JZMIEXBBSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OC3C(C(C(C(O3)CO)F)O)O)O)O
ACDLabs 10.04
O=P(OC1OC(C(F)C(O)C1O)CO)(O)OP(=O)(O)OCC3OC(N2C=CC(=O)NC2=O)C(O)C3O
CACTVS 3.341
OC[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)N3C=CC(=O)NC3=O)[C@H](O)[C@@H](O)[C@@H]1F
CACTVS 3.341
OC[CH]1O[CH](O[P](O)(=O)O[P](O)(=O)OC[CH]2O[CH]([CH](O)[CH]2O)N3C=CC(=O)NC3=O)[CH](O)[CH](O)[CH]1F
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)(O)O[P@@](=O)(O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)F)O)O)O)O
Formula
C15 H23 F N2 O16 P2
Name
URIDINE-5'-DIPHOSPHATE-4-DEOXY-4-FLUORO-ALPHA-D-GALACTOSE
ChEMBL
CHEMBL593125
DrugBank
DB04097
ZINC
ZINC000016051558
PDB chain
2cnb Chain A Residue 1382 [
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Receptor-Ligand Complex Structure
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PDB
2cnb
Trypanosoma Brucei Udp-Galactose-4-Epimerase in Ternary Complex with Nad+ and the Substrate Analogue Udp-4-Deoxy-4-Fluoro-Alpha-D-Galactose
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
L102 S142 Y173 F201 N202 H221 L222 P253 I254 F255 C266 R268 V312 R335 D338
Binding residue
(residue number reindexed from 1)
L104 S144 Y169 F197 N198 H217 L218 P238 I239 F240 C251 R253 V297 R320 D323
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S142 A143 A144 Y173 K177
Catalytic site (residue number reindexed from 1)
S144 A145 A146 Y169 K173
Enzyme Commision number
5.1.3.2
: UDP-glucose 4-epimerase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003978
UDP-glucose 4-epimerase activity
GO:0016853
isomerase activity
Biological Process
GO:0006012
galactose metabolic process
GO:0033499
galactose catabolic process via UDP-galactose
Cellular Component
GO:0005829
cytosol
GO:0020015
glycosome
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2cnb
,
PDBe:2cnb
,
PDBj:2cnb
PDBsum
2cnb
PubMed
16946458
UniProt
Q8T8E9
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