Structure of PDB 6om8 Chain L Binding Site BS02
Receptor Information
>6om8 Chain L (length=463) Species:
6239
(Caenorhabditis elegans) [
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GKVSKVVCVGAGYVGGPTCAMIAHKCPHITVTVVDMNTAKIAEWNSDKLP
IYEPGLDEIVFAARGRNLFFSSDIPKAIAEADLIFISVNTPTKMYGRGKG
MAPDLKYVESVSRTIAQYAGGPKIVVEKSTVPVKAAESIGCILREAQKNN
ENLKFQVLSNPEFLAEGTAMKDLANPDRVLIGGESSPEGLQAVAELVRIY
ENWVPRNRIITTNTWSSELSKLVANAFLAQRISSINSISAVCEATGAEIS
EVAHAVGYDTRIGSKFLQASVGFGGSCFQKDVLSLVYLCESLNLPQVADY
WQGVININNWQRRRFADKIIAELFNTVTDKKIAIFGFAFKKNTGDTRESS
AIHVIKHLMEEHAKLSVYDPKVQKSQMLNDLASVTSAQDVERLITVESDP
YAAARGAHAIVVLTEWDEFVELNYSQIHNDMQHPAAIFDGRLILDQKALR
EIGFRTFAIGTSP
Ligand information
Ligand ID
UDX
InChI
InChI=1S/C14H22N2O16P2/c17-5-3-28-13(11(22)8(5)19)31-34(26,27)32-33(24,25)29-4-6-9(20)10(21)12(30-6)16-2-1-7(18)15-14(16)23/h1-2,5-6,8-13,17,19-22H,3-4H2,(H,24,25)(H,26,27)(H,15,18,23)/t5-,6-,8+,9-,10-,11-,12-,13-/m1/s1
InChIKey
DQQDLYVHOTZLOR-OCIMBMBZSA-N
SMILES
Software
SMILES
CACTVS 3.341
O[C@@H]1CO[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]1O
ACDLabs 10.04
O=P(OC1OCC(O)C(O)C1O)(O)OP(=O)(O)OCC3OC(N2C=CC(=O)NC2=O)C(O)C3O
OpenEye OEToolkits 1.5.0
C1C(C(C(C(O1)OP(=O)(O)OP(=O)(O)OCC2C(C(C(O2)N3C=CC(=O)NC3=O)O)O)O)O)O
OpenEye OEToolkits 1.5.0
C1[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)N3C=CC(=O)NC3=O)O)O)O)O)O
CACTVS 3.341
O[CH]1CO[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]1O
Formula
C14 H22 N2 O16 P2
Name
URIDINE-5'-DIPHOSPHATE-XYLOPYRANOSE;
UDP-ALPHA-D-XYLOPYRANOSE
ChEMBL
DrugBank
DB01713
ZINC
ZINC000008551129
PDB chain
6om8 Chain L Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
6om8
Conservation of Atypical Allostery inC. elegansUDP-Glucose Dehydrogenase.
Resolution
2.449 Å
Binding residue
(original residue number in PDB)
E168 F169 L170 A171 E172 K227 I238 F272 Q274 S276 F279 G280 C283 F284 F345 K346 R447
Binding residue
(residue number reindexed from 1)
E162 F163 L164 A165 E166 K221 I232 F266 Q268 S270 F273 G274 C277 F278 F339 K340 R441
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
T136 E172 K227 N231 C283 D287
Catalytic site (residue number reindexed from 1)
T130 E166 K221 N225 C277 D281
Enzyme Commision number
1.1.1.22
: UDP-glucose 6-dehydrogenase.
Gene Ontology
Molecular Function
GO:0003979
UDP-glucose 6-dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0042802
identical protein binding
GO:0051287
NAD binding
Biological Process
GO:0002009
morphogenesis of an epithelium
GO:0006024
glycosaminoglycan biosynthetic process
GO:0006065
UDP-glucuronate biosynthetic process
GO:0009792
embryo development ending in birth or egg hatching
GO:0018991
egg-laying behavior
GO:0022414
reproductive process
GO:0040025
vulval development
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6om8
,
PDBe:6om8
,
PDBj:6om8
PDBsum
6om8
PubMed
31616809
UniProt
Q19905
|UGDH_CAEEL UDP-glucose 6-dehydrogenase (Gene Name=sqv-4)
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