Structure of PDB 6c58 Chain F Binding Site BS02
Receptor Information
>6c58 Chain F (length=459) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
FEIKKICCIGAGYVGGPTCSVIAHMCPEIRVTVVDVNESRINAWNSPTLP
IYEPGLKEVVESCRGKNLFFSTNIDDAIKEADLVFISVNTPTKTYGMGKG
RAADLKYIEACARRIVQNSNGYKIVTEKSTVPVRAAESIRRIFDANTKPN
LNLQVLSNPEFLAEGTAIKDLKNPDRVLIGGDETPEGQRAVQALCAVYEH
WVPREKILTTNTWSSELSKLAANLFLAQRISSINSISALCEATGADVEEV
ATAIGMDQRIGNKFLKASVGFGGSCFQKDVLNLVYLCEALNLPEVARYWQ
QVIDMNDYQRRRFASRIIDSLFNTVTDKKIAILGFAFKKDTGDTRESSSI
YISKYLMDEGAHLHIYDPKVPREQIVVDLSHPDQVSRLVTISKDPYEACD
GAHAVVICTEWDMFKELDYERIHKKMLKPAFIFDGRRVLDGLHNELQTIG
FQIETIGKK
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
6c58 Chain F Residue 501 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
6c58
The A225L Substitution of hUGDH alters structure and function
Resolution
2.198 Å
Binding residue
(original residue number in PDB)
T131 F162 L163 A164 E165 K220 I231 F265 K267 S269 F272 G273 C276 F277 F338 K339 R442
Binding residue
(residue number reindexed from 1)
T130 F161 L162 A163 E164 K219 I230 F264 K266 S268 F271 G272 C275 F276 F337 K338 R436
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
T131 E165 K220 N224 C276 D280
Catalytic site (residue number reindexed from 1)
T130 E164 K219 N223 C275 D279
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:0001702
gastrulation with mouth forming second
GO:0006024
glycosaminoglycan biosynthetic process
GO:0006065
UDP-glucuronate biosynthetic process
GO:0015012
heparan sulfate proteoglycan biosynthetic process
GO:0030206
chondroitin sulfate biosynthetic process
GO:0034214
protein hexamerization
GO:0048666
neuron development
Cellular Component
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005829
cytosol
GO:0070062
extracellular exosome
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:6c58
,
PDBe:6c58
,
PDBj:6c58
PDBsum
6c58
PubMed
UniProt
O60701
|UGDH_HUMAN UDP-glucose 6-dehydrogenase (Gene Name=UGDH)
[
Back to BioLiP
]