Structure of PDB 6c4j Chain E Binding Site BS01
Receptor Information
>6c4j Chain E (length=460) Species:
9606
(Homo sapiens) [
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MFEIKKICCIGAGYVGGPTCSVIAHMCPEIRVTVVDVNESRINAWNSPTL
PIYEPGLKEVVESCRGKNLFFSTNIDDAIKEADLVFISVNTPTKTYGMGK
GRALDLKYIEACARRIVQNSNGYKIVTEKSTVPVRAAESIRRIFDANTKP
NLNLQVLSNPEFLAEGTAIKDLKNPDRVLIGGDETPEGQRAVQALCAVYE
HWVPREKILTTNTWSSELSKLAANAFLAQRISSINSISALCEATGADVEE
VATAIGMDQRIGNKFLKASVGFGGSCFQKDVLNLVYLCEALNLPEVARYW
QQVIDMNDYQRRRFASRIIDSLFNTVTDKKIAILGFAFKKDTGDTRESSS
IYISKYLMDEGAHLHIYDPKVPREQIVVDLSHDQVSRLVTISKDPYEACD
GAHAVVICTEWDMFKELDYERIHKKMLKPAFIFDGRRVLDGLHNELQTIG
FQIETIGKKV
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
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)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)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)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]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)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
6c4j Chain E Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
6c4j
Hysteresis and Allostery in Human UDP-Glucose Dehydrogenase Require a Flexible Protein Core.
Resolution
2.53 Å
Binding residue
(original residue number in PDB)
G11 G13 Y14 V15 D36 R41 S88 V89 N90 T91 Y108 S130 T131 E161
Binding residue
(residue number reindexed from 1)
G11 G13 Y14 V15 D36 R41 S88 V89 N90 T91 Y108 S130 T131 E161
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
T131 E165 K220 N224 C276 D280
Catalytic site (residue number reindexed from 1)
T131 E165 K220 N224 C276 D280
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6c4j
,
PDBe:6c4j
,
PDBj:6c4j
PDBsum
6c4j
PubMed
30457329
UniProt
O60701
|UGDH_HUMAN UDP-glucose 6-dehydrogenase (Gene Name=UGDH)
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