Structure of PDB 3prj Chain D Binding Site BS01
Receptor Information
>3prj Chain D (length=458) Species:
9606
(Homo sapiens) [
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MFEIKKICCIGAGYVGGPTCSVIAHMCPEIRVTVVDVNESRINAWNSPTL
PIYEPGLKEVVESCRGKNLFFSTNIDDAIKEADLVFISVNTPTKTYGMGK
GRAADLKYIEACARRIVQNSNGYKIVTEKSTVPVRAAESIRRIFDANTKP
NLNLQVLSNPEFLAEGTAIKDLKNPDRVLIGGDETPEGQRAVQALCAVYE
HWVPREKILTTNTWSSELSKLAANAFLAQRISSINSISALCEATGADVEE
VATAIGMDQRIGNKFLKASVGFGGSCFQKDVLNLVYLCEALNLPEVARYW
QQVIDMNDYQRRRFASRIIDSLFNTVTDKKIAILGFAFKKDTGDTRESSS
IYISKYLMDEGAHLHIYDPKVPREQIVVDLSDQVSRLVTISKDPYEACDG
AHAVVICTEWDMFKELDYERIHKKMLKPAFIFDGRRVLDGLHNELQTIGF
QIETIGKK
Ligand information
Ligand ID
NAI
InChI
InChI=1S/C21H29N7O14P2/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/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BOPGDPNILDQYTO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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
Formula
C21 H29 N7 O14 P2
Name
1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE;
NADH
ChEMBL
CHEMBL1234616
DrugBank
DB00157
ZINC
ZINC000008215403
PDB chain
3prj Chain D Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
3prj
Role of Packing Defects in the Evolution of Allostery and Induced Fit in Human UDP-Glucose Dehydrogenase.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
I10 G11 G13 Y14 V15 D36 V37 R41 V89 N90 T91 C112 S130 T131 K279 R346
Binding residue
(residue number reindexed from 1)
I10 G11 G13 Y14 V15 D36 V37 R41 V89 N90 T91 C112 S130 T131 K279 R346
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:3prj
,
PDBe:3prj
,
PDBj:3prj
PDBsum
3prj
PubMed
21595445
UniProt
O60701
|UGDH_HUMAN UDP-glucose 6-dehydrogenase (Gene Name=UGDH)
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