Structure of PDB 6vp0 Chain C Binding Site BS04
Receptor Information
>6vp0 Chain C (length=404) Species:
9606
(Homo sapiens) [
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WELRCHRLQDSLFSSDSGFSNYRGILNWCVVMLILSNARLFLENLIKYGI
LVDPIQVVSLFLKDPYSWPAPCLVIAANVFAVAAFQVEKRLAVGALTEQA
GLLLHVANLATILCFPAAVVLLVESITPVGSLLALMAHTILFLKLFSYRD
VNSWCRRARAKHTVSYPDNLTYRDLYYFLFAPTLCYELNFPRSPRIRKRF
LLRRILEMLFFTQLQVGLIQQWMVPTIQNSMKPFKDMDYSRIIERLLKLA
VPNHLIWLIFFYWLFHSCLNAVAELMQFGDREFYRDWWNSESVTYFWQNW
NIPVHKWCIRHFYKPMLRRGSSKWMARTGVFLASAFFHEYLVSVPLRMFR
LWAFTGMMAQIPLAWFVGRFFQGNYGNAAVWLSLIIGQPIAVLMYVHDYY
VLNY
Ligand information
Ligand ID
AV0
InChI
InChI=1S/C47H88O22/c1-3-5-7-9-11-13-15-17-19-47(20-18-16-14-12-10-8-6-4-2,25-62-43-39(60)35(56)41(29(23-50)66-43)68-45-37(58)33(54)31(52)27(21-48)64-45)26-63-44-40(61)36(57)42(30(24-51)67-44)69-46-38(59)34(55)32(53)28(22-49)65-46/h27-46,48-61H,3-26H2,1-2H3/t27-,28-,29-,30-,31-,32-,33+,34+,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-/m1/s1
InChIKey
MADJBYLAYPCCOO-VWHTXWAPSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.6
CCCCCCCCCCC(CCCCCCCCCC)(CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O)O)CO[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O
ACDLabs 12.01
C2(C(C(O)C(OC1OC(CO)C(O)C(O)C1O)C(CO)O2)O)OCC(CCCCCCCCCC)(CCCCCCCCCC)COC4OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C4O
CACTVS 3.385
CCCCCCCCCCC(CCCCCCCCCC)(CO[C@@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O)CO[C@@H]3O[C@H](CO)[C@@H](O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O
CACTVS 3.385
CCCCCCCCCCC(CCCCCCCCCC)(CO[CH]1O[CH](CO)[CH](O[CH]2O[CH](CO)[CH](O)[CH](O)[CH]2O)[CH](O)[CH]1O)CO[CH]3O[CH](CO)[CH](O[CH]4O[CH](CO)[CH](O)[CH](O)[CH]4O)[CH](O)[CH]3O
OpenEye OEToolkits 2.0.6
CCCCCCCCCCC(CCCCCCCCCC)(COC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O)COC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O
Formula
C47 H88 O22
Name
Lauryl Maltose Neopentyl Glycol;
2,2-didecylpropane-1,3-bis-b-D-maltopyranoside;
2-decyl-2-{[(4-O-alpha-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]methyl}dodecyl4-O-alpha-D-glucopyranosyl-beta-D-glucopyranoside
ChEMBL
DrugBank
ZINC
PDB chain
6vp0 Chain C Residue 606 [
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Receptor-Ligand Complex Structure
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PDB
6vp0
Structure and mechanism of human diacylglycerol O-acyltransferase 1.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
Q290 L291 Q298 W299
Binding residue
(residue number reindexed from 1)
Q213 L214 Q221 W222
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.3.1.20
: diacylglycerol O-acyltransferase.
2.3.1.76
: retinol O-fatty-acyltransferase.
Gene Ontology
Molecular Function
GO:0003846
2-acylglycerol O-acyltransferase activity
GO:0004144
diacylglycerol O-acyltransferase activity
GO:0005515
protein binding
GO:0008374
O-acyltransferase activity
GO:0016746
acyltransferase activity
GO:0042802
identical protein binding
GO:0050252
retinol O-fatty-acyltransferase activity
Biological Process
GO:0006629
lipid metabolic process
GO:0006640
monoacylglycerol biosynthetic process
GO:0006641
triglyceride metabolic process
GO:0019432
triglyceride biosynthetic process
GO:0019915
lipid storage
GO:0034379
very-low-density lipoprotein particle assembly
GO:0035336
long-chain fatty-acyl-CoA metabolic process
GO:0042572
retinol metabolic process
GO:0046339
diacylglycerol metabolic process
GO:0046486
glycerolipid metabolic process
GO:0055089
fatty acid homeostasis
Cellular Component
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0035579
specific granule membrane
GO:0043231
intracellular membrane-bounded organelle
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6vp0
,
PDBe:6vp0
,
PDBj:6vp0
PDBsum
6vp0
PubMed
32433610
UniProt
O75907
|DGAT1_HUMAN Diacylglycerol O-acyltransferase 1 (Gene Name=DGAT1)
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