Structure of PDB 8y6i Chain A Binding Site BS03
Receptor Information
>8y6i Chain A (length=646) Species:
9606
(Homo sapiens) [
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PTVSVFSMFRYSNWLDKLYMVVGTLAAIIHGAGLPLMMLVFGEMTDIFAN
AGNLEDLMSNFMNLEEDMTRYAYYYSGIGAGVLVAAYIQVSFWCLAAGRQ
IHKIRKQFFHAIMRQEIGWFHDGELNTRLTDDVSKINEGIGDKIGMFFQS
MATFFTGFIVGFTRGWKLTLVILAISPVLGLSAAVWAKILSSFTDKELLA
YAKAGAVAEEVLAIRTVIAFGGQKKELERYNKNLEEAKRIGIKKAITANI
SIGAAFLLIYASYALAFWYGTTLVLSGEYSIGQVLTVFFSVLIGAFSVGQ
ASPSIEAFANARGAAYEIFKIIDNKPSIDSWRIMKLNLTEWPYFVVGVFC
AIINGGLQPAFAIIFSKIIGVFTRIDDPETKRQNSNLFSLLFLALGIISF
ITFFLQGFTFGKAGEILTKRLRYMVFRSMLRQDVSWFDDPKNTTGALTTR
LANDAAQVKGAIGSRLAVITQNIANLGTGIIISFIYGWQLTLLLLAIVPI
IAIAGVVEMKMLSGQEGSGKIATEAIENFRTVVSLTQEQKFEHMYAQSLQ
VPYRNSLRKAHIFGITFSFTQAMMYFSYAGCFRFGAYLVAHKLMSFEDVL
LVFSAVVFGAMAVGQVSSFAPDYAKAKISAAHIIMIIEKTPLIDSY
Ligand information
Ligand ID
CLR
InChI
InChI=1S/C27H46O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9,18-19,21-25,28H,6-8,10-17H2,1-5H3/t19-,21+,22+,23-,24+,25+,26+,27-/m1/s1
InChIKey
HVYWMOMLDIMFJA-DPAQBDIFSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C
CACTVS 3.341
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
ACDLabs 10.04
OC4CCC3(C(=CCC2C1C(C(C(C)CCCC(C)C)CC1)(C)CCC23)C4)C
OpenEye OEToolkits 1.5.0
CC(C)CCC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O)C)C
CACTVS 3.341
CC(C)CCC[CH](C)[CH]1CC[CH]2[CH]3CC=C4C[CH](O)CC[C]4(C)[CH]3CC[C]12C
Formula
C27 H46 O
Name
CHOLESTEROL
ChEMBL
CHEMBL112570
DrugBank
DB04540
ZINC
ZINC000003875383
PDB chain
8y6i Chain A Residue 1603 [
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Receptor-Ligand Complex Structure
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PDB
8y6i
Cryo-EM structure of P-glycoprotein bound to triple elacridar inhibitor molecules.
Resolution
2.54 Å
Binding residue
(original residue number in PDB)
I836 N839
Binding residue
(residue number reindexed from 1)
I469 N472
Annotation score
1
Enzymatic activity
Enzyme Commision number
7.6.2.1
: P-type phospholipid transporter.
7.6.2.2
: ABC-type xenobiotic transporter.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0008559
ABC-type xenobiotic transporter activity
GO:0015562
efflux transmembrane transporter activity
GO:0016887
ATP hydrolysis activity
GO:0022857
transmembrane transporter activity
GO:0031625
ubiquitin protein ligase binding
GO:0042626
ATPase-coupled transmembrane transporter activity
GO:0042910
xenobiotic transmembrane transporter activity
GO:0046943
carboxylic acid transmembrane transporter activity
GO:0090554
phosphatidylcholine floppase activity
GO:0090555
phosphatidylethanolamine flippase activity
GO:0099038
ceramide floppase activity
GO:0140326
ATPase-coupled intramembrane lipid transporter activity
GO:0140328
floppase activity
GO:0140359
ABC-type transporter activity
Biological Process
GO:0000086
G2/M transition of mitotic cell cycle
GO:0006805
xenobiotic metabolic process
GO:0006869
lipid transport
GO:0008218
bioluminescence
GO:0009410
response to xenobiotic stimulus
GO:0045332
phospholipid translocation
GO:0046865
terpenoid transport
GO:0055085
transmembrane transport
GO:0070633
transepithelial transport
GO:0072089
stem cell proliferation
GO:0099040
ceramide translocation
GO:0140115
export across plasma membrane
GO:0150104
transport across blood-brain barrier
GO:1905039
carboxylic acid transmembrane transport
GO:1990961
xenobiotic detoxification by transmembrane export across the plasma membrane
GO:1990962
xenobiotic transport across blood-brain barrier
GO:2001225
regulation of chloride transport
Cellular Component
GO:0005737
cytoplasm
GO:0005886
plasma membrane
GO:0009986
cell surface
GO:0016020
membrane
GO:0016324
apical plasma membrane
GO:0070062
extracellular exosome
GO:0098591
external side of apical plasma membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8y6i
,
PDBe:8y6i
,
PDBj:8y6i
PDBsum
8y6i
PubMed
38579618
UniProt
P08183
|MDR1_HUMAN ATP-dependent translocase ABCB1 (Gene Name=ABCB1)
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