Structure of PDB 5jmn Chain A Binding Site BS01
Receptor Information
>5jmn Chain A (length=1034) Species:
83333
(Escherichia coli K-12) [
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MPNFFIDRPIFAWVIAIIIMLAGGLAILKLPVAQYPTIAPPAVTISASYP
GADAKTVQDTVTQVIEQNMNGIDNLMYMSSNSDSTGTVQITLTFESGTDA
DIAQVQVQNKLQLAMPLLPQEVQQQGVSVEKSSSSFLMVVGVINTDGTMT
QEDISDYVAANMKDAISRTSGVGDVQLFGSQYAMRIWMNPNELNKFQLTP
VDVITAIKAQNAQVAAGQLGGTPPVKGQQLNASIIAQTRLTSTEEFGKIL
LKVNQDGSRVLLRDVAKIELGGENYDIIAEFNGQPASGLGIKLATGANAL
DTAAAIRAELAKMEPFFPSGLKIVYPYDTTPFVKISIHEVVKTLVEAIIL
VFLVMYLFLQNFRATLIPTIAVPVVLLGTFAVLAAFGFSINTLTMFGMVL
AIGLLVDDAIVVVENVERVMAEEGLPPKEATRKSMGQIQGALVGIAMVLS
AVFVPMAFFGGSTGAIYRQFSITIVSAMALSVLVALILTPALCATMLKPI
AKGDHGEGKKGFFGWFNRMFEKSTHHYTDSVGGILRSTGRYLVLYLIIVV
GMAYLFVRLPSSFLPDEDQGVFMTMVQLPAGATQERTQKVLNEVTHYYLT
KEKNNVESVFAVNGFGFAGRGQNTGIAFVSLKDWADRPGEENKVEAITMR
ATRAFSQIKDAMVFAFNLPAIVELGTATGFDFELIDQAGLGHEKLTQARN
QLLAEAAKHPDMLTSVRPNGLEDTPQFKIDIDQEKAQALGVSINDINTTL
GAAWGGSYVNDFIDRGRVKKVYVMSEAKYRMLPDDIGDWYVRAADGQMVP
FSAFSSSRWEYGSPRLERYNGLPSMEILGQAAPGKSTGEAMELMEQLASK
LPTGVGYDWTGMSYQERLSGNQAPSLYAISLIVVFLCLAALYESWSIPFS
VMLVVPLGVIGALLAATFRGLTNDVYFQVGLLTTIGLSAKNAILIVEFAK
DLMDKEGKGLIEATLDAVRMRLRPILMTSLAFILGVMPLVISTGAGSGAQ
NAVGTGVMGGMVTATVLAIFFVPVFFVVVRRRFS
Ligand information
Ligand ID
FUA
InChI
InChI=1S/C31H48O6/c1-17(2)9-8-10-20(28(35)36)26-22-15-24(34)27-29(5)13-12-23(33)18(3)21(29)11-14-30(27,6)31(22,7)16-25(26)37-19(4)32/h9,18,21-25,27,33-34H,8,10-16H2,1-7H3,(H,35,36)/b26-20-/t18-,21-,22-,23+,24+,25-,27-,29-,30-,31-/m0/s1
InChIKey
IECPWNUMDGFDKC-MZJAQBGESA-N
SMILES
Software
SMILES
CACTVS 3.341
C[C@@H]1[C@H](O)CC[C@@]2(C)[C@H]1CC[C@@]3(C)[C@H]2[C@H](O)C[C@H]4\C([C@H](C[C@]34C)OC(C)=O)=C(/CCC=C(C)C)C(O)=O
CACTVS 3.341
C[CH]1[CH](O)CC[C]2(C)[CH]1CC[C]3(C)[CH]2[CH](O)C[CH]4C([CH](C[C]34C)OC(C)=O)=C(CCC=C(C)C)C(O)=O
OpenEye OEToolkits 1.5.0
CC1C2CCC3(C(C2(CCC1O)C)C(CC4C3(CC(C4=C(CCC=C(C)C)C(=O)O)OC(=O)C)C)O)C
OpenEye OEToolkits 1.5.0
C[C@H]1[C@@H]2CC[C@]3([C@H]([C@]2(CC[C@H]1O)C)[C@@H](C[C@@H]\4[C@@]3(C[C@@H](/C4=C(/CCC=C(C)C)\C(=O)O)OC(=O)C)C)O)C
ACDLabs 10.04
O=C(O)/C(=C2/C1CC(O)C3C(C1(CC2OC(=O)C)C)(C)CCC4C(C)C(O)CCC34C)CC\C=C(/C)C
Formula
C31 H48 O6
Name
FUSIDIC ACID
ChEMBL
CHEMBL374975
DrugBank
DB02703
ZINC
ZINC000008143796
PDB chain
5jmn Chain A Residue 1101 [
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Receptor-Ligand Complex Structure
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PDB
5jmn
Transport of lipophilic carboxylates is mediated by transmembrane helix 2 in multidrug transporter AcrB.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
K334 H338
Binding residue
(residue number reindexed from 1)
K334 H338
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0015125
bile acid transmembrane transporter activity
GO:0015562
efflux transmembrane transporter activity
GO:0015567
alkane transmembrane transporter activity
GO:0022857
transmembrane transporter activity
GO:0042802
identical protein binding
GO:0042910
xenobiotic transmembrane transporter activity
GO:0042931
enterobactin transmembrane transporter activity
Biological Process
GO:0009410
response to xenobiotic stimulus
GO:0009636
response to toxic substance
GO:0015721
bile acid and bile salt transport
GO:0015895
alkane transport
GO:0015908
fatty acid transport
GO:0042908
xenobiotic transport
GO:0042930
enterobactin transport
GO:0046677
response to antibiotic
GO:0055085
transmembrane transport
GO:0140330
xenobiotic detoxification by transmembrane export across the cell outer membrane
Cellular Component
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0098567
periplasmic side of plasma membrane
GO:1990281
efflux pump complex
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5jmn
,
PDBe:5jmn
,
PDBj:5jmn
PDBsum
5jmn
PubMed
27982032
UniProt
P31224
|ACRB_ECOLI Multidrug efflux pump subunit AcrB (Gene Name=acrB)
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