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4DX7

Transport of drugs by the multidrug transporter AcrB involves an access and a deep binding pocket that are separated by a switch-loop

Functional Information from GO Data
ChainGOidnamespacecontents
A0005515molecular_functionprotein binding
A0005886cellular_componentplasma membrane
A0009410biological_processresponse to xenobiotic stimulus
A0009636biological_processresponse to toxic substance
A0015125molecular_functionbile acid transmembrane transporter activity
A0015562molecular_functionefflux transmembrane transporter activity
A0015567molecular_functionalkane transmembrane transporter activity
A0015721biological_processbile acid and bile salt transport
A0015895biological_processalkane transport
A0015908biological_processfatty acid transport
A0016020cellular_componentmembrane
A0022857molecular_functiontransmembrane transporter activity
A0042802molecular_functionidentical protein binding
A0042908biological_processxenobiotic transport
A0042910molecular_functionxenobiotic transmembrane transporter activity
A0042930biological_processenterobactin transport
A0042931molecular_functionenterobactin transmembrane transporter activity
A0046677biological_processresponse to antibiotic
A0055085biological_processtransmembrane transport
A0098567cellular_componentperiplasmic side of plasma membrane
A0140330biological_processxenobiotic detoxification by transmembrane export across the cell outer membrane
A1990281cellular_componentefflux pump complex
B0005515molecular_functionprotein binding
B0005886cellular_componentplasma membrane
B0009410biological_processresponse to xenobiotic stimulus
B0009636biological_processresponse to toxic substance
B0015125molecular_functionbile acid transmembrane transporter activity
B0015562molecular_functionefflux transmembrane transporter activity
B0015567molecular_functionalkane transmembrane transporter activity
B0015721biological_processbile acid and bile salt transport
B0015895biological_processalkane transport
B0015908biological_processfatty acid transport
B0016020cellular_componentmembrane
B0022857molecular_functiontransmembrane transporter activity
B0042802molecular_functionidentical protein binding
B0042908biological_processxenobiotic transport
B0042910molecular_functionxenobiotic transmembrane transporter activity
B0042930biological_processenterobactin transport
B0042931molecular_functionenterobactin transmembrane transporter activity
B0046677biological_processresponse to antibiotic
B0055085biological_processtransmembrane transport
B0098567cellular_componentperiplasmic side of plasma membrane
B0140330biological_processxenobiotic detoxification by transmembrane export across the cell outer membrane
B1990281cellular_componentefflux pump complex
C0005515molecular_functionprotein binding
C0005886cellular_componentplasma membrane
C0009410biological_processresponse to xenobiotic stimulus
C0009636biological_processresponse to toxic substance
C0015125molecular_functionbile acid transmembrane transporter activity
C0015562molecular_functionefflux transmembrane transporter activity
C0015567molecular_functionalkane transmembrane transporter activity
C0015721biological_processbile acid and bile salt transport
C0015895biological_processalkane transport
C0015908biological_processfatty acid transport
C0016020cellular_componentmembrane
C0022857molecular_functiontransmembrane transporter activity
C0042802molecular_functionidentical protein binding
C0042908biological_processxenobiotic transport
C0042910molecular_functionxenobiotic transmembrane transporter activity
C0042930biological_processenterobactin transport
C0042931molecular_functionenterobactin transmembrane transporter activity
C0046677biological_processresponse to antibiotic
C0055085biological_processtransmembrane transport
C0098567cellular_componentperiplasmic side of plasma membrane
C0140330biological_processxenobiotic detoxification by transmembrane export across the cell outer membrane
C1990281cellular_componentefflux pump complex
Functional Information from PDB Data
site_idAC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE LMT A 1101
ChainResidue
ALEU28
AVAL32
AVAL341
APRO373
APHE380
AHOH1304
AHOH1410
BLMT1101

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE LMT A 1102
ChainResidue
ASER561
ATYR877
ALEU881
AVAL884
AGLN928
AHOH1581
APHE556

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE LMT A 1103
ChainResidue
AGLY440
AGLY444
AALA890
ALEU891
CARG8

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE LMT A 1104
ChainResidue
AILE335
AHIS338
AGLU339
AILE349
AASP633
AHOH1275

site_idAC5
Number of Residues12
DetailsBINDING SITE FOR RESIDUE DM2 A 1105
ChainResidue
AMET575
AGLY616
APHE617
ATHR676
AASP681
AARG717
AASN719
AGLU826
AMET862
ADM21106
AHOH1532
AHOH1617

site_idAC6
Number of Residues10
DetailsBINDING SITE FOR RESIDUE DM2 A 1106
ChainResidue
AMET575
APHE617
APHE664
APHE666
ATHR676
AGLN830
ADM21105
AHOH1564
AHOH1609
AHOH1692

site_idAC7
Number of Residues2
DetailsBINDING SITE FOR RESIDUE D12 A 1107
ChainResidue
AARG8
BHOH1683

site_idAC8
Number of Residues2
DetailsBINDING SITE FOR RESIDUE D10 A 1108
ChainResidue
ATRP895
AD101109

site_idAC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE D10 A 1109
ChainResidue
APHE885
ATRP895
AD101108

site_idBC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE LMT B 1101
ChainResidue
ALEU28
ALMT1101
BPHE458
BASN871
BGLN872
BSER875
BLEU876

site_idBC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE LMT B 1102
ChainResidue
BSER530
BGLY533
BARG536
BSER537
BARG540
BTYR541

site_idBC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE LMU B 1103
ChainResidue
BASP566
BPHE617
BPHE628
BPHE664
BPHE666
BASN667
BLEU668
BPRO669
BVAL672
BHOH1549
BHOH1645

site_idBC4
Number of Residues9
DetailsBINDING SITE FOR RESIDUE DM2 B 1104
ChainResidue
BGLN89
BGLU130
BGLN176
BPHE178
BGLY179
BILE277
BVAL612
BPHE615
BHOH1692

site_idBC5
Number of Residues1
DetailsBINDING SITE FOR RESIDUE D10 B 1105
ChainResidue
CTRP895

site_idBC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL B 1106
ChainResidue
BARG239
BTYR758
BASN760
BASP761
BHOH1457
CPRO119
CGLN120

site_idBC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL B 1107
ChainResidue
BSER807
BHOH1357
BPRO783
BSER805
BSER806

site_idBC8
Number of Residues2
DetailsBINDING SITE FOR RESIDUE D12 B 1109
ChainResidue
BLYS29
CPHE458

site_idBC9
Number of Residues8
DetailsBINDING SITE FOR RESIDUE LMT C 1101
ChainResidue
CSER530
CGLY533
CARG536
CSER537
CARG540
CTYR541
CPHE1020
CHOH1540

site_idCC1
Number of Residues1
DetailsBINDING SITE FOR RESIDUE D12 C 1102
ChainResidue
CTRP895

site_idCC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL C 1103
ChainResidue
CARG185
CGLU273
CASN274
CGLY755
CGLY756
CTYR772
CHOH1340

site_idCC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE D10 C 1104
ChainResidue
BLYS29
CPHE458

site_idCC4
Number of Residues1
DetailsBINDING SITE FOR RESIDUE D12 C 1106
ChainResidue
CTRP13

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues462
DetailsTOPO_DOM: Cytoplasmic => ECO:0000269|PubMed:15919996
ChainResidueDetails
AMET1-PRO9
BGLU414-ILE438
BALA491-THR538
BALA889-PRO898
BLEU944-LEU972
BILE1019-HIS1049
CMET1-PRO9
CLEU357-THR365
CGLU414-ILE438
CALA491-THR538
CALA889-PRO898
ALEU357-THR365
CLEU944-LEU972
CILE1019-HIS1049
AGLU414-ILE438
AALA491-THR538
AALA889-PRO898
ALEU944-LEU972
AILE1019-HIS1049
BMET1-PRO9
BLEU357-THR365

site_idSWS_FT_FI2
Number of Residues54
DetailsTRANSMEM: Helical; Name=1
ChainResidueDetails
AILE10-LEU28
BILE10-LEU28
CILE10-LEU28

site_idSWS_FT_FI3
Number of Residues1932
DetailsTOPO_DOM: Periplasmic => ECO:0000269|PubMed:15919996
ChainResidueDetails
ALYS29-SER336
BPHE556-ASN871
BARG919-ASP924
BTHR993-GLY998
CLYS29-SER336
CPHE386-ASN391
CPHE458-ALA465
CPHE556-ASN871
CARG919-ASP924
CTHR993-GLY998
APHE386-ASN391
APHE458-ALA465
APHE556-ASN871
AARG919-ASP924
ATHR993-GLY998
BLYS29-SER336
BPHE386-ASN391
BPHE458-ALA465

site_idSWS_FT_FI4
Number of Residues57
DetailsTRANSMEM: Helical; Name=2
ChainResidueDetails
AILE337-TYR356
BILE337-TYR356
CILE337-TYR356

site_idSWS_FT_FI5
Number of Residues57
DetailsTRANSMEM: Helical; Name=3
ChainResidueDetails
ALEU366-ALA385
BLEU366-ALA385
CLEU366-ALA385

site_idSWS_FT_FI6
Number of Residues63
DetailsTRANSMEM: Helical; Name=4
ChainResidueDetails
ATHR392-VAL413
BTHR392-VAL413
CTHR392-VAL413

site_idSWS_FT_FI7
Number of Residues54
DetailsTRANSMEM: Helical; Name=5
ChainResidueDetails
AGLN439-ALA457
BGLN439-ALA457
CGLN439-ALA457

site_idSWS_FT_FI8
Number of Residues72
DetailsTRANSMEM: Helical; Name=6
ChainResidueDetails
AILE466-PRO490
BILE466-PRO490
CILE466-PRO490

site_idSWS_FT_FI9
Number of Residues48
DetailsTRANSMEM: Helical; Name=7
ChainResidueDetails
AGLY539-LEU555
BGLY539-LEU555
CGLY539-LEU555

site_idSWS_FT_FI10
Number of Residues48
DetailsTRANSMEM: Helical; Name=8
ChainResidueDetails
AGLN872-LEU888
BGLN872-LEU888
CGLN872-LEU888

site_idSWS_FT_FI11
Number of Residues57
DetailsTRANSMEM: Helical; Name=9
ChainResidueDetails
APHE899-PHE918
BPHE899-PHE918
CPHE899-PHE918

site_idSWS_FT_FI12
Number of Residues54
DetailsTRANSMEM: Helical; Name=10
ChainResidueDetails
AVAL925-ILE943
BVAL925-ILE943
CVAL925-ILE943

site_idSWS_FT_FI13
Number of Residues57
DetailsTRANSMEM: Helical; Name=11
ChainResidueDetails
AARG973-SER992
BARG973-SER992
CARG973-SER992

site_idSWS_FT_FI14
Number of Residues57
DetailsTRANSMEM: Helical; Name=12
ChainResidueDetails
AALA999-ALA1018
BALA999-ALA1018
CALA999-ALA1018

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PDB entries from 2024-11-06

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