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1O95

Ternary complex between trimethylamine dehydrogenase and electron transferring flavoprotein

Functional Information from GO Data
ChainGOidnamespacecontents
A0010181molecular_functionFMN binding
A0016491molecular_functionoxidoreductase activity
A0046872molecular_functionmetal ion binding
A0050470molecular_functiontrimethylamine dehydrogenase activity
A0051536molecular_functioniron-sulfur cluster binding
A0051539molecular_function4 iron, 4 sulfur cluster binding
B0010181molecular_functionFMN binding
B0016491molecular_functionoxidoreductase activity
B0046872molecular_functionmetal ion binding
B0050470molecular_functiontrimethylamine dehydrogenase activity
B0051536molecular_functioniron-sulfur cluster binding
B0051539molecular_function4 iron, 4 sulfur cluster binding
C0000166molecular_functionnucleotide binding
C0009055molecular_functionelectron transfer activity
D0009055molecular_functionelectron transfer activity
D0033539biological_processfatty acid beta-oxidation using acyl-CoA dehydrogenase
D0050660molecular_functionflavin adenine dinucleotide binding
E0000166molecular_functionnucleotide binding
E0009055molecular_functionelectron transfer activity
F0009055molecular_functionelectron transfer activity
F0033539biological_processfatty acid beta-oxidation using acyl-CoA dehydrogenase
F0050660molecular_functionflavin adenine dinucleotide binding
Functional Information from PDB Data
site_idAC1
Number of Residues19
DetailsBINDING SITE FOR RESIDUE FMN A 1730
ChainResidue
AVAL27
ATRP264
AASP267
AALA268
AVAL297
AARG299
ACYS320
AALA321
AARG322
APRO323
AILE352
APRO28
AHIS29
ACYS30
ATYR60
AGLU103
ATYR169
AHIS172
AARG222

site_idAC2
Number of Residues16
DetailsBINDING SITE FOR RESIDUE ADP A 1731
ChainResidue
AVAL395
AGLY396
AGLY398
APRO399
ASER400
AASP419
ATHR420
AGLY426
AHIS427
APRO469
AMET470
AALA486
ATHR487
AGLY488
AGLY673
AASP674

site_idAC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SF4 A 1732
ChainResidue
AARG322
AILE325
ACYS345
AILE346
AGLY347
ACYS348
AASN349
AVAL350
ACYS351
ACYS364
ATHR365

site_idAC4
Number of Residues20
DetailsBINDING SITE FOR RESIDUE FMN B 1730
ChainResidue
BVAL27
BPRO28
BHIS29
BCYS30
BGLU59
BTYR60
BGLU103
BTYR169
BHIS172
BARG222
BTRP264
BASP267
BVAL297
BARG299
BCYS320
BALA321
BARG322
BPRO323
BCYS351
BILE352

site_idAC5
Number of Residues15
DetailsBINDING SITE FOR RESIDUE ADP B 1731
ChainResidue
BVAL395
BGLY396
BGLY398
BPRO399
BSER400
BASP419
BTHR420
BGLY426
BHIS427
BMET470
BALA486
BTHR487
BGLY488
BGLY673
BASP674

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SF4 B 1732
ChainResidue
BARG322
BILE325
BCYS345
BILE346
BGLY347
BCYS348
BASN349
BVAL350
BCYS351
BCYS364
BTHR365

site_idAC7
Number of Residues15
DetailsBINDING SITE FOR RESIDUE AMP C 1236
ChainResidue
CALA118
CGLY119
CGLN121
CSER122
CTYR127
CALA128
CSER129
CTHR130
CALA6
CVAL7
CASN36
CASP39
CVAL62
CVAL64
CVAL100

site_idAC8
Number of Residues16
DetailsBINDING SITE FOR RESIDUE AMP E 1237
ChainResidue
EALA6
EVAL7
ELYS8
EASN36
EASP39
EVAL64
EVAL100
EALA118
EGLY119
EGLN121
ESER122
EALA126
ETYR127
EALA128
ESER129
ETHR130

Functional Information from PROSITE/UniProt
site_idPS00696
Number of Residues27
DetailsETF_ALPHA Electron transfer flavoprotein alpha-subunit signature. LYVAmGISGsIQHmaGmkhvptIiAVN
ChainResidueDetails
DLEU262-ASN288

site_idPS01065
Number of Residues22
DetailsETF_BETA Electron transfer flavoprotein beta-subunit signature. IrRelEGGmlQeVeincPaVLT
ChainResidueDetails
CILE160-THR181

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsActive site: {"description":"Proton donor","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues34
DetailsBinding site: {"evidences":[{"source":"PDB","id":"1DJN","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1DJQ","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1O94","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1O95","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2TMD","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues2
DetailsBinding site: {"description":"covalent","evidences":[{"source":"PubMed","id":"1551870","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"620783","evidenceCode":"ECO:0000305"},{"source":"PDB","id":"1O94","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1O95","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2TMD","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues6
DetailsBinding site: {"evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"PDB","id":"1DJQ","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"2TMD","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues2
DetailsModified residue: {"description":"S-6-FMN cysteine"}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues20
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"12567183","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1O94","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1O95","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1O96","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3CLR","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3CLS","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3CLU","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"PDB","id":"1O94","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1O95","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1O96","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3CLR","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3CLS","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3CLU","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ps9
ChainResidueDetails
ATYR174
AASP260

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ps9
ChainResidueDetails
BTYR174
BASP260

site_idCSA3
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ps9
ChainResidueDetails
AHIS172
ATYR169
AASP267

site_idCSA4
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ps9
ChainResidueDetails
BHIS172
BTYR169
BASP267

site_idMCSA1
Number of Residues4
DetailsM-CSA 114
ChainResidueDetails
ACYS30activator, alter redox potential, covalently attached
ATYR169activator, alter redox potential, electrostatic stabiliser, hydrogen bond donor
AHIS172activator, electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor
AASP267electrostatic stabiliser

site_idMCSA2
Number of Residues4
DetailsM-CSA 114
ChainResidueDetails
BCYS30activator, alter redox potential, covalently attached
BTYR169activator, alter redox potential, electrostatic stabiliser, hydrogen bond donor
BHIS172activator, electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor
BASP267electrostatic stabiliser

238582

PDB entries from 2025-07-09

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