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5PA1

rat catechol O-methyltransferase in complex with SAH and 6-(4-fluorophenyl)quinolin-8-ol

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0006584biological_processcatecholamine metabolic process
A0008171molecular_functionO-methyltransferase activity
A0016206molecular_functioncatechol O-methyltransferase activity
Functional Information from PDB Data
site_idAC1
Number of Residues5
Detailsbinding site for residue MG A 301
ChainResidue
AASP141
AASP169
AASN170
A7JS308
AHOH420

site_idAC2
Number of Residues3
Detailsbinding site for residue CL A 302
ChainResidue
AASP44
AALA45
ATYR200

site_idAC3
Number of Residues5
Detailsbinding site for residue SO4 A 303
ChainResidue
AGLY83
AARG85
ALYS111
ALYS128
APRO82

site_idAC4
Number of Residues5
Detailsbinding site for residue SO4 A 304
ChainResidue
ATRP143
ALYS144
A7JS308
AHOH408
AHOH508

site_idAC5
Number of Residues22
Detailsbinding site for residue SAH A 307
ChainResidue
AMET40
AASN41
AVAL42
AGLY66
AALA67
ATYR68
ATYR71
ASER72
AGLU90
AMET91
ATYR95
AGLY117
AALA118
ASER119
AGLN120
AASP141
AHIS142
ATRP143
A7JS308
AHOH430
AHOH489
AHOH526

site_idAC6
Number of Residues16
Detailsbinding site for residue 7JS A 308
ChainResidue
AALA97
AGLN100
AGLN101
AASP141
AHIS142
ATRP143
ALYS144
AASP169
AASN170
AGLU199
AMG301
ASO4304
AD1D305
ANHE306
ASAH307
AHOH420

site_idAC7
Number of Residues13
Detailsbinding site for residues D1D A 305 and NHE A 306
ChainResidue
AGLU37
ATRP38
AALA96
AALA97
AGLN100
AILE114
ALEU115
AASN116
AMET201
A7JS308
AHOH405
AHOH429
AHOH537

site_idAC8
Number of Residues13
Detailsbinding site for residues D1D A 305 and NHE A 306
ChainResidue
AGLU37
ATRP38
AALA96
AALA97
AGLN100
AILE114
ALEU115
AASN116
AMET201
A7JS308
AHOH405
AHOH429
AHOH537

site_idAC9
Number of Residues13
Detailsbinding site for residues D1D A 305 and NHE A 306
ChainResidue
AGLU37
ATRP38
AALA96
AALA97
AGLN100
AILE114
ALEU115
AASN116
AMET201
A7JS308
AHOH405
AHOH429
AHOH537

site_idAD1
Number of Residues13
Detailsbinding site for residues D1D A 305 and NHE A 306
ChainResidue
AGLN100
AILE114
ALEU115
AASN116
AMET201
A7JS308
AHOH405
AHOH429
AHOH537
AGLU37
ATRP38
AALA96
AALA97

site_idAD2
Number of Residues13
Detailsbinding site for residues D1D A 305 and NHE A 306
ChainResidue
AGLU37
ATRP38
AALA96
AALA97
AGLN100
AILE114
ALEU115
AASN116
AMET201
A7JS308
AHOH405
AHOH429
AHOH537

site_idAD3
Number of Residues13
Detailsbinding site for residues D1D A 305 and NHE A 306
ChainResidue
AGLU37
ATRP38
AALA96
AALA97
AGLN100
AILE114
ALEU115
AASN116
AMET201
A7JS308
AHOH405
AHOH429
AHOH537

site_idAD4
Number of Residues13
Detailsbinding site for residues D1D A 305 and NHE A 306
ChainResidue
AGLU37
ATRP38
AALA96
AALA97
AGLN100
AILE114
ALEU115
AASN116
AMET201
A7JS308
AHOH405
AHOH429
AHOH537

site_idAD5
Number of Residues13
Detailsbinding site for residues D1D A 305 and NHE A 306
ChainResidue
AGLU37
ATRP38
AALA96
AALA97
AGLN100
AILE114
ALEU115
AASN116
AMET201
A7JS308
AHOH405
AHOH429
AHOH537

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU01019","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"12237326","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues3
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU01019","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues7
DetailsBinding site: {}
ChainResidueDetails

Catalytic Information from CSA
site_idMCSA1
Number of Residues5
DetailsM-CSA 915
ChainResidueDetails
AASP141metal ligand
ALYS144proton shuttle (general acid/base)
AASP169metal ligand
AASN170metal ligand
AGLU199electrostatic stabiliser

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PDB entries from 2026-01-21

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