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6PS3

XFEL beta2 AR structure by ligand exchange from Timolol to Carvedilol.

Functional Information from GO Data
ChainGOidnamespacecontents
A0003796molecular_functionlysozyme activity
A0003824molecular_functioncatalytic activity
A0004930molecular_functionG protein-coupled receptor activity
A0004941molecular_functionbeta2-adrenergic receptor activity
A0006940biological_processregulation of smooth muscle contraction
A0007186biological_processG protein-coupled receptor signaling pathway
A0007189biological_processadenylate cyclase-activating G protein-coupled receptor signaling pathway
A0009253biological_processpeptidoglycan catabolic process
A0016020cellular_componentmembrane
A0016787molecular_functionhydrolase activity
A0016798molecular_functionhydrolase activity, acting on glycosyl bonds
A0016998biological_processcell wall macromolecule catabolic process
A0030430cellular_componenthost cell cytoplasm
A0031640biological_processkilling of cells of another organism
A0042742biological_processdefense response to bacterium
A0044659biological_processviral release from host cell by cytolysis
A0097746biological_processblood vessel diameter maintenance
Functional Information from PDB Data
site_idAC1
Number of Residues12
Detailsbinding site for residue CVD A 1201
ChainResidue
AHIS93
ATYR308
AASN312
ATYR316
AILE94
AASP113
ATYR199
ASER203
ASER207
APHE289
APHE290
AASN293

site_idAC2
Number of Residues5
Detailsbinding site for residue SO4 A 1202
ChainResidue
ATHR66
AVAL67
ATHR68
AARG131
ASER143

site_idAC3
Number of Residues3
Detailsbinding site for residue SO4 A 1203
ChainResidue
ALYS270
ALYS273
AARG328

site_idAC4
Number of Residues4
Detailsbinding site for residue SO4 A 1204
ChainResidue
APHE1114
ATHR1115
AASN1116
ASER1117

site_idAC5
Number of Residues4
Detailsbinding site for residue SO4 A 1205
ChainResidue
ATHR1142
APRO1143
AASN1144
AARG1145

site_idAC6
Number of Residues5
Detailsbinding site for residue CLR A 1206
ChainResidue
ATHR73
ACYS77
AARG151
ATRP158
AOLC1207

site_idAC7
Number of Residues3
Detailsbinding site for residue OLC A 1207
ChainResidue
AILE55
AGLN65
ACLR1206

site_idAC8
Number of Residues1
Detailsbinding site for residue OLC A 1208
ChainResidue
ASER41

site_idAC9
Number of Residues3
Detailsbinding site for residue OLC A 1209
ChainResidue
AGLN197
ALEU339
AOLA1213

site_idAD1
Number of Residues3
Detailsbinding site for residue OLC A 1210
ChainResidue
ATRP173
ALEU340
ALEU342

site_idAD2
Number of Residues2
Detailsbinding site for residue OLC A 1211
ChainResidue
AVAL126
APHE133

site_idAD3
Number of Residues1
Detailsbinding site for residue OLC A 1212
ChainResidue
ATRP122

site_idAD4
Number of Residues1
Detailsbinding site for residue OLA A 1213
ChainResidue
AOLC1209

site_idAD5
Number of Residues3
Detailsbinding site for residue OLA A 1214
ChainResidue
ATHR100
APHE217
AVAL218

site_idAD6
Number of Residues1
Detailsbinding site for residue OLA A 1215
ChainResidue
AVAL216

Functional Information from PROSITE/UniProt
site_idPS00237
Number of Residues17
DetailsG_PROTEIN_RECEP_F1_1 G-protein coupled receptors family 1 signature. ASIwTLCVIAVDRYFaI
ChainResidueDetails
AALA119-ILE135

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI2
Number of Residues23
DetailsTransmembrane: {"description":"Helical; Name=1"}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues32
DetailsTopological domain: {"description":"Cytoplasmic"}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues23
DetailsTransmembrane: {"description":"Helical; Name=2"}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues37
DetailsTopological domain: {"description":"Extracellular"}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues22
DetailsTransmembrane: {"description":"Helical; Name=3"}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues23
DetailsTransmembrane: {"description":"Helical; Name=4"}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues23
DetailsTransmembrane: {"description":"Helical; Name=5"}
ChainResidueDetails

site_idSWS_FT_FI9
Number of Residues23
DetailsTransmembrane: {"description":"Helical; Name=6"}
ChainResidueDetails

site_idSWS_FT_FI10
Number of Residues23
DetailsTransmembrane: {"description":"Helical; Name=7"}
ChainResidueDetails

site_idSWS_FT_FI11
Number of Residues5
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"18547522","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"3D4S","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI12
Number of Residues1
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"17952055","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17962520","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"2RH1","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI13
Number of Residues1
DetailsModified residue: {"description":"Phosphotyrosine","evidences":[{"source":"PubMed","id":"8521811","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI14
Number of Residues1
DetailsModified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"17525332","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI15
Number of Residues2
DetailsModified residue: {"description":"Phosphoserine; by PKA","evidences":[{"evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI16
Number of Residues1
DetailsLipidation: {"description":"S-palmitoyl cysteine","evidences":[{"source":"PubMed","id":"27481942","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI17
Number of Residues1
DetailsLipidation: {"description":"S-palmitoyl cysteine","evidences":[{"source":"PubMed","id":"17962520","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18547522","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"2540197","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"27481942","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

242842

PDB entries from 2025-10-08

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