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3OE9

Crystal structure of the chemokine CXCR4 receptor in complex with a small molecule antagonist IT1t in P1 spacegroup

Functional Information from GO Data
ChainGOidnamespacecontents
A0003796molecular_functionlysozyme activity
A0004930molecular_functionG protein-coupled receptor activity
A0007186biological_processG protein-coupled receptor signaling pathway
A0009253biological_processpeptidoglycan catabolic process
A0016020cellular_componentmembrane
A0016798molecular_functionhydrolase activity, acting on glycosyl bonds
A0016998biological_processcell wall macromolecule catabolic process
A0019955molecular_functioncytokine binding
A0030430cellular_componenthost cell cytoplasm
A0031640biological_processkilling of cells of another organism
A0042742biological_processdefense response to bacterium
A0044659biological_processviral release from host cell by cytolysis
B0003796molecular_functionlysozyme activity
B0004930molecular_functionG protein-coupled receptor activity
B0007186biological_processG protein-coupled receptor signaling pathway
B0009253biological_processpeptidoglycan catabolic process
B0016020cellular_componentmembrane
B0016798molecular_functionhydrolase activity, acting on glycosyl bonds
B0016998biological_processcell wall macromolecule catabolic process
B0019955molecular_functioncytokine binding
B0030430cellular_componenthost cell cytoplasm
B0031640biological_processkilling of cells of another organism
B0042742biological_processdefense response to bacterium
B0044659biological_processviral release from host cell by cytolysis
Functional Information from PDB Data
site_idAC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE ITD A 1500
ChainResidue
ALYS38
AGLU288
ATRP94
AASP97
AVAL112
AHIS113
AARG183
ACYS186
AASP187
AARG188

site_idAC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE ITD B 1500
ChainResidue
BTRP94
BASP97
BVAL112
BTYR116
BARG183
BILE185
BCYS186
BASP187
BARG188
BGLU288

Functional Information from PROSITE/UniProt
site_idPS00237
Number of Residues17
DetailsG_PROTEIN_RECEP_F1_1 G-protein coupled receptors family 1 signature. SSVwILAFISLDRYLaI
ChainResidueDetails
ASER122-ILE138

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues48
DetailsTRANSMEM: Helical; Name=1 => ECO:0000269|PubMed:20929726
ChainResidueDetails
AILE39-MET63
BILE39-MET63

site_idSWS_FT_FI2
Number of Residues72
DetailsTOPO_DOM: Cytoplasmic => ECO:0000269|PubMed:20929726
ChainResidueDetails
AGLY64-ARG77
ASER131-LYS154
BGLY64-ARG77
BSER131-LYS154

site_idSWS_FT_FI3
Number of Residues42
DetailsTRANSMEM: Helical; Name=2 => ECO:0000269|PubMed:20929726
ChainResidueDetails
ALEU78-VAL99
BLEU78-VAL99

site_idSWS_FT_FI4
Number of Residues100
DetailsTOPO_DOM: Extracellular => ECO:0000269|PubMed:20929726
ChainResidueDetails
AALA100-LYS110
AALA175-TRP195
AASP262-LYS282
BALA100-LYS110
BALA175-TRP195
BASP262-LYS282

site_idSWS_FT_FI5
Number of Residues38
DetailsTRANSMEM: Helical; Name=3 => ECO:0000269|PubMed:20929726
ChainResidueDetails
AALA111-ILE130
BALA111-ILE130

site_idSWS_FT_FI6
Number of Residues38
DetailsTRANSMEM: Helical; Name=4 => ECO:0000269|PubMed:20929726
ChainResidueDetails
AVAL155-PHE174
BVAL155-PHE174

site_idSWS_FT_FI7
Number of Residues40
DetailsTRANSMEM: Helical; Name=5 => ECO:0000269|PubMed:20929726
ChainResidueDetails
AVAL196-LEU216
BVAL196-LEU216

site_idSWS_FT_FI8
Number of Residues38
DetailsTRANSMEM: Helical; Name=6 => ECO:0000269|PubMed:20929726
ChainResidueDetails
AVAL242-ILE261
BVAL242-ILE261

site_idSWS_FT_FI9
Number of Residues38
DetailsTRANSMEM: Helical; Name=7 => ECO:0000269|PubMed:20929726
ChainResidueDetails
ATRP283-TYR302
BTRP283-TYR302

site_idSWS_FT_FI10
Number of Residues2
DetailsSITE: Chemokine binding
ChainResidueDetails
AASP171
BASP171

site_idSWS_FT_FI11
Number of Residues2
DetailsSITE: Chemokine binding => ECO:0000269|PubMed:20929726, ECO:0000305|PubMed:10825158
ChainResidueDetails
AGLU288
BGLU288

site_idSWS_FT_FI12
Number of Residues4
DetailsMOD_RES: Sulfotyrosine; partial => ECO:0000269|PubMed:18834145
ChainResidueDetails
ATYR7
ATYR12
BTYR7
BTYR12

site_idSWS_FT_FI13
Number of Residues2
DetailsMOD_RES: Sulfotyrosine => ECO:0000269|PubMed:12034737, ECO:0000269|PubMed:16725153, ECO:0000269|PubMed:18834145
ChainResidueDetails
ATYR21
BTYR21

site_idSWS_FT_FI14
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:18669648
ChainResidueDetails
ASER319
BSER319

site_idSWS_FT_FI15
Number of Residues2
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000269|PubMed:10756055
ChainResidueDetails
AASN11
BASN11

site_idSWS_FT_FI16
Number of Residues2
DetailsCARBOHYD: O-linked (Xyl...) (chondroitin sulfate) serine => ECO:0000269|PubMed:12034737
ChainResidueDetails
ASER18
BSER18

site_idSWS_FT_FI17
Number of Residues2
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255
ChainResidueDetails
AASN176
BASN176

Catalytic Information from CSA
site_idMCSA1
Number of Residues
DetailsM-CSA 921
ChainResidueDetails

site_idMCSA2
Number of Residues
DetailsM-CSA 921
ChainResidueDetails

222926

PDB entries from 2024-07-24

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