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6C7I

Crystal structure of human phosphodiesterase 2A with 1-(2-chloro-5-methoxy-phenyl)-N-isobutyl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline-8-carboxamide

Functional Information from GO Data
ChainGOidnamespacecontents
A0004114molecular_function3',5'-cyclic-nucleotide phosphodiesterase activity
A0007165biological_processsignal transduction
A0008081molecular_functionphosphoric diester hydrolase activity
B0004114molecular_function3',5'-cyclic-nucleotide phosphodiesterase activity
B0007165biological_processsignal transduction
B0008081molecular_functionphosphoric diester hydrolase activity
C0004114molecular_function3',5'-cyclic-nucleotide phosphodiesterase activity
C0007165biological_processsignal transduction
C0008081molecular_functionphosphoric diester hydrolase activity
D0004114molecular_function3',5'-cyclic-nucleotide phosphodiesterase activity
D0007165biological_processsignal transduction
D0008081molecular_functionphosphoric diester hydrolase activity
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue EP7 A 1001
ChainResidue
ATHR768
AHOH1119
AHOH1128
AHOH1142
AHOH1219
AHOH1237
AHOH1270
DLYS584
ALEU770
AASP808
ALEU809
AGLN812
AILE826
APHE830
AGLN859
APHE862

site_idAC2
Number of Residues6
Detailsbinding site for residue ZN A 1002
ChainResidue
AHIS660
AHIS696
AASP697
AASP808
AHOH1136
AHOH1249

site_idAC3
Number of Residues6
Detailsbinding site for residue MG A 1003
ChainResidue
AASP697
AHOH1134
AHOH1136
AHOH1176
AHOH1191
AHOH1265

site_idAC4
Number of Residues18
Detailsbinding site for residue EP7 B 1001
ChainResidue
BHIS656
BTHR768
BLEU770
BASP808
BLEU809
BGLN812
BILE826
BPHE830
BGLN859
BPHE862
BILE866
BHOH1106
BHOH1149
BHOH1151
BHOH1225
BHOH1248
BHOH1264
BHOH1343

site_idAC5
Number of Residues6
Detailsbinding site for residue ZN B 1002
ChainResidue
BHIS660
BHIS696
BASP697
BASP808
BHOH1110
BHOH1254

site_idAC6
Number of Residues6
Detailsbinding site for residue MG B 1003
ChainResidue
BASP697
BHOH1110
BHOH1119
BHOH1154
BHOH1165
BHOH1260

site_idAC7
Number of Residues12
Detailsbinding site for residue EP7 C 1001
ChainResidue
CTHR768
CLEU770
CASP808
CGLN812
CILE826
CPHE830
CPHE862
CHOH1113
CHOH1120
CHOH1169
CHOH1199
CHOH1222

site_idAC8
Number of Residues6
Detailsbinding site for residue ZN C 1002
ChainResidue
CHIS660
CHIS696
CASP697
CASP808
CHOH1103
CHOH1193

site_idAC9
Number of Residues6
Detailsbinding site for residue MG C 1003
ChainResidue
CASP697
CHOH1103
CHOH1134
CHOH1147
CHOH1192
CHOH1246

site_idAD1
Number of Residues15
Detailsbinding site for residue EP7 D 1001
ChainResidue
AASP588
AGLN591
DTHR768
DLEU770
DASP808
DLEU809
DGLN812
DILE826
DPHE830
DPHE862
DHOH1118
DHOH1175
DHOH1223
DHOH1253
DHOH1294

site_idAD2
Number of Residues6
Detailsbinding site for residue ZN D 1002
ChainResidue
DASP697
DASP808
DHOH1144
DHOH1184
DHIS660
DHIS696

site_idAD3
Number of Residues6
Detailsbinding site for residue MG D 1003
ChainResidue
DASP697
DHOH1140
DHOH1144
DHOH1168
DHOH1169
DHOH1251

Functional Information from PROSITE/UniProt
site_idPS00126
Number of Residues12
DetailsPDEASE_I_1 3'5'-cyclic nucleotide phosphodiesterase domain signature. HDLdHrGtnNsF
ChainResidueDetails
AHIS696-PHE707

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton donor => ECO:0000250|UniProtKB:O76083
ChainResidueDetails
ASER912
BSER912
CSER912
DSER912

site_idSWS_FT_FI2
Number of Residues20
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:Q922S4
ChainResidueDetails
APHE687
BGLN755
CPHE687
CGLY702
CSER721
CASN744
CGLN755
DPHE687
DGLY702
DSER721
DASN744
AGLY702
DGLN755
ASER721
AASN744
AGLN755
BPHE687
BGLY702
BSER721
BASN744

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:15938621, ECO:0000269|PubMed:19828435, ECO:0000269|PubMed:23899287, ECO:0007744|PDB:1Z1L, ECO:0007744|PDB:3IBJ, ECO:0007744|PDB:3ITM, ECO:0007744|PDB:3ITU, ECO:0007744|PDB:4HTX, ECO:0007744|PDB:4HTZ, ECO:0007744|PDB:4JIB
ChainResidueDetails
ALEU916
BLEU916
CLEU916
DLEU916

227344

PDB entries from 2024-11-13

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