Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

6C7E

Crystal structure of human phosphodiesterase 2A with 1-(2-chlorophenyl)-N,4-dimethyl-[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 Residues12
Detailsbinding site for residue EOG A 1001
ChainResidue
ALEU770
AHOH1167
AHOH1225
AHOH1276
ALEU809
AGLN812
AILE826
APHE830
AMET847
AGLN859
APHE862
AHOH1156

site_idAC2
Number of Residues6
Detailsbinding site for residue ZN A 1002
ChainResidue
AHIS660
AHIS696
AASP697
AASP808
AHOH1135
AHOH1260

site_idAC3
Number of Residues6
Detailsbinding site for residue MG A 1003
ChainResidue
AASP697
AHOH1128
AHOH1135
AHOH1180
AHOH1205
AHOH1280

site_idAC4
Number of Residues11
Detailsbinding site for residue EOG B 1001
ChainResidue
BLEU770
BLEU809
BGLN812
BILE826
BPHE830
BPHE862
BHOH1134
BHOH1146
BHOH1147
BHOH1216
BHOH1275

site_idAC5
Number of Residues6
Detailsbinding site for residue ZN B 1002
ChainResidue
BHIS660
BHIS696
BASP697
BASP808
BHOH1118
BHOH1268

site_idAC6
Number of Residues6
Detailsbinding site for residue MG B 1003
ChainResidue
BASP697
BHOH1118
BHOH1127
BHOH1151
BHOH1165
BHOH1267

site_idAC7
Number of Residues10
Detailsbinding site for residue EOG C 1001
ChainResidue
CLEU770
CLEU809
CGLN812
CILE826
CPHE830
CPHE862
CHOH1104
CHOH1160
CHOH1165
CHOH1239

site_idAC8
Number of Residues6
Detailsbinding site for residue ZN C 1002
ChainResidue
CHIS660
CHIS696
CASP697
CASP808
CHOH1107
CHOH1226

site_idAC9
Number of Residues6
Detailsbinding site for residue MG C 1003
ChainResidue
CASP697
CHOH1107
CHOH1134
CHOH1142
CHOH1164
CHOH1246

site_idAD1
Number of Residues9
Detailsbinding site for residue EOG D 1001
ChainResidue
DLEU770
DGLN812
DILE826
DPHE830
DPHE862
DHOH1137
DHOH1161
DHOH1182
DHOH1248

site_idAD2
Number of Residues6
Detailsbinding site for residue ZN D 1002
ChainResidue
DHIS660
DHIS696
DASP697
DASP808
DHOH1116
DHOH1227

site_idAD3
Number of Residues6
Detailsbinding site for residue MG D 1003
ChainResidue
DASP697
DHOH1116
DHOH1127
DHOH1195
DHOH1219
DHOH1272

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

222624

PDB entries from 2024-07-17

PDB statisticsPDBj update infoContact PDBjnumon