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

6W43

APE1 AP-endonuclease product complex R237C

Functional Information from GO Data
ChainGOidnamespacecontents
A0003677molecular_functionDNA binding
A0003824molecular_functioncatalytic activity
A0004518molecular_functionnuclease activity
A0004519molecular_functionendonuclease activity
A0006281biological_processDNA repair
B0003677molecular_functionDNA binding
B0003824molecular_functioncatalytic activity
B0004518molecular_functionnuclease activity
B0004519molecular_functionendonuclease activity
B0006281biological_processDNA repair
Functional Information from PDB Data
site_idAC1
Number of Residues5
Detailsbinding site for residue EDO A 401
ChainResidue
ALYS63
AGLU86
AGLU87
ALEU179
AHOH549

site_idAC2
Number of Residues7
Detailsbinding site for residue EDO A 402
ChainResidue
AHOH550
AHOH619
AHOH627
ALEU44
ATYR45
AASN277
AHOH532

site_idAC3
Number of Residues6
Detailsbinding site for residue MG A 403
ChainResidue
AGLU96
AHOH504
AHOH518
AHOH527
D3DR1
PDC10

site_idAC4
Number of Residues5
Detailsbinding site for residue CL A 404
ChainResidue
AGLU101
ATRP119
AHOH605
BHIS116
BARG136

site_idAC5
Number of Residues7
Detailsbinding site for residue PEG B 401
ChainResidue
ATYR144
AGLU149
AHOH553
AHOH574
BHIS116
BGLN117
BTYR118

site_idAC6
Number of Residues8
Detailsbinding site for residue EDO B 402
ChainResidue
BTHR97
BCYS99
BLEU104
BTRP119
BSER120
BALA121
BGLY130
BHOH612

site_idAC7
Number of Residues4
Detailsbinding site for residue EDO B 403
ChainResidue
BASP189
BPHE192
BPHE240
BHOH530

Functional Information from PROSITE/UniProt
site_idPS00726
Number of Residues10
DetailsAP_NUCLEASE_F1_1 AP endonucleases family 1 signature 1. PDILCLQETK
ChainResidueDetails
APRO89-LYS98

site_idPS00727
Number of Residues17
DetailsAP_NUCLEASE_F1_2 AP endonucleases family 1 signature 2. DSFRHlypntpyaYTFW
ChainResidueDetails
AASP251-TRP267

site_idPS00728
Number of Residues12
DetailsAP_NUCLEASE_F1_3 AP endonucleases family 1 signature 3. NvGwRLDYfLlS
ChainResidueDetails
AASN277-SER288

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: ACT_SITE => ECO:0000269|PubMed:15380100
ChainResidueDetails
BTYR171
ATYR171

site_idSWS_FT_FI2
Number of Residues2
DetailsACT_SITE: Proton donor/acceptor => ECO:0000269|PubMed:9351835, ECO:0007744|PDB:1BIX
ChainResidueDetails
BASP210
AASP210

site_idSWS_FT_FI3
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU00764
ChainResidueDetails
AHIS309
BHIS309

site_idSWS_FT_FI4
Number of Residues12
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00764
ChainResidueDetails
AASP210
AASN212
AASP308
AHIS309
BASN68
BGLU96
BASP210
BASN212
BASP308
BHIS309
AASN68
AGLU96

site_idSWS_FT_FI5
Number of Residues2
DetailsSITE: Transition state stabilizer => ECO:0000269|PubMed:8932375
ChainResidueDetails
BASN212
AASN212

site_idSWS_FT_FI6
Number of Residues2
DetailsSITE: Important for catalytic activity => ECO:0000269|PubMed:21762700, ECO:0000269|PubMed:9804799
ChainResidueDetails
BASP283
AASP283

site_idSWS_FT_FI7
Number of Residues2
DetailsSITE: Interaction with DNA substrate
ChainResidueDetails
BHIS309
AHIS309

site_idSWS_FT_FI8
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163
ChainResidueDetails
BSER54
ASER54

site_idSWS_FT_FI9
Number of Residues4
DetailsMOD_RES: S-nitrosocysteine; alternate => ECO:0000269|PubMed:17403694
ChainResidueDetails
BCYS65
BCYS93
ACYS65
ACYS93

site_idSWS_FT_FI10
Number of Residues2
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
BLYS197
ALYS197

site_idSWS_FT_FI11
Number of Residues2
DetailsMOD_RES: Phosphothreonine; by CDK5 => ECO:0000250|UniProtKB:P28352
ChainResidueDetails
BTHR233
ATHR233

site_idSWS_FT_FI12
Number of Residues2
DetailsMOD_RES: S-nitrosocysteine => ECO:0000269|PubMed:17403694
ChainResidueDetails
ACYS310
BCYS310

Catalytic Information from CSA
site_idMCSA1
Number of Residues8
DetailsM-CSA 510
ChainResidueDetails
AASP70metal ligand
AGLU96metal ligand
ATYR171electrostatic stabiliser, metal ligand
AASP210increase nucleophilicity, metal ligand, proton acceptor
AASN212
AASP283electrostatic stabiliser
AASP308metal ligand
AHIS309electrostatic stabiliser, metal ligand

site_idMCSA2
Number of Residues8
DetailsM-CSA 510
ChainResidueDetails
BASP70metal ligand
BGLU96metal ligand
BTYR171electrostatic stabiliser, metal ligand
BASP210increase nucleophilicity, metal ligand, proton acceptor
BASN212
BASP283electrostatic stabiliser
BASP308metal ligand
BHIS309electrostatic stabiliser, metal ligand

221051

PDB entries from 2024-06-12

PDB statisticsPDBj update infoContact PDBjnumon