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5WN5

APE1 exonuclease substrate complex with a C/T mismatch and Mn2+

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 Residues2
Detailsbinding site for residue MN E 101
ChainResidue
EDC6
EDG7

site_idAC2
Number of Residues4
Detailsbinding site for residue NA A 401
ChainResidue
APHE253
AARG281
AASP283
AHOH526

site_idAC3
Number of Residues2
Detailsbinding site for residue MN A 402
ChainResidue
AASP70
AGLU96

site_idAC4
Number of Residues4
Detailsbinding site for residue EDO A 403
ChainResidue
ATYR45
AASN277
ASER302
ALEU44

site_idAC5
Number of Residues4
Detailsbinding site for residue MN B 401
ChainResidue
BASP70
BGLU96
DC7R10
DHOH207

site_idAC6
Number of Residues4
Detailsbinding site for residue EDO B 402
ChainResidue
BLEU44
BTYR45
BARG274
BASN277

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
ATYR171
BTYR171

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

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
AASN68
BASN212
BASP308
BHIS309
AGLU96
AASP210
AASN212
AASP308
AHIS309
BASN68
BGLU96
BASP210

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

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

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

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

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

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

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

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

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PDB entries from 2024-10-30

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