DB code: M00186
CATH domain | 3.20.20.140 : TIM Barrel | Catalytic domain |
---|---|---|
-.-.-.- : | ||
-.-.-.- : | Catalytic domain | |
2.40.50.140 : OB fold (Dihydrolipoamide Acetyltransferase, E2P) | ||
-.-.-.- : | ||
3.30.420.10 : Nucleotidyltransferase; domain 5 | Catalytic domain | |
-.-.-.- : | ||
1.10.1110.10 : DNA Polymerase III; Chain A | ||
3.40.50.300 : Rossmann fold | Catalytic domain | |
1.20.272.10 : Zinc Finger, Delta Prime; domain 3 | ||
1.10.8.60 : Helicase, Ruva Protein; domain 3 | ||
-.-.-.- : | ||
-.-.-.- : | ||
3.40.50.300 : Rossmann fold | ||
1.20.272.20 : Zinc Finger, Delta Prime; domain 3 | ||
1.10.8.60 : Helicase, Ruva Protein; domain 3 | ||
3.40.50.300 : Rossmann fold | ||
1.10.8.10 : Helicase, Ruva Protein; domain 3 | ||
1.20.272.10 : Zinc Finger, Delta Prime; domain 3 | ||
3.40.50.10220 : Rossmann fold | ||
3.40.50.10110 : Rossmann fold | ||
3.10.150.10 : DNA Polymerase III; Chain A, domain 2 | ||
3.10.150.10 : DNA Polymerase III; Chain A, domain 2 | ||
3.10.150.10 : DNA Polymerase III; Chain A, domain 2 | ||
E.C. | 2.7.7.7 3.1.11.1 3.6.1.3 | |
CSA | 1j53 | |
M-CSA | 1j53 | |
MACiE |
CATH domain | Related DB codes (homologues) |
---|---|
3.40.50.300 : Rossmann fold | S00527 S00547 S00548 S00550 S00554 S00555 S00671 S00672 S00676 S00680 S00682 S00913 S00914 S00301 S00302 S00303 S00304 S00307 S00308 S00305 S00306 S00309 S00310 S00311 M00114 M00199 D00129 D00130 D00540 |
2.40.50.140 : OB fold (Dihydrolipoamide Acetyltransferase, E2P) | M00220 T00050 D00291 D00294 T00254 |
3.20.20.140 : TIM Barrel | S00231 S00232 D00673 D00675 D00801 D00873 M00030 M00225 M00226 |
3.30.420.10 : Nucleotidyltransferase; domain 5 | M00206 T00252 M00019 M00020 M00055 M00135 M00146 M00166 M00173 M00175 |
Uniprot Enzyme Name | UniprotKB | Protein name | Synonyms | Contains | RefSeq | Pfam |
---|---|---|---|---|---|
P10443 |
DNA polymerase III subunit alpha
|
EC
2.7.7.7
|
None |
NP_414726.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_488486.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF07733
(DNA_pol3_alpha)
PF02811 (PHP) PF01336 (tRNA_anti) [Graphical View] |
P03007 |
DNA polymerase III subunit epsilon
|
EC
2.7.7.7
|
None |
NP_414751.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_488512.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF00929
(RNase_T)
[Graphical View] |
P0ABS8 |
DNA polymerase III subunit theta
|
EC
2.7.7.7
|
None |
NP_416356.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_490104.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF06440
(DNA_pol3_theta)
[Graphical View] |
P06710 |
DNA polymerase III subunit tau
|
EC
2.7.7.7
|
DNA polymerase III subunit gamma
|
NP_415003.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_488761.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF12169
(DNA_pol3_gamma3)
PF12168 (DNA_pol3_tau_4) PF12170 (DNA_pol3_tau_5) [Graphical View] |
P28630 |
DNA polymerase III subunit delta
|
EC
2.7.7.7
|
None |
NP_415173.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_488931.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF06144
(DNA_pol3_delta)
[Graphical View] |
P28631 |
DNA polymerase III subunit delta''
|
EC
2.7.7.7
|
None |
NP_415617.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_489367.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF09115
(DNApol3-delta_C)
[Graphical View] |
P28632 |
DNA polymerase III subunit psi
|
EC
2.7.7.7
|
None |
NP_418789.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_492501.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF03603
(DNA_III_psi)
[Graphical View] |
P28905 |
DNA polymerase III subunit chi
|
EC
2.7.7.7
|
None |
NP_418680.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_492397.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF04364
(DNA_pol3_chi)
[Graphical View] |
P0A988 |
DNA polymerase III subunit beta
|
EC
2.7.7.7
|
None |
NP_418156.1
(Protein)
NC_000913.2 (DNA/RNA sequence) YP_491734.1 (Protein) NC_007779.1 (DNA/RNA sequence) |
PF00712
(DNA_pol3_beta)
PF02767 (DNA_pol3_beta_2) PF02768 (DNA_pol3_beta_3) [Graphical View] |
KEGG enzyme name |
---|
DNA-directed DNA polymerase
(EC 2.7.7.7 ) DNA polymerase I (EC 2.7.7.7 ) DNA polymerase II (EC 2.7.7.7 ) DNA polymerase III (EC 2.7.7.7 ) DNA polymerase alpha (EC 2.7.7.7 ) DNA polymerase beta (EC 2.7.7.7 ) DNA polymerase gamma (EC 2.7.7.7 ) DNA nucleotidyltransferase (DNA-directed) (EC 2.7.7.7 ) DNA nucleotidyltransferase (DNA-directed) (EC 2.7.7.7 ) deoxyribonucleate nucleotidyltransferase (EC 2.7.7.7 ) deoxynucleate polymerase (EC 2.7.7.7 ) deoxyribonucleic acid duplicase (EC 2.7.7.7 ) deoxyribonucleic acid polymerase (EC 2.7.7.7 ) deoxyribonucleic duplicase (EC 2.7.7.7 ) deoxyribonucleic polymerase (EC 2.7.7.7 ) deoxyribonucleic polymerase I (EC 2.7.7.7 ) DNA duplicase (EC 2.7.7.7 ) DNA nucleotidyltransferase (EC 2.7.7.7 ) DNA polymerase (EC 2.7.7.7 ) DNA replicase (EC 2.7.7.7 ) DNA-dependent DNA polymerase (EC 2.7.7.7 ) duplicase (EC 2.7.7.7 ) Klenow fragment (EC 2.7.7.7 ) sequenase (EC 2.7.7.7 ) Taq DNA polymerase (EC 2.7.7.7 ) Taq Pol I (EC 2.7.7.7 ) Tca DNA polymerase (EC 2.7.7.7 ) exodeoxyribonuclease I (EC 3.1.11.1 ) Escherichia coli exonuclease I (EC 3.1.11.1 ) E. coli exonuclease I (EC 3.1.11.1 ) exonuclease I (EC 3.1.11.1 ) adenosinetriphosphatase (EC 3.6.1.3 ) adenylpyrophosphatase (EC 3.6.1.3 ) ATP monophosphatase (EC 3.6.1.3 ) triphosphatase (EC 3.6.1.3 ) ATPase (EC 3.6.1.3 ) SV40 T-antigen (EC 3.6.1.3 ) adenosine 5'-triphosphatase (EC 3.6.1.3 ) ATP hydrolase (EC 3.6.1.3 ) ATPase (EC 3.6.1.3 ) complex V (mitochondrial electron transport) (EC 3.6.1.3 ) (Ca2+ + Mg2+)-ATPase (EC 3.6.1.3 ) HCO3--ATPase (EC 3.6.1.3 ) adenosine triphosphatase (EC 3.6.1.3 ) |
UniprotKB: Accession Number | Entry name | Activity | Subunit | Subcellular location | Cofactor |
---|---|---|---|---|---|
P10443 | DPO3A_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. | Cytoplasm. | |
P03007 | DPO3E_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. | Binds 2 divalent metal cations. Magnesium or manganese. | |
P0ABS8 | HOLE_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. | ||
P06710 | DPO3X_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. | ||
P28630 | HOLA_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. | ||
P28631 | HOLB_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. | ||
P28632 | HOLD_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. | ||
P28905 | HOLC_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. | ||
P0A988 | DPO3B_ECOLI | Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1). | The DNA polymerase holoenzyme is a complex that contains 10 different types of subunits. These subunits are organized into 3 functionally essential subassemblies: the pol III core, the beta sliding clamp processivity factor and the clamp-loading complex. The pol III core (subunits alpha,epsilon and theta) contains the polymerase and the 3''-5'' exonuclease proofreading activities. The polymerase is tethered to the template via the sliding clamp processivity factor. The clamp-loading complex assembles the beta processivity factor onto the primer template and plays a central role in the organization and communication at the replication fork. This complex contains delta, delta'', psi and chi, and copies of either or both of two different dnaX proteins, gamma and tau. The composition of the holoenzyme is, therefore: (alpha,epsilon,theta)[2]-(gamma/tau)[3]-delta,delta'', psi,chi- beta[4]. The beta chain is a homodimer when not associated with the other components. | Cytoplasm. |
KEGG Pathways | Map code | Pathways | E.C. |
---|---|---|
MAP00230 | Purine metabolism | 2.7.7.7 3.6.1.3 |
MAP00240 | Pyrimidine metabolism | 2.7.7.7 |
Compound table | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cofactors | Substrates | Products | Intermediates | |||||||||||||||
KEGG-id | C02148 | C00677 | C00039 | C00039 | C00001 | C00002 | C00013 | C00039 | C00039 | C01150 | C00008 | C00009 | ||||||
E.C. |
2.7.7.7
3.1.11.1 |
2.7.7.7
|
2.7.7.7
|
3.1.11.1
|
3.1.11.1
3.6.1.3 |
3.6.1.3
|
2.7.7.7
|
2.7.7.7
|
3.1.11.1
|
3.1.11.1
|
3.6.1.3
|
3.6.1.3
|
||||||
Compound | Divalent metal | Deoxynucleoside triphosphate | DNA(n) | DNA(n+1) | H2O | ATP | Pyrophosphate | DNA(n+1) | DNA(n) | 5'-Phosphomononucleotides | ADP | Orthophosphate | ||||||
Type | divalent metal (Ca2+, Mg2+) | nucleotide | nucleic acids | nucleic acids | H2O | amine group,nucleotide | phosphate group/phosphate ion | nucleic acids | nucleic acids | amine group,nucleotide | phosphate group/phosphate ion | |||||||
ChEBI |
15377 15377 |
15422 15422 |
29888 29888 |
16761 16761 |
26078 26078 |
|||||||||||||
PubChem |
22247451 962 22247451 962 |
5957 5957 |
1023 21961011 1023 21961011 |
6022 6022 |
1004 22486802 1004 22486802 |
|||||||||||||
1j53A | Bound:2x_MN | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Analogue:TMP_2100 | Bound:TMP_2000 | Unbound | Unbound | |||||||
1j54A | Bound:2x_MN | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Bound:TMP_2000 | Unbound | Unbound | |||||||
1du2A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
2ae9A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3A01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Analogue:SO4 | |||||||
1jr3B01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Analogue:SO4 | |||||||
1jr3C01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Analogue:SO4 | |||||||
1xxhB01 | Unbound | Unbound | Unbound | Unbound | Analogue:ATG | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhC01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Bound:PO4 | |||||||
1xxhD01 | Unbound | Unbound | Unbound | Unbound | Analogue:ATG | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhG01 | Unbound | Unbound | Unbound | Unbound | Analogue:ATG | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhH01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Bound:PO4 | |||||||
1xxhI01 | Unbound | Unbound | Unbound | Unbound | Analogue:ATG | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiB01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Bound:ADP | Unbound | |||||||
1xxiC01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Bound:PO4 | |||||||
1xxiD01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Bound:ADP | Unbound | |||||||
1xxiG01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiH01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiI01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Bound:ADP | Unbound | |||||||
1njfA01 | Unbound | Unbound | Unbound | Unbound | Analogue:ATG | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njfB01 | Unbound | Unbound | Unbound | Unbound | Analogue:ATG | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njfC01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Bound:ADP | Unbound | |||||||
1njfD01 | Unbound | Unbound | Unbound | Unbound | Analogue:ATG | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njgA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Analogue:SO4 | |||||||
1njgB01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Analogue:SO4 | |||||||
1jr3A02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3B02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3C02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhB02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhC02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhD02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhG02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhH02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhI02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiB02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiC02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiD02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiG02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiH02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiI02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3A03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3B03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3C03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhB03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhC03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhD03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhG03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhH03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhI03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiB03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiC03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiD03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiG03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiH03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiI03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njfA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njfB02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njfC02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njfD02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njgA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1njgB02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3D01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhF01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiF01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjC01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjD01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqlB | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3D02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhF02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiF02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjC02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjD02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3D03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhA03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhF03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiA03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiF03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjC03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjD03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1a5tA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3E01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhE01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhJ01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiE01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiJ01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1a5tA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3E02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhE02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhJ02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiE02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiJ02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1a5tA03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jr3E03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhE03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxhJ03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiE03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1xxiJ03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1em8B | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1em8D | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1em8A | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1em8C | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjB01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqlA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1mmiA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1mmiB01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1ok7A01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1ok7B01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1unnA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1unnB01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
2polA01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
2polB01 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjB02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqlA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1mmiA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1mmiB02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1ok7A02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1ok7B02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1unnA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1unnB02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
2polA02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
2polB02 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjA03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqjB03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1jqlA03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1mmiA03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1mmiB03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1ok7A03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1ok7B03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1unnA03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
1unnB03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
2polA03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | |||||||
2polB03 | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound | Unbound |
Reference for Active-site residues | ||
---|---|---|
resource | references | E.C. |
References for Catalytic Mechanism | ||
---|---|---|
References | Sections | No. of steps in catalysis |
[34]
|
Fig.5, p.540-543 |
References | |
---|---|
[1] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7118945 |
Journal | J Biol Chem |
Year | 1982 |
Volume | 257 |
Pages | 12310-5 |
Authors | Johanson KO, McHenry CS |
Title | The beta subunit of the DNA polymerase III holoenzyme becomes inaccessible to antibody after formation of an initiation complex with primed DNA. |
Related PDB | |
Related UniProtKB | |
[2] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 3037519 |
Journal | Proc Natl Acad Sci U S A |
Year | 1987 |
Volume | 84 |
Pages | 4389-92 |
Authors | Maki H, Kornberg A |
Title | Proofreading by DNA polymerase III of Escherichia coli depends on cooperative interaction of the polymerase and exonuclease subunits. |
Related PDB | |
Related UniProtKB | |
[3] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 3283128 |
Journal | J Biol Chem |
Year | 1988 |
Volume | 263 |
Pages | 6570-8 |
Authors | Maki H, Maki S, Kornberg A |
Title |
DNA Polymerase III holoenzyme of Escherichia coli. |
Related PDB | |
Related UniProtKB | |
[4] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 2243096 |
Journal | J Biol Chem |
Year | 1990 |
Volume | 265 |
Pages | 20356-63 |
Authors | Griep MA, McHenry CS |
Title | Dissociation of the DNA polymerase III holoenzyme beta 2 subunits is accompanied by conformational change at distal cysteines 333. |
Related PDB | |
Related UniProtKB | |
[5] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1918028 |
Journal | J Biol Chem |
Year | 1991 |
Volume | 266 |
Pages | 19127-30 |
Authors | McHenry CS |
Title |
DNA polymerase III holoenzyme. |
Related PDB | |
Related UniProtKB | |
[6] | |
Resource | |
Comments | REVIEW. |
Medline ID | 92246902 |
PubMed ID | 1575709 |
Journal | Bioessays |
Year | 1992 |
Volume | 14 |
Pages | 105-11 |
Authors | O'Donnell M |
Title |
Accessory protein function in the DNA polymerase III holoenzyme from E. |
Related PDB | |
Related UniProtKB | P28631 |
[7] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 1740452 |
Journal | J Biol Chem |
Year | 1992 |
Volume | 267 |
Pages | 4045-53 |
Authors | Zechner EL, Wu CA, Marians KJ |
Title |
Coordinated leading- and lagging-strand synthesis at the Escherichia coli DNA replication fork. |
Related PDB | |
Related UniProtKB | |
[8] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (2.5 ANGSTROMS) |
Medline ID | 92257585 |
PubMed ID | 1349852 |
Journal | Cell |
Year | 1992 |
Volume | 69 |
Pages | 425-37 |
Authors | Kong XP, Onrust R, O'Donnell M, Kuriyan J |
Title |
Three-dimensional structure of the beta subunit of E. |
Related PDB | 2pol |
Related UniProtKB | P00583 |
[9] | |
Resource | |
Comments | CHARACTERIZATION. |
Medline ID | 93280137 |
PubMed ID | 8505304 |
Journal | J Biol Chem |
Year | 1993 |
Volume | 268 |
Pages | 11766-72 |
Authors | Onrust R, O'Donnell M |
Title |
DNA polymerase III accessory proteins. |
Related PDB | |
Related UniProtKB | P28631 |
[10] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7903401 |
Journal | J Mol Biol |
Year | 1993 |
Volume | 234 |
Pages | 915-25 |
Authors | Kuriyan J, O'Donnell M |
Title | Sliding clamps of DNA polymerases. |
Related PDB | |
Related UniProtKB | |
[11] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8505305 |
Journal | J Biol Chem |
Year | 1993 |
Volume | 268 |
Pages | 11779-84 |
Authors | Xiao H, Dong Z, O'Donnell M |
Title |
DNA polymerase III accessory proteins. |
Related PDB | |
Related UniProtKB | |
[12] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8001157 |
Journal | Cell |
Year | 1994 |
Volume | 79 |
Pages | 1233-43 |
Authors | Krishna TS, Kong XP, Gary S, Burgers PM, Kuriyan J |
Title | Crystal structure of the eukaryotic DNA polymerase processivity factor PCNA. |
Related PDB | |
Related UniProtKB | |
[13] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 8300534 |
Journal | J Bacteriol |
Year | 1994 |
Volume | 176 |
Pages | 815-21 |
Authors | Slater SC, Lifsics MR, O'Donnell M, Maurer R |
Title |
holE, |
Related PDB | |
Related UniProtKB | |
[14] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7768937 |
Journal | J Biol Chem |
Year | 1995 |
Volume | 270 |
Pages | 13358-65 |
Authors | Naktinis V, Onrust R, Fang L, O'Donnell M |
Title |
Assembly of a chromosomal replication machine: two DNA polymerases, |
Related PDB | |
Related UniProtKB | |
[15] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7768938 |
Journal | J Biol Chem |
Year | 1995 |
Volume | 270 |
Pages | 13366-77 |
Authors | Onrust R, Finkelstein J, Turner J, Naktinis V, O'Donnell M |
Title |
Assembly of a chromosomal replication machine: two DNA polymerases, |
Related PDB | |
Related UniProtKB | |
[16] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7768939 |
Journal | J Biol Chem |
Year | 1995 |
Volume | 270 |
Pages | 13378-83 |
Authors | Xiao H, Naktinis V, O'Donnell M |
Title |
Assembly of a chromosomal replication machine: two DNA polymerases, |
Related PDB | |
Related UniProtKB | |
[17] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 7478986 |
Journal | Nucleic Acids Res |
Year | 1995 |
Volume | 23 |
Pages | 3613-20 |
Authors | Kelman Z, O'Donnell M |
Title | Structural and functional similarities of prokaryotic and eukaryotic DNA polymerase sliding clamps. |
Related PDB | |
Related UniProtKB | |
[18] | |
Resource | |
Comments | X-RAY CRYSTALLOGRAPHY (2.2 ANGSTROMS). |
Medline ID | 98028572 |
PubMed ID | 9363942 |
Journal | Cell |
Year | 1997 |
Volume | 91 |
Pages | 335-45 |
Authors | Guenther B, Onrust R, Sali A, O'Donnell M, Kuriyan J |
Title |
Crystal structure of the delta' subunit of the clamp-loader complex of E. |
Related PDB | 1a5t |
Related UniProtKB | P28631 |
[19] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9346941 |
Journal | J Biol Chem |
Year | 1997 |
Volume | 272 |
Pages | 27919-30 |
Authors | Bloom LB, Chen X, Fygenson DK, Turner J, O'Donnell M, Goodman MF |
Title |
Fidelity of Escherichia coli DNA polymerase III holoenzyme. |
Related PDB | |
Related UniProtKB | |
[20] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9753470 |
Journal | Biochemistry |
Year | 1998 |
Volume | 37 |
Pages | 13807-15 |
Authors | Terashima I, Suzuki N, Dasaradhi L, Tan CK, Downey KM, Shibutani S |
Title | Translesional synthesis on DNA templates containing an estrogen quinone-derived adduct: N2-(2-hydroxyestron-6-yl)-2'-deoxyguanosine and N6-(2-hydroxyestron-6-yl)-2'-deoxyadenosine. |
Related PDB | |
Related UniProtKB | |
[21] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 9685491 |
Journal | Nucleic Acids Res |
Year | 1998 |
Volume | 26 |
Pages | 3746-52 |
Authors | Aravind L, Koonin EV |
Title | Phosphoesterase domains associated with DNA polymerases of diverse origins. |
Related PDB | |
Related UniProtKB | |
[22] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11101526 |
Journal | EMBO J |
Year | 2000 |
Volume | 19 |
Pages | 6536-45 |
Authors | Pritchard AE, Dallmann HG, Glover BP, McHenry CS |
Title | A novel assembly mechanism for the DNA polymerase III holoenzyme DnaX complex: association of deltadelta' with DnaX(4) forms DnaX(3)deltadelta'. |
Related PDB | |
Related UniProtKB | |
[23] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 10794414 |
Journal | Protein Sci |
Year | 2000 |
Volume | 9 |
Pages | 721-33 |
Authors | Keniry MA, Berthon HA, Yang JY, Miles CS, Dixon NE |
Title | NMR solution structure of the theta subunit of DNA polymerase III from Escherichia coli. |
Related PDB | 1du2 |
Related UniProtKB | |
[24] | |
Resource | |
Comments | X-ray crystallography |
Medline ID | |
PubMed ID | 11525729 |
Journal | Cell |
Year | 2001 |
Volume | 106 |
Pages | 429-41 |
Authors | Jeruzalmi D, O'Donnell M, Kuriyan J |
Title |
Crystal structure of the processivity clamp loader gamma (gamma) complex of E. |
Related PDB | 1jr3 |
Related UniProtKB | |
[25] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11518714 |
Journal | J Biol Chem |
Year | 2001 |
Volume | 276 |
Pages | 40668-79 |
Authors | Song MS, Dallmann HG, McHenry CS |
Title | Carboxyl-terminal domain III of the delta' subunit of the DNA polymerase III holoenzyme binds delta. |
Related PDB | |
Related UniProtKB | |
[26] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11606586 |
Journal | J Biol Chem |
Year | 2001 |
Volume | 276 |
Pages | 48709-15 |
Authors | Song MS, McHenry CS |
Title | Carboxyl-terminal domain III of the delta' subunit of DNA polymerase III holoenzyme binds DnaX and supports cooperative DnaX complex assembly. |
Related PDB | |
Related UniProtKB | |
[27] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11572866 |
Journal | J Biol Chem |
Year | 2001 |
Volume | 276 |
Pages | 47185-94 |
Authors | Leu FP, O'Donnell M |
Title | Interplay of clamp loader subunits in opening the beta sliding clamp of Escherichia coli DNA polymerase III holoenzyme. |
Related PDB | |
Related UniProtKB | |
[28] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11279099 |
Journal | J Biol Chem |
Year | 2001 |
Volume | 276 |
Pages | 19182-9 |
Authors | Stewart J, Hingorani MM, Kelman Z, O'Donnell M |
Title | Mechanism of beta clamp opening by the delta subunit of Escherichia coli DNA polymerase III holoenzyme. |
Related PDB | |
Related UniProtKB | |
[29] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11719243 |
Journal | Curr Biol |
Year | 2001 |
Volume | 11 |
Pages | R935-46 |
Authors | O'Donnell M, Jeruzalmi D, Kuriyan J |
Title | Clamp loader structure predicts the architecture of DNA polymerase III holoenzyme and RFC. |
Related PDB | |
Related UniProtKB | |
[30] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11525728 |
Journal | Cell |
Year | 2001 |
Volume | 106 |
Pages | 417-28 |
Authors | Jeruzalmi D, Yurieva O, Zhao Y, Young M, Stewart J, Hingorani M, O'Donnell M, Kuriyan J |
Title |
Mechanism of processivity clamp opening by the delta subunit wrench of the clamp loader complex of E. |
Related PDB | 1jqj 1jql |
Related UniProtKB | |
[31] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11859073 |
Journal | J Biol Chem |
Year | 2002 |
Volume | 277 |
Pages | 17334-48 |
Authors | Bruck I, Yuzhakov A, Yurieva O, Jeruzalmi D, Skangalis M, Kuriyan J, O'Donnell M |
Title | Analysis of a multicomponent thermostable DNA polymerase III replicase from an extreme thermophile. |
Related PDB | |
Related UniProtKB | |
[32] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11809766 |
Journal | J Biol Chem |
Year | 2002 |
Volume | 277 |
Pages | 13246-56 |
Authors | Bullard JM, Pritchard AE, Song MS, Glover BP, Wieczorek A, Chen J, Janjic N, McHenry CS |
Title | A three-domain structure for the delta subunit of the DNA polymerase III holoenzyme delta domain III binds delta' and assembles into the DnaX complex. |
Related PDB | |
Related UniProtKB | |
[33] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11772007 |
Journal | Biochemistry |
Year | 2002 |
Volume | 41 |
Pages | 94-110 |
Authors | DeRose EF, Li D, Darden T, Harvey S, Perrino FW, Schaaper RM, London RE |
Title | Model for the catalytic domain of the proofreading epsilon subunit of Escherichia coli DNA polymerase III based on NMR structural data. |
Related PDB | |
Related UniProtKB | |
[34] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 11937058 |
Journal | Structure |
Year | 2002 |
Volume | 10 |
Pages | 535-46 |
Authors | Hamdan S, Carr PD, Brown SE, Ollis DL, Dixon NE |
Title | Structural basis for proofreading during replication of the Escherichia coli chromosome. |
Related PDB | 1j53 1j54 |
Related UniProtKB | |
[35] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 14592985 |
Journal | EMBO J |
Year | 2003 |
Volume | 22 |
Pages | 5883-92 |
Authors | Bunting KA, Roe SM, Pearl LH |
Title | Structural basis for recruitment of translesion DNA polymerase Pol IV/DinB to the beta-clamp. |
Related PDB | 1unn |
Related UniProtKB | |
[36] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 12832762 |
Journal | Acta Crystallogr D Biol Crystallogr |
Year | 2003 |
Volume | 59 |
Pages | 1192-9 |
Authors | Oakley AJ, Prosselkov P, Wijffels G, Beck JL, Wilce MC, Dixon NE |
Title | Flexibility revealed by the 1.85 A crystal structure of the beta sliding-clamp subunit of Escherichia coli DNA polymerase III. |
Related PDB | 1mmi |
Related UniProtKB | |
[37] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 12623013 |
Journal | Structure |
Year | 2003 |
Volume | 11 |
Pages | 253-63 |
Authors | Podobnik M, Weitze TF, O'Donnell M, Kuriyan J |
Title | Nucleotide-induced conformational changes in an isolated Escherichia coli DNA polymerase III clamp loader subunit. |
Related PDB | 1njf 1njg |
Related UniProtKB | |
[38] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 14717711 |
Journal | Eur J Biochem |
Year | 2004 |
Volume | 271 |
Pages | 439-49 |
Authors | Gulbis JM, Kazmirski SL, Finkelstein J, Kelman Z, O'Donnell M, Kuriyan J |
Title | Crystal structure of the chi:psi sub-assembly of the Escherichia coli DNA polymerase clamp-loader complex. |
Related PDB | 1em8 |
Related UniProtKB | |
[39] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 14610068 |
Journal | J Biol Chem |
Year | 2004 |
Volume | 279 |
Pages | 4386-93 |
Authors | Snyder AK, Williams CR, Johnson A, O'Donnell M, Bloom LB |
Title |
Mechanism of loading the Escherichia coli DNA polymerase III sliding clamp: II. |
Related PDB | |
Related UniProtKB | |
[40] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 15037068 |
Journal | J Mol Biol |
Year | 2004 |
Volume | 336 |
Pages | 1047-59 |
Authors | Goedken ER, Levitus M, Johnson A, Bustamante C, O'Donnell M, Kuriyan J |
Title | Fluorescence measurements on the E.coli DNA polymerase clamp loader: implications for conformational changes during ATP and clamp binding. |
Related PDB | |
Related UniProtKB | |
[41] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 14729336 |
Journal | J Mol Biol |
Year | 2004 |
Volume | 335 |
Pages | 1187-97 |
Authors | Burnouf DY, Olieric V, Wagner J, Fujii S, Reinbolt J, Fuchs RP, Dumas P |
Title | Structural and biochemical analysis of sliding clamp/ligand interactions suggest a competition between replicative and translesion DNA polymerases. |
Related PDB | 1ok7 |
Related UniProtKB | |
[42] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 15556993 |
Journal | Proc Natl Acad Sci U S A |
Year | 2004 |
Volume | 101 |
Pages | 16750-5 |
Authors | Kazmirski SL, Podobnik M, Weitze TF, O'Donnell M, Kuriyan J |
Title | Structural analysis of the inactive state of the Escherichia coli DNA polymerase clamp-loader complex. |
Related PDB | 1xxh 1xxi |
Related UniProtKB | |
[43] | |
Resource | |
Comments | |
Medline ID | |
PubMed ID | 16199579 |
Journal | J Bacteriol |
Year | 2005 |
Volume | 187 |
Pages | 7081-9 |
Authors | Mueller GA, Kirby TW, DeRose EF, Li D, Schaaper RM, London RE |
Title | Nuclear magnetic resonance solution structure of the Escherichia coli DNA polymerase III theta subunit. |
Related PDB | 2ae9 |
Related UniProtKB |
Comments |
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This enzyme belongs to the DNA polymerase type-C family.
This DNA enzyme is composed of 10 different types of subunits. According to the literature, (a) the pol III core (subunits alpha, (b) the clamp-loading complex (subunits delta, (c) the beta sliding clamp processivity factor (subunit beta) The pol III core contains the polymerase and the 3'-5' exonuclease proofreading activities. The clamp-loading complex (b) assembles the beta processivity factor (c) onto the primer template and plays a central role in the organization and communication at the replication fork. The composition of the enzyme is as follows: (a) (alpha, (b) (gamma/tau)[3]-(delta, (c) (beta[2])[2] The roles of the subunits are as follows: (a) (alpha, alpha subunit: A polymerase subunit. epsilon subunit: A proofreading subunit, theta subunit: This subunit might maintain fidelity. (b) (gamma/tau)[3]-(delta, gamma subunit: This subunit is a short vaiant of dnaX and interacts with delta subunit to transfer the beta subunit on the DNA. tau subunit: This subunit is a long vaiant of dnaX, delta subunit: This subunit interacts with gamma subunit to transfer the beta subunit on the DNA. delta' subunit: The function is unknown. chi subunit: The function is unknown. psi subunit: The function is unknown. (c) (beta[2])[2]; beta subunit: This subunit seems to be required for initiation of replication. |
Created | Updated |
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2005-03-30 | 2009-02-26 |