Results for property: Percent/Fold Effect
Detailed Results for Property
Use this page to examine all the the polymerases and references referring to the property: Percent/Fold Effect.
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| Polymerase | Kingdom | Family | Reference | Result | Context |
|---|---|---|---|---|---|
| T4 | Virus/Phage | B | Enzymatic synthesis of deoxyribonucleic acid. XXV. Purification and properties of deoxyribonucleic acid polymerase induced by infection with phage T4. | 96 % decrease | Reaction: 3-5' Exonuclease; Substrate: DNA template; Experimental conditions: GTP (0.2mM), ATP (0.2mM), CTP (0.2mM), TTP (0mM) |
| T4 | Virus/Phage | B | Enzymatic synthesis of deoxyribonucleic acid. XXV. Purification and properties of deoxyribonucleic acid polymerase induced by infection with phage T4. | 81 % decrease | Reaction: 3-5' Exonuclease; Substrate: DNA template; Experimental conditions: GTP (0.2mM), ATP (0.2mM), CTP (0mM) |
| T4 | Virus/Phage | B | Enzymatic synthesis of deoxyribonucleic acid. XXV. Purification and properties of deoxyribonucleic acid polymerase induced by infection with phage T4. | 49 % decrease | Reaction: 3-5' Exonuclease; Substrate: DNA template; Experimental conditions: GTP (0.2mM), ATP (0mM), CTP (0mM), TTP (0mM) |
| T4 | Virus/Phage | B | Enzymatic synthesis of deoxyribonucleic acid. XXV. Purification and properties of deoxyribonucleic acid polymerase induced by infection with phage T4. | 0 % decrease | Reaction: 3-5' Exonuclease; Substrate: DNA template; Experimental conditions: NTPs (0mM) |
| T4 | Virus/Phage | B | Enzymatic synthesis of deoxyribonucleic acid. XXV. Purification and properties of deoxyribonucleic acid polymerase induced by infection with phage T4. | 75 % decrease | Reaction: 3-5' Exonuclease; Substrate: DNA template; Experimental conditions: Mg++ (.1mM) |
| T4 | Virus/Phage | B | Enzymatic synthesis of deoxyribonucleic acid. XXV. Purification and properties of deoxyribonucleic acid polymerase induced by infection with phage T4. | 0 % decrease | Reaction: 3-5' Exonuclease; Substrate: DNA template; Experimental conditions: Mg++ (6mM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 94.5 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: CTP (0µM), GTP (0µM), ATP (0µM), TTP (0µM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 0 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: PP (.016mM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 94 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: NTPs (0mM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 99.5 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: CTP (.005µM), GTP (.005µM), ATP (0µM), TTP (.005µM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 67.5 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: CTP (.005µM), GTP (0µM), ATP (0µM), TTP (0µM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 99.8 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: CTP (.005µM), GTP (.005µM), ATP (0µM), TTP (0µM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 50 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: PP (3mM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 33 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: CTP (.005µM), GTP (.005µM), ATP (0µM), TTP (.005µM) |
| Eco Pol I | Eubacterium | A | Enzymic synthesis of deoxyribonucleic acid. | 97 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: NaCl (0.2 mg/mL) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. I. Preparation of substrates and partial purification of an enzyme from Escherichia coli. | 90 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: KF (50mM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. I. Preparation of substrates and partial purification of an enzyme from Escherichia coli. | 97 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: NaCl (200mM) |
| Eco Pol I | Eubacterium | A | Enzymic synthesis of deoxyribonucleic acid. | 30 % increase | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: pH (pH 8.7) |
| Eco Pol I | Eubacterium | A | ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEIC ACID, XVI. OLIGONUCLEOTIDES AS TEMPLATES AND THE MECHANISM OF THEIR REPLICATION. | 50 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Temp (20°C) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 38.5 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: CTP (.005µM), GTP (.005µM), ATP (0µM), TTP (0µM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 99.9 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: CTP (.005µM), GTP (0µM), ATP (0µM), TTP (0µM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. II. General properties of the reaction. | 95 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Mg++ (0mM) |
| Eco Pol I | Eubacterium | A | ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEIC ACID. XIV. FURTHER PURIFICATION AND PROPERTIES OF DEOXYRIBONUCLEIC ACID POLYMERASE OF ESCHERICHIA COLI. | 30 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: pH (pH 7) |
| Eco Pol I | Eubacterium | A | ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEIC ACID. XIV. FURTHER PURIFICATION AND PROPERTIES OF DEOXYRIBONUCLEIC ACID POLYMERASE OF ESCHERICHIA COLI. | 30 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: pH (pH 7.8) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. XXVII. Chemical modifications of deoxyribonucleic acid polymerase. | 920 % increase | Reaction: 5-3' Exonuclease; Substrate: DNA template; Experimental conditions: Hg(II) (1000mM), pH (pH 7.4) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. XXVII. Chemical modifications of deoxyribonucleic acid polymerase. | 98 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: Hg(II) (1000mM), pH (pH 7.4) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. XXVII. Chemical modifications of deoxyribonucleic acid polymerase. | 99.9 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Hg(II) (1000mM), pH (pH 7.4) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. XXVII. Chemical modifications of deoxyribonucleic acid polymerase. | 80 % decrease | Reaction: 5-3' Exonuclease; Substrate: DNA template; Experimental conditions: Hg(II) (1000mM), pH (pH 8.76), Temp (37°C) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. XXVII. Chemical modifications of deoxyribonucleic acid polymerase. | 42 % decrease | Reaction: 5-3' Exonuclease; Substrate: DNA template; Experimental conditions: Hg(II) (1000mM), Temp (37°C), pH (pH 6.5) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. 28. The pyrophosphate exchange and pyrophosphorolysis reactions of deoxyribonucleic acid polymerase. | 50 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: PP (1mM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. 28. The pyrophosphate exchange and pyrophosphorolysis reactions of deoxyribonucleic acid polymerase. | 85 % increase | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: PP (2mM) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. 28. The pyrophosphate exchange and pyrophosphorolysis reactions of deoxyribonucleic acid polymerase. | 0 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: pH (pH 6.5), Temp (37°C) |
| Eco Pol I | Eubacterium | A | Enzymatic synthesis of deoxyribonucleic acid. 28. The pyrophosphate exchange and pyrophosphorolysis reactions of deoxyribonucleic acid polymerase. | 95 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: pH (pH 9), Temp (37°C) |
| Eco Pol I | Eubacterium | A | Deoxyribonucleic acid polymerase: two distinct enzymes in one polypeptide. II. A proteolytic fragment containing the 5' leads to 3' exonuclease function. Restoration of intact enzyme functions from the two proteolytic fragments. | 9.75 fold increase | Reaction: 5-3' Exonuclease; Substrate: DNA template; Experimental conditions: TTP (.5mM) |
| Bsu | Eubacterium | ? | ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEIC ACID. XIV. FURTHER PURIFICATION AND PROPERTIES OF DEOXYRIBONUCLEIC ACID POLYMERASE OF ESCHERICHIA COLI. | 70 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Mg++ (.33mM) |
| Bsu | Eubacterium | ? | ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEIC ACID. XIV. FURTHER PURIFICATION AND PROPERTIES OF DEOXYRIBONUCLEIC ACID POLYMERASE OF ESCHERICHIA COLI. | 0 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Mg++ (7mM) |
| Bsu | Eubacterium | ? | ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEIC ACID. XIV. FURTHER PURIFICATION AND PROPERTIES OF DEOXYRIBONUCLEIC ACID POLYMERASE OF ESCHERICHIA COLI. | 50 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Mg++ (33mM) |
| Human Pol epsilon | Eukaryote | B | Further characterization of HeLa DNA polymerase epsilon. | 0 % decrease | Reaction: Nucleotide incorporation |
| Bovine pol alpha | Eukaryote | B | Calf thymus polymerase. | 100 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Mg++ (0mM) |
| Bovine pol alpha | Eukaryote | B | Calf thymus polymerase. | 100 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: Mg++ (0mM) |
| Bovine pol alpha | Eukaryote | B | Calf thymus polymerase. | 60 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: NTPs (0mM) |
| Bovine pol alpha | Eukaryote | B | Calf thymus polymerase. | 87 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: ATP (0mM), CTP (0mM), GTP (0mM), TTP (.025mM) |
| Bovine pol alpha | Eukaryote | B | Calf thymus polymerase. | 72 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: ATP (.025mM), CTP (0mM), GTP (.025mM), TTP (.025mM) |
| Bovine pol alpha | Eukaryote | B | Calf thymus polymerase. | 87 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: ATP (.025mM), CTP (.025mM), GTP (0mM), TTP (.025mM) |
| Bovine pol alpha | Eukaryote | B | Calf thymus polymerase. | 91 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: ATP (0mM), CTP (.025mM), GTP (.025mM), TTP (.025mM) |
| Bovine pol alpha | Eukaryote | B | Calf thymus polymerase. | 100 % decrease | Reaction: Pyrophosphorolysis; Substrate: DNA template; Experimental conditions: Temp (0°C) |
| Rat Liver Extract | Eukaryote | ? | Incorporation of thymidine into deoxyribonucleic acid by enzymes from rat tissues. | 50 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: PP (.01mM) |
| Rat Liver Extract | Eukaryote | ? | Incorporation of thymidine into deoxyribonucleic acid by enzymes from rat tissues. | 100 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: PP (1mM) |
| Rat Liver Extract | Eukaryote | ? | Incorporation of thymidine into deoxyribonucleic acid by enzymes from rat tissues. | 0 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: pH (pH 9) |
| Rat Liver Extract | Eukaryote | ? | Incorporation of thymidine into deoxyribonucleic acid by enzymes from rat tissues. | 19 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: pH (pH 7) |
| Rat Liver Extract | Eukaryote | ? | Incorporation of thymidine into deoxyribonucleic acid by enzymes from rat tissues. | 76 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: pH (pH 6) |
| Eco Pol III* | Eubacterium | C | A new form of DNA polymerase 3 and a copolymerase replicate a long, single-stranded primer-template. | 99 % decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Spermidine (0mM) |
| Eco Pol III* | Eubacterium | C | DNA polymerase 3 star requires ATP to start synthesis on a primed DNA. | 56 fold decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Mg++ (0mM) |
| Eco Pol III* | Eubacterium | C | DNA polymerase 3 star requires ATP to start synthesis on a primed DNA. | 9.33 fold decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: ATP (0mM) |
| Eco Pol III* | Eubacterium | C | DNA polymerase 3 star requires ATP to start synthesis on a primed DNA. | 560 fold decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: Spermidine (0mM) |
| Eco Pol III Holoenzyme | Eubacterium | C | A holoenzyme form of deoxyribonucleic acid polymerase III. Isolation and properties. | 290 fold decrease | Reaction: Nucleotide incorporation; Substrate: dNTPs; Experimental conditions: ATP (0mM) |