Entry
Name
DNA ligase (ATP, ADP or GTP);
poly(deoxyribonucleotide):poly(deoxyribonucleotide) ligase (ATP, ADP or GTP)
Class
Ligases;
Forming phosphoric-ester bonds;
Ligases that form phosphoric-ester bonds (only sub-subclass identified to date)
BRITE hierarchy
Sysname
poly(deoxyribonucleotide)-3'-hydroxyl:5'-phospho-poly(deoxyribonucleotide) ligase (ATP, ADP or GTP)
Reaction(IUBMB)
(1) ATP + (deoxyribonucleotide)n-3'-hydroxyl + 5'-phospho-(deoxyribonucleotide)m = (deoxyribonucleotide)n+m + AMP + diphosphate (overall reaction) [RN:
R00381 ];
(1a) ATP + [DNA ligase]-L-lysine = 5'-adenosyl [DNA ligase]-Nepsilon-phosphono-L-lysine + diphosphate;
(1b) 5'-adenosyl [DNA ligase]-Nepsilon-phosphono-L-lysine + 5'-phospho-(deoxyribonucleotide)m = 5'-(5'-diphosphoadenosine)-(deoxyribonucleotide)m + [DNA ligase]-L-lysine;
(1c) (deoxyribonucleotide)n-3'-hydroxyl + 5'-(5'-diphosphoadenosine)-(deoxyribonucleotide)m = (deoxyribonucleotide)n+m + AMP;
(2) ADP + (deoxyribonucleotide)n-3'-hydroxyl + 5'-phospho-(deoxyribonucleotide)m = (deoxyribonucleotide)n+m + AMP + phosphate (overall reaction) [RN:
R10822 ];
(2a) ADP + [DNA ligase]-L-lysine = 5'-adenosyl [DNA ligase]-Nepsilon-phosphono-L-lysine + phosphate;
(2b) 5'-adenosyl [DNA ligase]-Nepsilon-phosphono-L-lysine + 5'-phospho-(deoxyribonucleotide)m = 5'-(5'-diphosphoadenosine)-(deoxyribonucleotide)m + [DNA ligase]-L-lysine;
(2c) (deoxyribonucleotide)n-3'-hydroxyl + 5'-(5'-diphosphoadenosine)-(deoxyribonucleotide)m = (deoxyribonucleotide)n+m + AMP;
(3) GTP + (deoxyribonucleotide)n-3'-hydroxyl + 5'-phospho-(deoxyribonucleotide)m = (deoxyribonucleotide)n+m + GMP + diphosphate (overall reaction) [RN:
R10823 ];
(3a) GTP + [DNA ligase]-L-lysine = 5'-guanosyl [DNA ligase]-Nepsilon-phosphono-L-lysine + diphosphate;
(3b) 5'-guanosyl [DNA ligase]-Nepsilon-phosphono-L-lysine + 5'-phospho-(deoxyribonucleotide)m = 5'-(5'-diphosphoguanosine)-(deoxyribonucleotide)m + [DNA ligase]-L-lysine;
(3c) (deoxyribonucleotide)n-3'-hydroxyl + 5'-(5'-diphosphoguanosine)-(deoxyribonucleotide)m = (deoxyribonucleotide)n+m + GMP
Reaction(KEGG)
Substrate
ATP [CPD:
C00002 ];
(deoxyribonucleotide)n-3'-hydroxyl;
5'-phospho-(deoxyribonucleotide)m;
[DNA ligase]-L-lysine;
5'-adenosyl [DNA ligase]-Nepsilon-phosphono-L-lysine;
5'-(5'-diphosphoadenosine)-(deoxyribonucleotide)m;
ADP [CPD:
C00008 ];
GTP [CPD:
C00044 ];
5'-guanosyl [DNA ligase]-Nepsilon-phosphono-L-lysine;
5'-(5'-diphosphoguanosine)-(deoxyribonucleotide)m
Product
(deoxyribonucleotide)n+m [CPD:
C00039 ];
AMP [CPD:
C00020 ];
diphosphate [CPD:
C00013 ];
5'-adenosyl [DNA ligase]-Nepsilon-phosphono-L-lysine;
5'-(5'-diphosphoadenosine)-(deoxyribonucleotide)m;
[DNA ligase]-L-lysine;
phosphate [CPD:
C00009 ];
GMP [CPD:
C00144 ];
5'-guanosyl [DNA ligase]-Nepsilon-phosphono-L-lysine;
5'-(5'-diphosphoguanosine)-(deoxyribonucleotide)m
Comment
The enzymes from the archaea Hyperthermus butylicus and Sulfophobococcus zilligii are active with ATP, ADP or GTP. They show no activity with NAD+. The enzyme catalyses the ligation of DNA strands with 3'-hydroxyl and 5'-phosphate termini, forming a phosphodiester and sealing certain types of single-strand breaks in duplex DNA. Catalysis occurs by a three-step mechanism, starting with the activation of the enzyme by ATP, ADP, or GTP, forming a phosphoramide bond between adenylate/guanylate and a lysine residue. The nucleotide is then transferred to the 5'-phosphate terminus of the substrate, forming the capped structure 5'-(5'-diphosphoadenosine/guanosine)-[DNA]. Finally, the enzyme catalyses a nucleophilic attack of the 3'-OH terminus on the capped terminus, which results in formation of the phosphodiester bond and release of the nucleotide. Different from EC
6.5.1.1 , DNA ligase (ATP), and EC
6.5.1.6 , DNA ligase (ATP or NAD+), which cannot utilize GTP.
History
EC 6.5.1.7 created 2014, modified 2016
Orthology
Genes
PLEU : 114689303 114703897(Lig1)
MORG : 121439844 121441664 121449379(Lig1)
ACYG : 106049362 136789369
SANH : 107659894 107692877
CAUA : 113045080 113046266 113120958
CGIB : 127934752 127951483
MASI : 127440333 127442776
CCLU : 121535440 121581379(lig1)
LPIC : 129269256 129269260
AFIL : 140143591 140144306
AALB : 109422000 115256368
SGRE : 126314437 126353476
CEL : CELE_C29A12.3(lig-1)
CBR : CBG_09716(Cbr-lig-1)
BMY : BM_BM2459(Bma-lig-1)
AMIL : 114956663 122964488
CSAT : 104739397 104754994
BNA : 106346356 106401619 106416310 106420229
HSYR : 120113512 120206322
TPRA : 123919891 123919892
MSYL : 126588919 126615853
SSPL : 121742703 121746080
SHIS : 125194010 125214817 125217761
TAES : 123047568 123122620 123181261
MFLO : 136485068 136538891
PVIR : 120650687 120689521
PAUA : 133903470 133907699
VCN : VOLCADRAFT_83047(lig1)
CGR : 2889175(GVI51_I03135)
NCS : NCAS_0A14110(NCAS0A14110)
NDI : NDAI_0A01940(NDAI0A01940)
TPF : TPHA_0D04570(TPHA0D04570)
TBL : TBLA_0E02050(TBLA0E02050)
TDL : TDEL_0C02040(TDEL0C02040)
KAF : KAFR_0B00830(KAFR0B00830)
KNG : KNAG_0C03740(KNAG0C03740)
LBG : 92207468(LODBEIA_P22720)
CAL : CAALFM_C300830CA(CaO19.6155)
ASAU : 88171612(PUMCH_000543)
YLI : 2908208(YALI2_F00983g)
NTE : NEUTE1DRAFT41251(NEUTE1DRAFT_41251)
SMP : 10803803(SMAC4_05315)
PBEL : QC761_710060(cdc17)
PPSD : QC762_710060(cdc17)
PPSP : QC763_710060(cdc17)
PPSA : QC764_710060(cdc17)
RTHE : 98121936(VTJ83DRAFT_1163)
TATV : 25775377(TrAtP1_012317)
TASP : 36609533(TrAFT101_010394)
PLJ : 28883317(PLICBS_000701)
PTKZ : JDV02_007494(cdc17)
CDET : 87937426(CDEST_00923)
BFU : BCIN_13g00240(Bccdc9)
CPW : 9691755(D8B26_002328)
PNO : SNOG_06940(SNOG_06939)
PTRR : 6338758(PtrM4_011050)
ADAC : 96089937(ACET3X_009615)
CDEP : 91085813(L203_101600)
KMG : 30165936(I203_103417)
KNE : 92181189(IAR55_003931)
CCAC : CcaHIS019_0201890(cdc17)
ABP : AGABI1DRAFT51454(AGABI1DRAFT_51454)
ABV : AGABI2DRAFT214235(AGABI2DRAFT_214235)
SCM : SCHCO_02160311(SCHCODRAFT_02160311)
EHI : EHI_111060(1.t00017)
PLAG : 39743275(PADL01_1302900)
PBRS : 92373375(MKS88_005288)
PREL : PRELSG_1401800(LigI)
FCY : FRACYDRAFT_225386(Lig1_a)
TPS : THAPSDRAFT_268404(Lig1)
TCR : 506835.120 506945.80
LMAT : 92514011(LSCM1_03971)
LOI : 92358241(LSCM4_02274)
LEIS : 94178415(GH5_02916)
LENR : 94170507(CUR178_03261)
LEIN : 94187316(JIQ42_03641)
PHET : 94289234(JKF63_03136)
SSAO : 94300887(SS50377_26864)
MJK : N2V74_01590 N2V74_04270
TVO : TVG1298537(TVG1298537)
BARC : AOA65_0724(lig_1) AOA65_0957(lig_2)
BARB : AOA66_0283(lig_1) AOA66_0941(lig_2)
» show all
Taxonomy
Reference
Authors
Sun Y, Seo MS, Kim JH, Kim YJ, Kim GA, Lee JI, Lee JH, Kwon ST
Title
Novel DNA ligase with broad nucleotide cofactor specificity from the hyperthermophilic crenarchaeon Sulfophobococcus zilligii: influence of ancestral DNA ligase on cofactor utilization.
Journal
Sequence
Reference
Authors
Kim JH, Lee KK, Sun Y, Seo GJ, Cho SS, Kwon SH, Kwon ST
Title
Broad nucleotide cofactor specificity of DNA ligase from the hyperthermophilic crenarchaeon Hyperthermus butylicus and its evolutionary significance.
Journal
Sequence
Other DBs
ExplorEnz - The Enzyme Database: 6.5.1.7
ExPASy - ENZYME nomenclature database: 6.5.1.7
BRENDA, the Enzyme Database: 6.5.1.7
LinkDB
All DBs