DNA ligase

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (07:41, 12 June 2019) (edit) (undo)
 
(11 intermediate revisions not shown.)
Line 1: Line 1:
-
<StructureSection load='2hix' size='400' side='right' scene='DNA_ligase/Cv/1' caption='ATP-dependent DNA ligase complexed with ATP [[2hix]]'>
+
<StructureSection load='2hix' size='350' side='right' scene='44/443730/Cv/2' caption='ATP-dependent DNA ligase complexed with ATP [[2hix]]'>
 +
__TOC__
 +
== Function ==
-
'''DNA ligase''' (LigD) is an enzyme which repairs single-stranded breaks in a double-stranded DNA. LigD is activated , in a species-dependent manner, by hydrolysis of ATP or NAD+. Mammalian LigD I ligates the nascent DNA of the lagging strand; LigD III complexes with XRCC1 in the process of nucleotide excision repair; LigD IV complexes with XRCC4 and catalyzes the last step in the non-homologous DNA end joining. LigD contains several domains: adenylation domain; DNA-binding domain and the ca. 100 amino acid long BRCT motif. See more details in [[ATP-Dependent DNA Ligase (Bacteriophage T7)]].
+
'''DNA ligase''' (LigD) is an enzyme which repairs single-stranded breaks in a double-stranded DNA. LigD is activated, in a species-dependent manner, by hydrolysis of ATP or NAD+. See also [[ATP-dependent DNA ligase from bacteriophage T7]].<br />
 +
* Mammalian '''LigD I''' ligates the nascent DNA of the lagging strand.<br />
 +
* '''LigD III''' complexes with XRCC1 in the process of nucleotide excision repair.<br />
 +
* '''LigD IV''' complexes with XRCC4 and catalyzes the last step in the non-homologous DNA end joining.<br />
 +
See more details in [[ATP-Dependent DNA Ligase (Bacteriophage T7)]].
==Disease==
==Disease==
Line 8: Line 14:
A specific point mutation (46BR in the mouse Lig1 gene) in DNA ligase I has also been linked as a cause for genome instability and cancer in humans. One possible reason for this is the accumulation of DNA fragments that are no longer ligated by the mutant DNA ligase I enzyme.
A specific point mutation (46BR in the mouse Lig1 gene) in DNA ligase I has also been linked as a cause for genome instability and cancer in humans. One possible reason for this is the accumulation of DNA fragments that are no longer ligated by the mutant DNA ligase I enzyme.
-
</StructureSection>
 
-
== 3D Structures of DNA ligase ==
+
== Structural highlights ==
-
Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}}
+
Human LigD IV contains several domains: DNA-binding domain (residues 1-240); adenylation domain (residues 268-405) and the ca. 100 amino acid long BRCT motifs (residues 654-911). In the ATP-dependent LigD the ATP binds between 2 symmetry related LigD molecules.
-
{{#tree:id=OrganizedByTopic|openlevels=0|
+
*<scene name='44/443730/Cv/4'>ATP binding site</scene> in ATP-dependent DNA ligase from ''S. solfataricus'' ([[2hix]]). <ref>PMID:17052461</ref>
-
*ATP-dependent LigD
+
== 3D Structures of DNA ligase ==
 +
[[DNA ligase 3D structures]]
-
**[[3p4h]], [[3ta5]], [[3ta7]] – LigD N-terminal – ''Candidatus korarchaeum cryptofilum''<br />
+
</StructureSection>
-
**[[3gde]] – LigD – ''Archaeoglobus fulgidus''<br />
+
-
**[[2hiv]] – SsLigD – ''Sulfolobus solfataricus''<br />
+
-
**[[2hix]] - SsLigD + ATP<br />
+
-
**[[2cfm]] - LigD + AMP – ''Pyrococcus furiosus''<br />
+
-
**[[2fao]] - PaLigD polymerase domain – ''Pseudomonas aeruginosa''<br />
+
-
**[[2faq]], [[2far]] - PaLigD polymerase domain + ATP + Mn<br />
+
-
**[[1a0i]] – LigD + ATP – Bacteriophage T7<br />
+
-
**[[4eq5]] – LigD + AMP – ''Thermococcus sibiricus''
+
-
 
+
-
*NAD+-dependent LigD
+
-
 
+
-
**[[3jsl]], [[3jsn]] - LigD adenylation domain – ''Staphylococcus aureus''<br />
+
-
**[[3ba8]], [[3ba9]], [[3baa]], [[3bab]], [[3bac]], [[4eeq]], [[4efb]], [[4efe]], [[4lh6]], [[4lh7]] - EfLigD adenylation domain + NMN + inhibitor – ''Enterococcus faecalis''<br />
+
-
**[[1ta8]], [[1tae]] - EfLigD adenylation domain<br />
+
-
**[[1zau]] - MtLigD adenylation domain – ''Mycobacterium tuberculosis''<br />
+
-
**[[3sgi]] – MtLigD (mutant) + AMP<br />
+
-
**[[1v9p]], [[1dgs]] – LigD – ''Thermos filiformis''<br />
+
-
**[[1b04]] – LigD adenylation domain (mutant) – ''Geobacillus stearothermophilus''<br />
+
-
**[[4glw]] – LigD A + NMN + inhibitor – ''Streptococcus pneumoniae''<br />
+
-
**[[4glx]] – LigD + DNA + inhibitor - ''Escherichia coli''<br />
+
-
 
+
-
*LigD
+
-
 
+
-
**[[2q2t]] – CvLigD + DNA + AMP + CMP – Chlorella virus<br />
+
-
**[[2q2u]], [[ 1p8l]], [[ 1fvi]] - CvLigD + DNA + mononucleotide<br />
+
-
**[[2owo]] – LigD + DNA + AMP + CMP – ''Escherichia coli''<br />
+
-
**[[3qwu]] – LigD – ''Aquifex aeolicus''<br />
+
-
**[[3pn1]] – HiLigD adenylation domain + inhibitor – ''Haemophilus influenzae''<br />
+
-
**[[3uq8]] - HiLigD adenylation domain + NAD<br />
+
-
**[[1l7b]] – LigD BRCT domain – ''Thermos thermophilus'' - NMR<br />
+
-
**[[3rr5]] – LigD - ''Thermococcus''
+
-
 
+
-
*Mammalian LigD I
+
-
 
+
-
**[[1x9n]] – hLigD I + DNA + AMP + CMP – human<br />
+
-
**[[2od8]] – LigD I residues 32-53 + PCNA
+
-
 
+
-
*Mammalian LigD III
+
-
 
+
-
**[[3l2p]] – hLigD III residues 257-833 + DNA<br />
+
-
**[[1uw0]] - hLigD III zinc-finger domain residues 1-117 – NMR<br />
+
-
**[[1imo]], [[1in1]] - hLigD III BRCTdomain – NMR<br />
+
-
**[[3pc7]] - hLigD III BRCTdomain<br />
+
-
**[[3pc8]] - hLigD III BRCTdomain (mutant) + XRCC1<br />
+
-
**[[3qvg]] - hLigD III BRCTdomain + XRCC1
+
-
 
+
-
*Mammalian LigD IV
+
-
 
+
-
**[[3ii6]], [[ 1ik9]] – hLigD IV C-terminal BRCT domains + DNA repair protein XRCC4<br />
+
-
**[[3w5o]] - hLigD IV <br />
+
-
**[[2e2w]] - hLigD IV BRCT domain - NMR<br />
+
-
**[[1z56]] – LigD IV + ligase interacting factor 1 - yeast<br />
+
-
**[[3vnn]] - hLigD IV adenylation domain<br />
+
-
**[[4hto]] - hLigD IV DNA-binding domain<br />
+
-
**[[4htp]] - hLigD IV DNA-binding domain + artemis protein peptide<br />
+
-
**[[3w1b]], [[3w1g]] - hLigD IV + artemis protein peptide<br />
+
-
}}
+
-
==REFERENCES==
+
== References ==
 +
<references/>
''Elevated expression of DNA ligase I in human cancers., Sun DY, Urrabaz R, Nguyen M, Marty J, Stringer S, Cruz E, Medina-Gundrum L, Weitman S., Clinical Cancer Research. 2001; 7(12):4143-4148.''<br />
''Elevated expression of DNA ligase I in human cancers., Sun DY, Urrabaz R, Nguyen M, Marty J, Stringer S, Cruz E, Medina-Gundrum L, Weitman S., Clinical Cancer Research. 2001; 7(12):4143-4148.''<br />
''Replication failure, genome instability, and increased cancer susceptibility in mice with a point mutation in the DNA ligase I gene., Harrison C, Ketchen AM, Redhead NJ, O'Sullivan MJ, Melton DW., Cancer Research. 2002; 62(14):4065-4074.''
''Replication failure, genome instability, and increased cancer susceptibility in mice with a point mutation in the DNA ligase I gene., Harrison C, Ketchen AM, Redhead NJ, O'Sullivan MJ, Melton DW., Cancer Research. 2002; 62(14):4065-4074.''

Current revision

ATP-dependent DNA ligase complexed with ATP 2hix

Drag the structure with the mouse to rotate

References

  1. ↑ Pascal JM, Tsodikov OV, Hura GL, Song W, Cotner EA, Classen S, Tomkinson AE, Tainer JA, Ellenberger T. A flexible interface between DNA ligase and PCNA supports conformational switching and efficient ligation of DNA. Mol Cell. 2006 Oct 20;24(2):279-91. PMID:17052461 doi:10.1016/j.molcel.2006.08.015

Elevated expression of DNA ligase I in human cancers., Sun DY, Urrabaz R, Nguyen M, Marty J, Stringer S, Cruz E, Medina-Gundrum L, Weitman S., Clinical Cancer Research. 2001; 7(12):4143-4148.
Replication failure, genome instability, and increased cancer susceptibility in mice with a point mutation in the DNA ligase I gene., Harrison C, Ketchen AM, Redhead NJ, O'Sullivan MJ, Melton DW., Cancer Research. 2002; 62(14):4065-4074.

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky

Retrieved from "http://52.214.119.220/wiki/index.php/DNA_ligase"
Personal tools