6h2j

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (10:00, 23 October 2024) (edit) (undo)
 
Line 3: Line 3:
<StructureSection load='6h2j' size='340' side='right'caption='[[6h2j]], [[Resolution|resolution]] 2.60&Aring;' scene=''>
<StructureSection load='6h2j' size='340' side='right'caption='[[6h2j]], [[Resolution|resolution]] 2.60&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
-
<table><tr><td colspan='2'>[[6h2j]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/"bacillus_coli"_migula_1895 "bacillus coli" migula 1895]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6H2J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6H2J FirstGlance]. <br>
+
<table><tr><td colspan='2'>[[6h2j]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6H2J OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6H2J FirstGlance]. <br>
-
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ATP:ADENOSINE-5-TRIPHOSPHATE'>ATP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></td></tr>
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.6&#8491;</td></tr>
-
<tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr>
+
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ATP:ADENOSINE-5-TRIPHOSPHATE'>ATP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr>
-
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2w00|2w00]], [[5j3n|5j3n]]</td></tr>
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6h2j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6h2j OCA], [https://pdbe.org/6h2j PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6h2j RCSB], [https://www.ebi.ac.uk/pdbsum/6h2j PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6h2j ProSAT]</span></td></tr>
-
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">hsdR ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=562 "Bacillus coli" Migula 1895])</td></tr>
+
-
<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Type_I_site-specific_deoxyribonuclease Type I site-specific deoxyribonuclease], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.21.3 3.1.21.3] </span></td></tr>
+
-
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6h2j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6h2j OCA], [http://pdbe.org/6h2j PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6h2j RCSB], [http://www.ebi.ac.uk/pdbsum/6h2j PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6h2j ProSAT]</span></td></tr>
+
</table>
</table>
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/T1R1_ECOLX T1R1_ECOLX] The restriction (R) subunit of a type I restriction enzyme that recognizes 5'-GAAN(6)RTCG-3' (for EcoR124I) and 5'-GAAN(7)RTCG-3' (for EcoR124II) and cleaves a random distance away (PubMed:2784505). Subunit R is required for both nuclease and ATPase activities, but not for modification (Probable) (PubMed:12654995). After locating an unmethylated recognition site, the enzyme complex serves as a molecular motor that translocates DNA in an ATP-dependent manner until a collision occurs that triggers cleavage (PubMed:15300241). The enzyme undergoes major structural changes to bring the motor domains into contact with DNA, allowing DNA translocation. This prevents DNA access to the catalytic domains of both the R and M subunits, preventing both restriction and methylation (PubMed:32483229). The R(1)M(2)S(1) complex translocates an average of 555 bp/second on nicked DNA; the R(2)M(2)S(1) complex translocates at double that speed (PubMed:15300241). The 2 R subunit motors are independent and track along the helical pitch of the DNA, inducing positive supercoiling ahead of themselves (PubMed:15300241).<ref>PMID:15300241</ref> <ref>PMID:2784505</ref> <ref>PMID:32483229</ref> <ref>PMID:12654995</ref> <ref>PMID:32483229</ref>
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
Line 24: Line 23:
__TOC__
__TOC__
</StructureSection>
</StructureSection>
-
[[Category: Bacillus coli migula 1895]]
 
-
[[Category: Large Structures]]
 
-
[[Category: Type I site-specific deoxyribonuclease]]
 
-
[[Category: Ettrich, R H]]
 
-
[[Category: Grinkevich, P]]
 
-
[[Category: Mesters, J R]]
 
-
[[Category: C-terminal domain]]
 
-
[[Category: Ecor124]]
 
-
[[Category: Endonuclease]]
 
[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
-
[[Category: Hsdr]]
+
[[Category: Large Structures]]
-
[[Category: Hydrolase]]
+
[[Category: Ettrich RH]]
-
[[Category: Restriction-modification enzyme]]
+
[[Category: Grinkevich P]]
 +
[[Category: Mesters JR]]

Current revision

Crystal structure of the HsdR subunit of the EcoR124I restriction enzyme with the C-terminal domain

PDB ID 6h2j

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools