1i3d: Difference between revisions

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|PDB= 1i3d |SIZE=350|CAPTION= <scene name='initialview01'>1i3d</scene>, resolution 1.70Å

|SITE=

|LIGAND= <scene name='pdbligand=~~HEM~~:~~PROTOPORPHYRIN~~+~~IX+CONTAINING+FE~~'>~~HEM~~</scene> ~~and~~ <scene name='pdbligand=~~CMO~~:~~CARBON MONOXIDE~~'>~~CMO~~</scene>

|LIGAND= <scene name='pdbligand=CMO:CARBON+MONOXIDE'>CMO</scene>, <scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>

|ACTIVITY=

|GENE= HBG1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])

|DOMAIN=

|RELATEDENTRY=[[1i3e|1I3E]]

|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1i3d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1i3d OCA], [http://www.ebi.ac.uk/pdbsum/1i3d PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1i3d RCSB]</span>

}}

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==Disease==

Known ~~diseases~~ associated with this structure: ~~Aplasia of lacrimal and salivary glands~~ OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=~~602115 602115]], LADD syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602115 602115~~]]

Known disease associated with this structure: Fetal hemoglobin quantitative trait locus 1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142200 142200]]

==About this Structure==

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[[Category: Kidd, R D.]]

[[Category: Mathews, A J.]]

~~[[Category: CMO]]~~

~~[[Category: HEM]]~~

[[Category: oxygen transport]]

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on ~~Thu~~ Mar ~~20 11~~:44:59 2008''

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:13:59 2008''

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@@ Line 4: / Line 4: @@
 |PDB= 1i3d |SIZE=350|CAPTION= <scene name='initialview01'>1i3d</scene>, resolution 1.70&Aring;
 |SITE=
-|LIGAND= <scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene> and <scene name='pdbligand=CMO:CARBON MONOXIDE'>CMO</scene>
+|LIGAND= <scene name='pdbligand=CMO:CARBON+MONOXIDE'>CMO</scene>, <scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>
 |ACTIVITY=
 |GENE= HBG1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
+|DOMAIN=
+|RELATEDENTRY=[[1i3e|1I3E]]
+|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1i3d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1i3d OCA], [http://www.ebi.ac.uk/pdbsum/1i3d PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1i3d RCSB]</span>
 }}
@@ Line 16: / Line 19: @@
 ==Disease==
-Known diseases associated with this structure: Aplasia of lacrimal and salivary glands OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602115 602115]], LADD syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602115 602115]]
+Known disease associated with this structure: Fetal hemoglobin quantitative trait locus 1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142200 142200]]
 ==About this Structure==
@@ Line 30: / Line 33: @@
 [[Category: Kidd, R D.]]
 [[Category: Mathews, A J.]]
-[[Category: CMO]]
-[[Category: HEM]]
 [[Category: oxygen transport]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 11:44:59 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:13:59 2008''