This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


2dad

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 7: Line 7:
|ACTIVITY=
|ACTIVITY=
|GENE= AIM1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= AIM1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
 +
|DOMAIN=
 +
|RELATEDENTRY=
 +
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2dad FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2dad OCA], [http://www.ebi.ac.uk/pdbsum/2dad PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2dad RCSB]</span>
}}
}}
Line 13: Line 16:
==Disease==
==Disease==
-
Known diseases associated with this structure: Oculocutaneous albinism, type IV OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606202 606202]], Skin/hair/eye pigmentation 5, black/nonblack hair OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606202 606202]], Skin/hair/eye pigmentation 5, dark/fair skin OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606202 606202]], Skin/hair/eye pigmentation 5, dark/light eyes OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606202 606202]]
+
Known disease associated with this structure: Oculocutaneous albinism, type IV OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606202 606202]], Skin/hair/eye pigmentation 5, black/nonblack hair OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606202 606202]], Skin/hair/eye pigmentation 5, dark/fair skin OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606202 606202]], Skin/hair/eye pigmentation 5, dark/light eyes OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606202 606202]]
==About this Structure==
==About this Structure==
Line 34: Line 37:
[[Category: structural genomic]]
[[Category: structural genomic]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:24:50 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:31:59 2008''

Revision as of 23:32, 30 March 2008


PDB ID 2dad

Drag the structure with the mouse to rotate
Gene: AIM1 (Homo sapiens)
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Solution structure of the fifth crystall domain of the non-lens protein, Absent in melanoma 1


Disease

Known disease associated with this structure: Oculocutaneous albinism, type IV OMIM:[606202], Skin/hair/eye pigmentation 5, black/nonblack hair OMIM:[606202], Skin/hair/eye pigmentation 5, dark/fair skin OMIM:[606202], Skin/hair/eye pigmentation 5, dark/light eyes OMIM:[606202]

About this Structure

2DAD is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Mon Mar 31 02:31:59 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools