3bqq
From Proteopedia
(Difference between revisions)
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|ACTIVITY= | |ACTIVITY= | ||
|GENE= PSAP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |GENE= PSAP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
| + | |DOMAIN= | ||
| + | |RELATEDENTRY=[[3bqp|3BQP]] | ||
| + | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3bqq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3bqq OCA], [http://www.ebi.ac.uk/pdbsum/3bqq PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=3bqq RCSB]</span> | ||
}} | }} | ||
'''Crystal Structure of Human Saposin D (triclinic)''' | '''Crystal Structure of Human Saposin D (triclinic)''' | ||
| + | |||
| + | ==Disease== | ||
| + | Known disease associated with this structure: Combined SAP deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801 176801]], Gaucher disease, atypical OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801 176801]], Krabbe disease, atypical OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801 176801]], Metachromatic leukodystrophy due to SAP-b deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801 176801]] | ||
==About this Structure== | ==About this Structure== | ||
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[[Category: Popovic, K.]] | [[Category: Popovic, K.]] | ||
[[Category: Prive, G G.]] | [[Category: Prive, G G.]] | ||
| - | [[Category: acid ceramidase | + | [[Category: acid ceramidase,farber disease]] |
| - | + | ||
[[Category: lipid binding protein]] | [[Category: lipid binding protein]] | ||
[[Category: lipid metabolism]] | [[Category: lipid metabolism]] | ||
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[[Category: sphingolipid metabolism]] | [[Category: sphingolipid metabolism]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 05:28:23 2008'' |
Revision as of 02:28, 31 March 2008
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| , resolution 2.00Å | |||||||
|---|---|---|---|---|---|---|---|
| Gene: | PSAP (Homo sapiens) | ||||||
| Related: | 3BQP
| ||||||
| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
Crystal Structure of Human Saposin D (triclinic)
Disease
Known disease associated with this structure: Combined SAP deficiency OMIM:[176801], Gaucher disease, atypical OMIM:[176801], Krabbe disease, atypical OMIM:[176801], Metachromatic leukodystrophy due to SAP-b deficiency OMIM:[176801]
About this Structure
3BQQ 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 05:28:23 2008
