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TitleA structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1.
Journal, issue, pagesEmbo J., Vol. 30, Page 1659-1670, Year 2011
Publish dateJan 14, 2011 (structure data deposition date)
AuthorsHou, X. / Hagemann, N. / Schoebel, S. / Blankenfeldt, W. / Goody, R.S. / Erdmann, K.S. / Itzen, A.
External linksEmbo J. / PubMed:21378754
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-3qbt:
Crystal structure of OCRL1 540-678 in complex with Rab8a:GppNHp
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-MG:
Unknown entry

ChemComp-GNP:
PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER / GppNHp, GMPPNP, energy-carrying molecule analogue*YM

ChemComp-SO4:
SULFATE ION

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsPROTEIN TRANSPORT/HYDROLASE / Protein transport / vesicular trafficking / GTPase / Lowe syndrome / immunoglobulin fold / Rab8a / OCRL1 / endocytosis / clathrin / APPL1 / phosphoinositide / ASH / RhoGAP / PROTEIN TRANSPORT-HYDROLASE complex

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