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- SASDCP6: Small GTPase Rab5 conjugated with ubiquitin at K165 -

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Basic information

Entry
Database: SASBDB / ID: SASDCP6
SampleSmall GTPase Rab5 conjugated with ubiquitin at K165
  • Monoubiquitinated Rab5 at K165 (protein), mUbRab5K165, Homo sapiens
Biological speciesHomo sapiens (human)
CitationJournal: Elife / Year: 2017
Title: Site-specific monoubiquitination downregulates Rab5 by disrupting effector binding and guanine nucleotide conversion.
Authors: Donghyuk Shin / Wooju Na / Ji-Hyung Lee / Gyuhee Kim / Jiseok Baek / Seok Hee Park / Cheol Yong Choi / Sangho Lee /
Abstract: Rab GTPases, which are involved in intracellular trafficking pathways, have recently been reported to be ubiquitinated. However, the functions of ubiquitinated Rab proteins remain unexplored. Here we ...Rab GTPases, which are involved in intracellular trafficking pathways, have recently been reported to be ubiquitinated. However, the functions of ubiquitinated Rab proteins remain unexplored. Here we show that Rab5 is monoubiquitinated on K116, K140, and K165. Upon co-transfection with ubiquitin, Rab5 exhibited abnormalities in endosomal localization and EGF-induced EGF receptor degradation. Rab5 K140R and K165R mutants restored these abnormalities, whereas K116R did not. We derived structural models of individual monoubiquitinated Rab5 proteins (mUbRab5s) by solution scattering and observed different conformational flexibilities in a site-specific manner. Structural analysis combined with biochemical data revealed that interactions with downstream effectors were impeded in mUbRab5, whereas GDP release and GTP loading activities were altered in mUbRab5. By contrast, mUbRab5 apparently had no effect. We propose a regulatory mechanism of Rab5 where monoubiquitination downregulates effector recruitment and GDP/GTP conversion in a site-specific manner.
Contact author
  • Donghyuk Shin (Sungkyunkwan University, Seoul, SK)

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Models

Model #1455
Type: atomic / Radius of dummy atoms: 1.90 A / Chi-square value: 1.251
Search similar-shape structures of this assembly by Omokage search (details)
Model #1456
Type: atomic / Radius of dummy atoms: 1.90 A / Chi-square value: 1.251
Search similar-shape structures of this assembly by Omokage search (details)
Model #1457
Type: dummy / Radius of dummy atoms: 2.00 A / Chi-square value: 1.382
Search similar-shape structures of this assembly by Omokage search (details)

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Sample

SampleName: Small GTPase Rab5 conjugated with ubiquitin at K165 / Specimen concentration: 1.00-2.60
BufferName: 50 mM Tris-HCl, 150 mM NaCl, 10 mM MgCl2 / pH: 7.5
Entity #760Name: mUbRab5K165 / Type: protein / Description: Monoubiquitinated Rab5 at K165 / Formula weight: 32.205 / Num. of mol.: 1 / Source: Homo sapiens
Sequence: MQIFVKTLTG KTITLEVEPS DTIENVKAKI QDKEGIPPDQ QRLIFAGKQL EDGRTLSDYN IQKESTLHLV LRLRGGMASR GATRPNGPNT GNKICQFKLV LLGESAVGKS SLVLRFVKGQ FHEFQESTIG AAFLTQTVCL DDTTVKFEIW DTAGQERYHS LAPMYYRGAQ ...Sequence:
MQIFVKTLTG KTITLEVEPS DTIENVKAKI QDKEGIPPDQ QRLIFAGKQL EDGRTLSDYN IQKESTLHLV LRLRGGMASR GATRPNGPNT GNKICQFKLV LLGESAVGKS SLVLRFVKGQ FHEFQESTIG AAFLTQTVCL DDTTVKFEIW DTAGQERYHS LAPMYYRGAQ AAIVVYDITN EESFARAKNW VKELQRQASP NIVIALSGNK ADLANKRAVD FQEAQSYADD NSLLFMETSA KTSMNVNEIF MAIAKKLPKN EPQNPGANSA RGRGVDLTEP TQPTRNQCCS N

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Experimental information

BeamInstrument name: Pohang Accelerator Laboratory 4C / City: Pohang / : South Korea / Type of source: X-ray synchrotron / Wavelength: 0.124 Å / Dist. spec. to detc.: 3 mm
DetectorName: ADSC Quantum 315 / Type: CCD / Pixsize x: 315 mm
Scan
Title: Small GTPase Rab5 conjugated with ubiquitin at K165 / Measurement date: Nov 21, 2016 / Storage temperature: 4 °C / Cell temperature: 4 °C / Exposure time: 10 sec. / Number of frames: 6 / Unit: 1/A /
MinMax
Q0.0192 0.1487
Distance distribution function P(R)
Sofotware P(R): GNOM 5.0 / Number of points: 616 /
MinMax
Q0.019165 0.14867
P(R) point1 616
R0 93.69
Result
Experimental MW: 30 kDa / D max: 9.37 / Type of curve: merged
P(R)GuinierGuinier error
Forward scattering, I010.74 10.69 0.054
Radius of gyration, Rg2.781 nm2.723 nm0.034

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