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- SASDA76: NetrinVIV DCC56 complex (Netrin-1, NetrinVIV + Deleted in Colorec... -

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Basic information

Entry
Database: SASBDB / ID: SASDA76
SampleNetrinVIV DCC56 complex
  • Netrin-1 (protein), NetrinVIV, Homo sapiens
  • Deleted in Colorectal Cancer (FN5 & FN6) (protein), dcc56, Homo sapiens
Function / homology
Function and homology information


regulation of glial cell migration / chemorepulsion of axon / anterior/posterior axon guidance / Cdc42 protein signal transduction / Role of second messengers in netrin-1 signaling / Netrin-1 signaling / Regulation of commissural axon pathfinding by SLIT and ROBO / motor neuron migration / negative regulation of axon extension / substrate-dependent cell migration, cell extension ...regulation of glial cell migration / chemorepulsion of axon / anterior/posterior axon guidance / Cdc42 protein signal transduction / Role of second messengers in netrin-1 signaling / Netrin-1 signaling / Regulation of commissural axon pathfinding by SLIT and ROBO / motor neuron migration / negative regulation of axon extension / substrate-dependent cell migration, cell extension / Netrin mediated repulsion signals / mammary gland duct morphogenesis / positive regulation of cell motility / nuclear migration / DCC mediated attractive signaling / regulation of synapse assembly / inner ear morphogenesis / DSCAM interactions / basement membrane / glial cell proliferation / positive regulation of axon extension / positive regulation of glial cell proliferation / cell-cell adhesion / actin cytoskeleton / Ras protein signal transduction / DNA-binding transcription factor activity, RNA polymerase II-specific / RNA polymerase II cis-regulatory region sequence-specific DNA binding / apoptotic process / regulation of transcription by RNA polymerase II / extracellular region / nucleoplasm / cytosol
Similarity search - Function
Laminin, N-terminal / Laminin N-terminal (Domain VI) / Laminin N-terminal domain profile. / Laminin N-terminal domain (domain VI) / Laminin-type EGF-like (LE) domain profile. / Laminin-type EGF-like (LE) domain signature. / Laminin-type epidermal growth factor-like domai / Laminin EGF domain / Laminin-type EGF domain / Netrin C-terminal Domain ...Laminin, N-terminal / Laminin N-terminal (Domain VI) / Laminin N-terminal domain profile. / Laminin N-terminal domain (domain VI) / Laminin-type EGF-like (LE) domain profile. / Laminin-type EGF-like (LE) domain signature. / Laminin-type epidermal growth factor-like domai / Laminin EGF domain / Laminin-type EGF domain / Netrin C-terminal Domain / Netrin module, non-TIMP type / UNC-6/NTR/C345C module / Netrin domain / NTR domain profile. / Tissue inhibitor of metalloproteinases-like, OB-fold / EGF-like domain signature 1. / Galactose-binding-like domain superfamily
Similarity search - Domain/homology
Biological speciesHomo sapiens (human)
CitationJournal: Neuron / Year: 2014
Title: The crystal structure of netrin-1 in complex with DCC reveals the bifunctionality of netrin-1 as a guidance cue.
Authors: Lorenzo I Finci / Nina Krüger / Xiaqin Sun / Jie Zhang / Magda Chegkazi / Yu Wu / Gundolf Schenk / Haydyn D T Mertens / Dmitri I Svergun / Yan Zhang / Jia-Huai Wang / Rob Meijers /
Abstract: Netrin-1 is a guidance cue that can trigger either attraction or repulsion effects on migrating axons of neurons, depending on the repertoire of receptors available on the growth cone. How a single ...Netrin-1 is a guidance cue that can trigger either attraction or repulsion effects on migrating axons of neurons, depending on the repertoire of receptors available on the growth cone. How a single chemotropic molecule can act in such contradictory ways has long been a puzzle at the molecular level. Here we present the crystal structure of netrin-1 in complex with the Deleted in Colorectal Cancer (DCC) receptor. We show that one netrin-1 molecule can simultaneously bind to two DCC molecules through a DCC-specific site and through a unique generic receptor binding site, where sulfate ions staple together positively charged patches on both DCC and netrin-1. Furthermore, we demonstrate that UNC5A can replace DCC on the generic receptor binding site to switch the response from attraction to repulsion. We propose that the modularity of binding allows for the association of other netrin receptors at the generic binding site, eliciting alternative turning responses.
Contact author
  • Haydyn Mertens (EMBL-Hamburg, European Molecular Biology Laboratory (EMBL) - Hamburg outstation, Notkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany)

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Structure visualization

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Models

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Sample

SampleName: NetrinVIV DCC56 complex / Specimen concentration: 0.30-2.90 / Entity id: 113 / 114
BufferName: MES / Concentration: 25.00 mM / pH: 7 / Comment: MES/TRIS
Composition: NaCl 200.000 mM, Tris 50.000 mM, (NH4)2(SO4) 0.200 M ammonium sulfate, CaCl2 1.000 mM calcium chloride
Entity #113Name: NetrinVIV / Type: protein / Description: Netrin-1 / Formula weight: 49.1 / Num. of mol.: 1 / Source: Homo sapiens / References: UniProt: O95631
Sequence: GPGLSMFAGQ AAQPDPCSDE NGHPRRCIPD FVNAAFGKDV RVSSTCGRPP ARYCVVSERG EERLRSCHLC NASDPKKAHP PAFLTDLNNP HNLTCWQSEN YLQFPHNVTL TLSLGKKFEV TYVSLQFCSP RPESMAIYKS MDYGRTWVPF QFYSTQCRKM YNRPHRAPIT ...Sequence:
GPGLSMFAGQ AAQPDPCSDE NGHPRRCIPD FVNAAFGKDV RVSSTCGRPP ARYCVVSERG EERLRSCHLC NASDPKKAHP PAFLTDLNNP HNLTCWQSEN YLQFPHNVTL TLSLGKKFEV TYVSLQFCSP RPESMAIYKS MDYGRTWVPF QFYSTQCRKM YNRPHRAPIT KQNEQEAVCT DSHTDMRPLS GGLIAFSTLD GRPSAHDFDN SPVLQDWVTA TDIRVAFSRL HTFGDENEDD SELARDSYFY AVSDLQVGGR CKCNGHAARC VRDRDDSLVC DCRHNTAGPE CDRCKPFHYD RPWQRATARE ANECVACNCN LHARRCRFNM ELYKLSGRKS GGVCLNCRHN TAGRHCHYCK EGYYRDMGKP ITHRKACKAC DCHPVGAAGK TCNQTTGQCP CKDGVTGITC NRCAKGYQQS RSPIAPCIKE LHHHHHH
Entity #114Name: dcc56 / Type: protein / Description: Deleted in Colorectal Cancer (FN5 & FN6) / Formula weight: 25.5 / Num. of mol.: 1 / Source: Homo sapiens
Sequence: MLPPVGVQAV ALTHDAVRVS WADNSVPKNQ KTSEVRLYTV RWRTSFSASA KYKSEDTTSL SYTATGLKPN TMYEFSVMVT KNRRSSTWSM TAHATTYEAA PTSAPKDLTV ITREGKPRAV IVSWQPPLEA NGKITAYILF YTLDKNIPID DWIMETISGD RLTHQIMDLN ...Sequence:
MLPPVGVQAV ALTHDAVRVS WADNSVPKNQ KTSEVRLYTV RWRTSFSASA KYKSEDTTSL SYTATGLKPN TMYEFSVMVT KNRRSSTWSM TAHATTYEAA PTSAPKDLTV ITREGKPRAV IVSWQPPLEA NGKITAYILF YTLDKNIPID DWIMETISGD RLTHQIMDLN LDTMYYFRIQ ARNSKGVGPL SDPILFRTLK LEVLFQGPGG HHHHHHGGWS HPQFEK

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Experimental information

BeamInstrument name: PETRA III P12 / City: Hamburg / : Germany / Type of source: X-ray synchrotronSynchrotron / Wavelength: 0.12 Å / Dist. spec. to detc.: 3.1 mm
DetectorName: Pilatus 2M
Scan
Title: NetrinVIV DCC56 complex / Measurement date: Oct 31, 2013 / Storage temperature: 10 °C / Cell temperature: 10 °C / Exposure time: 0.05 sec. / Number of frames: 20 / Unit: 1/nm /
MinMax
Q0.0536 3.4949
Distance distribution function P(R)
Sofotware P(R): GNOM 4.5a / Number of points: 374 /
MinMax
Q0.07654 1.567
P(R) point12 385
R0 17.85
Result
Type of curve: single_conc /
ExperimentalPorod
MW49 kDa-
Volume-120 nm3

P(R)Guinier
Forward scattering, I01450 1370
Radius of gyration, Rg5.1 nm5.1 nm

MinMax
D-17
Guinier point12 80

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