Interpro : IPR000073 Alpha\/beta hydrolase fold-1 , IPR026151 Maspardin
PIRSF : No PIRSF
Pdoc : No Pdoc
Pfam : PF12697 Abhydrolase_6
Prints : No Print
EC Number : No EC Number
Title : OsMas1, a novel maspardin protein gene, confers the tolerance to salt and drought stresses by regulating ABA signaling in rice - Wang_2022_J.Integr.Agric__ |
Author(s) : Wang FB , Wan CZ , Niu HF , Qi MY , Li G , Zhang F , Hu LB , Ye YX , Wang ZX , Pei BL , Chen XH , Yuan CY |
Ref : J.Integr.Agric , : , 2022 |
Abstract : Wang_2022_J.Integr.Agric__ |
ESTHER : Wang_2022_J.Integr.Agric__ |
PubMedSearch : Wang_2022_J.Integr.Agric__ |
PubMedID: |
Gene_locus related to this paper: orysa-q33aq0 |
Title : Extracellular vesicles from Echinococcus granulosus larval stage: Isolation, characterization and uptake by dendritic cells - Nicolao_2019_PLoS.Negl.Trop.Dis_13_e0007032 |
Author(s) : Nicolao MC , Rodriguez Rodrigues C , Cumino AC |
Ref : PLoS Negl Trop Dis , 13 :e0007032 , 2019 |
Abstract : Nicolao_2019_PLoS.Negl.Trop.Dis_13_e0007032 |
ESTHER : Nicolao_2019_PLoS.Negl.Trop.Dis_13_e0007032 |
PubMedSearch : Nicolao_2019_PLoS.Negl.Trop.Dis_13_e0007032 |
PubMedID: 30615613 |
Gene_locus related to this paper: echgr-w6u7y4 |
Title : Loss of Maspardin Attenuates the Growth and Maturation of Mouse Cortical Neurons - Davenport_2016_Neurodegener.Dis_16_260 |
Author(s) : Davenport A , Bivona A , Latson W , Lemanski LF , Cheriyath V |
Ref : Neurodegener Dis , 16 :260 , 2016 |
Abstract : Davenport_2016_Neurodegener.Dis_16_260 |
ESTHER : Davenport_2016_Neurodegener.Dis_16_260 |
PubMedSearch : Davenport_2016_Neurodegener.Dis_16_260 |
PubMedID: 26978163 |
Title : A Novel alpha\/beta-Hydrolase Gene IbMas Enhances Salt Tolerance in Transgenic Sweetpotato - Liu_2014_PLoS.One_9_e115128 |
Author(s) : Liu D , Wang L , Zhai H , Song X , He S , Liu Q |
Ref : PLoS ONE , 9 :e115128 , 2014 |
Abstract : Liu_2014_PLoS.One_9_e115128 |
ESTHER : Liu_2014_PLoS.One_9_e115128 |
PubMedSearch : Liu_2014_PLoS.One_9_e115128 |
PubMedID: 25501819 |
Gene_locus related to this paper: ipoba-a0a076l3m2 |
Title : Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses - Ishiura_2014_J.Hum.Genet_59_163 |
Author(s) : Ishiura H , Takahashi Y , Hayashi T , Saito K , Furuya H , Watanabe M , Murata M , Suzuki M , Sugiura A , Sawai S , Shibuya K , Ueda N , Ichikawa Y , Kanazawa I , Goto J , Tsuji S |
Ref : J Hum Genet , 59 :163 , 2014 |
Abstract : Ishiura_2014_J.Hum.Genet_59_163 |
ESTHER : Ishiura_2014_J.Hum.Genet_59_163 |
PubMedSearch : Ishiura_2014_J.Hum.Genet_59_163 |
PubMedID: 24451228 |
Gene_locus related to this paper: human-SPG21 |
Title : Characterization of maspardin, responsible for human Mast syndrome, in an insect species and analysis of its evolution in metazoans - Chertemps_2012_Naturwiss_99_537 |
Author(s) : Chertemps T , Montagne N , Bozzolan F , Maria A , Durand N , Maibeche-Coisne M |
Ref : Naturwissenschaften , 99 :537 , 2012 |
Abstract : Chertemps_2012_Naturwiss_99_537 |
ESTHER : Chertemps_2012_Naturwiss_99_537 |
PubMedSearch : Chertemps_2012_Naturwiss_99_537 |
PubMedID: 22729480 |
Gene_locus related to this paper: spoli-a0a023pts0 |
Title : Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance - Finsterer_2012_J.Neurol.Sci_318_1 |
Author(s) : Finsterer J , Loscher W , Quasthoff S , Wanschitz J , Auer-Grumbach M , Stevanin G |
Ref : Journal of Neurology Sci , 318 :1 , 2012 |
Abstract : Finsterer_2012_J.Neurol.Sci_318_1 |
ESTHER : Finsterer_2012_J.Neurol.Sci_318_1 |
PubMedSearch : Finsterer_2012_J.Neurol.Sci_318_1 |
PubMedID: 22554690 |
Gene_locus related to this paper: human-SPG21 |
Title : [Study of the effect and mechanism of spastic paraplegia 21 protein on the replication of hepatitis B virus] - Gao_2011_Zhonghua.Gan.Zang.Bing.Za.Zhi_19_747 |
Author(s) : Gao GS , Weng PJ , Li RY , Ding SX |
Ref : Zhonghua Gan Zang Bing Za Zhi , 19 :747 , 2011 |
Abstract : Gao_2011_Zhonghua.Gan.Zang.Bing.Za.Zhi_19_747 |
ESTHER : Gao_2011_Zhonghua.Gan.Zang.Bing.Za.Zhi_19_747 |
PubMedSearch : Gao_2011_Zhonghua.Gan.Zang.Bing.Za.Zhi_19_747 |
PubMedID: 22409846 |
Gene_locus related to this paper: human-SPG21 |
Title : Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons - Soderblom_2010_Neurogenetics_11_369 |
Author(s) : Soderblom C , Stadler J , Jupille H , Blackstone C , Shupliakov O , Hanna MC |
Ref : Neurogenetics , 11 :369 , 2010 |
Abstract : Soderblom_2010_Neurogenetics_11_369 |
ESTHER : Soderblom_2010_Neurogenetics_11_369 |
PubMedSearch : Soderblom_2010_Neurogenetics_11_369 |
PubMedID: 20661613 |
Gene_locus related to this paper: human-SPG21 , mouse-SPG21 |
Title : Interaction of the SPG21 protein ACP33\/maspardin with the aldehyde dehydrogenase ALDH16A1 - Hanna_2009_Neurogenetics_10_217 |
Author(s) : Hanna MC , Blackstone C |
Ref : Neurogenetics , 10 :217 , 2009 |
Abstract : Hanna_2009_Neurogenetics_10_217 |
ESTHER : Hanna_2009_Neurogenetics_10_217 |
PubMedSearch : Hanna_2009_Neurogenetics_10_217 |
PubMedID: 19184135 |
Gene_locus related to this paper: human-SPG21 , mouse-SPG21 |
Title : Differential brain transcriptome of beta4 nAChR subunit-deficient mice: is it the effect of the null mutation or the background strain? - Kedmi_2007_Physiol.Genomics_28_213 |
Author(s) : Kedmi M , Orr-Urtreger A |
Ref : Physiol Genomics , 28 :213 , 2007 |
Abstract : Kedmi_2007_Physiol.Genomics_28_213 |
ESTHER : Kedmi_2007_Physiol.Genomics_28_213 |
PubMedSearch : Kedmi_2007_Physiol.Genomics_28_213 |
PubMedID: 16985005 |
Gene_locus related to this paper: human-SPG21 |
Title : Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia - Simpson_2003_Am.J.Hum.Genet_73_1147 |
Author(s) : Simpson MA , Cross H , Proukakis C , Pryde A , Hershberger R , Chatonnet A , Patton MA , Crosby AH |
Ref : American Journal of Human Genetics , 73 :1147 , 2003 |
Abstract : Simpson_2003_Am.J.Hum.Genet_73_1147 |
ESTHER : Simpson_2003_Am.J.Hum.Genet_73_1147 |
PubMedSearch : Simpson_2003_Am.J.Hum.Genet_73_1147 |
PubMedID: 14564668 |
Gene_locus related to this paper: human-SPG21 |
Title : Cloning of ACP33 as a novel intracellular ligand of CD4 - Zeitlmann_2001_J.Biol.Chem_276_9123 |
Author(s) : Zeitlmann L , Sirim P , Kremmer E , Kolanus W |
Ref : Journal of Biological Chemistry , 276 :9123 , 2001 |
Abstract : Zeitlmann_2001_J.Biol.Chem_276_9123 |
ESTHER : Zeitlmann_2001_J.Biol.Chem_276_9123 |
PubMedSearch : Zeitlmann_2001_J.Biol.Chem_276_9123 |
PubMedID: 11113139 |
Gene_locus related to this paper: human-SPG21 , mouse-SPG21 |
Title : The mast syndrome. A recessively inherited form of presenile dementia with motor disturbances - |
Author(s) : Cross HE , McKusick VA |
Ref : Archives of Neurology , 16 :1 , 1967 |
PubMedID: 6024251 |
Gene_locus related to this paper: human-SPG21 |
No structure scheme yet for this family
Genes Proteins in Maspardin-ACP33-SPG21_like family (150)
Fragments of genes in Maspardin-ACP33-SPG21_like family (25)
No fragment of genesNo substrate
No Inhibitor