SGID Silkworm Genome Informatics Database
Gene
KWMTBOMO13909
Annotation
PREDICTED:_probable_E3_SUMO-protein_ligase_RNF212_[Plutella_xylostella]
Full name
Probable E3 SUMO-protein ligase RNF212      
Alternative Name
Probable E3 SUMO-protein transferase RNF212
RING finger protein 212
Location in the cell
Extracellular   Reliability : 2.899
 

Sequence

CDS
ATGGATTGGATTCACTGTAATAAATGTTTTTCACAATTAGAACCAGGGATAACACTGCATCTCACATCATGTGGTCACATGTTCTGCAACAATTGTTTGGGCAACGGTCTAAAAGACAGCACGTGTCTAGTATGTCGAATGCCGTGTTCTGCTATGAAATTAGTGCCAGACATGAAACAAGAAATCCAAGATTACTTCACTGATCCTGAAGAGTTGATAAAGAAGTCTTGCGATGTGATACAGTTTCAAAGGCAGCATAGAAGGAGATTGCTCTCTTATCTATTACAATCGACAGAATATTTGGCCCTTCAACATACAATATTCCTCGTTATACCATAA
Protein
MDWIHCNKCFSQLEPGITLHLTSCGHMFCNNCLGNGLKDSTCLVCRMPCSAMKLVPDMKQEIQDYFTDPEELIKKSCDVIQFQRQHRRRLLSYLLQSTEYLALQHTIFLVIP

Summary

Description
SUMO E3 ligase that acts as a regulator of crossing-over during meiosis: required to couple chromosome synapsis to the formation of crossover-specific recombination complexes. Localizes to recombination sites and stabilizes meiosis-specific recombination factors, such as MutS-gamma complex proteins (MSH4 and MSH5) and TEX11. May mediate sumoylation of target proteins MSH4 and/or MSH5, leading to enhance their binding to recombination sites. Acts as a limiting factor for crossover designation and/or reinforcement and plays an antagonist role with CCNB1IP1/HEI10 in the regulation of meiotic recombination (By similarity).
SUMO E3 ligase that acts as a regulator of crossing-over during meiosis: required to couple chromosome synapsis to the formation of crossover-specific recombination complexes. Localizes to recombination sites and stabilizes meiosis-specific recombination factors, such as MutS-gamma complex proteins (MSH4 and MSH5) and TEX11. May mediate sumoylation of target proteins MSH4 and/or MSH5, leading to enhance their binding to recombination sites. Acts as a limiting factor for crossover designation and/or reinforcement and plays an antagonist role with CCNB1IP1/HEI10 in the regulation of meiotic recombination.
Keywords
Alternative splicing   Chromosome   Coiled coil   Complete proteome   Meiosis   Metal-binding   Nucleus   Polymorphism   Reference proteome   Transferase   Ubl conjugation pathway   Zinc   Zinc-finger  
Feature
chain  Probable E3 SUMO-protein ligase RNF212
splice variant  In isoform 4.
sequence variant  In dbSNP:rs17728127.
EC Number
2.3.2.-
EMBL
ODYU01002016    SOQ38999.1    AGBW02007799    OWR54553.1    RSAL01000081    RVE48582.1    + More
JTDY01004398    KOB68214.1    KQ417924    KOF89682.1    KB202284    ESO91101.1    DS235430    EEB15630.1    PYGN01000200    PSN51377.1    NEDP02076567    OWF36567.1    APGK01018569    APGK01018570    KB740081    ENN81615.1    GECU01000923    JAT06784.1    ENN81614.1    AHAT01001562    AHAT01001563    JH817484    EKC30858.1    AK096160    AC019103    AC092535    BC036250    BC050356    BC101258    BC101259    BC101260    BC101261    NBAG03000389    PNI30760.1    NDHI03003552    PNJ23623.1    KK115511    KFM65302.1    ACTA01067697    ACTA01075697    ACTA01083697    ACTA01091697    LSMT01000025    PFX32291.1    KK853123    KDR11067.1    AJFE02035425    AJFE02035426    AJFE02035427    AJFE02035428    AJFE02035429    AJFE02035430    AC194569    PNI30756.1    ABGA01011469    ABGA01011470    ABGA01011471    ABGA01011472    AAEX03002646    PNJ23620.1    PNI30761.1    CABD030026647    CABD030026648    CABD030026649    AQIA01053416    AQIA01053417    AQIA01053418    AQIA01053419    AQIA01053420    AQIA01053421    AQIB01147700    GECZ01017504    JAS52265.1    AHZZ02026141    JH169543    EHB07009.1    AEMK02000062    JSUE03032726    JSUE03032727    KN123337    KFO25691.1    GEDC01016713    JAS20585.1    GEBF01007067    JAN96565.1    FM207699    CAR63560.1    AEYP01079023    JXJN01024710    GEDC01009298    JAS28000.1    EAAA01002659    AABR07072361    AC117047    KK831536    KFP76862.1    UYSL01019922    VDL71338.1    AK089585    AC123743    PNJ23624.1    GDRN01076925    JAI62823.1    UYYA01000150    VDM52709.1    UYYG01001151    VDN55179.1    KQ971371    EFA10202.1    KK715081    KFQ35836.1    CYRY02046175    VCX41821.1    AANG04001605    QCYY01002627    ROT68851.1    KL218617    KFP07064.1    KK371807    KFV43944.1    JOJR01001659    RCN30109.1    KL225479    KFW72653.1   
Pfam
PF14634   zf-RING_5
Interpro
IPR017907   Znf_RING_CS        + More
IPR042123   Vilya/Cst9/RNF212       
IPR013083   Znf_RING/FYVE/PHD       
IPR001841   Znf_RING       
IPR036572   Doublecortin_dom_sf       
SUPFAM
SSF89837   SSF89837       
Gene 3D

Ontologies

Topology

Subcellular location
Nucleus   Associates to the synaptonemal complex. Localizes to a minority of double-strand breaks (DSBs) sites. Marks crossover sites during midpachynema (By similarity).   With evidence from 1 publications.
Chromosome   Associates to the synaptonemal complex. Localizes to a minority of double-strand breaks (DSBs) sites. Marks crossover sites during midpachynema (By similarity).   With evidence from 1 publications.
Length:
112
Number of predicted TMHs:
0
Exp number of AAs in TMHs:
3.54936
Exp number, first 60 AAs:
0.10563
Total prob of N-in:
0.48599
outside
1  -  112
 
 

Population Genetic Test Statistics

Pi
187.255451
Theta
127.716559
Tajima's D
1.40331
CLR
0.138179
CSRT
0.758462076896155
Interpretation
Uncertain
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