SGID Silkworm Genome Informatics Database
Gene
KWMTBOMO00391  Validated by peptides from experiments
Pre Gene Modal
BGIBMGA000722
Annotation
surfeit_1_isoform_1_[Bombyx_mori]
Full name
SURF1-like protein       + More
Surfeit locus protein 1      
Location in the cell
Mitochondrial   Reliability : 2.173
 

Sequence

CDS
ATGATACCAGTTACTTCCTTTACTCTTGGTTCATGGCAAGTGTACAGATGGCAATGGAAGCTGGGGCTCATTGACATGATGCAAGCTAAATCCAATGCTGTCCCAATCGACATGCCAAAAGACTTTTCAGAATTAGAAAAAATGGAATATTTACCAGTGAAAGTAAAAGGAGAATTTTTGCATGAAAAAGAGATATTAATAGGTCCTAGAGCACTCATAGAAGAGAGTTCTATCACCAATAGAGTTGGTTCACTTGTATCTGACCCGAAAAAAAACCAAGGGTGGTTGGTGATCACTCCGTTTAAGTTAGCTGACACAGGAGAAGTCATCTTGATAAACAGAGGTTGGATTCATCAAAATTTAAGGCCTAAAGAAAAGCGAGAGCCATCTTTAATAAAGGGTCCTGTTGAGCTAACTGGTGTTGTAAGGTTAACAGAGAAAAGAGCTCCTTTCATGCCTAAAAATAATCCAGAAAAAGGCTCATGGTTTTACAGAGATTTGGATCAGATGAGTGCTCATATTGGATGTTTGCCGATTTGGTTGGATGCAAAAGGTATCCCAGACCCACCTACTGGTTGGCCGATCCCAAATCAAACCAGAGTAACATTGCGGAATGAACACTTTTCGTACATTGTCACATGGTATTCTTTGTTTGCATTTACTAGTATTATGTGGCATCGTTTCTTCATTAGAAAGTTACCATTATTGTAA
Protein
MIPVTSFTLGSWQVYRWQWKLGLIDMMQAKSNAVPIDMPKDFSELEKMEYLPVKVKGEFLHEKEILIGPRALIEESSITNRVGSLVSDPKKNQGWLVITPFKLADTGEVILINRGWIHQNLRPKEKREPSLIKGPVELTGVVRLTEKRAPFMPKNNPEKGSWFYRDLDQMSAHIGCLPIWLDAKGIPDPPTGWPIPNQTRVTLRNEHFSYIVTWYSLFAFTSIMWHRFFIRKLPLL

Summary

Description
Probably involved in the biogenesis of the COX complex.
Component of the MITRAC (mitochondrial translation regulation assembly intermediate of cytochrome c oxidase complex) complex, that regulates cytochrome c oxidase assembly.
Subunit
Component of the MITRAC (mitochondrial translation regulation assembly intermediate of cytochrome c oxidase complex) complex, the core components of this complex being COA3/MITRAC12 and COX14. Interacts with COA3.
Similarity
Belongs to the SURF1 family.
Keywords
Complete proteome   Membrane   Mitochondrion   Mitochondrion inner membrane   Reference proteome   Transmembrane   Transmembrane helix   Alternative splicing   Charcot-Marie-Tooth disease   Disease mutation   Leigh syndrome   Neurodegeneration   Neuropathy   Polymorphism   Primary mitochondrial disease  
Feature
chain  Surfeit locus protein 1
splice variant  In isoform 2.
sequence variant  Found in a patient with LS; unknown pathological significance; dbSNP:rs116779216.
EMBL
DQ311414    ABD36358.1    BABH01007203    ODYU01011944    SOQ57979.1    KQ461196    + More
KPJ06350.1    AK403056    BAM19529.1    GDQN01003249    JAT87805.1    KQ459605    KPI91951.1    GAIX01012019    JAA80541.1    AGBW02015069    OWR40599.1    JTDY01001401    KOB73967.1    KQ971318    EFA00352.1    KQ980074    KYN17830.1    QOIP01000010    RLU18166.1    KQ978379    KYM94491.1    KQ434844    KZC08140.1    KQ976491    KYM83317.1    ADTU01016607    ADTU01016608    ADTU01016609    ADTU01016610    ADTU01016611    ADTU01016612    ADTU01016613    KK107374    EZA51578.1    GL888197    EGI65383.1    GL442742    EFN63126.1    GL450772    EFN80495.1    KQ414663    KOC65353.1    KV924374    PIO37833.1    KK853156    KDR10514.1    GACK01002859    JAA62175.1    AF182952    CH933809    EDW17955.2    KK946934    KFQ55160.1    AQIB01148009    GEZM01063898    JAV68927.1    GEFH01002139    JAP66442.1    KL205884    KFV76182.1    JO841576    AEO33193.1    KL390834    KFP91546.1    KL439664    KFW93858.1    AAEX03006771    KK719747    KFO65575.1    AHZZ02007956    AEYP01042389    AGTO01000703    GEDC01017941    JAS19357.1    KL448313    KFO82504.1    ACTA01065156    GL192776    EFB24908.1    AQIA01023131    KL218256    KFP03574.1    GFFV01003560    JAV36385.1    BC052500    AAH52500.1    KZ288311    PBC28531.1    CM004480    OCT67086.1    JSUE03013917    JU323145    JU473633    JV048058    AFE66901.1    AFH30437.1    AFI38129.1    AGTP01090843    CM001290    EHH57007.1    QUSF01000027    RLW00496.1    NDHI03003456    PNJ45241.1    AJFE02078062    PYGN01001366    PSN35363.1    KK733774    KFQ99310.1    KL351004    KFZ58908.1    M14689    AK002469    BC004755    LSYS01008925    OPJ67713.1    KL226358    KFM12774.1    JH001641    EGW06899.1    RAZU01000235    RLQ63946.1    AC195415    GABC01009972    GABF01010317    GABD01004870    NBAG03000232    JAA01366.1    JAA11828.1    JAA28230.1    PNI68719.1    CM001267    EHH23708.1    GGLE01004793    MBY08919.1    GEDV01006831    JAP81726.1    KV460434    OCA18146.1    GFPF01012168    MAA23314.1    JH169003    GEBF01001245    EHB05582.1    JAO02388.1    HQ205786    HQ205787    HQ205788    HQ205789    HQ205790    HQ205791    HQ205792    HQ205793    HQ205794    HQ205795    HQ205796    HQ205797    HQ205798    HQ205799    HQ205800    HQ205801    HQ205802    HQ205803    HQ205804    HQ205805    HQ205806    HQ205807    HQ205808    HQ205809    HQ205810    HQ205811    HQ205812    HQ205813    HQ205814    HQ205815    HQ205816    HQ205817    HQ205818    HQ205819    HQ205820    HQ205821    HQ205822    HQ205823    HQ205824    HQ205825    KU178341    ADP91654.1    ALQ33799.1    Z35093    AK291122    AL158826    BC028314    BC071658    KL507841    KFO85454.1   
Pfam
PF02104   SURF1
Interpro
IPR002994   Surf1/Shy1       

Ontologies

Topology

Subcellular location
Mitochondrion inner membrane  
Length:
236
Number of predicted TMHs:
1
Exp number of AAs in TMHs:
21.17245
Exp number, first 60 AAs:
0.00485
Total prob of N-in:
0.52654
inside
1  -  207
TMhelix
208  -  230
outside
231  -  236
 
 

Population Genetic Test Statistics

Pi
22.610906
Theta
27.122785
Tajima's D
-1.009077
CLR
0
CSRT
0.135993200339983
Interpretation
Uncertain
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