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Results for the Protein: P13639
119172

EF2_HUMAN RecName: Full=Elongation factor 2; Short=EF-2

Known Diseases associated with this Protein:
  SPINOCEREBELLAR ATAXIA 26 (1 FAMILY)
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1
1
1
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Tips:
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Default View:

FusA - COG0480
LepA - COG0481
PrfC - COG4108
TypA - COG1217
GTP_EFTU - pfam00009
TypA_BipA - cd01891
RF3 - cd04169
LepA - cd01890
EF2 - cd01885
Snu114p - cd04167
EF-G_bact - cd04170
TetM_like - cd04168
EF1_alpha - cd01883
SelB_euk - cd01889
GTP_translation_fact - cd00881
EF-G - cd01886
EF_Tu - cd01884
SelB - cd04171
IF2_eIF5B - cd01887
Ras_like_GTPase - cd00882
MMR_HSR1 - pfam01926
Translation_Factor_I - cd01342
eEF2_II_snRNP - cd04090
eEF2_snRNP_like_II - cd03700
GTP_EFTU_D2 - pfam03144
aeEF2_snRNP_like_IV - cd01681
EF2_IV_snRNP - cd01683
EFG_like_IV - cd01680
EFG_IV - pfam03764
EFG_C - pfam00679
EFG_C - smart00838
eEF2_C_snRNP - cd04098
Elongation_Factor_C - cd01514
Tet_C - cd03711
EFG_mtEFG_C - cd03713
eEF2_snRNP_like_C - cd04096
mtEFG1_C - cd04097


Swiss-Prot Protein: P13639
Identical to: NP_001952
   Default View:























Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
FusACOG04801e-2629844
LepACOG04813.4e-0711356
TypACOG12172.6e-0615513
TypA_BipAcd018911.6e-2218239
EF2cd018854.9e-16020361
LepAcd018909.8e-2920207
Snu114pcd041672.3e-5520361
RF3cd041692.6e-0720296
GTP_translation_factcd008814.7e-9621361
EF_Tucd018840.0002221207
EF1_alphacd018831.5e-0621229
EF-Gcd018864.6e-1121280
SelB_eukcd018897.1e-0621214
TetM_likecd041681e-1021225
EF-G_bactcd041703.7e-0721239
IF2_eIF5Bcd018876.4e-0623232
SelBcd041710.0008523208
Ras_like_GTPasecd008822.1e-2624356
Translation_Factor_Icd013423.7e-13394488
eEF2_snRNP_like_IIcd037006.9e-57394488
eEF2_II_snRNPcd040902.2e-28394487
aeEF2_snRNP_like_IVcd016812.2e-116574746
EF2_IV_snRNPcd016839.2e-71574747
EFG_like_IVcd016801.7e-47579737
Elongation_Factor_Ccd015141.2e-36742821
Tet_Ccd037112.4e-05742821
EFG_mtEFG_Ccd037135e-15742821
eEF2_snRNP_like_Ccd040969.5e-58742821
mtEFG1_Ccd040971.3e-07742810
eEF2_C_snRNPcd040981.7e-36742821
PrfCCOG41089.7e-0511387
GTP_EFTUpfam000092.2e-10817360
MMR_HSR1pfam019265.3e-0531159
GTP_EFTU_D2pfam031442.3e-13409486
EFG_IVpfam037644.8e-52620737
EFG_Cpfam006797.5e-30739828
EFG_Csmart008386e-26740826

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs2230560 Polymorphismp.HIS108GLNN/A
OMIM130610.0001 Diseasep.PRO596HISSPINOCEREBELLAR ATAXIA 26 (1 family)



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