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Results for the Protein: P36404
116241255
402

ARL2_HUMAN RecName: Full=ADP-ribosylation factor-like protein 2
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1
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1
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Default View:

Sar1 - cd00879
Arl5_Arl8 - cd04153
ARF - smart00177
Arf - pfam00025
Arl2 - cd04154
SAR - smart00178
Arl3 - cd04155
COG2229 - COG2229
COG1100 - COG1100
Arf6 - cd04149
Rab30 - cd04114
SRPRB - pfam09439
Rab8_Rab10_Rab13_lik - cd01867
Arl4_Arl7 - cd04152
Arf1_5_like - cd04150
RAB - smart00175
Rab1_Ypt1 - cd01869
Rab6 - cd01861
Rab - cd00154
Rab18 - cd01863
SR_beta - cd04105
Rab27A - cd04127
Rab4 - cd04113
Miro - pfam08477
Ras - pfam00071
Arl1 - cd04151
ARD1 - cd04158
Arl6 - cd04157
ARLTS1 - cd04156
Arl10_like - cd04159
Arfrp1 - cd04160
Arf_Arl - cd00878
Arl9_Arfrp2_like - cd04162
Arl2l1_Arl13_like - cd04161
Ras_like_GTPase - cd00882
Era_like - cd00880
MMR_HSR1 - pfam01926


Swiss-Prot Protein: P36404
Identical to: NP_001658
   Default View:







































Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
Sar1cd008791.5e-212176
Arl5_Arl8cd041534.6e-552175
Arl3cd041554.6e-913175
Arl2cd041548.9e-1333175
Arf6cd041494.4e-647175
COG1100COG11002.3e-197182
Rab30cd041140.0008910181
Rab8_Rab10_Rab13_likcd018670.0001114179
Arl4_Arl7cd041528.8e-1214183
Rabcd001541.1e-0717174
Rab6cd018610.00117180
Rab18cd018635.3e-0517176
Rab1_Ypt1cd018699.7e-0517179
SR_betacd041050.0009917179
Rab4cd041133e-0517176
Rab27Acd041278.2e-0517180
Arf1_5_likecd041503.4e-6117175
Arf_Arlcd008781.7e-8718175
Arl1cd041513.1e-7118175
ARLTS1cd041565.8e-5618175
Arl6cd041571.8e-3818175
ARD1cd041586.4e-4018183
Arl10_likecd041598.6e-2218175
Arfrp1cd041605.1e-4118175
Arl9_Arfrp2_likecd041622.2e-3618182
Arl2l1_Arl13_likecd041612.3e-3319175
Era_likecd008807.2e-0521180
Ras_like_GTPasecd008823.5e-3321174
Arfpfam000251.4e-1113176
COG2229COG22293e-057184
Raspfam000710.0001318178
MMR_HSR1pfam019260.0007228126
ARFsmart001779.5e-613178
SARsmart001782.8e-213176
SRPRBpfam094390.000114180
RABsmart001750.0002717179
Miropfam084772.6e-0518128

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs664226 Polymorphismp.VAL141ALAN/A



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