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Results for the Protein: NP_612198
27894285

proprotein convertase subtilisin/kexin type 6 isoform f preproprotein [Homo sapiens]
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AprE - COG1404
Peptidases_S8_Subtil - cd07483
Peptidases_S8_Protei - cd04059
Peptidases_S8_Thermi - cd07484
Peptidase_S8 - pfam00082
Peptidases_S8_11 - cd04843
Peptidases_S8_Fervid - cd07485
Peptidases_S8_C5a_Pe - cd07475
Peptidases_S8_PCSK9_ - cd04077
Peptidases_S8_Kp43_p - cd04842
Peptidases_S8_5 - cd07489
Peptidases_S8_12 - cd07480
Peptidases_S8_Autotr - cd04848
Peptidases_S8_1 - cd07487
Peptidases_S8_subtil - cd07474
Peptidases_S8_Bacill - cd07481
Peptidases_S8_Subtil - cd07473
Peptidases_S8_Subtil - cd07477
Peptidases_S8_8 - cd07492
Peptidases_S8_Lantib - cd07482
Peptidases_S8_13 - cd07496
Peptidases_S8_6 - cd07490
Peptidases_S8_S53 - cd00306
Peptidases_S8_15 - cd07498
Peptidases_S8_Subtil - cd04847
COG4935 - COG4935
P_proprotein - pfam01483


RefSeq Protein: NP_612198
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Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
Peptidases_S8_Subtilcd074830.00094100454
Peptidases_S8_Proteicd040591.5e-175160454
Peptidases_S8_Thermicd074841e-09161457
Peptidases_S8_11cd048433.8e-06184454
Peptidases_S8_C5a_Pecd074752.8e-05188488
Peptidases_S8_Fervidcd074855.5e-12188452
Peptidases_S8_PCSK9_cd040770.00026190455
Peptidases_S8_Kp43_pcd048426.2e-07191462
Peptidases_S8_5cd074895.7e-05192482
Peptidases_S8_12cd074800.00095194483
Peptidases_S8_Autotrcd048482e-12195454
Peptidases_S8_Subtilcd074732.5e-13196454
Peptidases_S8_subtilcd074741.9e-08196486
Peptidases_S8_Bacillcd074814.1e-06196454
Peptidases_S8_1cd074871.2e-07196454
Peptidases_S8_Lantibcd074829.9e-07198452
Peptidases_S8_13cd074961.5e-10198452
Peptidases_S8_8cd074921.4e-05198454
Peptidases_S8_Subtilcd074772.3e-09198452
Peptidases_S8_S53cd003065e-37199452
Peptidases_S8_Subtilcd048479.3e-05199454
Peptidases_S8_15cd074982.6e-14199452
Peptidases_S8_6cd074907.5e-05199454
Peptidase_S8pfam000821.2e-123179479
COG4935COG49353.1e-06497658
P_proproteinpfam014833.2e-38539622

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs45566435 Polymorphismp.CYS487ARGN/A
dbSNPrs1058260 Polymorphismp.CYS502ARGN/A
dbSNPrs1135911 Polymorphismp.GLU465LYSN/A
dbSNPrs20543 Polymorphismp.SER570PHEN/A



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