Amycolicicoccus subflavus (strain DSM 45089 / DQS3-9A1)
Average proteome isoelectric point is 6.3
Get precalculated fractions of proteins
Acidic |
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pI < 6.8 |
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6.8-7.4 |
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pI > 7.4 |
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Basic |
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All |
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Virtual 2D-PAGE plot for 4,703 proteins (isoelectric point calculated using IPC_method)
Get csv file with sequences according given criteria:
* You can choose from 18 different methods for calculating isoelectric point
Protein with the lowest isoelectric point:>tr|F6EJA3|F6EJA3_AMYSD Collagen alpha 2(I) chain
MGPSTTGPTIVGPTTVGPTIVGPTIVSPGGGSGAGGGNVVFNPVIAPVIAPVIAPVINPGAPGGGGGGGGGTAAPVTNVNNNTNNNIITTPPGGGGGDTTIIINNPPGGGGGDVTGPVTNIGDIGNIGDIGLGDISLGDIGLGDISLGDIGNLTGPILTDILTSGITLSEILPVNLLSDNVFGDLISAPS
IGDLTDIGNFVQNLTNIGVIDQSLAIGDIINSLANIGDVTGIGPVGDFLQDIAFLNDLTGIGQVGDFLQNLTGIGSIDPSLLQNITGIVQDVNLTDTDVLSNLVNVGDFLSNVSGIGDVTNIGQVLQNFANFGDLTNVGQVGDILSNLVNVGDPSSVIGDILTNAGDLSGIGEIGNILSGLSQIGDISNI
ANVADVLQQFAQIGDLSVFNSVLDGLTGVFDPTVTFNDLVDVLSNIGDINTLNATLTDVLNDFTGIGQIGDVLSGLVGLNNEGALGQIGDVLTAFGNIENLNAIGDVLSNIGNGSGVGELLTGDVTAINQIGDVLSNIGQIGDGANFTAIGSALENIANITDPTIIGQIGDFTNVGNLTDVGQIAGFFQD
IAQLSDISVLSPMFENIALLSDLIDAGDVTALNQINEILTNVASGNELTDVLSNIALISDPTVISQVGELLSGNQLGDITGIAGDFGNVSDVVTNLLSDNQLGDFAGQIGDVLSGNEVGDVISGIAGGNQVGDVLSGITALNDAAAVGQVGDILSNFAQVTDNTVITQIGEALSGNQFGDVLSNLAQFDP
VVLGQVGDVLSGFTAFSDPAVIGQVGDILSGNVGAIGQVGDVLSNLASAGDIASIGAIGDALQNFANLSDTSLLSDLISAGDFTAVGPLFENLAQLGDVNNLSVIGDILSGNVAQGGDVLNNIANADGVTQFGDVLSGIGSGNLAQIGDVLSGNVAQLSDFSDFAQVGDILSNLGALNDPVLIGQFGDIL
SGLASNNPVVISDVAEILSGNAAQFGPITTFLGDIASISDSTILGQIGDVLSGFGNMENLSGIGDLLSGNNGDILSDLVGIGDGNGIGQVGDVLSNLATVSDNLNVGALGAALQDIASIGDPSAMFGDILSGDVLSNISNFGDLGLAELNQVGAFFQDIAQVGDLTAIGQVFDSLVSLGDVANVGEIGDV
LSGFGLFNDVLSNLGSFGDNATIGSLGAALQDFANISDAALIGDVLSNIASGDPSAALGDVLSNIAQLGDITDNTVVGEVGDVLSNFAQITDPAIINDFSEALSGLGSWNQLGDLLAGNQFGDVLSGLAQIGDPTAIGQLGDVLIGIGNIENLGQFADVLNGDLFSGNVGEIGDVLSQLATLGDTANLTA
IGNTLQDFANITDPSVLSDILNPSSDIGDVLSGFTTGDFGQLTAFFSDLADIGDINVIGDVLSNVAQLSDIANGNAITDVLSGIAGGNEIGDVVGGIANGDNGVGQIGDVAAISLAQISDVLNGNQFGDVLSGDFGQIGDVLSGLTGISDPAVIAQVGDVLTGLAGGNDISDVLNGLTTGDFVSIGEIGD
VLSGIANADNVGQIGDVLSGFGNLENVGQFSEILSGLVGVGDFAPVTTLGSVLQDFANTGDISQVGTFFENITQNGDLNVLNPVLENISTLSDFGNITDISDVLSGFGNISDPTIVAPITDVLSGVANISDPTVIGQVGDVLSGLASGNEVGDVLSGLTGIGDGNSIGQLGDILSGLGSFGDVNGIGEIS
DVLSNFGGLANIGQVGDILSNFDAISDNLNIGSLAATLQNVAQMGDFAPFLQDVGQVGDIAGISAVFENLSALNEISNVGQISDVLSNIGNANEVGDVLSGLANANQLGDVLSGIANVSDPSVLGQIGDVLSGFGSGNEIGDVLSGLATITDPIVLGEVGDILSGIANLDNTQIGNVLSDLVDASDFANV
GQIGDVLSNLAGAGDFTNIGQIGDLLSNFGTIGDSFNIGEIGAVLQDIAQTGDISQLGAFVDTLGQMGDLNVLSPVFESITALNDISNIGQIGDVLSNFVEAGNANQLGDVLSGIANISDPTVVGQINDVLSSFGNANDVSDVLSDLIAVGDNATIGQIGDVLSSIGSFENVGQISESLNDLSALSDNLN
ISELSAVLQDVAQTGDIGQFAAFLQDVAQVGDIGQLGAVFENLSVLSDFANSSDIGDVLSGNANPVTEILPGDFSDIGQISDVLNDLSALNPAVVGQVGDVLSGFGNITDPTFIGQFGNVLNDLVDAGNENQLAPLLSDLIEVGDVTNIGQFSDILNDLSALNPSDIGQVGDVLSGLSGIDAGDVSGIGD
VLSGNAGQFGDVLSSLVALSDTVDIGNLGGALQDFANISDSTVLSDLFNGLAGGDPSAAIGDVLSGISAGDIGSITAFFDDLAQIGDFGDVSAVFDNISVLGDILSGNDIAGTISDIASGNAVFGQVGDFLNGVGTISDPSVIGEIGDVLSGLSAIGDPTIIGQFGDVLSGIVSGNQISDVLSGDFGQLG
PISSVIGDLTGISDPTVIGQVGDVLSDLVDAGDITNIGQVGDLLSGNAGEIGDVLSNLAALSDTVDVGNLGATLQDFANISDPSVLNDVIDSVINVSGDPSVVIGDVLSGLSAGDIGSLTAFFEDLAQVGDFGNVTAVIENLATLGDFGNIGQIGDFIANIGEIPGLGDLPGLGDLPGLGNLPGLGELPD
FSDVLDPSVIGDLTGGIGAVEFVGDISGSFSGAAEAVAGVAGAAAGAAEGAATAAGAVTGAFAAVGEAGGTLSGAFDGSAGAAAQAAGALSGGATALGDASGSLGGAFAGGAEALAGAAGGAAGAVSGAAGAAAGATGALAGTAGAASEVAGNLGGAFAGGAEAVGGAAGALAGSAGAVSDATGAVAGSA
GAAGQTAGTVAGAAAAAAGGAAAAAAGLAAVAAGGAEAIGGFTGMGEALAGAAGDLAGSAGAVGGVTGALAGSAGALGEAAGAAGAAMQGGATAAGDVAGALAGSAGAVGDVAGTAAAGLAGGAGAVGDVAGSLAGSAGALGEAAGAASGALAGGAEALGGAAGAFSGALESGADAAAGAAGAFAGAAGA
AGDVAGAVGSGLSGGAAAAGALAGSAGALGDVAGAVGGAATGGAGAVGDVAGALAGSASGLAGAAGGLTGAVEGGASAFGDAAGALAGSAGALGEAAGAATGAFAGGAQALGDAGTALAGSAGAVGDVAGALAGSAGAVGDVAGTLAGSAGALGEAAGAVGGAFAGGAEALGGAAGALAGSAGAVGDVAG
TLAGSAAAFGDVAGAGAGALAGGAEALGGVAGGLAGSAGAVGDVAGGLAGSAGALGEAAGGFAGAFEGGAAALGDAAGGLAGVAGAAGEAGGALAGAAGAAGDVAGALAGSAGAAGDVAGALAGSAGALGEAGGALAGSAGALGGAAGAIAGAAEAGAGIGGELGDTAFGLGGALAGGADAAAGAAGALS
GSAEALGGVAGGAAGAFAGGAEAVGGAAGALAGSAGALGGVAGGAAGAFAGGAEAVGGAAGALAGSAGALGGVAGGAAGAFAGGAEVVGGAAGALAGSAGAVGDVAGSAAGAFAGGAGALGEAGAGLAGSAGAVGDAAGAVAGSAGVVGDAAGALAGSAGAVGDAAGAFSGALAGGAEAIGGVAGAAAGS
AGAVGDVAGALAGSAGVVGDAAGAAAGAFSGGAEALGGAAGALAGSAGAVGDVAGTLAGSAGALGETAGAFTGAFEGGAGAVGDAAGALAGSAEVLGDTAGAFSGALQGGAAAAGSTAAALAGSAGALGDAAGSVGGALSGGADALASTAGAAAGSAGALGGLAGALGGAFGGGAAALGGVAGAAGAGLE
GGAGAAGGAAGALAGSAGALGETAGTLGGALAGGADAFGGATGALAGSAGALGDAAAAFSGALESGADAAGGLAGSAGVIGDVAGGLAGSAGALGDMAGAGGAALAGGAGAAAAAAGALAGSAGALGDVAGAAAGGAEAVGDVAGALAGTADAGGALAGSAGAIGDTAGAFTGAFQGGADALGGAGGALA
GSAGAVGDAAGGFAGAVDGGAGIIGDAAGVFAGTAGGTAEAVGGVTGAVAGGADALGGAAGALSGSTAFLGDATAGIAGAGGGAAEAVGGAAGAVSGGAEALGGAAGAVSGTLDGAAGITGGLTTAPDSVSSTSFSDGTDGFGGVTGTVTDTVGAVTDYSTYSAPVTEYIAPLPDYTAPVTDTVTSGAET
LGGTASGLTSGLTSGLSSGLSQTWDSGLTSAFDAPAGDSTDFIG
Molecular weight: 389.46 kDa
Isoelectric point according different methods:
Protein with the highest isoelectric point:>tr|F6EPG8|F6EPG8_AMYSD 50S ribosomal protein L34
MAKGKRTFQPNNRRRARVHGFRLRMRTRAGRSIISARRRKGRAELAV
Molecular weight: 5.55 kDa
Isoelectric point according different methods:
General Statistics
Number of major isoforms |
Number of additional isoforms |
Number of all proteins |
Number of amino acids |
Min. Seq. Length |
Max. Seq. Length |
Avg. Seq. Length |
Avg. Mol. Weight |
4,673 |
30 |
4,703 |
1,461,867 |
37 |
7,481 |
312.8 |
33.7 kDa |
Amino acid frequency
Ala |
Cys |
Asp |
Glu |
Phe |
Gly |
His |
Ile |
Lys |
Leu |
Met |
Asn |
Gln |
Pro |
Arg |
Ser |
Thr |
Val |
Trp |
Tyr |
12.48 |
0.78 |
5.93 |
5.9 |
3.19 |
8.69 |
2.26 |
4.67 |
2.28 |
9.98 |
2.05 |
2.23 |
3.0 |
5.47 |
7.28 |
5.88 |
5.94 |
8.48 |
1.44 |
2.08 |
Note: For statistics only major isoforms were used (in this case 4,673 proteins)
For dipeptide frequency statistics click
here