BDB -BiopanningDataSet Details

Biopanning Data

BiopanningDataSet ID: 19

Peptides:

Sequences

EQYQLAWPAMQS(3)
DQMMLPWPAVKL(2)
SQHPLPWPVLML(2)
WQHKIDLRYNGA(2)
WHYPPPYDLMRT(2)
LDQIVIPWPTPR(1)
DQWMMAWPSLTL(1)
SEQHLLKWPPWH(1)
EQQQLSWPPFLP(1)
SQIPMAWPLLSL(1)
TQYTMTWPFSWR(1)
WQQQMKWPSFTY(1)
WQIPVDWPPLPP(1)
WQMQLPWPPRLS(1)
GQMILPWPSPRA(1)
EQFPIAFPRYSI(1)
HQMVLTYPWVPT(1)
DQYVLTFPWTPR(1)
WQMPVNLPIRYP(1)
WQLKYPWISPVG(1)
HQIPIQIHSFAM(1)
DQSKVWLLPSWK(1)
WHYQVPQWLYRH(1)
WYHPLQLTPAPI(1)
WSHMLYLPGSAP(1)
WSHPMYLGPSAL(1)
YNAPSSFIPLVM(1)
NHPIYPHMLLSY(1)
WDSHILTYHVPY(1)

Sequences Features:

Motif:

Q-x(2)-[AVLIFYW]-x-W-P

Unique Sequence Number:

Experimental Method:

Phage display (common panning)

Sequencing Platform:

Sequencing Method:

Sanger sequencing

Rounds of Panning:

Reference:

PMID: 16636049

Target Name:

Coagulation factor XIII A chain

Template Name:

Not determined.

Structure of Target-Template Complex:

Not determined.

Structure of Target-Peptide Complex:

Not determined.

Library Name:

Ph.D.-12 phage display library (X12)

Affinity Measurement Method:

Affinity Measurement Description:

Brief Description:

BiopanningDataSet Comments:

This study further confirmed that the sequences were favored for transamidation using modified glutathione S-transferase (GST) for recombinant peptide-GST fusion proteins. Most of the fusion proteins exhibited a considerable increase in incorporation of primary amines over that of modified GST alone.

Curator:

Curation Date:

0000-00-00

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