Fold Recognition Example


Michael Tress
ProteinDesign Group.
Centro Nacional de Biotecnologia (C.N.B.- C.S.I.C.)
Tlf: +34-91-5854570. Fax: +34-91-5854506.

Madrid-May-05


The Query Sequence:

>BX842656_101
MLKNTSSNLDAPVARSCDFAMKKMDLRKAFTLIEPGPVTLVTTSAGGTNNVMTISWTMAV
DFTPKLAITTGPWNFSYKALTKSRECVIAIPTVDLLDKVVGVGTCSGKDTDKFDTFRLTP
IKGKYVEAPLIKECVANIECKVVDIIKKHDIVVLEGVAAYFDTSRKEKRTLHAVGDGTFV
VDGRTLDRKKQMRSKLLGIF


Procedure:

1.-Is this protein similar to a known structure? The results of "BLAST search against PDB.
There is no known structure with sequence similarity to our query.
2.- Get 1D prediction for the target This is the Predict protein [ OUTPUT]
3.-What can I get from annotation?: SwissProtFile.
In this case, swissprot indicates it is a hypothetical protein containing a Flavin reductase like domain.
3.-Results from some fold recognition steps
4.- How consistent is my fold assignment? Some of the predicted folds are structuraly related:
FSSP comparison results file
5.a- Fold Recognition on 1EJE_A structure Based on the secondary structure data, the protein might have 2 domains, one seems to be "all beta" and another the other one "mixed alpha-beta". The active site (FMN binding) of the query protein is located in the same spatial place as the template (1EJE_A) structure.
Alignment structure-sequence : text format
5.b- Mapping the query on 1EJE_A structure

YELLOW: B-Strands.
RED: Helices.
GREY: No secondary structure elements.

Note the loops (are missing)

5.c- Fold Recognition on 1EJE_A structure

A comparison between the predicted structure and the actual one:

RED: The predicted model.
GREEN: The template.
REST: FMN (flavin) group and Ni heteratms.

And, [HERE],the PDB file of the above comparison structure.