D-I-TASSER Q9BZF9-D1

D-I-TASSER results for Q9BZF9-D1

[Click result.zip to download all results on this page]

Input Sequence in FASTA format

>Q9BZF9 (295 residues)
MKSLKSRLRRQDVPGPASSGAAAASAHAADWNKYDDRLMKAAERGDVEKVTSILAKKGVN
PGKLDVEGRSVFHVVTSKGNLECLNAILIHGVDITTKNRFKYFESDHLGSGSHFSNRKED
MLLKQGQMYMADSQCTSPGIPAHMQSRSMLRPLELSLPSQTSYSENEILKKELEAMRTFC
ESAKQDRLKLQNELAHKVAECKALALECERVKEDSDEQIKQLEDALKDVQKRMYESEGKV
KQMQTHFLALKEHLTSEAASGNHRLTEELKDQLKDLKVKYEGASAEVGKLRNQIK

Predicted Secondary Structure

Sequence	20 40 60 80 100 120 140 160 180 200 220 240 260 280 \| \| \| \| \| \| \| \| \| \| \| \| \| \| MKSLKSRLRRQDVPGPASSGAAAASAHAADWNKYDDRLMKAAERGDVEKVTSILAKKGVNPGKLDVEGRSVFHVVTSKGNLECLNAILIHGVDITTKNRFKYFESDHLGSGSHFSNRKEDMLLKQGQMYMADSQCTSPGIPAHMQSRSMLRPLELSLPSQTSYSENEILKKELEAMRTFCESAKQDRLKLQNELAHKVAECKALALECERVKEDSDEQIKQLEDALKDVQKRMYESEGKVKQMQTHFLALKEHLTSEAASGNHRLTEELKDQLKDLKVKYEGASAEVGKLRNQIK
Prediction	CCHHHHHHCCCCCCCCCCCCCCCCCCCHHHCCCCCHHHHHHHHHCCHHHHHHHHHHCCCCCCCCCCCCCCHHHHHHHHCCHHHHHHHHHHCCCCCCCCCCCCCCHHHHHHHCCCHHHHHHHHHHCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCHHHHHHHHHHHHHHHHHHHCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCC
Confidence	9217898714556653212220000003214667628999999799999999999809998776899998899999919699999999909998754589992679999865644899999993898765456799931026886233223677622322222210111567889999999998735778899998755542211256778888999999999999999999998025267788999999988753112211468999999999999878778999999998709
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 120 140 160 180 200 220 240 260 280 \| \| \| \| \| \| \| \| \| \| \| \| \| \| MKSLKSRLRRQDVPGPASSGAAAASAHAADWNKYDDRLMKAAERGDVEKVTSILAKKGVNPGKLDVEGRSVFHVVTSKGNLECLNAILIHGVDITTKNRFKYFESDHLGSGSHFSNRKEDMLLKQGQMYMADSQCTSPGIPAHMQSRSMLRPLELSLPSQTSYSENEILKKELEAMRTFCESAKQDRLKLQNELAHKVAECKALALECERVKEDSDEQIKQLEDALKDVQKRMYESEGKVKQMQTHFLALKEHLTSEAASGNHRLTEELKDQLKDLKVKYEGASAEVGKLRNQIK
Prediction	4650354045453643444444444333441254343002004532162024003644040244175120000000232122004000633020123154522000000013223400120034404323143424102000222133233213212432334334432454243034214124542253344035424414433443531453255204403531550354136465515414531441454045554554453254046316534543551454155136528
	Values range from 0 (buried residue) to 8 (highly exposed residue)

Predicted Contact, Hydrogen and Distance Map Used in D-I-TASSER simulation

Contact Map

Distance Map

Hydrogen bond networks

D-I-TASSER simulation is guided by the consensus contact map (left figure), distance map (middle figure) and Hydrogen bond network (right figure) derived based on confidence scores of AttentionPotential. In the contact, distance map and hydrogen bond networks, the axes mark the residue index along the sequence. For the contact map, each dot represents a residue pair with predicted contact, while for the distance map and hydrogen bond network, a color scale represents a distance of 1-20+ angstroms or a angle of 0-180 degree.

Top 10 threading templates used by D-I-TASSER

Rank

PDB
hit

ID1

ID2

Cov

Norm.
Zscore

Download
alignment

                  20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280

                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |

SS
Seq

CCHHHHHHCCCCCCCCCCCCCCCCCCCHHHCCCCCHHHHHHHHHCCHHHHHHHHHHCCCCCCCCCCCCCCHHHHHHHHCCHHHHHHHHHHCCCCCCCCCCCCCCHHHHHHHCCCHHHHHHHHHHCCCCCCCCCCCCCCCCHHHHHHHHHHHHHHHHCCCCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCHHHHHHHHHHHHHHHHHHHCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCC
MKSLKSRLRRQDVPGPASSGAAAASAHAADWNKYDDRLMKAAERGDVEKVTSILAKKGVNPGKLDVEGRSVFHVVTSKGNLECLNAILIHGVDITTKNRFKYFESDHLGSGSHFSNRKEDMLLKQGQMYMADSQCTSPGIPAHMQSRSMLRPLELSLPSQTSYSENEILKKELEAMRTFCESAKQDRLKLQNELAHKVAECKALALECERVKEDSDEQIKQLEDALKDVQKRMYESEGKVKQMQTHFLALKEHLTSEAASGNHRLTEELKDQLKDLKVKYEGASAEVGKLRNQIK

3j5pB

0.09

3.56

1.10

EigenThreader

DRRSIFDAVAQSNCQELESNDTIALLLDVARKTQFVNLHIAIERRNMTLVTLLVENGADVQAAANYFGELPLSLAACTNQLAIVKFLLQNPADISARDSVGNTVLHALVEVATSMYNEILILGAKLHPTLKLEEITNRKGLTPLALAASSGKLPPYKLKNTVGDYFRVTGEILSVSGGVYFFFRGIQYFLQSVVLYFSQVASMVFSLAMGWTNMLYYTRQMGIYAVMIEKMILRDLCRFMFVYLVFLFGFSTAVVTLIEDGKYNLLLAYVILTYLLLNMLIALMGETVNKIAQES

6fesA1

0.19

0.11

3.62

1.39

FFAS-3D

-KKLLEAARAGQDDEVRILLANGADVNTAD-ETGFTPLHLAAWEGHLGIV-EVLLKNGADVNANDERGHTPLHLAAYTGHLEIVEVLLKNGAGVNATDVIGTAPLHLAAMWGHEE-IVEVLLKNGADARAQDKFGKT-------------------------------------PEDLARDNGYESVARLARK-----EIIRAVVDELKELIQNVNDDIKEVEK-----------------------------------------------------------------------

6fesA

0.12

4.11

0.44

CEthreader

GKKLLEAARAGQDDEVRILLANGADVNTADETGFT-PLHLAAWEGHLGIVEVLLKN-GADVNANDERGHTPLHLAAYTGHLEIVEVLLKNGAGVNATDVIGTAPLHLAAMWGHEEIVEVLLKNGADARAQDKFGKTPEDLARDNGYESVARLARKEIIRAVVDELKELIQNVNDDIKEVEKNPEDMEYWNKIYRLVHTMKEITETMGFSPVALVLEAIMMLVKLMLNSEIKITSDLPEDMEFWNLIYRLVHVMKEVTETMGFSSVAKVLHTIMNLVDKMLNSEIKITSDLIDKVK

6bbjA

0.10

3.63

1.07

EigenThreader

GKTCLTKALMNLNGGKNDTIPMLIDIAEKTGNLREFILHIAIERRCKHYVELLVEKGADVHAQARYFGELPLSLAACTNQPDIVHYLTEKKADIRRQDSRGNTVLHALVAIAKVYDLLVIKCVKLYPDSSLEAIFNNDSMSPLMMAAKLGKDGTPPYPYRTTMDYMRLAGEIVTLLTGVVFFITNIKDLFMIITAVLYLVGLAVMVFALVLGWMNALYFTRIMLQKILFKDLFRFLLVYLLFMIGYASALVSLLNPCRDSST------FSKFLLDLFKLTIGLLNMLIALMGETV

5le2A1

0.18

0.11

3.64

1.38

FFAS-3D

-KKLLEAARAGQDDEVRILLANGADVNTAD-ETGFTPLHLAAWEGHLGIV-EVLLKNGADVNANDERGHTPLHLAAYTGHLEIVEVLLKNGAGVNATDVIGTAPLHLAAMWGHLE-IVEVLLKNGADVRAQDKFGKT----------------------------------------PKDLARDNGNEWIRELLEKAERKLKDLDRKLLEAARAGHRDE--VEDLIKN-------------------------------------------------------------------

6fesA

0.14

0.13

4.28

0.86

SPARKS-K

DDEVRILLANGDVNTADETGFT--------------PLHLAAWEGHLGIVEVLLKN-GADVNANDERGHTPLHLAAYTGHLEIVEVLLKNGAGVNATDVIGTAPLHLAAMWGH--EEIVEVLLKNGADA--RAQDKFGKTPEDLARDN-----------GYESVARLARKEIIRAVVDELKELIQNVNDDIKEVEKDMEYWNKIYRLVHTMKEITETMLDMVTRLLDLMEQYIKMVVDALKILIEAVNVLIKMVEKNPEDGFSSVAKVLHTIMNLVDKMLDKVKKKLDMVTRELD

6fesA

0.14

0.12

4.20

0.96

CNFpred

QDDEVRILLANGADVNTADETG------------FTPLHLAAWEGHLGIVEVLLKN-GADVNANDERGHTPLHLAAYTGHLEIVEVLLKNGAGVNATDVIGTAPLHLAAMWGHE--EIVEVLLKNGADARAQD--KFGKTPEDLARDNGYESVARL-------ARKEIIRAVVDELKELIQNVNDDIKEVEKNDMEYWNKIYRLVHTMKEITETMGSPVALVLEAIMMLVKLMLNSSDLIDAVKKMLDMVTRLLDLMVD-----PNLNEEQYIKMVVDALKILIEAVNVLIKMVE

5nvrA

0.07

0.06

2.46

0.83

DEthreader

LAQDTLLSSS------------------VIYRWTTGALITAQVSFLRD-EKFGTFFLSEEIKPISTFTEI----NLIYEKLLLIRGFLKYPKLIETVTSWLPGEVLPRIGILITSIVVLLELLKKCVRIYCIIGLQQNYIADLWNCFSIKWTPGIIHLIVVLFTLVQAVEAHILIVTSFVSLVFNTLKFLELDENKVPHVSWSNFSLPGNPFCNNLLNLPFQTLVRWLLKQIIELLHLALEFCGNTGKLLAAVIE-EEKLKEPLL------------------------------

6fesA

0.11

4.01

0.71

MapAlign

QDDEVRILLANGADVNTADETGFTPLHLAAWEDVNTPLHLAAYTGHLEIVEVLLKNGAG-VNATDVIGTAPLHLAAMWGHEEIVEVLLKNGADARAQDKFGKTPEDLARDNGYVARLARKEIIRAVVDELKELIQNVNDDIKEVEKNPEDMEYWNKIYRLVHTMKEITESPVALVLEAIMMLVKLMDLIDAVKKMLDMVTRLLDLMEEQYIKMVVDALKILIEAVNVLIKMVEKNPE-DMEFWNLIYRLVHVMKEVTETMGFSSVAKVLHTIMNLVDKMLDLIDKVKKKLDMVT-

5le2A

0.15

4.93

0.92

MUSTER

DVRAQDKFGKTPKDLARDNGNELLEKAERKLKDLDRKLLEAARAGH-RDEVEDLIKNGADVNTADETGFTPLHLAAWEGHLGIVEVLLKNGADVNANDERGHTPLHLAAYTGHL-EIVEVLLKNGAGVNATDVIGTAPLHLAAMWGHLEIVEVLLKNGADVRLARDNGNEWIRELLEKAERKLKDLDRKLLEAARAHRDEVEDLIKNGADVNTADETGFTPLHLAAWEGHLGIVEVLLK-ADVNANDERGHTPLHLAAYTGHLEIVEVLLKNGAGVNATDVIAPLHLAAMWGHLE

(a)	ID1 is the number of template residues identical to query divided by number of aligned residues.
(b)	ID2 is the number of template residues identical to query divided by query sequence length.
(c)	Cov is equal the number of aligned template residues divided by query sequence length.
(d)	Norm. Zscore is the normalized Z-score of the threading alignments. A Normalized Z-score >1 means a good alignment and is highlighted in bold.
(e)	Download alignment lists the threading program used to identify the template, and provide the 3D structure of aligned regions of threading templates (threading[1-10].pdb.gz).
(f)	Template residues identical to query sequence are highlighted in color.

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.5677

(a)

D-I-TASSER simulations generate a large ensemble of structural conformations, i.e. decoys. These decoys are clustered by SPICKER based on pairwise structure similarity to report up to five final models from the five largest clusters. Models are ranked in descending order of cluster size. If the simulations converge well, it is possible to have less than 5 models generated, which is usually an indication of good model quality.

(b)

The model confidence is quantitatified by estimated TM-score (eTM-score), calculated based on significance of threading template alignments, contact map satisfaction rate, mean absolute error between distance of model and distance of AttentionPotential, and convergence of D-I-TASSER simulations. eTM-score is typically in the range of [0, 1], with higher eTM-score signifies higher model confidence.

Proteins with similar structure

Top 10 structural analogs in PDB (as identified by TM-align)

Rank	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov.	Download Alignment
1	5nvrA	0.52	5.56	0.071	0.817	model1_5nvrA.pdb.gz
2	6yvuA	0.51	5.51	0.088	0.763	model1_6yvuA.pdb.gz
3	1xi5A	0.50	5.65	0.091	0.780	model1_1xi5A.pdb.gz
4	6wcjL	0.46	5.75	0.060	0.739	model1_6wcjL.pdb.gz
5	5yz0A	0.46	5.66	0.050	0.722	model1_5yz0A.pdb.gz
6	2dfsA	0.46	4.87	0.043	0.647	model1_2dfsA.pdb.gz
7	7dl2A	0.46	6.46	0.047	0.800	model1_7dl2A.pdb.gz
8	6tgbA	0.45	6.11	0.052	0.749	model1_6tgbA.pdb.gz
9	5gncA	0.44	5.93	0.088	0.719	model1_5gncA.pdb.gz
10	3utmA	0.43	4.60	0.125	0.566	model1_3utmA.pdb.gz

(a)	Query structure is shown in cartoon, while the structural analog is displayed using backbone trace.
(b)	Ranking of proteins is based on TM-score of the structural alignment between the query structure and known structures in the PDB library.
(c)	RMSD^a is the RMSD between residues that are structurally aligned by TM-align.
(d)	IDEN^a is the percentage sequence identity in the structurally aligned region.
(e)	Cov. represents the coverage of the alignment by TM-align and is equal to the number of structurally aligned residues divided by length of the query protein.

Predicted Gene Ontology (GO) Terms

Molecular Function (MF)

GO term	Cscore^GO	Name
GO:0003824	0.45	catalytic activity
GO:0008092	0.43	cytoskeletal protein binding
GO:1901363	0.42	heterocyclic compound binding
GO:0097159	0.42	organic cyclic compound binding
GO:0035639	0.41	purine ribonucleoside triphosphate binding
GO:0032559	0.41	adenyl ribonucleotide binding
GO:0032550	0.41	purine ribonucleoside binding
GO:0016787	0.33	hydrolase activity
GO:0060090	0.32	binding, bridging
GO:0044877	0.32	macromolecular complex binding
GO:0016887	0.32	ATPase activity
GO:0005198	0.32	structural molecule activity
GO:0046872	0.31	metal ion binding
GO:0042623	0.31	ATPase activity, coupled
GO:0032403	0.31	protein complex binding

Download full result of the above consensus prediction.

Click the graph to show a high resolution version.

(a)

Cscore^GO is the confidence score of predicted GO terms. Cscore^GO values range in between [0-1]; where a higher value indicates a better confidence in predicting the function using the template.

(b)

The graph shows the predicted terms within the Gene Ontology hierachy for Molecular Function. Confidently predicted terms are color coded by Cscore^GO:

[0.4,0.5)

[0.5,0.6)

[0.6,0.7)

[0.7,0.8)

[0.8,0.9)

[0.9,1.0]

Biological Process (BP)

GO term	Cscore^GO	Name
GO:0065007	0.87	biological regulation
GO:0009987	0.55	cellular process
GO:0050794	0.54	regulation of cellular process
GO:0065008	0.52	regulation of biological quality

Download full result of the above consensus prediction.

Click the graph to show a high resolution version.

(a)

Cscore^GO is the confidence score of predicted GO terms. Cscore^GO values range in between [0-1]; where a higher value indicates a better confidence in predicting the function using the template.

(b)

The graph shows the predicted terms within the Gene Ontology hierachy for Biological Process. Confidently predicted terms are color coded by Cscore^GO:

[0.4,0.5)

[0.5,0.6)

[0.6,0.7)

[0.7,0.8)

[0.8,0.9)

[0.9,1.0]

Cellular Component (CC)

GO term	Cscore^GO	Name
GO:0044446	1.00	intracellular organelle part
GO:0043229	1.00	intracellular organelle
GO:0005737	0.83	cytoplasm
GO:0044444	0.81	cytoplasmic part
GO:0043227	0.72	membrane-bounded organelle
GO:0043231	0.71	intracellular membrane-bounded organelle
GO:0043234	0.68	protein complex
GO:0005634	0.62	nucleus
GO:0044430	0.51	cytoskeletal part
GO:0016459	0.50	myosin complex

Download full result of the above consensus prediction.

Click the graph to show a high resolution version.

(a)

Cscore^GO is the confidence score of predicted GO terms. Cscore^GO values range in between [0-1]; where a higher value indicates a better confidence in predicting the function using the template.

(b)

The graph shows the predicted terms within the Gene Ontology hierachy for Cellular Component. Confidently predicted terms are color coded by Cscore^GO:

[0.4,0.5)

[0.5,0.6)

[0.6,0.7)

[0.7,0.8)

[0.8,0.9)

[0.9,1.0]

Predicted Enzyme Commission (EC) Numbers

Top 5 enzyme homologs in PDB

Rank	Cscore^EC	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov.	EC Number	Predicted Active Site Residues
1	0.060	1ug9A	0.382	5.68	0.056	0.597	3.2.1.70	NA
2	0.060	3m07A	0.315	6.22	0.061	0.522	3.2.1.141	NA
3	0.060	3c5wA	0.301	5.16	0.037	0.448	3.1.3.16	NA
4	0.060	2nvrA	0.286	5.67	0.072	0.448	3.5.1.98	104
5	0.060	1y5mA	0.315	4.79	0.090	0.437	1.1.1.146	105,118

	Click on the radio buttons to visualize predicted active site residues.
(a)	Cscore^EC is the confidence score for the Enzyme Commission (EC) number prediction. Cscore^EC values range in between [0-1]; where a higher score indicates a more reliable EC number prediction.
(b)	TM-score is a measure of global structural similarity between query and template protein.
(c)	RMSD^a is the RMSD between residues that are structurally aligned by TM-align.
(d)	IDEN^a is the percentage sequence identity in the structurally aligned region.
(e)	Cov. represents the coverage of global structural alignment and is equal to the number of structurally aligned residues divided by length of the query protein.

Predicted Ligand Binding Sites

Template proteins with similar binding site:

Rank	Cscore^LB	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov.	BS-score	Lig. Name	Download Complex	Predicted binding site residues
1	0.02	2dvw0	0.395	3.56	0.132	0.475	0.54	III	complex1.pdb.gz	3,66,69,77,78,80,99,100,102,107,110,111
2	0.02	3b95B	0.381	3.59	0.156	0.458	0.57	III	complex2.pdb.gz	69,73,74,77,102,107,110
3	0.02	2rfmB	0.372	3.58	0.155	0.451	0.67	BU2	complex3.pdb.gz	62,91,92,93,94
4	0.02	2rfmB	0.372	3.58	0.155	0.451	0.67	BU2	complex4.pdb.gz	55,58,60,61,92
5	0.01	3depA	0.363	3.12	0.118	0.424	0.61	III	complex5.pdb.gz	69,78,102,107,110,111
6	0.01	2dzn0	0.381	3.69	0.103	0.461	0.58	III	complex6.pdb.gz	10,43,67,78,100,102,107,110
7	0.01	1h2u0	0.354	4.98	0.058	0.505	0.67	III	complex7.pdb.gz	54,58,91
8	0.01	2gl7A	0.341	5.17	0.082	0.495	0.51	III	complex8.pdb.gz	50,64,67,74,81

	Click on the radio buttons to visualize predicted binding site and residues.
(a)	Cscore^LB is the confidence score of predicted binding site. Cscore^LB values range in between [0-1]; where a higher score indicates a more reliable ligand-binding site prediction.
(b)	BS-score is a measure of local similarity (sequence & structure) between template binding site and predicted binding site in the query structure. Based on large scale benchmarking analysis, we have observed that a BS-score >1 reflects a significant local match between the predicted and template binding site.
(c)	TM-score is a measure of global structural similarity between query and template protein.
(d)	RMSD^a the RMSD between residues that are structurally aligned by TM-align.
(e)	IDEN^a is the percentage sequence identity in the structurally aligned region.
(f)	Cov. represents the coverage of global structural alignment and is equal to the number of structurally aligned residues divided by length of the query protein.

[Click result.zip to download all results on this page]

References:
1.	Wei Zheng, Chengxin Zhang, Yang Li, Robin Pearce, Eric W. Bell, Yang Zhang. Folding non-homology proteins by coupling deep-learning contact maps with I-TASSER assembly simulations. In preparation, 2020.