D-I-TASSER P11309-D1

D-I-TASSER results for P11309-D1

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

Input Sequence in FASTA format

>P11309 (122 residues)
MLLSKINSLAHLRAAPCNDLHATKLAPGKEKEPLESQYQVGPLLGSGGFGSVYSGIRVSD
NLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLIL
ER

Predicted Secondary Structure

Sequence	20 40 60 80 100 120 \| \| \| \| \| \| MLLSKINSLAHLRAAPCNDLHATKLAPGKEKEPLESQYQVGPLLGSGGFGSVYSGIRVSDNLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLILER
Prediction	CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSSSSSSSSCCCSSSSSSSSCCCCCSSSSSSSSHHHCCCCCCCCHHHHHHHHHHHHHHHCCCCCCSSSSSSSSSCCCSSSSSSCC
Confidence	97676787100246899988877678765456323546998786316886999999989997899999974655401013214789999999998277999771899999739979999719
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 120 \| \| \| \| \| \| MLLSKINSLAHLRAAPCNDLHATKLAPGKEKEPLESQYQVGPLLGSGGFGSVYSGIRVSDNLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLILER
Prediction	62354354444355463753635545656556505640502530352220302203437454400001032640463454743540430040043056513000101211247630000028
	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

                   |                   |                   |                   |                   |                   |

SS
Seq

CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSSSSSSSSCCCSSSSSSSSCCCCCSSSSSSSSHHHCCCCCCCCHHHHHHHHHHHHHHHCCCCCCSSSSSSSSSCCCSSSSSSCC
MLLSKINSLAHLRAAPCNDLHATKLAPGKEKEPLESQYQVGPLLGSGGFGSVYSGIRVSDNLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLILER

3kvwA

0.17

0.16

5.11

1.17

DEthreader

ENTPMTPQAM-YMKLTAFEHH-EI--FSYPEIHVAYRYEVLKVIGKGSFGQVVKAYDHKVHQHVALKMVRN--EK---RF--HRQAAEEIRILEHLRKQDMNVIHMLENFTFRNHICMTFEL

3f2aA1

1.00

0.75

20.89

1.95

SPARKS-K

-------------------------------EPLESQYQVGPLLGSGGFGSVYSGIRVSDNLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLILER

6vg3A1

0.21

0.15

4.67

0.37

MapAlign

------------------------------MHFPRSSLQPITTLGKSEFGEVFLAKAQGLETLVLVKSLQ---SKDEQQQ---LDFRRELEMFGKLN--HANVVRLLGLCREAEPHYMVLEY

2bcjA

0.18

5.84

0.20

CEthreader

CQNLRGDVFQKFIESDKFTRFCQWKNVELNIHLTMNDFSVHRIIGRGGFGEVYGCRKADTGKMYAMKCLDKKRIKMKQGETL---ALNERIMLSLVSTDCPFIVCMSYAFHTPDKLSFILDL

3p1aA2

0.20

0.19

6.02

1.84

MUSTER

---QLQPRRVSFRGEASETLQSPGYDPSRPESFFQQSFQRLSRLGHGSYGEVFKVRSKEDGRLYAVKRSM----SPFRGPKDRARKLAEVGSHEKVG-QHPCCVRLEQAWEEGGILYLQTEL

3i7bA

0.25

0.17

5.34

0.64

HHsearch

--------------------------------IFSDRYKGQRVLGKGSFGEVILCKDKITGQECAVKVISKRQVKQKTD---KESLLREVQLLKQLDH--PNIMKLYEFFEDKGYFYLVGEV

3f2aA1

1.00

0.75

20.89

1.67

FFAS-3D

-------------------------------EPLESQYQVGPLLGSGGFGSVYSGIRVSDNLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLILER

2acxA

0.21

0.20

6.27

0.65

EigenThreader

LSHTGPDLIPEVPRQLVTNCTQRLEQGPCKDLVTKNTFRQYRVLGKGGFGEVCACQVRATGKMYACKKLEKKRIKKR---KGEAMALNEKQILEKVNSR--FVVSLAYAYETKDALCLVLTL

1koaA

0.23

0.16

4.87

1.55

CNFpred

---------------------------------VLDHYDIHEELGTGAFGVVHRVTERATGNNFAAKFVMTPHE------SDKETVRKEIQTMSVLRHP--TLVNLHDAFEDDNEMVMIYEF

2vd5A

0.18

0.14

4.54

1.17

DEthreader

--------------------GA--LAEVRLKRLQRDDFEILKVIGRGAFSEVAVVKMKQTGQVYAMKIMNKWDMLKR--GE-VSCFREERDVLVNG-D-RRWITQLHFAFQDENYLYLVMEY

(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	0.7263

(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	3a7hB	0.69	1.69	0.202	0.770	model1_3a7hB.pdb.gz
2	2vd5A	0.69	2.67	0.186	0.836	model1_2vd5A.pdb.gz
3	2f2uA	0.68	2.34	0.138	0.820	model1_2f2uA.pdb.gz
4	3hkoA	0.67	1.99	0.247	0.762	model1_3hkoA.pdb.gz
5	3tkuA1	0.67	2.70	0.155	0.811	model1_3tkuA1.pdb.gz
6	4dn5A	0.67	3.26	0.128	0.869	model1_4dn5A.pdb.gz
7	1u5rA	0.67	2.20	0.211	0.779	model1_1u5rA.pdb.gz
8	1cdkA	0.66	2.40	0.176	0.770	model1_1cdkA.pdb.gz
9	3c0gB1	0.66	1.25	0.161	0.713	model1_3c0gB1.pdb.gz
10	7akgA1	0.66	2.06	0.263	0.762	model1_7akgA1.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:0004672	0.99	protein kinase activity
GO:0004674	0.98	protein serine/threonine kinase activity

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:0009987	0.99	cellular process
GO:0008152	0.98	metabolic process
GO:0044260	0.97	cellular macromolecule metabolic process
GO:0044238	0.97	primary metabolic process
GO:0065007	0.96	biological regulation
GO:0050789	0.96	regulation of biological process
GO:0006468	0.96	protein phosphorylation
GO:0050794	0.95	regulation of cellular process
GO:0046777	0.85	protein autophosphorylation
GO:0048519	0.77	negative regulation of biological process
GO:0051726	0.76	regulation of cell cycle
GO:0048523	0.76	negative regulation of cellular process
GO:0043067	0.75	regulation of programmed cell death
GO:0043066	0.74	negative regulation of apoptotic process
GO:0007346	0.74	regulation of mitotic cell cycle

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:0044424	1.00	intracellular part
GO:0005737	0.95	cytoplasm
GO:0043226	0.56	organelle
GO:0043229	0.55	intracellular organelle
GO:0043227	0.52	membrane-bounded organelle
GO:0043231	0.51	intracellular membrane-bounded organelle

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	2w4kA	0.665	1.99	0.297	0.746	2.7.11.1	NA
2	0.060	1f0qA	0.620	2.18	0.202	0.730	2.7.11.1	61
3	0.060	1lufA	0.623	2.37	0.185	0.754	2.7.10.1	NA
4	0.060	1gzkA	0.574	1.46	0.234	0.631	2.7.11.1 2.7.1.-	NA
5	0.060	3e3bX	0.625	1.97	0.175	0.721	2.7.11.1	NA

	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	0.18	3a7hB	0.692	1.69	0.202	0.770	0.86	ATP	complex1.pdb.gz	44,47,52,65,67,121
2	0.16	3ndmD	0.689	2.47	0.175	0.836	0.83	3ND	complex2.pdb.gz	44,45,46,47,50,51,52,65,67,104,120,121
3	0.06	1xh9A	0.664	2.29	0.185	0.770	1.40	BU3	complex3.pdb.gz	49,50,51,68,70,73,115

	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.