D-I-TASSER A0A1B0GX49-D1

D-I-TASSER results for A0A1B0GX49-D1

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

Input Sequence in FASTA format

>A0A1B0GX49 (114 residues)
MSIRLLCCVAFSLLWAGPVTAGITQAPTSQILAAGRSMTLRCTQDMRHNAMYWYRQDLGL
GLRLIHYSNTAGTTGKGEVPDGYSVSRANTDDFPLTLASAVPSQTSVYFCASSD

Predicted Secondary Structure

Sequence	20 40 60 80 100 \| \| \| \| \| MSIRLLCCVAFSLLWAGPVTAGITQAPTSQILAAGRSMTLRCTQDMRHNAMYWYRQDLGLGLRLIHYSNTAGTTGKGEVPDGYSVSRANTDDFPLTLASAVPSQTSVYFCASSD
Prediction	CCCSSHHHHHHHHHCCCCCCCSSSSCCCCSSSSCCCSSSSSSSSCCCCCSSSSSSCCCCCCCSSSSSSCCCCCCCCCCCCCCCCCSCCCCCCSSSSSCCCCCCCCSSSSSSCCC
Confidence	995300656666754476564078578814421893099999945898717997618999966899983654346788999842156899962688814890035565545049
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 60 80 100 \| \| \| \| \| MSIRLLCCVAFSLLWAGPVTAGITQAPTSQILAAGRSMTLRCTQDMRHNAMYWYRQDLGLGLRLIHYSNTAGTTGKGEVPDGYSVSRANTDDFPLTLASAVPSQTSVYFCASSD
Prediction	833311120212121133341403033443344445513040424462420201224475413001111344456675147403172486450404054344612032141338
	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 DeepPotential. 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

                   |                   |                   |                   |                   |

SS
Seq

CCCSSHHHHHHHHHCCCCCCCSSSSCCCCSSSSCCCSSSSSSSSCCCCCSSSSSSCCCCCCCSSSSSSCCCCCCCCCCCCCCCCCSCCCCCCSSSSSCCCCCCCCSSSSSSCCC
MSIRLLCCVAFSLLWAGPVTAGITQAPTSQILAAGRSMTLRCTQDMRHNAMYWYRQDLGLGLRLIHYSNTAGTTGKGEVPDGYSVSRANTDDFPLTLASAVPSQTSVYFCASSD

3tf7C

0.44

0.42

12.32

1.33

DEthreader

PDARV--LWYVQGPQMLL--AAVTQSPRNKVTVTGENVTLSCRQTNSHNYMYWYRQDTGHELRLIYYSYGGNLQIGDVPD-GYKATRTTQEDFFLTLESASPSQTSLYFCASSD

6v0yE1

0.28

0.23

6.97

1.17

SPARKS-K

---------------------AVFQTPNYHVTQVGNEVSFNCKQTLGHDTMYWYKQDSKKLLKIMFSYNNKQLIVNETVPRRFSPQSSDKAHLNLRIKSVEPEDSAVYLCASSL

6wl2C1

0.27

0.22

6.73

1.72

FFAS-3D

---------------------GVVQSPRHIIKEKGGRSVLTCIPISGHSNVVWYQQTLGKELKFLIQHYEKVERDKGFLPCRFSVQQFDDYHSEMNMSALELEDSAMYFCASS-

4pjhF

0.68

0.55

15.74

1.65

CNFpred

---------------------GVTQTPKFQVLKTGQSMTLQCAQDMNHNSMYWYRQDPGMGLRLIYYSASEGTTDKGEVPNGYNVSRLNKREFSLRLESAAPSQTSVYFCASSG

3wbdA

0.17

5.46

1.33

DEthreader

PL-SL--IYLQKSPKPLGSQIQLQQSG-PELVRPGASVKISCKASYTFTYIHWVKQRPGEGLEWIGWIYPSNTKYNEKFKGKATLTVDTSSTAYMQLSSLTSEDSAVYFCARGG

3he6D1

0.57

0.46

13.37

1.10

SPARKS-K

---------------------AVTQSPRNKVAVTGGKVTLSCNQTNNHNNMYWYRQDTGHGLRLIHYSYGAGSTEKGDIPDGYKASRPSQENFSLILELATPSQTSVYFCASGD

7ckwN

0.25

0.20

6.26

0.47

MapAlign

--------------------VQLQESGG-GLVQPGGSLRLSCAASFSNYKMNWVRQAPGKGLEWVSDISQSGSISYTSVKGRFTISRDAKNTLYLQMNSLKPEDTAVYYCARCP

6vy5H

0.23

0.19

6.04

0.26

CEthreader

-------------------EVQLLESGG-GLIQPGGSLRLSCAASFSRFTMSWVRQPPGKGPEWVSGISGGHTYYADSVKGRFTISRDNKNTLYLQMNSLKAEDTAVYYCAKDG

3tf7C2

0.56

0.46

13.38

0.96

MUSTER

--------------------AAVTQSPRNKVTVTGENVTLSCRQTNSHNYMYWYRQDTGHELRLIYYSYGAGNLQIGDVPDGYKATRTTQEDFFLTLESASPSQTSLYFCASSD

3tf7C2

0.56

0.46

13.38

0.40

HHsearch

--------------------AAVTQSPRNKVTVTGENVTLSCRQTNSHNYMYWYRQDTGHELRLIYYSYGAGNLQIGDVPDGYKATRTTQEDFFLTLESASPSQTSLYFCASSD

(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	0.7775

(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 DeepPotential, 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	3tf7C	0.82	1.75	0.444	0.903	model1_3tf7C.pdb.gz
2	3wbdA	0.80	1.95	0.173	0.912	model1_3wbdA.pdb.gz
3	2gjjA	0.79	2.19	0.120	0.921	model1_2gjjA.pdb.gz
4	5lx9H	0.79	1.93	0.210	0.895	model1_5lx9H.pdb.gz
5	5npiA	0.79	2.05	0.189	0.903	model1_5npiA.pdb.gz
6	6ehwB	0.79	1.90	0.238	0.895	model1_6ehwB.pdb.gz
7	5wn9H	0.79	1.83	0.248	0.895	model1_5wn9H.pdb.gz
8	3uzeA	0.79	1.88	0.238	0.895	model1_3uzeA.pdb.gz
9	7jumI	0.78	1.97	0.257	0.895	model1_7jumI.pdb.gz
10	5b3nA	0.78	2.19	0.236	0.903	model1_5b3nA.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:0003823	0.80	antigen binding
GO:0005102	0.68	receptor binding
GO:0003824	0.63	catalytic activity
GO:0008236	0.62	serine-type peptidase activity
GO:0004175	0.62	endopeptidase 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:0050896	0.96	response to stimulus
GO:0002376	0.95	immune system process
GO:0006955	0.94	immune response
GO:0002377	0.64	immunoglobulin production
GO:0065007	0.50	biological regulation
GO:0050789	0.50	regulation of biological process

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:0044421	0.91	extracellular region part
GO:0044464	0.82	cell part
GO:0044425	0.79	membrane part
GO:0016020	0.75	membrane
GO:0005615	0.64	extracellular space
GO:0005886	0.62	plasma membrane

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	0.089	1zv5A	0.720	1.81	0.215	0.816	3.2.1.17	NA
2	0.075	1rjcA	0.685	2.10	0.250	0.807	3.2.1.17	36
3	0.072	2bk8A	0.583	2.05	0.130	0.675	2.7.11.1	54
4	0.067	2wwmD	0.590	2.29	0.145	0.693	2.7.11.1	41,95,99
5	0.067	2gqhA	0.529	2.53	0.159	0.667	2.7.11.1	106

	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	0.10	1kcsL	0.734	1.40	0.286	0.798	0.53	III	complex1.pdb.gz	56,57,58,62
2	0.08	1nd0A	0.727	1.42	0.231	0.798	0.51	DP4	complex2.pdb.gz	55,56,57,61
3	0.05	1mf22	0.735	1.36	0.264	0.798	0.51	III	complex3.pdb.gz	50,52,54,56,60,61,62,64,67,68,109
4	0.05	1cbvL	0.739	1.30	0.275	0.798	0.54	QNA	complex4.pdb.gz	35,99,100
5	0.05	3cfbA	0.711	1.49	0.278	0.789	0.51	SPB	complex5.pdb.gz	58,59,60
6	0.05	3cfbL	0.708	1.51	0.278	0.789	0.51	SPB	complex6.pdb.gz	59,61,63
7	0.04	1himL	0.715	1.80	0.202	0.825	0.66	III	complex7.pdb.gz	68,69,74,75,77,112

	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, Qiqige Wuyun, Yang Li, Quancheng Liu, Xiaogen Zhou, Yiheng Zhu, P. Lydia Freddolino, Yang Zhang. Integrating deep learning potentials with I-TASSER for single- and multi-domain protein structure prediction. Submitted. 2023.