D-I-TASSER Q2M3R5

D-I-TASSER results for Q2M3R5

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

Summary of the Protein

Uniprot ID: Q2M3R5
Protein Name: Solute carrier family 35 member G1
Gene Name: SLC35G1

Input Sequence in FASTA format

>Q2M3R5 (365 residues)
MRPQDSTGVAELQEPGLPLTDDAPPGATEEPAAAEAAGAPDRGRCWLCLSSPCCSRTEPE
AKKKAPCPGLGLFYTLLSAFLFSVGSLFVKKVQDVHAVEISAFRCVFQMLVVIPCLIYRK
TGFIGPKGQRIFLILRGVLGSTAMMLIYYAYQTMSLADATVITFSSPVFTSIFAWICLKE
KYSPWDALFTVFTITGVILIVRPPFLFGSDTSGMEESYSGHLKGTFAAIGSAVFAASTLV
ILRKMGKSVDYFLSIWYYVVLGLVESVIILSVLGEWSLPYCGLDRLFLIFIGLFGLGGQI
FITKALQIEKAGPVAIMKTMDVVFAFIFQIIFFNNVPTWWTVGGALCVVASNVGAAIRKW
YQSSK

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

Contact Map

Distance Map

D-I-TASSER simulation is guided by the consensus contact map (left figure) and distance map (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.

Information of Domain

No. of Domain	Domain	Domain Boundary	Length of Domain	Models of Domain	Sequence
1	Q2M3R5-D1	1-365	365		MRPQDSTGVAELQEPGLPLTDDAPPGATEEPAAAEAAGAPDRGRCWLCLSSPCCSRTEPEAKKKAPCPGLGLFYTLLSAFLFSVGSLFVKKVQDVHAVEISAFRCVFQMLVVIPCLIYRKTGFIGPKGQRIFLILRGVLGSTAMMLIYYAYQTMSLADATVITFSSPVFTSIFAWICLKEKYSPWDALFTVFTITGVILIVRPPFLFGSDTSGMEESYSGHLKGTFAAIGSAVFAASTLVILRKMGKSVDYFLSIWYYVVLGLVESVIILSVLGEWSLPYCGLDRLFLIFIGLFGLGGQIFITKALQIEKAGPVAIMKTMDVVFAFIFQIIFFNNVPTWWTVGGALCVVASNVGAAIRKWYQSSK

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.7895

(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	6ukjA	0.71	2.67	0.105	0.797	model1_6ukjA.pdb.gz
2	5y78A	0.70	2.82	0.138	0.792	model1_5y78A.pdb.gz
3	5ogeA	0.68	3.19	0.121	0.794	model1_5ogeA.pdb.gz
4	5i20A	0.67	3.13	0.116	0.781	model1_5i20A.pdb.gz
5	6i1rA	0.65	3.60	0.125	0.775	model1_6i1rA.pdb.gz
6	6oh2A	0.63	3.22	0.105	0.732	model1_6oh2A.pdb.gz
7	3bkkA	0.43	6.53	0.043	0.685	model1_3bkkA.pdb.gz
8	2c6fA	0.43	6.45	0.055	0.679	model1_2c6fA.pdb.gz
9	6s1yA	0.43	6.48	0.046	0.679	model1_6s1yA.pdb.gz
10	1j36A	0.42	6.63	0.064	0.685	model1_1j36A.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	0.49	catalytic activity
GO:0016787	0.42	hydrolase activity
GO:0043167	0.41	ion binding
GO:0046872	0.40	metal ion binding
GO:0070011	0.38	peptidase activity, acting on L-amino acid peptides
GO:0046914	0.38	transition metal ion binding
GO:0008238	0.36	exopeptidase activity
GO:1901363	0.32	heterocyclic compound binding
GO:0097159	0.32	organic cyclic compound 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:0009987	1.00	cellular process
GO:0006810	1.00	transport
GO:0044699	0.96	single-organism process
GO:0044763	0.94	single-organism cellular process
GO:0065007	0.92	biological regulation
GO:1990034	0.91	calcium ion export from cell
GO:0051480	0.91	regulation of cytosolic calcium ion concentration

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:0005886	1.00	plasma membrane
GO:0005789	1.00	endoplasmic reticulum 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	0.060	1i1iP	0.377	7.12	0.043	0.663	3.4.24.16	NA
2	0.060	1r1jA	0.357	6.40	0.035	0.573	3.4.24.11	233
3	0.060	3fg3A	0.413	5.76	0.034	0.600	4.2.1.92 1.13.11.40	NA
4	0.060	1s4bP	0.365	7.46	0.067	0.668	3.4.24.15	NA
5	0.060	1dmtA	0.357	6.43	0.031	0.573	3.4.24.11	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	0.11	2x94A	0.425	6.59	0.064	0.685	0.25	X94	complex1.pdb.gz	137,138,141,293,296
2	0.06	1jnqA	0.405	6.21	0.053	0.636	0.27	UUU	complex2.pdb.gz	81,82,86,147,295,299,302
3	0.06	1j36A	0.423	6.63	0.064	0.685	0.25	LPR	complex3.pdb.gz	140,143,144,148,295
4	0.01	2xydA	0.428	6.49	0.052	0.685	0.18	3ES	complex4.pdb.gz	137,140,141,238,252,297,300
5	0.01	1ik3A	0.405	5.76	0.029	0.589	0.17	13S	complex5.pdb.gz	78,81,82,85,86,90,149,292,301
6	0.01	3ahoA	0.424	6.72	0.031	0.690	0.16	3A2	complex6.pdb.gz	133,137,254,255,258
7	0.01	1loxA	0.386	6.14	0.031	0.573	0.35	RS7	complex7.pdb.gz	80,83,85,86,151,164,295,298
8	0.01	1hu9A	0.421	5.95	0.038	0.633	0.37	4HM	complex8.pdb.gz	101,105,109,138,300
9	0.01	1uzeA	0.319	7.41	0.035	0.581	0.21	EAL	complex9.pdb.gz	144,145,289,292,295
10	0.01	3dy5A	0.410	5.91	0.026	0.606	0.22	HEM	complex10.pdb.gz	277,278,288,291,292,295,296,299

	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.