D-I-TASSER Q16851

D-I-TASSER results for Q16851

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

Summary of the Protein

Uniprot ID: Q16851
Protein Name: UTP--glucose-1-phosphate uridylyltransferase
Gene Name: UGP2

Input Sequence in FASTA format

>Q16851 (508 residues)
MSRFVQDLSKAMSQDGASQFQEVIRQELELSVKKELEKILTTASSHEFEHTKKDLDGFRK
LFHRFLQEKGPSVDWGKIQRPPEDSIQPYEKIKARGLPDNISSVLNKLVVVKLNGGLGTS
MGCKGPKSLIGVRNENTFLDLTVQQIEHLNKTYNTDVPLVLMNSFNTDEDTKKILQKYNH
CRVKIYTFNQSRYPRINKESLLPVAKDVSYSGENTEAWYPPGHGDIYASFYNSGLLDTFI
GEGKEYIFVSNIDNLGATVDLYILNHLMNPPNGKRCEFVMEVTNKTRADVKGGTLTQYEG
KLRLVEIAQVPKAHVDEFKSVSKFKIFNTNNLWISLAAVKRLQEQNAIDMEIIVNAKTLD
GGLNVIQLETAVGAAIKSFENSLGINVPRSRFLPVKTTSDLLLVMSNLYSLNAGSLTMSE
KREFPTVPLVKLGSSFTKVQDYLRRFESIPDMLELDHLTVSGDVTFGKNVSLKGTVIIIA
NHGDRIDIPPGAVLENKIVSGNLRILDH

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	Q16851-D1	1-72	72		MSRFVQDLSKAMSQDGASQFQEVIRQELELSVKKELEKILTTASSHEFEHTKKDLDGFRKLFHRFLQEKGPS
2	Q16851-D2	73-422	350		VDWGKIQRPPEDSIQPYEKIKARGLPDNISSVLNKLVVVKLNGGLGTSMGCKGPKSLIGVRNENTFLDLTVQQIEHLNKTYNTDVPLVLMNSFNTDEDTKKILQKYNHCRVKIYTFNQSRYPRINKESLLPVAKDVSYSGENTEAWYPPGHGDIYASFYNSGLLDTFIGEGKEYIFVSNIDNLGATVDLYILNHLMNPPNGKRCEFVMEVTNKTRADVKGGTLTQYEGKLRLVEIAQVPKAHVDEFKSVSKFKIFNTNNLWISLAAVKRLQEQNAIDMEIIVNAKTLDGGLNVIQLETAVGAAIKSFENSLGINVPRSRFLPVKTTSDLLLVMSNLYSLNAGSLTMSEKR
3	Q16851-D3	423-508	86		EFPTVPLVKLGSSFTKVQDYLRRFESIPDMLELDHLTVSGDVTFGKNVSLKGTVIIIANHGDRIDIPPGAVLENKIVSGNLRILDH

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.68

(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	2icyB	0.89	1.52	0.532	0.909	model1_2icyB.pdb.gz
2	2i5kB	0.87	1.79	0.554	0.905	model1_2i5kB.pdb.gz
3	3r2wA	0.86	2.01	0.957	0.905	model1_3r2wA.pdb.gz
4	2oefA	0.80	2.65	0.354	0.866	model1_2oefA.pdb.gz
5	3gueA	0.79	3.41	0.348	0.894	model1_3gueA.pdb.gz
6	1jv3A	0.65	4.01	0.156	0.756	model1_1jv3A.pdb.gz
7	3ogzA	0.65	4.89	0.151	0.797	model1_3ogzA.pdb.gz
8	2yqjA	0.65	3.68	0.138	0.736	model1_2yqjA.pdb.gz
9	4bqhA	0.64	3.64	0.155	0.730	model1_4bqhA.pdb.gz
10	4bmaA	0.64	3.78	0.171	0.730	model1_4bmaA.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	1.00	catalytic activity
GO:0070569	0.98	uridylyltransferase activity
GO:0003983	0.51	UTP:glucose-1-phosphate uridylyltransferase 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:0008152	0.98	metabolic process
GO:0071704	0.97	organic substance metabolic process
GO:0044238	0.96	primary metabolic process
GO:0009987	0.96	cellular process
GO:0044237	0.93	cellular metabolic process
GO:0034641	0.84	cellular nitrogen compound metabolic process
GO:1901135	0.83	carbohydrate derivative metabolic process
GO:0006139	0.83	nucleobase-containing compound metabolic process
GO:0009225	0.81	nucleotide-sugar metabolic process
GO:1901576	0.70	organic substance biosynthetic process
GO:0044699	0.68	single-organism process
GO:0044249	0.68	cellular biosynthetic process
GO:1901362	0.56	organic cyclic compound biosynthetic process
GO:0044710	0.56	single-organism metabolic process
GO:0044271	0.56	cellular nitrogen compound biosynthetic process
GO:0018130	0.56	heterocycle biosynthetic process
GO:1901137	0.55	carbohydrate derivative biosynthetic process
GO:0034654	0.55	nucleobase-containing compound biosynthetic process
GO:0009226	0.54	nucleotide-sugar biosynthetic 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:0044464	1.00	cell part
GO:0044424	0.99	intracellular part
GO:0044444	0.90	cytoplasmic part
GO:0005829	0.72	cytosol

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	0.569	2icyB	0.886	1.52	0.532	0.909	2.7.7.9	113,117,119,122,165,170,189,220,223,251,367,369
2	0.565	2i5kB	0.872	1.79	0.554	0.905	2.7.7.9	113,115,117,119,122,127,137,139,165,168,170,189,220
3	0.508	2oefA	0.797	2.65	0.354	0.866	2.7.7.9	113,115,117,119,123,127,129,161,165,220,223,251,253,396
4	0.234	2yqjA	0.646	3.68	0.138	0.736	2.7.7.23	119,127,167,220,369,396
5	0.227	1jv3A	0.652	4.01	0.156	0.756	2.7.7.23	113,119,369,396

	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	0.85	2icxA	0.867	1.49	0.535	0.894	1.75	UTP	complex1.pdb.gz	113,115,116,127,190,220,222,223,251,252,253,396
2	0.52	1jv3A	0.652	4.01	0.156	0.756	1.14	UD2	complex2.pdb.gz	113,115,116,162,190,220,222,223,251,252,293,306,328,329,330,371,373,392,396
3	0.09	1g0rC	0.407	3.27	0.105	0.461	1.17	THM	complex3.pdb.gz	113,115,128,190,220,221,222,223,253
4	0.08	1yp4A	0.465	4.20	0.091	0.549	0.98	ADP	complex4.pdb.gz	113,115,116,162,221,223,251,252,253,371,373
5	0.05	2ggqA	0.421	4.16	0.092	0.492	0.90	TTP	complex5.pdb.gz	113,115,116,117,118,119,120,127,190,222,226,369

	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.