D-I-TASSER P21108

D-I-TASSER results for P21108

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

Summary of the Protein

Uniprot ID: P21108
Protein Name: Ribose-phosphate pyrophosphokinase 3
Gene Name: PRPS1L1

Input Sequence in FASTA format

>P21108 (318 residues)
MPNIKIFSGSSHQDLSQKIADRLGLELGKVVTKKFSNQETCVEIDESVRGEDVYIVQSGC
GEINDSLMELLIMINACKIASASRVTAVIPCFPYARQDKKDKSRSPISAKLVANMLSIAG
ADHIITMDLHASQIQGFFDIPVDNLYAEPTVLKWIRENIPEWKNCIIVSPDAGGAKRVTS
IADQLNVDFALIHKERKKANEVDCIVLVGDVNDRVAILVDDMADTCVTICLAADKLLSAG
ATRVYAILTHGIFSGPAISRINTACFEAVVVTNTIPQDEKMKHCSKIRVIDISMILAEAI
RRTHNGESVSYLFSHVPL

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	P21108-D1	1-146	146		MPNIKIFSGSSHQDLSQKIADRLGLELGKVVTKKFSNQETCVEIDESVRGEDVYIVQSGCGEINDSLMELLIMINACKIASASRVTAVIPCFPYARQDKKDKSRSPISAKLVANMLSIAGADHIITMDLHASQIQGFFDIPVDNLY
2	P21108-D2	147-318	172		AEPTVLKWIRENIPEWKNCIIVSPDAGGAKRVTSIADQLNVDFALIHKERKKANEVDCIVLVGDVNDRVAILVDDMADTCVTICLAADKLLSAGATRVYAILTHGIFSGPAISRINTACFEAVVVTNTIPQDEKMKHCSKIRVIDISMILAEAIRRTHNGESVSYLFSHVPL

Top 1 final models from D-I-TASSER

Click to view	Rank^a	Download	Estimated TM-score^b
	1	model1.pdb.gz	0.89

(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	2hcrB	0.94	1.24	0.942	0.969	model1_2hcrB.pdb.gz
2	5t3oA	0.93	1.30	0.466	0.965	model1_5t3oA.pdb.gz
3	4s2uA	0.92	1.64	0.467	0.956	model1_4s2uA.pdb.gz
4	2c4kA	0.91	1.36	0.480	0.950	model1_2c4kA.pdb.gz
5	1dkrB	0.91	1.62	0.468	0.947	model1_1dkrB.pdb.gz
6	5mp7A	0.91	1.25	0.424	0.934	model1_5mp7A.pdb.gz
7	3dahC	0.88	1.70	0.472	0.931	model1_3dahC.pdb.gz
8	3lpnA	0.81	2.09	0.232	0.880	model1_3lpnA.pdb.gz
9	4twbA	0.80	2.13	0.266	0.874	model1_4twbA.pdb.gz
10	1u9yA	0.78	2.11	0.271	0.859	model1_1u9yA.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	0.96	catalytic activity
GO:0004749	0.94	ribose phosphate diphosphokinase activity
GO:1901363	0.74	heterocyclic compound binding
GO:0097159	0.74	organic cyclic compound binding
GO:0000166	0.67	nucleotide binding
GO:0035639	0.66	purine ribonucleoside triphosphate binding
GO:0032555	0.66	purine ribonucleotide binding
GO:0032550	0.66	purine ribonucleoside binding
GO:0005524	0.64	ATP binding
GO:0042803	0.58	protein homodimerization 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	0.88	cellular process
GO:0008152	0.88	metabolic process
GO:0071704	0.85	organic substance metabolic process
GO:0044699	0.85	single-organism process
GO:0044237	0.84	cellular metabolic process
GO:0044238	0.70	primary metabolic process
GO:1901576	0.68	organic substance biosynthetic process
GO:0006807	0.65	nitrogen compound metabolic process
GO:0006796	0.63	phosphate-containing compound metabolic process
GO:0019637	0.62	organophosphate metabolic process
GO:0044710	0.61	single-organism metabolic process
GO:0090407	0.60	organophosphate biosynthetic process
GO:0044281	0.60	small molecule metabolic process
GO:0034641	0.60	cellular nitrogen compound metabolic process
GO:0044763	0.57	single-organism cellular process
GO:1901135	0.56	carbohydrate derivative metabolic process
GO:0006139	0.56	nucleobase-containing compound metabolic process
GO:1901137	0.54	carbohydrate derivative biosynthetic process
GO:0019693	0.54	ribose phosphate metabolic process
GO:0046390	0.52	ribose phosphate biosynthetic process
GO:0032502	0.52	developmental process
GO:1901564	0.51	organonitrogen compound metabolic 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	0.95	cell part
GO:0044424	0.90	intracellular part
GO:0044444	0.67	cytoplasmic part
GO:0043226	0.53	organelle
GO:0032991	0.51	macromolecular 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	0.409	1u9yC	0.785	2.11	0.271	0.859	2.7.6.1	210
2	0.164	2h06B	0.939	1.30	0.942	0.969	2.7.6.1	57,67,91,94,97,108,110,128,130,132,136,138,142,222,249,252,274
3	0.060	1gdhA	0.523	4.58	0.061	0.714	1.1.1.29	NA
4	0.060	2a9fA	0.509	5.10	0.080	0.736	1.1.1.39	NA
5	0.060	2j6iA	0.525	5.05	0.074	0.748	1.2.1.2	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	0.01	1gz3B	0.548	5.48	0.075	0.808	0.12	ATP	complex1.pdb.gz	96,97,134
2	0.01	1do8A	0.541	5.71	0.071	0.824	0.10	NAD	complex2.pdb.gz	79,80,120
3	0.01	1gz3A	0.549	5.32	0.085	0.802	0.14	ATP	complex3.pdb.gz	54,86,87,88,123
4	0.01	1do8B	0.548	5.49	0.071	0.808	0.11	NAD	complex4.pdb.gz	3,5,78,120,121,122
5	0.01	1gz3C	0.543	5.59	0.065	0.821	0.15	ATP	complex5.pdb.gz	67,68,112,116,117

	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.