D-I-TASSER Q96G75-D3

D-I-TASSER results for Q96G75-D3

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

Input Sequence in FASTA format

>Q96G75 (58 residues)
FACPILRQQTSDSNPPIKLICGHVISRDALNKLINGGKLKCPYCPMEQNPADGKRIIF

Predicted Secondary Structure

Sequence	20 40 \| \| FACPILRQQTSDSNPPIKLICGHVISRDALNKLINGGKLKCPYCPMEQNPADGKRIIF
Prediction	CCCCCCCCCCCCCCCCSSSCCCCSHHHHHHHHHHHCCCCCCCCCCCCCCHHHCSSCCC
Confidence	9787341317888984674086321799999998189124998966679888645119
	H:Helix; S:Strand; C:Coil

Predicted Solvent Accessibility

Sequence	20 40 \| \| FACPILRQQTSDSNPPIKLICGHVISRDALNKLINGGKLKCPYCPMEQNPADGKRIIF
Prediction	7603034543377433330412201035005403764414033135634274046227
	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

                   |                   |

SS
Seq

CCCCCCCCCCCCCCCCSSSCCCCSHHHHHHHHHHHCCCCCCCCCCCCCCHHHCSSCCC
FACPILRQQTSDSNPPIKLICGHVISRDALNKLINGGKLKCPYCPMEQNPADGKRIIF

7l3lA

0.15

0.14

4.67

1.33

DEthreader

YKCAFCHSVL---HNPHQTGCGHRFCQHCILSLRELTVPICPVDKEVIKSQEVFKDNR

1g25A

0.21

6.59

2.37

SPARKS-K

QGCPRCKTYRNPSLKLMVNVCGHTLCESCVDLLFVRGAGNCPECGTPLRKSNFRVQLF

7l3lA

0.15

0.14

4.67

0.76

MapAlign

YKCAFCHSVL---HNPHQTGCGHRFCQHCILSLRENTVPICPVDKEVIKSQEVFKDCK

7l3lA

0.15

0.14

4.67

0.49

CEthreader

YKCAFCHSVL---HNPHQTGCGHRFCQHCILSLRELTVPICPVDKEVIKSQEVFKDNC

1g25A

0.21

6.59

2.32

MUSTER

QGCPRCKTTKNPSLKLMVNVCGHTLCESCVDLLFVRGAGNCPECGTPLRKSNFRVQLF

6nmiH

0.19

6.12

1.11

HHsearch

QGCPRCKTTYRNPSKLMVNVCGHTLCESCVDLLFVRGAGNCPECGTPLRKSNFRVQLF

4r7eA

0.18

0.17

5.60

0.88

FFAS-3D

VYCSLCSKNWKN---MAIKTCGHVFCENCCKERLAARMRKCPTCNKAFSSNDLLTVHL

4ap4A

0.25

0.24

7.50

0.72

EigenThreader

VSCPICMDGYSEIVLIVSTECGHVFCSQCLRDSLK-NANTCPTCRKKINHKRYHPIYI

5vo0A

0.22

0.21

6.53

1.72

CNFpred

YECPICLMGLR---SAVQTPCGHRFCDSCIRKSIRDTGQKCPVDNEVLLEEQLFPDNF

2h0dB

0.18

0.17

5.60

1.33

DEthreader

LMCPICLDML---KNTMTTECLHRFCADCIITALRSGNKECPTCRKKLSKRSLRPDPA

(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	0.8091

(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	2h0dB	0.84	1.03	0.182	0.948	model1_2h0dB.pdb.gz
2	7l3lA	0.83	1.08	0.145	0.948	model1_7l3lA.pdb.gz
3	3hcsA1	0.82	1.26	0.200	0.948	model1_3hcsA1.pdb.gz
4	6wi7A	0.82	1.08	0.182	0.948	model1_6wi7A.pdb.gz
5	4s3oC	0.81	1.05	0.148	0.931	model1_4s3oC.pdb.gz
6	4r8pL	0.81	1.23	0.182	0.948	model1_4r8pL.pdb.gz
7	5h7rD	0.81	1.15	0.241	0.931	model1_5h7rD.pdb.gz
8	6yxeA	0.81	1.28	0.200	0.948	model1_6yxeA.pdb.gz
9	5vo0D	0.81	1.32	0.200	0.948	model1_5vo0D.pdb.gz
10	6l8nA2	0.81	1.86	0.224	1.000	model1_6l8nA2.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	0.85	catalytic activity
GO:0019787	0.77	ubiquitin-like protein transferase activity
GO:0004842	0.76	ubiquitin-protein transferase activity
GO:0043167	0.58	ion binding
GO:0061630	0.57	ubiquitin protein ligase activity
GO:0046872	0.57	metal ion binding
GO:0008270	0.56	zinc ion binding
GO:0016874	0.53	ligase activity
GO:1901363	0.51	heterocyclic compound binding
GO:0097159	0.51	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	0.99	cellular process
GO:0071704	0.97	organic substance metabolic process
GO:0044238	0.97	primary metabolic process
GO:0044260	0.96	cellular macromolecule metabolic process
GO:0019538	0.95	protein metabolic process
GO:0016567	0.90	protein ubiquitination
GO:0065007	0.86	biological regulation
GO:0050789	0.86	regulation of biological process
GO:0050794	0.84	regulation of cellular process
GO:0019222	0.76	regulation of metabolic process
GO:0080090	0.75	regulation of primary metabolic process
GO:0031323	0.75	regulation of cellular metabolic process
GO:1901575	0.66	organic substance catabolic process
GO:0019941	0.65	modification-dependent protein catabolic process
GO:0006511	0.64	ubiquitin-dependent protein catabolic process
GO:0060255	0.61	regulation of macromolecule metabolic process
GO:0000209	0.61	protein polyubiquitination
GO:0048519	0.60	negative regulation of biological process
GO:0048523	0.59	negative regulation of cellular process
GO:0048518	0.59	positive regulation of biological process
GO:0031326	0.58	regulation of cellular biosynthetic process
GO:0048522	0.57	positive regulation of cellular process
GO:0010604	0.55	positive regulation of macromolecule metabolic process
GO:0051246	0.54	regulation of protein metabolic process
GO:0043161	0.54	proteasome-mediated ubiquitin-dependent protein catabolic process
GO:0031325	0.54	positive regulation of cellular metabolic process
GO:0032268	0.53	regulation of cellular protein metabolic process
GO:0051247	0.52	positive regulation of protein metabolic process
GO:0044699	0.52	single-organism process
GO:0031324	0.52	negative regulation of cellular metabolic process
GO:0032270	0.51	positive regulation of cellular protein 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	1.00	cell part
GO:0044424	0.99	intracellular part
GO:0043229	0.85	intracellular organelle
GO:0043227	0.82	membrane-bounded organelle
GO:0043231	0.81	intracellular membrane-bounded organelle
GO:0044446	0.74	intracellular organelle part
GO:0044444	0.74	cytoplasmic part
GO:0005634	0.74	nucleus
GO:0032991	0.73	macromolecular complex
GO:0044428	0.62	nuclear part
GO:0043234	0.62	protein complex
GO:0005737	0.61	cytoplasm
GO:0005829	0.57	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	0.060	1eawA	0.442	2.75	0.089	0.690	3.4.21.109 3.4.21.-	NA
2	0.060	1ptqA	0.486	2.17	0.135	0.638	2.7.11.13	NA
3	0.060	3clyA	0.353	4.08	0.067	0.655	2.7.10.1	NA
4	0.060	1weoA	0.560	2.50	0.167	0.862	2.4.1.12	21,37,42
5	0.060	1e7dA	0.495	2.30	0.034	0.655	3.1.22.4	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:

Click to view	Rank	Cscore^LB	PDB Hit	TM-score	RMSD^a	IDEN^a	Cov.	BS-score	Lig. Name	Download Complex	Predicted binding site residues
	1	0.34	2eciA	0.728	1.78	0.200	0.931	1.46	ZN	complex1.pdb.gz	21,23,41,43,44

	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.