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I-TASSER results for job id S693368

(Click on S693368_results.tar.bz2 to download the tarball file including all modeling results listed on this page. Click on Annotation of I-TASSER Output to read the instructions for how to interpret the results on this page. Model results are kept on the server for 60 days, there is no way to retrieve the modeling data older than 2 months)

  Submitted Sequence in FASTA format

>protein
MDSFYEKPMERSRGTPLTRMLLSGEMTQERQSELTSKERFDRWMINEGYRRFFVFVFAVL
QVLVFSFAAVNFSRKENLVTARNTFGFTFVIARSAALVLHVNIALILFPVCRTLISLARQ
TPLNGIIQFDKNITFHIVTAWSIVFWSWVHTVAHWNNFAQISAKNNLGFYGFLVANLVSG
PGWTGYVMLVALMGMVMTSMEKPRRANYERFWYTHHMFIVFFFFWSIHGAFCMIQPDFAP
FCSSVGPSAIGVFWQYWMYGGFAYLAERIAREVRGRHRTVISKVVQHPSNVCEIQIKKAN
TKTRAGQYIFLCCPAVSLWQYHPFTLTSAPEEDYISIHMRIVGDFTRELATVLGCELGGK
DKVKGSNVVGTGADGIDPALRRVLPRVYVDGPFGSASEDVFKYEISMLVGAGIGVTPFAS
ILKSIWYRMNYPKERTRLSKVYFFWICRDFGSFEWFRSLLLAIEAQDVDQRIDIHTYLTA
RIKADDAVNIMINDANAEKDAITGLRSPTNFGRPNWDMIFRGVRKLHTPAECGVFFCGPK
GLGSALHIFCNKYSDPGFSFVWGKENF

  Predicted Secondary Structure

Sequence                  20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380                 400                 420                 440                 460                 480                 500                 520                 540                 560
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |       
MDSFYEKPMERSRGTPLTRMLLSGEMTQERQSELTSKERFDRWMINEGYRRFFVFVFAVLQVLVFSFAAVNFSRKENLVTARNTFGFTFVIARSAALVLHVNIALILFPVCRTLISLARQTPLNGIIQFDKNITFHIVTAWSIVFWSWVHTVAHWNNFAQISAKNNLGFYGFLVANLVSGPGWTGYVMLVALMGMVMTSMEKPRRANYERFWYTHHMFIVFFFFWSIHGAFCMIQPDFAPFCSSVGPSAIGVFWQYWMYGGFAYLAERIAREVRGRHRTVISKVVQHPSNVCEIQIKKANTKTRAGQYIFLCCPAVSLWQYHPFTLTSAPEEDYISIHMRIVGDFTRELATVLGCELGGKDKVKGSNVVGTGADGIDPALRRVLPRVYVDGPFGSASEDVFKYEISMLVGAGIGVTPFASILKSIWYRMNYPKERTRLSKVYFFWICRDFGSFEWFRSLLLAIEAQDVDQRIDIHTYLTARIKADDAVNIMINDANAEKDAITGLRSPTNFGRPNWDMIFRGVRKLHTPAECGVFFCGPKGLGSALHIFCNKYSDPGFSFVWGKENF
PredictionCCCCCCCCCCCCCCCCCCHHHCCCCCCCCCCCCCCCHHHSSSSSSCCCHHHSSSHHHHHHHHHHHHHHHHHHCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCHHHHCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCHHHHHHHHCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHSSCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCSSSSSSSSCCCCSSSSSSCCCCCCCCCCCSSSSSSCCCCCCCCCCCCCCCCCCCCCSSSSSSSCCCCHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSSSSCCCCCCCCCHHHCCCSSSSSCCCCHHHHHHHHHHHHHHHHHCCCCCCCCSSSSSSSCCCHHHHHHHHHHHHHHHHHCCCCSSSSSSSSCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHHHHHHHCCCCSSSSSSSCCHHHHHHHHHHHHHHCCCCCSSSSSSSCC
Conf.Score964234888866688856011142124466665333414436894266263210579999999999999986157765106766788999999999999999999999999999999824524323677788999999999999999999999998765421467400334334421477640269999999999999989998662789999999999999999998642210354320454336888899999999999999999888764303432688889759973899982788885897289999478983545764001146799616999835862777899873056765434444433454323454446667548975899888867522980899973865777899999999745302345677537998630888887744999999974463664799999887766666543113553235565556665323467789999999986279970899991948999999999998579997799997069
H:Helix; S:Strand; C:Coil

  Predicted Solvent Accessibility

Sequence                  20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380                 400                 420                 440                 460                 480                 500                 520                 540                 560
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |       
MDSFYEKPMERSRGTPLTRMLLSGEMTQERQSELTSKERFDRWMINEGYRRFFVFVFAVLQVLVFSFAAVNFSRKENLVTARNTFGFTFVIARSAALVLHVNIALILFPVCRTLISLARQTPLNGIIQFDKNITFHIVTAWSIVFWSWVHTVAHWNNFAQISAKNNLGFYGFLVANLVSGPGWTGYVMLVALMGMVMTSMEKPRRANYERFWYTHHMFIVFFFFWSIHGAFCMIQPDFAPFCSSVGPSAIGVFWQYWMYGGFAYLAERIAREVRGRHRTVISKVVQHPSNVCEIQIKKANTKTRAGQYIFLCCPAVSLWQYHPFTLTSAPEEDYISIHMRIVGDFTRELATVLGCELGGKDKVKGSNVVGTGADGIDPALRRVLPRVYVDGPFGSASEDVFKYEISMLVGAGIGVTPFASILKSIWYRMNYPKERTRLSKVYFFWICRDFGSFEWFRSLLLAIEAQDVDQRIDIHTYLTARIKADDAVNIMINDANAEKDAITGLRSPTNFGRPNWDMIFRGVRKLHTPAECGVFFCGPKGLGSALHIFCNKYSDPGFSFVWGKENF
Prediction634124424543333313221234423454433133233021001132000000011102000000000000024331111220120010000000000000000000022100000012120000011120010000000100100010000000000101222322010001010232111000000200210000000100211010000001100000010000000000122211000000020000000000000000000000000112220200211124330020103236031200000000000002100000000001375200010103331033014103633433442343333433343243444321110000001001132133010000000000000000001000322444644131010000000133410200240043035323521020000001324454334232434646333133142323214220340044016424521000000013200420240034126650202012125
Values range from 0 (buried residue) to 9 (highly exposed residue)

   Predicted normalized B-factor

(B-factor is a value to indicate the extent of the inherent thermal mobility of residues/atoms in proteins. In I-TASSER, this value is deduced from threading template proteins from the PDB in combination with the sequence profiles derived from sequence databases. The reported B-factor profile in the figure below corresponds to the normalized B-factor of the target protein, defined by B=(B'-u)/s, where B' is the raw B-factor value, u and s are respectively the mean and standard deviation of the raw B-factors along the sequence. Click here to read more about predicted normalized B-factor)


  Top 10 threading templates used by I-TASSER

(I-TASSER modeling starts from the structure templates identified by LOMETS from the PDB library. LOMETS is a meta-server threading approach containing multiple threading programs, where each threading program can generate tens of thousands of template alignments. I-TASSER only uses the templates of the highest significance in the threading alignments, the significance of which are measured by the Z-score, i.e. the difference between the raw and average scores in the unit of standard deviation. The templates in this section are the 10 best templates selected from the LOMETS threading programs. Usually, one template of the highest Z-score is selected from each threading program, where the threading programs are sorted by the average performance in the large-scale benchmark test experiments.)

Rank PDB
Hit
Iden1Iden2CovNorm.
Z-score
Download
Align.
                   20                  40                  60                  80                 100                 120                 140                 160                 180                 200                 220                 240                 260                 280                 300                 320                 340                 360                 380                 400                 420                 440                 460                 480                 500                 520                 540                 560
                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |                   |       
Sec.Str
Seq
CCCCCCCCCCCCCCCCCCHHHCCCCCCCCCCCCCCCHHHSSSSSSCCCHHHSSSHHHHHHHHHHHHHHHHHHCCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCHHHHCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCHHHHHHHHCCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHSSCCCCCHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCSSSSSSSSCCCCSSSSSSCCCCCCCCCCCSSSSSSCCCCCCCCCCCCCCCCCCCCCSSSSSSSCCCCHHHHHHHHHCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCSSSSSCCCCCCCCCHHHCCCSSSSSCCCCHHHHHHHHHHHHHHHHHCCCCCCCCSSSSSSSCCCHHHHHHHHHHHHHHHHHCCCCSSSSSSSSCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHHHHHHHHHHHCCCCSSSSSSSCCHHHHHHHHHHHHHHCCCCCSSSSSSSCC
MDSFYEKPMERSRGTPLTRMLLSGEMTQERQSELTSKERFDRWMINEGYRRFFVFVFAVLQVLVFSFAAVNFSRKENLVTARNTFGFTFVIARSAALVLHVNIALILFPVCRTLISLARQTPLNGIIQFDKNITFHIVTAWSIVFWSWVHTVAHWNNFAQISAKNNLGFYGFLVANLVSGPGWTGYVMLVALMGMVMTSMEKPRRANYERFWYTHHMFIVFFFFWSIHGAFCMIQPDFAPFCSSVGPSAIGVFWQYWMYGGFAYLAERIAREVRGRHRTVISKVVQHPSNVCEIQIKKANTKTRAGQYIFLCCPAVSLWQYHPFTLTSAPEEDYISIHMRIVGDFTRELATVLGCELGGKDKVKGSNVVGTGADGIDPALRRVLPRVYVDGPFGSASEDVFKYEISMLVGAGIGVTPFASILKSIWYRMNYPKERTRLSKVYFFWICRDFGSFEWFRSLLLAIEAQDVDQRIDIHTYLTARIKADDAVNIMINDANAEKDAITGLRSPTNFGRPNWDMIFRGVRKLHTPAECGVFFCGPKGLGSALHIFCNKYSDPGFSFVWGKENF
16wxvA 0.30 0.34 0.88 5.30Download ----------------LVSLLSAWIVARLRKRNHQTVQQFKRFIENYRRHIGCVAVFYTITGALFLERAYYYAFAAHHSGITDTTRVGIILSRGTAASISFMFSYILLTMCRNLITFLRETFLNRYIPFDAAVDFHRLIASTAIILTVLHSAGHVVNVYLFSISPLSVLSCYYWWFFQTVPGLTGVLLLLALAIMYVFASHHFRRRSFRGFWLTHHLYIFLYILLIIHGSFALIQMP--------------RFHIFFLVPAIIYVGDKLVSLSRKKVEISVVKAELLPSGVTHLRFQRPQFEYKSGQWVRIACLALGTTEYHPFTLTSAPHEDTLSLHIRAAGPWTTRLREIYS--------------------------PPRYPKLYLDGPFGEGHQEWHKFEVSVLVGGGIGVTPFASILKDLVFKSS----VSCCKKIYFIWVTRTQRQFEWLADIIREVEENDRQDLVSVHIYITQLAEKFDLRVL-------NRSLFTGLRSITHFGRPPFEPFFNSLQEVHP-QKIGVFSCGPPGMTKNVEKACQLINRQD--FSHHYENF
27m68A 0.07 0.28 0.89 0.86Download AISLRRADALGIDFGDDENIAHREQGKVKWNIYLEYAKACNPKSVCVFILFIVISMFLSVMGNVWLKHWSEVNSRYGAIYFALGIGSALATLIQTIVLWVFCTIHASKYLHNLMTNSVLRAPMTFFETTPIGRILNRFSNDIYKVDALLGRTFSQFFVNAVKVTFTITVICATTW------QFIFIIIPLSVFYIYYQQYYLRTSRELRRLDSITRSPIYSHFQETLGGLATVRGYSQQKRFSHINQCRIDNNMSYPSINANRWLAYRLELIGSIIILGAATLSVFLKQG-----------TLTAGMVGLSLSYALQI-------------TQTLNWIVRMTVEVETNIVSVERIKEYAD-------LKSEAPLIVESQGDIKFNNYSTRYRPELVLKHIIKPNEKVGIVGGAGKSSLTLALFRM---IEASEGNIVIDNIAILSIIPQRENIEAIWRALELSH------------------------LKEHVLSMSNDGLDAQLTEGGGNLSVGQRQLLCLARAMLVPSKILVLDQATVETDKVVQETIRTAFKDRTILTIAHRLN
37d3e 0.29 0.34 0.90 3.71Download WEDFHFMLRL----LFT-------EAHREKFSCHQTVQQFKRFIENYRRHIGCVAVFYAIAGGLFLERAYYYAFAAHHTGITDTTRVGIILSRGTAASISFMFSYILLTMCRNLITFLRETFLNRYVPFDAAVDFHRLIASTAIVLTVLHSVGHVVNVYLFSISPLQKYYWW---FFQTVPGLTGVVLLLILAIMYVFASHHFRRRSFRGFWLTHHLYILLYVLLIIHGSFALIQL--------------PRFHIFFLVPAIIYGGDKLVSLSRKKVEISVVKAELLPSGVTHLRFQRPGFEYKSGQWVRIACLALGTTEYHPFTLTSAPHEDTLSLHIRAAGPWTTRLREIYSAP--------------------------TYPKLYLDGPFGEGHQEWHKFEVSVLVGGGIGVTPFASILKDLVFKSSVS-CQVFCKKIYFIWVTRTQRQFEWLADIIREVEENDHQDLVSVHIYITQLAEKFDLRTTMLYQKVLNRSLFTGLRSITHFGRPPFEPFFNSLQEVHPVRKIGVFSCGPPGMTKNVEKACQLINRDRTHFSHHYENF
47d3e 0.28 0.34 0.91 3.00Download WEDFHFMLRLLF---------TEAHEKFQRSCLHQTVQQFKRFIENYRRHIGCVAVFYAIAGGLFLERAYYYAFAAHHTGITDTTRVGIILSRGTAASISFMFSYILLTMCRNLITFLRETFLNRYVPFDAAVDFHRLIASTAIVLTVLHSVGHVVNVYLFSISPLSVLQKYYWWFFQTVPGLTGVVLLLILAIMYVFASHHFRRRSFRGFWLTHHLYILLYV-LLIIHGSFALIQ-------------LPRFHIFFLVPAIIYGGDKLVSLSRKKVEISVVKAELLPSGVTHLRFQRPGFEYKSGQWVRIACLALGTTEYHPFTLTSAPHEDTLSLHIRAAGPWTTRLREIYSAP--------------------------TYPKLYLDGPFGEGHQEWHKFEVSVLVGGGIGVTPFASILKDLVFKSSVS-CQVFCKKIYFIWVTRTQRQFEWLADIIREVEENDHQDLVSVHIYITQLAEKFDLRTTMLFQKVLNRSLFTGLRSITHFGRPPFEPFFNSLQEVHPQRKIGVFSCGPPGMTKNVEKACQLINRDRTHFSHHYENF
56wxrA 0.28 0.33 0.88 2.32Download SQLSAKGLPACAPLFIPLVSLLSAWIVARLRKRHQTVQQFKRFIENYRRHIGCVAVFYTITGALFLERAYYYAFAAHHSGITDTTRVGIILSRGTAASISFMFSYILLTMCRNLITFLRETFLNRYIPFDAAVDFHRLIASTAIILTVLHSAGHVVNVYLFSISGSEFPQKYYWWFFQTVPGLTGVLLLLALAIMYVFASHHFRRRSFRGFWLTHHLYIFLYILLIIHGSFALIQMP--------------RFHIFFLVPAIIYVGDKLVSLSRKKVEISVVKAELLPSGVTHLRFQRPQFEYKSGQWVRIACLALGTTEYHPFTLTSAPHEDTLSLHIRAAGPWTTRLREIYS--------------------------PPRYPKLYLDGPFGEGHQEWHKFEVSVLVGGGIGVTPFASILKDLVFKSSVSC----CKKIYFIWVTRTQRQFEWLADIIREVEENDRQDLVSVHIYITQLAEKFDLR-----------------------GRPPFEPFFNSLQEVHP-QKIGVFSCGPPGMTKNVEKACQLINRQ-THFSHHYENF
67d3e 0.30 0.34 0.87 4.54Download ----------------------------------QTVQQFKRFIENYRRHIGCVAVFYAIAGGLFLERAYYYAFAAHHTGITDTTRVGIILSRGTAASISFMFSYILLTMCRNLITFLRETFLNRYVPFDAAVDFHRLIASTAIVLTVLHSVGHVVNVYLFSISPLSVPQKYYWWFFQTVPGLTGVVLLLILAIMYVFASHHFRRRSFRGFWLTHHLYILLYVLLIIHGSFALIQ--------------LPRFHIFFLVPAIIYGGDKLVSLSRKKVEISVVKAELLPSGVTHLRFQRPGFEYKSGQWVRIACLALGTTEYHPFTLTSAPHEDTLSLHIRAAGPWTTRLREIYSAP--------------------------TYPKLYLDGPFGEGHQEWHKFEVSVLVGGGIGVTPFASILKDLVFKSSVS-CQVFCKKIYFIWVTRTQRQFEWLADIIREVEENDHQDLVSVHIYITQLAEKFDLRTTMLFQKVLNRSLFTGLRSITHFGRPPFEPFFNSLQEVHPQRKIGVFSCGPPGMTKNVEKACQLINRQRTHFSHHYEN-
75o0xA 0.38 0.21 0.45 4.28Download ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------GSEPTFVVNASLLPSKVLGLQVQRPSFNYQPGDYLFIKCPGISKFEWHPFTISSAPEMPDLTLHIRAVGSWTGKLYQLIREQREEWIRSG-------------SSQSLPGVPVYIDGPYGTPSTHIFESKYAILICAGIGVTPFASILKSILHRNQQNPAKMPLKKVHFYWLNREQKAFEWFVELLSKIEAEDTNNLFDLNLYLTLITGLKSRTKTG---------------------RPDWEEIFKDVAKQHAPDNVEVFFCGPTGLALQLRHLCTKYG-----FGYRKENF
86wxrA 0.29 0.33 0.88 1.36Download LSAKGLPACAPLFIRDYFESLLSAWIVARLRKRHQTVQQFKRFIENYRRHIGCVAVFYTITGALFLERAYYYAFAAHHSGITDTTRVGIILSRGTAASISFMFSYILLTMCRNLITFLRETFLNRYIPFDAAVDFHRLIASTAIILTVLHSAGHVVNVYLFSISPSEFPQKYYWWFFQTVPGLTGVLLLLALAIMYVFASHHFRRRSFRGFWLTHHLYIFLYILLIIHGSFALIQMP--------------RFHIFFLVPAIIYVGDKLVSLSRKKVEISVVKAELLPSGVTHLRFQRPGFEYKSGQWVRIACLALGTTEYHPFTLTSAPHEDTLSLHIRAAGPWTTRLREIYSPPR--------------------------YPKLYLDGPFGEGHQEWHKFEVSVLVGGGIGVTPFASILKDLVFKSS----VSCCKKIYFIWVTRTQRQFEWLADIIREVEENDRQDLVSVHIYITQLAEKFD-----------------------LRGRPPFEPFFNSLQEVH-PQKIGVFSCGPPGMTKNVEKACQLINR-QTHFSHHYENF
97v6yA 0.08 0.19 0.96 1.56Download KAANLETNVEELWVEVGGRVSRELNYTRQKIGEEATTTTLDDILKSFSDVSVIRVASGYLLMLAYACLTMLRWDCSKSQGAVGLAGVLLVALSVAAATTQVLPFLALGVGVDDVFLLAHAFSETGQNKRIPFEDRTGECLKRTGASVALTSISNVTAFFMAALIPI--------------------PALRAFSLQAAVVVVFNFAMVLLIFPAILSMDLYRREDRRLDIFCCFTKWTLSSFAEKHYAPFLLKPKAKVVVILLFLGLLGVSLYGTTRVRDGLDLTDIVPREYNMYIVTQKADYPNIQHLLYDLHKSFSNVKYVMLEENKQLPQMWLHYFRDWLQGLQDAFDSDWETGRIMPNNYKNGSDDGVLAYKLLVQTGSRDK-----PIDISQLTKQRLVDADGIINPSAFYIYLTAWVSNDPVAYAASQANIRPHRPFYLNGLRDTSDFVEAIEKVRVICNNYTSLGLSSYPNGYPFLFWEQYISLRHWLLLSISVVLACTFLVCAVFLLNPWELFGMMGLIGIKLSAVPVVIAIGDKNHRAMLALEHMFAAGSEFDFIVRYF
106wxrA 0.28 0.33 0.88 6.78Download LSAKGLPAAPLFIRDYFEVSLLSAWIVARLRKRHQTVQQFKRFIENYRRHIGCVAVFYTITGALFLERAYYYAFAAHHSGITDTTRVGIILSRGTAASISFMFSYILLTMCRNLITFLRETFLNRYIPFDAAVDFHRLIASTAIILTVLHSAGHVVNVYLFSISPSEFPQKYYWWFFQTVPGLTGVLLLLALAIMYVFASHHFRRRSFRGFWLTHHLYIFLYILLIIHGSFALIQMPR--------------FHIFFLVPAIIYVGDKLVSLSRKKVEISVVKAELLPSGVTHLRFQRPQFEYKSGQWVRIACLALGTTEYHPFTLTSAPHEDTLSLHIRAAGPWTTRLREI--------------------------YSPPRYPKLYLDGPFGEGHQEWHKFEVSVLVGGGIGVTPFASILKDLVFKSSVSC----CKKIYFIWVTRTQRQFEWLADIIREVEENDRQDLVSVHIYITQLAEKFDLR-----------------------GRPPFEPFFNSLQEVHP-QKIGVFSCGPPGMTKNVEKACQLINR-QTHFSHHYENF
(a)All the residues are colored in black; however, those residues in template which are identical to the residue in the query sequence are highlighted in color. Coloring scheme is based on the property of amino acids, where polar are brightly coloured while non-polar residues are colored in dark shade. (more about the colors used)
(b)Rank of templates represents the top ten threading templates used by I-TASSER.
(c)Ident1 is the percentage sequence identity of the templates in the threading aligned region with the query sequence.
(d)Ident2 is the percentage sequence identity of the whole template chains with query sequence.
(e)Cov represents the coverage of the threading alignment and is equal to the number of aligned residues divided by the length of query protein.
(f)Norm. Z-score is the normalized Z-score of the threading alignments. Alignment with a Normalized Z-score >1 mean a good alignment and vice versa.
(g)Download Align. provides the 3D structure of the aligned regions of the threading templates.
(h)The top 10 alignments reported above (in order of their ranking) are from the following threading programs:
       1: FFAS-3D   2: SPARKS-X   3: HHSEARCH2   4: HHSEARCH I   5: Neff-PPAS   6: HHSEARCH   7: pGenTHREADER   8: wdPPAS   9: PROSPECT2   10: SP3   

   Top 5 final models predicted by I-TASSER

(For each target, I-TASSER simulations generate a large ensemble of structural conformations, called decoys. To select the final models, I-TASSER uses the SPICKER program to cluster all the decoys based on the pair-wise structure similarity, and reports up to five models which corresponds to the five largest structure clusters. The confidence of each model is quantitatively measured by C-score that is calculated based on the significance of threading template alignments and the convergence parameters of the structure assembly simulations. C-score is typically in the range of [-5, 2], where a C-score of a higher value signifies a model with a higher confidence and vice-versa. TM-score and RMSD are estimated based on C-score and protein length following the correlation observed between these qualities. Since the top 5 models are ranked by the cluster size, it is possible that the lower-rank models have a higher C-score in rare cases. Although the first model has a better quality in most cases, it is also possible that the lower-rank models have a better quality than the higher-rank models as seen in our benchmark tests. If the I-TASSER simulations converge, it is possible to have less than 5 clusters generated; this is usually an indication that the models have a good quality because of the converged simulations.)
    (By right-click on the images, you can export image file or change the configurations, e.g. modifying the background color or stopping the spin of your models)
  • Download Model 1
  • C-score=0.08 (Read more about C-score)
  • Estimated TM-score = 0.72±0.11
  • Estimated RMSD = 7.4±4.3Å

  • Download Model 2
  • C-score = -1.04

  • Download Model 3
  • C-score = -1.37

  • Download Model 4
  • C-score = -0.93


  Proteins structurally close to the target in the PDB (as identified by TM-align)

(After the structure assembly simulation, I-TASSER uses the TM-align structural alignment program to match the first I-TASSER model to all structures in the PDB library. This section reports the top 10 proteins from the PDB that have the closest structural similarity, i.e. the highest TM-score, to the predicted I-TASSER model. Due to the structural similarity, these proteins often have similar function to the target. However, users are encouraged to use the data in the next section 'Predicted function using COACH' to infer the function of the target protein, since COACH has been extensively trained to derive biological functions from multi-source of sequence and structure features which has on average a higher accuracy than the function annotations derived only from the global structure comparison.)


Top 10 Identified stuctural analogs in PDB

Click
to view
RankPDB HitTM-scoreRMSDaIDENaCovAlignment
17d3eA0.899 1.060.2860.908Download
26wxrA0.802 1.310.2770.820Download
32bf4A0.462 5.510.0640.593Download
46t1tA0.453 5.420.0700.577Download
51gvhA0.437 4.990.1220.543Download
61tllA0.433 5.300.0630.550Download
71ja1A0.429 6.000.0600.566Download
85o0xA0.411 2.690.4090.448Download
94g1bA0.410 5.110.0880.515Download
105gxuA0.408 5.240.0630.513Download

(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)RMSDa is the RMSD between residues that are structurally aligned by TM-align.
(d)IDENa 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 function using COFACTOR and COACH

(This section reports biological annotations of the target protein by COFACTOR and COACH based on the I-TASSER structure prediction. While COFACTOR deduces protein functions (ligand-binding sites, EC and GO) using structure comparison and protein-protein networks, COACH is a meta-server approach that combines multiple function annotation results (on ligand-binding sites) from the COFACTOR, TM-SITE and S-SITE programs.)

  Ligand binding sites


Click
to view
RankC-scoreCluster
size
PDB
Hit
Lig
Name
Download
Complex
Ligand Binding Site Residues
10.22 12 4eh1A FAD Rep, Mult 308,322,323,324,325,338,339,340,342,343,344,345,346,416,566
20.06 3 4yaoA 2AM Rep, Mult 412,447,448,479,480,513,542,545
30.04 2 3w2eA NAD Rep, Mult 340,342,412,413,414,446,447,448,479,513,537,538,539,540,541,542,566
40.04 2 2BF4A 2BF4A03 Rep, Mult 340,342,412,413,447,448,449,450,452,453,539
50.04 2 1TLLA 1TLLA00 Rep, Mult 53,106,107,108,109,110,111,127,128,129,130,131,132,133,134,135,136


Download the residue-specific ligand binding probability, which is estimated by SVM.
Download the all possible binding ligands and detailed prediction summary.
Download the templates clustering results.
(a)C-score is the confidence score of the prediction. C-score ranges [0-1], where a higher score indicates a more reliable prediction.
(b)Cluster size is the total number of templates in a cluster.
(c)Lig Name is name of possible binding ligand. Click the name to view its information in the BioLiP database.
(d)Rep is a single complex structure with the most representative ligand in the cluster, i.e., the one listed in the Lig Name column.
Mult is the complex structures with all potential binding ligands in the cluster.

  Enzyme Commission (EC) numbers and active sites


Click
to view
RankCscoreECPDB
Hit
TM-scoreRMSDaIDENaCovEC NumberActive Site Residues
10.2671ja1A0.429 6.000.0600.566 1.6.2.4  NA
20.2581cqxA0.370 5.840.1260.494 1.14.12.17  NA
30.1952bf4A0.462 5.510.0640.593 1.6.2.4  NA
40.1861gvhA0.437 4.990.1220.543 1.14.12.17  392
50.1831tllA0.433 5.300.0630.550 1.14.13.39  NA

 Click on the radio buttons to visualize predicted active site residues.
(a)CscoreEC is the confidence score for the EC number prediction. CscoreEC 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)RMSDa is the RMSD between residues that are structurally aligned by TM-align.
(d)IDENa 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.

  Gene Ontology (GO) terms
Top 10 homologous GO templates in PDB 
RankCscoreGOTM-scoreRMSDaIDENaCovPDB HitAssociated GO Terms
1 0.200.4622 5.51 0.06 0.592bf4A GO:0016491 GO:0005515 GO:0006696 GO:0016021 GO:0008610 GO:0005886 GO:0006694 GO:0016020 GO:0005789 GO:0005783 GO:0005739 GO:0055114 GO:0003958 GO:0016126 GO:0009055 GO:0005741 GO:0005792 GO:0005506 GO:0010181
2 0.190.4367 4.99 0.12 0.541gvhA GO:0019825 GO:0016491 GO:0008941 GO:0009636 GO:0006810 GO:0020037 GO:0015671 GO:0071949 GO:0005737 GO:0005506 GO:0055114 GO:0005344 GO:0046872 GO:0051409
3 0.180.4290 6.00 0.06 0.571ja1A GO:0018393 GO:0032770 GO:0071372 GO:0070988 GO:0043602 GO:0005792 GO:0004128 GO:0005625 GO:0032332 GO:0055114 GO:0090181 GO:0005789 GO:0050661 GO:0042493 GO:0043154 GO:0019395 GO:0046210 GO:0045542 GO:0090346 GO:0016787 GO:0009055 GO:0009437 GO:0007584 GO:0071371 GO:0047726 GO:0003420 GO:0060192 GO:0071375 GO:0090031 GO:0009812 GO:0010181 GO:0005783 GO:0016491 GO:0045880 GO:0043066 GO:0019899 GO:0005624 GO:0005739 GO:0003958 GO:0050660 GO:0016020 GO:0005506
4 0.180.4333 5.30 0.06 0.551tllA GO:0005506 GO:0010181 GO:0016491 GO:0055114
5 0.170.4034 5.01 0.07 0.503fjoA GO:0005739 GO:0006694 GO:0003958 GO:0005789 GO:0008610 GO:0016491 GO:0005741 GO:0016126 GO:0055114 GO:0005783 GO:0016020 GO:0005886 GO:0016021 GO:0005792 GO:0005515 GO:0009055 GO:0006696 GO:0005506 GO:0010181
6 0.170.3703 5.84 0.13 0.491cqxA GO:0005737 GO:0006810 GO:0046872 GO:0071949 GO:0020037 GO:0051409 GO:0055114 GO:0008941 GO:0016491 GO:0019825 GO:0005506 GO:0009636 GO:0015671 GO:0005344
7 0.160.3739 4.18 0.09 0.441f20A GO:0016491 GO:0055114
8 0.160.3551 7.17 0.06 0.551kblA GO:0050242 GO:0000166 GO:0016310 GO:0046872 GO:0016740 GO:0005524 GO:0016301 GO:0003824 GO:0016772 GO:0016874
9 0.160.3744 3.64 0.12 0.431krhA GO:0019439 GO:0008860 GO:0016491 GO:0046872 GO:0051536 GO:0055114 GO:0051537 GO:0009055
10 0.160.3555 7.65 0.04 0.582zxqA GO:0007155


Consensus prediction of GO terms
 
Molecular Function GO:0005506 GO:0010181 GO:0003958 GO:0009055 GO:0046906 GO:0022892 GO:0016708 GO:0016675 GO:0005515
GO-Score 0.64 0.56 0.46 0.46 0.37 0.37 0.37 0.37 0.34
Biological Process GO:0015669 GO:0042127 GO:0018394 GO:0006577 GO:0042981 GO:0046209 GO:0043281 GO:0042126 GO:0043069 GO:0046886
GO-Score 0.37 0.37 0.37 0.37 0.37 0.37 0.37 0.37 0.37 0.37
Cellular Component GO:0005792 GO:0005789 GO:0016021 GO:0005886 GO:0005741
GO-Score 0.46 0.46 0.34 0.34 0.34

(a)CscoreGO is a combined measure for evaluating global and local similarity between query and template protein. It's range is [0-1] and higher values indicate more confident predictions.
(b)TM-score is a measure of global structural similarity between query and template protein.
(c)RMSDa is the RMSD between residues that are structurally aligned by TM-align.
(d)IDENa 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.
(f)The second table shows a consensus GO terms amongst the top scoring templates. The GO-Score associated with each prediction is defined as the average weight of the GO term, where the weights are assigned based on CscoreGO of the template.


[Click on S693368_results.tar.bz2 to download the tarball file including all modeling results listed on this page]



Please cite the following articles when you use the I-TASSER server:
  • 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. Cell Reports Methods, 1: 100014 (2021).
  • Chengxin Zhang, Peter L. Freddolino, and Yang Zhang. COFACTOR: improved protein function prediction by combining structure, sequence and protein-protein interaction information. Nucleic Acids Research, 45: W291-299 (2017).
  • Jianyi Yang, Yang Zhang. I-TASSER server: new development for protein structure and function predictions, Nucleic Acids Research, 43: W174-W181, 2015.