Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 11 |
GO:0099080 | supramolecular complex | 2 | 11 |
GO:0099081 | supramolecular polymer | 3 | 11 |
GO:0099512 | supramolecular fiber | 4 | 11 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
Related structures:
AlphaFold database: Q4QBU1
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 15 |
GO:0007018 | microtubule-based movement | 3 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0006810 | transport | 3 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003774 | cytoskeletal motor activity | 1 | 15 |
GO:0003777 | microtubule motor activity | 2 | 15 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 15 |
GO:0005515 | protein binding | 2 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0008017 | microtubule binding | 5 | 15 |
GO:0008092 | cytoskeletal protein binding | 3 | 15 |
GO:0015631 | tubulin binding | 4 | 15 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140657 | ATP-dependent activity | 1 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0008574 | plus-end-directed microtubule motor activity | 3 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.518 |
CLV_PCSK_FUR_1 | 428 | 432 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 775 | 777 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 817 | 819 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 430 | 432 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 817 | 819 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 764 | 768 | PF00082 | 0.478 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.435 |
DEG_SCF_FBW7_2 | 409 | 414 | PF00400 | 0.366 |
DOC_CKS1_1 | 741 | 746 | PF01111 | 0.439 |
DOC_CYCLIN_RxL_1 | 456 | 466 | PF00134 | 0.470 |
DOC_MAPK_gen_1 | 428 | 438 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 532 | 540 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 815 | 824 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.233 |
DOC_MAPK_MEF2A_6 | 817 | 826 | PF00069 | 0.410 |
DOC_MIT_MIM_1 | 696 | 704 | PF04212 | 0.552 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 783 | 787 | PF00917 | 0.540 |
DOC_USP7_UBL2_3 | 316 | 320 | PF12436 | 0.253 |
DOC_USP7_UBL2_3 | 856 | 860 | PF12436 | 0.426 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 740 | 745 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 227 | 234 | PF00244 | 0.267 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 284 | 292 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 569 | 573 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 619 | 628 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 703 | 711 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 731 | 739 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 825 | 830 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 877 | 883 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 441 | 458 | PF00022 | 0.497 |
LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.277 |
LIG_APCC_ABBA_1 | 381 | 386 | PF00400 | 0.249 |
LIG_APCC_ABBAyCdc20_2 | 127 | 133 | PF00400 | 0.366 |
LIG_BIR_III_4 | 154 | 158 | PF00653 | 0.253 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.268 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.254 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.277 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.277 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.243 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.488 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.456 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.233 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.487 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.616 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.680 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.383 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.408 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.356 |
LIG_FHA_2 | 708 | 714 | PF00498 | 0.674 |
LIG_FHA_2 | 751 | 757 | PF00498 | 0.732 |
LIG_Integrin_RGD_1 | 661 | 663 | PF01839 | 0.445 |
LIG_LIR_Gen_1 | 115 | 122 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 401 | 409 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 48 | 57 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 682 | 690 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 94 | 102 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 682 | 686 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 727 | 733 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.289 |
LIG_NRBOX | 145 | 151 | PF00104 | 0.233 |
LIG_NRBOX | 388 | 394 | PF00104 | 0.277 |
LIG_NRBOX | 728 | 734 | PF00104 | 0.434 |
LIG_PCNA_yPIPBox_3 | 143 | 151 | PF02747 | 0.407 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.366 |
LIG_SH2_NCK_1 | 53 | 57 | PF00017 | 0.253 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.268 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.216 |
LIG_SH2_STAT3 | 479 | 482 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.169 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.249 |
LIG_SH3_3 | 881 | 887 | PF00018 | 0.466 |
LIG_SUMO_SIM_par_1 | 189 | 195 | PF11976 | 0.250 |
LIG_SUMO_SIM_par_1 | 830 | 836 | PF11976 | 0.326 |
LIG_SxIP_EBH_1 | 375 | 385 | PF03271 | 0.238 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.309 |
LIG_TRAF2_1 | 273 | 276 | PF00917 | 0.655 |
LIG_TRAF2_1 | 526 | 529 | PF00917 | 0.359 |
LIG_TRAF2_1 | 630 | 633 | PF00917 | 0.510 |
LIG_TRAF2_2 | 744 | 749 | PF00917 | 0.505 |
LIG_UBA3_1 | 846 | 853 | PF00899 | 0.487 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.451 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.367 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.280 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.275 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.728 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.389 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.262 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.310 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.257 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.596 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.492 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.525 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.277 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.277 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.249 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.139 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.690 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.249 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.373 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.397 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.464 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.334 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.531 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.480 |
MOD_CK2_1 | 783 | 789 | PF00069 | 0.494 |
MOD_Cter_Amidation | 298 | 301 | PF01082 | 0.545 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.438 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.227 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.153 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.295 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.640 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.266 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.268 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.677 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.506 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.277 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.387 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.480 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.300 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.355 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.703 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.288 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.249 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.372 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.694 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.529 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.589 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.494 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.595 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.277 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.277 |
MOD_N-GLC_1 | 707 | 712 | PF02516 | 0.498 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.292 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.476 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.538 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.233 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.519 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.527 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.630 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.424 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.550 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.485 |
MOD_NEK2_1 | 724 | 729 | PF00069 | 0.433 |
MOD_NEK2_1 | 852 | 857 | PF00069 | 0.492 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.272 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.366 |
MOD_NEK2_2 | 750 | 755 | PF00069 | 0.535 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.326 |
MOD_NEK2_2 | 864 | 869 | PF00069 | 0.460 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.415 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.697 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.704 |
MOD_PIKK_1 | 572 | 578 | PF00454 | 0.518 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.571 |
MOD_PIKK_1 | 644 | 650 | PF00454 | 0.457 |
MOD_PIKK_1 | 737 | 743 | PF00454 | 0.586 |
MOD_PIKK_1 | 754 | 760 | PF00454 | 0.453 |
MOD_PIKK_1 | 854 | 860 | PF00454 | 0.603 |
MOD_PIKK_1 | 878 | 884 | PF00454 | 0.592 |
MOD_PK_1 | 825 | 831 | PF00069 | 0.411 |
MOD_PKA_1 | 619 | 625 | PF00069 | 0.395 |
MOD_PKA_1 | 775 | 781 | PF00069 | 0.521 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.278 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.404 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.327 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.703 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.277 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.259 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.558 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.506 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.426 |
MOD_PKA_2 | 699 | 705 | PF00069 | 0.615 |
MOD_PKA_2 | 720 | 726 | PF00069 | 0.454 |
MOD_PKA_2 | 754 | 760 | PF00069 | 0.612 |
MOD_PKA_2 | 775 | 781 | PF00069 | 0.521 |
MOD_PKA_2 | 878 | 884 | PF00069 | 0.423 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.312 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.305 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.405 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.268 |
MOD_Plk_1 | 582 | 588 | PF00069 | 0.556 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.422 |
MOD_Plk_1 | 707 | 713 | PF00069 | 0.493 |
MOD_Plk_2-3 | 257 | 263 | PF00069 | 0.586 |
MOD_Plk_2-3 | 33 | 39 | PF00069 | 0.366 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.268 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.436 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.243 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.251 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.440 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.559 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.480 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.329 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.349 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.345 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.373 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.354 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.296 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.552 |
MOD_ProDKin_1 | 740 | 746 | PF00069 | 0.435 |
MOD_SUMO_rev_2 | 529 | 536 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 602 | 609 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 809 | 816 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_1 | 623 | 628 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 693 | 698 | PF01217 | 0.598 |
TRG_DiLeu_BaEn_4 | 529 | 535 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_4 | 633 | 639 | PF01217 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 501 | 506 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 652 | 657 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 728 | 733 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 792 | 797 | PF01217 | 0.399 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.249 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 790 | 793 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 877 | 880 | PF00400 | 0.595 |
TRG_NES_CRM1_1 | 124 | 140 | PF08389 | 0.271 |
TRG_NES_CRM1_1 | 529 | 543 | PF08389 | 0.493 |
TRG_NES_CRM1_1 | 664 | 677 | PF08389 | 0.402 |
TRG_NES_CRM1_1 | 820 | 835 | PF08389 | 0.422 |
TRG_NLS_Bipartite_1 | 300 | 322 | PF00514 | 0.508 |
TRG_NLS_MonoExtN_4 | 316 | 322 | PF00514 | 0.253 |
TRG_NLS_MonoExtN_4 | 428 | 434 | PF00514 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 601 | 606 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 795 | 799 | PF00026 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A068FIK2 | Gossypium hirsutum | 28% | 86% |
A0A0N1HVM1 | Leptomonas seymouri | 63% | 96% |
A0A0S4INA4 | Bodo saltans | 41% | 100% |
A0A1X0NUN6 | Trypanosomatidae | 41% | 95% |
A0A3Q8IG88 | Leishmania donovani | 31% | 100% |
A0A3S7WX05 | Leishmania donovani | 92% | 100% |
A0A422N2N4 | Trypanosoma rangeli | 42% | 100% |
A4H4I4 | Leishmania braziliensis | 24% | 100% |
A4HCA1 | Leishmania braziliensis | 78% | 100% |
A4HZT3 | Leishmania infantum | 92% | 100% |
A4IBA7 | Leishmania infantum | 31% | 100% |
E9AF32 | Leishmania major | 31% | 100% |
E9AVN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9B687 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O35787 | Rattus norvegicus | 29% | 81% |
Q9LPC6 | Arabidopsis thaliana | 25% | 100% |
V5BLH7 | Trypanosoma cruzi | 43% | 100% |