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: 6 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 21 |
GO:0099080 | supramolecular complex | 2 | 21 |
GO:0099081 | supramolecular polymer | 3 | 21 |
GO:0099512 | supramolecular fiber | 4 | 21 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 21 |
GO:0110165 | cellular anatomical entity | 1 | 21 |
GO:0000922 | spindle pole | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005819 | spindle | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AJ89
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 21 |
GO:0007018 | microtubule-based movement | 3 | 21 |
GO:0009987 | cellular process | 1 | 21 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007019 | microtubule depolymerization | 5 | 2 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0007052 | mitotic spindle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022411 | cellular component disassembly | 4 | 2 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 2 |
GO:0032984 | protein-containing complex disassembly | 5 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051261 | protein depolymerization | 6 | 2 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 21 |
GO:0003774 | cytoskeletal motor activity | 1 | 21 |
GO:0003777 | microtubule motor activity | 2 | 21 |
GO:0005488 | binding | 1 | 21 |
GO:0005515 | protein binding | 2 | 21 |
GO:0005524 | ATP binding | 5 | 21 |
GO:0008017 | microtubule binding | 5 | 21 |
GO:0008092 | cytoskeletal protein binding | 3 | 21 |
GO:0015631 | tubulin binding | 4 | 21 |
GO:0017076 | purine nucleotide binding | 4 | 21 |
GO:0030554 | adenyl nucleotide binding | 5 | 21 |
GO:0032553 | ribonucleotide binding | 3 | 21 |
GO:0032555 | purine ribonucleotide binding | 4 | 21 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 21 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 21 |
GO:0036094 | small molecule binding | 2 | 21 |
GO:0043167 | ion binding | 2 | 21 |
GO:0043168 | anion binding | 3 | 21 |
GO:0097159 | organic cyclic compound binding | 2 | 21 |
GO:0097367 | carbohydrate derivative binding | 2 | 21 |
GO:0140657 | ATP-dependent activity | 1 | 21 |
GO:1901265 | nucleoside phosphate binding | 3 | 21 |
GO:1901363 | heterocyclic compound binding | 2 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 152 | 156 | PF00656 | 0.315 |
CLV_C14_Caspase3-7 | 79 | 83 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.569 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.548 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 127 | 129 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 451 | 453 | PF00082 | 0.437 |
CLV_PCSK_PC1ET2_1 | 545 | 547 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 569 | 571 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.469 |
CLV_PCSK_PC7_1 | 477 | 483 | PF00082 | 0.555 |
CLV_PCSK_PC7_1 | 565 | 571 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.427 |
CLV_Separin_Metazoa | 409 | 413 | PF03568 | 0.277 |
DEG_APCC_DBOX_1 | 276 | 284 | PF00400 | 0.225 |
DEG_SPOP_SBC_1 | 667 | 671 | PF00917 | 0.471 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.549 |
DOC_CYCLIN_RxL_1 | 378 | 388 | PF00134 | 0.313 |
DOC_MAPK_gen_1 | 127 | 136 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 165 | 173 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 127 | 136 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 165 | 173 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 330 | 339 | PF00069 | 0.348 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.622 |
DOC_USP7_UBL2_3 | 338 | 342 | PF12436 | 0.358 |
DOC_USP7_UBL2_3 | 346 | 350 | PF12436 | 0.181 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.790 |
LIG_14-3-3_CanoR_1 | 105 | 115 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 174 | 183 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 23 | 32 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 251 | 260 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 452 | 460 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 481 | 487 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 504 | 509 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 512 | 518 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 625 | 635 | PF00244 | 0.523 |
LIG_Actin_WH2_1 | 47 | 62 | PF00022 | 0.329 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.460 |
LIG_BRCT_BRCA1_1 | 668 | 672 | PF00533 | 0.479 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.475 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.360 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.313 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.313 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.630 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.475 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.436 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.324 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.216 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.186 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.517 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.277 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.384 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.414 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.532 |
LIG_Integrin_isoDGR_2 | 275 | 277 | PF01839 | 0.238 |
LIG_LIR_Gen_1 | 147 | 156 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 247 | 255 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 352 | 357 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 587 | 592 | PF02991 | 0.477 |
LIG_NRBOX | 269 | 275 | PF00104 | 0.280 |
LIG_PCNA_TLS_4 | 632 | 639 | PF02747 | 0.525 |
LIG_PDZ_Class_1 | 667 | 672 | PF00595 | 0.476 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.277 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.474 |
LIG_RPA_C_Fungi | 620 | 632 | PF08784 | 0.523 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.216 |
LIG_SH2_NCK_1 | 241 | 245 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.374 |
LIG_SH3_2 | 530 | 535 | PF14604 | 0.786 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.755 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.780 |
LIG_SH3_3 | 556 | 562 | PF00018 | 0.544 |
LIG_SH3_3 | 661 | 667 | PF00018 | 0.439 |
LIG_SUMO_SIM_par_1 | 382 | 388 | PF11976 | 0.277 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.422 |
LIG_UBA3_1 | 132 | 138 | PF00899 | 0.412 |
LIG_UBA3_1 | 334 | 342 | PF00899 | 0.238 |
LIG_UBA3_1 | 383 | 387 | PF00899 | 0.313 |
LIG_WRC_WIRS_1 | 259 | 264 | PF05994 | 0.277 |
LIG_WRC_WIRS_1 | 635 | 640 | PF05994 | 0.530 |
LIG_WW_3 | 501 | 505 | PF00397 | 0.439 |
MOD_CDK_SPK_2 | 526 | 531 | PF00069 | 0.739 |
MOD_CDK_SPxxK_3 | 90 | 97 | PF00069 | 0.582 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.514 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.313 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.423 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.283 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.364 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.313 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.587 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.579 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.610 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.668 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.559 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.447 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.299 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.320 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.242 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.302 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.364 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.525 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.740 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.478 |
MOD_Cter_Amidation | 275 | 278 | PF01082 | 0.401 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.699 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.465 |
MOD_GlcNHglycan | 157 | 161 | PF01048 | 0.246 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.318 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.291 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.234 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.307 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.591 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.694 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.728 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.510 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.269 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.325 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.266 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.150 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.215 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.588 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.681 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.556 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.586 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.615 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.717 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.748 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.635 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.630 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.469 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.558 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.379 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.225 |
MOD_N-GLC_1 | 379 | 384 | PF02516 | 0.313 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.387 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.477 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.303 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.288 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.423 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.660 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.682 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.506 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.313 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.451 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.563 |
MOD_PIKK_1 | 637 | 643 | PF00454 | 0.558 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.686 |
MOD_PKA_1 | 127 | 133 | PF00069 | 0.391 |
MOD_PKA_1 | 174 | 180 | PF00069 | 0.351 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.372 |
MOD_PKA_1 | 481 | 487 | PF00069 | 0.679 |
MOD_PKA_1 | 504 | 510 | PF00069 | 0.616 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.491 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.391 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.372 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.385 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.225 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.313 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.313 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.690 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.598 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.644 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.572 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.571 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.633 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.561 |
MOD_PKB_1 | 104 | 112 | PF00069 | 0.539 |
MOD_PKB_1 | 137 | 145 | PF00069 | 0.315 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.313 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.280 |
MOD_Plk_2-3 | 305 | 311 | PF00069 | 0.216 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.475 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.314 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.313 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.317 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.384 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.300 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.255 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.688 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.528 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.313 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.673 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.755 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.783 |
MOD_SUMO_for_1 | 600 | 603 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 161 | 169 | PF00179 | 0.376 |
MOD_SUMO_rev_2 | 331 | 339 | PF00179 | 0.225 |
MOD_SUMO_rev_2 | 445 | 453 | PF00179 | 0.178 |
TRG_DiLeu_BaEn_1 | 622 | 627 | PF01217 | 0.394 |
TRG_DiLeu_BaEn_2 | 387 | 393 | PF01217 | 0.372 |
TRG_DiLeu_LyEn_5 | 622 | 627 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 582 | 585 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 623 | 626 | PF00400 | 0.574 |
TRG_NLS_Bipartite_1 | 127 | 141 | PF00514 | 0.384 |
TRG_NLS_MonoExtC_3 | 126 | 131 | PF00514 | 0.541 |
TRG_NLS_MonoExtN_4 | 127 | 132 | PF00514 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 281 | 285 | PF00026 | 0.246 |
TRG_Pf-PMV_PEXEL_1 | 293 | 297 | PF00026 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 584 | 588 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 625 | 630 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6P6 | Leptomonas seymouri | 73% | 100% |
A0A0S4IP49 | Bodo saltans | 26% | 83% |
A0A0S4JS40 | Bodo saltans | 52% | 79% |
A0A1X0P2U1 | Trypanosomatidae | 47% | 96% |
A0A3R7MC35 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H4S8 | Leishmania donovani | 96% | 100% |
A0A3S7WST0 | Leishmania donovani | 46% | 92% |
A0A3S7WY84 | Leishmania donovani | 40% | 100% |
A0A3S7X9Y1 | Leishmania donovani | 34% | 100% |
A0A422NY45 | Trypanosoma rangeli | 47% | 96% |
A4H337 | Leishmania braziliensis | 88% | 100% |
A4H7F1 | Leishmania braziliensis | 46% | 100% |
A4HAQ7 | Leishmania braziliensis | 26% | 100% |
A4HDC2 | Leishmania braziliensis | 40% | 100% |
A4HND6 | Leishmania braziliensis | 33% | 100% |
A4HRC5 | Leishmania infantum | 96% | 100% |
A4HSA6 | Leishmania infantum | 32% | 100% |
A4HVT9 | Leishmania infantum | 46% | 92% |
A4I0Q2 | Leishmania infantum | 40% | 100% |
A4IC09 | Leishmania infantum | 34% | 100% |
C9ZXH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 97% |
E9ABZ2 | Leishmania major | 95% | 100% |
E9AFU7 | Leishmania major | 34% | 100% |
E9API5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 93% |
E9AWQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q4QFZ3 | Leishmania major | 46% | 100% |
Q5R9Y9 | Pongo abelii | 39% | 90% |
Q940Y8 | Arabidopsis thaliana | 40% | 98% |
V5D311 | Trypanosoma cruzi | 47% | 99% |