Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 12 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0099080 | supramolecular complex | 2 | 12 |
GO:0099081 | supramolecular polymer | 3 | 12 |
GO:0099512 | supramolecular fiber | 4 | 12 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QJ61
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 14 |
GO:0007018 | microtubule-based movement | 3 | 14 |
GO:0009987 | cellular process | 1 | 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003774 | cytoskeletal motor activity | 1 | 14 |
GO:0003777 | microtubule motor activity | 2 | 14 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0005488 | binding | 1 | 14 |
GO:0005515 | protein binding | 2 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0008017 | microtubule binding | 5 | 14 |
GO:0008092 | cytoskeletal protein binding | 3 | 14 |
GO:0015631 | tubulin binding | 4 | 14 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.439 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.684 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.410 |
CLV_PCSK_PC7_1 | 197 | 203 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.730 |
CLV_Separin_Metazoa | 57 | 61 | PF03568 | 0.628 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.751 |
DEG_SCF_FBW7_2 | 556 | 562 | PF00400 | 0.477 |
DEG_SPOP_SBC_1 | 347 | 351 | PF00917 | 0.342 |
DEG_SPOP_SBC_1 | 359 | 363 | PF00917 | 0.205 |
DEG_SPOP_SBC_1 | 624 | 628 | PF00917 | 0.743 |
DOC_CKS1_1 | 556 | 561 | PF01111 | 0.576 |
DOC_CYCLIN_RxL_1 | 392 | 399 | PF00134 | 0.418 |
DOC_CYCLIN_yCln2_LP_2 | 159 | 165 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 289 | 298 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 305 | 314 | PF00069 | 0.272 |
DOC_MAPK_gen_1 | 364 | 373 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 489 | 499 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 364 | 373 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 492 | 499 | PF00069 | 0.572 |
DOC_PP1_RVXF_1 | 365 | 371 | PF00149 | 0.357 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.412 |
DOC_PP2B_LxvP_1 | 159 | 162 | PF13499 | 0.380 |
DOC_PP2B_LxvP_1 | 527 | 530 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 59 | 62 | PF13499 | 0.663 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.760 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.275 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 616 | 621 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 197 | 203 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 268 | 278 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 378 | 384 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 38 | 46 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 444 | 448 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 48 | 53 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 566 | 572 | PF00244 | 0.778 |
LIG_14-3-3_CanoR_1 | 587 | 592 | PF00244 | 0.780 |
LIG_14-3-3_CanoR_1 | 616 | 620 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.586 |
LIG_14-3-3_CterR_2 | 668 | 672 | PF00244 | 0.727 |
LIG_Actin_WH2_2 | 182 | 199 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 366 | 382 | PF00022 | 0.384 |
LIG_Actin_WH2_2 | 509 | 526 | PF00022 | 0.554 |
LIG_APCC_ABBA_1 | 248 | 253 | PF00400 | 0.286 |
LIG_APCC_ABBA_1 | 323 | 328 | PF00400 | 0.384 |
LIG_BIR_III_2 | 426 | 430 | PF00653 | 0.307 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.412 |
LIG_Clathr_ClatBox_1 | 368 | 372 | PF01394 | 0.384 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.373 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.315 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.437 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.743 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.275 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.646 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.275 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.475 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.358 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.442 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.747 |
LIG_Integrin_RGD_1 | 207 | 209 | PF01839 | 0.233 |
LIG_LIR_Apic_2 | 590 | 594 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 117 | 128 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 246 | 255 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 292 | 298 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.371 |
LIG_MLH1_MIPbox_1 | 275 | 279 | PF16413 | 0.412 |
LIG_NRBOX | 254 | 260 | PF00104 | 0.384 |
LIG_NRBOX | 447 | 453 | PF00104 | 0.286 |
LIG_Pex14_2 | 323 | 327 | PF04695 | 0.419 |
LIG_REV1ctd_RIR_1 | 324 | 334 | PF16727 | 0.412 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.412 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.357 |
LIG_SH2_CRK | 365 | 369 | PF00017 | 0.414 |
LIG_SH2_PTP2 | 247 | 250 | PF00017 | 0.414 |
LIG_SH2_SRC | 251 | 254 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 484 | 488 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.359 |
LIG_SH3_2 | 439 | 444 | PF14604 | 0.419 |
LIG_SH3_2 | 75 | 80 | PF14604 | 0.679 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.398 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.382 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.630 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.737 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.752 |
LIG_SUMO_SIM_anti_2 | 136 | 142 | PF11976 | 0.377 |
LIG_SUMO_SIM_anti_2 | 292 | 300 | PF11976 | 0.358 |
LIG_SUMO_SIM_anti_2 | 656 | 662 | PF11976 | 0.682 |
LIG_SUMO_SIM_par_1 | 292 | 300 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 402 | 408 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 656 | 662 | PF11976 | 0.628 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.386 |
LIG_TRAF2_1 | 508 | 511 | PF00917 | 0.552 |
LIG_TYR_ITIM | 181 | 186 | PF00017 | 0.412 |
LIG_TYR_ITIM | 31 | 36 | PF00017 | 0.530 |
MOD_CDC14_SPxK_1 | 593 | 596 | PF00782 | 0.623 |
MOD_CDK_SPK_2 | 561 | 566 | PF00069 | 0.761 |
MOD_CDK_SPxK_1 | 590 | 596 | PF00069 | 0.628 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.769 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.286 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.286 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.387 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.302 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.282 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.363 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.286 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.337 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.678 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.669 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.740 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.747 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.786 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.337 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.314 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.442 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.364 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.605 |
MOD_CK2_1 | 623 | 629 | PF00069 | 0.744 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.297 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.288 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.355 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.357 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.326 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.364 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.441 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.377 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.401 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.286 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.419 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.743 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.677 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.714 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.730 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.753 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.700 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.363 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.426 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.402 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.394 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.431 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.414 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.338 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.356 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.302 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.709 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.331 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.637 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.649 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.608 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.749 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.673 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.275 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.328 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.414 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.377 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.453 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.254 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.374 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.680 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.632 |
MOD_NEK2_2 | 251 | 256 | PF00069 | 0.408 |
MOD_NEK2_2 | 274 | 279 | PF00069 | 0.403 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.352 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.790 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.233 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.371 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.301 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.522 |
MOD_PKA_1 | 197 | 203 | PF00069 | 0.440 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.403 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.653 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.316 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.363 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.694 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.275 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.773 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.743 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.275 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.328 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.292 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.339 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.263 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.226 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.362 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.359 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.330 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.749 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.774 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.674 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.795 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.399 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.419 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.326 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.275 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.659 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.522 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.643 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.610 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.760 |
MOD_ProDKin_1 | 616 | 622 | PF00069 | 0.734 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.712 |
MOD_SUMO_rev_2 | 25 | 32 | PF00179 | 0.498 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_3 | 117 | 123 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 523 | 525 | PF00400 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVM1 | Leptomonas seymouri | 27% | 72% |
A0A0N1HY56 | Leptomonas seymouri | 51% | 98% |
A0A0S4ILK1 | Bodo saltans | 28% | 79% |
A0A0S4JUR0 | Bodo saltans | 26% | 77% |
A0A0S4KL43 | Bodo saltans | 30% | 100% |
A0A1X0NJN6 | Trypanosomatidae | 39% | 100% |
A0A1X0NQ03 | Trypanosomatidae | 25% | 81% |
A0A1X0P9E3 | Trypanosomatidae | 29% | 100% |
A0A3Q8IBS7 | Leishmania donovani | 26% | 100% |
A0A3Q8IHG6 | Leishmania donovani | 26% | 100% |
A0A3R7MC35 | Trypanosoma rangeli | 39% | 100% |
A0A3R7RD86 | Trypanosoma rangeli | 27% | 84% |
A0A3S5H5N6 | Leishmania donovani | 92% | 100% |
A0A3S5IRH3 | Trypanosoma rangeli | 26% | 100% |
A0A3S7X2P9 | Leishmania donovani | 26% | 100% |
A0A422NE49 | Trypanosoma rangeli | 26% | 76% |
A0A422NEQ8 | Trypanosoma rangeli | 26% | 89% |
A4H4I4 | Leishmania braziliensis | 76% | 100% |
A4HAQ7 | Leishmania braziliensis | 28% | 100% |
A4HCA1 | Leishmania braziliensis | 24% | 75% |
A4HHY2 | Leishmania braziliensis | 27% | 100% |
A4HSA6 | Leishmania infantum | 24% | 100% |
A4HSQ9 | Leishmania infantum | 92% | 100% |
A4I4V2 | Leishmania infantum | 26% | 100% |
A4I562 | Leishmania infantum | 26% | 100% |
C9ZQI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZU98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 83% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 90% |
D0A7F3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 68% |
D0A992 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 73% |
E9AKP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AVN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 76% |
F4IL57 | Arabidopsis thaliana | 27% | 68% |
F4J2M6 | Arabidopsis thaliana | 26% | 70% |
O14343 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 76% |
P46864 | Arabidopsis thaliana | 25% | 90% |
P46865 | Leishmania chagasi | 28% | 70% |
P46870 | Chlamydomonas reinhardtii | 28% | 87% |
P53086 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 83% |
P97329 | Mus musculus | 24% | 76% |
Q0IMS9 | Oryza sativa subsp. japonica | 26% | 70% |
Q29RT6 | Bos taurus | 24% | 76% |
Q4Q7S4 | Leishmania major | 27% | 100% |
Q6PFD6 | Mus musculus | 27% | 81% |
Q6ZMV9 | Homo sapiens | 24% | 83% |
Q75HV1 | Oryza sativa subsp. japonica | 26% | 80% |
V5B325 | Trypanosoma cruzi | 25% | 81% |
V5BK25 | Trypanosoma cruzi | 29% | 93% |
V5BLH7 | Trypanosoma cruzi | 26% | 78% |