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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A0A3Q8IDI3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0005215 | transporter activity | 1 | 5 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 5 |
GO:0022804 | active transmembrane transporter activity | 3 | 5 |
GO:0022857 | transmembrane transporter activity | 2 | 5 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 5 |
GO:0140657 | ATP-dependent activity | 1 | 5 |
GO:0140359 | ABC-type transporter activity | 3 | 4 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.465 |
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.444 |
CLV_C14_Caspase3-7 | 296 | 300 | PF00656 | 0.460 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.370 |
CLV_PCSK_FUR_1 | 166 | 170 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.246 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.442 |
DEG_APCC_DBOX_1 | 232 | 240 | PF00400 | 0.536 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.249 |
DOC_AGCK_PIF_2 | 549 | 554 | PF00069 | 0.427 |
DOC_CYCLIN_RxL_1 | 578 | 587 | PF00134 | 0.227 |
DOC_CYCLIN_yCln2_LP_2 | 252 | 258 | PF00134 | 0.505 |
DOC_MAPK_gen_1 | 233 | 239 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 395 | 404 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 450 | 457 | PF00069 | 0.210 |
DOC_MAPK_MEF2A_6 | 482 | 489 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 499 | 507 | PF00069 | 0.237 |
DOC_MAPK_MEF2A_6 | 521 | 529 | PF00069 | 0.210 |
DOC_MAPK_NFAT4_5 | 234 | 242 | PF00069 | 0.459 |
DOC_MAPK_NFAT4_5 | 450 | 458 | PF00069 | 0.210 |
DOC_MAPK_RevD_3 | 87 | 100 | PF00069 | 0.432 |
DOC_PP1_RVXF_1 | 396 | 402 | PF00149 | 0.604 |
DOC_PP1_RVXF_1 | 502 | 508 | PF00149 | 0.353 |
DOC_PP1_RVXF_1 | 579 | 586 | PF00149 | 0.231 |
DOC_PP1_SILK_1 | 327 | 332 | PF00149 | 0.561 |
DOC_PP1_SILK_1 | 586 | 591 | PF00149 | 0.334 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.496 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.622 |
DOC_PP4_FxxP_1 | 630 | 633 | PF00568 | 0.334 |
DOC_SPAK_OSR1_1 | 197 | 201 | PF12202 | 0.451 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.309 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.220 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.731 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 17 | 21 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 353 | 357 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 602 | 607 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 622 | 630 | PF00244 | 0.285 |
LIG_Actin_WH2_2 | 576 | 592 | PF00022 | 0.310 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.648 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.548 |
LIG_BRCT_BRCA1_1 | 48 | 52 | PF00533 | 0.697 |
LIG_CaM_IQ_9 | 261 | 277 | PF13499 | 0.460 |
LIG_EH1_1 | 424 | 432 | PF00400 | 0.230 |
LIG_EH1_1 | 491 | 499 | PF00400 | 0.478 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.554 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.483 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.550 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.236 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.247 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.329 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.560 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.482 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.482 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.386 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.563 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.549 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.595 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.457 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.686 |
LIG_GBD_Chelix_1 | 416 | 424 | PF00786 | 0.321 |
LIG_HP1_1 | 247 | 251 | PF01393 | 0.463 |
LIG_IRF3_LxIS_1 | 481 | 488 | PF10401 | 0.485 |
LIG_LIR_Apic_2 | 628 | 633 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 185 | 193 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 293 | 303 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 380 | 387 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 452 | 461 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 553 | 562 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 553 | 557 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 645 | 649 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.667 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.289 |
LIG_PCNA_yPIPBox_3 | 469 | 481 | PF02747 | 0.443 |
LIG_Pex14_1 | 421 | 425 | PF04695 | 0.237 |
LIG_Pex14_1 | 548 | 552 | PF04695 | 0.502 |
LIG_PTB_Apo_2 | 186 | 193 | PF02174 | 0.511 |
LIG_PTB_Apo_2 | 357 | 364 | PF02174 | 0.493 |
LIG_PTB_Apo_2 | 556 | 563 | PF02174 | 0.267 |
LIG_PTB_Phospho_1 | 357 | 363 | PF10480 | 0.495 |
LIG_PTB_Phospho_1 | 556 | 562 | PF10480 | 0.267 |
LIG_SH2_CRK | 565 | 569 | PF00017 | 0.265 |
LIG_SH2_CRK | 593 | 597 | PF00017 | 0.248 |
LIG_SH2_PTP2 | 486 | 489 | PF00017 | 0.442 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 363 | 366 | PF00017 | 0.499 |
LIG_SH2_STAT3 | 638 | 641 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.186 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 643 | 646 | PF00017 | 0.252 |
LIG_SH3_2 | 23 | 28 | PF14604 | 0.631 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.747 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.599 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.443 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.419 |
LIG_SH3_5 | 550 | 554 | PF00018 | 0.465 |
LIG_SH3_CIN85_PxpxPR_1 | 23 | 28 | PF14604 | 0.554 |
LIG_SUMO_SIM_anti_2 | 246 | 254 | PF11976 | 0.535 |
LIG_SUMO_SIM_anti_2 | 299 | 307 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 335 | 342 | PF11976 | 0.583 |
LIG_SUMO_SIM_anti_2 | 553 | 559 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 657 | 663 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 180 | 185 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 246 | 254 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 347 | 352 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 433 | 439 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 523 | 528 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 572 | 578 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 660 | 665 | PF11976 | 0.268 |
LIG_SxIP_EBH_1 | 572 | 581 | PF03271 | 0.378 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.772 |
LIG_TYR_ITIM | 591 | 596 | PF00017 | 0.408 |
LIG_TYR_ITSM | 217 | 224 | PF00017 | 0.360 |
LIG_UBA3_1 | 477 | 483 | PF00899 | 0.289 |
LIG_WRC_WIRS_1 | 533 | 538 | PF05994 | 0.343 |
LIG_WW_1 | 393 | 396 | PF00397 | 0.484 |
LIG_WW_3 | 25 | 29 | PF00397 | 0.563 |
LIG_WW_3 | 392 | 396 | PF00397 | 0.344 |
MOD_CDK_SPxxK_3 | 21 | 28 | PF00069 | 0.455 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.419 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.621 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.334 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.740 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.575 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.371 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.559 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.526 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.295 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.369 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.527 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.686 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.702 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.354 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.222 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.715 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.440 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.542 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.714 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.425 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.342 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.691 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.309 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.634 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.613 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.538 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.508 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.515 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.644 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.484 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.348 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.357 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.327 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.525 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.426 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.259 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.635 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.527 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.394 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.249 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.355 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.475 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.672 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.719 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.500 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.363 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.274 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.391 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.289 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.755 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.257 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.340 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.211 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.284 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.384 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.257 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.247 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.736 |
MOD_NEK2_2 | 633 | 638 | PF00069 | 0.362 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.382 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.274 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.585 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.629 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.455 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.447 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.195 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.604 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.374 |
MOD_PKB_1 | 275 | 283 | PF00069 | 0.453 |
MOD_PKB_1 | 375 | 383 | PF00069 | 0.351 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.340 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.695 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.447 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.370 |
MOD_Plk_2-3 | 201 | 207 | PF00069 | 0.361 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.638 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.310 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.428 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.482 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.366 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.414 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.148 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.482 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.562 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.272 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.251 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.275 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.280 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.241 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.527 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.433 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.349 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.518 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.682 |
MOD_SUMO_for_1 | 468 | 471 | PF00179 | 0.361 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.330 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.191 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.392 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.762 |
TRG_ER_diArg_1 | 601 | 604 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 365 | 369 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 395 | 400 | PF00026 | 0.319 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I194 | Leptomonas seymouri | 56% | 83% |
A0A0S4IZ09 | Bodo saltans | 35% | 100% |
A0A0S4KMF6 | Bodo saltans | 24% | 85% |
A0A1X0P4K0 | Trypanosomatidae | 33% | 100% |
A0A3R7MIF6 | Trypanosoma rangeli | 33% | 100% |
A4HFU5 | Leishmania braziliensis | 77% | 100% |
A4I2W2 | Leishmania infantum | 98% | 100% |
D3ZCM3 | Rattus norvegicus | 22% | 100% |
E9ADE9 | Leishmania major | 91% | 100% |
P45843 | Drosophila melanogaster | 23% | 100% |
Q4GZT4 | Bos taurus | 21% | 100% |
Q91WA9 | Mus musculus | 21% | 100% |
Q99P81 | Mus musculus | 22% | 100% |
V5B0X3 | Trypanosoma cruzi | 34% | 100% |
V5BLN9 | Trypanosoma cruzi | 24% | 99% |