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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HKQ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.727 |
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.438 |
CLV_C14_Caspase3-7 | 489 | 493 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 573 | 577 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 614 | 618 | PF00656 | 0.491 |
CLV_C14_Caspase3-7 | 647 | 651 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.488 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.459 |
CLV_PCSK_FUR_1 | 118 | 122 | PF00082 | 0.500 |
CLV_PCSK_FUR_1 | 176 | 180 | PF00082 | 0.524 |
CLV_PCSK_FUR_1 | 706 | 710 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.320 |
CLV_PCSK_PC7_1 | 164 | 170 | PF00082 | 0.606 |
CLV_PCSK_PC7_1 | 244 | 250 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 727 | 731 | PF00082 | 0.419 |
CLV_Separin_Metazoa | 23 | 27 | PF03568 | 0.536 |
DEG_APCC_DBOX_1 | 129 | 137 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 623 | 631 | PF00400 | 0.430 |
DEG_SPOP_SBC_1 | 181 | 185 | PF00917 | 0.410 |
DOC_CYCLIN_RxL_1 | 248 | 260 | PF00134 | 0.582 |
DOC_CYCLIN_RxL_1 | 559 | 573 | PF00134 | 0.334 |
DOC_CYCLIN_yCln2_LP_2 | 347 | 353 | PF00134 | 0.274 |
DOC_MAPK_gen_1 | 63 | 72 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 253 | 261 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 364 | 373 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 63 | 72 | PF00069 | 0.516 |
DOC_MAPK_NFAT4_5 | 63 | 71 | PF00069 | 0.491 |
DOC_PP1_RVXF_1 | 679 | 686 | PF00149 | 0.385 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.268 |
DOC_PP2B_LxvP_1 | 628 | 631 | PF13499 | 0.431 |
DOC_PP2B_LxvP_1 | 713 | 716 | PF13499 | 0.444 |
DOC_PP4_FxxP_1 | 415 | 418 | PF00568 | 0.427 |
DOC_PP4_FxxP_1 | 672 | 675 | PF00568 | 0.446 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.565 |
DOC_USP7_UBL2_3 | 555 | 559 | PF12436 | 0.561 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.296 |
LIG_14-3-3_CanoR_1 | 146 | 154 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 308 | 314 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 422 | 427 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 537 | 543 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 653 | 660 | PF00244 | 0.432 |
LIG_Actin_WH2_2 | 234 | 250 | PF00022 | 0.490 |
LIG_Actin_WH2_2 | 419 | 434 | PF00022 | 0.529 |
LIG_ActinCP_TwfCPI_2 | 415 | 424 | PF01115 | 0.509 |
LIG_AP2alpha_2 | 658 | 660 | PF02296 | 0.563 |
LIG_BRCT_BRCA1_1 | 148 | 152 | PF00533 | 0.575 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 287 | 291 | PF00533 | 0.425 |
LIG_deltaCOP1_diTrp_1 | 337 | 342 | PF00928 | 0.314 |
LIG_deltaCOP1_diTrp_1 | 721 | 726 | PF00928 | 0.405 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.521 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.452 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.280 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.481 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.602 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.377 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.512 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.496 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.481 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.640 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.495 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.543 |
LIG_GBD_Chelix_1 | 261 | 269 | PF00786 | 0.511 |
LIG_GBD_Chelix_1 | 597 | 605 | PF00786 | 0.519 |
LIG_LIR_Apic_2 | 412 | 418 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 273 | 283 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.518 |
LIG_MYND_1 | 625 | 629 | PF01753 | 0.431 |
LIG_NRBOX | 585 | 591 | PF00104 | 0.581 |
LIG_Pex14_2 | 278 | 282 | PF04695 | 0.311 |
LIG_Pex14_2 | 672 | 676 | PF04695 | 0.506 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 469 | 473 | PF00017 | 0.461 |
LIG_SH2_STAT3 | 116 | 119 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.362 |
LIG_SH3_1 | 709 | 715 | PF00018 | 0.463 |
LIG_SH3_1 | 717 | 723 | PF00018 | 0.404 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.479 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.550 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.567 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.430 |
LIG_SH3_3 | 676 | 682 | PF00018 | 0.371 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.443 |
LIG_SH3_3 | 717 | 723 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 258 | 264 | PF11976 | 0.529 |
LIG_SUMO_SIM_anti_2 | 319 | 325 | PF11976 | 0.368 |
LIG_TRAF2_1 | 101 | 104 | PF00917 | 0.325 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.524 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.478 |
LIG_TRAF2_2 | 675 | 680 | PF00917 | 0.346 |
LIG_UBA3_1 | 265 | 274 | PF00899 | 0.411 |
LIG_UBA3_1 | 601 | 610 | PF00899 | 0.422 |
MOD_CDK_SPxK_1 | 231 | 237 | PF00069 | 0.542 |
MOD_CDK_SPxxK_3 | 351 | 358 | PF00069 | 0.315 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.480 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.567 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.643 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.506 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.473 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.374 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.774 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.531 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.481 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.385 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.392 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.341 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.663 |
MOD_GlcNHglycan | 492 | 496 | PF01048 | 0.634 |
MOD_GlcNHglycan | 498 | 502 | PF01048 | 0.630 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.689 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.362 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.398 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.336 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.749 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.792 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.621 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.587 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.481 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.489 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.609 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.523 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.587 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.706 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.557 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.407 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.472 |
MOD_NEK2_1 | 685 | 690 | PF00069 | 0.421 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.553 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.443 |
MOD_NEK2_2 | 53 | 58 | PF00069 | 0.514 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.434 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.299 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.394 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.558 |
MOD_PIKK_1 | 544 | 550 | PF00454 | 0.607 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.515 |
MOD_PK_1 | 309 | 315 | PF00069 | 0.577 |
MOD_PKA_1 | 551 | 557 | PF00069 | 0.596 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.335 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.562 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.479 |
MOD_PKB_1 | 167 | 175 | PF00069 | 0.544 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.493 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.480 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.428 |
MOD_Plk_2-3 | 608 | 614 | PF00069 | 0.392 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.414 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.495 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.487 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.390 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.437 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.728 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.761 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.697 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.293 |
MOD_SUMO_for_1 | 329 | 332 | PF00179 | 0.527 |
MOD_SUMO_for_1 | 558 | 561 | PF00179 | 0.544 |
MOD_SUMO_rev_2 | 606 | 611 | PF00179 | 0.383 |
TRG_AP2beta_CARGO_1 | 280 | 289 | PF09066 | 0.246 |
TRG_DiLeu_BaEn_1 | 585 | 590 | PF01217 | 0.505 |
TRG_DiLeu_BaEn_4 | 463 | 469 | PF01217 | 0.348 |
TRG_DiLeu_BaLyEn_6 | 342 | 347 | PF01217 | 0.249 |
TRG_DiLeu_BaLyEn_6 | 597 | 602 | PF01217 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 679 | 684 | PF01217 | 0.392 |
TRG_DiLeu_LyEn_5 | 585 | 590 | PF01217 | 0.505 |
TRG_DiLeu_LyEn_5 | 623 | 628 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 551 | 553 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 706 | 709 | PF00400 | 0.462 |
TRG_NLS_MonoExtC_3 | 660 | 665 | PF00514 | 0.565 |
TRG_NLS_MonoExtN_4 | 240 | 246 | PF00514 | 0.525 |
TRG_NLS_MonoExtN_4 | 659 | 665 | PF00514 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.528 |
TRG_Pf-PMV_PEXEL_1 | 441 | 445 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 466 | 471 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 588 | 592 | PF00026 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 653 | 658 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I355 | Leptomonas seymouri | 72% | 87% |
A0A0S4JPP8 | Bodo saltans | 43% | 93% |
A0A1X0NS88 | Trypanosomatidae | 50% | 92% |
A0A3R7LBC9 | Trypanosoma rangeli | 53% | 97% |
A0A3S7X5U8 | Leishmania donovani | 85% | 93% |
A4I888 | Leishmania infantum | 85% | 93% |
D0AAF7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 97% |
E9B346 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 93% |
Q4Q508 | Leishmania major | 85% | 100% |
V5AUT0 | Trypanosoma cruzi | 54% | 89% |