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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4Q3H7
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 9 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006399 | tRNA metabolic process | 7 | 9 |
GO:0006400 | tRNA modification | 6 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008033 | tRNA processing | 8 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009451 | RNA modification | 5 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0016556 | mRNA modification | 6 | 2 |
GO:0031119 | tRNA pseudouridine synthesis | 7 | 6 |
GO:0034470 | ncRNA processing | 7 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034660 | ncRNA metabolic process | 6 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:1990481 | mRNA pseudouridine synthesis | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0009982 | pseudouridine synthase activity | 4 | 9 |
GO:0016853 | isomerase activity | 2 | 9 |
GO:0016866 | intramolecular transferase activity | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.774 |
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.774 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.765 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 665 | 667 | PF00675 | 0.434 |
CLV_PCSK_FUR_1 | 51 | 55 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 187 | 189 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.730 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.754 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.558 |
CLV_PCSK_PC7_1 | 604 | 610 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.806 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.786 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.482 |
CLV_Separin_Metazoa | 562 | 566 | PF03568 | 0.357 |
DEG_ODPH_VHL_1 | 245 | 257 | PF01847 | 0.533 |
DEG_SCF_FBW7_2 | 319 | 326 | PF00400 | 0.698 |
DOC_CYCLIN_RxL_1 | 436 | 446 | PF00134 | 0.567 |
DOC_CYCLIN_RxL_1 | 86 | 95 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 50 | 60 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 664 | 672 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 686 | 694 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 127 | 136 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 53 | 62 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 664 | 672 | PF00069 | 0.386 |
DOC_PP1_RVXF_1 | 251 | 258 | PF00149 | 0.633 |
DOC_PP1_RVXF_1 | 691 | 697 | PF00149 | 0.513 |
DOC_PP2B_LxvP_1 | 535 | 538 | PF13499 | 0.337 |
DOC_PP4_FxxP_1 | 244 | 247 | PF00568 | 0.466 |
DOC_PP4_FxxP_1 | 499 | 502 | PF00568 | 0.438 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.415 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.162 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 127 | 133 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 269 | 274 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 354 | 360 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 388 | 394 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 467 | 473 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 505 | 511 | PF00244 | 0.438 |
LIG_Actin_WH2_2 | 238 | 255 | PF00022 | 0.611 |
LIG_Actin_WH2_2 | 678 | 695 | PF00022 | 0.464 |
LIG_AP2alpha_2 | 476 | 478 | PF02296 | 0.381 |
LIG_BRCT_BRCA1_1 | 474 | 478 | PF00533 | 0.376 |
LIG_Clathr_ClatBox_1 | 110 | 114 | PF01394 | 0.519 |
LIG_deltaCOP1_diTrp_1 | 492 | 499 | PF00928 | 0.414 |
LIG_eIF4E_1 | 597 | 603 | PF01652 | 0.369 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.415 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.797 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.568 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.593 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.542 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.598 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.431 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.743 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.480 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.353 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.788 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.391 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.423 |
LIG_GBD_Chelix_1 | 668 | 676 | PF00786 | 0.388 |
LIG_LIR_Apic_2 | 222 | 226 | PF02991 | 0.384 |
LIG_LIR_Apic_2 | 24 | 28 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 243 | 247 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 426 | 431 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 227 | 236 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 405 | 414 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 448 | 456 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 622 | 629 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 99 | 110 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 464 | 469 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 622 | 626 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.245 |
LIG_LYPXL_yS_3 | 80 | 83 | PF13949 | 0.464 |
LIG_MYND_1 | 28 | 32 | PF01753 | 0.590 |
LIG_PCNA_yPIPBox_3 | 104 | 118 | PF02747 | 0.521 |
LIG_RPA_C_Fungi | 661 | 673 | PF08784 | 0.464 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.478 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.509 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.492 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.402 |
LIG_SH2_GRB2like | 213 | 216 | PF00017 | 0.506 |
LIG_SH2_GRB2like | 451 | 454 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 201 | 205 | PF00017 | 0.373 |
LIG_SH2_SRC | 138 | 141 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 399 | 403 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 510 | 514 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.393 |
LIG_SH3_1 | 26 | 32 | PF00018 | 0.671 |
LIG_SH3_1 | 609 | 615 | PF00018 | 0.438 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.367 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.457 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.628 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.815 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.357 |
LIG_SH3_3 | 609 | 615 | PF00018 | 0.357 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.476 |
LIG_SUMO_SIM_anti_2 | 131 | 136 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 342 | 351 | PF11976 | 0.754 |
LIG_SUMO_SIM_par_1 | 356 | 363 | PF11976 | 0.756 |
LIG_SUMO_SIM_par_1 | 647 | 652 | PF11976 | 0.598 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.771 |
LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.493 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.783 |
LIG_TRAF2_1 | 481 | 484 | PF00917 | 0.454 |
LIG_TRAF2_1 | 509 | 512 | PF00917 | 0.422 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.402 |
LIG_UBA3_1 | 574 | 580 | PF00899 | 0.357 |
LIG_WRC_WIRS_1 | 225 | 230 | PF05994 | 0.381 |
LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.445 |
LIG_WW_3 | 266 | 270 | PF00397 | 0.736 |
MOD_CDK_SPxK_1 | 348 | 354 | PF00069 | 0.710 |
MOD_CDK_SPxK_1 | 35 | 41 | PF00069 | 0.543 |
MOD_CDK_SPxxK_3 | 452 | 459 | PF00069 | 0.357 |
MOD_CDK_SPxxK_3 | 498 | 505 | PF00069 | 0.438 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.443 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.520 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.768 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.732 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.438 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.700 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.542 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.431 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.407 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.791 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.786 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.766 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.690 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.454 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.238 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.367 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.391 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.430 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.480 |
MOD_Cter_Amidation | 262 | 265 | PF01082 | 0.715 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.661 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.818 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.749 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.508 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.436 |
MOD_GlcNHglycan | 625 | 629 | PF01048 | 0.465 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.618 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.516 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.752 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.647 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.750 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.785 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.340 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.339 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.430 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.499 |
MOD_N-GLC_1 | 452 | 457 | PF02516 | 0.332 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.580 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.514 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.422 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.357 |
MOD_NEK2_2 | 461 | 466 | PF00069 | 0.395 |
MOD_NEK2_2 | 684 | 689 | PF00069 | 0.390 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.476 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.797 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.441 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.753 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.714 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.585 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.467 |
MOD_Plk_2-3 | 512 | 518 | PF00069 | 0.492 |
MOD_Plk_2-3 | 79 | 85 | PF00069 | 0.456 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.567 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.586 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.357 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.422 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.357 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.767 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.749 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.543 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.357 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.412 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.162 |
MOD_SUMO_rev_2 | 15 | 20 | PF00179 | 0.765 |
MOD_SUMO_rev_2 | 182 | 189 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_1 | 185 | 190 | PF01217 | 0.413 |
TRG_DiLeu_LyEn_5 | 185 | 190 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 623 | 626 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 607 | 609 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 664 | 666 | PF00400 | 0.473 |
TRG_NLS_Bipartite_1 | 281 | 302 | PF00514 | 0.756 |
TRG_NLS_MonoCore_2 | 282 | 287 | PF00514 | 0.767 |
TRG_NLS_MonoExtC_3 | 49 | 54 | PF00514 | 0.569 |
TRG_NLS_MonoExtN_4 | 281 | 287 | PF00514 | 0.759 |
TRG_NLS_MonoExtN_4 | 297 | 302 | PF00514 | 0.716 |
TRG_NLS_MonoExtN_4 | 51 | 58 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 89 | 93 | PF00026 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I609 | Leptomonas seymouri | 68% | 100% |
A0A3Q8IKM7 | Leishmania donovani | 95% | 100% |
A0A422N797 | Trypanosoma rangeli | 42% | 100% |
A4H7D9 | Leishmania braziliensis | 81% | 92% |
A4I9K1 | Leishmania infantum | 95% | 100% |
D0A1W0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9B4J9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |