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:0005634 | nucleus | 5 | 2 |
GO:0005730 | nucleolus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QJG6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003724 | RNA helicase activity | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.465 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.727 |
CLV_PCSK_FUR_1 | 180 | 184 | PF00082 | 0.158 |
CLV_PCSK_FUR_1 | 521 | 525 | PF00082 | 0.593 |
CLV_PCSK_FUR_1 | 556 | 560 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 555 | 557 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 619 | 621 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.627 |
CLV_Separin_Metazoa | 349 | 353 | PF03568 | 0.417 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.481 |
DEG_SCF_FBW7_2 | 74 | 81 | PF00400 | 0.406 |
DOC_CDC14_PxL_1 | 319 | 327 | PF14671 | 0.386 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.473 |
DOC_CKS1_1 | 75 | 80 | PF01111 | 0.406 |
DOC_CYCLIN_RxL_1 | 129 | 136 | PF00134 | 0.483 |
DOC_CYCLIN_RxL_1 | 144 | 158 | PF00134 | 0.407 |
DOC_CYCLIN_RxL_1 | 180 | 190 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 175 | 178 | PF00134 | 0.473 |
DOC_MAPK_DCC_7 | 397 | 406 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 130 | 137 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 180 | 187 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 428 | 438 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 452 | 460 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 98 | 105 | PF00069 | 0.405 |
DOC_MAPK_HePTP_8 | 394 | 406 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 347 | 355 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 397 | 406 | PF00069 | 0.417 |
DOC_PP1_RVXF_1 | 181 | 188 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 175 | 178 | PF13499 | 0.451 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.541 |
DOC_PP2B_LxvP_1 | 314 | 317 | PF13499 | 0.316 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.406 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.539 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.406 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.473 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.480 |
DOC_USP7_UBL2_3 | 576 | 580 | PF12436 | 0.574 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.406 |
LIG_14-3-3_CanoR_1 | 11 | 20 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 159 | 166 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 194 | 199 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 217 | 223 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 595 | 603 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 98 | 103 | PF00244 | 0.405 |
LIG_APCC_ABBA_1 | 406 | 411 | PF00400 | 0.417 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.317 |
LIG_BIR_III_4 | 67 | 71 | PF00653 | 0.452 |
LIG_eIF4E_1 | 69 | 75 | PF01652 | 0.406 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.425 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.415 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.443 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.426 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.362 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.465 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.426 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.454 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.310 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.413 |
LIG_FHA_2 | 560 | 566 | PF00498 | 0.611 |
LIG_LIR_Apic_2 | 301 | 306 | PF02991 | 0.574 |
LIG_LIR_Apic_2 | 459 | 464 | PF02991 | 0.420 |
LIG_LIR_Apic_2 | 53 | 59 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 3 | 9 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 310 | 320 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 81 | 92 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.406 |
LIG_LYPXL_SIV_4 | 323 | 331 | PF13949 | 0.452 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.473 |
LIG_NRBOX | 364 | 370 | PF00104 | 0.510 |
LIG_PDZ_Class_3 | 620 | 625 | PF00595 | 0.540 |
LIG_RPA_C_Plants | 496 | 507 | PF08784 | 0.514 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.406 |
LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.510 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.510 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 442 | 446 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.421 |
LIG_SH3_2 | 294 | 299 | PF14604 | 0.573 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.457 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.581 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.448 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.435 |
LIG_SUMO_SIM_anti_2 | 260 | 265 | PF11976 | 0.493 |
LIG_SUMO_SIM_anti_2 | 434 | 441 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 443 | 448 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 468 | 477 | PF11976 | 0.475 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.476 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.477 |
LIG_TYR_ITIM | 149 | 154 | PF00017 | 0.510 |
LIG_TYR_ITIM | 82 | 87 | PF00017 | 0.406 |
LIG_WRC_WIRS_1 | 378 | 383 | PF05994 | 0.426 |
MOD_CDC14_SPxK_1 | 615 | 618 | PF00782 | 0.627 |
MOD_CDK_SPxK_1 | 124 | 130 | PF00069 | 0.406 |
MOD_CDK_SPxK_1 | 612 | 618 | PF00069 | 0.633 |
MOD_CDK_SPxK_1 | 74 | 80 | PF00069 | 0.406 |
MOD_CDK_SPxxK_3 | 460 | 467 | PF00069 | 0.495 |
MOD_CDK_SPxxK_3 | 612 | 619 | PF00069 | 0.611 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.542 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.678 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.741 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.406 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.420 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.605 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.646 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.593 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.723 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.548 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.507 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.416 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.711 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.589 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.678 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.755 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.424 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.354 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.212 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.754 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.683 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.681 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.688 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.776 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.491 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.539 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.499 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.718 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.506 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.539 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.638 |
MOD_LATS_1 | 192 | 198 | PF00433 | 0.620 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.630 |
MOD_N-GLC_2 | 343 | 345 | PF02516 | 0.206 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.438 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.481 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.648 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.781 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.461 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.357 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.417 |
MOD_PIKK_1 | 566 | 572 | PF00454 | 0.722 |
MOD_PIKK_1 | 596 | 602 | PF00454 | 0.616 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.406 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.548 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.599 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.417 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.611 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.638 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.685 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.422 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.421 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.400 |
MOD_Plk_2-3 | 158 | 164 | PF00069 | 0.456 |
MOD_Plk_2-3 | 255 | 261 | PF00069 | 0.479 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.399 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.467 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.406 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.406 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.452 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.430 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.384 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.299 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.344 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.406 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.355 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.607 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.492 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.736 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.643 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.406 |
MOD_SUMO_rev_2 | 445 | 454 | PF00179 | 0.366 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 171 | 176 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 556 | 559 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 97 | 100 | PF00400 | 0.405 |
TRG_NLS_Bipartite_1 | 558 | 580 | PF00514 | 0.684 |
TRG_NLS_Bipartite_1 | 605 | 622 | PF00514 | 0.617 |
TRG_NLS_MonoExtC_3 | 554 | 559 | PF00514 | 0.562 |
TRG_NLS_MonoExtC_3 | 575 | 580 | PF00514 | 0.615 |
TRG_NLS_MonoExtC_3 | 617 | 622 | PF00514 | 0.613 |
TRG_NLS_MonoExtN_4 | 616 | 622 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.206 |
TRG_Pf-PMV_PEXEL_1 | 585 | 590 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 80 | 85 | PF00026 | 0.206 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2T9 | Leptomonas seymouri | 72% | 100% |
A0A0S4J5D6 | Bodo saltans | 49% | 100% |
A0A0S4KKU4 | Bodo saltans | 30% | 90% |
A0A1X0NVK0 | Trypanosomatidae | 28% | 87% |
A0A1X0P0F9 | Trypanosomatidae | 56% | 100% |
A0A3R7KKL1 | Trypanosoma rangeli | 31% | 87% |
A0A3R7M1K3 | Trypanosoma rangeli | 29% | 87% |
A0A3S5H5H4 | Leishmania donovani | 95% | 100% |
A0A3S5H6T7 | Leishmania donovani | 29% | 100% |
A0A3S7X5R1 | Leishmania donovani | 28% | 81% |
A0A422NDK5 | Trypanosoma rangeli | 56% | 100% |
A2XVF7 | Oryza sativa subsp. indica | 30% | 75% |
A3AVH5 | Oryza sativa subsp. japonica | 30% | 75% |
A4H481 | Leishmania braziliensis | 79% | 99% |
A4HKL3 | Leishmania braziliensis | 27% | 81% |
A4HSF8 | Leishmania infantum | 95% | 100% |
A4HWB0 | Leishmania infantum | 29% | 100% |
A4I846 | Leishmania infantum | 28% | 81% |
A4R5B8 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 33% | 68% |
A4REU9 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 31% | 82% |
A7ESL7 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 33% | 68% |
A7TJ71 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 28% | 81% |
C9ZNU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 98% |
D0A4H6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
D0A6Z3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0AAB3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 86% |
E9AKE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AQ10 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 96% |
P26802 | Drosophila melanogaster | 29% | 91% |
Q0DLB9 | Oryza sativa subsp. japonica | 26% | 100% |
Q4HZ42 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 33% | 70% |
Q4IJH1 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 30% | 100% |
Q4Q552 | Leishmania major | 28% | 81% |
Q4QFH1 | Leishmania major | 32% | 100% |
Q6C835 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 78% |
Q6FU81 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 94% |
Q76PD3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q7FGZ2 | Arabidopsis thaliana | 29% | 100% |
Q7XJN0 | Arabidopsis thaliana | 28% | 100% |
Q8W4E1 | Arabidopsis thaliana | 27% | 100% |
Q93Y39 | Arabidopsis thaliana | 33% | 76% |
V5CZW7 | Trypanosoma cruzi | 58% | 100% |
V5DCA1 | Trypanosoma cruzi | 27% | 87% |