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:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AQG1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 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:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0003724 | RNA helicase activity | 3 | 2 |
GO:0003743 | translation initiation factor activity | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004386 | helicase activity | 2 | 6 |
GO:0008135 | translation factor activity, RNA binding | 3 | 2 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0045182 | translation regulator activity | 1 | 2 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 6 |
GO:0140657 | ATP-dependent activity | 1 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.466 |
CLV_PCSK_FUR_1 | 10 | 14 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 471 | 473 | PF00082 | 0.199 |
CLV_PCSK_PC1ET2_1 | 626 | 628 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.485 |
CLV_PCSK_PC7_1 | 218 | 224 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.331 |
DEG_APCC_DBOX_1 | 112 | 120 | PF00400 | 0.466 |
DEG_APCC_DBOX_1 | 583 | 591 | PF00400 | 0.287 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.457 |
DEG_SPOP_SBC_1 | 606 | 610 | PF00917 | 0.380 |
DOC_CKS1_1 | 176 | 181 | PF01111 | 0.391 |
DOC_CYCLIN_RxL_1 | 646 | 657 | PF00134 | 0.472 |
DOC_MAPK_DCC_7 | 412 | 422 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 166 | 176 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 296 | 302 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 385 | 391 | PF00069 | 0.258 |
DOC_MAPK_MEF2A_6 | 113 | 120 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 642 | 651 | PF00069 | 0.376 |
DOC_PP1_RVXF_1 | 393 | 400 | PF00149 | 0.283 |
DOC_PP1_RVXF_1 | 45 | 52 | PF00149 | 0.321 |
DOC_PP1_RVXF_1 | 81 | 88 | PF00149 | 0.465 |
DOC_PP2B_LxvP_1 | 27 | 30 | PF13499 | 0.404 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.415 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.289 |
DOC_PP2B_LxvP_1 | 569 | 572 | PF13499 | 0.474 |
DOC_PP4_FxxP_1 | 505 | 508 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.473 |
DOC_SPAK_OSR1_1 | 249 | 253 | PF12202 | 0.359 |
DOC_SPAK_OSR1_1 | 362 | 366 | PF12202 | 0.297 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.421 |
DOC_USP7_UBL2_3 | 292 | 296 | PF12436 | 0.724 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.402 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 267 | 271 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 289 | 299 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 402 | 407 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 555 | 560 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 612 | 622 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 627 | 633 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 64 | 69 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 94 | 103 | PF00244 | 0.568 |
LIG_Actin_WH2_2 | 608 | 625 | PF00022 | 0.387 |
LIG_APCC_ABBA_1 | 329 | 334 | PF00400 | 0.270 |
LIG_BRCT_BRCA1_1 | 238 | 242 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 552 | 556 | PF00533 | 0.550 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.406 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.413 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.417 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.359 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.474 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.445 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.481 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.353 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.504 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.399 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.403 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.725 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.326 |
LIG_LIR_Apic_2 | 258 | 264 | PF02991 | 0.341 |
LIG_LIR_Apic_2 | 597 | 602 | PF02991 | 0.451 |
LIG_LIR_Apic_2 | 641 | 647 | PF02991 | 0.419 |
LIG_LIR_Apic_2 | 84 | 90 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 181 | 189 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 247 | 257 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 28 | 38 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 315 | 324 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 434 | 443 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 315 | 319 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.523 |
LIG_MYND_3 | 186 | 190 | PF01753 | 0.417 |
LIG_Pex14_2 | 143 | 147 | PF04695 | 0.504 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.287 |
LIG_Pex14_2 | 390 | 394 | PF04695 | 0.425 |
LIG_Pex14_2 | 466 | 470 | PF04695 | 0.465 |
LIG_PTB_Apo_2 | 45 | 52 | PF02174 | 0.321 |
LIG_SH2_NCK_1 | 261 | 265 | PF00017 | 0.569 |
LIG_SH2_PTP2 | 599 | 602 | PF00017 | 0.266 |
LIG_SH2_SRC | 501 | 504 | PF00017 | 0.399 |
LIG_SH2_SRC | 599 | 602 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 332 | 336 | PF00017 | 0.293 |
LIG_SH2_STAT3 | 374 | 377 | PF00017 | 0.296 |
LIG_SH2_STAT3 | 614 | 617 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.540 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.504 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.411 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.511 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.392 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.401 |
LIG_SH3_4 | 564 | 571 | PF00018 | 0.469 |
LIG_SUMO_SIM_anti_2 | 529 | 535 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 250 | 256 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 345 | 351 | PF11976 | 0.485 |
LIG_TRAF2_1 | 595 | 598 | PF00917 | 0.473 |
LIG_UBA3_1 | 185 | 194 | PF00899 | 0.350 |
LIG_UBA3_1 | 2 | 9 | PF00899 | 0.359 |
LIG_UBA3_1 | 378 | 386 | PF00899 | 0.304 |
LIG_UBA3_1 | 414 | 419 | PF00899 | 0.369 |
LIG_UBA3_1 | 43 | 47 | PF00899 | 0.376 |
LIG_UBA3_1 | 621 | 626 | PF00899 | 0.302 |
MOD_CDC14_SPxK_1 | 121 | 124 | PF00782 | 0.262 |
MOD_CDC14_SPxK_1 | 287 | 290 | PF00782 | 0.544 |
MOD_CDK_SPK_2 | 175 | 180 | PF00069 | 0.322 |
MOD_CDK_SPK_2 | 284 | 289 | PF00069 | 0.534 |
MOD_CDK_SPxK_1 | 118 | 124 | PF00069 | 0.289 |
MOD_CDK_SPxK_1 | 284 | 290 | PF00069 | 0.536 |
MOD_CDK_SPxxK_3 | 260 | 267 | PF00069 | 0.350 |
MOD_CDK_SPxxK_3 | 282 | 289 | PF00069 | 0.522 |
MOD_CDK_SPxxK_3 | 323 | 330 | PF00069 | 0.435 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.515 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.494 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.412 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.256 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.592 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.327 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.376 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.718 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.418 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.262 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.500 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.556 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.352 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.391 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.681 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.287 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.257 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.492 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.543 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.600 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.404 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.279 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.316 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.331 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.262 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.374 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.461 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.327 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.199 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.540 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.552 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.548 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.462 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.300 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.376 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.330 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.318 |
MOD_NEK2_2 | 340 | 345 | PF00069 | 0.324 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.586 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.414 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.357 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.255 |
MOD_PK_1 | 402 | 408 | PF00069 | 0.361 |
MOD_PK_1 | 527 | 533 | PF00069 | 0.303 |
MOD_PKA_1 | 290 | 296 | PF00069 | 0.608 |
MOD_PKA_1 | 563 | 569 | PF00069 | 0.609 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.595 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.383 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.524 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.460 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.770 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.229 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.429 |
MOD_Plk_2-3 | 18 | 24 | PF00069 | 0.429 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.238 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.233 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.348 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.245 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.287 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.289 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.259 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.353 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.346 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.657 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.453 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.348 |
MOD_SUMO_rev_2 | 16 | 21 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 545 | 551 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 634 | 643 | PF00179 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 324 | 329 | PF01217 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 410 | 415 | PF01217 | 0.350 |
TRG_DiLeu_LyEn_5 | 184 | 189 | PF01217 | 0.206 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.271 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.772 |
TRG_NLS_MonoCore_2 | 449 | 454 | PF00514 | 0.255 |
TRG_NLS_MonoExtC_3 | 449 | 454 | PF00514 | 0.376 |
TRG_NLS_MonoExtC_3 | 8 | 13 | PF00514 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 124 | 128 | PF00026 | 0.259 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 652 | 657 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8C1 | Leptomonas seymouri | 73% | 98% |
A0A0S4JMG7 | Bodo saltans | 41% | 87% |
A0A1X0NZ55 | Trypanosomatidae | 55% | 100% |
A0A3R7LSE5 | Trypanosoma rangeli | 53% | 100% |
A0A3S7WTP8 | Leishmania donovani | 93% | 100% |
A4H8D2 | Leishmania braziliensis | 84% | 100% |
A4HWQ4 | Leishmania infantum | 93% | 100% |
A7F8V8 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 23% | 75% |
C9ZPS7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 98% |
E9AKE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q2NL08 | Bos taurus | 23% | 100% |
Q4QF15 | Leishmania major | 92% | 100% |
Q6ZPL9 | Mus musculus | 23% | 100% |
Q8NHQ9 | Homo sapiens | 23% | 100% |
V5BBA0 | Trypanosoma cruzi | 55% | 100% |
V5CZW7 | Trypanosoma cruzi | 25% | 100% |