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 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HIU4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0000245 | spliceosomal complex assembly | 7 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0050684 | regulation of mRNA processing | 7 | 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:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 4 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 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:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 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 | 114 | 118 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 581 | 585 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 587 | 591 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 683 | 687 | PF00656 | 0.675 |
CLV_C14_Caspase3-7 | 700 | 704 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.573 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 16 | 18 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.741 |
DEG_APCC_DBOX_1 | 267 | 275 | PF00400 | 0.279 |
DEG_SCF_FBW7_1 | 293 | 300 | PF00400 | 0.357 |
DOC_ANK_TNKS_1 | 105 | 112 | PF00023 | 0.672 |
DOC_CKS1_1 | 294 | 299 | PF01111 | 0.357 |
DOC_MAPK_gen_1 | 178 | 186 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 411 | 420 | PF00069 | 0.264 |
DOC_MAPK_HePTP_8 | 408 | 420 | PF00069 | 0.264 |
DOC_MAPK_MEF2A_6 | 411 | 420 | PF00069 | 0.264 |
DOC_PP1_RVXF_1 | 158 | 165 | PF00149 | 0.264 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.700 |
DOC_PP4_FxxP_1 | 308 | 311 | PF00568 | 0.490 |
DOC_PP4_FxxP_1 | 526 | 529 | PF00568 | 0.264 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.597 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.621 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.654 |
DOC_USP7_UBL2_3 | 325 | 329 | PF12436 | 0.491 |
DOC_USP7_UBL2_3 | 337 | 341 | PF12436 | 0.455 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.628 |
DOC_USP7_UBL2_3 | 514 | 518 | PF12436 | 0.277 |
DOC_USP7_UBL2_3 | 66 | 70 | PF12436 | 0.528 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 665 | 674 | PF00244 | 0.520 |
LIG_APCC_ABBA_1 | 239 | 244 | PF00400 | 0.279 |
LIG_BRCT_BRCA1_1 | 614 | 618 | PF00533 | 0.663 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.478 |
LIG_Clathr_ClatBox_1 | 271 | 275 | PF01394 | 0.279 |
LIG_CtBP_PxDLS_1 | 473 | 477 | PF00389 | 0.279 |
LIG_deltaCOP1_diTrp_1 | 378 | 386 | PF00928 | 0.584 |
LIG_deltaCOP1_diTrp_1 | 429 | 438 | PF00928 | 0.314 |
LIG_EH1_1 | 298 | 306 | PF00400 | 0.424 |
LIG_eIF4E_1 | 198 | 204 | PF01652 | 0.264 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.264 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.264 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.480 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.608 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.475 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.670 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.601 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.538 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.266 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.679 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.511 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.411 |
LIG_FHA_2 | 728 | 734 | PF00498 | 0.650 |
LIG_Integrin_RGD_1 | 358 | 360 | PF01839 | 0.659 |
LIG_LIR_Apic_2 | 410 | 416 | PF02991 | 0.264 |
LIG_LIR_Apic_2 | 525 | 529 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 179 | 186 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.235 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.357 |
LIG_LIR_LC3C_4 | 55 | 59 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.188 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.208 |
LIG_LIR_Nem_3 | 549 | 554 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 556 | 562 | PF02991 | 0.423 |
LIG_Pex14_2 | 167 | 171 | PF04695 | 0.264 |
LIG_PTB_Apo_2 | 150 | 157 | PF02174 | 0.420 |
LIG_PTB_Apo_2 | 625 | 632 | PF02174 | 0.542 |
LIG_PTB_Phospho_1 | 150 | 156 | PF10480 | 0.424 |
LIG_PTB_Phospho_1 | 625 | 631 | PF10480 | 0.547 |
LIG_Rb_pABgroove_1 | 233 | 241 | PF01858 | 0.326 |
LIG_RPA_C_Fungi | 150 | 162 | PF08784 | 0.190 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.330 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.264 |
LIG_SH2_CRK | 336 | 340 | PF00017 | 0.449 |
LIG_SH2_CRK | 559 | 563 | PF00017 | 0.534 |
LIG_SH2_GRB2like | 487 | 490 | PF00017 | 0.348 |
LIG_SH2_NCK_1 | 193 | 197 | PF00017 | 0.279 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.264 |
LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 592 | 596 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.523 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.536 |
LIG_SUMO_SIM_anti_2 | 279 | 286 | PF11976 | 0.279 |
LIG_SUMO_SIM_anti_2 | 300 | 306 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 458 | 467 | PF11976 | 0.264 |
LIG_SUMO_SIM_par_1 | 244 | 251 | PF11976 | 0.264 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.594 |
LIG_TYR_ITIM | 500 | 505 | PF00017 | 0.409 |
LIG_UBA3_1 | 301 | 306 | PF00899 | 0.395 |
LIG_UBA3_1 | 527 | 532 | PF00899 | 0.190 |
MOD_CDK_SPK_2 | 293 | 298 | PF00069 | 0.279 |
MOD_CDK_SPxxK_3 | 531 | 538 | PF00069 | 0.298 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.409 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.515 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.631 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.703 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.264 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.190 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.190 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.640 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.709 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.540 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.720 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.524 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.409 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.281 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.629 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.579 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.303 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.632 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.545 |
MOD_CK2_1 | 727 | 733 | PF00069 | 0.650 |
MOD_CMANNOS | 171 | 174 | PF00535 | 0.264 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.264 |
MOD_GlcNHglycan | 571 | 577 | PF01048 | 0.650 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.510 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.544 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.750 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.393 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.538 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.253 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.649 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.663 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.609 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.696 |
MOD_GSK3_1 | 734 | 741 | PF00069 | 0.636 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.327 |
MOD_N-GLC_1 | 602 | 607 | PF02516 | 0.712 |
MOD_N-GLC_1 | 627 | 632 | PF02516 | 0.540 |
MOD_N-GLC_2 | 396 | 398 | PF02516 | 0.264 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.733 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.302 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.469 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.264 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.190 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.540 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.665 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.484 |
MOD_PIKK_1 | 698 | 704 | PF00454 | 0.743 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.694 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.791 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.640 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.663 |
MOD_Plk_1 | 585 | 591 | PF00069 | 0.522 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.495 |
MOD_Plk_2-3 | 580 | 586 | PF00069 | 0.810 |
MOD_Plk_2-3 | 691 | 697 | PF00069 | 0.809 |
MOD_Plk_2-3 | 734 | 740 | PF00069 | 0.718 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.264 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.280 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.448 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.531 |
MOD_Plk_4 | 641 | 647 | PF00069 | 0.583 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.475 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.324 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.392 |
MOD_SUMO_for_1 | 287 | 290 | PF00179 | 0.264 |
MOD_SUMO_for_1 | 340 | 343 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 194 | 204 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 281 | 289 | PF00179 | 0.279 |
MOD_SUMO_rev_2 | 321 | 327 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 342 | 347 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 593 | 602 | PF00179 | 0.635 |
MOD_SUMO_rev_2 | 690 | 700 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 718 | 727 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_1 | 343 | 348 | PF01217 | 0.586 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_1 | 662 | 667 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_2 | 521 | 527 | PF01217 | 0.279 |
TRG_DiLeu_BaEn_4 | 622 | 628 | PF01217 | 0.552 |
TRG_DiLeu_BaEn_4 | 669 | 675 | PF01217 | 0.628 |
TRG_DiLeu_LyEn_5 | 60 | 65 | PF01217 | 0.483 |
TRG_DiLeu_LyEn_5 | 662 | 667 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.198 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 559 | 562 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.519 |
TRG_NLS_Bipartite_1 | 16 | 30 | PF00514 | 0.672 |
TRG_NLS_MonoCore_2 | 67 | 72 | PF00514 | 0.468 |
TRG_NLS_MonoExtC_3 | 24 | 29 | PF00514 | 0.662 |
TRG_NLS_MonoExtC_3 | 516 | 521 | PF00514 | 0.322 |
TRG_NLS_MonoExtC_3 | 67 | 73 | PF00514 | 0.648 |
TRG_NLS_MonoExtN_4 | 23 | 30 | PF00514 | 0.664 |
TRG_NLS_MonoExtN_4 | 514 | 521 | PF00514 | 0.322 |
TRG_NLS_MonoExtN_4 | 66 | 72 | PF00514 | 0.721 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 495 | 499 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 665 | 669 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1H8 | Leptomonas seymouri | 80% | 100% |
A0A0S4JMD1 | Bodo saltans | 55% | 96% |
A0A1X0P1B0 | Trypanosomatidae | 60% | 100% |
A0A3R7KF70 | Trypanosoma rangeli | 58% | 100% |
A0A3S7X404 | Leishmania donovani | 84% | 99% |
A4I649 | Leishmania infantum | 83% | 99% |
C9ZRG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9B1D2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4Q6T0 | Leishmania major | 84% | 100% |
V5B752 | Trypanosoma cruzi | 64% | 100% |