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: 3 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AX39
Term | Name | Level | Count |
---|---|---|---|
GO:0006066 | alcohol metabolic process | 3 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0019751 | polyol metabolic process | 4 | 7 |
GO:0032957 | inositol trisphosphate metabolic process | 5 | 7 |
GO:0043647 | inositol phosphate metabolic process | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044281 | small molecule metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 7 |
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006020 | inositol metabolic process | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0046835 | carbohydrate phosphorylation | 4 | 1 |
GO:0052746 | obsolete inositol phosphorylation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0000287 | magnesium ion binding | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0047325 | inositol tetrakisphosphate 1-kinase activity | 6 | 7 |
GO:0051765 | inositol tetrakisphosphate kinase activity | 5 | 7 |
GO:0051766 | inositol trisphosphate kinase activity | 5 | 7 |
GO:0052725 | inositol-1,3,4-trisphosphate 6-kinase activity | 6 | 7 |
GO:0052726 | inositol-1,3,4-trisphosphate 5-kinase activity | 6 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.519 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 689 | 691 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.630 |
CLV_PCSK_FUR_1 | 224 | 228 | PF00082 | 0.433 |
CLV_PCSK_FUR_1 | 94 | 98 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 688 | 690 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 688 | 690 | PF00082 | 0.654 |
CLV_PCSK_PC7_1 | 222 | 228 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.454 |
CLV_Separin_Metazoa | 470 | 474 | PF03568 | 0.516 |
DEG_APCC_DBOX_1 | 226 | 234 | PF00400 | 0.577 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.270 |
DEG_APCC_DBOX_1 | 359 | 367 | PF00400 | 0.316 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.658 |
DEG_SCF_FBW7_1 | 505 | 511 | PF00400 | 0.373 |
DEG_SPOP_SBC_1 | 439 | 443 | PF00917 | 0.567 |
DOC_CKS1_1 | 202 | 207 | PF01111 | 0.448 |
DOC_CKS1_1 | 505 | 510 | PF01111 | 0.368 |
DOC_CKS1_1 | 605 | 610 | PF01111 | 0.441 |
DOC_MAPK_gen_1 | 141 | 148 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 224 | 233 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 141 | 148 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 387 | 394 | PF00069 | 0.370 |
DOC_MAPK_NFAT4_5 | 141 | 149 | PF00069 | 0.413 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.488 |
DOC_PP4_FxxP_1 | 202 | 205 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 502 | 505 | PF00568 | 0.389 |
DOC_PP4_MxPP_1 | 10 | 13 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.494 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.280 |
LIG_14-3-3_CanoR_1 | 100 | 109 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 111 | 121 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 403 | 408 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 473 | 482 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 577 | 584 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 614 | 621 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 689 | 694 | PF00244 | 0.621 |
LIG_BRCT_BRCA1_1 | 609 | 613 | PF00533 | 0.524 |
LIG_BRCT_BRCA1_1 | 615 | 619 | PF00533 | 0.427 |
LIG_Clathr_ClatBox_1 | 230 | 234 | PF01394 | 0.369 |
LIG_deltaCOP1_diTrp_1 | 497 | 502 | PF00928 | 0.395 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.658 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.396 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.495 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.369 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.534 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.395 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.601 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.403 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.469 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.670 |
LIG_LIR_Apic_2 | 201 | 205 | PF02991 | 0.394 |
LIG_LIR_Apic_2 | 268 | 274 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 298 | 307 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 34 | 41 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 497 | 505 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 507 | 517 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 34 | 38 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 497 | 502 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.529 |
LIG_NRBOX | 247 | 253 | PF00104 | 0.359 |
LIG_PTB_Apo_2 | 124 | 131 | PF02174 | 0.359 |
LIG_PTB_Phospho_1 | 131 | 137 | PF10480 | 0.279 |
LIG_SH2_CRK | 369 | 373 | PF00017 | 0.391 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.426 |
LIG_SH2_CRK | 646 | 650 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 510 | 514 | PF00017 | 0.411 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 137 | 140 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.385 |
LIG_SH3_2 | 468 | 473 | PF14604 | 0.513 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.384 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.427 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.413 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.711 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.650 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.536 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.389 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.325 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.674 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.564 |
LIG_SUMO_SIM_anti_2 | 190 | 196 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 391 | 396 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 534 | 539 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 228 | 234 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 409 | 416 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 627 | 633 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 634 | 639 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 658 | 664 | PF11976 | 0.373 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.505 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.627 |
LIG_TYR_ITIM | 562 | 567 | PF00017 | 0.524 |
LIG_UBA3_1 | 230 | 238 | PF00899 | 0.280 |
LIG_UBA3_1 | 656 | 663 | PF00899 | 0.431 |
LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.376 |
LIG_WRC_WIRS_1 | 296 | 301 | PF05994 | 0.450 |
LIG_WW_3 | 470 | 474 | PF00397 | 0.516 |
MOD_CAAXbox | 691 | 694 | PF01239 | 0.648 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.522 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.309 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.478 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.443 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.434 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.718 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.565 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.660 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.634 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.646 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.688 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.589 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.584 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.448 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.666 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.609 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.529 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.688 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.573 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.660 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.450 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.687 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.780 |
MOD_GlcNHglycan | 519 | 523 | PF01048 | 0.403 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.440 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.471 |
MOD_GlcNHglycan | 65 | 69 | PF01048 | 0.566 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.673 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.624 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.506 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.544 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.567 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.489 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.600 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.467 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.612 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.638 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.374 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.481 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.594 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.573 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.630 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.605 |
MOD_LATS_1 | 401 | 407 | PF00433 | 0.530 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.671 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.532 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.555 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.668 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.417 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.363 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.356 |
MOD_NEK2_2 | 661 | 666 | PF00069 | 0.396 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.558 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.410 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.581 |
MOD_PIKK_1 | 607 | 613 | PF00454 | 0.443 |
MOD_PKA_1 | 220 | 226 | PF00069 | 0.499 |
MOD_PKA_1 | 96 | 102 | PF00069 | 0.617 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.490 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.499 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.512 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.555 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.522 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.533 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.634 |
MOD_PKB_1 | 111 | 119 | PF00069 | 0.481 |
MOD_PKB_1 | 94 | 102 | PF00069 | 0.758 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.523 |
MOD_Plk_2-3 | 478 | 484 | PF00069 | 0.475 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.395 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.501 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.380 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.423 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.369 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.615 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.381 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.419 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.657 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.587 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.562 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.370 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.717 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.273 |
MOD_SUMO_rev_2 | 149 | 155 | PF00179 | 0.516 |
MOD_SUMO_rev_2 | 166 | 170 | PF00179 | 0.518 |
TRG_DiLeu_BaEn_1 | 237 | 242 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_2 | 356 | 362 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 482 | 487 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 625 | 630 | PF01217 | 0.279 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 646 | 649 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.628 |
TRG_NES_CRM1_1 | 658 | 669 | PF08389 | 0.466 |
TRG_NLS_MonoCore_2 | 218 | 223 | PF00514 | 0.311 |
TRG_NLS_MonoCore_2 | 686 | 691 | PF00514 | 0.606 |
TRG_NLS_MonoExtN_4 | 216 | 223 | PF00514 | 0.311 |
TRG_NLS_MonoExtN_4 | 687 | 692 | PF00514 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 209 | 213 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 48 | 53 | PF00026 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCV4 | Leptomonas seymouri | 49% | 100% |
A0A3S5H7D6 | Leishmania donovani | 87% | 97% |
A4HDQ5 | Leishmania braziliensis | 66% | 98% |
A4I101 | Leishmania infantum | 87% | 98% |
Q4QAD7 | Leishmania major | 86% | 100% |