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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4QAD7
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 2 |
GO:0006020 | inositol metabolic process | 4 | 2 |
GO:0006066 | alcohol metabolic process | 3 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016310 | phosphorylation | 5 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0019751 | polyol metabolic process | 4 | 8 |
GO:0032957 | inositol trisphosphate metabolic process | 5 | 8 |
GO:0043647 | inositol phosphate metabolic process | 4 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 8 |
GO:0046835 | carbohydrate phosphorylation | 4 | 2 |
GO:0052746 | obsolete inositol phosphorylation | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0000287 | magnesium ion binding | 5 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016301 | kinase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0047325 | inositol tetrakisphosphate 1-kinase activity | 6 | 8 |
GO:0051765 | inositol tetrakisphosphate kinase activity | 5 | 8 |
GO:0051766 | inositol trisphosphate kinase activity | 5 | 8 |
GO:0052725 | inositol-1,3,4-trisphosphate 6-kinase activity | 6 | 8 |
GO:0052726 | inositol-1,3,4-trisphosphate 5-kinase activity | 6 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.777 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 700 | 702 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.763 |
CLV_PCSK_FUR_1 | 235 | 239 | PF00082 | 0.558 |
CLV_PCSK_FUR_1 | 94 | 98 | PF00082 | 0.819 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 699 | 701 | PF00082 | 0.796 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.760 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 699 | 701 | PF00082 | 0.796 |
CLV_PCSK_PC7_1 | 233 | 239 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 237 | 245 | PF00400 | 0.608 |
DEG_APCC_DBOX_1 | 255 | 263 | PF00400 | 0.317 |
DEG_APCC_DBOX_1 | 370 | 378 | PF00400 | 0.448 |
DEG_COP1_1 | 352 | 360 | PF00400 | 0.452 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.739 |
DEG_SCF_FBW7_1 | 516 | 522 | PF00400 | 0.500 |
DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.605 |
DOC_CKS1_1 | 213 | 218 | PF01111 | 0.585 |
DOC_CKS1_1 | 516 | 521 | PF01111 | 0.494 |
DOC_CYCLIN_RxL_1 | 128 | 138 | PF00134 | 0.500 |
DOC_MAPK_gen_1 | 141 | 148 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 235 | 244 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 141 | 148 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 235 | 244 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 398 | 405 | PF00069 | 0.499 |
DOC_MAPK_NFAT4_5 | 141 | 149 | PF00069 | 0.520 |
DOC_PP2B_PxIxI_1 | 239 | 245 | PF00149 | 0.480 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.530 |
DOC_PP4_FxxP_1 | 513 | 516 | PF00568 | 0.499 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 672 | 676 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.648 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 100 | 109 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 111 | 120 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 131 | 136 | PF00244 | 0.211 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 414 | 419 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 598 | 608 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 625 | 632 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 700 | 705 | PF00244 | 0.785 |
LIG_BIR_III_2 | 458 | 462 | PF00653 | 0.579 |
LIG_BRCT_BRCA1_1 | 620 | 624 | PF00533 | 0.628 |
LIG_BRCT_BRCA1_1 | 626 | 630 | PF00533 | 0.494 |
LIG_Clathr_ClatBox_1 | 241 | 245 | PF01394 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 508 | 513 | PF00928 | 0.480 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.826 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.509 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.494 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.444 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.444 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.669 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.525 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.598 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.566 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.788 |
LIG_FHA_2 | 691 | 697 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 212 | 216 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 279 | 285 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 34 | 41 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 508 | 516 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 518 | 528 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 34 | 38 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 508 | 513 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.597 |
LIG_NRBOX | 258 | 264 | PF00104 | 0.486 |
LIG_PTB_Apo_2 | 124 | 131 | PF02174 | 0.488 |
LIG_SH2_CRK | 380 | 384 | PF00017 | 0.528 |
LIG_SH2_CRK | 521 | 525 | PF00017 | 0.531 |
LIG_SH2_CRK | 657 | 661 | PF00017 | 0.557 |
LIG_SH2_GRB2like | 509 | 512 | PF00017 | 0.343 |
LIG_SH2_NCK_1 | 521 | 525 | PF00017 | 0.504 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.464 |
LIG_SH2_STAT3 | 137 | 140 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.459 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.510 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.479 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.715 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.509 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.455 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.695 |
LIG_SUMO_SIM_anti_2 | 201 | 207 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 402 | 407 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 47 | 53 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 545 | 550 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 239 | 245 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 643 | 650 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 669 | 675 | PF11976 | 0.490 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.595 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.707 |
LIG_TYR_ITIM | 573 | 578 | PF00017 | 0.600 |
LIG_UBA3_1 | 667 | 674 | PF00899 | 0.494 |
LIG_WRC_WIRS_1 | 210 | 215 | PF05994 | 0.504 |
LIG_WRC_WIRS_1 | 307 | 312 | PF05994 | 0.535 |
MOD_CAAXbox | 702 | 705 | PF01239 | 0.794 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.509 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.545 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.613 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.512 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.359 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.567 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.673 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.761 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.740 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.746 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.690 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.549 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.745 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.795 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.706 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.794 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.576 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.646 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.800 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.680 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.622 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.713 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.511 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.646 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.802 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.773 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.775 |
MOD_GlcNHglycan | 530 | 534 | PF01048 | 0.532 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.571 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.718 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.702 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.365 |
MOD_GlcNHglycan | 65 | 69 | PF01048 | 0.676 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.743 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.530 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.689 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.660 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.572 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.599 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.727 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.511 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.590 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.457 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.623 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.752 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.680 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.258 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.672 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.716 |
MOD_LATS_1 | 412 | 418 | PF00433 | 0.663 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.727 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.634 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.687 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.694 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.766 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.527 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.449 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.602 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.698 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.627 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.451 |
MOD_NEK2_2 | 601 | 606 | PF00069 | 0.753 |
MOD_NEK2_2 | 672 | 677 | PF00069 | 0.481 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.685 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.485 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.641 |
MOD_PIKK_1 | 618 | 624 | PF00454 | 0.483 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.630 |
MOD_PKA_1 | 96 | 102 | PF00069 | 0.758 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.608 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.630 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.706 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.596 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.551 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.762 |
MOD_PKB_1 | 111 | 119 | PF00069 | 0.473 |
MOD_PKB_1 | 94 | 102 | PF00069 | 0.817 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.599 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.587 |
MOD_Plk_1 | 493 | 499 | PF00069 | 0.594 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.495 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.639 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.471 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.569 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.725 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.511 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.553 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.713 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.686 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.493 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.753 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.705 |
MOD_SUMO_rev_2 | 149 | 155 | PF00179 | 0.635 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_1 | 47 | 52 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_2 | 367 | 373 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.552 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.770 |
TRG_NES_CRM1_1 | 669 | 680 | PF08389 | 0.604 |
TRG_NLS_MonoCore_2 | 697 | 702 | PF00514 | 0.712 |
TRG_NLS_MonoExtC_3 | 230 | 235 | PF00514 | 0.578 |
TRG_NLS_MonoExtN_4 | 698 | 703 | PF00514 | 0.781 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 371 | 375 | PF00026 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCV4 | Leptomonas seymouri | 48% | 100% |
A0A1X0NVY7 | Trypanosomatidae | 24% | 100% |
A0A3S5H7D6 | Leishmania donovani | 93% | 98% |
A4HDQ5 | Leishmania braziliensis | 69% | 100% |
A4I101 | Leishmania infantum | 93% | 99% |
E9AX39 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |