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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4H4B8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006396 | RNA processing | 6 | 8 |
GO:0006399 | tRNA metabolic process | 7 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008033 | tRNA processing | 8 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0034470 | ncRNA processing | 7 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0034660 | ncRNA metabolic process | 6 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0031590 | wybutosine metabolic process | 4 | 1 |
GO:0031591 | wybutosine biosynthetic process | 5 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1901657 | glycosyl compound metabolic process | 4 | 1 |
GO:1901659 | glycosyl compound biosynthetic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0010181 | FMN binding | 4 | 8 |
GO:0016829 | lyase activity | 2 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 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:0051536 | iron-sulfur cluster binding | 3 | 8 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 8 |
GO:0051540 | metal cluster binding | 2 | 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_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.717 |
CLV_C14_Caspase3-7 | 695 | 699 | PF00656 | 0.311 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 831 | 833 | PF00675 | 0.638 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.356 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 620 | 622 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 774 | 778 | PF00082 | 0.431 |
DEG_APCC_DBOX_1 | 48 | 56 | PF00400 | 0.593 |
DEG_MDM2_SWIB_1 | 627 | 635 | PF02201 | 0.517 |
DEG_MDM2_SWIB_1 | 777 | 785 | PF02201 | 0.469 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.605 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.470 |
DOC_MAPK_DCC_7 | 514 | 524 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 599 | 609 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 643 | 654 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 516 | 524 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 599 | 607 | PF00069 | 0.522 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.430 |
DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.475 |
DOC_PP2B_LxvP_1 | 611 | 614 | PF13499 | 0.426 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.477 |
DOC_SPAK_OSR1_1 | 221 | 225 | PF12202 | 0.421 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.481 |
DOC_USP7_UBL2_3 | 639 | 643 | PF12436 | 0.496 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 807 | 812 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 273 | 283 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 285 | 289 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 460 | 466 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 548 | 555 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 633 | 641 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 651 | 655 | PF00244 | 0.422 |
LIG_Actin_WH2_2 | 267 | 283 | PF00022 | 0.493 |
LIG_Actin_WH2_2 | 604 | 622 | PF00022 | 0.556 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.376 |
LIG_BRCT_BRCA1_1 | 509 | 513 | PF00533 | 0.556 |
LIG_Clathr_ClatBox_1 | 769 | 773 | PF01394 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 778 | 784 | PF00928 | 0.470 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.609 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.450 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.509 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.228 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.350 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.473 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.510 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.350 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.371 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.517 |
LIG_FHA_1 | 826 | 832 | PF00498 | 0.644 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.496 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.430 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.598 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.501 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.517 |
LIG_FHA_2 | 693 | 699 | PF00498 | 0.311 |
LIG_FHA_2 | 781 | 787 | PF00498 | 0.451 |
LIG_FHA_2 | 800 | 806 | PF00498 | 0.278 |
LIG_GBD_Chelix_1 | 18 | 26 | PF00786 | 0.557 |
LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 676 | 685 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 786 | 794 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 799 | 809 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 476 | 480 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 676 | 680 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 783 | 787 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 788 | 794 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 799 | 804 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 805 | 809 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 810 | 816 | PF02991 | 0.394 |
LIG_LYPXL_S_1 | 434 | 438 | PF13949 | 0.493 |
LIG_LYPXL_S_1 | 568 | 572 | PF13949 | 0.317 |
LIG_LYPXL_yS_3 | 435 | 438 | PF13949 | 0.502 |
LIG_LYPXL_yS_3 | 569 | 572 | PF13949 | 0.517 |
LIG_MAD2 | 829 | 837 | PF02301 | 0.660 |
LIG_NRBOX | 5 | 11 | PF00104 | 0.367 |
LIG_Pex14_2 | 627 | 631 | PF04695 | 0.517 |
LIG_Pex14_2 | 777 | 781 | PF04695 | 0.487 |
LIG_PTB_Apo_2 | 588 | 595 | PF02174 | 0.517 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.390 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.442 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.556 |
LIG_SH2_CRK | 724 | 728 | PF00017 | 0.584 |
LIG_SH2_CRK | 806 | 810 | PF00017 | 0.433 |
LIG_SH2_GRB2like | 187 | 190 | PF00017 | 0.249 |
LIG_SH2_NCK_1 | 806 | 810 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 177 | 181 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 666 | 670 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 787 | 791 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 97 | 100 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 685 | 688 | PF00017 | 0.376 |
LIG_SH3_2 | 72 | 77 | PF14604 | 0.567 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.377 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.501 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.479 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.549 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.516 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.545 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.793 |
LIG_SH3_4 | 602 | 609 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 740 | 748 | PF11976 | 0.632 |
LIG_SUMO_SIM_par_1 | 768 | 773 | PF11976 | 0.442 |
LIG_TRAF2_1 | 615 | 618 | PF00917 | 0.556 |
LIG_TRAF2_1 | 748 | 751 | PF00917 | 0.646 |
LIG_TRAF2_2 | 595 | 600 | PF00917 | 0.490 |
LIG_TYR_ITIM | 21 | 26 | PF00017 | 0.566 |
LIG_TYR_ITIM | 433 | 438 | PF00017 | 0.487 |
LIG_TYR_ITIM | 567 | 572 | PF00017 | 0.517 |
LIG_TYR_ITIM | 804 | 809 | PF00017 | 0.497 |
LIG_UBA3_1 | 769 | 774 | PF00899 | 0.451 |
LIG_WRC_WIRS_1 | 584 | 589 | PF05994 | 0.538 |
LIG_WRC_WIRS_1 | 706 | 711 | PF05994 | 0.249 |
LIG_WW_1 | 259 | 262 | PF00397 | 0.477 |
LIG_WW_3 | 192 | 196 | PF00397 | 0.430 |
MOD_CDK_SPxK_1 | 542 | 548 | PF00069 | 0.517 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.459 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.473 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.581 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.376 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.520 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.376 |
MOD_CK1_1 | 796 | 802 | PF00069 | 0.528 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.469 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.430 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.517 |
MOD_CMANNOS | 781 | 784 | PF00535 | 0.392 |
MOD_GlcNHglycan | 143 | 149 | PF01048 | 0.512 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.504 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.810 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.714 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.404 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.481 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.452 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.471 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.587 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.775 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.593 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.544 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.517 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.376 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.249 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.574 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.520 |
MOD_N-GLC_1 | 480 | 485 | PF02516 | 0.472 |
MOD_N-GLC_2 | 164 | 166 | PF02516 | 0.430 |
MOD_N-GLC_2 | 496 | 498 | PF02516 | 0.317 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.362 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.392 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.379 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.736 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.424 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.517 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.517 |
MOD_NEK2_1 | 793 | 798 | PF00069 | 0.465 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.628 |
MOD_NEK2_2 | 292 | 297 | PF00069 | 0.566 |
MOD_NEK2_2 | 473 | 478 | PF00069 | 0.411 |
MOD_OFUCOSY | 332 | 339 | PF10250 | 0.536 |
MOD_OFUCOSY | 354 | 359 | PF10250 | 0.557 |
MOD_OFUCOSY | 760 | 766 | PF10250 | 0.416 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.380 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.430 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.609 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.764 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.535 |
MOD_PIKK_1 | 480 | 486 | PF00454 | 0.432 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.463 |
MOD_PK_1 | 370 | 376 | PF00069 | 0.510 |
MOD_PKA_1 | 297 | 303 | PF00069 | 0.627 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.311 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.430 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.520 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.525 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.445 |
MOD_PKA_2 | 650 | 656 | PF00069 | 0.517 |
MOD_PKA_2 | 835 | 841 | PF00069 | 0.639 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.249 |
MOD_Plk_1 | 799 | 805 | PF00069 | 0.511 |
MOD_Plk_1 | 825 | 831 | PF00069 | 0.563 |
MOD_Plk_2-3 | 800 | 806 | PF00069 | 0.495 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.430 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.437 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.457 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.368 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.517 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.538 |
MOD_Plk_4 | 650 | 656 | PF00069 | 0.517 |
MOD_Plk_4 | 780 | 786 | PF00069 | 0.403 |
MOD_Plk_4 | 835 | 841 | PF00069 | 0.539 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.376 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.517 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.504 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.693 |
MOD_ProDKin_1 | 807 | 813 | PF00069 | 0.443 |
MOD_SUMO_rev_2 | 596 | 604 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 612 | 622 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 676 | 683 | PF00179 | 0.376 |
TRG_DiLeu_BaEn_1 | 429 | 434 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.635 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 724 | 727 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 787 | 790 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 791 | 794 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 806 | 809 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 466 | 469 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 752 | 755 | PF00400 | 0.592 |
TRG_NES_CRM1_1 | 600 | 612 | PF08389 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 624 | 628 | PF00026 | 0.317 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I710 | Leptomonas seymouri | 66% | 96% |
A0A3S5H5J8 | Leishmania donovani | 81% | 100% |
A4HSJ7 | Leishmania infantum | 81% | 100% |
C9ZU99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AKI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QJC7 | Leishmania major | 80% | 96% |