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. | yes | yes: 20 |
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. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IF24
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 12 |
GO:0009889 | regulation of biosynthetic process | 4 | 12 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0031323 | regulation of cellular metabolic process | 4 | 12 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 12 |
GO:0034248 | regulation of amide metabolic process | 5 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051246 | regulation of protein metabolic process | 5 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004519 | endonuclease activity | 5 | 1 |
GO:0004520 | DNA endonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016888 | endodeoxyribonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0017108 | 5'-flap endonuclease activity | 7 | 1 |
GO:0048256 | flap endonuclease activity | 6 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.711 |
CLV_C14_Caspase3-7 | 457 | 461 | PF00656 | 0.431 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.413 |
CLV_PCSK_FUR_1 | 331 | 335 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.635 |
CLV_PCSK_PC7_1 | 266 | 272 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.435 |
CLV_Separin_Metazoa | 540 | 544 | PF03568 | 0.435 |
CLV_Separin_Metazoa | 84 | 88 | PF03568 | 0.613 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.649 |
DOC_CYCLIN_yCln2_LP_2 | 359 | 365 | PF00134 | 0.584 |
DOC_MAPK_DCC_7 | 385 | 395 | PF00069 | 0.435 |
DOC_MAPK_DCC_7 | 435 | 444 | PF00069 | 0.411 |
DOC_MAPK_FxFP_2 | 640 | 643 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 435 | 444 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 724 | 731 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 494 | 501 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 311 | 314 | PF13499 | 0.637 |
DOC_PP2B_LxvP_1 | 359 | 362 | PF13499 | 0.574 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.599 |
DOC_PP4_FxxP_1 | 341 | 344 | PF00568 | 0.598 |
DOC_PP4_FxxP_1 | 526 | 529 | PF00568 | 0.435 |
DOC_PP4_FxxP_1 | 640 | 643 | PF00568 | 0.331 |
DOC_SPAK_OSR1_1 | 154 | 158 | PF12202 | 0.588 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.381 |
DOC_USP7_MATH_2 | 125 | 131 | PF00917 | 0.709 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.611 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 622 | 627 | PF00244 | 0.484 |
LIG_AP_GAE_1 | 249 | 255 | PF02883 | 0.668 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.655 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.660 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.610 |
LIG_BRCT_BRCA1_1 | 496 | 500 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 585 | 589 | PF00533 | 0.478 |
LIG_BRCT_BRCA1_1 | 599 | 603 | PF00533 | 0.420 |
LIG_BRCT_BRCA1_1 | 646 | 650 | PF00533 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 410 | 420 | PF00928 | 0.435 |
LIG_EH1_1 | 610 | 618 | PF00400 | 0.378 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.471 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.458 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.341 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.644 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.435 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.435 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.427 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.661 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.665 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.697 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.599 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.340 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.305 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.435 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.356 |
LIG_LIR_Apic_2 | 188 | 193 | PF02991 | 0.600 |
LIG_LIR_Apic_2 | 524 | 529 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 226 | 235 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 249 | 258 | PF02991 | 0.668 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 625 | 635 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 688 | 699 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 704 | 713 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 74 | 82 | PF02991 | 0.577 |
LIG_LIR_LC3C_4 | 549 | 554 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 272 | 277 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 443 | 449 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 497 | 503 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 532 | 537 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 625 | 631 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 682 | 687 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 688 | 694 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 704 | 708 | PF02991 | 0.331 |
LIG_MLH1_MIPbox_1 | 187 | 191 | PF16413 | 0.655 |
LIG_PCNA_yPIPBox_3 | 484 | 494 | PF02747 | 0.397 |
LIG_Pex14_1 | 413 | 417 | PF04695 | 0.331 |
LIG_Pex14_1 | 585 | 589 | PF04695 | 0.435 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.654 |
LIG_Pex14_2 | 151 | 155 | PF04695 | 0.690 |
LIG_Pex14_2 | 349 | 353 | PF04695 | 0.431 |
LIG_Pex14_2 | 500 | 504 | PF04695 | 0.435 |
LIG_Pex14_2 | 642 | 646 | PF04695 | 0.435 |
LIG_Pex14_2 | 687 | 691 | PF04695 | 0.435 |
LIG_Pex14_2 | 730 | 734 | PF04695 | 0.450 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.443 |
LIG_SH2_CRK | 534 | 538 | PF00017 | 0.356 |
LIG_SH2_CRK | 705 | 709 | PF00017 | 0.378 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.608 |
LIG_SH2_CRK | 793 | 797 | PF00017 | 0.579 |
LIG_SH2_NCK_1 | 705 | 709 | PF00017 | 0.378 |
LIG_SH2_NCK_1 | 76 | 80 | PF00017 | 0.608 |
LIG_SH2_SRC | 699 | 702 | PF00017 | 0.435 |
LIG_SH2_SRC | 793 | 796 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.691 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 654 | 657 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.670 |
LIG_SH3_2 | 281 | 286 | PF14604 | 0.719 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.720 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.711 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.450 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.378 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.438 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.680 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.346 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.338 |
LIG_SH3_3 | 749 | 755 | PF00018 | 0.575 |
LIG_SH3_3 | 756 | 762 | PF00018 | 0.656 |
LIG_SUMO_SIM_anti_2 | 204 | 209 | PF11976 | 0.663 |
LIG_SUMO_SIM_anti_2 | 549 | 556 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 535 | 540 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 61 | 68 | PF11976 | 0.640 |
LIG_SxIP_EBH_1 | 572 | 583 | PF03271 | 0.342 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.684 |
LIG_TRAF2_1 | 662 | 665 | PF00917 | 0.435 |
LIG_TRFH_1 | 399 | 403 | PF08558 | 0.431 |
LIG_TYR_ITIM | 481 | 486 | PF00017 | 0.497 |
LIG_TYR_ITIM | 703 | 708 | PF00017 | 0.431 |
LIG_UBA3_1 | 401 | 407 | PF00899 | 0.511 |
LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.524 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.495 |
LIG_WRC_WIRS_1 | 469 | 474 | PF05994 | 0.478 |
LIG_WW_3 | 794 | 798 | PF00397 | 0.712 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.531 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.540 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.524 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.646 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.402 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.580 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.546 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.366 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.511 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.454 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.590 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.425 |
MOD_GlcNHglycan | 249 | 255 | PF01048 | 0.569 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.428 |
MOD_GlcNHglycan | 379 | 383 | PF01048 | 0.511 |
MOD_GlcNHglycan | 512 | 516 | PF01048 | 0.462 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.412 |
MOD_GlcNHglycan | 645 | 649 | PF01048 | 0.428 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.569 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.501 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.526 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.583 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.531 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.297 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.636 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.453 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.380 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.495 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.462 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.393 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.511 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.585 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.538 |
MOD_N-GLC_2 | 107 | 109 | PF02516 | 0.556 |
MOD_N-GLC_2 | 580 | 582 | PF02516 | 0.431 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.468 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.528 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.520 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.428 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.676 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.372 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.436 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.471 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.511 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.553 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.532 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.490 |
MOD_NEK2_2 | 324 | 329 | PF00069 | 0.580 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.501 |
MOD_PIKK_1 | 364 | 370 | PF00454 | 0.460 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.627 |
MOD_PK_1 | 572 | 578 | PF00069 | 0.366 |
MOD_PKA_1 | 270 | 276 | PF00069 | 0.595 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.530 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.588 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.518 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.498 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.485 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.566 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.511 |
MOD_Plk_1 | 559 | 565 | PF00069 | 0.431 |
MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.568 |
MOD_Plk_2-3 | 527 | 533 | PF00069 | 0.511 |
MOD_Plk_2-3 | 701 | 707 | PF00069 | 0.511 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.508 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.609 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.533 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.629 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.496 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.372 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.534 |
MOD_Plk_4 | 650 | 656 | PF00069 | 0.476 |
MOD_Plk_4 | 679 | 685 | PF00069 | 0.398 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.477 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.666 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.431 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.419 |
MOD_SUMO_rev_2 | 15 | 22 | PF00179 | 0.494 |
MOD_SUMO_rev_2 | 297 | 303 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 97 | 103 | PF00179 | 0.573 |
TRG_DiLeu_BaEn_1 | 298 | 303 | PF01217 | 0.510 |
TRG_DiLeu_BaEn_1 | 533 | 538 | PF01217 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 354 | 359 | PF01217 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.293 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 705 | 708 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 239 | 242 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.511 |
TRG_NES_CRM1_1 | 679 | 692 | PF08389 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 608 | 612 | PF00026 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 715 | 720 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P424 | Leptomonas seymouri | 76% | 99% |
A0A0S4JHW4 | Bodo saltans | 30% | 100% |
A0A1X0P1K6 | Trypanosomatidae | 37% | 100% |
A0A3R7MIQ4 | Trypanosoma rangeli | 37% | 100% |
A4HIT1 | Leishmania braziliensis | 95% | 100% |
A4I633 | Leishmania infantum | 100% | 100% |
C9ZRF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B1B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
Q4Q6U6 | Leishmania major | 98% | 100% |
Q587E3 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 37% | 100% |
V5BX20 | Trypanosoma cruzi | 39% | 100% |