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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HDY0
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 2 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043043 | peptide biosynthetic process | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0043604 | amide biosynthetic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 2 |
GO:0005198 | structural molecule activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 481 | 485 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.626 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.795 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.813 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.707 |
CLV_PCSK_FUR_1 | 577 | 581 | PF00082 | 0.812 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.862 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.813 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.779 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.795 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.813 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.862 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.749 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.668 |
CLV_PCSK_PC7_1 | 419 | 425 | PF00082 | 0.786 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.611 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.494 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.732 |
DEG_SCF_FBW7_1 | 453 | 460 | PF00400 | 0.545 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 626 | 630 | PF00917 | 0.491 |
DOC_CKS1_1 | 209 | 214 | PF01111 | 0.604 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.833 |
DOC_CYCLIN_yCln2_LP_2 | 459 | 465 | PF00134 | 0.541 |
DOC_CYCLIN_yCln2_LP_2 | 542 | 548 | PF00134 | 0.602 |
DOC_MAPK_DCC_7 | 678 | 688 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 127 | 134 | PF00069 | 0.699 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.474 |
DOC_MAPK_RevD_3 | 282 | 296 | PF00069 | 0.602 |
DOC_PP1_RVXF_1 | 493 | 500 | PF00149 | 0.664 |
DOC_PP2B_LxvP_1 | 542 | 545 | PF13499 | 0.628 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.789 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.840 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 149 | 153 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.815 |
LIG_14-3-3_CanoR_1 | 182 | 191 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 205 | 210 | PF00244 | 0.854 |
LIG_14-3-3_CanoR_1 | 325 | 331 | PF00244 | 0.825 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 401 | 409 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 411 | 416 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.562 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.595 |
LIG_BRCT_BRCA1_1 | 445 | 449 | PF00533 | 0.582 |
LIG_CtBP_PxDLS_1 | 645 | 651 | PF00389 | 0.277 |
LIG_CtBP_PxDLS_1 | 84 | 88 | PF00389 | 0.545 |
LIG_EVH1_2 | 457 | 461 | PF00568 | 0.545 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.732 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.755 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.625 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.658 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.760 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.578 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.414 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.544 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.552 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.584 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.525 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.600 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.576 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.436 |
LIG_HCF-1_HBM_1 | 383 | 386 | PF13415 | 0.479 |
LIG_IBAR_NPY_1 | 90 | 92 | PF08397 | 0.806 |
LIG_KLC1_Yacidic_2 | 660 | 664 | PF13176 | 0.530 |
LIG_LIR_Apic_2 | 635 | 641 | PF02991 | 0.530 |
LIG_LIR_Apic_2 | 96 | 100 | PF02991 | 0.812 |
LIG_LIR_Gen_1 | 194 | 204 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 52 | 62 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.657 |
LIG_MYND_1 | 430 | 434 | PF01753 | 0.628 |
LIG_PDZ_Class_2 | 697 | 702 | PF00595 | 0.576 |
LIG_Pex14_2 | 561 | 565 | PF04695 | 0.571 |
LIG_PTAP_UEV_1 | 433 | 438 | PF05743 | 0.586 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.797 |
LIG_SH2_CRK | 638 | 642 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 197 | 201 | PF00017 | 0.614 |
LIG_SH2_NCK_1 | 45 | 49 | PF00017 | 0.534 |
LIG_SH2_SRC | 197 | 200 | PF00017 | 0.614 |
LIG_SH2_SRC | 482 | 485 | PF00017 | 0.735 |
LIG_SH2_SRC | 642 | 645 | PF00017 | 0.530 |
LIG_SH2_SRC | 662 | 665 | PF00017 | 0.199 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.748 |
LIG_SH2_STAP1 | 482 | 486 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 514 | 518 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.751 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.748 |
LIG_SH3_1 | 343 | 349 | PF00018 | 0.833 |
LIG_SH3_1 | 638 | 644 | PF00018 | 0.530 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.656 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.721 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.710 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.833 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.748 |
LIG_SH3_3 | 638 | 644 | PF00018 | 0.389 |
LIG_SH3_3 | 679 | 685 | PF00018 | 0.530 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.814 |
LIG_SUMO_SIM_anti_2 | 521 | 528 | PF11976 | 0.647 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.569 |
LIG_SUMO_SIM_par_1 | 65 | 75 | PF11976 | 0.540 |
LIG_SUMO_SIM_par_1 | 684 | 690 | PF11976 | 0.530 |
LIG_SxIP_EBH_1 | 19 | 33 | PF03271 | 0.823 |
LIG_TYR_ITIM | 195 | 200 | PF00017 | 0.573 |
LIG_WW_3 | 438 | 442 | PF00397 | 0.564 |
MOD_CDC14_SPxK_1 | 293 | 296 | PF00782 | 0.860 |
MOD_CDC14_SPxK_1 | 298 | 301 | PF00782 | 0.765 |
MOD_CDC14_SPxK_1 | 332 | 335 | PF00782 | 0.858 |
MOD_CDC14_SPxK_1 | 34 | 37 | PF00782 | 0.794 |
MOD_CDK_SPK_2 | 290 | 295 | PF00069 | 0.676 |
MOD_CDK_SPK_2 | 329 | 334 | PF00069 | 0.739 |
MOD_CDK_SPxK_1 | 290 | 296 | PF00069 | 0.859 |
MOD_CDK_SPxK_1 | 31 | 37 | PF00069 | 0.799 |
MOD_CDK_SPxK_1 | 329 | 335 | PF00069 | 0.859 |
MOD_CDK_SPxK_1 | 342 | 348 | PF00069 | 0.650 |
MOD_CDK_SPxxK_3 | 300 | 307 | PF00069 | 0.652 |
MOD_CDK_SPxxK_3 | 327 | 334 | PF00069 | 0.743 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.491 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.629 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.616 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.763 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.716 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.661 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.705 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.666 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.737 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.689 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.628 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.823 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.791 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.433 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.477 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.553 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.570 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.555 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.528 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.696 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.797 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.433 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.834 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.698 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.777 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.489 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.737 |
MOD_GlcNHglycan | 239 | 243 | PF01048 | 0.550 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.596 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.786 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.656 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.641 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.751 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.584 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.540 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.573 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.614 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.741 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.379 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.530 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.472 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.625 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.597 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.705 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.674 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.746 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.599 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.744 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.810 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.559 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.666 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.588 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.495 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.424 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.591 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.623 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.657 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.549 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.645 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.649 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.380 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.456 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.747 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.578 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.551 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.569 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.731 |
MOD_PK_1 | 169 | 175 | PF00069 | 0.580 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.493 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.813 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.569 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.643 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.823 |
MOD_PKB_1 | 580 | 588 | PF00069 | 0.554 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.688 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.752 |
MOD_Plk_2-3 | 522 | 528 | PF00069 | 0.433 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.588 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.649 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.433 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.671 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.780 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.813 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.673 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.777 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.759 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.625 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.764 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.617 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.772 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.831 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.542 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.483 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.643 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.443 |
TRG_DiLeu_BaEn_2 | 609 | 615 | PF01217 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 459 | 464 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.796 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.801 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.807 |
TRG_ER_diArg_1 | 490 | 493 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.691 |
TRG_NES_CRM1_1 | 198 | 210 | PF08389 | 0.685 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 136 | 140 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 495 | 500 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WYR3 | Leishmania donovani | 71% | 100% |
A4I176 | Leishmania infantum | 71% | 100% |
E9AXB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4QA62 | Leishmania major | 69% | 97% |