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 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QA62
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 3 |
GO:0006518 | peptide metabolic process | 4 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009058 | biosynthetic process | 2 | 3 |
GO:0009059 | macromolecule biosynthetic process | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 3 |
GO:0043043 | peptide biosynthetic process | 5 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043603 | amide metabolic process | 3 | 3 |
GO:0043604 | amide biosynthetic process | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044249 | cellular biosynthetic process | 3 | 3 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 3 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 3 |
GO:1901576 | organic substance biosynthetic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 3 |
GO:0005198 | structural molecule activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 502 | 506 | PF00656 | 0.494 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.472 |
CLV_PCSK_FUR_1 | 560 | 564 | PF00082 | 0.685 |
CLV_PCSK_FUR_1 | 571 | 575 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.803 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.803 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.677 |
CLV_PCSK_PC7_1 | 338 | 344 | PF00082 | 0.688 |
CLV_PCSK_PC7_1 | 419 | 425 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.482 |
DEG_COP1_1 | 78 | 86 | PF00400 | 0.537 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.656 |
DEG_SCF_FBW7_2 | 300 | 306 | PF00400 | 0.686 |
DEG_SPOP_SBC_1 | 152 | 156 | PF00917 | 0.614 |
DEG_SPOP_SBC_1 | 325 | 329 | PF00917 | 0.615 |
DEG_SPOP_SBC_1 | 609 | 613 | PF00917 | 0.598 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.658 |
DOC_CKS1_1 | 300 | 305 | PF01111 | 0.683 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.694 |
DOC_CKS1_1 | 434 | 439 | PF01111 | 0.618 |
DOC_CYCLIN_yCln2_LP_2 | 265 | 271 | PF00134 | 0.660 |
DOC_CYCLIN_yCln2_LP_2 | 525 | 531 | PF00134 | 0.472 |
DOC_MAPK_DCC_7 | 661 | 671 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 127 | 134 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 571 | 580 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 426 | 434 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 571 | 580 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 477 | 483 | PF00149 | 0.512 |
DOC_PP2B_LxvP_1 | 525 | 528 | PF13499 | 0.500 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.575 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 204 | 209 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 365 | 374 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 539 | 545 | PF00244 | 0.470 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.587 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.694 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.667 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.631 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.498 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.459 |
LIG_IBAR_NPY_1 | 90 | 92 | PF08397 | 0.681 |
LIG_KLC1_Yacidic_2 | 643 | 647 | PF13176 | 0.446 |
LIG_LIR_Apic_2 | 618 | 624 | PF02991 | 0.540 |
LIG_LIR_Apic_2 | 96 | 100 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 538 | 546 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 584 | 590 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.541 |
LIG_LYPXL_yS_3 | 63 | 66 | PF13949 | 0.509 |
LIG_PDZ_Class_2 | 680 | 685 | PF00595 | 0.455 |
LIG_Pex14_2 | 544 | 548 | PF04695 | 0.447 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.683 |
LIG_SH2_CRK | 621 | 625 | PF00017 | 0.507 |
LIG_SH2_SRC | 625 | 628 | PF00017 | 0.497 |
LIG_SH2_SRC | 645 | 648 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.492 |
LIG_SH3_1 | 342 | 348 | PF00018 | 0.719 |
LIG_SH3_1 | 361 | 367 | PF00018 | 0.541 |
LIG_SH3_1 | 621 | 627 | PF00018 | 0.505 |
LIG_SH3_2 | 100 | 105 | PF14604 | 0.605 |
LIG_SH3_2 | 300 | 305 | PF14604 | 0.683 |
LIG_SH3_2 | 468 | 473 | PF14604 | 0.527 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.635 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.695 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.674 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.630 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.670 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.719 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.541 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.668 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.605 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.523 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.488 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.621 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.563 |
LIG_SUMO_SIM_anti_2 | 504 | 511 | PF11976 | 0.626 |
LIG_SUMO_SIM_par_1 | 411 | 416 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 667 | 673 | PF11976 | 0.434 |
LIG_SxIP_EBH_1 | 19 | 33 | PF03271 | 0.704 |
LIG_WRC_WIRS_1 | 532 | 537 | PF05994 | 0.315 |
LIG_WRC_WIRS_1 | 541 | 546 | PF05994 | 0.303 |
LIG_WW_3 | 292 | 296 | PF00397 | 0.590 |
MOD_CDC14_SPxK_1 | 292 | 295 | PF00782 | 0.731 |
MOD_CDC14_SPxK_1 | 331 | 334 | PF00782 | 0.743 |
MOD_CDC14_SPxK_1 | 34 | 37 | PF00782 | 0.692 |
MOD_CDC14_SPxK_1 | 363 | 366 | PF00782 | 0.664 |
MOD_CDK_SPK_2 | 328 | 333 | PF00069 | 0.659 |
MOD_CDK_SPK_2 | 341 | 346 | PF00069 | 0.581 |
MOD_CDK_SPK_2 | 360 | 365 | PF00069 | 0.595 |
MOD_CDK_SPxK_1 | 289 | 295 | PF00069 | 0.734 |
MOD_CDK_SPxK_1 | 299 | 305 | PF00069 | 0.631 |
MOD_CDK_SPxK_1 | 31 | 37 | PF00069 | 0.693 |
MOD_CDK_SPxK_1 | 328 | 334 | PF00069 | 0.735 |
MOD_CDK_SPxK_1 | 341 | 347 | PF00069 | 0.604 |
MOD_CDK_SPxK_1 | 360 | 366 | PF00069 | 0.594 |
MOD_CDK_SPxxK_3 | 294 | 301 | PF00069 | 0.631 |
MOD_CDK_SPxxK_3 | 326 | 333 | PF00069 | 0.661 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.635 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.653 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.685 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.708 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.639 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.641 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.649 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.735 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.721 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.575 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.686 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.676 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.542 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.478 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.574 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.639 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.542 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.724 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.693 |
MOD_Cter_Amidation | 246 | 249 | PF01082 | 0.577 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.695 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.548 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.673 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.609 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.575 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.727 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.583 |
MOD_GlcNHglycan | 276 | 281 | PF01048 | 0.611 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.634 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.792 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.678 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.564 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.610 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.475 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.517 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.611 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.635 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.463 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.467 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.639 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.626 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.676 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.680 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.720 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.611 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.729 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.767 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.627 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.582 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.743 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.532 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.314 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.503 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.463 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.554 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.556 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.613 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.642 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.672 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.535 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.670 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.494 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.657 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.663 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.534 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.684 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.651 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.650 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.670 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.660 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.530 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.572 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.652 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.614 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.707 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.728 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.550 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.662 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.624 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.609 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.806 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.643 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.686 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.551 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.692 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.619 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.667 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.489 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.516 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.535 |
TRG_DiLeu_BaEn_2 | 592 | 598 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.684 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.561 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.502 |
TRG_NES_CRM1_1 | 197 | 209 | PF08389 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 136 | 140 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WYR3 | Leishmania donovani | 89% | 100% |
A4HDY0 | Leishmania braziliensis | 69% | 98% |
A4I176 | Leishmania infantum | 89% | 100% |
E9AXB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |