| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H724
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006355 | regulation of DNA-templated transcription | 6 | 11 |
| GO:0009889 | regulation of biosynthetic process | 4 | 11 |
| GO:0010468 | regulation of gene expression | 5 | 11 |
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 11 |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 11 |
| GO:0019222 | regulation of metabolic process | 3 | 11 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 11 |
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 11 |
| GO:0050789 | regulation of biological process | 2 | 11 |
| GO:0050794 | regulation of cellular process | 3 | 11 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 11 |
| GO:0051252 | regulation of RNA metabolic process | 5 | 11 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 |
| GO:0065007 | biological regulation | 1 | 11 |
| GO:0080090 | regulation of primary metabolic process | 4 | 11 |
| GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 11 |
| GO:2001141 | regulation of RNA biosynthetic process | 6 | 11 |
| GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
| GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
| GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
| GO:0009892 | negative regulation of metabolic process | 4 | 1 |
| GO:0009893 | positive regulation of metabolic process | 4 | 1 |
| GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
| GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
| GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
| GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
| GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
| GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
| GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
| GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
| GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 |
| GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
| GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
| GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
| GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 |
| GO:0048518 | positive regulation of biological process | 3 | 1 |
| GO:0048519 | negative regulation of biological process | 3 | 1 |
| GO:0048522 | positive regulation of cellular process | 4 | 1 |
| GO:0048523 | negative regulation of cellular process | 4 | 1 |
| GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
| GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
| GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
| GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
| GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 |
| GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
| GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 |
| GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 |
| GO:0004402 | histone acetyltransferase activity | 4 | 11 |
| GO:0008080 | N-acetyltransferase activity | 6 | 11 |
| GO:0016407 | acetyltransferase activity | 5 | 11 |
| GO:0016410 | N-acyltransferase activity | 5 | 11 |
| GO:0016740 | transferase activity | 2 | 11 |
| GO:0016746 | acyltransferase activity | 3 | 11 |
| GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 11 |
| GO:0034212 | peptide N-acetyltransferase activity | 7 | 11 |
| GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 11 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
| GO:0003712 | transcription coregulator activity | 2 | 1 |
| GO:0005488 | binding | 1 | 1 |
| GO:0005515 | protein binding | 2 | 1 |
| GO:0042393 | histone binding | 3 | 1 |
| GO:0140110 | transcription regulator activity | 1 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 539 | 543 | PF00656 | 0.801 |
| CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.442 |
| CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.325 |
| CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.554 |
| CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.796 |
| CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.782 |
| CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.654 |
| CLV_PCSK_FUR_1 | 528 | 532 | PF00082 | 0.596 |
| CLV_PCSK_FUR_1 | 67 | 71 | PF00082 | 0.649 |
| CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.442 |
| CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.325 |
| CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.633 |
| CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.797 |
| CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.760 |
| CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.693 |
| CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.654 |
| CLV_PCSK_PC1ET2_1 | 602 | 604 | PF00082 | 0.737 |
| CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.360 |
| CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.313 |
| CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.358 |
| CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.335 |
| CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.543 |
| DEG_APCC_DBOX_1 | 313 | 321 | PF00400 | 0.454 |
| DEG_APCC_DBOX_1 | 440 | 448 | PF00400 | 0.564 |
| DEG_APCC_DBOX_1 | 465 | 473 | PF00400 | 0.592 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.591 |
| DEG_SPOP_SBC_1 | 522 | 526 | PF00917 | 0.674 |
| DOC_CKS1_1 | 252 | 257 | PF01111 | 0.552 |
| DOC_MAPK_MEF2A_6 | 459 | 467 | PF00069 | 0.673 |
| DOC_MAPK_MEF2A_6 | 473 | 480 | PF00069 | 0.428 |
| DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.552 |
| DOC_PP4_FxxP_1 | 204 | 207 | PF00568 | 0.415 |
| DOC_PP4_FxxP_1 | 496 | 499 | PF00568 | 0.684 |
| DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.722 |
| DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.671 |
| DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.673 |
| DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.415 |
| DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.522 |
| DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.393 |
| DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.650 |
| DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.768 |
| DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.763 |
| DOC_USP7_UBL2_3 | 588 | 592 | PF12436 | 0.519 |
| DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.376 |
| DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.525 |
| DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.496 |
| DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.768 |
| DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.499 |
| LIG_14-3-3_CanoR_1 | 283 | 288 | PF00244 | 0.496 |
| LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.443 |
| LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.371 |
| LIG_14-3-3_CanoR_1 | 391 | 396 | PF00244 | 0.561 |
| LIG_14-3-3_CanoR_1 | 456 | 465 | PF00244 | 0.658 |
| LIG_14-3-3_CanoR_1 | 466 | 470 | PF00244 | 0.605 |
| LIG_14-3-3_CanoR_1 | 535 | 541 | PF00244 | 0.770 |
| LIG_14-3-3_CanoR_1 | 571 | 577 | PF00244 | 0.624 |
| LIG_APCC_ABBA_1 | 40 | 45 | PF00400 | 0.553 |
| LIG_APCC_ABBA_1 | 427 | 432 | PF00400 | 0.405 |
| LIG_APCC_ABBA_1 | 478 | 483 | PF00400 | 0.438 |
| LIG_BIR_III_4 | 354 | 358 | PF00653 | 0.374 |
| LIG_BRCT_BRCA1_1 | 232 | 236 | PF00533 | 0.472 |
| LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.380 |
| LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.496 |
| LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.375 |
| LIG_CSL_BTD_1 | 202 | 205 | PF09270 | 0.506 |
| LIG_deltaCOP1_diTrp_1 | 114 | 120 | PF00928 | 0.440 |
| LIG_EH1_1 | 30 | 38 | PF00400 | 0.442 |
| LIG_eIF4E_1 | 438 | 444 | PF01652 | 0.562 |
| LIG_FHA_1 | 164 | 170 | PF00498 | 0.474 |
| LIG_FHA_1 | 32 | 38 | PF00498 | 0.553 |
| LIG_FHA_1 | 392 | 398 | PF00498 | 0.539 |
| LIG_FHA_1 | 480 | 486 | PF00498 | 0.547 |
| LIG_FHA_1 | 571 | 577 | PF00498 | 0.650 |
| LIG_FHA_1 | 578 | 584 | PF00498 | 0.587 |
| LIG_FHA_2 | 149 | 155 | PF00498 | 0.763 |
| LIG_FHA_2 | 326 | 332 | PF00498 | 0.684 |
| LIG_FHA_2 | 347 | 353 | PF00498 | 0.371 |
| LIG_FHA_2 | 466 | 472 | PF00498 | 0.563 |
| LIG_FHA_2 | 55 | 61 | PF00498 | 0.517 |
| LIG_FHA_2 | 579 | 585 | PF00498 | 0.635 |
| LIG_LIR_Apic_2 | 493 | 499 | PF02991 | 0.667 |
| LIG_LIR_Gen_1 | 114 | 125 | PF02991 | 0.444 |
| LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.458 |
| LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.526 |
| LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.471 |
| LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.440 |
| LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.370 |
| LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.462 |
| LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.480 |
| LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.506 |
| LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.562 |
| LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.471 |
| LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.559 |
| LIG_LIR_Nem_3 | 453 | 457 | PF02991 | 0.664 |
| LIG_LIR_Nem_3 | 492 | 497 | PF02991 | 0.574 |
| LIG_MLH1_MIPbox_1 | 232 | 236 | PF16413 | 0.505 |
| LIG_NRBOX | 484 | 490 | PF00104 | 0.424 |
| LIG_Pex14_1 | 116 | 120 | PF04695 | 0.546 |
| LIG_Pex14_1 | 48 | 52 | PF04695 | 0.550 |
| LIG_Pex14_2 | 200 | 204 | PF04695 | 0.447 |
| LIG_Pex14_2 | 600 | 604 | PF04695 | 0.602 |
| LIG_PTB_Apo_2 | 25 | 32 | PF02174 | 0.446 |
| LIG_REV1ctd_RIR_1 | 233 | 242 | PF16727 | 0.538 |
| LIG_SH2_CRK | 249 | 253 | PF00017 | 0.542 |
| LIG_SH2_CRK | 454 | 458 | PF00017 | 0.439 |
| LIG_SH2_CRK | 497 | 501 | PF00017 | 0.593 |
| LIG_SH2_CRK | 615 | 619 | PF00017 | 0.741 |
| LIG_SH2_PTP2 | 242 | 245 | PF00017 | 0.547 |
| LIG_SH2_PTP2 | 307 | 310 | PF00017 | 0.562 |
| LIG_SH2_SRC | 305 | 308 | PF00017 | 0.562 |
| LIG_SH2_SRC | 319 | 322 | PF00017 | 0.587 |
| LIG_SH2_SRC | 497 | 500 | PF00017 | 0.689 |
| LIG_SH2_STAP1 | 117 | 121 | PF00017 | 0.426 |
| LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.482 |
| LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.625 |
| LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.516 |
| LIG_SH2_STAT3 | 198 | 201 | PF00017 | 0.473 |
| LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.356 |
| LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.463 |
| LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.377 |
| LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.324 |
| LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.406 |
| LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.526 |
| LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.413 |
| LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.483 |
| LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.392 |
| LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.686 |
| LIG_SH2_STAT6 | 267 | 271 | PF00017 | 0.562 |
| LIG_SH3_3 | 149 | 155 | PF00018 | 0.675 |
| LIG_SH3_3 | 199 | 205 | PF00018 | 0.502 |
| LIG_SH3_3 | 307 | 313 | PF00018 | 0.496 |
| LIG_SH3_3 | 315 | 321 | PF00018 | 0.467 |
| LIG_SH3_3 | 379 | 385 | PF00018 | 0.534 |
| LIG_SH3_3 | 423 | 429 | PF00018 | 0.496 |
| LIG_SUMO_SIM_anti_2 | 165 | 171 | PF11976 | 0.470 |
| LIG_SUMO_SIM_par_1 | 486 | 493 | PF11976 | 0.558 |
| LIG_SUMO_SIM_par_1 | 573 | 581 | PF11976 | 0.661 |
| LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.443 |
| LIG_TRAF2_1 | 468 | 471 | PF00917 | 0.347 |
| LIG_TRFH_1 | 120 | 124 | PF08558 | 0.553 |
| LIG_TYR_ITIM | 211 | 216 | PF00017 | 0.519 |
| LIG_WRC_WIRS_1 | 392 | 397 | PF05994 | 0.562 |
| MOD_CDK_SPxxK_3 | 251 | 258 | PF00069 | 0.529 |
| MOD_CK1_1 | 102 | 108 | PF00069 | 0.541 |
| MOD_CK1_1 | 140 | 146 | PF00069 | 0.755 |
| MOD_CK1_1 | 165 | 171 | PF00069 | 0.690 |
| MOD_CK1_1 | 326 | 332 | PF00069 | 0.684 |
| MOD_CK1_1 | 503 | 509 | PF00069 | 0.716 |
| MOD_CK1_1 | 517 | 523 | PF00069 | 0.760 |
| MOD_CK1_1 | 543 | 549 | PF00069 | 0.663 |
| MOD_CK1_1 | 596 | 602 | PF00069 | 0.476 |
| MOD_CK2_1 | 148 | 154 | PF00069 | 0.743 |
| MOD_CK2_1 | 325 | 331 | PF00069 | 0.666 |
| MOD_CK2_1 | 465 | 471 | PF00069 | 0.560 |
| MOD_CK2_1 | 54 | 60 | PF00069 | 0.557 |
| MOD_CK2_1 | 578 | 584 | PF00069 | 0.581 |
| MOD_CK2_1 | 89 | 95 | PF00069 | 0.658 |
| MOD_DYRK1A_RPxSP_1 | 425 | 429 | PF00069 | 0.496 |
| MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.640 |
| MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.726 |
| MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.716 |
| MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.685 |
| MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.381 |
| MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.668 |
| MOD_GlcNHglycan | 512 | 517 | PF01048 | 0.714 |
| MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.719 |
| MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.649 |
| MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.480 |
| MOD_GlcNHglycan | 608 | 613 | PF01048 | 0.560 |
| MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.695 |
| MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.684 |
| MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.455 |
| MOD_GSK3_1 | 13 | 20 | PF00069 | 0.598 |
| MOD_GSK3_1 | 132 | 139 | PF00069 | 0.693 |
| MOD_GSK3_1 | 230 | 237 | PF00069 | 0.386 |
| MOD_GSK3_1 | 335 | 342 | PF00069 | 0.429 |
| MOD_GSK3_1 | 376 | 383 | PF00069 | 0.477 |
| MOD_GSK3_1 | 421 | 428 | PF00069 | 0.489 |
| MOD_GSK3_1 | 430 | 437 | PF00069 | 0.465 |
| MOD_GSK3_1 | 500 | 507 | PF00069 | 0.652 |
| MOD_GSK3_1 | 514 | 521 | PF00069 | 0.690 |
| MOD_GSK3_1 | 536 | 543 | PF00069 | 0.712 |
| MOD_GSK3_1 | 73 | 80 | PF00069 | 0.595 |
| MOD_GSK3_1 | 99 | 106 | PF00069 | 0.505 |
| MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.754 |
| MOD_NEK2_1 | 103 | 108 | PF00069 | 0.525 |
| MOD_NEK2_1 | 196 | 201 | PF00069 | 0.404 |
| MOD_NEK2_1 | 292 | 297 | PF00069 | 0.487 |
| MOD_NEK2_1 | 31 | 36 | PF00069 | 0.570 |
| MOD_NEK2_1 | 346 | 351 | PF00069 | 0.449 |
| MOD_NEK2_1 | 434 | 439 | PF00069 | 0.492 |
| MOD_NEK2_1 | 443 | 448 | PF00069 | 0.500 |
| MOD_NEK2_1 | 540 | 545 | PF00069 | 0.777 |
| MOD_NEK2_1 | 578 | 583 | PF00069 | 0.557 |
| MOD_NEK2_1 | 75 | 80 | PF00069 | 0.725 |
| MOD_NEK2_2 | 86 | 91 | PF00069 | 0.713 |
| MOD_PIKK_1 | 14 | 20 | PF00454 | 0.490 |
| MOD_PKA_1 | 455 | 461 | PF00069 | 0.660 |
| MOD_PKA_1 | 531 | 537 | PF00069 | 0.547 |
| MOD_PKA_2 | 185 | 191 | PF00069 | 0.492 |
| MOD_PKA_2 | 313 | 319 | PF00069 | 0.440 |
| MOD_PKA_2 | 346 | 352 | PF00069 | 0.368 |
| MOD_PKA_2 | 455 | 461 | PF00069 | 0.638 |
| MOD_PKA_2 | 465 | 471 | PF00069 | 0.604 |
| MOD_PKA_2 | 570 | 576 | PF00069 | 0.656 |
| MOD_PKB_1 | 389 | 397 | PF00069 | 0.558 |
| MOD_Plk_1 | 335 | 341 | PF00069 | 0.530 |
| MOD_Plk_1 | 374 | 380 | PF00069 | 0.562 |
| MOD_Plk_1 | 578 | 584 | PF00069 | 0.614 |
| MOD_Plk_1 | 608 | 614 | PF00069 | 0.636 |
| MOD_Plk_4 | 165 | 171 | PF00069 | 0.470 |
| MOD_Plk_4 | 221 | 227 | PF00069 | 0.480 |
| MOD_Plk_4 | 283 | 289 | PF00069 | 0.497 |
| MOD_Plk_4 | 391 | 397 | PF00069 | 0.562 |
| MOD_Plk_4 | 430 | 436 | PF00069 | 0.507 |
| MOD_Plk_4 | 484 | 490 | PF00069 | 0.519 |
| MOD_Plk_4 | 572 | 578 | PF00069 | 0.537 |
| MOD_Plk_4 | 99 | 105 | PF00069 | 0.526 |
| MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.377 |
| MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.527 |
| MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.496 |
| MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.769 |
| MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.497 |
| MOD_SUMO_for_1 | 606 | 609 | PF00179 | 0.479 |
| MOD_SUMO_rev_2 | 483 | 488 | PF00179 | 0.292 |
| MOD_SUMO_rev_2 | 539 | 546 | PF00179 | 0.538 |
| TRG_DiLeu_BaEn_1 | 294 | 299 | PF01217 | 0.405 |
| TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.306 |
| TRG_DiLeu_BaEn_1 | 471 | 476 | PF01217 | 0.571 |
| TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.562 |
| TRG_DiLeu_LyEn_5 | 46 | 51 | PF01217 | 0.306 |
| TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.451 |
| TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.432 |
| TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.438 |
| TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.446 |
| TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.435 |
| TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.560 |
| TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.471 |
| TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.444 |
| TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.592 |
| TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.424 |
| TRG_ER_diArg_1 | 389 | 392 | PF00400 | 0.581 |
| TRG_ER_diArg_1 | 407 | 410 | PF00400 | 0.421 |
| TRG_ER_diArg_1 | 439 | 441 | PF00400 | 0.496 |
| TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.568 |
| TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.694 |
| TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.566 |
| TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.615 |
| TRG_Pf-PMV_PEXEL_1 | 258 | 263 | PF00026 | 0.286 |
| TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.334 |
| TRG_Pf-PMV_PEXEL_1 | 473 | 477 | PF00026 | 0.553 |
| TRG_Pf-PMV_PEXEL_1 | 603 | 608 | PF00026 | 0.720 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I4F2 | Leptomonas seymouri | 55% | 100% |
| A0A0S4JFL5 | Bodo saltans | 30% | 100% |
| A0A1X0NNC2 | Trypanosomatidae | 42% | 100% |
| A0A3R7KIN4 | Trypanosoma rangeli | 40% | 100% |
| A0A3S7WSE3 | Leishmania donovani | 81% | 100% |
| A4HVF3 | Leishmania infantum | 81% | 100% |
| E9AP51 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
| Q4QGD7 | Leishmania major | 80% | 100% |
| V5B9B5 | Trypanosoma cruzi | 42% | 100% |