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: A0A3S7WSE3
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 | 540 | 544 | PF00656 | 0.807 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.779 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.559 |
CLV_PCSK_FUR_1 | 67 | 71 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.819 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 527 | 529 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 603 | 605 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.422 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 441 | 449 | PF00400 | 0.564 |
DEG_APCC_DBOX_1 | 466 | 474 | PF00400 | 0.592 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.573 |
DOC_CKS1_1 | 253 | 258 | PF01111 | 0.548 |
DOC_CKS1_1 | 616 | 621 | PF01111 | 0.672 |
DOC_CYCLIN_RxL_1 | 5 | 15 | PF00134 | 0.403 |
DOC_MAPK_gen_1 | 593 | 601 | PF00069 | 0.653 |
DOC_MAPK_MEF2A_6 | 460 | 468 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 474 | 481 | PF00069 | 0.381 |
DOC_PP2B_LxvP_1 | 215 | 218 | PF13499 | 0.569 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.411 |
DOC_PP4_FxxP_1 | 497 | 500 | PF00568 | 0.654 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.533 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 284 | 289 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 315 | 319 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 392 | 397 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 534 | 541 | PF00244 | 0.799 |
LIG_14-3-3_CanoR_1 | 572 | 578 | PF00244 | 0.583 |
LIG_APCC_ABBA_1 | 40 | 45 | PF00400 | 0.582 |
LIG_APCC_ABBA_1 | 479 | 484 | PF00400 | 0.453 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.475 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.509 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.375 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.488 |
LIG_CSL_BTD_1 | 203 | 206 | PF09270 | 0.492 |
LIG_deltaCOP1_diTrp_1 | 114 | 120 | PF00928 | 0.445 |
LIG_eIF4E_1 | 439 | 445 | PF01652 | 0.562 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.553 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.546 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.544 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.652 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.811 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.466 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.715 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.560 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.554 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.586 |
LIG_GSK3_LRP6_1 | 519 | 525 | PF00069 | 0.733 |
LIG_LIR_Apic_2 | 494 | 500 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 114 | 125 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 240 | 250 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 304 | 314 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 249 | 253 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 493 | 498 | PF02991 | 0.544 |
LIG_MLH1_MIPbox_1 | 233 | 237 | PF16413 | 0.508 |
LIG_PCNA_PIPBox_1 | 433 | 442 | PF02747 | 0.480 |
LIG_PCNA_yPIPBox_3 | 333 | 344 | PF02747 | 0.607 |
LIG_PCNA_yPIPBox_3 | 426 | 440 | PF02747 | 0.480 |
LIG_Pex14_1 | 116 | 120 | PF04695 | 0.550 |
LIG_Pex14_1 | 48 | 52 | PF04695 | 0.574 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.401 |
LIG_Pex14_2 | 601 | 605 | PF04695 | 0.581 |
LIG_PTB_Apo_2 | 103 | 110 | PF02174 | 0.543 |
LIG_PTB_Phospho_1 | 103 | 109 | PF10480 | 0.550 |
LIG_REV1ctd_RIR_1 | 234 | 243 | PF16727 | 0.540 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.543 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.536 |
LIG_SH2_CRK | 616 | 620 | PF00017 | 0.747 |
LIG_SH2_NCK_1 | 616 | 620 | PF00017 | 0.669 |
LIG_SH2_PTP2 | 243 | 246 | PF00017 | 0.555 |
LIG_SH2_PTP2 | 308 | 311 | PF00017 | 0.562 |
LIG_SH2_SRC | 306 | 309 | PF00017 | 0.562 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.587 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.658 |
LIG_SH2_STAP1 | 117 | 121 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.634 |
LIG_SH2_STAT3 | 199 | 202 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.699 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.623 |
LIG_SH2_STAT6 | 268 | 272 | PF00017 | 0.562 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.764 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.722 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.495 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.496 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.455 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.534 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.494 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.759 |
LIG_SUMO_SIM_par_1 | 337 | 343 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 487 | 494 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 574 | 580 | PF11976 | 0.646 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.610 |
LIG_TRFH_1 | 120 | 124 | PF08558 | 0.555 |
LIG_TYR_ITIM | 212 | 217 | PF00017 | 0.502 |
LIG_WRC_WIRS_1 | 393 | 398 | PF05994 | 0.562 |
MOD_CDK_SPxxK_3 | 252 | 259 | PF00069 | 0.524 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.526 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.778 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.715 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.694 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.725 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.549 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.755 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.546 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.627 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.742 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.788 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.411 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.698 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.555 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.564 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.528 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.553 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.662 |
MOD_DYRK1A_RPxSP_1 | 426 | 430 | PF00069 | 0.496 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.613 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.696 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.476 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.696 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.370 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.645 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.745 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.717 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.618 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.581 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.621 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.687 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.653 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.635 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.765 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.389 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.492 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.495 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.482 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.482 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.490 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.466 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.623 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.706 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.496 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.710 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.470 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.748 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.746 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.680 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.478 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.568 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.597 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.491 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.496 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.525 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.805 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.528 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.560 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.714 |
MOD_PIKK_1 | 541 | 547 | PF00454 | 0.717 |
MOD_PKA_1 | 456 | 462 | PF00069 | 0.664 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.476 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.432 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.642 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.603 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.653 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.728 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.629 |
MOD_PKB_1 | 390 | 398 | PF00069 | 0.558 |
MOD_PKB_1 | 532 | 540 | PF00069 | 0.594 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.562 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.585 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.502 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.490 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.546 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.509 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.509 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.536 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.567 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.778 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.383 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.524 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.494 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.773 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.670 |
TRG_DiLeu_BaEn_1 | 472 | 477 | PF01217 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.562 |
TRG_NLS_MonoCore_2 | 592 | 597 | PF00514 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 474 | 478 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 604 | 609 | PF00026 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 8 | 13 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4F2 | Leptomonas seymouri | 57% | 100% |
A0A0S4JFL5 | Bodo saltans | 30% | 100% |
A0A1X0NNC2 | Trypanosomatidae | 43% | 100% |
A0A3R7KIN4 | Trypanosoma rangeli | 41% | 100% |
A4H724 | Leishmania braziliensis | 81% | 100% |
A4HVF3 | Leishmania infantum | 100% | 100% |
E9AP51 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QGD7 | Leishmania major | 95% | 100% |
V5B9B5 | Trypanosoma cruzi | 42% | 100% |