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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HBC8
Term | Name | Level | Count |
---|---|---|---|
GO:0044145 | modulation of formation of structure involved in a symbiotic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.490 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.804 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.786 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 607 | 609 | PF00082 | 0.594 |
CLV_PCSK_PC7_1 | 633 | 639 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.390 |
CLV_Separin_Metazoa | 197 | 201 | PF03568 | 0.385 |
DEG_APCC_DBOX_1 | 104 | 112 | PF00400 | 0.378 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 430 | 438 | PF00400 | 0.689 |
DEG_APCC_DBOX_1 | 482 | 490 | PF00400 | 0.503 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.685 |
DEG_SPOP_SBC_1 | 272 | 276 | PF00917 | 0.692 |
DOC_CYCLIN_RxL_1 | 481 | 491 | PF00134 | 0.350 |
DOC_CYCLIN_yCln2_LP_2 | 627 | 630 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 102 | 110 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 27 | 34 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 36 | 44 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 430 | 436 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 607 | 613 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 36 | 44 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 326 | 332 | PF00149 | 0.410 |
DOC_PP2B_LxvP_1 | 167 | 170 | PF13499 | 0.625 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 533 | 536 | PF13499 | 0.662 |
DOC_PP2B_LxvP_1 | 627 | 630 | PF13499 | 0.530 |
DOC_PP2B_PxIxI_1 | 535 | 541 | PF00149 | 0.462 |
DOC_PP4_FxxP_1 | 591 | 594 | PF00568 | 0.745 |
DOC_PP4_FxxP_1 | 668 | 671 | PF00568 | 0.702 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.650 |
DOC_USP7_UBL2_3 | 658 | 662 | PF12436 | 0.775 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 131 | 136 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 328 | 338 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 598 | 604 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 88 | 93 | PF00244 | 0.519 |
LIG_Actin_WH2_2 | 89 | 107 | PF00022 | 0.368 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 181 | 185 | PF00533 | 0.288 |
LIG_BRCT_BRCA1_1 | 445 | 449 | PF00533 | 0.676 |
LIG_BRCT_BRCA1_1 | 587 | 591 | PF00533 | 0.752 |
LIG_EH1_1 | 479 | 487 | PF00400 | 0.572 |
LIG_EVH1_1 | 628 | 632 | PF00568 | 0.535 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.673 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.535 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.529 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.568 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.445 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.641 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.561 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.457 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.696 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.518 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.494 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.766 |
LIG_GBD_Chelix_1 | 342 | 350 | PF00786 | 0.517 |
LIG_Integrin_RGD_1 | 633 | 635 | PF01839 | 0.592 |
LIG_LIR_Apic_2 | 588 | 594 | PF02991 | 0.719 |
LIG_LIR_Gen_1 | 116 | 123 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 228 | 236 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 664 | 669 | PF02991 | 0.506 |
LIG_LYPXL_yS_3 | 666 | 669 | PF13949 | 0.503 |
LIG_MYND_1 | 626 | 630 | PF01753 | 0.525 |
LIG_NRBOX | 189 | 195 | PF00104 | 0.473 |
LIG_NRBOX | 345 | 351 | PF00104 | 0.314 |
LIG_NRBOX | 485 | 491 | PF00104 | 0.364 |
LIG_NRBOX | 71 | 77 | PF00104 | 0.594 |
LIG_Pex14_2 | 668 | 672 | PF04695 | 0.701 |
LIG_Rb_LxCxE_1 | 238 | 259 | PF01857 | 0.603 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.492 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.553 |
LIG_SH2_STAT3 | 218 | 221 | PF00017 | 0.511 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.683 |
LIG_SH3_1 | 497 | 503 | PF00018 | 0.378 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.378 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.752 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.610 |
LIG_SH3_4 | 658 | 665 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 188 | 194 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 57 | 63 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 2 | 8 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 376 | 381 | PF11976 | 0.677 |
LIG_SUMO_SIM_par_1 | 52 | 59 | PF11976 | 0.588 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.331 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.522 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.729 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.648 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.657 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.598 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.742 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.662 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.477 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.648 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.525 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.610 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.537 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.574 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.662 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.562 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.632 |
MOD_Cter_Amidation | 428 | 431 | PF01082 | 0.681 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.502 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.675 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.365 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.427 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.662 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.618 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.711 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.708 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.520 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.599 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.667 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.680 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.679 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.278 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.669 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.717 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.579 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.620 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.631 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.630 |
MOD_N-GLC_1 | 464 | 469 | PF02516 | 0.635 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.689 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.384 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.420 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.349 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.594 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.574 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.488 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.515 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.666 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.640 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.568 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.618 |
MOD_NEK2_2 | 536 | 541 | PF00069 | 0.471 |
MOD_PKA_1 | 131 | 137 | PF00069 | 0.464 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.390 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.591 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.644 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.625 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.594 |
MOD_Plk_2-3 | 106 | 112 | PF00069 | 0.635 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.602 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.472 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.493 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.609 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.546 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.547 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.574 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.625 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.376 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.661 |
MOD_SUMO_for_1 | 661 | 664 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 125 | 134 | PF00179 | 0.610 |
MOD_SUMO_rev_2 | 616 | 626 | PF00179 | 0.445 |
TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.565 |
TRG_DiLeu_BaEn_2 | 105 | 111 | PF01217 | 0.633 |
TRG_DiLeu_BaEn_2 | 608 | 614 | PF01217 | 0.633 |
TRG_DiLeu_BaEn_2 | 663 | 669 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 480 | 485 | PF01217 | 0.588 |
TRG_DiLeu_LyEn_5 | 623 | 628 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.645 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.533 |
TRG_NLS_MonoExtC_3 | 35 | 41 | PF00514 | 0.619 |
TRG_NLS_MonoExtN_4 | 27 | 33 | PF00514 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 473 | 477 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 487 | 491 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 612 | 616 | PF00026 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7E6 | Leptomonas seymouri | 45% | 100% |
A0A0S4KLZ0 | Bodo saltans | 27% | 84% |
A0A1X0PAG6 | Trypanosomatidae | 34% | 100% |
A0A3Q8IIY0 | Leishmania donovani | 74% | 100% |
A0A422NVB5 | Trypanosoma rangeli | 30% | 100% |
A4IAH6 | Leishmania infantum | 73% | 100% |
C9ZLR4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B5K0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q2D6 | Leishmania major | 72% | 98% |
V5BRF7 | Trypanosoma cruzi | 32% | 100% |