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: Q4Q2D6
Term | Name | Level | Count |
---|---|---|---|
GO:0044145 | modulation of formation of structure involved in a symbiotic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.671 |
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.639 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 628 | 630 | PF00675 | 0.798 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.780 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 598 | 600 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 629 | 633 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.689 |
CLV_Separin_Metazoa | 197 | 201 | PF03568 | 0.383 |
DEG_APCC_DBOX_1 | 432 | 440 | PF00400 | 0.724 |
DEG_APCC_DBOX_1 | 484 | 492 | PF00400 | 0.495 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.687 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.705 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.601 |
DOC_MAPK_gen_1 | 102 | 110 | PF00069 | 0.636 |
DOC_MAPK_gen_1 | 352 | 360 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 36 | 44 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 432 | 438 | PF00069 | 0.632 |
DOC_MAPK_gen_1 | 598 | 604 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 613 | 621 | PF00069 | 0.671 |
DOC_MAPK_MEF2A_6 | 286 | 293 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 352 | 360 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 36 | 44 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 613 | 621 | PF00069 | 0.634 |
DOC_MAPK_NFAT4_5 | 286 | 294 | PF00069 | 0.469 |
DOC_PP2B_LxvP_1 | 289 | 292 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 535 | 538 | PF13499 | 0.655 |
DOC_PP4_FxxP_1 | 582 | 585 | PF00568 | 0.747 |
DOC_PP4_FxxP_1 | 659 | 662 | PF00568 | 0.692 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 631 | 635 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.685 |
DOC_USP7_UBL2_3 | 649 | 653 | PF12436 | 0.750 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 589 | 595 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 64 | 69 | PF00244 | 0.597 |
LIG_Actin_WH2_2 | 196 | 213 | PF00022 | 0.466 |
LIG_Actin_WH2_2 | 474 | 491 | PF00022 | 0.509 |
LIG_APCC_ABBA_1 | 58 | 63 | PF00400 | 0.583 |
LIG_BRCT_BRCA1_1 | 447 | 451 | PF00533 | 0.702 |
LIG_BRCT_BRCA1_1 | 578 | 582 | PF00533 | 0.737 |
LIG_CaM_IQ_9 | 550 | 565 | PF13499 | 0.580 |
LIG_EH1_1 | 481 | 489 | PF00400 | 0.569 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.458 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.726 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.624 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.623 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.554 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.477 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.719 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.530 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.636 |
LIG_GBD_Chelix_1 | 343 | 351 | PF00786 | 0.531 |
LIG_LIR_Apic_2 | 579 | 585 | PF02991 | 0.714 |
LIG_LIR_Apic_2 | 81 | 86 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 116 | 123 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 228 | 236 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 67 | 76 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 634 | 639 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.528 |
LIG_NRBOX | 189 | 195 | PF00104 | 0.490 |
LIG_NRBOX | 71 | 77 | PF00104 | 0.583 |
LIG_PDZ_Class_2 | 660 | 665 | PF00595 | 0.700 |
LIG_Pex14_2 | 659 | 663 | PF04695 | 0.689 |
LIG_Rb_LxCxE_1 | 238 | 259 | PF01857 | 0.640 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.553 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.687 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.689 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.644 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.749 |
LIG_SUMO_SIM_anti_2 | 180 | 189 | PF11976 | 0.517 |
LIG_SUMO_SIM_anti_2 | 228 | 235 | PF11976 | 0.534 |
LIG_SUMO_SIM_anti_2 | 89 | 94 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.670 |
LIG_SUMO_SIM_par_1 | 531 | 541 | PF11976 | 0.637 |
LIG_SUMO_SIM_par_1 | 56 | 63 | PF11976 | 0.534 |
LIG_TRAF2_1 | 476 | 479 | PF00917 | 0.571 |
MOD_CDK_SPxK_1 | 637 | 643 | PF00069 | 0.546 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.603 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.783 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.680 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.571 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.644 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.736 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.723 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.588 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.702 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.554 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.555 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.574 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.636 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.534 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.674 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.599 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.642 |
MOD_Cter_Amidation | 129 | 132 | PF01082 | 0.606 |
MOD_Cter_Amidation | 430 | 433 | PF01082 | 0.719 |
MOD_Cter_Amidation | 626 | 629 | PF01082 | 0.713 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.537 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.720 |
MOD_GlcNHglycan | 262 | 266 | PF01048 | 0.737 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.446 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.519 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.629 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.704 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.711 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.708 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.706 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.473 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.654 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.717 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.687 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.717 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.661 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.677 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.737 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.665 |
MOD_N-GLC_1 | 550 | 555 | PF02516 | 0.644 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.621 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.445 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.396 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.420 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.561 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.591 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.678 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.495 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.507 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.516 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.564 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.716 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.590 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.601 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.673 |
MOD_PK_1 | 148 | 154 | PF00069 | 0.776 |
MOD_PK_1 | 156 | 162 | PF00069 | 0.719 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.675 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.603 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.650 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.734 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.624 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.634 |
MOD_Plk_2-3 | 106 | 112 | PF00069 | 0.648 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.591 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.644 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.566 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.592 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.734 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.774 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.587 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.687 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.477 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.626 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.646 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.603 |
TRG_DiLeu_BaEn_1 | 181 | 186 | PF01217 | 0.479 |
TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.582 |
TRG_DiLeu_BaEn_2 | 105 | 111 | PF01217 | 0.643 |
TRG_DiLeu_BaEn_2 | 505 | 511 | PF01217 | 0.372 |
TRG_DiLeu_BaEn_2 | 599 | 605 | PF01217 | 0.635 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.538 |
TRG_DiLeu_BaLyEn_6 | 482 | 487 | PF01217 | 0.580 |
TRG_DiLeu_LyEn_5 | 71 | 76 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 351 | 353 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.702 |
TRG_NES_CRM1_1 | 181 | 195 | PF08389 | 0.472 |
TRG_NLS_MonoExtC_3 | 35 | 41 | PF00514 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 30 | 35 | PF00026 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 475 | 479 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 603 | 607 | PF00026 | 0.627 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7E6 | Leptomonas seymouri | 47% | 100% |
A0A0S4KLZ0 | Bodo saltans | 27% | 83% |
A0A1X0PAG6 | Trypanosomatidae | 35% | 100% |
A0A3Q8IIY0 | Leishmania donovani | 90% | 98% |
A0A422NVB5 | Trypanosoma rangeli | 32% | 100% |
A4HBC8 | Leishmania braziliensis | 72% | 99% |
A4IAH6 | Leishmania infantum | 90% | 98% |
C9ZLR4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B5K0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
V5BRF7 | Trypanosoma cruzi | 33% | 100% |