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: A4HWP7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.722 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.439 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.608 |
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.664 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 376 | 378 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 418 | 420 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.545 |
CLV_PCSK_PC7_1 | 414 | 420 | PF00082 | 0.589 |
CLV_PCSK_PC7_1 | 5 | 11 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.716 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.639 |
DEG_SCF_FBW7_1 | 460 | 467 | PF00400 | 0.601 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.660 |
DOC_CYCLIN_RxL_1 | 414 | 426 | PF00134 | 0.610 |
DOC_CYCLIN_RxL_1 | 507 | 517 | PF00134 | 0.753 |
DOC_CYCLIN_yCln2_LP_2 | 134 | 140 | PF00134 | 0.460 |
DOC_MAPK_DCC_7 | 173 | 181 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 272 | 279 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 532 | 539 | PF00069 | 0.565 |
DOC_PP1_RVXF_1 | 119 | 126 | PF00149 | 0.434 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.422 |
DOC_PP4_FxxP_1 | 76 | 79 | PF00568 | 0.466 |
DOC_PP4_MxPP_1 | 71 | 74 | PF00568 | 0.396 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.642 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.779 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 431 | 439 | PF00244 | 0.588 |
LIG_Actin_WH2_2 | 228 | 245 | PF00022 | 0.544 |
LIG_BIR_III_2 | 517 | 521 | PF00653 | 0.540 |
LIG_eIF4E_1 | 55 | 61 | PF01652 | 0.383 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.422 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.424 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.663 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.374 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.622 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.501 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.756 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.690 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.671 |
LIG_Integrin_RGD_1 | 106 | 108 | PF01839 | 0.649 |
LIG_LIR_Apic_2 | 139 | 144 | PF02991 | 0.371 |
LIG_LIR_Apic_2 | 343 | 348 | PF02991 | 0.713 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 288 | 297 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 426 | 434 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 473 | 482 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 288 | 292 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.588 |
LIG_MYND_1 | 526 | 530 | PF01753 | 0.697 |
LIG_PTB_Apo_2 | 149 | 156 | PF02174 | 0.420 |
LIG_PTB_Apo_2 | 64 | 71 | PF02174 | 0.484 |
LIG_REV1ctd_RIR_1 | 437 | 446 | PF16727 | 0.691 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.402 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.402 |
LIG_SH2_GRB2like | 150 | 153 | PF00017 | 0.424 |
LIG_SH2_GRB2like | 249 | 252 | PF00017 | 0.521 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.341 |
LIG_SH2_PTP2 | 345 | 348 | PF00017 | 0.705 |
LIG_SH2_SRC | 345 | 348 | PF00017 | 0.705 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.463 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.709 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.591 |
LIG_SH3_1 | 345 | 351 | PF00018 | 0.696 |
LIG_SH3_2 | 35 | 40 | PF14604 | 0.456 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.442 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.452 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.707 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.439 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.702 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.762 |
LIG_SUMO_SIM_anti_2 | 115 | 120 | PF11976 | 0.589 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 199 | 205 | PF11976 | 0.550 |
LIG_TRAF2_1 | 357 | 360 | PF00917 | 0.646 |
LIG_TRAF2_2 | 450 | 455 | PF00917 | 0.708 |
LIG_TRFH_1 | 133 | 137 | PF08558 | 0.456 |
LIG_TYR_ITIM | 292 | 297 | PF00017 | 0.406 |
MOD_CDC14_SPxK_1 | 46 | 49 | PF00782 | 0.524 |
MOD_CDK_SPK_2 | 531 | 536 | PF00069 | 0.558 |
MOD_CDK_SPxK_1 | 43 | 49 | PF00069 | 0.509 |
MOD_CDK_SPxK_1 | 526 | 532 | PF00069 | 0.659 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.690 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.661 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.661 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.563 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.576 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.661 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.662 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.744 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.545 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.634 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.659 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.572 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.500 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.533 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.573 |
MOD_GlcNHglycan | 380 | 384 | PF01048 | 0.697 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.586 |
MOD_GlcNHglycan | 492 | 496 | PF01048 | 0.655 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.551 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.635 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.674 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.443 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.674 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.540 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.585 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.424 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.586 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.691 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.646 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.367 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.446 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.654 |
MOD_PIKK_1 | 448 | 454 | PF00454 | 0.725 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.622 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.615 |
MOD_PKB_1 | 377 | 385 | PF00069 | 0.659 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.508 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.559 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.478 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.384 |
MOD_Plk_2-3 | 337 | 343 | PF00069 | 0.701 |
MOD_Plk_2-3 | 354 | 360 | PF00069 | 0.640 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.628 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.602 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.510 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.388 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.642 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.440 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.647 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.710 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.781 |
MOD_SUMO_for_1 | 489 | 492 | PF00179 | 0.727 |
MOD_SUMO_rev_2 | 89 | 96 | PF00179 | 0.564 |
TRG_DiLeu_BaEn_4 | 262 | 268 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 533 | 538 | PF01217 | 0.672 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.496 |
TRG_NLS_MonoExtC_3 | 3 | 8 | PF00514 | 0.595 |
TRG_NLS_MonoExtC_3 | 374 | 379 | PF00514 | 0.660 |
TRG_NLS_MonoExtN_4 | 2 | 8 | PF00514 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 12 | 17 | PF00026 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 419 | 424 | PF00026 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 536 | 540 | PF00026 | 0.664 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P791 | Leptomonas seymouri | 66% | 100% |
A0A1X0NGQ9 | Trypanosomatidae | 40% | 92% |
A0A3R7L2Y6 | Trypanosoma rangeli | 43% | 91% |
A0A3S5H6W3 | Leishmania donovani | 100% | 100% |
A4H8C6 | Leishmania braziliensis | 79% | 100% |
C9ZTQ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 87% |
E9AQF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QF21 | Leishmania major | 90% | 100% |
V5DPP9 | Trypanosoma cruzi | 43% | 92% |