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: Q4QF21
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.564 |
CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.443 |
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.546 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.352 |
CLV_PCSK_PC1ET2_1 | 376 | 378 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 418 | 420 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.514 |
CLV_PCSK_PC7_1 | 414 | 420 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 5 | 11 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.570 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.565 |
DOC_CYCLIN_RxL_1 | 414 | 426 | PF00134 | 0.610 |
DOC_CYCLIN_RxL_1 | 507 | 517 | PF00134 | 0.622 |
DOC_CYCLIN_yCln2_LP_2 | 134 | 140 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 272 | 279 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 119 | 126 | PF00149 | 0.461 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.384 |
DOC_PP4_FxxP_1 | 76 | 79 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.622 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.765 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 431 | 439 | PF00244 | 0.554 |
LIG_Actin_WH2_2 | 228 | 245 | PF00022 | 0.517 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.591 |
LIG_BRCT_BRCA1_1 | 464 | 468 | PF00533 | 0.477 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.349 |
LIG_eIF4E_1 | 55 | 61 | PF01652 | 0.338 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.374 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.431 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.607 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.622 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.336 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.458 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.613 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.464 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.539 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.748 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.665 |
LIG_Integrin_RGD_1 | 106 | 108 | PF01839 | 0.567 |
LIG_LIR_Apic_2 | 139 | 144 | PF02991 | 0.325 |
LIG_LIR_Apic_2 | 343 | 348 | PF02991 | 0.689 |
LIG_LIR_Apic_2 | 67 | 73 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 288 | 297 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 382 | 390 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 426 | 434 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 473 | 482 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 288 | 292 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.529 |
LIG_MYND_1 | 526 | 530 | PF01753 | 0.583 |
LIG_PTB_Apo_2 | 149 | 156 | PF02174 | 0.335 |
LIG_REV1ctd_RIR_1 | 437 | 446 | PF16727 | 0.552 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.377 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.362 |
LIG_SH2_GRB2like | 150 | 153 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 249 | 252 | PF00017 | 0.489 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.294 |
LIG_SH2_PTP2 | 345 | 348 | PF00017 | 0.684 |
LIG_SH2_SRC | 345 | 348 | PF00017 | 0.603 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.561 |
LIG_SH3_2 | 35 | 40 | PF14604 | 0.438 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.390 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.441 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.408 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.592 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.733 |
LIG_SUMO_SIM_anti_2 | 115 | 120 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.487 |
LIG_TRAF2_2 | 450 | 455 | PF00917 | 0.677 |
LIG_TRFH_1 | 133 | 137 | PF08558 | 0.446 |
LIG_TYR_ITIM | 292 | 297 | PF00017 | 0.370 |
MOD_CDK_SPxK_1 | 526 | 532 | PF00069 | 0.566 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.674 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.575 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.501 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.525 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.605 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.360 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.568 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.708 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.416 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.631 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.696 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.539 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.498 |
MOD_GlcNHglycan | 196 | 200 | PF01048 | 0.470 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.467 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.554 |
MOD_GlcNHglycan | 380 | 384 | PF01048 | 0.618 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.561 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.466 |
MOD_GlcNHglycan | 492 | 496 | PF01048 | 0.703 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.364 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.542 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.590 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.503 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.432 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.781 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.526 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.561 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.379 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.559 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.565 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.360 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.436 |
MOD_PIKK_1 | 448 | 454 | PF00454 | 0.694 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.632 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.663 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.599 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.570 |
MOD_PKB_1 | 377 | 385 | PF00069 | 0.581 |
MOD_PKB_1 | 391 | 399 | PF00069 | 0.584 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.466 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.564 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.508 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.331 |
MOD_Plk_2-3 | 337 | 343 | PF00069 | 0.668 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.622 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.583 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.485 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.370 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.410 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.549 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.670 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.768 |
MOD_SUMO_for_1 | 489 | 492 | PF00179 | 0.699 |
MOD_SUMO_rev_2 | 89 | 96 | PF00179 | 0.542 |
TRG_DiLeu_BaEn_4 | 262 | 268 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 533 | 538 | PF01217 | 0.613 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 84 | 87 | PF00400 | 0.449 |
TRG_NES_CRM1_1 | 34 | 48 | PF08389 | 0.438 |
TRG_NES_CRM1_1 | 503 | 517 | PF08389 | 0.509 |
TRG_NLS_MonoExtC_3 | 3 | 8 | PF00514 | 0.622 |
TRG_NLS_MonoExtC_3 | 374 | 379 | PF00514 | 0.591 |
TRG_NLS_MonoExtN_4 | 2 | 8 | PF00514 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 12 | 17 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 419 | 424 | PF00026 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 536 | 540 | PF00026 | 0.594 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P791 | Leptomonas seymouri | 63% | 100% |
A0A1X0NGQ9 | Trypanosomatidae | 40% | 92% |
A0A3R7L2Y6 | Trypanosoma rangeli | 39% | 91% |
A0A3S5H6W3 | Leishmania donovani | 90% | 100% |
A4H8C6 | Leishmania braziliensis | 77% | 100% |
A4HWP7 | Leishmania infantum | 90% | 100% |
C9ZTQ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 87% |
E9AQF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5DPP9 | Trypanosoma cruzi | 44% | 92% |