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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q4E2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.660 |
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.566 |
CLV_PCSK_FUR_1 | 176 | 180 | PF00082 | 0.514 |
CLV_PCSK_FUR_1 | 362 | 366 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 364 | 366 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.596 |
CLV_PCSK_PC7_1 | 285 | 291 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.655 |
DEG_APCC_DBOX_1 | 178 | 186 | PF00400 | 0.550 |
DEG_APCC_DBOX_1 | 403 | 411 | PF00400 | 0.488 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.523 |
DOC_CKS1_1 | 358 | 363 | PF01111 | 0.594 |
DOC_CYCLIN_RxL_1 | 176 | 184 | PF00134 | 0.425 |
DOC_CYCLIN_RxL_1 | 288 | 299 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 155 | 161 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 222 | 228 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 205 | 213 | PF00069 | 0.670 |
DOC_MAPK_gen_1 | 288 | 298 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 479 | 489 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 479 | 487 | PF00069 | 0.543 |
DOC_PP2B_LxvP_1 | 211 | 214 | PF13499 | 0.666 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.550 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.455 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.768 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 288 | 298 | PF00244 | 0.623 |
LIG_APCC_ABBA_1 | 336 | 341 | PF00400 | 0.545 |
LIG_BIR_III_4 | 118 | 122 | PF00653 | 0.649 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.459 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.474 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.499 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.712 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.543 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.533 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.427 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.461 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.622 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.557 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.437 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.589 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.583 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.515 |
LIG_LIR_Gen_1 | 446 | 456 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.715 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.438 |
LIG_LYPXL_S_1 | 156 | 160 | PF13949 | 0.559 |
LIG_LYPXL_yS_3 | 105 | 108 | PF13949 | 0.693 |
LIG_LYPXL_yS_3 | 157 | 160 | PF13949 | 0.543 |
LIG_PDZ_Class_2 | 485 | 490 | PF00595 | 0.588 |
LIG_PTAP_UEV_1 | 306 | 311 | PF05743 | 0.544 |
LIG_SH2_CRK | 473 | 477 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.462 |
LIG_SH3_1 | 177 | 183 | PF00018 | 0.424 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.582 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.687 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.553 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.529 |
LIG_SUMO_SIM_par_1 | 294 | 299 | PF11976 | 0.551 |
LIG_TYR_ITSM | 101 | 108 | PF00017 | 0.614 |
MOD_CDK_SPK_2 | 308 | 313 | PF00069 | 0.581 |
MOD_CDK_SPK_2 | 357 | 362 | PF00069 | 0.522 |
MOD_CDK_SPK_2 | 91 | 96 | PF00069 | 0.667 |
MOD_CDK_SPxxK_3 | 357 | 364 | PF00069 | 0.597 |
MOD_CDK_SPxxK_3 | 463 | 470 | PF00069 | 0.467 |
MOD_CDK_SPxxK_3 | 472 | 479 | PF00069 | 0.419 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.690 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.549 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.710 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.398 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.715 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.492 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.579 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.780 |
MOD_Cter_Amidation | 44 | 47 | PF01082 | 0.479 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.715 |
MOD_GlcNHglycan | 306 | 310 | PF01048 | 0.650 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.641 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.609 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.585 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.659 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.739 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.710 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.515 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.627 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.477 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.716 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.401 |
MOD_N-GLC_1 | 85 | 90 | PF02516 | 0.736 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.494 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.479 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.516 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.592 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.474 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.517 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.755 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.486 |
MOD_PK_1 | 32 | 38 | PF00069 | 0.557 |
MOD_PKA_1 | 289 | 295 | PF00069 | 0.617 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.466 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.564 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.482 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.497 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.767 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.692 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.728 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.474 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.670 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.649 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.753 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.593 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.596 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.463 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.429 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.766 |
TRG_DiLeu_BaEn_2 | 22 | 28 | PF01217 | 0.627 |
TRG_DiLeu_BaLyEn_6 | 177 | 182 | PF01217 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 397 | 402 | PF01217 | 0.581 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.711 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.540 |
TRG_NES_CRM1_1 | 405 | 420 | PF08389 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 179 | 184 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 294 | 299 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUL5 | Leptomonas seymouri | 37% | 100% |
A0A1X0P1W2 | Trypanosomatidae | 24% | 100% |
A0A3Q8IHD2 | Leishmania donovani | 90% | 100% |
A0A3R7K4P6 | Trypanosoma rangeli | 25% | 100% |
A4HLA3 | Leishmania braziliensis | 73% | 100% |
A4I8S9 | Leishmania infantum | 90% | 100% |
E9B3P5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5BJY6 | Trypanosoma cruzi | 26% | 100% |