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: A4I8S9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 125 | 129 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.654 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.579 |
CLV_PCSK_FUR_1 | 361 | 365 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.581 |
CLV_PCSK_PC7_1 | 284 | 290 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.658 |
DEG_APCC_DBOX_1 | 177 | 185 | PF00400 | 0.608 |
DEG_APCC_DBOX_1 | 402 | 410 | PF00400 | 0.486 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.537 |
DOC_CKS1_1 | 357 | 362 | PF01111 | 0.533 |
DOC_CYCLIN_RxL_1 | 287 | 298 | PF00134 | 0.570 |
DOC_CYCLIN_yCln2_LP_2 | 221 | 227 | PF00134 | 0.617 |
DOC_MAPK_gen_1 | 204 | 212 | PF00069 | 0.667 |
DOC_MAPK_gen_1 | 287 | 297 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 478 | 488 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 478 | 486 | PF00069 | 0.490 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.653 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.459 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.422 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.754 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 382 | 386 | PF00244 | 0.395 |
LIG_APCC_ABBA_1 | 335 | 340 | PF00400 | 0.530 |
LIG_BIR_III_4 | 117 | 121 | PF00653 | 0.691 |
LIG_BRCT_BRCA1_1 | 274 | 278 | PF00533 | 0.537 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.500 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.698 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.596 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.488 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.450 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.587 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.513 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.542 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.629 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.561 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.671 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.552 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.707 |
LIG_LIR_Gen_1 | 142 | 152 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.716 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.472 |
LIG_LYPXL_S_1 | 155 | 159 | PF13949 | 0.624 |
LIG_LYPXL_yS_3 | 104 | 107 | PF13949 | 0.742 |
LIG_LYPXL_yS_3 | 156 | 159 | PF13949 | 0.607 |
LIG_PDZ_Class_2 | 484 | 489 | PF00595 | 0.539 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.352 |
LIG_SH2_CRK | 472 | 476 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.426 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.587 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.624 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.605 |
LIG_TYR_ITSM | 100 | 107 | PF00017 | 0.648 |
MOD_CDK_SPK_2 | 307 | 312 | PF00069 | 0.628 |
MOD_CDK_SPK_2 | 356 | 361 | PF00069 | 0.512 |
MOD_CDK_SPK_2 | 90 | 95 | PF00069 | 0.703 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.539 |
MOD_CDK_SPxxK_3 | 462 | 469 | PF00069 | 0.479 |
MOD_CDK_SPxxK_3 | 471 | 478 | PF00069 | 0.393 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.675 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.724 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.360 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.736 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.560 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.572 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.454 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.417 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.669 |
MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.700 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.580 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.677 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.719 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.732 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.564 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.714 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.519 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.742 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.654 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.481 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.529 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.574 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.717 |
MOD_PK_1 | 32 | 38 | PF00069 | 0.575 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.602 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.642 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.522 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.457 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.757 |
MOD_PKB_1 | 236 | 244 | PF00069 | 0.489 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.652 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.679 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.713 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.628 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.617 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.752 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.659 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.539 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.475 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.400 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.754 |
TRG_DiLeu_BaEn_1 | 16 | 21 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_2 | 22 | 28 | PF01217 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 176 | 181 | PF01217 | 0.644 |
TRG_DiLeu_BaLyEn_6 | 396 | 401 | PF01217 | 0.552 |
TRG_DiLeu_LyEn_5 | 16 | 21 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.700 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.523 |
TRG_ER_diArg_1 | 286 | 289 | PF00400 | 0.556 |
TRG_NES_CRM1_1 | 404 | 419 | PF08389 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 178 | 183 | PF00026 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 293 | 298 | PF00026 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUL5 | Leptomonas seymouri | 37% | 100% |
A0A1X0P1W2 | Trypanosomatidae | 23% | 100% |
A0A3Q8IHD2 | Leishmania donovani | 100% | 100% |
A0A3R7K4P6 | Trypanosoma rangeli | 24% | 100% |
A4HLA3 | Leishmania braziliensis | 72% | 100% |
E9B3P5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q4E2 | Leishmania major | 90% | 100% |
V5BJY6 | Trypanosoma cruzi | 25% | 100% |