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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q593
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.640 |
CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.541 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.594 |
DEG_APCC_DBOX_1 | 357 | 365 | PF00400 | 0.639 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.494 |
DOC_CYCLIN_RxL_1 | 355 | 365 | PF00134 | 0.641 |
DOC_CYCLIN_yCln2_LP_2 | 154 | 160 | PF00134 | 0.562 |
DOC_CYCLIN_yCln2_LP_2 | 85 | 91 | PF00134 | 0.481 |
DOC_MAPK_MEF2A_6 | 367 | 374 | PF00069 | 0.640 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.559 |
DOC_PP2B_LxvP_1 | 24 | 27 | PF13499 | 0.461 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.543 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.645 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.503 |
DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.669 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.646 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.619 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 186 | 192 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 95 | 105 | PF00244 | 0.420 |
LIG_Actin_WH2_2 | 121 | 139 | PF00022 | 0.667 |
LIG_Actin_WH2_2 | 79 | 97 | PF00022 | 0.471 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.508 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.622 |
LIG_CtBP_PxDLS_1 | 75 | 79 | PF00389 | 0.407 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.414 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.675 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.658 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.628 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.572 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.465 |
LIG_FXI_DFP_1 | 172 | 176 | PF00024 | 0.610 |
LIG_IRF3_LxIS_1 | 289 | 296 | PF10401 | 0.646 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.646 |
LIG_LIR_Apic_2 | 28 | 32 | PF02991 | 0.554 |
LIG_LIR_Apic_2 | 50 | 54 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 190 | 197 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.543 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.608 |
LIG_SH2_CRK | 10 | 14 | PF00017 | 0.532 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.626 |
LIG_SH2_SRC | 192 | 195 | PF00017 | 0.603 |
LIG_SH2_STAP1 | 192 | 196 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 347 | 351 | PF00017 | 0.598 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.571 |
LIG_SH3_1 | 179 | 185 | PF00018 | 0.634 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.634 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.652 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.466 |
LIG_TYR_ITSM | 188 | 195 | PF00017 | 0.571 |
LIG_WRC_WIRS_1 | 26 | 31 | PF05994 | 0.541 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.512 |
MOD_CDK_SPK_2 | 279 | 284 | PF00069 | 0.566 |
MOD_CDK_SPxxK_3 | 279 | 286 | PF00069 | 0.557 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.583 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.630 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.617 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.691 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.436 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.580 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.711 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.515 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.490 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.744 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.749 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.713 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.757 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.717 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.663 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.599 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.665 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.695 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.677 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.613 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.679 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.585 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.629 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.633 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.573 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.664 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.486 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.598 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.522 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.588 |
MOD_NEK2_2 | 76 | 81 | PF00069 | 0.512 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.517 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.508 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.609 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.521 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.733 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.443 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.382 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.619 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.638 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.652 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.477 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.506 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.502 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.647 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.523 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.633 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.618 |
MOD_SUMO_rev_2 | 36 | 45 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 369 | 375 | PF00179 | 0.604 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.652 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.644 |
TRG_Pf-PMV_PEXEL_1 | 62 | 67 | PF00026 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I475 | Leptomonas seymouri | 55% | 100% |
A0A1X0NUD6 | Trypanosomatidae | 29% | 100% |
A0A3Q8IGT2 | Leishmania donovani | 89% | 100% |
A4I801 | Leishmania infantum | 89% | 100% |
E9B2W3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5BF21 | Trypanosoma cruzi | 29% | 100% |