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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9ALN4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.543 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.747 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.681 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.647 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.622 |
DEG_SPOP_SBC_1 | 100 | 104 | PF00917 | 0.657 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.756 |
DOC_CKS1_1 | 23 | 28 | PF01111 | 0.490 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.611 |
DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 33 | 40 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.461 |
DOC_PP4_FxxP_1 | 378 | 381 | PF00568 | 0.684 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.522 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.643 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.571 |
LIG_BIR_III_4 | 154 | 158 | PF00653 | 0.367 |
LIG_BIR_III_4 | 243 | 247 | PF00653 | 0.699 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.559 |
LIG_deltaCOP1_diTrp_1 | 202 | 210 | PF00928 | 0.531 |
LIG_deltaCOP1_diTrp_1 | 9 | 18 | PF00928 | 0.419 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.684 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.582 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.663 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.710 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.648 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.387 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.455 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.403 |
LIG_PDZ_Class_1 | 442 | 447 | PF00595 | 0.709 |
LIG_PTB_Apo_2 | 334 | 341 | PF02174 | 0.616 |
LIG_SH2_NCK_1 | 28 | 32 | PF00017 | 0.544 |
LIG_SH2_PTP2 | 174 | 177 | PF00017 | 0.518 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.530 |
LIG_SH3_1 | 39 | 45 | PF00018 | 0.521 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.536 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.642 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.462 |
LIG_SH3_4 | 380 | 387 | PF00018 | 0.658 |
LIG_SUMO_SIM_anti_2 | 412 | 418 | PF11976 | 0.654 |
LIG_SUMO_SIM_par_1 | 410 | 418 | PF11976 | 0.648 |
LIG_WRC_WIRS_1 | 315 | 320 | PF05994 | 0.718 |
LIG_WRC_WIRS_1 | 332 | 337 | PF05994 | 0.410 |
LIG_WW_3 | 340 | 344 | PF00397 | 0.634 |
MOD_CDK_SPxxK_3 | 342 | 349 | PF00069 | 0.655 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.538 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.638 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.539 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.729 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.613 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.620 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.635 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.520 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.694 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.615 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.602 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.465 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.466 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.593 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.622 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.609 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.719 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.575 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.660 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.566 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.475 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.412 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.467 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.718 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.611 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.564 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.460 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.555 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.690 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.500 |
MOD_PKB_1 | 22 | 30 | PF00069 | 0.490 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.637 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.639 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.522 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.490 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.564 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.496 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.642 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.652 |
MOD_SUMO_for_1 | 379 | 382 | PF00179 | 0.684 |
MOD_SUMO_for_1 | 403 | 406 | PF00179 | 0.707 |
MOD_SUMO_rev_2 | 231 | 240 | PF00179 | 0.659 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.508 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.713 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 431 | 435 | PF00026 | 0.722 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q6 | Leptomonas seymouri | 65% | 95% |
A0A0S4KK06 | Bodo saltans | 26% | 92% |
A0A1X0NJ10 | Trypanosomatidae | 33% | 100% |
A0A3Q8IRG7 | Leishmania donovani | 95% | 100% |
A0A3R7NSU2 | Trypanosoma rangeli | 33% | 100% |
A4HHJ0 | Leishmania braziliensis | 88% | 100% |
A4I4P8 | Leishmania infantum | 95% | 100% |
C9ZN48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AE51 | Leishmania major | 95% | 100% |
V5BIJ5 | Trypanosoma cruzi | 32% | 100% |