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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9ALZ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 211 | 215 | PF00656 | 0.669 |
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 306 | 310 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.712 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.443 |
CLV_PCSK_FUR_1 | 289 | 293 | PF00082 | 0.383 |
CLV_PCSK_FUR_1 | 470 | 474 | PF00082 | 0.530 |
CLV_PCSK_FUR_1 | 528 | 532 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 530 | 532 | PF00082 | 0.451 |
CLV_PCSK_PC7_1 | 465 | 471 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.448 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.676 |
DOC_ANK_TNKS_1 | 400 | 407 | PF00023 | 0.778 |
DOC_CYCLIN_RxL_1 | 189 | 198 | PF00134 | 0.625 |
DOC_CYCLIN_RxL_1 | 530 | 539 | PF00134 | 0.645 |
DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.654 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.674 |
DOC_USP7_UBL2_3 | 105 | 109 | PF12436 | 0.571 |
DOC_USP7_UBL2_3 | 117 | 121 | PF12436 | 0.479 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 134 | 140 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 163 | 172 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 23 | 27 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 373 | 379 | PF00244 | 0.760 |
LIG_14-3-3_CanoR_1 | 391 | 399 | PF00244 | 0.584 |
LIG_APCC_ABBA_1 | 293 | 298 | PF00400 | 0.604 |
LIG_APCC_ABBAyCdc20_2 | 292 | 298 | PF00400 | 0.601 |
LIG_deltaCOP1_diTrp_1 | 602 | 610 | PF00928 | 0.784 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.310 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.620 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.728 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.472 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.511 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.676 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.569 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.629 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 275 | 284 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 536 | 545 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.673 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 536 | 541 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.513 |
LIG_PDZ_Class_3 | 608 | 613 | PF00595 | 0.698 |
LIG_SH2_PTP2 | 187 | 190 | PF00017 | 0.630 |
LIG_SH2_PTP2 | 60 | 63 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 18 | 22 | PF00017 | 0.770 |
LIG_SH2_STAP1 | 423 | 427 | PF00017 | 0.675 |
LIG_SH2_STAT3 | 452 | 455 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.530 |
LIG_SH3_1 | 410 | 416 | PF00018 | 0.741 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.683 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.723 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.733 |
LIG_SUMO_SIM_anti_2 | 441 | 451 | PF11976 | 0.573 |
LIG_TRAF2_1 | 464 | 467 | PF00917 | 0.744 |
LIG_TYR_ITIM | 58 | 63 | PF00017 | 0.671 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.297 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.676 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.736 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.677 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.469 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.429 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.518 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.578 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.732 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.661 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.782 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.453 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.464 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.551 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.457 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.555 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.524 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.423 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.467 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.485 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.575 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.521 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.692 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.782 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.651 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.644 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.651 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.580 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.430 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.679 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.679 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.606 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.589 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.411 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.340 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.580 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.205 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.724 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.608 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.738 |
MOD_PKB_1 | 86 | 94 | PF00069 | 0.535 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.598 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.687 |
MOD_Plk_2-3 | 491 | 497 | PF00069 | 0.782 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.655 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.691 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.800 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.366 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.454 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.662 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.645 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.667 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.619 |
MOD_SUMO_rev_2 | 161 | 171 | PF00179 | 0.683 |
TRG_DiLeu_BaEn_1 | 445 | 450 | PF01217 | 0.742 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.677 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.677 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.673 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.723 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 401 | 405 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7X5 | Leptomonas seymouri | 46% | 100% |
A0A3S7X291 | Leishmania donovani | 86% | 99% |
A4HH89 | Leishmania braziliensis | 70% | 100% |
A4I4D5 | Leishmania infantum | 85% | 99% |
E9ADT4 | Leishmania major | 86% | 100% |