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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9B6E9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.616 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.596 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.748 |
CLV_PCSK_PC1ET2_1 | 491 | 493 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.469 |
CLV_Separin_Metazoa | 299 | 303 | PF03568 | 0.283 |
DEG_APCC_DBOX_1 | 293 | 301 | PF00400 | 0.572 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.578 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.463 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.649 |
DEG_SCF_FBW7_1 | 59 | 66 | PF00400 | 0.622 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.662 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.777 |
DOC_CYCLIN_RxL_1 | 136 | 146 | PF00134 | 0.551 |
DOC_MAPK_gen_1 | 137 | 144 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 348 | 356 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 29 | 36 | PF00069 | 0.489 |
DOC_MAPK_NFAT4_5 | 29 | 37 | PF00069 | 0.496 |
DOC_MAPK_RevD_3 | 479 | 493 | PF00069 | 0.489 |
DOC_PP1_RVXF_1 | 137 | 144 | PF00149 | 0.475 |
DOC_PP1_RVXF_1 | 346 | 352 | PF00149 | 0.529 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.497 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.675 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.698 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.542 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 150 | 159 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 308 | 316 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 348 | 354 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 465 | 470 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.659 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.565 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.547 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.567 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.504 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.478 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.559 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.573 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.288 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.577 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.748 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.762 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.718 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.472 |
LIG_IRF3_LxIS_1 | 160 | 167 | PF10401 | 0.684 |
LIG_LIR_Apic_2 | 424 | 430 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 373 | 383 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 408 | 418 | PF02991 | 0.684 |
LIG_LIR_LC3C_4 | 366 | 371 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.555 |
LIG_MLH1_MIPbox_1 | 467 | 471 | PF16413 | 0.537 |
LIG_NRBOX | 480 | 486 | PF00104 | 0.516 |
LIG_PCNA_yPIPBox_3 | 139 | 152 | PF02747 | 0.617 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.540 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.412 |
LIG_Pex14_2 | 467 | 471 | PF04695 | 0.429 |
LIG_PTB_Apo_2 | 369 | 376 | PF02174 | 0.447 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.595 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.458 |
LIG_SH2_SRC | 391 | 394 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 325 | 329 | PF00017 | 0.628 |
LIG_SH2_STAT3 | 325 | 328 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.502 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 366 | 373 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 366 | 373 | PF11976 | 0.554 |
LIG_TRFH_1 | 351 | 355 | PF08558 | 0.437 |
LIG_TYR_ITIM | 136 | 141 | PF00017 | 0.592 |
LIG_TYR_ITIM | 484 | 489 | PF00017 | 0.536 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.539 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.697 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.750 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.739 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.733 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.786 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.577 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.595 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.677 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.701 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.744 |
MOD_Cter_Amidation | 489 | 492 | PF01082 | 0.544 |
MOD_Cter_Amidation | 78 | 81 | PF01082 | 0.498 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.641 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.742 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.736 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.785 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.550 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.651 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.669 |
MOD_GlcNHglycan | 449 | 453 | PF01048 | 0.727 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.733 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.685 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.708 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.698 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.668 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.434 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.640 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.676 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.760 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.557 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.679 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.722 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.641 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.529 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.561 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.617 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.532 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.612 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.709 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.573 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.687 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.566 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.502 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.747 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.570 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.409 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.530 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.527 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.700 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.619 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.421 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.614 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.430 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.617 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.565 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.741 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.715 |
MOD_SUMO_rev_2 | 178 | 185 | PF00179 | 0.663 |
TRG_DiLeu_BaEn_1 | 381 | 386 | PF01217 | 0.540 |
TRG_DiLeu_BaEn_4 | 387 | 393 | PF01217 | 0.589 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.560 |
TRG_NLS_MonoExtN_4 | 488 | 495 | PF00514 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 399 | 403 | PF00026 | 0.646 |
TRG_Pf-PMV_PEXEL_1 | 493 | 498 | PF00026 | 0.339 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBR0 | Leptomonas seymouri | 52% | 97% |
A0A1X0P6J4 | Trypanosomatidae | 23% | 100% |
A0A3S7X9M3 | Leishmania donovani | 93% | 100% |
A0A422P2R2 | Trypanosoma rangeli | 28% | 100% |
A4HMT7 | Leishmania braziliensis | 73% | 100% |
A4IBD8 | Leishmania infantum | 93% | 100% |
C9ZZ79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AF94 | Leishmania major | 92% | 100% |
V5BTJ6 | Trypanosoma cruzi | 28% | 100% |