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: A0A3S7X9M3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.620 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.736 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.736 |
CLV_PCSK_PC1ET2_1 | 491 | 493 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.455 |
DEG_APCC_DBOX_1 | 293 | 301 | PF00400 | 0.576 |
DEG_APCC_DBOX_1 | 349 | 357 | PF00400 | 0.580 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.448 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.645 |
DEG_SCF_FBW7_1 | 59 | 66 | PF00400 | 0.638 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.686 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.783 |
DEG_SPOP_SBC_1 | 74 | 78 | PF00917 | 0.705 |
DOC_CYCLIN_RxL_1 | 136 | 146 | PF00134 | 0.550 |
DOC_MAPK_gen_1 | 137 | 144 | PF00069 | 0.585 |
DOC_MAPK_RevD_3 | 479 | 493 | PF00069 | 0.489 |
DOC_PP1_RVXF_1 | 137 | 144 | PF00149 | 0.473 |
DOC_PP1_RVXF_1 | 346 | 352 | PF00149 | 0.528 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.655 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.831 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.722 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 150 | 159 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 348 | 354 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 465 | 470 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.666 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.569 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.547 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.560 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.500 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.574 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.571 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.292 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.741 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.791 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.557 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.739 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.497 |
LIG_IRF3_LxIS_1 | 160 | 167 | PF10401 | 0.695 |
LIG_LIR_Apic_2 | 424 | 430 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 373 | 383 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 408 | 418 | PF02991 | 0.686 |
LIG_LIR_LC3C_4 | 367 | 371 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.582 |
LIG_MLH1_MIPbox_1 | 467 | 471 | PF16413 | 0.537 |
LIG_NRBOX | 480 | 486 | PF00104 | 0.521 |
LIG_PCNA_yPIPBox_3 | 139 | 152 | PF02747 | 0.615 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.545 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.630 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.408 |
LIG_Pex14_2 | 467 | 471 | PF04695 | 0.445 |
LIG_PTB_Apo_2 | 369 | 376 | PF02174 | 0.443 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.592 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.488 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.445 |
LIG_SH2_SRC | 391 | 394 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 325 | 329 | PF00017 | 0.627 |
LIG_SH2_STAT3 | 325 | 328 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.505 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.480 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 364 | 370 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 367 | 373 | PF11976 | 0.549 |
LIG_TRAF2_1 | 117 | 120 | PF00917 | 0.447 |
LIG_TRFH_1 | 351 | 355 | PF08558 | 0.447 |
LIG_TYR_ITIM | 136 | 141 | PF00017 | 0.588 |
LIG_TYR_ITIM | 484 | 489 | PF00017 | 0.535 |
MOD_CDK_SPK_2 | 70 | 75 | PF00069 | 0.704 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.530 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.675 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.809 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.735 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.743 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.789 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.510 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.591 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.595 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.683 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.697 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.759 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.363 |
MOD_Cter_Amidation | 489 | 492 | PF01082 | 0.536 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.629 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.727 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.712 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.796 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.608 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.577 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.625 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.658 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.729 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.697 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.730 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.755 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.756 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.442 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.646 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.670 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.773 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.549 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.683 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.738 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.656 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.700 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.537 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.561 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.628 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.727 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.533 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.607 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.694 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.564 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.674 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.750 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.510 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.739 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.559 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.535 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.710 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.612 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.428 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.770 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.613 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.437 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.570 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.690 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.731 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.688 |
MOD_SUMO_rev_2 | 178 | 185 | PF00179 | 0.658 |
TRG_DiLeu_BaEn_1 | 381 | 386 | PF01217 | 0.541 |
TRG_DiLeu_BaEn_4 | 387 | 393 | PF01217 | 0.578 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.453 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.553 |
TRG_NLS_MonoExtN_4 | 488 | 495 | PF00514 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 399 | 403 | PF00026 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBR0 | Leptomonas seymouri | 51% | 97% |
A0A1X0P6J4 | Trypanosomatidae | 24% | 100% |
A0A422P2R2 | Trypanosoma rangeli | 27% | 100% |
A4HMT7 | Leishmania braziliensis | 75% | 100% |
A4IBD8 | Leishmania infantum | 99% | 100% |
C9ZZ79 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AF94 | Leishmania major | 93% | 100% |
E9B6E9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BTJ6 | Trypanosoma cruzi | 30% | 100% |