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 |
Related structures:
AlphaFold database: A0A3Q8IRH8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.781 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.773 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.826 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.765 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.559 |
CLV_PCSK_FUR_1 | 217 | 221 | PF00082 | 0.708 |
CLV_PCSK_FUR_1 | 269 | 273 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.826 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.670 |
CLV_PCSK_PC7_1 | 296 | 302 | PF00082 | 0.696 |
CLV_PCSK_PC7_1 | 389 | 395 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.552 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.696 |
DOC_CYCLIN_RxL_1 | 88 | 98 | PF00134 | 0.580 |
DOC_MAPK_DCC_7 | 37 | 46 | PF00069 | 0.750 |
DOC_MAPK_gen_1 | 243 | 253 | PF00069 | 0.591 |
DOC_MAPK_gen_1 | 269 | 276 | PF00069 | 0.660 |
DOC_MAPK_gen_1 | 404 | 412 | PF00069 | 0.628 |
DOC_MAPK_MEF2A_6 | 190 | 199 | PF00069 | 0.721 |
DOC_MAPK_MEF2A_6 | 246 | 255 | PF00069 | 0.620 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.750 |
DOC_MAPK_MEF2A_6 | 92 | 99 | PF00069 | 0.558 |
DOC_MAPK_NFAT4_5 | 248 | 256 | PF00069 | 0.583 |
DOC_PP1_RVXF_1 | 255 | 261 | PF00149 | 0.506 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.688 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.805 |
DOC_USP7_UBL2_3 | 282 | 286 | PF12436 | 0.687 |
DOC_USP7_UBL2_3 | 381 | 385 | PF12436 | 0.725 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 311 | 320 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 43 | 52 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 96 | 100 | PF00244 | 0.669 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.612 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.544 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.544 |
LIG_BIR_III_4 | 330 | 334 | PF00653 | 0.711 |
LIG_eIF4E_1 | 236 | 242 | PF01652 | 0.496 |
LIG_FAT_LD_1 | 128 | 136 | PF03623 | 0.564 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.699 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.759 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.747 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.562 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.571 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.649 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.741 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.716 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.748 |
LIG_IRF3_LxIS_1 | 197 | 204 | PF10401 | 0.657 |
LIG_LIR_Apic_2 | 353 | 359 | PF02991 | 0.695 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.512 |
LIG_MAD2 | 16 | 24 | PF02301 | 0.707 |
LIG_MYND_2 | 4 | 8 | PF01753 | 0.544 |
LIG_NRBOX | 90 | 96 | PF00104 | 0.663 |
LIG_Pex14_2 | 412 | 416 | PF04695 | 0.571 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.639 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.657 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.766 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.671 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.790 |
LIG_SH3_4 | 381 | 388 | PF00018 | 0.727 |
LIG_SUMO_SIM_anti_2 | 168 | 174 | PF11976 | 0.635 |
LIG_SUMO_SIM_par_1 | 192 | 198 | PF11976 | 0.674 |
LIG_SUMO_SIM_par_1 | 199 | 205 | PF11976 | 0.663 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.766 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.762 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.734 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.686 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.728 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.776 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.765 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.748 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.744 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.733 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.730 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.768 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.805 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.558 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.760 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.710 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.709 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.816 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.749 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.787 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.618 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.637 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.669 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.655 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.672 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.714 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.658 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.795 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.508 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.728 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.632 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.507 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.790 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.692 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.683 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.611 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.653 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.843 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.607 |
MOD_PKA_1 | 368 | 374 | PF00069 | 0.640 |
MOD_PKA_1 | 389 | 395 | PF00069 | 0.735 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.810 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.720 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.772 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.527 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.723 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.853 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.765 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.667 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.741 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.649 |
MOD_Plk_2-3 | 111 | 117 | PF00069 | 0.777 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.777 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.760 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.631 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.762 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.683 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.693 |
TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.749 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 269 | 272 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.731 |
TRG_NLS_Bipartite_1 | 271 | 287 | PF00514 | 0.599 |
TRG_NLS_Bipartite_1 | 368 | 384 | PF00514 | 0.633 |
TRG_NLS_MonoCore_2 | 281 | 286 | PF00514 | 0.627 |
TRG_NLS_MonoCore_2 | 379 | 384 | PF00514 | 0.725 |
TRG_NLS_MonoExtC_3 | 281 | 286 | PF00514 | 0.725 |
TRG_NLS_MonoExtN_4 | 282 | 287 | PF00514 | 0.723 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCW7 | Leptomonas seymouri | 29% | 100% |
A4HHK6 | Leishmania braziliensis | 54% | 95% |
A4I4R7 | Leishmania infantum | 100% | 100% |
E9AE69 | Leishmania major | 84% | 100% |
E9ALL6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |