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: 1, no: 3 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9APP9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 295 | 299 | PF00656 | 0.456 |
CLV_C14_Caspase3-7 | 451 | 455 | PF00656 | 0.637 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.356 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.644 |
DEG_SCF_FBW7_1 | 15 | 22 | PF00400 | 0.641 |
DOC_ANK_TNKS_1 | 449 | 456 | PF00023 | 0.640 |
DOC_CYCLIN_RxL_1 | 403 | 417 | PF00134 | 0.641 |
DOC_CYCLIN_yCln2_LP_2 | 37 | 43 | PF00134 | 0.587 |
DOC_MAPK_gen_1 | 407 | 416 | PF00069 | 0.640 |
DOC_MAPK_HePTP_8 | 108 | 120 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 111 | 120 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 409 | 418 | PF00069 | 0.637 |
DOC_PP1_RVXF_1 | 273 | 280 | PF00149 | 0.369 |
DOC_PP1_RVXF_1 | 60 | 66 | PF00149 | 0.613 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.451 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.640 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 266 | 270 | PF00244 | 0.482 |
LIG_Actin_WH2_2 | 253 | 268 | PF00022 | 0.466 |
LIG_APCC_ABBA_1 | 65 | 70 | PF00400 | 0.609 |
LIG_BIR_III_4 | 319 | 323 | PF00653 | 0.464 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.598 |
LIG_Clathr_ClatBox_1 | 413 | 417 | PF01394 | 0.631 |
LIG_deltaCOP1_diTrp_1 | 323 | 326 | PF00928 | 0.448 |
LIG_EVH1_2 | 28 | 32 | PF00568 | 0.602 |
LIG_FAT_LD_1 | 381 | 389 | PF03623 | 0.356 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.386 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.449 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.311 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.307 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.643 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.443 |
LIG_GBD_Chelix_1 | 195 | 203 | PF00786 | 0.631 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.613 |
LIG_LYPXL_yS_3 | 183 | 186 | PF13949 | 0.442 |
LIG_NRBOX | 115 | 121 | PF00104 | 0.337 |
LIG_NRBOX | 383 | 389 | PF00104 | 0.356 |
LIG_Pex14_2 | 288 | 292 | PF04695 | 0.448 |
LIG_Pex14_2 | 81 | 85 | PF04695 | 0.614 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.312 |
LIG_SH2_GRB2like | 289 | 292 | PF00017 | 0.411 |
LIG_SH2_SRC | 296 | 299 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.633 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.650 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.610 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.356 |
LIG_Sin3_3 | 115 | 122 | PF02671 | 0.308 |
LIG_SUMO_SIM_anti_2 | 382 | 389 | PF11976 | 0.415 |
LIG_SUMO_SIM_anti_2 | 415 | 420 | PF11976 | 0.628 |
LIG_SUMO_SIM_par_1 | 412 | 417 | PF11976 | 0.637 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.654 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.602 |
LIG_TYR_ITSM | 179 | 186 | PF00017 | 0.450 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.636 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.518 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.564 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.401 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.373 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.485 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.593 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.514 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.701 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.602 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.768 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.672 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.595 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.560 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.717 |
MOD_GlcNHglycan | 424 | 428 | PF01048 | 0.482 |
MOD_GlcNHglycan | 438 | 443 | PF01048 | 0.517 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.400 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.520 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.641 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.450 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.379 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.468 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.412 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.373 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.513 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.748 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.762 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.649 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.662 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.605 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.710 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.598 |
MOD_N-GLC_1 | 444 | 449 | PF02516 | 0.438 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.403 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.523 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.502 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.473 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.372 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.714 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.490 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.484 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.525 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.666 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.605 |
MOD_NEK2_2 | 161 | 166 | PF00069 | 0.439 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.470 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.365 |
MOD_PIKK_1 | 362 | 368 | PF00454 | 0.486 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.698 |
MOD_PK_1 | 49 | 55 | PF00069 | 0.602 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.616 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.473 |
MOD_PKB_1 | 446 | 454 | PF00069 | 0.724 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.452 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.604 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.443 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.440 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.391 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.376 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.719 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.460 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.282 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.604 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.437 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.639 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.639 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.409 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.456 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.617 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.615 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I9R5 | Leishmania donovani | 89% | 100% |
A4HVZ7 | Leishmania infantum | 90% | 100% |
Q4QFT0 | Leishmania major | 76% | 100% |