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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9APP7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 13 |
GO:0005216 | monoatomic ion channel activity | 4 | 13 |
GO:0005227 | calcium activated cation channel activity | 6 | 13 |
GO:0005261 | monoatomic cation channel activity | 5 | 13 |
GO:0005267 | potassium channel activity | 6 | 13 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 13 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 13 |
GO:0015079 | potassium ion transmembrane transporter activity | 6 | 13 |
GO:0015267 | channel activity | 4 | 13 |
GO:0015269 | calcium-activated potassium channel activity | 7 | 13 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 13 |
GO:0016286 | small conductance calcium-activated potassium channel activity | 8 | 13 |
GO:0022803 | passive transmembrane transporter activity | 3 | 13 |
GO:0022836 | gated channel activity | 5 | 13 |
GO:0022839 | monoatomic ion gated channel activity | 6 | 13 |
GO:0022857 | transmembrane transporter activity | 2 | 13 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 13 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 13 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.304 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.395 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.534 |
DEG_MDM2_SWIB_1 | 201 | 208 | PF02201 | 0.388 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.624 |
DEG_SCF_FBW7_1 | 369 | 376 | PF00400 | 0.734 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.677 |
DEG_SPOP_SBC_1 | 435 | 439 | PF00917 | 0.721 |
DOC_MAPK_gen_1 | 312 | 321 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 41 | 49 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 315 | 323 | PF00069 | 0.613 |
DOC_PP4_MxPP_1 | 128 | 131 | PF00568 | 0.500 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.282 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.706 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 160 | 167 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 247 | 254 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 398 | 404 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 494 | 502 | PF00244 | 0.728 |
LIG_Actin_WH2_2 | 356 | 372 | PF00022 | 0.633 |
LIG_APCC_ABBA_1 | 401 | 406 | PF00400 | 0.697 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.539 |
LIG_CaM_IQ_9 | 299 | 314 | PF13499 | 0.516 |
LIG_Clathr_ClatBox_1 | 30 | 34 | PF01394 | 0.634 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.609 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.284 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.560 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.625 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.788 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.610 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.604 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.292 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.555 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.620 |
LIG_GBD_Chelix_1 | 202 | 210 | PF00786 | 0.400 |
LIG_GBD_Chelix_1 | 70 | 78 | PF00786 | 0.376 |
LIG_LIR_Gen_1 | 112 | 122 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 144 | 154 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 320 | 328 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.703 |
LIG_MYND_3 | 442 | 446 | PF01753 | 0.691 |
LIG_Pex14_1 | 244 | 248 | PF04695 | 0.304 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.622 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.448 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.157 |
LIG_SH2_PTP2 | 152 | 155 | PF00017 | 0.310 |
LIG_SH2_SRC | 152 | 155 | PF00017 | 0.342 |
LIG_SH2_SRC | 220 | 223 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.630 |
LIG_SH3_1 | 413 | 419 | PF00018 | 0.578 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.610 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.706 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.746 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.755 |
LIG_SUMO_SIM_anti_2 | 478 | 485 | PF11976 | 0.644 |
LIG_SUMO_SIM_par_1 | 29 | 34 | PF11976 | 0.618 |
LIG_SUMO_SIM_par_1 | 74 | 79 | PF11976 | 0.294 |
LIG_TRAF2_1 | 421 | 424 | PF00917 | 0.626 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.261 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.327 |
MOD_CDK_SPK_2 | 373 | 378 | PF00069 | 0.707 |
MOD_CDK_SPK_2 | 408 | 413 | PF00069 | 0.660 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.516 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.523 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.613 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.574 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.502 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.670 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.673 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.693 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.723 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.655 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.251 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.571 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.707 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.558 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.524 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.477 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.643 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.398 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.345 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.512 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.647 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.577 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.650 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.683 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.608 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.710 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.695 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.706 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.742 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.662 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.593 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.277 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.441 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.518 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.271 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.187 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.546 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.507 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.549 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.765 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.606 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.379 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.279 |
MOD_NEK2_2 | 106 | 111 | PF00069 | 0.620 |
MOD_NEK2_2 | 55 | 60 | PF00069 | 0.340 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.577 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.704 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.608 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.545 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.319 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.612 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.654 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.749 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.348 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.338 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.621 |
MOD_Plk_2-3 | 216 | 222 | PF00069 | 0.261 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.326 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.322 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.543 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.467 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.519 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.289 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.344 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.517 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.648 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.271 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.418 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.616 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.547 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.689 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.680 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.668 |
MOD_SUMO_for_1 | 311 | 314 | PF00179 | 0.529 |
MOD_SUMO_for_1 | 343 | 346 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 400 | 409 | PF00179 | 0.669 |
TRG_DiLeu_BaEn_1 | 446 | 451 | PF01217 | 0.656 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.264 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 336 | 341 | PF00026 | 0.328 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3W7 | Leptomonas seymouri | 62% | 98% |
A0A0S4IWT9 | Bodo saltans | 31% | 95% |
A0A0S4IZM8 | Bodo saltans | 35% | 100% |
A0A1X0NNP7 | Trypanosomatidae | 28% | 94% |
A0A1X0NP80 | Trypanosomatidae | 40% | 100% |
A0A3Q8I9U0 | Leishmania donovani | 90% | 100% |
A0A422NNJ1 | Trypanosoma rangeli | 41% | 100% |
A0A422NNK5 | Trypanosoma rangeli | 31% | 98% |
A4H7L1 | Leishmania braziliensis | 74% | 100% |
A4HVZ5 | Leishmania infantum | 90% | 100% |
Q4QFT2 | Leishmania major | 90% | 100% |