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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9APP8
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 | 11 |
GO:0005216 | monoatomic ion channel activity | 4 | 11 |
GO:0005227 | calcium activated cation channel activity | 6 | 11 |
GO:0005261 | monoatomic cation channel activity | 5 | 11 |
GO:0005267 | potassium channel activity | 6 | 11 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 11 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 11 |
GO:0015079 | potassium ion transmembrane transporter activity | 6 | 11 |
GO:0015267 | channel activity | 4 | 11 |
GO:0015269 | calcium-activated potassium channel activity | 7 | 11 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 11 |
GO:0016286 | small conductance calcium-activated potassium channel activity | 8 | 11 |
GO:0022803 | passive transmembrane transporter activity | 3 | 11 |
GO:0022836 | gated channel activity | 5 | 11 |
GO:0022839 | monoatomic ion gated channel activity | 6 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 11 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 11 |
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 | 285 | 289 | PF00656 | 0.334 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.499 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.536 |
CLV_PCSK_PC7_1 | 65 | 71 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.440 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.586 |
DEG_SPOP_SBC_1 | 500 | 504 | PF00917 | 0.758 |
DOC_CKS1_1 | 192 | 197 | PF01111 | 0.360 |
DOC_MAPK_gen_1 | 259 | 268 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 361 | 370 | PF00069 | 0.626 |
DOC_MAPK_gen_1 | 388 | 396 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 453 | 462 | PF00069 | 0.691 |
DOC_MAPK_HePTP_8 | 256 | 268 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 215 | 223 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 259 | 268 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 455 | 464 | PF00069 | 0.686 |
DOC_MAPK_MEF2A_6 | 76 | 83 | PF00069 | 0.626 |
DOC_PP1_RVXF_1 | 311 | 318 | PF00149 | 0.296 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.358 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.660 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.681 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.283 |
LIG_14-3-3_CanoR_1 | 172 | 178 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 235 | 244 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 261 | 267 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 28 | 32 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 361 | 370 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 48 | 56 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 530 | 538 | PF00244 | 0.632 |
LIG_Actin_WH2_2 | 96 | 113 | PF00022 | 0.556 |
LIG_APCC_ABBAyCdc20_2 | 76 | 82 | PF00400 | 0.594 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.580 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.408 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.579 |
LIG_CaM_IQ_9 | 365 | 381 | PF13499 | 0.588 |
LIG_CtBP_PxDLS_1 | 546 | 550 | PF00389 | 0.689 |
LIG_deltaCOP1_diTrp_1 | 288 | 294 | PF00928 | 0.283 |
LIG_EH1_1 | 181 | 189 | PF00400 | 0.481 |
LIG_EH1_1 | 344 | 352 | PF00400 | 0.664 |
LIG_EH1_1 | 476 | 484 | PF00400 | 0.499 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.345 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.419 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.480 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.559 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.460 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.353 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.601 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.531 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.670 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.622 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.539 |
LIG_KLC1_Yacidic_2 | 77 | 82 | PF13176 | 0.613 |
LIG_LIR_Gen_1 | 177 | 188 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 293 | 302 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 323 | 332 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 333 | 340 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 51 | 60 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 77 | 88 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.643 |
LIG_NRBOX | 395 | 401 | PF00104 | 0.584 |
LIG_Pex14_1 | 320 | 324 | PF04695 | 0.345 |
LIG_Pex14_2 | 13 | 17 | PF04695 | 0.584 |
LIG_PTB_Apo_2 | 163 | 170 | PF02174 | 0.588 |
LIG_PTB_Apo_2 | 222 | 229 | PF02174 | 0.400 |
LIG_PTB_Phospho_1 | 222 | 228 | PF10480 | 0.432 |
LIG_SH2_CRK | 217 | 221 | PF00017 | 0.378 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.597 |
LIG_SH2_GRB2like | 222 | 225 | PF00017 | 0.475 |
LIG_SH2_PTP2 | 204 | 207 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 80 | 83 | PF00017 | 0.661 |
LIG_SH2_SRC | 80 | 83 | PF00017 | 0.646 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.645 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 392 | 396 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.644 |
LIG_SH3_1 | 379 | 385 | PF00018 | 0.668 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.443 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.668 |
LIG_SUMO_SIM_anti_2 | 480 | 486 | PF11976 | 0.700 |
LIG_SUMO_SIM_anti_2 | 98 | 104 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 115 | 120 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 122 | 128 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 392 | 397 | PF11976 | 0.621 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.336 |
LIG_UBA3_1 | 123 | 131 | PF00899 | 0.186 |
LIG_UBA3_1 | 148 | 153 | PF00899 | 0.378 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.420 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.447 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.569 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.537 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.397 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.326 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.524 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.422 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.584 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.594 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.782 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.592 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.655 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.354 |
MOD_Cter_Amidation | 67 | 70 | PF01082 | 0.619 |
MOD_DYRK1A_RPxSP_1 | 28 | 32 | PF00069 | 0.563 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.532 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.504 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.512 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.408 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.434 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.539 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.612 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.645 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.662 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.487 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.481 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.474 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.679 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.634 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.408 |
MOD_N-GLC_1 | 282 | 287 | PF02516 | 0.407 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.567 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.489 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.323 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.500 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.329 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.411 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.388 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.348 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.394 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.493 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.426 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.279 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.655 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.702 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.750 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.635 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.435 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.407 |
MOD_PK_1 | 215 | 221 | PF00069 | 0.447 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.564 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.741 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.507 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.575 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.512 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.537 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.342 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.435 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.441 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.545 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.477 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.339 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.280 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.390 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.489 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.247 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.403 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.424 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.418 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.579 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.598 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.320 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.409 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.690 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.336 |
MOD_SUMO_rev_2 | 519 | 529 | PF00179 | 0.635 |
TRG_DiLeu_BaEn_1 | 480 | 485 | PF01217 | 0.369 |
TRG_DiLeu_BaLyEn_6 | 62 | 67 | PF01217 | 0.579 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 360 | 363 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.629 |
TRG_NLS_MonoCore_2 | 46 | 51 | PF00514 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 419 | 423 | PF00026 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4A8 | Leptomonas seymouri | 65% | 100% |
A0A0S4IWT9 | Bodo saltans | 34% | 100% |
A0A1X0NNP7 | Trypanosomatidae | 41% | 100% |
A0A3S7WSZ6 | Leishmania donovani | 92% | 100% |
A0A422NNK5 | Trypanosoma rangeli | 40% | 100% |
A4H7L2 | Leishmania braziliensis | 77% | 100% |
A4HVZ6 | Leishmania infantum | 92% | 100% |
Q4QFT1 | Leishmania major | 93% | 100% |
V5BNC5 | Trypanosoma cruzi | 41% | 100% |