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:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: Q4QFT2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
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:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005516 | calmodulin binding | 3 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.304 |
CLV_C14_Caspase3-7 | 426 | 430 | PF00656 | 0.692 |
CLV_MEL_PAP_1 | 3 | 9 | PF00089 | 0.359 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.374 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.579 |
DEG_MDM2_SWIB_1 | 201 | 208 | PF02201 | 0.388 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.615 |
DEG_SCF_FBW7_1 | 369 | 376 | PF00400 | 0.734 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.682 |
DOC_CDC14_PxL_1 | 439 | 447 | PF14671 | 0.592 |
DOC_MAPK_gen_1 | 312 | 321 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 315 | 323 | PF00069 | 0.613 |
DOC_PP4_MxPP_1 | 128 | 131 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.722 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 160 | 167 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 247 | 254 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 398 | 404 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 494 | 502 | PF00244 | 0.727 |
LIG_Actin_WH2_2 | 258 | 275 | PF00022 | 0.196 |
LIG_Actin_WH2_2 | 356 | 372 | PF00022 | 0.634 |
LIG_APCC_ABBA_1 | 401 | 406 | PF00400 | 0.695 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.537 |
LIG_CaM_IQ_9 | 299 | 314 | PF13499 | 0.516 |
LIG_Clathr_ClatBox_1 | 30 | 34 | PF01394 | 0.632 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.608 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.286 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.559 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.630 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.799 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.636 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.582 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.330 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.557 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.646 |
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 | 136 | 147 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 151 | 158 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 320 | 328 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.703 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.702 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.518 |
LIG_MYND_3 | 442 | 446 | PF01753 | 0.683 |
LIG_Pex14_1 | 244 | 248 | PF04695 | 0.304 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.625 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.417 |
LIG_SH2_PTP2 | 152 | 155 | PF00017 | 0.347 |
LIG_SH2_SRC | 152 | 155 | PF00017 | 0.342 |
LIG_SH2_SRC | 220 | 223 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.639 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.710 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.744 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.580 |
LIG_SUMO_SIM_anti_2 | 478 | 485 | PF11976 | 0.645 |
LIG_SUMO_SIM_par_1 | 29 | 34 | PF11976 | 0.614 |
LIG_SUMO_SIM_par_1 | 74 | 79 | PF11976 | 0.329 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.261 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.327 |
MOD_CDK_SPK_2 | 373 | 378 | PF00069 | 0.709 |
MOD_CDK_SPK_2 | 388 | 393 | PF00069 | 0.684 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.517 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.532 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.612 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.582 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.509 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.667 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.680 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.691 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.754 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.653 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.251 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.572 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.730 |
MOD_Cter_Amidation | 396 | 399 | PF01082 | 0.525 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.581 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.539 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.475 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.662 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.465 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.511 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.651 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.572 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.509 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.658 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.718 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.685 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.652 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.703 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.706 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.722 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.667 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.591 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.465 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.528 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.291 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.299 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.552 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.506 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.548 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.744 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.780 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.614 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.664 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.264 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.320 |
MOD_NEK2_2 | 106 | 111 | PF00069 | 0.627 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.577 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.702 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.477 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.604 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.582 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.319 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.615 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.650 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.753 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.338 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.714 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.609 |
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 | 0.542 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.469 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.531 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.302 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.371 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.511 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.648 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.285 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.418 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.547 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.692 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.696 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.671 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.666 |
MOD_SUMO_for_1 | 311 | 314 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 400 | 409 | PF00179 | 0.687 |
TRG_DiLeu_BaEn_1 | 446 | 451 | PF01217 | 0.648 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.264 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 336 | 341 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 448 | 453 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3W7 | Leptomonas seymouri | 63% | 98% |
A0A0S4IWT9 | Bodo saltans | 31% | 95% |
A0A0S4IZM8 | Bodo saltans | 35% | 100% |
A0A1X0NNP7 | Trypanosomatidae | 28% | 94% |
A0A1X0NP80 | Trypanosomatidae | 38% | 100% |
A0A3Q8I9U0 | Leishmania donovani | 96% | 100% |
A0A422NNJ1 | Trypanosoma rangeli | 40% | 100% |
A0A422NNK5 | Trypanosoma rangeli | 31% | 98% |
A4H7L1 | Leishmania braziliensis | 76% | 100% |
A4HVZ5 | Leishmania infantum | 96% | 100% |
E9APP7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |