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:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4QFT1
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 | 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:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005516 | calmodulin binding | 3 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.353 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.533 |
CLV_PCSK_PC7_1 | 10 | 16 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.515 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.643 |
DEG_SPOP_SBC_1 | 189 | 193 | PF00917 | 0.559 |
DEG_SPOP_SBC_1 | 445 | 449 | PF00917 | 0.748 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.336 |
DOC_MAPK_gen_1 | 204 | 213 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 306 | 315 | PF00069 | 0.625 |
DOC_MAPK_gen_1 | 333 | 341 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 398 | 407 | PF00069 | 0.635 |
DOC_MAPK_gen_1 | 421 | 429 | PF00069 | 0.647 |
DOC_MAPK_HePTP_8 | 201 | 213 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 160 | 168 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 204 | 213 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 21 | 28 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 400 | 409 | PF00069 | 0.638 |
DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.279 |
DOC_PP4_FxxP_1 | 120 | 123 | PF00568 | 0.334 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.652 |
DOC_USP7_UBL2_3 | 17 | 21 | PF12436 | 0.631 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.270 |
LIG_14-3-3_CanoR_1 | 117 | 123 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 160 | 165 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 306 | 315 | PF00244 | 0.574 |
LIG_Actin_WH2_2 | 41 | 58 | PF00022 | 0.537 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.552 |
LIG_CaM_IQ_9 | 310 | 326 | PF13499 | 0.595 |
LIG_CtBP_PxDLS_1 | 491 | 495 | PF00389 | 0.653 |
LIG_deltaCOP1_diTrp_1 | 233 | 239 | PF00928 | 0.265 |
LIG_EH1_1 | 126 | 134 | PF00400 | 0.449 |
LIG_EH1_1 | 289 | 297 | PF00400 | 0.647 |
LIG_EVH1_2 | 140 | 144 | PF00568 | 0.398 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.522 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.546 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.415 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.342 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.621 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.463 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.388 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.498 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.613 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.526 |
LIG_GBD_Chelix_1 | 64 | 72 | PF00786 | 0.355 |
LIG_LIR_Gen_1 | 122 | 133 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 139 | 150 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 177 | 185 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 22 | 33 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 268 | 277 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 278 | 285 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.673 |
LIG_LIR_Gen_1 | 403 | 414 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 403 | 409 | PF02991 | 0.520 |
LIG_MLH1_MIPbox_1 | 121 | 125 | PF16413 | 0.355 |
LIG_NRBOX | 340 | 346 | PF00104 | 0.581 |
LIG_Pex14_1 | 265 | 269 | PF04695 | 0.330 |
LIG_PTB_Apo_2 | 108 | 115 | PF02174 | 0.553 |
LIG_PTB_Apo_2 | 167 | 174 | PF02174 | 0.384 |
LIG_PTB_Apo_2 | 24 | 31 | PF02174 | 0.541 |
LIG_PTB_Apo_2 | 73 | 80 | PF02174 | 0.374 |
LIG_PTB_Phospho_1 | 167 | 173 | PF10480 | 0.399 |
LIG_PTB_Phospho_1 | 24 | 30 | PF10480 | 0.536 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.355 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.586 |
LIG_SH2_GRB2like | 167 | 170 | PF00017 | 0.448 |
LIG_SH2_GRB2like | 25 | 28 | PF00017 | 0.532 |
LIG_SH2_PTP2 | 25 | 28 | PF00017 | 0.608 |
LIG_SH2_SRC | 25 | 28 | PF00017 | 0.592 |
LIG_SH2_SRC | 30 | 33 | PF00017 | 0.622 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.612 |
LIG_SH3_1 | 324 | 330 | PF00018 | 0.656 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.657 |
LIG_SUMO_SIM_anti_2 | 425 | 431 | PF11976 | 0.665 |
LIG_SUMO_SIM_anti_2 | 43 | 49 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 337 | 342 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 67 | 73 | PF11976 | 0.404 |
LIG_TRAF2_1 | 29 | 32 | PF00917 | 0.635 |
LIG_TYR_ITIM | 245 | 250 | PF00017 | 0.330 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.487 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.538 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.387 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.244 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.526 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.530 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.586 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.437 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.540 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.517 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.569 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.363 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.683 |
MOD_Cter_Amidation | 12 | 15 | PF01082 | 0.557 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.487 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.483 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.388 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.406 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.522 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.614 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.612 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.503 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.475 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.463 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.536 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.679 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.589 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.469 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.399 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.424 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.657 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.388 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.630 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.386 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.405 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.349 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.379 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.512 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.423 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.553 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.612 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.684 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.672 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.308 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.404 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.393 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.419 |
MOD_PK_1 | 160 | 166 | PF00069 | 0.433 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.486 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.383 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.540 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.511 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.315 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.388 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.468 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.363 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.396 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.442 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.453 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.457 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.540 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.468 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.322 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.282 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.311 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.391 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.318 |
MOD_SUMO_rev_2 | 464 | 474 | PF00179 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 7 | 12 | PF01217 | 0.511 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 305 | 308 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.602 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4A8 | Leptomonas seymouri | 72% | 90% |
A0A0S4IWT9 | Bodo saltans | 30% | 94% |
A0A1X0NNP7 | Trypanosomatidae | 44% | 93% |
A0A3S7WSZ6 | Leishmania donovani | 95% | 100% |
A0A422NNK5 | Trypanosoma rangeli | 41% | 97% |
A4H7L2 | Leishmania braziliensis | 79% | 90% |
A4HVZ6 | Leishmania infantum | 95% | 100% |
E9APP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 90% |
V5BNC5 | Trypanosoma cruzi | 42% | 97% |