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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005774 | vacuolar membrane | 5 | 7 |
GO:0016020 | membrane | 2 | 8 |
GO:0031090 | organelle membrane | 3 | 7 |
GO:0098588 | bounding membrane of organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: Q4QFV8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006812 | monoatomic cation transport | 5 | 2 |
GO:0006816 | calcium ion transport | 7 | 2 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 2 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 2 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019725 | cellular homeostasis | 2 | 2 |
GO:0030001 | metal ion transport | 6 | 2 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0042592 | homeostatic process | 3 | 2 |
GO:0048878 | chemical homeostasis | 4 | 2 |
GO:0050801 | monoatomic ion homeostasis | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 2 |
GO:0055074 | calcium ion homeostasis | 8 | 2 |
GO:0055080 | monoatomic cation homeostasis | 6 | 2 |
GO:0055082 | intracellular chemical homeostasis | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0070588 | calcium ion transmembrane transport | 6 | 2 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 2 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 2 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 2 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 2 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 2 |
GO:0098771 | inorganic ion homeostasis | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 8 |
GO:0005451 | obsolete monoatomic cation:proton antiporter activity | 5 | 4 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 8 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 8 |
GO:0015078 | proton transmembrane transporter activity | 5 | 4 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 4 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 4 |
GO:0015297 | antiporter activity | 5 | 4 |
GO:0015298 | obsolete solute:monoatomic cation antiporter activity | 5 | 4 |
GO:0015299 | obsolete solute:proton antiporter activity | 6 | 4 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 4 |
GO:0015368 | calcium:monoatomic cation antiporter activity | 7 | 4 |
GO:0015369 | calcium:proton antiporter activity | 8 | 4 |
GO:0022804 | active transmembrane transporter activity | 3 | 4 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 4 |
GO:0022857 | transmembrane transporter activity | 2 | 8 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 4 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 4 |
GO:0051139 | metal cation:proton antiporter activity | 7 | 4 |
GO:0140828 | metal cation:monoatomic cation antiporter activity | 6 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.754 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.686 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.686 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.389 |
CLV_Separin_Metazoa | 316 | 320 | PF03568 | 0.512 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.723 |
DOC_CDC14_PxL_1 | 413 | 421 | PF14671 | 0.460 |
DOC_CKS1_1 | 251 | 256 | PF01111 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 427 | 433 | PF00134 | 0.345 |
DOC_CYCLIN_yCln2_LP_2 | 79 | 85 | PF00134 | 0.346 |
DOC_MAPK_MEF2A_6 | 139 | 147 | PF00069 | 0.610 |
DOC_MAPK_MEF2A_6 | 361 | 370 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 74 | 83 | PF00069 | 0.327 |
DOC_MAPK_NFAT4_5 | 74 | 82 | PF00069 | 0.264 |
DOC_PP1_RVXF_1 | 169 | 176 | PF00149 | 0.338 |
DOC_PP1_RVXF_1 | 456 | 462 | PF00149 | 0.596 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.410 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.475 |
DOC_PP2B_LxvP_1 | 427 | 430 | PF13499 | 0.395 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.346 |
DOC_PP2B_PxIxI_1 | 368 | 374 | PF00149 | 0.260 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.362 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.362 |
DOC_SPAK_OSR1_1 | 333 | 337 | PF12202 | 0.460 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.187 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.528 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.375 |
LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 33 | 42 | PF00244 | 0.570 |
LIG_Actin_WH2_2 | 305 | 321 | PF00022 | 0.635 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.565 |
LIG_CAP-Gly_1 | 490 | 494 | PF01302 | 0.384 |
LIG_CSL_BTD_1 | 79 | 82 | PF09270 | 0.435 |
LIG_CtBP_PxDLS_1 | 305 | 309 | PF00389 | 0.483 |
LIG_CtBP_PxDLS_1 | 430 | 434 | PF00389 | 0.364 |
LIG_eIF4E_1 | 72 | 78 | PF01652 | 0.260 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.397 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.727 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.659 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.391 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.331 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.479 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.384 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.595 |
LIG_IRF3_LxIS_1 | 207 | 212 | PF10401 | 0.591 |
LIG_LIR_Apic_2 | 172 | 178 | PF02991 | 0.358 |
LIG_LIR_Apic_2 | 226 | 232 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 158 | 167 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 331 | 341 | PF02991 | 0.531 |
LIG_LIR_LC3C_4 | 135 | 138 | PF02991 | 0.574 |
LIG_LIR_LC3C_4 | 446 | 450 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.681 |
LIG_NRBOX | 184 | 190 | PF00104 | 0.460 |
LIG_PCNA_yPIPBox_3 | 126 | 139 | PF02747 | 0.417 |
LIG_RPA_C_Fungi | 266 | 278 | PF08784 | 0.341 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.410 |
LIG_SH2_CRK | 412 | 416 | PF00017 | 0.476 |
LIG_SH2_CRK | 471 | 475 | PF00017 | 0.362 |
LIG_SH2_GRB2like | 132 | 135 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 330 | 334 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 471 | 475 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 310 | 313 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.436 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.460 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.570 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.532 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.381 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.701 |
LIG_SUMO_SIM_anti_2 | 236 | 241 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 119 | 125 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 126 | 131 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 351 | 356 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 429 | 434 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 85 | 90 | PF11976 | 0.302 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.340 |
MOD_CDK_SPxK_1 | 250 | 256 | PF00069 | 0.467 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.479 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.694 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.449 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.646 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.614 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.503 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.600 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.465 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.672 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.669 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.663 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.707 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.720 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.704 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.394 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.520 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.663 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.707 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.303 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.410 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.371 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.332 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.305 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.333 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.329 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.723 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.418 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.495 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.333 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.525 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.568 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.423 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.568 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.725 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.276 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.454 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.460 |
MOD_Plk_2-3 | 203 | 209 | PF00069 | 0.499 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.344 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.373 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.348 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.387 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.320 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.442 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.723 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.493 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.389 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.452 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.213 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.410 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.420 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.577 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.467 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.598 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.724 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.375 |
TRG_DiLeu_BaEn_1 | 463 | 468 | PF01217 | 0.341 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.329 |
TRG_ER_diArg_1 | 248 | 250 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 458 | 461 | PF00400 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 460 | 465 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT55 | Leptomonas seymouri | 61% | 100% |
A0A0S4J0Y4 | Bodo saltans | 28% | 100% |
A0A1X0NNQ4 | Trypanosomatidae | 34% | 100% |
A0A3Q8ID24 | Leishmania donovani | 93% | 100% |
A4HVW9 | Leishmania infantum | 93% | 100% |
E9APM0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
O59768 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q39253 | Arabidopsis thaliana | 23% | 100% |
Q39254 | Arabidopsis thaliana | 24% | 100% |
Q5KQN0 | Oryza sativa subsp. japonica | 24% | 100% |
Q6K1C4 | Oryza sativa subsp. japonica | 25% | 100% |
Q75XW3 | Aphanothece halophytica | 26% | 100% |
Q945S5 | Arabidopsis thaliana | 22% | 100% |