Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 15 |
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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005886 | plasma membrane | 3 | 3 |
Related structures:
AlphaFold database: A4HJV1
Term | Name | Level | Count |
---|---|---|---|
GO:0000041 | transition metal ion transport | 7 | 3 |
GO:0006810 | transport | 3 | 3 |
GO:0006811 | monoatomic ion transport | 4 | 3 |
GO:0006812 | monoatomic cation transport | 5 | 3 |
GO:0006829 | zinc ion transport | 8 | 3 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0006882 | intracellular zinc ion homeostasis | 7 | 1 |
GO:0009987 | cellular process | 1 | 3 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030001 | metal ion transport | 6 | 3 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 3 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0046916 | obsolete intracellular transition metal ion homeostasis | 7 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055069 | obsolete zinc ion homeostasis | 8 | 1 |
GO:0055076 | obsolete transition metal ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 3 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071577 | zinc ion transmembrane transport | 6 | 3 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 3 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 3 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 3 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 20 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 20 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 20 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 20 |
GO:0022857 | transmembrane transporter activity | 2 | 20 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 20 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 20 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 3 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 3 |
GO:0005381 | iron ion transmembrane transporter activity | 7 | 1 |
GO:0015093 | ferrous iron transmembrane transporter activity | 8 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.451 |
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.367 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.159 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.180 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.359 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.359 |
DEG_APCC_DBOX_1 | 301 | 309 | PF00400 | 0.435 |
DOC_MAPK_gen_1 | 300 | 309 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 380 | 389 | PF00069 | 0.468 |
DOC_MAPK_HePTP_8 | 383 | 395 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 275 | 283 | PF00069 | 0.273 |
DOC_MAPK_MEF2A_6 | 300 | 309 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 382 | 391 | PF00069 | 0.499 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.189 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.199 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.275 |
LIG_14-3-3_CanoR_1 | 244 | 253 | PF00244 | 0.463 |
LIG_Actin_WH2_2 | 193 | 210 | PF00022 | 0.359 |
LIG_BIR_III_4 | 189 | 193 | PF00653 | 0.519 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.307 |
LIG_CtBP_PxDLS_1 | 236 | 240 | PF00389 | 0.459 |
LIG_EH_1 | 43 | 47 | PF12763 | 0.370 |
LIG_eIF4E_1 | 357 | 363 | PF01652 | 0.319 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.209 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.179 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.487 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.261 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.347 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.192 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.340 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.282 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.397 |
LIG_GBD_Chelix_1 | 23 | 31 | PF00786 | 0.201 |
LIG_LIR_Gen_1 | 106 | 117 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 17 | 27 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 338 | 347 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 388 | 397 | PF02991 | 0.192 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.204 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.264 |
LIG_MLH1_MIPbox_1 | 6 | 10 | PF16413 | 0.277 |
LIG_NRBOX | 22 | 28 | PF00104 | 0.162 |
LIG_PDZ_Wminus1_1 | 405 | 407 | PF00595 | 0.420 |
LIG_Pex14_2 | 283 | 287 | PF04695 | 0.338 |
LIG_Pex14_2 | 390 | 394 | PF04695 | 0.309 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.359 |
LIG_SH2_PTP2 | 37 | 40 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.278 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.498 |
LIG_SUMO_SIM_anti_2 | 129 | 135 | PF11976 | 0.359 |
LIG_SUMO_SIM_anti_2 | 17 | 25 | PF11976 | 0.162 |
LIG_SUMO_SIM_anti_2 | 303 | 309 | PF11976 | 0.490 |
LIG_SUMO_SIM_anti_2 | 342 | 349 | PF11976 | 0.275 |
LIG_SUMO_SIM_anti_2 | 91 | 98 | PF11976 | 0.162 |
LIG_SUMO_SIM_par_1 | 129 | 135 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 17 | 25 | PF11976 | 0.180 |
LIG_SUMO_SIM_par_1 | 342 | 349 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 360 | 366 | PF11976 | 0.177 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.162 |
LIG_TYR_ITIM | 191 | 196 | PF00017 | 0.359 |
LIG_UBA3_1 | 174 | 179 | PF00899 | 0.359 |
MOD_CDK_SPxK_1 | 167 | 173 | PF00069 | 0.359 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.538 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.416 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.358 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.422 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.240 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.200 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.324 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.344 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.350 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.514 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.425 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.381 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.563 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.388 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.329 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.402 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.243 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.274 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.492 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.427 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.255 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.338 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.365 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.459 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.344 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.336 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.339 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.346 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.354 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.471 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.261 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.388 |
MOD_PK_1 | 161 | 167 | PF00069 | 0.394 |
MOD_PKA_1 | 385 | 391 | PF00069 | 0.393 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.401 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.466 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.362 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.374 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.356 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.319 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.286 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.230 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.453 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.275 |
MOD_SUMO_rev_2 | 271 | 277 | PF00179 | 0.290 |
MOD_SUMO_rev_2 | 294 | 301 | PF00179 | 0.325 |
TRG_DiLeu_LyEn_5 | 273 | 278 | PF01217 | 0.275 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.496 |
TRG_NES_CRM1_1 | 57 | 70 | PF08389 | 0.162 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.176 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E9 | Leptomonas seymouri | 41% | 100% |
A0A0N1PCU5 | Leptomonas seymouri | 55% | 95% |
A0A1X0NSI7 | Trypanosomatidae | 33% | 100% |
A0A3S7X1N7 | Leishmania donovani | 36% | 88% |
A0A3S7X501 | Leishmania donovani | 59% | 94% |
A4HGP7 | Leishmania braziliensis | 40% | 89% |
A4HJU9 | Leishmania braziliensis | 64% | 100% |
A4HJV0 | Leishmania braziliensis | 63% | 100% |
A4I3R9 | Leishmania infantum | 36% | 88% |
A4I7B1 | Leishmania infantum | 59% | 94% |
D0A885 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B012 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 90% |
E9B2A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 94% |
E9B2A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 94% |
O82643 | Arabidopsis thaliana | 24% | 100% |
O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
Q12436 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 96% |
Q4Q5V0 | Leishmania major | 57% | 100% |
Q4Q5V1 | Leishmania major | 57% | 100% |
Q4Q873 | Leishmania major | 36% | 100% |
V5DCU2 | Trypanosoma cruzi | 36% | 100% |