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: 30 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 5 |
GO:0016020 | membrane | 2 | 31 |
GO:0110165 | cellular anatomical entity | 1 | 31 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: Q4Q5V1
Term | Name | Level | Count |
---|---|---|---|
GO:0000041 | transition metal ion transport | 7 | 5 |
GO:0006810 | transport | 3 | 5 |
GO:0006811 | monoatomic ion transport | 4 | 5 |
GO:0006812 | monoatomic cation transport | 5 | 5 |
GO:0006829 | zinc ion transport | 8 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0030001 | metal ion transport | 6 | 5 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 5 |
GO:0051179 | localization | 1 | 5 |
GO:0051234 | establishment of localization | 2 | 5 |
GO:0055085 | transmembrane transport | 2 | 5 |
GO:0071577 | zinc ion transmembrane transport | 6 | 5 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 5 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 5 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 5 |
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:0019725 | cellular homeostasis | 2 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
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: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:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 31 |
GO:0005381 | iron ion transmembrane transporter activity | 7 | 2 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 5 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 31 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 31 |
GO:0015093 | ferrous iron transmembrane transporter activity | 8 | 2 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 31 |
GO:0022857 | transmembrane transporter activity | 2 | 31 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 31 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 31 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.432 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.338 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.288 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 340 | 346 | PF00134 | 0.311 |
DOC_MAPK_DCC_7 | 294 | 304 | PF00069 | 0.221 |
DOC_MAPK_gen_1 | 405 | 414 | PF00069 | 0.463 |
DOC_MAPK_HePTP_8 | 322 | 334 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 300 | 308 | PF00069 | 0.243 |
DOC_MAPK_MEF2A_6 | 325 | 334 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 407 | 416 | PF00069 | 0.480 |
DOC_MAPK_RevD_3 | 280 | 295 | PF00069 | 0.222 |
DOC_PP1_RVXF_1 | 128 | 135 | PF00149 | 0.177 |
DOC_PP1_RVXF_1 | 409 | 416 | PF00149 | 0.516 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.384 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.447 |
DOC_USP7_UBL2_3 | 160 | 164 | PF12436 | 0.549 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.405 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.249 |
LIG_14-3-3_CanoR_1 | 206 | 215 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 268 | 278 | PF00244 | 0.451 |
LIG_eIF4E_1 | 133 | 139 | PF01652 | 0.323 |
LIG_eIF4E_1 | 382 | 388 | PF01652 | 0.303 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.380 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.408 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.358 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.411 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.559 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.336 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.350 |
LIG_GBD_Chelix_1 | 139 | 147 | PF00786 | 0.304 |
LIG_GBD_Chelix_1 | 332 | 340 | PF00786 | 0.300 |
LIG_LIR_Gen_1 | 363 | 372 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.338 |
LIG_LYPXL_yS_3 | 86 | 89 | PF13949 | 0.421 |
LIG_PDZ_Wminus1_1 | 430 | 432 | PF00595 | 0.461 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.368 |
LIG_Pex14_2 | 415 | 419 | PF04695 | 0.268 |
LIG_Pex14_2 | 61 | 65 | PF04695 | 0.361 |
LIG_SH2_CRK | 129 | 133 | PF00017 | 0.254 |
LIG_SH2_SRC | 269 | 272 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.469 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.481 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.451 |
LIG_SUMO_SIM_anti_2 | 329 | 334 | PF11976 | 0.538 |
LIG_SUMO_SIM_anti_2 | 367 | 374 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 100 | 106 | PF11976 | 0.280 |
LIG_SUMO_SIM_par_1 | 230 | 235 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 367 | 374 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 385 | 391 | PF11976 | 0.183 |
LIG_SxIP_EBH_1 | 66 | 78 | PF03271 | 0.327 |
MOD_CDK_SPK_2 | 232 | 237 | PF00069 | 0.362 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.284 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.555 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.521 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.290 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.375 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.502 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.697 |
MOD_GlcNHglycan | 246 | 251 | PF01048 | 0.309 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.307 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.712 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.347 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.368 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.477 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.409 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.581 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.464 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.307 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.237 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.463 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.279 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.523 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.269 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.323 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.310 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.316 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.264 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.353 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.240 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.295 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.365 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.421 |
MOD_PKA_1 | 294 | 300 | PF00069 | 0.197 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.497 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.421 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.229 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.308 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.283 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.407 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.302 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.462 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.564 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.553 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.249 |
MOD_SUMO_for_1 | 163 | 166 | PF00179 | 0.435 |
MOD_SUMO_for_1 | 170 | 173 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 199 | 209 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 225 | 230 | PF00179 | 0.369 |
MOD_SUMO_rev_2 | 296 | 302 | PF00179 | 0.270 |
MOD_SUMO_rev_2 | 319 | 327 | PF00179 | 0.295 |
TRG_DiLeu_BaLyEn_6 | 198 | 203 | PF01217 | 0.369 |
TRG_DiLeu_LyEn_5 | 298 | 303 | PF01217 | 0.249 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.226 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.613 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCU5 | Leptomonas seymouri | 55% | 100% |
A0A1X0NSB9 | Trypanosomatidae | 34% | 100% |
A0A1X0NSI7 | Trypanosomatidae | 35% | 100% |
A0A3R7LZX6 | Trypanosoma rangeli | 33% | 100% |
A0A3S7X1N7 | Leishmania donovani | 39% | 93% |
A0A3S7X501 | Leishmania donovani | 90% | 100% |
A0A422MUI2 | Trypanosoma rangeli | 34% | 100% |
A4HGP7 | Leishmania braziliensis | 42% | 100% |
A4HJU9 | Leishmania braziliensis | 72% | 100% |
A4HJV0 | Leishmania braziliensis | 72% | 100% |
A4HJV1 | Leishmania braziliensis | 57% | 100% |
A4HM27 | Leishmania braziliensis | 31% | 100% |
A4I3R9 | Leishmania infantum | 39% | 94% |
A4I7B1 | Leishmania infantum | 90% | 100% |
D0A885 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A886 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
D0A887 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
D0A888 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
D0A889 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B012 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 96% |
E9B2A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9B2A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9B4F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
O04089 | Arabidopsis thaliana | 27% | 100% |
O82643 | Arabidopsis thaliana | 26% | 100% |
O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
P32804 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
Q12436 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q4Q3L6 | Leishmania major | 34% | 88% |
Q4Q5V0 | Leishmania major | 99% | 100% |
Q4Q873 | Leishmania major | 40% | 100% |
Q6L8F7 | Oryza sativa subsp. japonica | 27% | 100% |
Q6L8F9 | Oryza sativa subsp. japonica | 24% | 100% |
Q6L8G1 | Oryza sativa subsp. japonica | 23% | 100% |
Q8LE59 | Arabidopsis thaliana | 27% | 100% |
Q8W246 | Arabidopsis thaliana | 24% | 100% |
V5AWN3 | Trypanosoma cruzi | 34% | 100% |
V5BC34 | Trypanosoma cruzi | 35% | 100% |
V5DCU2 | Trypanosoma cruzi | 40% | 100% |