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: 27 |
NetGPI | no | yes: 0, no: 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 28 |
GO:0110165 | cellular anatomical entity | 1 | 28 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005886 | plasma membrane | 3 | 3 |
Related structures:
AlphaFold database: A4HJV0
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 | 28 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 28 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 28 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 28 |
GO:0022857 | transmembrane transporter activity | 2 | 28 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 28 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 28 |
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 | 170 | 174 | PF00656 | 0.438 |
CLV_MEL_PAP_1 | 18 | 24 | PF00089 | 0.527 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.170 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.321 |
DEG_APCC_DBOX_1 | 320 | 328 | PF00400 | 0.417 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.466 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 399 | 408 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 78 | 86 | PF00069 | 0.533 |
DOC_MAPK_HePTP_8 | 402 | 414 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 294 | 302 | PF00069 | 0.254 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 401 | 410 | PF00069 | 0.479 |
DOC_MAPK_RevD_3 | 64 | 79 | PF00069 | 0.159 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.337 |
DOC_USP7_UBL2_3 | 160 | 164 | PF12436 | 0.545 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.256 |
LIG_14-3-3_CanoR_1 | 13 | 22 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 181 | 191 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 263 | 272 | PF00244 | 0.458 |
LIG_CtBP_PxDLS_1 | 255 | 259 | PF00389 | 0.482 |
LIG_eIF4E_1 | 133 | 139 | PF01652 | 0.299 |
LIG_eIF4E_1 | 376 | 382 | PF01652 | 0.312 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.401 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.307 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.324 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.570 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.450 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.249 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.349 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.181 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.316 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.440 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.264 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.386 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.295 |
LIG_LIR_Gen_1 | 357 | 366 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 407 | 416 | PF02991 | 0.181 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.293 |
LIG_PDZ_Wminus1_1 | 424 | 426 | PF00595 | 0.472 |
LIG_Pex14_1 | 82 | 86 | PF04695 | 0.362 |
LIG_Pex14_2 | 302 | 306 | PF04695 | 0.347 |
LIG_Pex14_2 | 409 | 413 | PF04695 | 0.262 |
LIG_Pex14_2 | 61 | 65 | PF04695 | 0.338 |
LIG_Pex14_2 | 86 | 90 | PF04695 | 0.362 |
LIG_SH2_CRK | 129 | 133 | PF00017 | 0.275 |
LIG_SH2_SRC | 27 | 30 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.464 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.372 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.461 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.553 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.413 |
LIG_SUMO_SIM_anti_2 | 322 | 328 | PF11976 | 0.533 |
LIG_SUMO_SIM_anti_2 | 361 | 368 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 100 | 106 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 361 | 368 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 379 | 385 | PF11976 | 0.178 |
LIG_SxIP_EBH_1 | 66 | 79 | PF03271 | 0.351 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.275 |
MOD_CDK_SPK_2 | 229 | 234 | PF00069 | 0.372 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.313 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.286 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.417 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.413 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.500 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.262 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.449 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.482 |
MOD_Cter_Amidation | 76 | 79 | PF01082 | 0.276 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.372 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.337 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.179 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.681 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.310 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.379 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.343 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.431 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.392 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.204 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.253 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.480 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.364 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.295 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.513 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.300 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.485 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.337 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.327 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.304 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.356 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.343 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.308 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.471 |
MOD_PKA_1 | 404 | 410 | PF00069 | 0.382 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.352 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.463 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.259 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.237 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.368 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.312 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.315 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.316 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.540 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.256 |
MOD_SUMO_for_1 | 163 | 166 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 173 | 179 | PF00179 | 0.362 |
MOD_SUMO_rev_2 | 290 | 296 | PF00179 | 0.289 |
MOD_SUMO_rev_2 | 313 | 320 | PF00179 | 0.301 |
TRG_DiLeu_LyEn_5 | 292 | 297 | PF01217 | 0.256 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.231 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 321 | 325 | PF00026 | 0.166 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCU5 | Leptomonas seymouri | 58% | 99% |
A0A1X0NR51 | Trypanosomatidae | 42% | 100% |
A0A1X0NSB9 | Trypanosomatidae | 36% | 100% |
A0A1X0NSI7 | Trypanosomatidae | 37% | 100% |
A0A3S7X1N7 | Leishmania donovani | 41% | 92% |
A0A3S7X501 | Leishmania donovani | 75% | 99% |
A0A3S7X7B0 | Leishmania donovani | 33% | 100% |
A0A422MUI2 | Trypanosoma rangeli | 35% | 100% |
A4HGP7 | Leishmania braziliensis | 44% | 92% |
A4HJU9 | Leishmania braziliensis | 96% | 100% |
A4HJV1 | Leishmania braziliensis | 63% | 100% |
A4HM27 | Leishmania braziliensis | 31% | 100% |
A4I3R9 | Leishmania infantum | 41% | 92% |
A4I7B1 | Leishmania infantum | 75% | 99% |
A4I9G1 | Leishmania infantum | 34% | 100% |
D0A885 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B012 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 95% |
E9B2A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 99% |
E9B2A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 99% |
E9B4F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
O04089 | Arabidopsis thaliana | 27% | 100% |
O81123 | Arabidopsis thaliana | 25% | 100% |
O81850 | Arabidopsis thaliana | 23% | 100% |
O82643 | Arabidopsis thaliana | 25% | 100% |
O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
P32804 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
Q12436 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
Q4Q5V0 | Leishmania major | 72% | 100% |
Q4Q5V1 | Leishmania major | 72% | 100% |
Q4Q873 | Leishmania major | 42% | 100% |
Q6L8G0 | Oryza sativa subsp. japonica | 27% | 100% |
Q6L8G1 | Oryza sativa subsp. japonica | 23% | 100% |
Q8LE59 | Arabidopsis thaliana | 27% | 100% |
Q9FIS2 | Arabidopsis thaliana | 27% | 100% |
V5AWN3 | Trypanosoma cruzi | 35% | 100% |
V5BC34 | Trypanosoma cruzi | 36% | 100% |
V5DCU2 | Trypanosoma cruzi | 43% | 100% |