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. | yes | 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: 33 |
NetGPI | no | yes: 0, no: 33 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 34 |
GO:0110165 | cellular anatomical entity | 1 | 34 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005886 | plasma membrane | 3 | 4 |
Related structures:
AlphaFold database: E9B012
Term | Name | Level | Count |
---|---|---|---|
GO:0000041 | transition metal ion transport | 7 | 4 |
GO:0006810 | transport | 3 | 4 |
GO:0006811 | monoatomic ion transport | 4 | 4 |
GO:0006812 | monoatomic cation transport | 5 | 4 |
GO:0006829 | zinc ion transport | 8 | 4 |
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 | 4 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030001 | metal ion transport | 6 | 4 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 4 |
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 | 4 |
GO:0051234 | establishment of localization | 2 | 4 |
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 | 4 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071577 | zinc ion transmembrane transport | 6 | 4 |
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 | 4 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 4 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 4 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 34 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 34 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 34 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 34 |
GO:0022857 | transmembrane transporter activity | 2 | 34 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 34 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 34 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 4 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 4 |
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 | 79 | 83 | PF00656 | 0.625 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.371 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.319 |
CLV_PCSK_PC1ET2_1 | 423 | 425 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.284 |
CLV_PCSK_PC7_1 | 424 | 430 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.580 |
DOC_MAPK_gen_1 | 125 | 132 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 125 | 132 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 318 | 326 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 345 | 354 | PF00069 | 0.574 |
DOC_MAPK_NFAT4_5 | 345 | 353 | PF00069 | 0.514 |
DOC_PP4_FxxP_1 | 358 | 361 | PF00568 | 0.340 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.300 |
DOC_USP7_MATH_2 | 28 | 34 | PF00917 | 0.401 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.195 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.642 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.559 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.402 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.402 |
LIG_Clathr_ClatBox_1 | 405 | 409 | PF01394 | 0.463 |
LIG_CtBP_PxDLS_1 | 279 | 283 | PF00389 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 178 | 184 | PF00928 | 0.242 |
LIG_eIF4E_1 | 400 | 406 | PF01652 | 0.360 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.402 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.364 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.293 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.403 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.280 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.434 |
LIG_FXI_DFP_1 | 407 | 411 | PF00024 | 0.199 |
LIG_LIR_Apic_2 | 357 | 361 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 178 | 188 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 381 | 390 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 41 | 49 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 381 | 386 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.469 |
LIG_PDZ_Wminus1_1 | 448 | 450 | PF00595 | 0.382 |
LIG_Pex14_1 | 180 | 184 | PF04695 | 0.490 |
LIG_Pex14_2 | 326 | 330 | PF04695 | 0.418 |
LIG_Pex14_2 | 403 | 407 | PF04695 | 0.406 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.242 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.377 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.242 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.548 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.336 |
LIG_SH3_1 | 213 | 219 | PF00018 | 0.438 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.546 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.580 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.377 |
LIG_SUMO_SIM_anti_2 | 349 | 354 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 5 | 10 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 147 | 152 | PF11976 | 0.340 |
LIG_SxIP_EBH_1 | 113 | 126 | PF03271 | 0.376 |
LIG_TYR_ITIM | 42 | 47 | PF00017 | 0.369 |
LIG_TYR_ITSM | 379 | 386 | PF00017 | 0.242 |
LIG_UBA3_1 | 119 | 125 | PF00899 | 0.272 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.312 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.435 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.247 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.330 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.341 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.447 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.556 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.567 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.569 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.253 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.636 |
MOD_Cter_Amidation | 123 | 126 | PF01082 | 0.372 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.214 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.465 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.275 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.726 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.399 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.712 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.384 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.351 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.741 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.817 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.785 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.681 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.336 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.201 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.435 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.529 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.482 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.624 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.423 |
MOD_N-GLC_2 | 226 | 228 | PF02516 | 0.238 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.352 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.329 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.378 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.366 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.321 |
MOD_NEK2_2 | 340 | 345 | PF00069 | 0.476 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.559 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.549 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.635 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.441 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.359 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.269 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.259 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.364 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.351 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.195 |
TRG_DiLeu_BaEn_2 | 177 | 183 | PF01217 | 0.286 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 10 | 15 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCU5 | Leptomonas seymouri | 41% | 100% |
A0A1X0NR51 | Trypanosomatidae | 45% | 100% |
A0A1X0NSB9 | Trypanosomatidae | 38% | 100% |
A0A1X0NSI7 | Trypanosomatidae | 37% | 100% |
A0A3R7LZX6 | Trypanosoma rangeli | 39% | 100% |
A0A3S7X1N7 | Leishmania donovani | 83% | 97% |
A0A3S7X501 | Leishmania donovani | 41% | 100% |
A0A3S7X7B0 | Leishmania donovani | 36% | 100% |
A0A422MUI2 | Trypanosoma rangeli | 38% | 100% |
A4HGP7 | Leishmania braziliensis | 79% | 100% |
A4HJU9 | Leishmania braziliensis | 44% | 100% |
A4HJV0 | Leishmania braziliensis | 44% | 100% |
A4HJV1 | Leishmania braziliensis | 37% | 100% |
A4HM27 | Leishmania braziliensis | 33% | 94% |
A4I3R9 | Leishmania infantum | 84% | 97% |
A4I7B1 | Leishmania infantum | 41% | 100% |
A4I9G1 | Leishmania infantum | 35% | 100% |
D0A885 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A886 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A887 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A888 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A889 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9B2A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B2A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9B4F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
O04089 | Arabidopsis thaliana | 29% | 100% |
O23039 | Arabidopsis thaliana | 29% | 100% |
O81123 | Arabidopsis thaliana | 24% | 100% |
O81850 | Arabidopsis thaliana | 24% | 100% |
O82643 | Arabidopsis thaliana | 28% | 100% |
O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
P32804 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
Q0DHE3 | Oryza sativa subsp. japonica | 25% | 100% |
Q12436 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
Q38856 | Arabidopsis thaliana | 23% | 100% |
Q4Q3L6 | Leishmania major | 34% | 94% |
Q4Q5V0 | Leishmania major | 41% | 100% |
Q4Q5V1 | Leishmania major | 41% | 100% |
Q4Q873 | Leishmania major | 83% | 99% |
Q6L8F7 | Oryza sativa subsp. japonica | 28% | 100% |
Q6L8G0 | Oryza sativa subsp. japonica | 28% | 100% |
Q6L8G1 | Oryza sativa subsp. japonica | 30% | 100% |
Q75HB1 | Oryza sativa subsp. japonica | 29% | 100% |
Q7XLD4 | Oryza sativa subsp. japonica | 30% | 100% |
Q8S3W4 | Arabidopsis thaliana | 23% | 100% |
Q8W245 | Arabidopsis thaliana | 24% | 100% |
Q8W246 | Arabidopsis thaliana | 27% | 100% |
Q9FIS2 | Arabidopsis thaliana | 25% | 100% |
Q9SLG3 | Arabidopsis thaliana | 28% | 100% |
V5AWN3 | Trypanosoma cruzi | 37% | 100% |
V5BC34 | Trypanosoma cruzi | 37% | 100% |
V5DCU2 | Trypanosoma cruzi | 47% | 100% |