Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 4 |
Forrest at al. (procyclic) | yes | 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: A4I3R9
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 | 55 | 59 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 79 | 83 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.397 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.606 |
DOC_CYCLIN_yCln2_LP_2 | 370 | 376 | PF00134 | 0.383 |
DOC_MAPK_gen_1 | 137 | 144 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 24 | 31 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 137 | 144 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 330 | 338 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 357 | 366 | PF00069 | 0.600 |
DOC_MAPK_NFAT4_5 | 357 | 365 | PF00069 | 0.540 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.463 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.326 |
DOC_USP7_MATH_2 | 28 | 34 | PF00917 | 0.381 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.484 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.586 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.430 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.430 |
LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.256 |
LIG_Clathr_ClatBox_1 | 417 | 421 | PF01394 | 0.489 |
LIG_deltaCOP1_diTrp_1 | 190 | 196 | PF00928 | 0.268 |
LIG_eIF4E_1 | 412 | 418 | PF01652 | 0.386 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.428 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.319 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.307 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.455 |
LIG_GBD_Chelix_1 | 300 | 308 | PF00786 | 0.406 |
LIG_GBD_Chelix_1 | 362 | 370 | PF00786 | 0.372 |
LIG_LIR_Gen_1 | 190 | 200 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 393 | 402 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.403 |
LIG_PDZ_Wminus1_1 | 460 | 462 | PF00595 | 0.405 |
LIG_Pex14_1 | 192 | 196 | PF04695 | 0.516 |
LIG_Pex14_2 | 31 | 35 | PF04695 | 0.343 |
LIG_Pex14_2 | 338 | 342 | PF04695 | 0.444 |
LIG_Pex14_2 | 415 | 419 | PF04695 | 0.432 |
LIG_PTB_Apo_2 | 235 | 242 | PF02174 | 0.437 |
LIG_SH2_CRK | 395 | 399 | PF00017 | 0.268 |
LIG_SH2_NCK_1 | 395 | 399 | PF00017 | 0.268 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.575 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.362 |
LIG_SH3_1 | 225 | 231 | PF00018 | 0.464 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.573 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.443 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.614 |
LIG_SUMO_SIM_anti_2 | 361 | 366 | PF11976 | 0.501 |
LIG_SxIP_EBH_1 | 125 | 138 | PF03271 | 0.402 |
LIG_TYR_ITSM | 391 | 398 | PF00017 | 0.268 |
LIG_UBA3_1 | 131 | 137 | PF00899 | 0.298 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.367 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.479 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.592 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.288 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.476 |
MOD_Cter_Amidation | 135 | 138 | PF01082 | 0.399 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.698 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.675 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.425 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.410 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.378 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.657 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.661 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.844 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.362 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.407 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.555 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.382 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.454 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.647 |
MOD_N-GLC_2 | 238 | 240 | PF02516 | 0.264 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.378 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.404 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.348 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.392 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.347 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.401 |
MOD_NEK2_2 | 352 | 357 | PF00069 | 0.502 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.549 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.575 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.484 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.468 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.385 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.285 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.391 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.407 |
TRG_DiLeu_BaEn_2 | 189 | 195 | PF01217 | 0.313 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 10 | 15 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCU5 | Leptomonas seymouri | 40% | 100% |
A0A1X0NR51 | Trypanosomatidae | 34% | 100% |
A0A1X0NSB9 | Trypanosomatidae | 37% | 100% |
A0A1X0NSI7 | Trypanosomatidae | 38% | 100% |
A0A3R7LZX6 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X1N7 | Leishmania donovani | 99% | 100% |
A0A3S7X501 | Leishmania donovani | 40% | 100% |
A0A3S7X7B0 | Leishmania donovani | 35% | 100% |
A0A422MUI2 | Trypanosoma rangeli | 37% | 100% |
A4HGP7 | Leishmania braziliensis | 80% | 100% |
A4HJU9 | Leishmania braziliensis | 41% | 100% |
A4HJV0 | Leishmania braziliensis | 41% | 100% |
A4HJV1 | Leishmania braziliensis | 36% | 99% |
A4HM27 | Leishmania braziliensis | 33% | 94% |
A4I7B1 | Leishmania infantum | 40% | 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% |
E9B012 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 97% |
E9B2A5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B2A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B4F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 93% |
O04089 | Arabidopsis thaliana | 27% | 100% |
O23039 | Arabidopsis thaliana | 29% | 100% |
O64738 | Arabidopsis thaliana | 26% | 100% |
O81123 | Arabidopsis thaliana | 24% | 100% |
O81850 | Arabidopsis thaliana | 25% | 100% |
O82643 | Arabidopsis thaliana | 27% | 100% |
O94639 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
P32804 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
Q38856 | Arabidopsis thaliana | 24% | 100% |
Q4Q3L6 | Leishmania major | 33% | 92% |
Q4Q5V0 | Leishmania major | 39% | 100% |
Q4Q5V1 | Leishmania major | 39% | 100% |
Q4Q873 | Leishmania major | 86% | 96% |
Q6L8G0 | Oryza sativa subsp. japonica | 28% | 100% |
Q6L8G1 | Oryza sativa subsp. japonica | 28% | 100% |
Q75HB1 | Oryza sativa subsp. japonica | 29% | 100% |
Q7XLD4 | Oryza sativa subsp. japonica | 26% | 100% |
Q8S3W4 | Arabidopsis thaliana | 22% | 100% |
Q8W245 | Arabidopsis thaliana | 22% | 100% |
Q8W246 | Arabidopsis thaliana | 28% | 100% |
Q9FIS2 | Arabidopsis thaliana | 26% | 100% |
Q9SLG3 | Arabidopsis thaliana | 28% | 100% |
V5AWN3 | Trypanosoma cruzi | 38% | 100% |
V5BC34 | Trypanosoma cruzi | 36% | 100% |
V5DCU2 | Trypanosoma cruzi | 45% | 100% |