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: A0A3S7X1N7
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 | 0.617 |
CLV_C14_Caspase3-7 | 79 | 83 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.411 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.622 |
DOC_CYCLIN_yCln2_LP_2 | 372 | 378 | PF00134 | 0.383 |
DOC_MAPK_gen_1 | 139 | 146 | PF00069 | 0.637 |
DOC_MAPK_gen_1 | 24 | 31 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 139 | 146 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 332 | 340 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 359 | 368 | PF00069 | 0.615 |
DOC_MAPK_NFAT4_5 | 359 | 367 | PF00069 | 0.551 |
DOC_PP2B_LxvP_1 | 372 | 375 | PF13499 | 0.452 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.338 |
DOC_USP7_MATH_2 | 28 | 34 | PF00917 | 0.466 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.701 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.455 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.455 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.455 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.282 |
LIG_Clathr_ClatBox_1 | 419 | 423 | PF01394 | 0.501 |
LIG_deltaCOP1_diTrp_1 | 192 | 198 | PF00928 | 0.285 |
LIG_eIF4E_1 | 414 | 420 | PF01652 | 0.391 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.434 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.352 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.319 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.493 |
LIG_GBD_Chelix_1 | 302 | 310 | PF00786 | 0.259 |
LIG_GBD_Chelix_1 | 364 | 372 | PF00786 | 0.374 |
LIG_LIR_Gen_1 | 192 | 202 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 316 | 321 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.428 |
LIG_PDZ_Wminus1_1 | 462 | 464 | PF00595 | 0.418 |
LIG_Pex14_1 | 194 | 198 | PF04695 | 0.532 |
LIG_Pex14_2 | 31 | 35 | PF04695 | 0.443 |
LIG_Pex14_2 | 340 | 344 | PF04695 | 0.451 |
LIG_Pex14_2 | 417 | 421 | PF04695 | 0.439 |
LIG_PTB_Apo_2 | 237 | 244 | PF02174 | 0.459 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.285 |
LIG_SH2_NCK_1 | 397 | 401 | PF00017 | 0.285 |
LIG_SH2_SRC | 149 | 152 | PF00017 | 0.587 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.368 |
LIG_SH3_1 | 227 | 233 | PF00018 | 0.482 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.586 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.539 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.641 |
LIG_SUMO_SIM_anti_2 | 363 | 368 | PF11976 | 0.515 |
LIG_SxIP_EBH_1 | 127 | 140 | PF03271 | 0.408 |
LIG_TYR_ITSM | 393 | 400 | PF00017 | 0.285 |
LIG_UBA3_1 | 133 | 139 | PF00899 | 0.310 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.380 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.634 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.607 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.302 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.691 |
MOD_Cter_Amidation | 137 | 140 | PF01082 | 0.397 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.790 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.776 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.436 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.542 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.383 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.865 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.825 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.856 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.368 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.507 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.594 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.534 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.394 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.677 |
MOD_N-GLC_2 | 240 | 242 | PF02516 | 0.282 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.398 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.410 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.355 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.410 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.359 |
MOD_NEK2_2 | 354 | 359 | PF00069 | 0.515 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.588 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.691 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.494 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.390 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.299 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.402 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.420 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.442 |
TRG_DiLeu_BaEn_2 | 191 | 197 | PF01217 | 0.324 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 10 | 15 | PF00026 | 0.623 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCU5 | Leptomonas seymouri | 40% | 100% |
A0A1X0NR51 | Trypanosomatidae | 46% | 100% |
A0A1X0NSB9 | Trypanosomatidae | 37% | 100% |
A0A1X0NSI7 | Trypanosomatidae | 38% | 100% |
A0A3R7LZX6 | Trypanosoma rangeli | 41% | 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% |
A4I3R9 | Leishmania infantum | 99% | 100% |
A4I7B1 | Leishmania infantum | 41% | 100% |
A4I9G1 | Leishmania infantum | 35% | 92% |
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) | 83% | 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 | 84% | 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 | 21% | 100% |
Q8W246 | Arabidopsis thaliana | 28% | 100% |
Q9FIS2 | Arabidopsis thaliana | 26% | 100% |
Q9SLG3 | Arabidopsis thaliana | 29% | 100% |
V5AWN3 | Trypanosoma cruzi | 38% | 100% |
V5BC34 | Trypanosoma cruzi | 36% | 100% |
V5DCU2 | Trypanosoma cruzi | 44% | 100% |