Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034702 | monoatomic ion channel complex | 4 | 1 |
GO:0034703 | cation channel complex | 5 | 1 |
GO:0034704 | calcium channel complex | 6 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:1902495 | transmembrane transporter complex | 3 | 1 |
GO:1990246 | uniplex complex | 4 | 1 |
GO:1990351 | transporter complex | 2 | 1 |
GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: A0A3S5H5W0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006811 | monoatomic ion transport | 4 | 12 |
GO:0006812 | monoatomic cation transport | 5 | 12 |
GO:0006816 | calcium ion transport | 7 | 12 |
GO:0006851 | mitochondrial calcium ion transmembrane transport | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0030001 | metal ion transport | 6 | 12 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0055085 | transmembrane transport | 2 | 12 |
GO:0070588 | calcium ion transmembrane transport | 6 | 12 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 12 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 12 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 12 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 12 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0036444 | calcium import into the mitochondrion | 5 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051560 | mitochondrial calcium ion homeostasis | 8 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055074 | calcium 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:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.304 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.615 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.624 |
DOC_CDC14_PxL_1 | 275 | 283 | PF14671 | 0.266 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.407 |
DOC_CYCLIN_RxL_1 | 132 | 145 | PF00134 | 0.491 |
DOC_CYCLIN_RxL_1 | 146 | 159 | PF00134 | 0.312 |
DOC_USP7_MATH_2 | 322 | 328 | PF00917 | 0.507 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.415 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 193 | 201 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 270 | 276 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 325 | 329 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.391 |
LIG_APCC_ABBA_1 | 243 | 248 | PF00400 | 0.401 |
LIG_BIR_III_4 | 77 | 81 | PF00653 | 0.260 |
LIG_deltaCOP1_diTrp_1 | 179 | 185 | PF00928 | 0.292 |
LIG_DLG_GKlike_1 | 162 | 169 | PF00625 | 0.479 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.537 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.404 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.391 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.514 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.476 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.422 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.284 |
LIG_LIR_Apic_2 | 13 | 17 | PF02991 | 0.344 |
LIG_LIR_Apic_2 | 8 | 12 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 121 | 127 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 199 | 209 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 287 | 294 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 304 | 314 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 81 | 91 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.154 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 184 | 188 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.230 |
LIG_NRBOX | 91 | 97 | PF00104 | 0.245 |
LIG_PCNA_yPIPBox_3 | 142 | 155 | PF02747 | 0.447 |
LIG_Pex14_1 | 181 | 185 | PF04695 | 0.289 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.365 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.621 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.621 |
LIG_SH2_NCK_1 | 9 | 13 | PF00017 | 0.479 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.461 |
LIG_SH2_STAT3 | 246 | 249 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.212 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.319 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.372 |
LIG_SUMO_SIM_anti_2 | 285 | 290 | PF11976 | 0.237 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 230 | 235 | PF11976 | 0.349 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.310 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.481 |
LIG_TYR_ITIM | 214 | 219 | PF00017 | 0.501 |
LIG_TYR_ITIM | 28 | 33 | PF00017 | 0.371 |
LIG_UBA3_1 | 106 | 114 | PF00899 | 0.277 |
LIG_UBA3_1 | 307 | 315 | PF00899 | 0.329 |
MOD_CDC14_SPxK_1 | 55 | 58 | PF00782 | 0.493 |
MOD_CDK_SPxK_1 | 52 | 58 | PF00069 | 0.469 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.485 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.341 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.592 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.484 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.334 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.415 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.383 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.483 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.260 |
MOD_GlcNHglycan | 113 | 117 | PF01048 | 0.401 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.466 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.395 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.572 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.356 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.512 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.378 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.531 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.466 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.425 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.261 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.327 |
MOD_PKA_1 | 162 | 168 | PF00069 | 0.431 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.343 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.349 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.480 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.633 |
MOD_Plk_2-3 | 230 | 236 | PF00069 | 0.342 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.451 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.332 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.469 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.409 |
MOD_SUMO_rev_2 | 319 | 328 | PF00179 | 0.565 |
TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_1 | 200 | 205 | PF01217 | 0.410 |
TRG_DiLeu_BaEn_1 | 88 | 93 | PF01217 | 0.245 |
TRG_DiLeu_BaEn_2 | 301 | 307 | PF01217 | 0.250 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.275 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.286 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.383 |
TRG_NES_CRM1_1 | 235 | 248 | PF08389 | 0.424 |
TRG_NLS_MonoCore_2 | 33 | 38 | PF00514 | 0.497 |
TRG_NLS_MonoExtC_3 | 310 | 315 | PF00514 | 0.381 |
TRG_NLS_MonoExtN_4 | 311 | 316 | PF00514 | 0.391 |
TRG_NLS_MonoExtN_4 | 34 | 39 | PF00514 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 152 | 157 | PF00026 | 0.363 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P773 | Leptomonas seymouri | 75% | 79% |
A0A0S4IPF8 | Bodo saltans | 43% | 87% |
A0A1X0NK53 | Trypanosomatidae | 49% | 86% |
A0A422NT64 | Trypanosoma rangeli | 47% | 86% |
A4H4V4 | Leishmania braziliensis | 87% | 100% |
A4HT58 | Leishmania infantum | 100% | 100% |
A4IG32 | Danio rerio | 22% | 71% |
C9ZUW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 72% |
E9AL21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4QIT3 | Leishmania major | 97% | 100% |
Q4R518 | Macaca fascicularis | 21% | 72% |
Q8CD10 | Mus musculus | 21% | 80% |
Q8IYU8 | Homo sapiens | 22% | 79% |
Q99P63 | Rattus norvegicus | 21% | 80% |
Q9BPX6 | Homo sapiens | 21% | 72% |
Q9SZ45 | Arabidopsis thaliana | 27% | 69% |
V5B8U7 | Trypanosoma cruzi | 49% | 74% |
V5BRA1 | Trypanosoma cruzi | 24% | 74% |