Homologous to plant metal transporters (likely Mg2+ transporters)
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:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4HKU5
Term | Name | Level | Count |
---|---|---|---|
GO:0010960 | magnesium ion homeostasis | 8 | 12 |
GO:0042592 | homeostatic process | 3 | 12 |
GO:0048878 | chemical homeostasis | 4 | 12 |
GO:0050801 | monoatomic ion homeostasis | 5 | 12 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 12 |
GO:0055080 | monoatomic cation homeostasis | 6 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0065008 | regulation of biological quality | 2 | 12 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 12 |
GO:0098771 | inorganic ion homeostasis | 6 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.268 |
CLV_PCSK_FUR_1 | 62 | 66 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.300 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.261 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.535 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.429 |
DOC_CDC14_PxL_1 | 302 | 310 | PF14671 | 0.378 |
DOC_CYCLIN_yCln2_LP_2 | 8 | 14 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 98 | 104 | PF00134 | 0.422 |
DOC_MAPK_DCC_7 | 301 | 310 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 301 | 310 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 61 | 70 | PF00069 | 0.473 |
DOC_MAPK_HePTP_8 | 298 | 310 | PF00069 | 0.245 |
DOC_MAPK_HePTP_8 | 58 | 70 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 295 | 302 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 303 | 310 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 6 | 14 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 61 | 70 | PF00069 | 0.493 |
DOC_MAPK_RevD_3 | 46 | 62 | PF00069 | 0.470 |
DOC_PP1_RVXF_1 | 153 | 160 | PF00149 | 0.275 |
DOC_PP1_RVXF_1 | 284 | 291 | PF00149 | 0.399 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.399 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.463 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.250 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.554 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.363 |
LIG_Actin_WH2_2 | 223 | 238 | PF00022 | 0.414 |
LIG_APCC_ABBA_1 | 112 | 117 | PF00400 | 0.201 |
LIG_APCC_ABBA_1 | 243 | 248 | PF00400 | 0.392 |
LIG_APCC_ABBA_1 | 267 | 272 | PF00400 | 0.322 |
LIG_Clathr_ClatBox_1 | 80 | 84 | PF01394 | 0.336 |
LIG_EH1_1 | 136 | 144 | PF00400 | 0.449 |
LIG_eIF4E_1 | 137 | 143 | PF01652 | 0.449 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.297 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.443 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.365 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.379 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.336 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.336 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.420 |
LIG_IRF3_LxIS_1 | 32 | 39 | PF10401 | 0.415 |
LIG_KLC1_Yacidic_2 | 364 | 369 | PF13176 | 0.347 |
LIG_LIR_Gen_1 | 15 | 25 | PF02991 | 0.451 |
LIG_LIR_LC3C_4 | 24 | 28 | PF02991 | 0.449 |
LIG_LIR_LC3C_4 | 79 | 82 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.335 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.398 |
LIG_NRBOX | 94 | 100 | PF00104 | 0.397 |
LIG_RPA_C_Fungi | 242 | 254 | PF08784 | 0.502 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.595 |
LIG_SH2_NCK_1 | 270 | 274 | PF00017 | 0.477 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.651 |
LIG_SH3_1 | 303 | 309 | PF00018 | 0.525 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.431 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.475 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.444 |
LIG_Sin3_3 | 136 | 143 | PF02671 | 0.410 |
LIG_SUMO_SIM_anti_2 | 108 | 114 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 24 | 30 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 352 | 359 | PF11976 | 0.532 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 10 | 15 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 140 | 146 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 222 | 228 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 36 | 42 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 78 | 85 | PF11976 | 0.343 |
LIG_TYR_ITIM | 135 | 140 | PF00017 | 0.384 |
LIG_WRC_WIRS_1 | 379 | 384 | PF05994 | 0.653 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.466 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.342 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.457 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.329 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.348 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.422 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.456 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.581 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.449 |
MOD_Cter_Amidation | 59 | 62 | PF01082 | 0.402 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.327 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.449 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.495 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.486 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.478 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.422 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.328 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.704 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.498 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.613 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.688 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.196 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.422 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.305 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.513 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.505 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.376 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.607 |
MOD_NEK2_2 | 241 | 246 | PF00069 | 0.473 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.540 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.445 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.677 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.501 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.496 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.368 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.378 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.430 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.522 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.362 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.306 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.440 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.472 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.543 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.636 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.318 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.475 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.439 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.466 |
TRG_DiLeu_BaEn_1 | 284 | 289 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_4 | 194 | 200 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 283 | 288 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 303 | 308 | PF01217 | 0.217 |
TRG_DiLeu_BaLyEn_6 | 62 | 67 | PF01217 | 0.422 |
TRG_DiLeu_LyEn_5 | 89 | 94 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.594 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.362 |
TRG_NES_CRM1_1 | 89 | 103 | PF08389 | 0.332 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8N1 | Leptomonas seymouri | 67% | 100% |
A0A0N1I1M9 | Leptomonas seymouri | 35% | 95% |
A0A0N1PDI6 | Leptomonas seymouri | 23% | 67% |
A0A0S4IPA6 | Bodo saltans | 26% | 100% |
A0A0S4IPI7 | Bodo saltans | 33% | 81% |
A0A0S4JSF9 | Bodo saltans | 24% | 75% |
A0A1X0NRR8 | Trypanosomatidae | 39% | 92% |
A0A1X0P1F1 | Trypanosomatidae | 24% | 100% |
A0A1X0PAL3 | Trypanosomatidae | 24% | 71% |
A0A3Q8IL77 | Leishmania donovani | 23% | 66% |
A0A3Q8ITK0 | Leishmania donovani | 87% | 100% |
A0A3R7LBY6 | Trypanosoma rangeli | 25% | 100% |
A0A422NS01 | Trypanosoma rangeli | 24% | 71% |
A0A422NYJ0 | Trypanosoma rangeli | 38% | 86% |
A4HAY2 | Leishmania braziliensis | 23% | 68% |
A4HIN7 | Leishmania braziliensis | 26% | 100% |
A4I8C4 | Leishmania infantum | 88% | 100% |
A4IA41 | Leishmania infantum | 23% | 66% |
C9ZM59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 72% |
E9B177 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B383 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9B555 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 66% |
Q4Q2T0 | Leishmania major | 24% | 66% |
Q4Q4X2 | Leishmania major | 87% | 100% |
Q4V3C7 | Arabidopsis thaliana | 27% | 81% |
Q67XQ0 | Arabidopsis thaliana | 28% | 82% |
Q8RY60 | Arabidopsis thaliana | 29% | 76% |
Q8VZI2 | Arabidopsis thaliana | 32% | 95% |
Q9LTD8 | Arabidopsis thaliana | 28% | 81% |
Q9ZQR4 | Arabidopsis thaliana | 27% | 95% |
Q9ZVS8 | Arabidopsis thaliana | 28% | 81% |
V5BKR5 | Trypanosoma cruzi | 24% | 70% |
V5DM70 | Trypanosoma cruzi | 38% | 89% |
V5DNW3 | Trypanosoma cruzi | 25% | 100% |