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: Q4Q4X2
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_C14_Caspase3-7 | 337 | 341 | PF00656 | 0.373 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.269 |
CLV_PCSK_FUR_1 | 62 | 66 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.256 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.289 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.262 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.536 |
DOC_CDC14_PxL_1 | 302 | 310 | PF14671 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 8 | 14 | PF00134 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 98 | 104 | PF00134 | 0.423 |
DOC_MAPK_DCC_7 | 301 | 310 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 301 | 310 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 61 | 70 | PF00069 | 0.463 |
DOC_MAPK_HePTP_8 | 58 | 70 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 301 | 310 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 61 | 70 | PF00069 | 0.520 |
DOC_PP1_RVXF_1 | 153 | 160 | PF00149 | 0.283 |
DOC_PP1_RVXF_1 | 284 | 291 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.400 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.467 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.555 |
DOC_USP7_UBL2_3 | 45 | 49 | PF12436 | 0.500 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.450 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 360 | 364 | PF00244 | 0.390 |
LIG_Actin_WH2_2 | 223 | 238 | PF00022 | 0.412 |
LIG_APCC_ABBA_1 | 243 | 248 | PF00400 | 0.393 |
LIG_APCC_ABBA_1 | 267 | 272 | PF00400 | 0.326 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.470 |
LIG_Clathr_ClatBox_1 | 80 | 84 | PF01394 | 0.337 |
LIG_EH1_1 | 136 | 144 | PF00400 | 0.450 |
LIG_eIF4E_1 | 137 | 143 | PF01652 | 0.450 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.313 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.431 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.366 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.246 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.171 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.519 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.329 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.305 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.361 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.425 |
LIG_IRF3_LxIS_1 | 32 | 39 | PF10401 | 0.415 |
LIG_LIR_Gen_1 | 15 | 25 | PF02991 | 0.447 |
LIG_LIR_LC3C_4 | 24 | 28 | PF02991 | 0.450 |
LIG_LIR_LC3C_4 | 79 | 82 | PF02991 | 0.396 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.408 |
LIG_RPA_C_Fungi | 242 | 254 | PF08784 | 0.506 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.597 |
LIG_SH2_NCK_1 | 270 | 274 | PF00017 | 0.479 |
LIG_SH2_SRC | 186 | 189 | PF00017 | 0.468 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.620 |
LIG_SH3_1 | 303 | 309 | PF00018 | 0.528 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.432 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.476 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.448 |
LIG_Sin3_3 | 136 | 143 | PF02671 | 0.411 |
LIG_SUMO_SIM_anti_2 | 108 | 114 | PF11976 | 0.388 |
LIG_SUMO_SIM_anti_2 | 24 | 30 | PF11976 | 0.428 |
LIG_SUMO_SIM_anti_2 | 352 | 359 | PF11976 | 0.529 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 10 | 15 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 222 | 228 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 332 | 338 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 36 | 42 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 78 | 85 | PF11976 | 0.320 |
LIG_TYR_ITIM | 135 | 140 | PF00017 | 0.388 |
LIG_WRC_WIRS_1 | 379 | 384 | PF05994 | 0.664 |
LIG_WW_3 | 197 | 201 | PF00397 | 0.678 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.450 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.637 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.545 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.342 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.456 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.585 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.349 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.423 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.452 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.450 |
MOD_Cter_Amidation | 59 | 62 | PF01082 | 0.403 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.340 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.450 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.494 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.515 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.423 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.346 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.750 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.469 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.592 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.617 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.422 |
MOD_N-GLC_1 | 385 | 390 | PF02516 | 0.649 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.281 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.320 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.343 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.510 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.524 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.412 |
MOD_NEK2_2 | 241 | 246 | PF00069 | 0.475 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.545 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.445 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.725 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.501 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.495 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.502 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.349 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.676 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.372 |
MOD_Plk_1 | 385 | 391 | PF00069 | 0.620 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.391 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.307 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.437 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.495 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.476 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.699 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.319 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.475 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.440 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.470 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.450 |
TRG_DiLeu_BaEn_1 | 284 | 289 | PF01217 | 0.428 |
TRG_DiLeu_BaLyEn_6 | 283 | 288 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 303 | 308 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 62 | 67 | PF01217 | 0.423 |
TRG_DiLeu_LyEn_5 | 89 | 94 | PF01217 | 0.423 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.569 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.363 |
TRG_NES_CRM1_1 | 89 | 103 | PF08389 | 0.333 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8N1 | Leptomonas seymouri | 70% | 100% |
A0A0N1I1M9 | Leptomonas seymouri | 35% | 95% |
A0A0N1PDI6 | Leptomonas seymouri | 22% | 67% |
A0A0S4IPA6 | Bodo saltans | 25% | 100% |
A0A0S4IPI7 | Bodo saltans | 35% | 81% |
A0A0S4JSF9 | Bodo saltans | 24% | 75% |
A0A1X0NRR8 | Trypanosomatidae | 39% | 92% |
A0A1X0P1F1 | Trypanosomatidae | 23% | 100% |
A0A1X0PAL3 | Trypanosomatidae | 22% | 71% |
A0A3Q8IL77 | Leishmania donovani | 22% | 66% |
A0A3Q8ITK0 | Leishmania donovani | 96% | 100% |
A0A3R7LBY6 | Trypanosoma rangeli | 27% | 100% |
A0A422NS01 | Trypanosoma rangeli | 23% | 71% |
A0A422NYJ0 | Trypanosoma rangeli | 38% | 86% |
A4HAY2 | Leishmania braziliensis | 21% | 68% |
A4HIN7 | Leishmania braziliensis | 24% | 89% |
A4HKU5 | Leishmania braziliensis | 87% | 100% |
A4I8C4 | Leishmania infantum | 97% | 100% |
A4IA41 | Leishmania infantum | 22% | 66% |
C9ZM59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 72% |
E9B177 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 80% |
E9B383 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9B555 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 66% |
Q4Q2T0 | Leishmania major | 22% | 66% |
Q4V3C7 | Arabidopsis thaliana | 30% | 81% |
Q67XQ0 | Arabidopsis thaliana | 29% | 82% |
Q8RY60 | Arabidopsis thaliana | 28% | 76% |
Q8VZI2 | Arabidopsis thaliana | 31% | 95% |
Q9LTD8 | Arabidopsis thaliana | 26% | 81% |
Q9ZQR4 | Arabidopsis thaliana | 29% | 95% |
Q9ZVS8 | Arabidopsis thaliana | 30% | 81% |
V5BKR5 | Trypanosoma cruzi | 23% | 70% |
V5DM70 | Trypanosoma cruzi | 37% | 89% |
V5DNW3 | Trypanosoma cruzi | 26% | 100% |