A bacterial-type Mg2+ transporter found in kinetoplastids.. Expanded extensively on multiple lineages, especially T cruzi
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9B013
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 5 |
GO:0006811 | monoatomic ion transport | 4 | 5 |
GO:0006812 | monoatomic cation transport | 5 | 5 |
GO:0015693 | magnesium ion transport | 7 | 5 |
GO:0030001 | metal ion transport | 6 | 5 |
GO:0051179 | localization | 1 | 5 |
GO:0051234 | establishment of localization | 2 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 5 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 5 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 5 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 5 |
GO:0022857 | transmembrane transporter activity | 2 | 5 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 5 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 199 | 203 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.409 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.611 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.736 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.629 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.392 |
DEG_SPOP_SBC_1 | 637 | 641 | PF00917 | 0.399 |
DOC_ANK_TNKS_1 | 307 | 314 | PF00023 | 0.483 |
DOC_CDC14_PxL_1 | 110 | 118 | PF14671 | 0.486 |
DOC_CDC14_PxL_1 | 619 | 627 | PF14671 | 0.340 |
DOC_CKS1_1 | 288 | 293 | PF01111 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 115 | 118 | PF00134 | 0.483 |
DOC_CYCLIN_yCln2_LP_2 | 418 | 424 | PF00134 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 540 | 546 | PF00134 | 0.564 |
DOC_MAPK_DCC_7 | 112 | 121 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 190 | 196 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 516 | 524 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 532 | 541 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 112 | 121 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 178 | 187 | PF00069 | 0.329 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.518 |
DOC_PP2B_LxvP_1 | 539 | 542 | PF13499 | 0.536 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.528 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.520 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.453 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 638 | 643 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 191 | 197 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 35 | 45 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 551 | 559 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 561 | 567 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 582 | 588 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 594 | 602 | PF00244 | 0.466 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.483 |
LIG_BIR_III_2 | 160 | 164 | PF00653 | 0.502 |
LIG_BRCT_BRCA1_1 | 298 | 302 | PF00533 | 0.390 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.412 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.453 |
LIG_CaM_IQ_9 | 477 | 492 | PF13499 | 0.265 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.413 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.428 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.511 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.547 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.388 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.321 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.470 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.463 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.330 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.406 |
LIG_HP1_1 | 291 | 295 | PF01393 | 0.397 |
LIG_LIR_Gen_1 | 108 | 118 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 42 | 53 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 641 | 651 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 94 | 104 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 640 | 646 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.496 |
LIG_MAD2 | 534 | 542 | PF02301 | 0.521 |
LIG_MYND_1 | 114 | 118 | PF01753 | 0.483 |
LIG_NRBOX | 535 | 541 | PF00104 | 0.514 |
LIG_Pex14_1 | 375 | 379 | PF04695 | 0.402 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.459 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.345 |
LIG_SH2_CRK | 663 | 667 | PF00017 | 0.567 |
LIG_SH2_CRK | 668 | 672 | PF00017 | 0.570 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.599 |
LIG_SH2_NCK_1 | 96 | 100 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.452 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.562 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.433 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.603 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.418 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.449 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.486 |
LIG_SUMO_SIM_anti_2 | 290 | 296 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 461 | 471 | PF11976 | 0.259 |
LIG_SUMO_SIM_anti_2 | 610 | 616 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 336 | 342 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 369 | 376 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 652 | 657 | PF11976 | 0.329 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.454 |
LIG_TYR_ITIM | 661 | 666 | PF00017 | 0.483 |
LIG_WRC_WIRS_1 | 301 | 306 | PF05994 | 0.415 |
LIG_WRC_WIRS_1 | 430 | 435 | PF05994 | 0.391 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.537 |
MOD_CDK_SPxxK_3 | 446 | 453 | PF00069 | 0.415 |
MOD_CDK_SPxxK_3 | 544 | 551 | PF00069 | 0.586 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.464 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.556 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.516 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.564 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.463 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.537 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.476 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.527 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.450 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.452 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.469 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.395 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.585 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.465 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.446 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.571 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.344 |
MOD_CK2_1 | 632 | 638 | PF00069 | 0.405 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.493 |
MOD_Cter_Amidation | 409 | 412 | PF01082 | 0.719 |
MOD_DYRK1A_RPxSP_1 | 453 | 457 | PF00069 | 0.375 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.667 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.719 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.716 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.660 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.757 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.704 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.728 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.604 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.327 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.650 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.312 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.334 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.533 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.514 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.502 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.435 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.506 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.519 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.497 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.400 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.467 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.453 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.448 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.483 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.447 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.537 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.555 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.352 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.644 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.580 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.691 |
MOD_N-GLC_1 | 583 | 588 | PF02516 | 0.332 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.484 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.404 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.488 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.460 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.414 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.448 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.545 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.551 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.553 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.326 |
MOD_NEK2_2 | 164 | 169 | PF00069 | 0.519 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.471 |
MOD_PIKK_1 | 607 | 613 | PF00454 | 0.528 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.446 |
MOD_PK_1 | 192 | 198 | PF00069 | 0.467 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.612 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.468 |
MOD_PKB_1 | 190 | 198 | PF00069 | 0.516 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.415 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.438 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.390 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.200 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.536 |
MOD_Plk_2-3 | 208 | 214 | PF00069 | 0.492 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.418 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.324 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.506 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.621 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.459 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.534 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.509 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.418 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.553 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.471 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.440 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.528 |
MOD_ProDKin_1 | 638 | 644 | PF00069 | 0.364 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 591 | 596 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.689 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.612 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 207 | 212 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 534 | 538 | PF00026 | 0.317 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5F0 | Leptomonas seymouri | 44% | 93% |
A0A3Q8IEP9 | Leishmania donovani | 86% | 100% |
A4HGP8 | Leishmania braziliensis | 65% | 99% |
A4I3S1 | Leishmania infantum | 86% | 100% |
Q4Q872 | Leishmania major | 83% | 100% |