A bacterial-type Mg2+ transporter found in kinetoplastids.. Expanded extensively on multiple lineages, especially T cruzi
Transporters, divalent cation transporter, putative Uncharacterized
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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I3S1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0006811 | monoatomic ion transport | 4 | 6 |
GO:0006812 | monoatomic cation transport | 5 | 6 |
GO:0015693 | magnesium ion transport | 7 | 6 |
GO:0030001 | metal ion transport | 6 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 6 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 6 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 6 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 6 |
GO:0022857 | transmembrane transporter activity | 2 | 6 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 6 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.342 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.583 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.511 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.382 |
DEG_SPOP_SBC_1 | 637 | 641 | PF00917 | 0.257 |
DOC_ANK_TNKS_1 | 307 | 314 | PF00023 | 0.385 |
DOC_CDC14_PxL_1 | 110 | 118 | PF14671 | 0.404 |
DOC_CDC14_PxL_1 | 619 | 627 | PF14671 | 0.267 |
DOC_CKS1_1 | 288 | 293 | PF01111 | 0.314 |
DOC_CKS1_1 | 448 | 453 | PF01111 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 115 | 118 | PF00134 | 0.401 |
DOC_CYCLIN_yCln2_LP_2 | 418 | 424 | PF00134 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 540 | 546 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 516 | 524 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 532 | 541 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 439 | 448 | PF00069 | 0.343 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.435 |
DOC_PP2B_LxvP_1 | 539 | 542 | PF13499 | 0.412 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.428 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.341 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 638 | 643 | PF00397 | 0.226 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.389 |
LIG_14-3-3_CanoR_1 | 120 | 128 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 35 | 45 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 551 | 559 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 561 | 567 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 582 | 588 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 594 | 602 | PF00244 | 0.324 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.395 |
LIG_BIR_III_2 | 160 | 164 | PF00653 | 0.421 |
LIG_BRCT_BRCA1_1 | 298 | 302 | PF00533 | 0.303 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.377 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.309 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.397 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.427 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.315 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.248 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.395 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.257 |
LIG_HP1_1 | 291 | 295 | PF01393 | 0.285 |
LIG_LIR_Gen_1 | 42 | 53 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 641 | 651 | PF02991 | 0.209 |
LIG_LIR_Gen_1 | 94 | 101 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 640 | 646 | PF02991 | 0.205 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.389 |
LIG_MAD2 | 534 | 542 | PF02301 | 0.402 |
LIG_MYND_1 | 114 | 118 | PF01753 | 0.400 |
LIG_NRBOX | 535 | 541 | PF00104 | 0.402 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.380 |
LIG_SH2_CRK | 663 | 667 | PF00017 | 0.493 |
LIG_SH2_CRK | 668 | 672 | PF00017 | 0.489 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.498 |
LIG_SH2_PTP2 | 254 | 257 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.357 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.479 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.446 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.348 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.503 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.316 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.445 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.300 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.387 |
LIG_SUMO_SIM_anti_2 | 172 | 182 | PF11976 | 0.269 |
LIG_SUMO_SIM_anti_2 | 462 | 471 | PF11976 | 0.185 |
LIG_SUMO_SIM_anti_2 | 610 | 616 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 172 | 182 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 336 | 342 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 652 | 657 | PF11976 | 0.256 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.379 |
LIG_TYR_ITIM | 661 | 666 | PF00017 | 0.406 |
LIG_WRC_WIRS_1 | 301 | 306 | PF05994 | 0.302 |
MOD_CDK_SPK_2 | 397 | 402 | PF00069 | 0.403 |
MOD_CDK_SPxK_1 | 447 | 453 | PF00069 | 0.372 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.463 |
MOD_CDK_SPxxK_3 | 544 | 551 | PF00069 | 0.457 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.379 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.387 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.475 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.427 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.492 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.390 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.463 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.399 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.454 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.387 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.377 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.389 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.322 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.459 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.357 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.395 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.308 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.499 |
MOD_CK2_1 | 632 | 638 | PF00069 | 0.257 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.401 |
MOD_Cter_Amidation | 409 | 412 | PF01082 | 0.622 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.580 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.607 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.582 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.529 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.635 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.535 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.687 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.629 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.254 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.579 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.201 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.386 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.454 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.418 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.439 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.363 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.430 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.389 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.434 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.299 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.400 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.379 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.366 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.352 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.378 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.374 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.419 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.384 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.422 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.205 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.379 |
MOD_LATS_1 | 229 | 235 | PF00433 | 0.417 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.558 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.618 |
MOD_N-GLC_1 | 583 | 588 | PF02516 | 0.222 |
MOD_N-GLC_2 | 458 | 460 | PF02516 | 0.520 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.392 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.314 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.406 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.312 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.375 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.431 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.422 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.423 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.253 |
MOD_NEK2_2 | 164 | 169 | PF00069 | 0.436 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.423 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.395 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.405 |
MOD_PIKK_1 | 607 | 613 | PF00454 | 0.402 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.388 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.342 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.486 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.356 |
MOD_PKB_1 | 190 | 198 | PF00069 | 0.449 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.319 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.402 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.352 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.422 |
MOD_Plk_2-3 | 213 | 219 | PF00069 | 0.464 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.323 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.251 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.394 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.366 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.434 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.435 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.322 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.454 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.373 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.402 |
MOD_ProDKin_1 | 638 | 644 | PF00069 | 0.226 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 591 | 596 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.510 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 485 | 490 | PF00026 | 0.195 |
TRG_Pf-PMV_PEXEL_1 | 534 | 538 | PF00026 | 0.202 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5F0 | Leptomonas seymouri | 44% | 93% |
A0A3Q8IEP9 | Leishmania donovani | 100% | 100% |
A4HGP8 | Leishmania braziliensis | 67% | 99% |
E9B013 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q872 | Leishmania major | 90% | 100% |