Homologous to animal Na+ / H+ exchangers.. Interestingly most heavily expanded in Strigomonas species and the non-parazitic Bodo saltans
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
Related structures:
AlphaFold database: E9AI47
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 14 |
GO:0005451 | obsolete monoatomic cation:proton antiporter activity | 5 | 14 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 14 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 14 |
GO:0015078 | proton transmembrane transporter activity | 5 | 14 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 14 |
GO:0015297 | antiporter activity | 5 | 14 |
GO:0015298 | obsolete solute:monoatomic cation antiporter activity | 5 | 14 |
GO:0015299 | obsolete solute:proton antiporter activity | 6 | 14 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 14 |
GO:0022804 | active transmembrane transporter activity | 3 | 14 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 14 |
GO:0022857 | transmembrane transporter activity | 2 | 14 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 745 | 749 | PF00656 | 0.751 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.482 |
CLV_PCSK_FUR_1 | 569 | 573 | PF00082 | 0.197 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 727 | 729 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 734 | 736 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.535 |
DEG_COP1_1 | 24 | 34 | PF00400 | 0.623 |
DEG_SCF_SKP2-CKS1_1 | 727 | 734 | PF00560 | 0.570 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.621 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.612 |
DOC_MAPK_DCC_7 | 309 | 319 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 647 | 654 | PF00069 | 0.543 |
DOC_MAPK_HePTP_8 | 261 | 273 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 242 | 249 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 257 | 265 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 349 | 356 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 471 | 478 | PF00069 | 0.315 |
DOC_MAPK_MEF2A_6 | 647 | 654 | PF00069 | 0.543 |
DOC_PP1_RVXF_1 | 262 | 268 | PF00149 | 0.432 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.605 |
DOC_PP2B_LxvP_1 | 311 | 314 | PF13499 | 0.359 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.777 |
DOC_SPAK_OSR1_1 | 631 | 635 | PF12202 | 0.452 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.709 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.560 |
DOC_USP7_UBL2_3 | 605 | 609 | PF12436 | 0.364 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 728 | 733 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.747 |
LIG_14-3-3_CanoR_1 | 54 | 59 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 631 | 637 | PF00244 | 0.356 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.608 |
LIG_BRCT_BRCA1_1 | 162 | 166 | PF00533 | 0.578 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.596 |
LIG_BRCT_BRCA1_1 | 613 | 617 | PF00533 | 0.260 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.746 |
LIG_Clathr_ClatBox_1 | 503 | 507 | PF01394 | 0.397 |
LIG_CtBP_PxDLS_1 | 140 | 144 | PF00389 | 0.615 |
LIG_deltaCOP1_diTrp_1 | 232 | 241 | PF00928 | 0.617 |
LIG_EH1_1 | 497 | 505 | PF00400 | 0.411 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.259 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.299 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.531 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.418 |
LIG_FHA_1 | 633 | 639 | PF00498 | 0.354 |
LIG_FHA_2 | 689 | 695 | PF00498 | 0.329 |
LIG_FHA_2 | 760 | 766 | PF00498 | 0.772 |
LIG_GBD_Chelix_1 | 270 | 278 | PF00786 | 0.224 |
LIG_GBD_Chelix_1 | 298 | 306 | PF00786 | 0.452 |
LIG_GBD_Chelix_1 | 669 | 677 | PF00786 | 0.452 |
LIG_LIR_Apic_2 | 218 | 223 | PF02991 | 0.556 |
LIG_LIR_Apic_2 | 48 | 53 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 208 | 215 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 526 | 537 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 584 | 593 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 703 | 714 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 589 | 593 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 703 | 709 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 715 | 719 | PF02991 | 0.369 |
LIG_MLH1_MIPbox_1 | 613 | 617 | PF16413 | 0.285 |
LIG_MYND_1 | 177 | 181 | PF01753 | 0.492 |
LIG_PALB2_WD40_1 | 216 | 224 | PF16756 | 0.481 |
LIG_Pex14_1 | 235 | 239 | PF04695 | 0.546 |
LIG_Pex14_1 | 457 | 461 | PF04695 | 0.346 |
LIG_Pex14_2 | 612 | 616 | PF04695 | 0.264 |
LIG_Pex14_2 | 632 | 636 | PF04695 | 0.457 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.758 |
LIG_PTB_Apo_2 | 165 | 172 | PF02174 | 0.615 |
LIG_PTB_Apo_2 | 392 | 399 | PF02174 | 0.373 |
LIG_PTB_Apo_2 | 510 | 517 | PF02174 | 0.485 |
LIG_PTB_Apo_2 | 610 | 617 | PF02174 | 0.277 |
LIG_PTB_Phospho_1 | 165 | 171 | PF10480 | 0.493 |
LIG_PTB_Phospho_1 | 510 | 516 | PF10480 | 0.494 |
LIG_REV1ctd_RIR_1 | 539 | 549 | PF16727 | 0.452 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.583 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.445 |
LIG_SH2_GRB2like | 695 | 698 | PF00017 | 0.321 |
LIG_SH2_NCK_1 | 537 | 541 | PF00017 | 0.452 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.612 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 537 | 541 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 695 | 699 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 706 | 709 | PF00017 | 0.346 |
LIG_SH3_2 | 71 | 76 | PF14604 | 0.606 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.726 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.724 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.294 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.325 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.276 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.388 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.627 |
LIG_SH3_3 | 766 | 772 | PF00018 | 0.622 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.717 |
LIG_Sin3_3 | 294 | 301 | PF02671 | 0.224 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.409 |
LIG_TRFH_1 | 210 | 214 | PF08558 | 0.496 |
LIG_TYR_ITIM | 535 | 540 | PF00017 | 0.224 |
LIG_UBA3_1 | 462 | 471 | PF00899 | 0.407 |
LIG_UBA3_1 | 598 | 605 | PF00899 | 0.373 |
LIG_UBA3_1 | 677 | 686 | PF00899 | 0.476 |
LIG_WRC_WIRS_1 | 633 | 638 | PF05994 | 0.346 |
LIG_WRC_WIRS_1 | 713 | 718 | PF05994 | 0.397 |
MOD_CDK_SPxK_1 | 728 | 734 | PF00069 | 0.472 |
MOD_CDK_SPxxK_3 | 728 | 735 | PF00069 | 0.482 |
MOD_CDK_SPxxK_3 | 94 | 101 | PF00069 | 0.507 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.751 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.622 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.648 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.537 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.585 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.357 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.766 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.408 |
MOD_CK1_1 | 741 | 747 | PF00069 | 0.733 |
MOD_CK2_1 | 688 | 694 | PF00069 | 0.393 |
MOD_CK2_1 | 759 | 765 | PF00069 | 0.767 |
MOD_Cter_Amidation | 250 | 253 | PF01082 | 0.508 |
MOD_DYRK1A_RPxSP_1 | 94 | 98 | PF00069 | 0.509 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.599 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.371 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.349 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.383 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.379 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.382 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.422 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.746 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.700 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.669 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.672 |
MOD_GlcNHglycan | 8 | 12 | PF01048 | 0.740 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.671 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.677 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.676 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.624 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.787 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.333 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.339 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.404 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.675 |
MOD_GSK3_1 | 759 | 766 | PF00069 | 0.659 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.455 |
MOD_N-GLC_1 | 612 | 617 | PF02516 | 0.411 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.729 |
MOD_N-GLC_2 | 522 | 524 | PF02516 | 0.457 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.619 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.338 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.306 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.385 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.353 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.322 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.280 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.340 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.381 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.380 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.330 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.210 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.305 |
MOD_NEK2_1 | 708 | 713 | PF00069 | 0.377 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.742 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.528 |
MOD_PK_1 | 252 | 258 | PF00069 | 0.545 |
MOD_PKA_1 | 252 | 258 | PF00069 | 0.545 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.500 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.773 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.757 |
MOD_PKA_2 | 738 | 744 | PF00069 | 0.733 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.634 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.493 |
MOD_Plk_1 | 612 | 618 | PF00069 | 0.428 |
MOD_Plk_2-3 | 685 | 691 | PF00069 | 0.397 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.484 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.481 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.351 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.420 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.362 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.336 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.232 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.777 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.365 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.373 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.403 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.323 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.537 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.662 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.335 |
MOD_ProDKin_1 | 728 | 734 | PF00069 | 0.472 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.713 |
MOD_SUMO_for_1 | 504 | 507 | PF00179 | 0.359 |
MOD_SUMO_for_1 | 726 | 729 | PF00179 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 220 | 225 | PF01217 | 0.331 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 706 | 709 | PF00928 | 0.336 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 569 | 572 | PF00400 | 0.224 |
TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 281 | 285 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1I3 | Leptomonas seymouri | 76% | 97% |
A0A0S4IUH4 | Bodo saltans | 40% | 100% |
A0A0S4IYS7 | Bodo saltans | 46% | 100% |
A0A0S4J2L9 | Bodo saltans | 49% | 100% |
A0A1X0NSQ8 | Trypanosomatidae | 64% | 100% |
A0A1X0P4B5 | Trypanosomatidae | 26% | 98% |
A0A3Q8I9W9 | Leishmania donovani | 86% | 100% |
A0A422N0A8 | Trypanosoma rangeli | 59% | 100% |
A4HW40 | Leishmania infantum | 86% | 100% |
C9ZP87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
D0A5M2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 98% |
E9APU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QFN7 | Leishmania major | 86% | 100% |
V5BES3 | Trypanosoma cruzi | 62% | 100% |
V5BN48 | Trypanosoma cruzi | 26% | 98% |