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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: Q4QFN7
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 15 |
GO:0005451 | obsolete monoatomic cation:proton antiporter activity | 5 | 15 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 15 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 15 |
GO:0015078 | proton transmembrane transporter activity | 5 | 15 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 15 |
GO:0015297 | antiporter activity | 5 | 15 |
GO:0015298 | obsolete solute:monoatomic cation antiporter activity | 5 | 15 |
GO:0015299 | obsolete solute:proton antiporter activity | 6 | 15 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 15 |
GO:0022804 | active transmembrane transporter activity | 3 | 15 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 15 |
GO:0022857 | transmembrane transporter activity | 2 | 15 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.124 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.298 |
CLV_PCSK_FUR_1 | 557 | 561 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 559 | 561 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.331 |
DOC_ANK_TNKS_1 | 46 | 53 | PF00023 | 0.442 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.273 |
DOC_MAPK_DCC_7 | 130 | 140 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 468 | 475 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 170 | 177 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.247 |
DOC_MAPK_MEF2A_6 | 468 | 475 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 63 | 70 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 78 | 86 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.379 |
DOC_PP2B_LxvP_1 | 132 | 135 | PF13499 | 0.261 |
DOC_SPAK_OSR1_1 | 452 | 456 | PF12202 | 0.408 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.782 |
DOC_USP7_UBL2_3 | 183 | 187 | PF12436 | 0.504 |
DOC_USP7_UBL2_3 | 426 | 430 | PF12436 | 0.240 |
DOC_USP7_UBL2_3 | 544 | 548 | PF12436 | 0.609 |
DOC_USP7_UBL2_3 | 555 | 559 | PF12436 | 0.649 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 390 | 395 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 452 | 458 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 632 | 636 | PF00244 | 0.551 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 53 | 62 | PF00928 | 0.565 |
LIG_EH1_1 | 318 | 326 | PF00400 | 0.266 |
LIG_eIF4E_1 | 110 | 116 | PF01652 | 0.279 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.195 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.292 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.465 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.282 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.712 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.617 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.289 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.728 |
LIG_GBD_Chelix_1 | 119 | 127 | PF00786 | 0.382 |
LIG_GBD_Chelix_1 | 490 | 498 | PF00786 | 0.408 |
LIG_LIR_Apic_2 | 39 | 44 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 29 | 36 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 356 | 365 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 405 | 414 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 524 | 535 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 640 | 646 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 405 | 409 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 640 | 645 | PF02991 | 0.595 |
LIG_PDZ_Class_1 | 641 | 646 | PF00595 | 0.597 |
LIG_Pex14_1 | 278 | 282 | PF04695 | 0.261 |
LIG_Pex14_2 | 433 | 437 | PF04695 | 0.203 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.105 |
LIG_PTB_Apo_2 | 213 | 220 | PF02174 | 0.302 |
LIG_PTB_Apo_2 | 331 | 338 | PF02174 | 0.418 |
LIG_PTB_Apo_2 | 431 | 438 | PF02174 | 0.217 |
LIG_PTB_Phospho_1 | 331 | 337 | PF10480 | 0.426 |
LIG_REV1ctd_RIR_1 | 360 | 370 | PF16727 | 0.408 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.520 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.398 |
LIG_SH2_CRK | 642 | 646 | PF00017 | 0.596 |
LIG_SH2_GRB2like | 516 | 519 | PF00017 | 0.267 |
LIG_SH2_NCK_1 | 358 | 362 | PF00017 | 0.408 |
LIG_SH2_NCK_1 | 642 | 646 | PF00017 | 0.596 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.243 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 516 | 520 | PF00017 | 0.211 |
LIG_SH2_STAP1 | 642 | 646 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.199 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.273 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.235 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.235 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.243 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.341 |
LIG_SUMO_SIM_anti_2 | 113 | 119 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 115 | 121 | PF11976 | 0.343 |
LIG_TRFH_1 | 31 | 35 | PF08558 | 0.419 |
LIG_UBA3_1 | 283 | 292 | PF00899 | 0.322 |
LIG_UBA3_1 | 419 | 426 | PF00899 | 0.303 |
LIG_UBA3_1 | 498 | 507 | PF00899 | 0.439 |
MOD_CDC14_SPxK_1 | 610 | 613 | PF00782 | 0.526 |
MOD_CDK_SPxK_1 | 607 | 613 | PF00069 | 0.532 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.284 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.384 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.669 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.562 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.475 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.320 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.745 |
MOD_Cter_Amidation | 504 | 507 | PF01082 | 0.369 |
MOD_Cter_Amidation | 71 | 74 | PF01082 | 0.448 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.285 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.278 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.313 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.258 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.363 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.664 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.642 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.725 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.266 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.282 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.249 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.570 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.597 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.735 |
MOD_N-GLC_1 | 433 | 438 | PF02516 | 0.373 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.733 |
MOD_N-GLC_2 | 343 | 345 | PF02516 | 0.434 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.438 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.162 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.333 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.268 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.233 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.258 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.302 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.218 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.216 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.137 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.180 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.665 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.712 |
MOD_PK_1 | 603 | 609 | PF00069 | 0.541 |
MOD_PK_1 | 73 | 79 | PF00069 | 0.499 |
MOD_PKA_1 | 506 | 512 | PF00069 | 0.132 |
MOD_PKA_1 | 559 | 565 | PF00069 | 0.639 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.499 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.433 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.647 |
MOD_PKA_2 | 628 | 634 | PF00069 | 0.530 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.440 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.539 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.373 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.561 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.726 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.280 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.362 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.279 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.247 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.163 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.411 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.281 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.303 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.310 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.195 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.276 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.674 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.286 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.508 |
TRG_ER_diArg_1 | 637 | 639 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7H5 | Leptomonas seymouri | 32% | 71% |
A0A0N1I1I3 | Leptomonas seymouri | 74% | 79% |
A0A0S4IUH4 | Bodo saltans | 41% | 93% |
A0A0S4IYS7 | Bodo saltans | 46% | 100% |
A0A0S4J2L9 | Bodo saltans | 50% | 100% |
A0A1X0NSQ8 | Trypanosomatidae | 64% | 90% |
A0A1X0P4B5 | Trypanosomatidae | 29% | 80% |
A0A3Q8I9W9 | Leishmania donovani | 95% | 100% |
A0A3R7NWD7 | Trypanosoma rangeli | 28% | 86% |
A0A422N0A8 | Trypanosoma rangeli | 59% | 96% |
A4HW40 | Leishmania infantum | 95% | 100% |
A4IHB9 | Xenopus tropicalis | 26% | 100% |
C9ZP87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
D0A5M2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 81% |
E9AI47 | Leishmania braziliensis | 86% | 82% |
E9APU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4R7S2 | Macaca fascicularis | 25% | 100% |
Q4ZJI4 | Homo sapiens | 24% | 100% |
Q5BKR2 | Mus musculus | 25% | 100% |
Q5R6B8 | Pongo abelii | 24% | 100% |
Q86UD5 | Homo sapiens | 24% | 100% |
V5BES3 | Trypanosoma cruzi | 62% | 96% |
V5BN48 | Trypanosoma cruzi | 28% | 81% |