LeishMANIAdb
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Ion_trans domain-containing protein

Quick info Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Ion_trans domain-containing protein
Gene product:
ion transport protein, putative
Species:
Leishmania braziliensis
UniProt:
A4H9A2_LEIBR
TriTrypDb:
LbrM.17.1590 , LBRM2903_170023500 *
Length:
665

Localization

Secreted promastigote
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
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 1
NetGPI no yes: 0, no: 1
Cellular components
Term Name Level Count
GO:0016020 membrane 2 2
GO:0110165 cellular anatomical entity 1 2

Expansion

Sequence features

A4H9A2
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4H9A2

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0005215 transporter activity 1 2
GO:0005216 monoatomic ion channel activity 4 2
GO:0015075 monoatomic ion transmembrane transporter activity 3 2
GO:0015267 channel activity 4 2
GO:0015318 inorganic molecular entity transmembrane transporter activity 3 2
GO:0022803 passive transmembrane transporter activity 3 2
GO:0022857 transmembrane transporter activity 2 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 29 33 PF00656 0.563
CLV_C14_Caspase3-7 654 658 PF00656 0.784
CLV_MEL_PAP_1 500 506 PF00089 0.521
CLV_NRD_NRD_1 478 480 PF00675 0.510
CLV_NRD_NRD_1 50 52 PF00675 0.750
CLV_NRD_NRD_1 550 552 PF00675 0.459
CLV_NRD_NRD_1 627 629 PF00675 0.582
CLV_NRD_NRD_1 93 95 PF00675 0.820
CLV_PCSK_KEX2_1 386 388 PF00082 0.650
CLV_PCSK_KEX2_1 478 480 PF00082 0.510
CLV_PCSK_KEX2_1 50 52 PF00082 0.750
CLV_PCSK_KEX2_1 626 628 PF00082 0.593
CLV_PCSK_PC1ET2_1 386 388 PF00082 0.650
CLV_PCSK_SKI1_1 294 298 PF00082 0.650
CLV_PCSK_SKI1_1 349 353 PF00082 0.449
CLV_PCSK_SKI1_1 636 640 PF00082 0.573
DEG_APCC_DBOX_1 566 574 PF00400 0.730
DOC_CYCLIN_RxL_1 346 354 PF00134 0.650
DOC_CYCLIN_yCln2_LP_2 141 147 PF00134 0.630
DOC_CYCLIN_yCln2_LP_2 341 347 PF00134 0.650
DOC_MAPK_gen_1 386 393 PF00069 0.387
DOC_MAPK_gen_1 478 485 PF00069 0.709
DOC_MAPK_gen_1 551 557 PF00069 0.685
DOC_MAPK_gen_1 567 575 PF00069 0.567
DOC_MAPK_gen_1 626 635 PF00069 0.780
DOC_MAPK_MEF2A_6 321 329 PF00069 0.549
DOC_MAPK_MEF2A_6 598 606 PF00069 0.730
DOC_MAPK_RevD_3 35 51 PF00069 0.543
DOC_MAPK_RevD_3 371 387 PF00069 0.549
DOC_MAPK_RevD_3 464 479 PF00069 0.726
DOC_PP2B_LxvP_1 141 144 PF13499 0.629
DOC_PP2B_LxvP_1 529 532 PF13499 0.648
DOC_PP2B_LxvP_1 639 642 PF13499 0.764
DOC_PP4_FxxP_1 462 465 PF00568 0.660
DOC_USP7_MATH_1 193 197 PF00917 0.641
DOC_USP7_MATH_1 259 263 PF00917 0.650
DOC_USP7_MATH_1 558 562 PF00917 0.749
DOC_USP7_MATH_1 615 619 PF00917 0.802
DOC_USP7_MATH_1 640 644 PF00917 0.761
DOC_USP7_MATH_1 652 656 PF00917 0.668
DOC_WW_Pin1_4 314 319 PF00397 0.549
DOC_WW_Pin1_4 610 615 PF00397 0.792
LIG_14-3-3_CanoR_1 180 187 PF00244 0.651
LIG_14-3-3_CanoR_1 216 226 PF00244 0.651
LIG_14-3-3_CanoR_1 349 359 PF00244 0.650
LIG_14-3-3_CanoR_1 423 428 PF00244 0.449
LIG_14-3-3_CanoR_1 569 575 PF00244 0.710
LIG_Actin_WH2_2 305 323 PF00022 0.549
LIG_APCC_ABBA_1 464 469 PF00400 0.749
LIG_BIR_II_1 1 5 PF00653 0.774
LIG_BRCT_BRCA1_1 643 647 PF00533 0.775
LIG_Clathr_ClatBox_1 397 401 PF01394 0.449
LIG_deltaCOP1_diTrp_1 142 151 PF00928 0.630
LIG_EH1_1 240 248 PF00400 0.549
LIG_EH1_1 345 353 PF00400 0.650
LIG_FHA_1 228 234 PF00498 0.615
LIG_FHA_1 243 249 PF00498 0.287
LIG_FHA_1 295 301 PF00498 0.387
LIG_FHA_1 321 327 PF00498 0.549
LIG_FHA_1 356 362 PF00498 0.523
LIG_FHA_1 368 374 PF00498 0.366
LIG_FHA_1 376 382 PF00498 0.218
LIG_FHA_1 435 441 PF00498 0.549
LIG_FHA_1 459 465 PF00498 0.549
LIG_FHA_1 507 513 PF00498 0.754
LIG_FHA_1 88 94 PF00498 0.625
LIG_FHA_2 187 193 PF00498 0.640
LIG_FHA_2 27 33 PF00498 0.572
LIG_FHA_2 572 578 PF00498 0.668
LIG_GBD_Chelix_1 445 453 PF00786 0.549
LIG_LIR_Apic_2 156 161 PF02991 0.641
LIG_LIR_Apic_2 461 465 PF02991 0.549
LIG_LIR_Gen_1 103 113 PF02991 0.621
LIG_LIR_Gen_1 134 144 PF02991 0.639
LIG_LIR_Gen_1 31 42 PF02991 0.547
LIG_LIR_Gen_1 364 373 PF02991 0.549
LIG_LIR_Gen_1 388 397 PF02991 0.449
LIG_LIR_Gen_1 406 416 PF02991 0.224
LIG_LIR_Gen_1 432 440 PF02991 0.449
LIG_LIR_Gen_1 441 450 PF02991 0.392
LIG_LIR_Gen_1 8 18 PF02991 0.549
LIG_LIR_Nem_3 103 108 PF02991 0.619
LIG_LIR_Nem_3 134 140 PF02991 0.644
LIG_LIR_Nem_3 182 187 PF02991 0.649
LIG_LIR_Nem_3 31 37 PF02991 0.552
LIG_LIR_Nem_3 364 368 PF02991 0.549
LIG_LIR_Nem_3 388 392 PF02991 0.449
LIG_LIR_Nem_3 406 411 PF02991 0.224
LIG_LIR_Nem_3 432 436 PF02991 0.449
LIG_LIR_Nem_3 437 442 PF02991 0.462
LIG_LIR_Nem_3 577 582 PF02991 0.666
LIG_LIR_Nem_3 8 13 PF02991 0.549
LIG_Pex14_2 438 442 PF04695 0.549
LIG_Pex14_2 647 651 PF04695 0.788
LIG_SH2_CRK 137 141 PF00017 0.644
LIG_SH2_CRK 184 188 PF00017 0.648
LIG_SH2_CRK 34 38 PF00017 0.547
LIG_SH2_CRK 433 437 PF00017 0.449
LIG_SH2_CRK 579 583 PF00017 0.664
LIG_SH2_CRK 649 653 PF00017 0.782
LIG_SH2_GRB2like 137 140 PF00017 0.643
LIG_SH2_NCK_1 365 369 PF00017 0.549
LIG_SH2_NCK_1 433 437 PF00017 0.449
LIG_SH2_SRC 137 140 PF00017 0.643
LIG_SH2_SRC 541 544 PF00017 0.638
LIG_SH2_STAP1 105 109 PF00017 0.617
LIG_SH2_STAP1 137 141 PF00017 0.644
LIG_SH2_STAP1 34 38 PF00017 0.547
LIG_SH2_STAP1 541 545 PF00017 0.640
LIG_SH2_STAT3 38 41 PF00017 0.542
LIG_SH2_STAT5 253 256 PF00017 0.549
LIG_SH2_STAT5 295 298 PF00017 0.449
LIG_SH2_STAT5 382 385 PF00017 0.449
LIG_SH2_STAT5 596 599 PF00017 0.714
LIG_SH2_STAT5 649 652 PF00017 0.784
LIG_SH2_STAT5 86 89 PF00017 0.635
LIG_SH3_1 158 164 PF00018 0.646
LIG_SH3_3 137 143 PF00018 0.639
LIG_SH3_3 158 164 PF00018 0.646
LIG_SH3_3 220 226 PF00018 0.652
LIG_SH3_3 312 318 PF00018 0.549
LIG_SH3_3 389 395 PF00018 0.449
LIG_SH3_5 75 79 PF00018 0.612
LIG_SUMO_SIM_anti_2 336 343 PF11976 0.650
LIG_SUMO_SIM_anti_2 358 364 PF11976 0.462
LIG_SUMO_SIM_anti_2 629 636 PF11976 0.776
LIG_SUMO_SIM_par_1 245 250 PF11976 0.549
LIG_SUMO_SIM_par_1 267 273 PF11976 0.650
LIG_SUMO_SIM_par_1 311 317 PF11976 0.462
LIG_SUMO_SIM_par_1 358 364 PF11976 0.549
LIG_SUMO_SIM_par_1 369 375 PF11976 0.357
LIG_SUMO_SIM_par_1 394 401 PF11976 0.449
LIG_TYR_ITIM 539 544 PF00017 0.535
LIG_TYR_ITIM 594 599 PF00017 0.629
LIG_UBA3_1 632 636 PF00899 0.730
LIG_WRC_WIRS_1 439 444 PF05994 0.549
LIG_WRC_WIRS_1 459 464 PF05994 0.199
MOD_CDK_SPxxK_3 314 321 PF00069 0.549
MOD_CK1_1 212 218 PF00069 0.817
MOD_CK1_1 314 320 PF00069 0.462
MOD_CK1_1 434 440 PF00069 0.549
MOD_CK1_1 610 616 PF00069 0.750
MOD_CK2_1 277 283 PF00069 0.549
MOD_CK2_1 571 577 PF00069 0.596
MOD_CK2_1 615 621 PF00069 0.765
MOD_GlcNHglycan 279 282 PF01048 0.549
MOD_GlcNHglycan 353 356 PF01048 0.549
MOD_GlcNHglycan 425 428 PF01048 0.549
MOD_GlcNHglycan 433 436 PF01048 0.410
MOD_GlcNHglycan 559 563 PF01048 0.700
MOD_GlcNHglycan 609 612 PF01048 0.754
MOD_GlcNHglycan 75 78 PF01048 0.777
MOD_GlcNHglycan 90 93 PF01048 0.529
MOD_GSK3_1 179 186 PF00069 0.832
MOD_GSK3_1 205 212 PF00069 0.807
MOD_GSK3_1 351 358 PF00069 0.462
MOD_GSK3_1 434 441 PF00069 0.549
MOD_GSK3_1 454 461 PF00069 0.199
MOD_GSK3_1 502 509 PF00069 0.666
MOD_GSK3_1 511 518 PF00069 0.566
MOD_GSK3_1 84 91 PF00069 0.805
MOD_N-GLC_1 423 428 PF02516 0.549
MOD_N-GLC_1 79 84 PF02516 0.790
MOD_NEK2_1 242 247 PF00069 0.549
MOD_NEK2_1 254 259 PF00069 0.339
MOD_NEK2_1 311 316 PF00069 0.510
MOD_NEK2_1 320 325 PF00069 0.431
MOD_NEK2_1 350 355 PF00069 0.549
MOD_NEK2_1 438 443 PF00069 0.549
MOD_NEK2_1 525 530 PF00069 0.544
MOD_NEK2_1 557 562 PF00069 0.679
MOD_NEK2_1 602 607 PF00069 0.689
MOD_NEK2_1 647 652 PF00069 0.741
MOD_NEK2_1 84 89 PF00069 0.807
MOD_NEK2_2 33 38 PF00069 0.685
MOD_OFUCOSY 565 572 PF10250 0.688
MOD_PK_1 387 393 PF00069 0.462
MOD_PKA_1 94 100 PF00069 0.781
MOD_PKA_2 153 159 PF00069 0.817
MOD_PKA_2 166 172 PF00069 0.615
MOD_PKA_2 179 185 PF00069 0.604
MOD_PKA_2 320 326 PF00069 0.549
MOD_PKA_2 502 508 PF00069 0.669
MOD_PKA_2 568 574 PF00069 0.656
MOD_Plk_1 387 393 PF00069 0.549
MOD_Plk_1 589 595 PF00069 0.589
MOD_Plk_1 79 85 PF00069 0.729
MOD_Plk_2-3 401 407 PF00069 0.492
MOD_Plk_4 109 115 PF00069 0.528
MOD_Plk_4 205 211 PF00069 0.808
MOD_Plk_4 242 248 PF00069 0.549
MOD_Plk_4 259 265 PF00069 0.252
MOD_Plk_4 327 333 PF00069 0.549
MOD_Plk_4 33 39 PF00069 0.684
MOD_Plk_4 367 373 PF00069 0.549
MOD_Plk_4 434 440 PF00069 0.549
MOD_Plk_4 444 450 PF00069 0.375
MOD_Plk_4 454 460 PF00069 0.199
MOD_Plk_4 496 502 PF00069 0.616
MOD_Plk_4 79 85 PF00069 0.791
MOD_Plk_4 94 100 PF00069 0.519
MOD_ProDKin_1 314 320 PF00069 0.549
MOD_ProDKin_1 610 616 PF00069 0.750
TRG_DiLeu_BaEn_1 142 147 PF01217 0.799
TRG_DiLeu_BaEn_1 629 634 PF01217 0.725
TRG_DiLeu_BaLyEn_6 233 238 PF01217 0.718
TRG_DiLeu_BaLyEn_6 315 320 PF01217 0.549
TRG_DiLeu_BaLyEn_6 392 397 PF01217 0.549
TRG_ENDOCYTIC_2 105 108 PF00928 0.785
TRG_ENDOCYTIC_2 137 140 PF00928 0.820
TRG_ENDOCYTIC_2 184 187 PF00928 0.828
TRG_ENDOCYTIC_2 34 37 PF00928 0.687
TRG_ENDOCYTIC_2 365 368 PF00928 0.549
TRG_ENDOCYTIC_2 433 436 PF00928 0.549
TRG_ENDOCYTIC_2 541 544 PF00928 0.533
TRG_ENDOCYTIC_2 579 582 PF00928 0.573
TRG_ENDOCYTIC_2 596 599 PF00928 0.416
TRG_ER_diArg_1 478 480 PF00400 0.633
TRG_ER_diArg_1 49 51 PF00400 0.691
TRG_ER_diArg_1 62 65 PF00400 0.546
TRG_ER_diArg_1 625 628 PF00400 0.750
TRG_NES_CRM1_1 521 535 PF08389 0.555

Homologs

Protein Taxonomy Sequence identity Coverage
C9D7C2 APIME 21% 35%
O35505 CAVPO 21% 31%
O57483 LITCT 26% 39%
P07293 RABIT 25% 36%
P15381 RABIT 22% 31%
P22002 RAT 21% 31%
P27732 RAT 21% 30%
P54282 RAT 20% 30%
P91645 DROME 21% 36%
Q01815 MOUSE 22% 31%
Q02485 RAT 25% 36%
Q02789 MOUSE 27% 36%
Q13698 HUMAN 26% 36%
Q99246 MOUSE 22% 31%

Download

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS