LeishMANIAdb
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Putative cation transporter

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

Quick info

Protein:
Putative cation transporter
Gene product:
cation transporter, putative
Species:
Leishmania braziliensis
UniProt:
A4HFQ2_LEIBR
TriTrypDb:
LbrM.27.1380
Length:
663

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: 11
NetGPI no yes: 0, no: 11
Cellular components
Term Name Level Count
GO:0016020 membrane 2 12
GO:0110165 cellular anatomical entity 1 12
GO:0005794 Golgi apparatus 5 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0043229 intracellular organelle 3 1
GO:0043231 intracellular membrane-bounded organelle 4 1
GO:0005886 plasma membrane 3 1

Expansion

Sequence features

A4HFQ2
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HFQ2

Function

Biological processes
Term Name Level Count
GO:0006873 intracellular monoatomic ion homeostasis 4 7
GO:0006875 obsolete intracellular metal ion homeostasis 6 7
GO:0006882 intracellular zinc ion homeostasis 7 7
GO:0009987 cellular process 1 8
GO:0019725 cellular homeostasis 2 7
GO:0030003 intracellular monoatomic cation homeostasis 5 7
GO:0042592 homeostatic process 3 7
GO:0046916 obsolete intracellular transition metal ion homeostasis 7 7
GO:0048878 chemical homeostasis 4 7
GO:0050801 monoatomic ion homeostasis 5 7
GO:0055065 obsolete metal ion homeostasis 7 7
GO:0055069 obsolete zinc ion homeostasis 8 7
GO:0055076 obsolete transition metal ion homeostasis 8 7
GO:0055080 monoatomic cation homeostasis 6 7
GO:0055082 intracellular chemical homeostasis 3 7
GO:0065007 biological regulation 1 7
GO:0065008 regulation of biological quality 2 7
GO:0072503 obsolete cellular divalent inorganic cation homeostasis 6 7
GO:0072507 obsolete divalent inorganic cation homeostasis 7 7
GO:0098771 inorganic ion homeostasis 6 7
GO:0006810 transport 3 2
GO:0006811 monoatomic ion transport 4 2
GO:0006812 monoatomic cation transport 5 2
GO:0030001 metal ion transport 6 2
GO:0051179 localization 1 2
GO:0051234 establishment of localization 2 2
GO:0000041 transition metal ion transport 7 1
GO:0006829 zinc ion transport 8 1
GO:0034220 monoatomic ion transmembrane transport 3 1
GO:0055085 transmembrane transport 2 1
GO:0071577 zinc ion transmembrane transport 6 1
GO:0098655 monoatomic cation transmembrane transport 4 1
GO:0098660 inorganic ion transmembrane transport 4 1
GO:0098662 inorganic cation transmembrane transport 5 1
Molecular functions
Term Name Level Count
GO:0005215 transporter activity 1 12
GO:0005385 zinc ion transmembrane transporter activity 7 8
GO:0008324 monoatomic cation transmembrane transporter activity 4 12
GO:0015075 monoatomic ion transmembrane transporter activity 3 12
GO:0015318 inorganic molecular entity transmembrane transporter activity 3 8
GO:0022857 transmembrane transporter activity 2 12
GO:0022890 inorganic cation transmembrane transporter activity 4 8
GO:0046873 metal ion transmembrane transporter activity 5 8
GO:0046915 transition metal ion transmembrane transporter activity 6 8

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 325 329 PF00656 0.637
CLV_NRD_NRD_1 14 16 PF00675 0.360
CLV_NRD_NRD_1 161 163 PF00675 0.397
CLV_NRD_NRD_1 241 243 PF00675 0.556
CLV_NRD_NRD_1 589 591 PF00675 0.264
CLV_PCSK_KEX2_1 14 16 PF00082 0.360
CLV_PCSK_KEX2_1 161 163 PF00082 0.407
CLV_PCSK_SKI1_1 322 326 PF00082 0.426
CLV_PCSK_SKI1_1 572 576 PF00082 0.275
CLV_PCSK_SKI1_1 590 594 PF00082 0.305
CLV_PCSK_SKI1_1 615 619 PF00082 0.298
DEG_Nend_UBRbox_2 1 3 PF02207 0.580
DOC_CYCLIN_RxL_1 319 330 PF00134 0.520
DOC_CYCLIN_RxL_1 569 580 PF00134 0.475
DOC_CYCLIN_RxL_1 588 596 PF00134 0.507
DOC_MAPK_DCC_7 21 31 PF00069 0.561
DOC_MAPK_gen_1 366 376 PF00069 0.422
DOC_MAPK_MEF2A_6 366 374 PF00069 0.425
DOC_PP1_RVXF_1 320 327 PF00149 0.607
DOC_PP1_RVXF_1 99 105 PF00149 0.552
DOC_PP2B_LxvP_1 464 467 PF13499 0.254
DOC_PP2B_LxvP_1 576 579 PF13499 0.524
DOC_PP4_FxxP_1 463 466 PF00568 0.265
DOC_USP7_MATH_1 285 289 PF00917 0.320
DOC_USP7_MATH_1 300 304 PF00917 0.361
DOC_USP7_MATH_1 327 331 PF00917 0.651
DOC_USP7_MATH_1 338 342 PF00917 0.595
DOC_USP7_MATH_1 390 394 PF00917 0.271
DOC_USP7_MATH_1 549 553 PF00917 0.329
DOC_WW_Pin1_4 45 50 PF00397 0.570
DOC_WW_Pin1_4 601 606 PF00397 0.510
LIG_14-3-3_CanoR_1 118 127 PF00244 0.400
LIG_14-3-3_CanoR_1 14 22 PF00244 0.566
LIG_14-3-3_CanoR_1 161 169 PF00244 0.585
LIG_14-3-3_CanoR_1 583 592 PF00244 0.477
LIG_APCC_ABBA_1 658 663 PF00400 0.522
LIG_BIR_III_4 494 498 PF00653 0.406
LIG_BRCT_BRCA1_1 397 401 PF00533 0.251
LIG_CtBP_PxDLS_1 26 30 PF00389 0.551
LIG_EH1_1 255 263 PF00400 0.280
LIG_eIF4E_1 34 40 PF01652 0.550
LIG_FHA_1 131 137 PF00498 0.508
LIG_FHA_1 189 195 PF00498 0.206
LIG_FHA_1 2 8 PF00498 0.571
LIG_FHA_1 219 225 PF00498 0.472
LIG_FHA_1 266 272 PF00498 0.244
LIG_FHA_1 276 282 PF00498 0.399
LIG_FHA_1 375 381 PF00498 0.280
LIG_FHA_1 568 574 PF00498 0.477
LIG_FHA_1 594 600 PF00498 0.504
LIG_FHA_1 638 644 PF00498 0.533
LIG_FHA_1 79 85 PF00498 0.251
LIG_FHA_1 92 98 PF00498 0.369
LIG_FHA_2 106 112 PF00498 0.595
LIG_FHA_2 323 329 PF00498 0.632
LIG_LIR_Gen_1 175 181 PF02991 0.219
LIG_LIR_Gen_1 303 311 PF02991 0.262
LIG_LIR_Gen_1 398 405 PF02991 0.247
LIG_LIR_Gen_1 470 479 PF02991 0.262
LIG_LIR_Gen_1 87 97 PF02991 0.290
LIG_LIR_Nem_3 175 179 PF02991 0.292
LIG_LIR_Nem_3 296 302 PF02991 0.424
LIG_LIR_Nem_3 303 308 PF02991 0.239
LIG_LIR_Nem_3 367 371 PF02991 0.406
LIG_LIR_Nem_3 437 442 PF02991 0.301
LIG_LIR_Nem_3 470 476 PF02991 0.262
LIG_LIR_Nem_3 562 567 PF02991 0.293
LIG_LIR_Nem_3 87 92 PF02991 0.290
LIG_LIR_Nem_3 94 99 PF02991 0.495
LIG_NRBOX 193 199 PF00104 0.212
LIG_NRBOX 522 528 PF00104 0.271
LIG_PCNA_yPIPBox_3 272 281 PF02747 0.556
LIG_PCNA_yPIPBox_3 349 362 PF02747 0.534
LIG_Pex14_1 85 89 PF04695 0.271
LIG_REV1ctd_RIR_1 93 99 PF16727 0.211
LIG_SH2_CRK 195 199 PF00017 0.211
LIG_SH2_PTP2 176 179 PF00017 0.212
LIG_SH2_PTP2 454 457 PF00017 0.271
LIG_SH2_SRC 34 37 PF00017 0.549
LIG_SH2_SRC 519 522 PF00017 0.271
LIG_SH2_STAP1 415 419 PF00017 0.317
LIG_SH2_STAP1 581 585 PF00017 0.532
LIG_SH2_STAT5 176 179 PF00017 0.212
LIG_SH2_STAT5 3 6 PF00017 0.569
LIG_SH2_STAT5 34 37 PF00017 0.549
LIG_SH2_STAT5 454 457 PF00017 0.292
LIG_SH2_STAT5 473 476 PF00017 0.271
LIG_SH2_STAT5 519 522 PF00017 0.271
LIG_SH2_STAT5 632 635 PF00017 0.564
LIG_SH3_3 599 605 PF00018 0.505
LIG_SH3_3 94 100 PF00018 0.425
LIG_Sin3_3 556 563 PF02671 0.280
LIG_SUMO_SIM_anti_2 175 184 PF11976 0.212
LIG_SUMO_SIM_anti_2 249 255 PF11976 0.265
LIG_SUMO_SIM_anti_2 28 33 PF11976 0.548
LIG_SUMO_SIM_anti_2 306 313 PF11976 0.310
LIG_SUMO_SIM_anti_2 36 42 PF11976 0.547
LIG_SUMO_SIM_anti_2 377 382 PF11976 0.243
LIG_SUMO_SIM_anti_2 529 537 PF11976 0.271
LIG_SUMO_SIM_anti_2 555 562 PF11976 0.285
LIG_SUMO_SIM_par_1 175 184 PF11976 0.269
LIG_SUMO_SIM_par_1 356 363 PF11976 0.541
LIG_SUMO_SIM_par_1 36 42 PF11976 0.553
LIG_SUMO_SIM_par_1 377 384 PF11976 0.212
LIG_SUMO_SIM_par_1 473 478 PF11976 0.271
LIG_SUMO_SIM_par_1 555 562 PF11976 0.294
LIG_SUMO_SIM_par_1 572 577 PF11976 0.470
LIG_TYR_ITIM 174 179 PF00017 0.305
LIG_TYR_ITIM 32 37 PF00017 0.550
LIG_UBA3_1 236 243 PF00899 0.433
LIG_WRC_WIRS_1 277 282 PF05994 0.406
LIG_WRC_WIRS_1 86 91 PF05994 0.271
LIG_WRC_WIRS_1 92 97 PF05994 0.271
MOD_CDK_SPK_2 601 606 PF00069 0.527
MOD_CK1_1 105 111 PF00069 0.572
MOD_CK1_1 276 282 PF00069 0.424
MOD_CK1_1 288 294 PF00069 0.295
MOD_CK1_1 330 336 PF00069 0.644
MOD_CK1_1 42 48 PF00069 0.570
MOD_CK1_1 552 558 PF00069 0.271
MOD_CK1_1 577 583 PF00069 0.526
MOD_CK1_1 79 85 PF00069 0.265
MOD_CK2_1 207 213 PF00069 0.212
MOD_CK2_1 300 306 PF00069 0.357
MOD_CK2_1 631 637 PF00069 0.506
MOD_GlcNHglycan 120 123 PF01048 0.287
MOD_GlcNHglycan 130 133 PF01048 0.250
MOD_GlcNHglycan 17 20 PF01048 0.366
MOD_GlcNHglycan 202 205 PF01048 0.324
MOD_GlcNHglycan 258 261 PF01048 0.271
MOD_GlcNHglycan 287 290 PF01048 0.269
MOD_GlcNHglycan 312 315 PF01048 0.305
MOD_GlcNHglycan 340 343 PF01048 0.410
MOD_GlcNHglycan 500 503 PF01048 0.237
MOD_GlcNHglycan 551 554 PF01048 0.271
MOD_GlcNHglycan 561 564 PF01048 0.271
MOD_GlcNHglycan 576 579 PF01048 0.352
MOD_GlcNHglycan 633 636 PF01048 0.437
MOD_GlcNHglycan 65 68 PF01048 0.245
MOD_GlcNHglycan 74 77 PF01048 0.576
MOD_GlcNHglycan 78 81 PF01048 0.619
MOD_GSK3_1 114 121 PF00069 0.617
MOD_GSK3_1 130 137 PF00069 0.425
MOD_GSK3_1 160 167 PF00069 0.617
MOD_GSK3_1 300 307 PF00069 0.365
MOD_GSK3_1 353 360 PF00069 0.543
MOD_GSK3_1 38 45 PF00069 0.563
MOD_GSK3_1 528 535 PF00069 0.271
MOD_GSK3_1 627 634 PF00069 0.565
MOD_GSK3_1 637 644 PF00069 0.593
MOD_GSK3_1 72 79 PF00069 0.357
MOD_N-GLC_1 188 193 PF02516 0.552
MOD_N-GLC_1 353 358 PF02516 0.336
MOD_N-GLC_1 583 588 PF02516 0.308
MOD_N-GLC_1 627 632 PF02516 0.367
MOD_N-GLC_1 654 659 PF02516 0.312
MOD_NEK2_1 1 6 PF00069 0.573
MOD_NEK2_1 128 133 PF00069 0.273
MOD_NEK2_1 160 165 PF00069 0.605
MOD_NEK2_1 235 240 PF00069 0.340
MOD_NEK2_1 256 261 PF00069 0.294
MOD_NEK2_1 273 278 PF00069 0.578
MOD_NEK2_1 310 315 PF00069 0.294
MOD_NEK2_1 345 350 PF00069 0.596
MOD_NEK2_1 374 379 PF00069 0.274
MOD_NEK2_1 39 44 PF00069 0.565
MOD_NEK2_1 405 410 PF00069 0.274
MOD_NEK2_1 456 461 PF00069 0.294
MOD_NEK2_1 475 480 PF00069 0.279
MOD_NEK2_1 526 531 PF00069 0.286
MOD_NEK2_1 567 572 PF00069 0.477
MOD_NEK2_1 574 579 PF00069 0.544
MOD_NEK2_1 593 598 PF00069 0.461
MOD_NEK2_1 609 614 PF00069 0.466
MOD_NEK2_1 63 68 PF00069 0.262
MOD_NEK2_1 69 74 PF00069 0.447
MOD_NEK2_1 78 83 PF00069 0.376
MOD_NEK2_2 91 96 PF00069 0.212
MOD_PIKK_1 160 166 PF00454 0.555
MOD_PKA_2 13 19 PF00069 0.558
MOD_PKA_2 160 166 PF00069 0.614
MOD_PKA_2 76 82 PF00069 0.390
MOD_Plk_1 114 120 PF00069 0.572
MOD_Plk_1 188 194 PF00069 0.206
MOD_Plk_1 327 333 PF00069 0.618
MOD_Plk_1 353 359 PF00069 0.600
MOD_Plk_1 615 621 PF00069 0.496
MOD_Plk_1 654 660 PF00069 0.508
MOD_Plk_4 169 175 PF00069 0.298
MOD_Plk_4 228 234 PF00069 0.321
MOD_Plk_4 27 33 PF00069 0.550
MOD_Plk_4 276 282 PF00069 0.435
MOD_Plk_4 288 294 PF00069 0.359
MOD_Plk_4 327 333 PF00069 0.594
MOD_Plk_4 353 359 PF00069 0.583
MOD_Plk_4 374 380 PF00069 0.329
MOD_Plk_4 406 412 PF00069 0.367
MOD_Plk_4 418 424 PF00069 0.295
MOD_Plk_4 528 534 PF00069 0.290
MOD_Plk_4 654 660 PF00069 0.508
MOD_Plk_4 79 85 PF00069 0.248
MOD_Plk_4 91 97 PF00069 0.271
MOD_ProDKin_1 45 51 PF00069 0.570
MOD_ProDKin_1 601 607 PF00069 0.508
MOD_SUMO_rev_2 363 371 PF00179 0.543
MOD_SUMO_rev_2 421 428 PF00179 0.448
TRG_DiLeu_BaEn_1 115 120 PF01217 0.559
TRG_DiLeu_BaEn_1 247 252 PF01217 0.382
TRG_DiLeu_BaEn_1 306 311 PF01217 0.271
TRG_DiLeu_BaEn_1 470 475 PF01217 0.248
TRG_DiLeu_BaEn_2 366 372 PF01217 0.448
TRG_DiLeu_BaLyEn_6 562 567 PF01217 0.271
TRG_DiLeu_LyEn_5 115 120 PF01217 0.559
TRG_ENDOCYTIC_2 176 179 PF00928 0.305
TRG_ENDOCYTIC_2 195 198 PF00928 0.211
TRG_ENDOCYTIC_2 34 37 PF00928 0.549
TRG_ENDOCYTIC_2 368 371 PF00928 0.406
TRG_ENDOCYTIC_2 436 439 PF00928 0.448
TRG_ENDOCYTIC_2 454 457 PF00928 0.271
TRG_ENDOCYTIC_2 473 476 PF00928 0.271
TRG_ENDOCYTIC_2 519 522 PF00928 0.271
TRG_ER_diArg_1 13 15 PF00400 0.556
TRG_ER_diArg_1 160 162 PF00400 0.606
TRG_Pf-PMV_PEXEL_1 591 595 PF00026 0.269

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1PB11 Leptomonas seymouri 55% 100%
A0A3Q8IDA3 Leishmania donovani 78% 100%
A0A3Q8IGB8 Leishmania donovani 23% 100%
A4HJM3 Leishmania braziliensis 24% 100%
A4I2S7 Leishmania infantum 77% 100%
A4I745 Leishmania infantum 24% 100%
E9ADA5 Leishmania major 79% 100%
E9AZ30 Leishmania mexicana (strain MHOM/GT/2001/U1103) 78% 100%
E9B239 Leishmania mexicana (strain MHOM/GT/2001/U1103) 24% 100%
Q4Q622 Leishmania major 24% 100%

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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