LeishMANIAdb
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Uncharacterized protein

Quick info Annotations Function or PPIs Localization Phosphorylation Expansion Sequence features Structure Putative motif mimicry Homologs Download

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein - conserved
Species:
Leishmania infantum
UniProt:
A4I6Y6_LEIIN
TriTrypDb:
LINF_310028800
Length:
768

Annotations

LeishMANIAdb annotations

A bacterial-type Mg2+ transporter found in kinetoplastids.. Expanded extensively on multiple lineages, especially T cruzi

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: 6
NetGPI no yes: 0, no: 6
Cellular components
Term Name Level Count
GO:0016020 membrane 2 6
GO:0110165 cellular anatomical entity 1 6

Phosphorylation

Amastigote: 47
Promastigote: 317, 334
Promastigote/Amastigote: 15, 352

Expansion

Sequence features

A4I6Y6
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4I6Y6

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 177 181 PF00656 0.434
CLV_C14_Caspase3-7 239 243 PF00656 0.475
CLV_C14_Caspase3-7 542 546 PF00656 0.544
CLV_C14_Caspase3-7 558 562 PF00656 0.569
CLV_C14_Caspase3-7 611 615 PF00656 0.688
CLV_NRD_NRD_1 10 12 PF00675 0.709
CLV_NRD_NRD_1 410 412 PF00675 0.677
CLV_NRD_NRD_1 426 428 PF00675 0.774
CLV_NRD_NRD_1 564 566 PF00675 0.368
CLV_NRD_NRD_1 571 573 PF00675 0.397
CLV_NRD_NRD_1 577 579 PF00675 0.452
CLV_NRD_NRD_1 604 606 PF00675 0.398
CLV_NRD_NRD_1 63 65 PF00675 0.678
CLV_NRD_NRD_1 761 763 PF00675 0.406
CLV_NRD_NRD_1 98 100 PF00675 0.796
CLV_PCSK_FUR_1 423 427 PF00082 0.755
CLV_PCSK_FUR_1 61 65 PF00082 0.698
CLV_PCSK_KEX2_1 271 273 PF00082 0.734
CLV_PCSK_KEX2_1 410 412 PF00082 0.677
CLV_PCSK_KEX2_1 423 425 PF00082 0.742
CLV_PCSK_KEX2_1 426 428 PF00082 0.773
CLV_PCSK_KEX2_1 564 566 PF00082 0.370
CLV_PCSK_KEX2_1 570 572 PF00082 0.392
CLV_PCSK_KEX2_1 577 579 PF00082 0.456
CLV_PCSK_KEX2_1 63 65 PF00082 0.678
CLV_PCSK_KEX2_1 98 100 PF00082 0.796
CLV_PCSK_PC1ET2_1 271 273 PF00082 0.734
CLV_PCSK_PC7_1 59 65 PF00082 0.698
CLV_PCSK_SKI1_1 136 140 PF00082 0.670
CLV_PCSK_SKI1_1 364 368 PF00082 0.729
CLV_PCSK_SKI1_1 564 568 PF00082 0.360
CLV_PCSK_SKI1_1 577 581 PF00082 0.362
CLV_PCSK_SKI1_1 81 85 PF00082 0.696
DEG_APCC_DBOX_1 159 167 PF00400 0.455
DEG_APCC_DBOX_1 237 245 PF00400 0.464
DEG_SCF_FBW7_1 376 383 PF00400 0.438
DEG_SPOP_SBC_1 109 113 PF00917 0.505
DOC_MAPK_gen_1 440 448 PF00069 0.427
DOC_PP1_RVXF_1 575 582 PF00149 0.581
DOC_PP1_RVXF_1 682 688 PF00149 0.600
DOC_PP2B_LxvP_1 500 503 PF13499 0.523
DOC_PP4_MxPP_1 648 651 PF00568 0.555
DOC_USP7_MATH_1 109 113 PF00917 0.518
DOC_USP7_MATH_1 236 240 PF00917 0.472
DOC_USP7_MATH_1 300 304 PF00917 0.466
DOC_USP7_MATH_1 306 310 PF00917 0.435
DOC_USP7_MATH_1 349 353 PF00917 0.413
DOC_USP7_MATH_1 412 416 PF00917 0.481
DOC_USP7_MATH_1 438 442 PF00917 0.479
DOC_USP7_MATH_1 484 488 PF00917 0.457
DOC_USP7_MATH_1 494 498 PF00917 0.500
DOC_USP7_MATH_1 612 616 PF00917 0.657
DOC_WW_Pin1_4 251 256 PF00397 0.447
DOC_WW_Pin1_4 376 381 PF00397 0.482
DOC_WW_Pin1_4 425 430 PF00397 0.492
DOC_WW_Pin1_4 482 487 PF00397 0.507
DOC_WW_Pin1_4 604 609 PF00397 0.680
DOC_WW_Pin1_4 732 737 PF00397 0.398
DOC_WW_Pin1_4 81 86 PF00397 0.494
LIG_14-3-3_CanoR_1 11 17 PF00244 0.469
LIG_14-3-3_CanoR_1 160 164 PF00244 0.403
LIG_14-3-3_CanoR_1 235 245 PF00244 0.481
LIG_14-3-3_CanoR_1 314 321 PF00244 0.489
LIG_14-3-3_CanoR_1 353 359 PF00244 0.590
LIG_14-3-3_CanoR_1 364 371 PF00244 0.472
LIG_14-3-3_CanoR_1 39 45 PF00244 0.489
LIG_14-3-3_CanoR_1 411 417 PF00244 0.481
LIG_14-3-3_CanoR_1 52 56 PF00244 0.453
LIG_14-3-3_CanoR_1 691 699 PF00244 0.599
LIG_Actin_WH2_2 156 174 PF00022 0.484
LIG_BIR_II_1 1 5 PF00653 0.600
LIG_BRCT_BRCA1_1 129 133 PF00533 0.497
LIG_Clathr_ClatBox_1 550 554 PF01394 0.603
LIG_deltaCOP1_diTrp_1 328 335 PF00928 0.469
LIG_eIF4E_1 705 711 PF01652 0.331
LIG_FHA_1 160 166 PF00498 0.475
LIG_FHA_1 280 286 PF00498 0.477
LIG_FHA_1 377 383 PF00498 0.453
LIG_FHA_1 390 396 PF00498 0.361
LIG_FHA_1 400 406 PF00498 0.500
LIG_FHA_1 675 681 PF00498 0.495
LIG_FHA_1 759 765 PF00498 0.481
LIG_FHA_1 82 88 PF00498 0.448
LIG_FHA_2 328 334 PF00498 0.470
LIG_FHA_2 404 410 PF00498 0.453
LIG_FHA_2 609 615 PF00498 0.687
LIG_GBD_Chelix_1 285 293 PF00786 0.686
LIG_KLC1_Yacidic_2 444 449 PF13176 0.423
LIG_LIR_Apic_2 487 493 PF02991 0.449
LIG_LIR_Gen_1 207 217 PF02991 0.449
LIG_LIR_Gen_1 282 292 PF02991 0.446
LIG_LIR_Gen_1 46 55 PF02991 0.533
LIG_LIR_Gen_1 461 470 PF02991 0.392
LIG_LIR_Gen_1 515 526 PF02991 0.343
LIG_LIR_Gen_1 697 707 PF02991 0.517
LIG_LIR_Gen_1 735 746 PF02991 0.289
LIG_LIR_Nem_3 180 185 PF02991 0.419
LIG_LIR_Nem_3 207 213 PF02991 0.454
LIG_LIR_Nem_3 282 287 PF02991 0.488
LIG_LIR_Nem_3 46 51 PF02991 0.499
LIG_LIR_Nem_3 461 465 PF02991 0.399
LIG_LIR_Nem_3 468 473 PF02991 0.381
LIG_LIR_Nem_3 515 521 PF02991 0.343
LIG_LIR_Nem_3 525 531 PF02991 0.335
LIG_LIR_Nem_3 695 701 PF02991 0.588
LIG_LIR_Nem_3 734 740 PF02991 0.383
LIG_LIR_Nem_3 752 757 PF02991 0.201
LIG_NRBOX 288 294 PF00104 0.444
LIG_PDZ_Class_2 763 768 PF00595 0.624
LIG_Pex14_1 331 335 PF04695 0.464
LIG_REV1ctd_RIR_1 14 23 PF16727 0.508
LIG_RPA_C_Fungi 566 578 PF08784 0.419
LIG_SH2_CRK 490 494 PF00017 0.563
LIG_SH2_CRK 528 532 PF00017 0.428
LIG_SH2_CRK 757 761 PF00017 0.331
LIG_SH2_NCK_1 490 494 PF00017 0.563
LIG_SH2_PTP2 284 287 PF00017 0.601
LIG_SH2_PTP2 705 708 PF00017 0.371
LIG_SH2_SRC 447 450 PF00017 0.514
LIG_SH2_SRC 765 768 PF00017 0.529
LIG_SH2_STAP1 131 135 PF00017 0.618
LIG_SH2_STAP1 245 249 PF00017 0.581
LIG_SH2_STAP1 681 685 PF00017 0.402
LIG_SH2_STAT3 475 478 PF00017 0.520
LIG_SH2_STAT5 284 287 PF00017 0.615
LIG_SH2_STAT5 386 389 PF00017 0.523
LIG_SH2_STAT5 447 450 PF00017 0.664
LIG_SH2_STAT5 458 461 PF00017 0.558
LIG_SH2_STAT5 50 53 PF00017 0.692
LIG_SH2_STAT5 530 533 PF00017 0.423
LIG_SH2_STAT5 681 684 PF00017 0.403
LIG_SH2_STAT5 705 708 PF00017 0.357
LIG_SH2_STAT5 759 762 PF00017 0.485
LIG_SH2_STAT5 765 768 PF00017 0.485
LIG_SH3_1 426 432 PF00018 0.618
LIG_SH3_3 187 193 PF00018 0.590
LIG_SH3_3 2 8 PF00018 0.536
LIG_SH3_3 23 29 PF00018 0.629
LIG_SH3_3 275 281 PF00018 0.656
LIG_SH3_3 385 391 PF00018 0.546
LIG_SH3_3 426 432 PF00018 0.668
LIG_SH3_3 483 489 PF00018 0.581
LIG_SH3_3 706 712 PF00018 0.371
LIG_SUMO_SIM_par_1 549 554 PF11976 0.489
LIG_TYR_ITIM 526 531 PF00017 0.287
MOD_CDK_SPxxK_3 251 258 PF00069 0.557
MOD_CDK_SPxxK_3 485 492 PF00069 0.657
MOD_CDK_SPxxK_3 81 88 PF00069 0.621
MOD_CK1_1 110 116 PF00069 0.663
MOD_CK1_1 117 123 PF00069 0.610
MOD_CK1_1 15 21 PF00069 0.596
MOD_CK1_1 313 319 PF00069 0.544
MOD_CK1_1 356 362 PF00069 0.675
MOD_CK1_1 468 474 PF00069 0.602
MOD_CK1_1 480 486 PF00069 0.500
MOD_CK1_1 508 514 PF00069 0.371
MOD_CK1_1 604 610 PF00069 0.629
MOD_CK1_1 616 622 PF00069 0.524
MOD_CK1_1 690 696 PF00069 0.466
MOD_CK1_1 70 76 PF00069 0.660
MOD_CK2_1 314 320 PF00069 0.732
MOD_CK2_1 327 333 PF00069 0.562
MOD_GlcNHglycan 142 145 PF01048 0.616
MOD_GlcNHglycan 148 151 PF01048 0.555
MOD_GlcNHglycan 200 203 PF01048 0.692
MOD_GlcNHglycan 206 209 PF01048 0.546
MOD_GlcNHglycan 298 301 PF01048 0.560
MOD_GlcNHglycan 308 311 PF01048 0.565
MOD_GlcNHglycan 316 319 PF01048 0.635
MOD_GlcNHglycan 359 362 PF01048 0.593
MOD_GlcNHglycan 40 43 PF01048 0.607
MOD_GlcNHglycan 406 409 PF01048 0.602
MOD_GlcNHglycan 414 417 PF01048 0.626
MOD_GlcNHglycan 496 499 PF01048 0.595
MOD_GlcNHglycan 500 503 PF01048 0.596
MOD_GlcNHglycan 505 508 PF01048 0.590
MOD_GlcNHglycan 614 618 PF01048 0.592
MOD_GlcNHglycan 625 628 PF01048 0.588
MOD_GlcNHglycan 630 633 PF01048 0.546
MOD_GSK3_1 104 111 PF00069 0.703
MOD_GSK3_1 112 119 PF00069 0.622
MOD_GSK3_1 146 153 PF00069 0.602
MOD_GSK3_1 155 162 PF00069 0.514
MOD_GSK3_1 215 222 PF00069 0.561
MOD_GSK3_1 266 273 PF00069 0.669
MOD_GSK3_1 288 295 PF00069 0.669
MOD_GSK3_1 296 303 PF00069 0.672
MOD_GSK3_1 306 313 PF00069 0.525
MOD_GSK3_1 327 334 PF00069 0.542
MOD_GSK3_1 349 356 PF00069 0.584
MOD_GSK3_1 376 383 PF00069 0.698
MOD_GSK3_1 389 396 PF00069 0.423
MOD_GSK3_1 399 406 PF00069 0.524
MOD_GSK3_1 480 487 PF00069 0.583
MOD_GSK3_1 494 501 PF00069 0.606
MOD_GSK3_1 508 515 PF00069 0.240
MOD_GSK3_1 517 524 PF00069 0.308
MOD_GSK3_1 604 611 PF00069 0.587
MOD_GSK3_1 612 619 PF00069 0.543
MOD_GSK3_1 67 74 PF00069 0.774
MOD_GSK3_1 675 682 PF00069 0.533
MOD_GSK3_1 685 692 PF00069 0.447
MOD_GSK3_1 711 718 PF00069 0.242
MOD_GSK3_1 732 739 PF00069 0.433
MOD_GSK3_1 745 752 PF00069 0.228
MOD_LATS_1 106 112 PF00433 0.637
MOD_LATS_1 69 75 PF00433 0.661
MOD_N-GLC_1 12 17 PF02516 0.584
MOD_N-GLC_1 31 36 PF02516 0.484
MOD_N-GLC_1 675 680 PF02516 0.396
MOD_N-GLC_1 685 690 PF02516 0.425
MOD_N-GLC_1 731 736 PF02516 0.351
MOD_N-GLC_1 74 79 PF02516 0.653
MOD_N-GLC_1 81 86 PF02516 0.594
MOD_NEK2_1 215 220 PF00069 0.507
MOD_NEK2_1 292 297 PF00069 0.592
MOD_NEK2_1 335 340 PF00069 0.505
MOD_NEK2_1 381 386 PF00069 0.568
MOD_NEK2_1 403 408 PF00069 0.554
MOD_NEK2_1 465 470 PF00069 0.447
MOD_NEK2_1 505 510 PF00069 0.607
MOD_NEK2_1 51 56 PF00069 0.573
MOD_NEK2_1 513 518 PF00069 0.298
MOD_NEK2_1 521 526 PF00069 0.322
MOD_NEK2_1 601 606 PF00069 0.643
MOD_NEK2_1 679 684 PF00069 0.415
MOD_NEK2_1 687 692 PF00069 0.488
MOD_NEK2_2 155 160 PF00069 0.578
MOD_PIKK_1 150 156 PF00454 0.567
MOD_PIKK_1 364 370 PF00454 0.668
MOD_PKA_1 271 277 PF00069 0.641
MOD_PKA_2 107 113 PF00069 0.616
MOD_PKA_2 117 123 PF00069 0.514
MOD_PKA_2 159 165 PF00069 0.582
MOD_PKA_2 237 243 PF00069 0.584
MOD_PKA_2 271 277 PF00069 0.641
MOD_PKA_2 313 319 PF00069 0.605
MOD_PKA_2 38 44 PF00069 0.613
MOD_PKA_2 51 57 PF00069 0.560
MOD_PKA_2 591 597 PF00069 0.512
MOD_PKA_2 612 618 PF00069 0.566
MOD_PKA_2 62 68 PF00069 0.581
MOD_PKA_2 690 696 PF00069 0.489
MOD_PKA_2 70 76 PF00069 0.519
MOD_PKA_2 97 103 PF00069 0.696
MOD_Plk_1 12 18 PF00069 0.588
MOD_Plk_1 127 133 PF00069 0.628
MOD_Plk_1 31 37 PF00069 0.551
MOD_Plk_1 327 333 PF00069 0.589
MOD_Plk_1 675 681 PF00069 0.391
MOD_Plk_2-3 540 546 PF00069 0.425
MOD_Plk_4 12 18 PF00069 0.588
MOD_Plk_4 288 294 PF00069 0.549
MOD_Plk_4 31 37 PF00069 0.551
MOD_Plk_4 381 387 PF00069 0.539
MOD_Plk_4 465 471 PF00069 0.443
MOD_Plk_4 508 514 PF00069 0.388
MOD_Plk_4 517 523 PF00069 0.321
MOD_Plk_4 531 537 PF00069 0.421
MOD_Plk_4 543 549 PF00069 0.396
MOD_Plk_4 637 643 PF00069 0.492
MOD_Plk_4 656 662 PF00069 0.426
MOD_Plk_4 675 681 PF00069 0.332
MOD_Plk_4 697 703 PF00069 0.331
MOD_Plk_4 711 717 PF00069 0.227
MOD_Plk_4 749 755 PF00069 0.331
MOD_ProDKin_1 251 257 PF00069 0.555
MOD_ProDKin_1 376 382 PF00069 0.601
MOD_ProDKin_1 425 431 PF00069 0.616
MOD_ProDKin_1 482 488 PF00069 0.637
MOD_ProDKin_1 604 610 PF00069 0.603
MOD_ProDKin_1 732 738 PF00069 0.482
MOD_ProDKin_1 81 87 PF00069 0.619
TRG_DiLeu_BaEn_1 288 293 PF01217 0.550
TRG_DiLeu_BaEn_4 247 253 PF01217 0.573
TRG_DiLeu_BaLyEn_6 377 382 PF01217 0.614
TRG_DiLeu_BaLyEn_6 546 551 PF01217 0.492
TRG_DiLeu_BaLyEn_6 575 580 PF01217 0.425
TRG_ENDOCYTIC_2 284 287 PF00928 0.591
TRG_ENDOCYTIC_2 528 531 PF00928 0.434
TRG_ENDOCYTIC_2 698 701 PF00928 0.464
TRG_ENDOCYTIC_2 705 708 PF00928 0.305
TRG_ENDOCYTIC_2 757 760 PF00928 0.331
TRG_ER_diArg_1 423 426 PF00400 0.640
TRG_ER_diArg_1 472 475 PF00400 0.478
TRG_ER_diArg_1 563 565 PF00400 0.449
TRG_ER_diArg_1 569 572 PF00400 0.443
TRG_ER_diArg_1 577 579 PF00400 0.535
TRG_ER_diArg_1 602 605 PF00400 0.458
TRG_ER_diArg_1 61 64 PF00400 0.602
TRG_ER_diArg_1 98 101 PF00400 0.760
TRG_Pf-PMV_PEXEL_1 258 263 PF00026 0.573
TRG_Pf-PMV_PEXEL_1 577 582 PF00026 0.437

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1HZK3 Leptomonas seymouri 45% 100%
A0A3S7X4P2 Leishmania donovani 99% 100%
A4HJX2 Leishmania braziliensis 60% 100%
E9B207 Leishmania mexicana (strain MHOM/GT/2001/U1103) 85% 100%
Q4Q654 Leishmania major 90% 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