LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania major
UniProt:
Q4QBI6_LEIMA
TriTrypDb:
LmjF.22.1610 , LMJLV39_220022100 , LMJSD75_220022700 *
Length:
723

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: 9
NetGPI no yes: 0, no: 9
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

Q4QBI6
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QBI6

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 496 500 PF00656 0.452
CLV_NRD_NRD_1 210 212 PF00675 0.447
CLV_NRD_NRD_1 27 29 PF00675 0.484
CLV_NRD_NRD_1 398 400 PF00675 0.736
CLV_NRD_NRD_1 531 533 PF00675 0.553
CLV_NRD_NRD_1 634 636 PF00675 0.590
CLV_NRD_NRD_1 75 77 PF00675 0.491
CLV_PCSK_FUR_1 529 533 PF00082 0.474
CLV_PCSK_KEX2_1 131 133 PF00082 0.387
CLV_PCSK_KEX2_1 210 212 PF00082 0.447
CLV_PCSK_KEX2_1 362 364 PF00082 0.606
CLV_PCSK_KEX2_1 531 533 PF00082 0.498
CLV_PCSK_KEX2_1 592 594 PF00082 0.419
CLV_PCSK_KEX2_1 633 635 PF00082 0.643
CLV_PCSK_KEX2_1 720 722 PF00082 0.636
CLV_PCSK_PC1ET2_1 131 133 PF00082 0.387
CLV_PCSK_PC1ET2_1 362 364 PF00082 0.569
CLV_PCSK_PC1ET2_1 592 594 PF00082 0.400
CLV_PCSK_PC1ET2_1 720 722 PF00082 0.622
CLV_PCSK_SKI1_1 128 132 PF00082 0.467
CLV_PCSK_SKI1_1 320 324 PF00082 0.450
CLV_PCSK_SKI1_1 603 607 PF00082 0.465
CLV_PCSK_SKI1_1 615 619 PF00082 0.381
CLV_Separin_Metazoa 526 530 PF03568 0.410
DEG_SPOP_SBC_1 701 705 PF00917 0.627
DOC_CKS1_1 432 437 PF01111 0.692
DOC_CYCLIN_RxL_1 128 139 PF00134 0.377
DOC_CYCLIN_yCln2_LP_2 432 438 PF00134 0.583
DOC_MAPK_gen_1 237 246 PF00069 0.424
DOC_MAPK_MEF2A_6 158 167 PF00069 0.466
DOC_MAPK_MEF2A_6 240 248 PF00069 0.396
DOC_PP1_RVXF_1 129 136 PF00149 0.474
DOC_PP1_RVXF_1 613 619 PF00149 0.454
DOC_PP4_FxxP_1 219 222 PF00568 0.389
DOC_PP4_FxxP_1 261 264 PF00568 0.466
DOC_USP7_MATH_1 179 183 PF00917 0.475
DOC_USP7_MATH_1 325 329 PF00917 0.517
DOC_USP7_MATH_1 419 423 PF00917 0.653
DOC_USP7_MATH_1 439 443 PF00917 0.639
DOC_USP7_MATH_1 546 550 PF00917 0.554
DOC_USP7_MATH_1 569 573 PF00917 0.418
DOC_USP7_MATH_1 584 588 PF00917 0.513
DOC_USP7_MATH_1 605 609 PF00917 0.408
DOC_USP7_MATH_1 671 675 PF00917 0.617
DOC_USP7_MATH_1 719 723 PF00917 0.643
DOC_USP7_MATH_1 88 92 PF00917 0.494
DOC_WW_Pin1_4 138 143 PF00397 0.580
DOC_WW_Pin1_4 168 173 PF00397 0.441
DOC_WW_Pin1_4 218 223 PF00397 0.589
DOC_WW_Pin1_4 251 256 PF00397 0.477
DOC_WW_Pin1_4 272 277 PF00397 0.533
DOC_WW_Pin1_4 284 289 PF00397 0.542
DOC_WW_Pin1_4 382 387 PF00397 0.758
DOC_WW_Pin1_4 431 436 PF00397 0.724
DOC_WW_Pin1_4 46 51 PF00397 0.445
DOC_WW_Pin1_4 95 100 PF00397 0.679
LIG_14-3-3_CanoR_1 158 163 PF00244 0.536
LIG_14-3-3_CanoR_1 210 218 PF00244 0.497
LIG_14-3-3_CanoR_1 28 34 PF00244 0.417
LIG_14-3-3_CanoR_1 388 392 PF00244 0.557
LIG_14-3-3_CanoR_1 424 432 PF00244 0.644
LIG_14-3-3_CanoR_1 623 628 PF00244 0.426
LIG_Actin_WH2_2 117 133 PF00022 0.391
LIG_Actin_WH2_2 544 560 PF00022 0.312
LIG_BIR_II_1 1 5 PF00653 0.393
LIG_BRCT_BRCA1_1 347 351 PF00533 0.431
LIG_BRCT_BRCA1_1 571 575 PF00533 0.453
LIG_BRCT_BRCA1_1 581 585 PF00533 0.541
LIG_CSL_BTD_1 58 61 PF09270 0.323
LIG_CtBP_PxDLS_1 276 280 PF00389 0.400
LIG_EH1_1 521 529 PF00400 0.443
LIG_eIF4E_1 522 528 PF01652 0.439
LIG_FHA_1 11 17 PF00498 0.504
LIG_FHA_1 151 157 PF00498 0.303
LIG_FHA_1 252 258 PF00498 0.418
LIG_FHA_1 28 34 PF00498 0.512
LIG_FHA_1 321 327 PF00498 0.589
LIG_FHA_1 469 475 PF00498 0.554
LIG_FHA_1 485 491 PF00498 0.472
LIG_FHA_1 584 590 PF00498 0.528
LIG_FHA_2 521 527 PF00498 0.385
LIG_FHA_2 548 554 PF00498 0.417
LIG_FHA_2 651 657 PF00498 0.415
LIG_FHA_2 95 101 PF00498 0.576
LIG_Integrin_RGD_1 37 39 PF01839 0.487
LIG_LIR_Apic_2 258 264 PF02991 0.443
LIG_LIR_Apic_2 271 276 PF02991 0.310
LIG_LIR_Gen_1 461 472 PF02991 0.523
LIG_LIR_Nem_3 461 467 PF02991 0.539
LIG_MYND_1 58 62 PF01753 0.431
LIG_SH2_CRK 121 125 PF00017 0.439
LIG_SH2_CRK 512 516 PF00017 0.467
LIG_SH2_STAP1 12 16 PF00017 0.366
LIG_SH2_STAP1 81 85 PF00017 0.352
LIG_SH2_STAT3 32 35 PF00017 0.407
LIG_SH2_STAT5 12 15 PF00017 0.477
LIG_SH2_STAT5 17 20 PF00017 0.406
LIG_SH2_STAT5 32 35 PF00017 0.235
LIG_SH2_STAT5 473 476 PF00017 0.393
LIG_SH2_STAT5 522 525 PF00017 0.404
LIG_SH2_STAT5 594 597 PF00017 0.449
LIG_SH2_STAT5 664 667 PF00017 0.499
LIG_SH3_3 157 163 PF00018 0.441
LIG_SH3_3 432 438 PF00018 0.777
LIG_SH3_3 55 61 PF00018 0.374
LIG_SH3_3 679 685 PF00018 0.668
LIG_SUMO_SIM_anti_2 523 529 PF11976 0.450
LIG_SUMO_SIM_anti_2 656 663 PF11976 0.468
LIG_SUMO_SIM_par_1 123 129 PF11976 0.366
LIG_SUMO_SIM_par_1 165 171 PF11976 0.457
LIG_SUMO_SIM_par_1 543 550 PF11976 0.450
LIG_TRAF2_1 275 278 PF00917 0.493
LIG_TRFH_1 260 264 PF08558 0.453
LIG_TYR_ITIM 119 124 PF00017 0.442
LIG_TYR_ITIM 510 515 PF00017 0.366
MOD_CDC14_SPxK_1 385 388 PF00782 0.509
MOD_CDK_SPK_2 251 256 PF00069 0.391
MOD_CDK_SPxK_1 382 388 PF00069 0.537
MOD_CDK_SPxxK_3 168 175 PF00069 0.436
MOD_CK1_1 137 143 PF00069 0.522
MOD_CK1_1 146 152 PF00069 0.478
MOD_CK1_1 202 208 PF00069 0.498
MOD_CK1_1 221 227 PF00069 0.550
MOD_CK1_1 284 290 PF00069 0.518
MOD_CK1_1 336 342 PF00069 0.587
MOD_CK1_1 381 387 PF00069 0.756
MOD_CK1_1 422 428 PF00069 0.684
MOD_CK1_1 462 468 PF00069 0.479
MOD_CK1_1 479 485 PF00069 0.540
MOD_CK1_1 492 498 PF00069 0.571
MOD_CK1_1 578 584 PF00069 0.406
MOD_CK1_1 91 97 PF00069 0.728
MOD_CK2_1 272 278 PF00069 0.530
MOD_CK2_1 407 413 PF00069 0.692
MOD_CK2_1 520 526 PF00069 0.484
MOD_CK2_1 584 590 PF00069 0.509
MOD_CK2_1 650 656 PF00069 0.429
MOD_CK2_1 660 666 PF00069 0.492
MOD_CK2_1 94 100 PF00069 0.508
MOD_GlcNHglycan 175 178 PF01048 0.576
MOD_GlcNHglycan 202 205 PF01048 0.454
MOD_GlcNHglycan 214 217 PF01048 0.468
MOD_GlcNHglycan 283 286 PF01048 0.526
MOD_GlcNHglycan 335 338 PF01048 0.580
MOD_GlcNHglycan 347 350 PF01048 0.576
MOD_GlcNHglycan 371 374 PF01048 0.664
MOD_GlcNHglycan 408 412 PF01048 0.611
MOD_GlcNHglycan 427 430 PF01048 0.535
MOD_GlcNHglycan 445 448 PF01048 0.594
MOD_GlcNHglycan 476 479 PF01048 0.656
MOD_GlcNHglycan 481 484 PF01048 0.632
MOD_GlcNHglycan 491 494 PF01048 0.382
MOD_GlcNHglycan 534 537 PF01048 0.542
MOD_GlcNHglycan 571 574 PF01048 0.442
MOD_GlcNHglycan 581 584 PF01048 0.595
MOD_GlcNHglycan 607 610 PF01048 0.476
MOD_GlcNHglycan 678 681 PF01048 0.642
MOD_GlcNHglycan 90 93 PF01048 0.586
MOD_GSK3_1 134 141 PF00069 0.438
MOD_GSK3_1 142 149 PF00069 0.475
MOD_GSK3_1 217 224 PF00069 0.488
MOD_GSK3_1 251 258 PF00069 0.445
MOD_GSK3_1 268 275 PF00069 0.517
MOD_GSK3_1 309 316 PF00069 0.534
MOD_GSK3_1 332 339 PF00069 0.535
MOD_GSK3_1 357 364 PF00069 0.508
MOD_GSK3_1 369 376 PF00069 0.655
MOD_GSK3_1 377 384 PF00069 0.631
MOD_GSK3_1 407 414 PF00069 0.717
MOD_GSK3_1 419 426 PF00069 0.694
MOD_GSK3_1 439 446 PF00069 0.597
MOD_GSK3_1 458 465 PF00069 0.466
MOD_GSK3_1 474 481 PF00069 0.558
MOD_GSK3_1 575 582 PF00069 0.575
MOD_GSK3_1 656 663 PF00069 0.553
MOD_GSK3_1 665 672 PF00069 0.642
MOD_GSK3_1 91 98 PF00069 0.656
MOD_N-GLC_1 10 15 PF02516 0.377
MOD_N-GLC_1 381 386 PF02516 0.652
MOD_NEK2_1 120 125 PF00069 0.320
MOD_NEK2_1 194 199 PF00069 0.448
MOD_NEK2_1 279 284 PF00069 0.554
MOD_NEK2_1 308 313 PF00069 0.451
MOD_NEK2_1 330 335 PF00069 0.494
MOD_NEK2_1 377 382 PF00069 0.698
MOD_NEK2_1 458 463 PF00069 0.579
MOD_NEK2_1 575 580 PF00069 0.501
MOD_NEK2_1 660 665 PF00069 0.571
MOD_NEK2_1 669 674 PF00069 0.638
MOD_NEK2_1 713 718 PF00069 0.630
MOD_NEK2_2 126 131 PF00069 0.396
MOD_NEK2_2 354 359 PF00069 0.298
MOD_NEK2_2 459 464 PF00069 0.376
MOD_PIKK_1 158 164 PF00454 0.561
MOD_PKA_2 209 215 PF00069 0.444
MOD_PKA_2 255 261 PF00069 0.433
MOD_PKA_2 27 33 PF00069 0.393
MOD_PKA_2 291 297 PF00069 0.363
MOD_PKA_2 387 393 PF00069 0.536
MOD_PKA_2 423 429 PF00069 0.712
MOD_PKA_2 468 474 PF00069 0.486
MOD_Plk_1 10 16 PF00069 0.400
MOD_Plk_1 179 185 PF00069 0.469
MOD_Plk_1 401 407 PF00069 0.594
MOD_Plk_1 422 428 PF00069 0.580
MOD_Plk_1 43 49 PF00069 0.579
MOD_Plk_1 650 656 PF00069 0.460
MOD_Plk_1 665 671 PF00069 0.577
MOD_Plk_4 120 126 PF00069 0.328
MOD_Plk_4 194 200 PF00069 0.482
MOD_Plk_4 313 319 PF00069 0.451
MOD_Plk_4 354 360 PF00069 0.411
MOD_Plk_4 459 465 PF00069 0.570
MOD_Plk_4 468 474 PF00069 0.444
MOD_Plk_4 52 58 PF00069 0.286
MOD_Plk_4 520 526 PF00069 0.422
MOD_Plk_4 623 629 PF00069 0.465
MOD_ProDKin_1 138 144 PF00069 0.580
MOD_ProDKin_1 168 174 PF00069 0.450
MOD_ProDKin_1 218 224 PF00069 0.592
MOD_ProDKin_1 251 257 PF00069 0.470
MOD_ProDKin_1 272 278 PF00069 0.530
MOD_ProDKin_1 284 290 PF00069 0.532
MOD_ProDKin_1 382 388 PF00069 0.761
MOD_ProDKin_1 431 437 PF00069 0.724
MOD_ProDKin_1 46 52 PF00069 0.449
MOD_ProDKin_1 95 101 PF00069 0.668
MOD_SUMO_rev_2 21 31 PF00179 0.492
TRG_DiLeu_BaEn_1 656 661 PF01217 0.506
TRG_DiLeu_BaLyEn_6 612 617 PF01217 0.465
TRG_ENDOCYTIC_2 12 15 PF00928 0.364
TRG_ENDOCYTIC_2 121 124 PF00928 0.461
TRG_ENDOCYTIC_2 512 515 PF00928 0.356
TRG_ENDOCYTIC_2 522 525 PF00928 0.319
TRG_ENDOCYTIC_2 81 84 PF00928 0.350
TRG_ER_diArg_1 209 211 PF00400 0.471
TRG_ER_diArg_1 509 512 PF00400 0.384
TRG_ER_diArg_1 530 532 PF00400 0.481
TRG_ER_diArg_1 633 635 PF00400 0.550
TRG_NES_CRM1_1 109 122 PF08389 0.345

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1IJC5 Leptomonas seymouri 48% 100%
A0A1X0NTM2 Trypanosomatidae 26% 100%
A0A3S7WXI7 Leishmania donovani 90% 99%
A0A422N4V7 Trypanosoma rangeli 23% 100%
A4HCK2 Leishmania braziliensis 75% 89%
A4I020 Leishmania infantum 91% 99%
E9AVZ3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 88% 99%
V5B7G6 Trypanosoma cruzi 26% 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