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 donovani
UniProt:
A0A3Q8ICJ7_LEIDO
TriTrypDb:
LdBPK_231040.1 , LdCL_230017200 , LDHU3_23.1400
Length:
776

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
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

A0A3Q8ICJ7
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3Q8ICJ7

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 208 212 PF00656 0.419
CLV_C14_Caspase3-7 566 570 PF00656 0.421
CLV_NRD_NRD_1 187 189 PF00675 0.379
CLV_NRD_NRD_1 313 315 PF00675 0.627
CLV_NRD_NRD_1 422 424 PF00675 0.379
CLV_NRD_NRD_1 536 538 PF00675 0.552
CLV_NRD_NRD_1 592 594 PF00675 0.479
CLV_NRD_NRD_1 633 635 PF00675 0.455
CLV_PCSK_KEX2_1 187 189 PF00082 0.379
CLV_PCSK_KEX2_1 313 315 PF00082 0.627
CLV_PCSK_KEX2_1 422 424 PF00082 0.398
CLV_PCSK_KEX2_1 536 538 PF00082 0.552
CLV_PCSK_KEX2_1 592 594 PF00082 0.479
CLV_PCSK_KEX2_1 622 624 PF00082 0.514
CLV_PCSK_KEX2_1 633 635 PF00082 0.356
CLV_PCSK_PC1ET2_1 622 624 PF00082 0.514
CLV_PCSK_SKI1_1 179 183 PF00082 0.412
CLV_PCSK_SKI1_1 22 26 PF00082 0.482
CLV_PCSK_SKI1_1 231 235 PF00082 0.371
CLV_PCSK_SKI1_1 573 577 PF00082 0.388
CLV_PCSK_SKI1_1 711 715 PF00082 0.550
CLV_PCSK_SKI1_1 761 765 PF00082 0.583
CLV_PCSK_SKI1_1 87 91 PF00082 0.461
CLV_Separin_Metazoa 762 766 PF03568 0.577
DEG_APCC_DBOX_1 230 238 PF00400 0.366
DEG_APCC_DBOX_1 760 768 PF00400 0.580
DEG_SCF_FBW7_1 315 320 PF00400 0.601
DEG_SIAH_1 269 277 PF03145 0.591
DOC_CKS1_1 112 117 PF01111 0.555
DOC_CYCLIN_RxL_1 176 185 PF00134 0.413
DOC_CYCLIN_RxL_1 19 29 PF00134 0.490
DOC_CYCLIN_RxL_1 228 235 PF00134 0.374
DOC_MAPK_gen_1 403 411 PF00069 0.358
DOC_MAPK_gen_1 735 744 PF00069 0.643
DOC_MAPK_MEF2A_6 405 413 PF00069 0.349
DOC_MAPK_RevD_3 173 188 PF00069 0.361
DOC_MAPK_RevD_3 407 423 PF00069 0.347
DOC_PP2B_PxIxI_1 227 233 PF00149 0.375
DOC_SPAK_OSR1_1 357 361 PF12202 0.387
DOC_USP7_MATH_1 212 216 PF00917 0.370
DOC_USP7_MATH_1 253 257 PF00917 0.558
DOC_USP7_MATH_1 279 283 PF00917 0.681
DOC_USP7_MATH_1 293 297 PF00917 0.567
DOC_USP7_MATH_1 445 449 PF00917 0.427
DOC_USP7_MATH_1 468 472 PF00917 0.389
DOC_USP7_MATH_1 479 483 PF00917 0.482
DOC_USP7_MATH_1 552 556 PF00917 0.632
DOC_USP7_UBL2_3 239 243 PF12436 0.399
DOC_USP7_UBL2_3 618 622 PF12436 0.511
DOC_WW_Pin1_4 111 116 PF00397 0.606
DOC_WW_Pin1_4 133 138 PF00397 0.594
DOC_WW_Pin1_4 272 277 PF00397 0.662
DOC_WW_Pin1_4 282 287 PF00397 0.648
DOC_WW_Pin1_4 289 294 PF00397 0.626
DOC_WW_Pin1_4 295 300 PF00397 0.550
DOC_WW_Pin1_4 313 318 PF00397 0.558
DOC_WW_Pin1_4 398 403 PF00397 0.416
DOC_WW_Pin1_4 584 589 PF00397 0.477
DOC_WW_Pin1_4 696 701 PF00397 0.500
LIG_14-3-3_CanoR_1 467 473 PF00244 0.386
LIG_14-3-3_CanoR_1 476 485 PF00244 0.475
LIG_14-3-3_CanoR_1 486 490 PF00244 0.559
LIG_14-3-3_CanoR_1 521 529 PF00244 0.567
LIG_14-3-3_CanoR_1 557 561 PF00244 0.606
LIG_14-3-3_CanoR_1 623 630 PF00244 0.611
LIG_14-3-3_CanoR_1 644 650 PF00244 0.368
LIG_14-3-3_CanoR_1 670 675 PF00244 0.461
LIG_Actin_WH2_1 433 449 PF00022 0.416
LIG_Actin_WH2_2 432 449 PF00022 0.417
LIG_APCC_ABBA_1 614 619 PF00400 0.415
LIG_BRCT_BRCA1_1 355 359 PF00533 0.370
LIG_BRCT_BRCA1_1 430 434 PF00533 0.425
LIG_EH1_1 640 648 PF00400 0.442
LIG_FHA_1 124 130 PF00498 0.564
LIG_FHA_1 170 176 PF00498 0.457
LIG_FHA_1 35 41 PF00498 0.413
LIG_FHA_1 404 410 PF00498 0.345
LIG_FHA_1 511 517 PF00498 0.615
LIG_FHA_1 609 615 PF00498 0.384
LIG_FHA_1 83 89 PF00498 0.530
LIG_FHA_2 169 175 PF00498 0.403
LIG_FHA_2 206 212 PF00498 0.396
LIG_FHA_2 219 225 PF00498 0.416
LIG_FHA_2 51 57 PF00498 0.499
LIG_FHA_2 686 692 PF00498 0.436
LIG_GBD_Chelix_1 330 338 PF00786 0.417
LIG_LIR_Apic_2 724 729 PF02991 0.535
LIG_LIR_Gen_1 316 327 PF02991 0.540
LIG_LIR_Gen_1 431 442 PF02991 0.417
LIG_LIR_Gen_1 574 584 PF02991 0.381
LIG_LIR_Nem_3 114 120 PF02991 0.584
LIG_LIR_Nem_3 185 189 PF02991 0.427
LIG_LIR_Nem_3 218 223 PF02991 0.559
LIG_LIR_Nem_3 29 35 PF02991 0.473
LIG_LIR_Nem_3 316 322 PF02991 0.603
LIG_LIR_Nem_3 380 386 PF02991 0.338
LIG_LIR_Nem_3 431 437 PF02991 0.388
LIG_LIR_Nem_3 574 580 PF02991 0.380
LIG_MLH1_MIPbox_1 355 359 PF16413 0.370
LIG_NRBOX 67 73 PF00104 0.464
LIG_NRP_CendR_1 773 776 PF00754 0.632
LIG_PCNA_PIPBox_1 213 222 PF02747 0.303
LIG_Pex14_2 391 395 PF04695 0.408
LIG_SH2_CRK 117 121 PF00017 0.491
LIG_SH2_CRK 200 204 PF00017 0.418
LIG_SH2_CRK 319 323 PF00017 0.581
LIG_SH2_CRK 35 39 PF00017 0.425
LIG_SH2_CRK 4 8 PF00017 0.521
LIG_SH2_CRK 726 730 PF00017 0.552
LIG_SH2_NCK_1 241 245 PF00017 0.355
LIG_SH2_NCK_1 4 8 PF00017 0.521
LIG_SH2_STAP1 200 204 PF00017 0.450
LIG_SH2_STAP1 241 245 PF00017 0.406
LIG_SH2_STAP1 374 378 PF00017 0.423
LIG_SH2_STAT3 148 151 PF00017 0.522
LIG_SH2_STAT5 148 151 PF00017 0.522
LIG_SH2_STAT5 180 183 PF00017 0.349
LIG_SH2_STAT5 220 223 PF00017 0.450
LIG_SH2_STAT5 236 239 PF00017 0.475
LIG_SH2_STAT5 241 244 PF00017 0.537
LIG_SH2_STAT5 319 322 PF00017 0.652
LIG_SH2_STAT5 35 38 PF00017 0.427
LIG_SH2_STAT5 579 582 PF00017 0.378
LIG_SH3_1 134 140 PF00018 0.661
LIG_SH3_1 283 289 PF00018 0.582
LIG_SH3_3 106 112 PF00018 0.557
LIG_SH3_3 134 140 PF00018 0.749
LIG_SH3_3 283 289 PF00018 0.595
LIG_SH3_3 76 82 PF00018 0.458
LIG_Sin3_3 525 532 PF02671 0.619
LIG_SUMO_SIM_anti_2 610 616 PF11976 0.385
LIG_SUMO_SIM_par_1 214 221 PF11976 0.441
LIG_TRAF2_1 244 247 PF00917 0.452
LIG_TYR_ITIM 184 189 PF00017 0.427
LIG_UBA3_1 233 239 PF00899 0.365
LIG_UBA3_1 64 73 PF00899 0.348
MOD_CDK_SPK_2 398 403 PF00069 0.386
MOD_CDK_SPxxK_3 111 118 PF00069 0.601
MOD_CDK_SPxxK_3 398 405 PF00069 0.403
MOD_CK1_1 282 288 PF00069 0.644
MOD_CK1_1 291 297 PF00069 0.642
MOD_CK1_1 333 339 PF00069 0.474
MOD_CK1_1 481 487 PF00069 0.523
MOD_CK1_1 488 494 PF00069 0.561
MOD_CK1_1 49 55 PF00069 0.468
MOD_CK1_1 499 505 PF00069 0.505
MOD_CK1_1 556 562 PF00069 0.648
MOD_CK2_1 212 218 PF00069 0.382
MOD_CK2_1 346 352 PF00069 0.405
MOD_CK2_1 685 691 PF00069 0.438
MOD_Cter_Amidation 590 593 PF01082 0.475
MOD_GlcNHglycan 253 256 PF01048 0.544
MOD_GlcNHglycan 396 399 PF01048 0.468
MOD_GlcNHglycan 443 446 PF01048 0.382
MOD_GlcNHglycan 447 450 PF01048 0.436
MOD_GlcNHglycan 487 490 PF01048 0.648
MOD_GlcNHglycan 501 504 PF01048 0.572
MOD_GlcNHglycan 66 71 PF01048 0.410
MOD_GSK3_1 165 172 PF00069 0.511
MOD_GSK3_1 287 294 PF00069 0.611
MOD_GSK3_1 302 309 PF00069 0.585
MOD_GSK3_1 313 320 PF00069 0.662
MOD_GSK3_1 394 401 PF00069 0.488
MOD_GSK3_1 403 410 PF00069 0.389
MOD_GSK3_1 441 448 PF00069 0.408
MOD_GSK3_1 46 53 PF00069 0.461
MOD_GSK3_1 477 484 PF00069 0.481
MOD_GSK3_1 485 492 PF00069 0.540
MOD_GSK3_1 499 506 PF00069 0.751
MOD_GSK3_1 552 559 PF00069 0.671
MOD_N-GLC_1 468 473 PF02516 0.447
MOD_N-GLC_1 623 628 PF02516 0.438
MOD_NEK2_1 182 187 PF00069 0.507
MOD_NEK2_1 407 412 PF00069 0.401
MOD_NEK2_1 43 48 PF00069 0.551
MOD_NEK2_1 485 490 PF00069 0.535
MOD_NEK2_1 501 506 PF00069 0.644
MOD_NEK2_1 685 690 PF00069 0.433
MOD_NEK2_2 34 39 PF00069 0.426
MOD_NEK2_2 468 473 PF00069 0.376
MOD_PIKK_1 147 153 PF00454 0.516
MOD_PIKK_1 50 56 PF00454 0.516
MOD_PIKK_1 82 88 PF00454 0.534
MOD_PK_1 3 9 PF00069 0.592
MOD_PKA_2 485 491 PF00069 0.567
MOD_PKA_2 506 512 PF00069 0.578
MOD_PKA_2 520 526 PF00069 0.513
MOD_PKA_2 556 562 PF00069 0.602
MOD_PKB_1 668 676 PF00069 0.463
MOD_Plk_1 165 171 PF00069 0.452
MOD_Plk_1 429 435 PF00069 0.411
MOD_Plk_1 468 474 PF00069 0.426
MOD_Plk_1 553 559 PF00069 0.654
MOD_Plk_1 66 72 PF00069 0.414
MOD_Plk_2-3 678 684 PF00069 0.442
MOD_Plk_4 165 171 PF00069 0.487
MOD_Plk_4 212 218 PF00069 0.374
MOD_Plk_4 330 336 PF00069 0.410
MOD_Plk_4 407 413 PF00069 0.397
MOD_Plk_4 43 49 PF00069 0.403
MOD_Plk_4 496 502 PF00069 0.565
MOD_Plk_4 670 676 PF00069 0.466
MOD_ProDKin_1 111 117 PF00069 0.602
MOD_ProDKin_1 133 139 PF00069 0.594
MOD_ProDKin_1 272 278 PF00069 0.664
MOD_ProDKin_1 282 288 PF00069 0.650
MOD_ProDKin_1 289 295 PF00069 0.626
MOD_ProDKin_1 313 319 PF00069 0.739
MOD_ProDKin_1 398 404 PF00069 0.409
MOD_ProDKin_1 584 590 PF00069 0.475
MOD_ProDKin_1 696 702 PF00069 0.507
TRG_DiLeu_BaEn_1 524 529 PF01217 0.620
TRG_DiLeu_BaEn_1 610 615 PF01217 0.383
TRG_DiLeu_BaEn_1 67 72 PF01217 0.456
TRG_DiLeu_BaEn_1 701 706 PF01217 0.530
TRG_DiLeu_BaLyEn_6 374 379 PF01217 0.375
TRG_ENDOCYTIC_2 117 120 PF00928 0.488
TRG_ENDOCYTIC_2 186 189 PF00928 0.473
TRG_ENDOCYTIC_2 200 203 PF00928 0.309
TRG_ENDOCYTIC_2 220 223 PF00928 0.308
TRG_ENDOCYTIC_2 319 322 PF00928 0.590
TRG_ENDOCYTIC_2 35 38 PF00928 0.463
TRG_ENDOCYTIC_2 4 7 PF00928 0.531
TRG_ENDOCYTIC_2 669 672 PF00928 0.390
TRG_ER_diArg_1 186 188 PF00400 0.376
TRG_ER_diArg_1 228 231 PF00400 0.379
TRG_ER_diArg_1 313 315 PF00400 0.582
TRG_ER_diArg_1 422 424 PF00400 0.398
TRG_ER_diArg_1 474 477 PF00400 0.413
TRG_ER_diArg_1 592 594 PF00400 0.479
TRG_NES_CRM1_1 62 78 PF08389 0.501
TRG_Pf-PMV_PEXEL_1 22 26 PF00026 0.481
TRG_Pf-PMV_PEXEL_1 231 235 PF00026 0.371
TRG_Pf-PMV_PEXEL_1 368 373 PF00026 0.454
TRG_Pf-PMV_PEXEL_1 422 426 PF00026 0.399
TRG_Pf-PMV_PEXEL_1 592 597 PF00026 0.411
TRG_Pf-PMV_PEXEL_1 623 627 PF00026 0.491
TRG_Pf-PMV_PEXEL_1 735 739 PF00026 0.620
TRG_Pf-PMV_PEXEL_1 743 747 PF00026 0.604
TRG_Pf-PMV_PEXEL_1 761 766 PF00026 0.461

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6B3 Leptomonas seymouri 57% 88%
A4HCV7 Leishmania braziliensis 80% 100%
A4I0D7 Leishmania infantum 99% 100%
E9AWA1 Leishmania mexicana (strain MHOM/GT/2001/U1103) 91% 100%
Q4QB78 Leishmania major 95% 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