LeishMANIAdb
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F-box domain-containing protein

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

Quick info

Protein:
F-box domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania braziliensis
UniProt:
A4H5W6_LEIBR
TriTrypDb:
LbrM.09.1450 , LBRM2903_090021100 *
Length:
661

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: 10
NetGPI no yes: 0, no: 10
Cellular components
Term Name Level Count
GO:0016020 membrane 2 10
GO:0110165 cellular anatomical entity 1 10

Expansion

Sequence features

A4H5W6
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4H5W6

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 112 116 PF00656 0.691
CLV_NRD_NRD_1 126 128 PF00675 0.521
CLV_NRD_NRD_1 195 197 PF00675 0.402
CLV_NRD_NRD_1 206 208 PF00675 0.397
CLV_NRD_NRD_1 488 490 PF00675 0.620
CLV_NRD_NRD_1 504 506 PF00675 0.493
CLV_PCSK_KEX2_1 126 128 PF00082 0.398
CLV_PCSK_KEX2_1 206 208 PF00082 0.458
CLV_PCSK_KEX2_1 348 350 PF00082 0.538
CLV_PCSK_KEX2_1 488 490 PF00082 0.582
CLV_PCSK_KEX2_1 5 7 PF00082 0.477
CLV_PCSK_KEX2_1 504 506 PF00082 0.493
CLV_PCSK_PC1ET2_1 348 350 PF00082 0.633
CLV_PCSK_PC1ET2_1 5 7 PF00082 0.475
CLV_PCSK_PC7_1 484 490 PF00082 0.438
CLV_PCSK_SKI1_1 206 210 PF00082 0.388
CLV_PCSK_SKI1_1 213 217 PF00082 0.425
CLV_PCSK_SKI1_1 271 275 PF00082 0.641
CLV_PCSK_SKI1_1 348 352 PF00082 0.607
CLV_PCSK_SKI1_1 35 39 PF00082 0.422
CLV_PCSK_SKI1_1 388 392 PF00082 0.500
CLV_PCSK_SKI1_1 397 401 PF00082 0.531
CLV_PCSK_SKI1_1 41 45 PF00082 0.453
CLV_PCSK_SKI1_1 505 509 PF00082 0.662
DEG_SCF_FBW7_1 42 48 PF00400 0.710
DEG_SPOP_SBC_1 78 82 PF00917 0.666
DOC_CKS1_1 398 403 PF01111 0.263
DOC_CKS1_1 42 47 PF01111 0.688
DOC_CKS1_1 549 554 PF01111 0.255
DOC_CYCLIN_yCln2_LP_2 47 53 PF00134 0.574
DOC_MAPK_MEF2A_6 275 282 PF00069 0.390
DOC_MAPK_MEF2A_6 349 358 PF00069 0.252
DOC_MAPK_MEF2A_6 593 602 PF00069 0.563
DOC_PP1_RVXF_1 239 246 PF00149 0.557
DOC_PP1_RVXF_1 316 323 PF00149 0.436
DOC_PP2B_LxvP_1 47 50 PF13499 0.573
DOC_USP7_MATH_1 273 277 PF00917 0.387
DOC_USP7_MATH_1 304 308 PF00917 0.646
DOC_USP7_MATH_1 344 348 PF00917 0.441
DOC_USP7_MATH_1 366 370 PF00917 0.478
DOC_USP7_UBL2_3 193 197 PF12436 0.587
DOC_WW_Pin1_4 298 303 PF00397 0.221
DOC_WW_Pin1_4 397 402 PF00397 0.398
DOC_WW_Pin1_4 41 46 PF00397 0.700
DOC_WW_Pin1_4 411 416 PF00397 0.384
DOC_WW_Pin1_4 548 553 PF00397 0.330
DOC_WW_Pin1_4 63 68 PF00397 0.762
LIG_14-3-3_CanoR_1 388 393 PF00244 0.316
LIG_14-3-3_CanoR_1 504 510 PF00244 0.396
LIG_14-3-3_CanoR_1 557 561 PF00244 0.405
LIG_14-3-3_CanoR_1 6 11 PF00244 0.635
LIG_Actin_WH2_2 9 25 PF00022 0.565
LIG_AP2alpha_2 453 455 PF02296 0.439
LIG_APCC_ABBA_1 155 160 PF00400 0.642
LIG_APCC_ABBA_1 419 424 PF00400 0.271
LIG_BRCT_BRCA1_1 428 432 PF00533 0.330
LIG_BRCT_BRCA1_1 91 95 PF00533 0.640
LIG_Clathr_ClatBox_1 156 160 PF01394 0.663
LIG_Clathr_ClatBox_1 420 424 PF01394 0.329
LIG_deltaCOP1_diTrp_1 533 542 PF00928 0.357
LIG_eIF4E_1 204 210 PF01652 0.507
LIG_FHA_1 210 216 PF00498 0.682
LIG_FHA_1 281 287 PF00498 0.307
LIG_FHA_1 289 295 PF00498 0.288
LIG_FHA_1 314 320 PF00498 0.546
LIG_FHA_1 32 38 PF00498 0.627
LIG_FHA_1 42 48 PF00498 0.743
LIG_FHA_1 5 11 PF00498 0.665
LIG_FHA_1 576 582 PF00498 0.275
LIG_FHA_1 613 619 PF00498 0.284
LIG_FHA_1 647 653 PF00498 0.314
LIG_FHA_1 80 86 PF00498 0.648
LIG_FHA_2 110 116 PF00498 0.647
LIG_FHA_2 214 220 PF00498 0.572
LIG_FHA_2 290 296 PF00498 0.459
LIG_FHA_2 389 395 PF00498 0.332
LIG_FHA_2 549 555 PF00498 0.331
LIG_FHA_2 63 69 PF00498 0.659
LIG_IRF3_LxIS_1 294 301 PF10401 0.196
LIG_LIR_Apic_2 496 502 PF02991 0.335
LIG_LIR_Gen_1 283 293 PF02991 0.293
LIG_LIR_Gen_1 374 382 PF02991 0.282
LIG_LIR_Gen_1 400 408 PF02991 0.339
LIG_LIR_Gen_1 508 514 PF02991 0.411
LIG_LIR_Gen_1 533 541 PF02991 0.363
LIG_LIR_Gen_1 649 657 PF02991 0.404
LIG_LIR_Nem_3 283 288 PF02991 0.397
LIG_LIR_Nem_3 374 378 PF02991 0.284
LIG_LIR_Nem_3 384 390 PF02991 0.291
LIG_LIR_Nem_3 450 455 PF02991 0.448
LIG_LIR_Nem_3 508 512 PF02991 0.402
LIG_LIR_Nem_3 533 539 PF02991 0.365
LIG_LIR_Nem_3 545 549 PF02991 0.324
LIG_LIR_Nem_3 565 570 PF02991 0.303
LIG_LIR_Nem_3 649 653 PF02991 0.404
LIG_MYND_1 45 49 PF01753 0.656
LIG_NRBOX 647 653 PF00104 0.196
LIG_PCNA_yPIPBox_3 275 286 PF02747 0.334
LIG_Pex14_1 542 546 PF04695 0.360
LIG_REV1ctd_RIR_1 1 10 PF16727 0.705
LIG_SH2_CRK 180 184 PF00017 0.637
LIG_SH2_CRK 482 486 PF00017 0.373
LIG_SH2_CRK 536 540 PF00017 0.429
LIG_SH2_CRK 570 574 PF00017 0.335
LIG_SH2_GRB2like 180 183 PF00017 0.594
LIG_SH2_NCK_1 536 540 PF00017 0.420
LIG_SH2_PTP2 546 549 PF00017 0.321
LIG_SH2_PTP2 656 659 PF00017 0.289
LIG_SH2_SRC 158 161 PF00017 0.585
LIG_SH2_SRC 448 451 PF00017 0.313
LIG_SH2_STAP1 180 184 PF00017 0.621
LIG_SH2_STAP1 427 431 PF00017 0.383
LIG_SH2_STAP1 448 452 PF00017 0.448
LIG_SH2_STAP1 536 540 PF00017 0.332
LIG_SH2_STAP1 564 568 PF00017 0.308
LIG_SH2_STAT3 367 370 PF00017 0.318
LIG_SH2_STAT5 158 161 PF00017 0.572
LIG_SH2_STAT5 189 192 PF00017 0.655
LIG_SH2_STAT5 204 207 PF00017 0.499
LIG_SH2_STAT5 220 223 PF00017 0.586
LIG_SH2_STAT5 265 268 PF00017 0.383
LIG_SH2_STAT5 402 405 PF00017 0.356
LIG_SH2_STAT5 422 425 PF00017 0.205
LIG_SH2_STAT5 536 539 PF00017 0.415
LIG_SH2_STAT5 546 549 PF00017 0.319
LIG_SH2_STAT5 630 633 PF00017 0.342
LIG_SH2_STAT5 656 659 PF00017 0.314
LIG_SH3_3 296 302 PF00018 0.289
LIG_SH3_3 373 379 PF00018 0.376
LIG_SH3_3 39 45 PF00018 0.729
LIG_SUMO_SIM_anti_2 283 292 PF11976 0.365
LIG_SUMO_SIM_anti_2 295 301 PF11976 0.252
LIG_SUMO_SIM_par_1 283 292 PF11976 0.308
LIG_SUMO_SIM_par_1 295 301 PF11976 0.265
LIG_SUMO_SIM_par_1 388 396 PF11976 0.364
LIG_SUMO_SIM_par_1 473 478 PF11976 0.288
LIG_SUMO_SIM_par_1 6 12 PF11976 0.634
LIG_TRFH_1 375 379 PF08558 0.309
LIG_TYR_ITIM 15 20 PF00017 0.670
LIG_TYR_ITIM 534 539 PF00017 0.458
LIG_TYR_ITIM 568 573 PF00017 0.404
LIG_UBA3_1 586 593 PF00899 0.459
LIG_WRC_WIRS_1 282 287 PF05994 0.336
LIG_WRC_WIRS_1 372 377 PF05994 0.335
MOD_CK1_1 109 115 PF00069 0.618
MOD_CK1_1 61 67 PF00069 0.709
MOD_CK1_1 9 15 PF00069 0.641
MOD_CK2_1 133 139 PF00069 0.599
MOD_CK2_1 289 295 PF00069 0.361
MOD_CK2_1 388 394 PF00069 0.390
MOD_CK2_1 548 554 PF00069 0.321
MOD_CK2_1 655 661 PF00069 0.336
MOD_Cter_Amidation 124 127 PF01082 0.385
MOD_DYRK1A_RPxSP_1 41 45 PF00069 0.661
MOD_GlcNHglycan 101 104 PF01048 0.381
MOD_GlcNHglycan 147 150 PF01048 0.434
MOD_GlcNHglycan 308 311 PF01048 0.349
MOD_GlcNHglycan 336 339 PF01048 0.327
MOD_GlcNHglycan 360 363 PF01048 0.643
MOD_GlcNHglycan 406 409 PF01048 0.567
MOD_GlcNHglycan 428 431 PF01048 0.562
MOD_GlcNHglycan 435 438 PF01048 0.517
MOD_GlcNHglycan 468 471 PF01048 0.652
MOD_GlcNHglycan 618 621 PF01048 0.316
MOD_GlcNHglycan 90 94 PF01048 0.450
MOD_GSK3_1 141 148 PF00069 0.679
MOD_GSK3_1 209 216 PF00069 0.677
MOD_GSK3_1 269 276 PF00069 0.395
MOD_GSK3_1 294 301 PF00069 0.414
MOD_GSK3_1 304 311 PF00069 0.668
MOD_GSK3_1 328 335 PF00069 0.233
MOD_GSK3_1 352 359 PF00069 0.412
MOD_GSK3_1 388 395 PF00069 0.340
MOD_GSK3_1 41 48 PF00069 0.684
MOD_GSK3_1 510 517 PF00069 0.307
MOD_GSK3_1 58 65 PF00069 0.597
MOD_GSK3_1 612 619 PF00069 0.394
MOD_GSK3_1 66 73 PF00069 0.664
MOD_GSK3_1 89 96 PF00069 0.645
MOD_LATS_1 87 93 PF00433 0.711
MOD_N-GLC_1 425 430 PF02516 0.558
MOD_N-GLC_1 433 438 PF02516 0.513
MOD_N-GLC_1 466 471 PF02516 0.641
MOD_NEK2_1 209 214 PF00069 0.717
MOD_NEK2_1 22 27 PF00069 0.618
MOD_NEK2_1 236 241 PF00069 0.513
MOD_NEK2_1 269 274 PF00069 0.384
MOD_NEK2_1 280 285 PF00069 0.261
MOD_NEK2_1 287 292 PF00069 0.193
MOD_NEK2_1 294 299 PF00069 0.224
MOD_NEK2_1 327 332 PF00069 0.246
MOD_NEK2_1 339 344 PF00069 0.384
MOD_NEK2_1 358 363 PF00069 0.386
MOD_NEK2_1 4 9 PF00069 0.703
MOD_NEK2_1 60 65 PF00069 0.760
MOD_NEK2_1 616 621 PF00069 0.370
MOD_NEK2_1 95 100 PF00069 0.638
MOD_PIKK_1 366 372 PF00454 0.308
MOD_PIKK_1 475 481 PF00454 0.340
MOD_PKA_2 22 28 PF00069 0.619
MOD_PKA_2 514 520 PF00069 0.368
MOD_PKA_2 556 562 PF00069 0.342
MOD_PKB_1 386 394 PF00069 0.305
MOD_Plk_1 294 300 PF00069 0.322
MOD_Plk_1 356 362 PF00069 0.390
MOD_Plk_1 433 439 PF00069 0.328
MOD_Plk_1 93 99 PF00069 0.668
MOD_Plk_2-3 352 358 PF00069 0.402
MOD_Plk_4 281 287 PF00069 0.345
MOD_Plk_4 289 295 PF00069 0.309
MOD_Plk_4 328 334 PF00069 0.348
MOD_Plk_4 371 377 PF00069 0.413
MOD_Plk_4 594 600 PF00069 0.606
MOD_Plk_4 612 618 PF00069 0.376
MOD_Plk_4 626 632 PF00069 0.366
MOD_Plk_4 646 652 PF00069 0.341
MOD_ProDKin_1 298 304 PF00069 0.221
MOD_ProDKin_1 397 403 PF00069 0.402
MOD_ProDKin_1 41 47 PF00069 0.700
MOD_ProDKin_1 411 417 PF00069 0.351
MOD_ProDKin_1 548 554 PF00069 0.335
MOD_ProDKin_1 63 69 PF00069 0.761
MOD_SUMO_for_1 225 228 PF00179 0.645
TRG_ENDOCYTIC_2 17 20 PF00928 0.675
TRG_ENDOCYTIC_2 180 183 PF00928 0.611
TRG_ENDOCYTIC_2 402 405 PF00928 0.329
TRG_ENDOCYTIC_2 482 485 PF00928 0.292
TRG_ENDOCYTIC_2 536 539 PF00928 0.415
TRG_ENDOCYTIC_2 546 549 PF00928 0.323
TRG_ENDOCYTIC_2 564 567 PF00928 0.334
TRG_ENDOCYTIC_2 570 573 PF00928 0.313
TRG_ENDOCYTIC_2 656 659 PF00928 0.190
TRG_ER_diArg_1 117 120 PF00400 0.657
TRG_ER_diArg_1 205 207 PF00400 0.591
TRG_ER_diArg_1 504 506 PF00400 0.312
TRG_NES_CRM1_1 150 160 PF08389 0.628

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P8M8 Leptomonas seymouri 64% 100%
A0A1X0NIN6 Trypanosomatidae 43% 100%
A0A3Q8I8N7 Leishmania donovani 80% 100%
A0A3R7N0K0 Trypanosoma rangeli 45% 100%
A4HU61 Leishmania infantum 80% 100%
D0A9P3 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 38% 100%
E9AMZ1 Leishmania mexicana (strain MHOM/GT/2001/U1103) 79% 100%
Q4QHN6 Leishmania major 81% 100%
V5BI21 Trypanosoma cruzi 44% 92%

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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