LeishMANIAdb
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Guanine nucleotide-binding protein subunit beta-like protein

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

Quick info

Protein:
Guanine nucleotide-binding protein subunit beta-like protein
Gene product:
WD domain, G-beta repeat, putative
Species:
Leishmania braziliensis
UniProt:
A4HLH8_LEIBR
TriTrypDb:
LbrM.33.1440 , LBRM2903_330019400
Length:
634

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: 16
NetGPI no yes: 0, no: 16
Cellular components
Term Name Level Count
GO:0005840 ribosome 5 14
GO:0032991 protein-containing complex 1 14
GO:0043226 organelle 2 14
GO:0043228 non-membrane-bounded organelle 3 14
GO:0043229 intracellular organelle 3 14
GO:0043232 intracellular non-membrane-bounded organelle 4 14
GO:0110165 cellular anatomical entity 1 14
GO:1990904 ribonucleoprotein complex 2 14
GO:0035869 ciliary transition zone 2 2

Expansion

Sequence features

A4HLH8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HLH8

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_NRD_NRD_1 253 255 PF00675 0.406
CLV_NRD_NRD_1 420 422 PF00675 0.513
CLV_NRD_NRD_1 430 432 PF00675 0.436
CLV_NRD_NRD_1 630 632 PF00675 0.722
CLV_NRD_NRD_1 77 79 PF00675 0.469
CLV_PCSK_FUR_1 75 79 PF00082 0.483
CLV_PCSK_KEX2_1 403 405 PF00082 0.526
CLV_PCSK_KEX2_1 430 432 PF00082 0.566
CLV_PCSK_KEX2_1 630 632 PF00082 0.729
CLV_PCSK_KEX2_1 77 79 PF00082 0.495
CLV_PCSK_PC1ET2_1 403 405 PF00082 0.561
CLV_PCSK_SKI1_1 158 162 PF00082 0.338
CLV_PCSK_SKI1_1 374 378 PF00082 0.519
CLV_PCSK_SKI1_1 542 546 PF00082 0.646
CLV_PCSK_SKI1_1 622 626 PF00082 0.510
CLV_Separin_Metazoa 427 431 PF03568 0.570
DEG_APCC_DBOX_1 373 381 PF00400 0.440
DEG_APCC_DBOX_1 429 437 PF00400 0.597
DEG_SIAH_1 590 598 PF03145 0.499
DOC_CDC14_PxL_1 1 9 PF14671 0.465
DOC_MAPK_DCC_7 467 477 PF00069 0.497
DOC_MAPK_gen_1 421 428 PF00069 0.495
DOC_MAPK_gen_1 6 14 PF00069 0.475
DOC_MAPK_gen_1 77 87 PF00069 0.511
DOC_MAPK_MEF2A_6 357 364 PF00069 0.348
DOC_MAPK_NFAT4_5 357 365 PF00069 0.343
DOC_PP2B_LxvP_1 445 448 PF13499 0.600
DOC_PP2B_LxvP_1 470 473 PF13499 0.740
DOC_PP2B_LxvP_1 511 514 PF13499 0.602
DOC_PP2B_LxvP_1 525 528 PF13499 0.749
DOC_PP2B_LxvP_1 562 565 PF13499 0.613
DOC_USP7_MATH_1 139 143 PF00917 0.461
DOC_USP7_MATH_1 176 180 PF00917 0.492
DOC_USP7_MATH_1 372 376 PF00917 0.619
DOC_USP7_MATH_1 439 443 PF00917 0.464
DOC_USP7_MATH_1 466 470 PF00917 0.619
DOC_USP7_MATH_1 485 489 PF00917 0.690
DOC_USP7_MATH_1 506 510 PF00917 0.682
DOC_USP7_MATH_1 521 525 PF00917 0.736
DOC_USP7_MATH_1 526 530 PF00917 0.770
DOC_USP7_MATH_1 534 538 PF00917 0.725
DOC_USP7_UBL2_3 399 403 PF12436 0.574
DOC_WW_Pin1_4 468 473 PF00397 0.607
DOC_WW_Pin1_4 486 491 PF00397 0.660
DOC_WW_Pin1_4 536 541 PF00397 0.678
LIG_14-3-3_CanoR_1 249 254 PF00244 0.438
LIG_14-3-3_CanoR_1 421 427 PF00244 0.599
LIG_14-3-3_CanoR_1 467 471 PF00244 0.499
LIG_14-3-3_CanoR_1 499 504 PF00244 0.637
LIG_14-3-3_CanoR_1 536 540 PF00244 0.754
LIG_14-3-3_CanoR_1 6 14 PF00244 0.498
LIG_14-3-3_CterR_2 630 634 PF00244 0.719
LIG_Actin_WH2_2 239 256 PF00022 0.521
LIG_APCC_ABBA_1 106 111 PF00400 0.472
LIG_BIR_II_1 1 5 PF00653 0.571
LIG_BRCT_BRCA1_1 140 144 PF00533 0.344
LIG_Clathr_ClatBox_1 578 582 PF01394 0.533
LIG_EVH1_1 511 515 PF00568 0.541
LIG_EVH1_1 562 566 PF00568 0.631
LIG_EVH1_2 563 567 PF00568 0.510
LIG_FHA_1 183 189 PF00498 0.493
LIG_FHA_1 338 344 PF00498 0.649
LIG_FHA_1 423 429 PF00498 0.467
LIG_FHA_1 43 49 PF00498 0.458
LIG_FHA_1 435 441 PF00498 0.463
LIG_FHA_1 481 487 PF00498 0.645
LIG_FHA_1 60 66 PF00498 0.542
LIG_FHA_1 608 614 PF00498 0.667
LIG_FHA_1 623 629 PF00498 0.654
LIG_FHA_1 7 13 PF00498 0.620
LIG_FHA_2 14 20 PF00498 0.609
LIG_GBD_Chelix_1 279 287 PF00786 0.429
LIG_Integrin_RGD_1 133 135 PF01839 0.404
LIG_LIR_Gen_1 44 55 PF02991 0.536
LIG_LIR_Gen_1 79 88 PF02991 0.413
LIG_LIR_LC3C_4 361 364 PF02991 0.462
LIG_LIR_Nem_3 552 558 PF02991 0.733
LIG_LIR_Nem_3 79 85 PF02991 0.413
LIG_LIR_Nem_3 86 91 PF02991 0.479
LIG_LYPXL_SIV_4 344 352 PF13949 0.586
LIG_SH2_CRK 88 92 PF00017 0.524
LIG_SH2_SRC 171 174 PF00017 0.493
LIG_SH2_SRC 555 558 PF00017 0.627
LIG_SH2_STAP1 109 113 PF00017 0.505
LIG_SH2_STAP1 339 343 PF00017 0.682
LIG_SH2_STAT3 339 342 PF00017 0.616
LIG_SH2_STAT5 109 112 PF00017 0.506
LIG_SH2_STAT5 127 130 PF00017 0.338
LIG_SH2_STAT5 166 169 PF00017 0.450
LIG_SH2_STAT5 303 306 PF00017 0.455
LIG_SH2_STAT5 339 342 PF00017 0.548
LIG_SH2_STAT5 345 348 PF00017 0.539
LIG_SH3_1 444 450 PF00018 0.593
LIG_SH3_3 444 450 PF00018 0.666
LIG_SH3_3 472 478 PF00018 0.693
LIG_SH3_3 484 490 PF00018 0.678
LIG_SH3_3 494 500 PF00018 0.665
LIG_SH3_3 507 513 PF00018 0.649
LIG_SH3_3 515 521 PF00018 0.678
LIG_SH3_3 560 566 PF00018 0.664
LIG_SH3_3 585 591 PF00018 0.597
LIG_SH3_3 593 599 PF00018 0.524
LIG_SH3_3 602 608 PF00018 0.668
LIG_SUMO_SIM_anti_2 361 367 PF11976 0.577
LIG_SUMO_SIM_anti_2 425 430 PF11976 0.548
LIG_SUMO_SIM_par_1 361 367 PF11976 0.458
LIG_TRAF2_1 407 410 PF00917 0.520
LIG_WRC_WIRS_1 373 378 PF05994 0.520
LIG_WW_2 447 450 PF00397 0.478
LIG_WW_3 496 500 PF00397 0.583
LIG_WW_3 539 543 PF00397 0.520
MOD_CDC14_SPxK_1 539 542 PF00782 0.517
MOD_CDK_SPxK_1 536 542 PF00069 0.525
MOD_CK1_1 13 19 PF00069 0.704
MOD_CK1_1 142 148 PF00069 0.351
MOD_CK1_1 192 198 PF00069 0.572
MOD_CK1_1 275 281 PF00069 0.503
MOD_CK1_1 289 295 PF00069 0.449
MOD_CK1_1 366 372 PF00069 0.509
MOD_CK1_1 41 47 PF00069 0.544
MOD_CK1_1 458 464 PF00069 0.711
MOD_CK1_1 481 487 PF00069 0.729
MOD_CK1_1 489 495 PF00069 0.738
MOD_CK1_1 571 577 PF00069 0.597
MOD_DYRK1A_RPxSP_1 536 540 PF00069 0.524
MOD_GlcNHglycan 102 105 PF01048 0.505
MOD_GlcNHglycan 123 126 PF01048 0.460
MOD_GlcNHglycan 178 181 PF01048 0.301
MOD_GlcNHglycan 192 195 PF01048 0.509
MOD_GlcNHglycan 206 209 PF01048 0.504
MOD_GlcNHglycan 210 213 PF01048 0.433
MOD_GlcNHglycan 221 224 PF01048 0.367
MOD_GlcNHglycan 225 228 PF01048 0.409
MOD_GlcNHglycan 263 266 PF01048 0.413
MOD_GlcNHglycan 291 294 PF01048 0.511
MOD_GlcNHglycan 306 309 PF01048 0.418
MOD_GlcNHglycan 366 369 PF01048 0.532
MOD_GlcNHglycan 441 444 PF01048 0.624
MOD_GlcNHglycan 482 486 PF01048 0.692
MOD_GlcNHglycan 491 494 PF01048 0.622
MOD_GlcNHglycan 504 507 PF01048 0.695
MOD_GlcNHglycan 582 586 PF01048 0.644
MOD_GSK3_1 117 124 PF00069 0.459
MOD_GSK3_1 138 145 PF00069 0.392
MOD_GSK3_1 178 185 PF00069 0.504
MOD_GSK3_1 188 195 PF00069 0.586
MOD_GSK3_1 204 211 PF00069 0.486
MOD_GSK3_1 215 222 PF00069 0.477
MOD_GSK3_1 306 313 PF00069 0.489
MOD_GSK3_1 34 41 PF00069 0.426
MOD_GSK3_1 481 488 PF00069 0.797
MOD_GSK3_1 498 505 PF00069 0.684
MOD_GSK3_1 547 554 PF00069 0.728
MOD_GSK3_1 6 13 PF00069 0.575
MOD_GSK3_1 622 629 PF00069 0.669
MOD_GSK3_1 83 90 PF00069 0.355
MOD_N-GLC_1 272 277 PF02516 0.287
MOD_N-GLC_1 289 294 PF02516 0.272
MOD_N-GLC_1 42 47 PF02516 0.518
MOD_NEK2_1 144 149 PF00069 0.452
MOD_NEK2_1 304 309 PF00069 0.430
MOD_NEK2_1 38 43 PF00069 0.430
MOD_NEK2_1 581 586 PF00069 0.763
MOD_NEK2_1 99 104 PF00069 0.425
MOD_NEK2_2 83 88 PF00069 0.380
MOD_PIKK_1 144 150 PF00454 0.474
MOD_PIKK_1 338 344 PF00454 0.633
MOD_PIKK_1 398 404 PF00454 0.541
MOD_PIKK_1 544 550 PF00454 0.723
MOD_PKA_2 204 210 PF00069 0.563
MOD_PKA_2 248 254 PF00069 0.311
MOD_PKA_2 383 389 PF00069 0.554
MOD_PKA_2 434 440 PF00069 0.545
MOD_PKA_2 466 472 PF00069 0.493
MOD_PKA_2 498 504 PF00069 0.636
MOD_PKA_2 535 541 PF00069 0.825
MOD_PKA_2 571 577 PF00069 0.527
MOD_PKA_2 76 82 PF00069 0.354
MOD_Plk_1 142 148 PF00069 0.421
MOD_Plk_1 182 188 PF00069 0.492
MOD_Plk_1 275 281 PF00069 0.486
MOD_Plk_1 289 295 PF00069 0.409
MOD_Plk_1 310 316 PF00069 0.452
MOD_Plk_1 42 48 PF00069 0.479
MOD_Plk_1 481 487 PF00069 0.648
MOD_Plk_4 275 281 PF00069 0.491
MOD_Plk_4 42 48 PF00069 0.513
MOD_Plk_4 506 512 PF00069 0.628
MOD_Plk_4 83 89 PF00069 0.424
MOD_ProDKin_1 468 474 PF00069 0.611
MOD_ProDKin_1 486 492 PF00069 0.661
MOD_ProDKin_1 536 542 PF00069 0.681
MOD_SUMO_rev_2 19 29 PF00179 0.495
MOD_SUMO_rev_2 416 423 PF00179 0.622
TRG_DiLeu_BaEn_1 173 178 PF01217 0.579
TRG_DiLeu_BaEn_1 358 363 PF01217 0.525
TRG_DiLeu_BaLyEn_6 152 157 PF01217 0.306
TRG_ENDOCYTIC_2 200 203 PF00928 0.542
TRG_ENDOCYTIC_2 391 394 PF00928 0.640
TRG_ENDOCYTIC_2 555 558 PF00928 0.627
TRG_ENDOCYTIC_2 88 91 PF00928 0.520
TRG_ER_diArg_1 429 431 PF00400 0.583
TRG_ER_diArg_1 5 8 PF00400 0.466
TRG_ER_diArg_1 630 632 PF00400 0.722
TRG_ER_diArg_1 74 77 PF00400 0.651
TRG_Pf-PMV_PEXEL_1 168 173 PF00026 0.293
TRG_Pf-PMV_PEXEL_1 357 361 PF00026 0.528

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I367 Leptomonas seymouri 70% 93%
A0A0S4JA89 Bodo saltans 35% 72%
A0A1X0P0X2 Trypanosomatidae 39% 96%
A0A1X0P178 Trypanosomatidae 36% 100%
A0A3Q8IGU1 Leishmania donovani 74% 100%
A0A3R7M637 Trypanosoma rangeli 33% 100%
A0A3S7X6R5 Leishmania donovani 29% 73%
A4HLH9 Leishmania braziliensis 31% 82%
A4I8Y8 Leishmania infantum 74% 100%
A4I8Y9 Leishmania infantum 28% 74%
D0A4Y6 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 34% 86%
E9B3V7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
E9B3V8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 32% 72%
Q4Q466 Leishmania major 28% 74%
Q4Q467 Leishmania major 74% 96%

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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