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 infantum
UniProt:
A4I8Y8_LEIIN
TriTrypDb:
LINF_330019900
Length:
621

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: 12
NetGPI no yes: 0, no: 12
Cellular components
Term Name Level Count
GO:0005840 ribosome 5 10
GO:0032991 protein-containing complex 1 10
GO:0043226 organelle 2 10
GO:0043228 non-membrane-bounded organelle 3 10
GO:0043229 intracellular organelle 3 10
GO:0043232 intracellular non-membrane-bounded organelle 4 10
GO:0110165 cellular anatomical entity 1 10
GO:1990904 ribonucleoprotein complex 2 10
GO:0035869 ciliary transition zone 2 2

Expansion

Sequence features

A4I8Y8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4I8Y8

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 375 379 PF00656 0.434
CLV_NRD_NRD_1 116 118 PF00675 0.440
CLV_NRD_NRD_1 253 255 PF00675 0.361
CLV_NRD_NRD_1 420 422 PF00675 0.549
CLV_NRD_NRD_1 430 432 PF00675 0.474
CLV_NRD_NRD_1 617 619 PF00675 0.691
CLV_NRD_NRD_1 77 79 PF00675 0.448
CLV_PCSK_FUR_1 75 79 PF00082 0.455
CLV_PCSK_KEX2_1 116 118 PF00082 0.346
CLV_PCSK_KEX2_1 403 405 PF00082 0.584
CLV_PCSK_KEX2_1 430 432 PF00082 0.606
CLV_PCSK_KEX2_1 617 619 PF00082 0.645
CLV_PCSK_KEX2_1 77 79 PF00082 0.448
CLV_PCSK_PC1ET2_1 403 405 PF00082 0.553
CLV_PCSK_SKI1_1 17 21 PF00082 0.491
CLV_PCSK_SKI1_1 238 242 PF00082 0.429
CLV_PCSK_SKI1_1 374 378 PF00082 0.426
CLV_Separin_Metazoa 427 431 PF03568 0.435
DEG_APCC_DBOX_1 373 381 PF00400 0.417
DEG_APCC_DBOX_1 429 437 PF00400 0.470
DEG_SPOP_SBC_1 449 453 PF00917 0.490
DEG_SPOP_SBC_1 497 501 PF00917 0.705
DOC_MAPK_gen_1 233 242 PF00069 0.440
DOC_MAPK_gen_1 421 428 PF00069 0.438
DOC_MAPK_gen_1 77 87 PF00069 0.459
DOC_PP2B_LxvP_1 537 540 PF13499 0.602
DOC_PP2B_LxvP_1 575 578 PF13499 0.660
DOC_USP7_MATH_1 139 143 PF00917 0.403
DOC_USP7_MATH_1 161 165 PF00917 0.476
DOC_USP7_MATH_1 176 180 PF00917 0.543
DOC_USP7_MATH_1 366 370 PF00917 0.402
DOC_USP7_MATH_1 372 376 PF00917 0.363
DOC_USP7_MATH_1 448 452 PF00917 0.611
DOC_USP7_MATH_1 455 459 PF00917 0.506
DOC_USP7_MATH_1 464 468 PF00917 0.616
DOC_USP7_MATH_1 507 511 PF00917 0.557
DOC_USP7_MATH_1 531 535 PF00917 0.695
DOC_USP7_MATH_1 608 612 PF00917 0.590
DOC_USP7_UBL2_3 399 403 PF12436 0.530
DOC_WW_Pin1_4 466 471 PF00397 0.528
DOC_WW_Pin1_4 487 492 PF00397 0.747
DOC_WW_Pin1_4 499 504 PF00397 0.754
DOC_WW_Pin1_4 521 526 PF00397 0.647
DOC_WW_Pin1_4 8 13 PF00397 0.649
LIG_14-3-3_CanoR_1 249 254 PF00244 0.405
LIG_14-3-3_CanoR_1 336 346 PF00244 0.499
LIG_14-3-3_CanoR_1 421 427 PF00244 0.464
LIG_14-3-3_CanoR_1 511 516 PF00244 0.604
LIG_14-3-3_CanoR_1 549 554 PF00244 0.639
LIG_14-3-3_CterR_2 617 621 PF00244 0.701
LIG_Actin_WH2_2 239 256 PF00022 0.452
LIG_APCC_ABBA_1 106 111 PF00400 0.431
LIG_BRCT_BRCA1_1 140 144 PF00533 0.326
LIG_CtBP_PxDLS_1 492 496 PF00389 0.515
LIG_EVH1_1 575 579 PF00568 0.655
LIG_FHA_1 183 189 PF00498 0.470
LIG_FHA_1 338 344 PF00498 0.472
LIG_FHA_1 410 416 PF00498 0.448
LIG_FHA_1 421 427 PF00498 0.478
LIG_FHA_1 43 49 PF00498 0.388
LIG_FHA_1 435 441 PF00498 0.452
LIG_FHA_1 60 66 PF00498 0.533
LIG_FHA_2 405 411 PF00498 0.418
LIG_FHA_2 469 475 PF00498 0.723
LIG_Integrin_RGD_1 133 135 PF01839 0.374
LIG_LIR_Gen_1 211 220 PF02991 0.266
LIG_LIR_Gen_1 44 55 PF02991 0.498
LIG_LIR_Gen_1 86 95 PF02991 0.459
LIG_LIR_Nem_3 211 216 PF02991 0.259
LIG_LIR_Nem_3 565 571 PF02991 0.673
LIG_LIR_Nem_3 86 91 PF02991 0.456
LIG_LYPXL_SIV_4 344 352 PF13949 0.536
LIG_PCNA_yPIPBox_3 225 238 PF02747 0.333
LIG_SH2_CRK 88 92 PF00017 0.461
LIG_SH2_SRC 171 174 PF00017 0.487
LIG_SH2_SRC 568 571 PF00017 0.593
LIG_SH2_STAP1 109 113 PF00017 0.464
LIG_SH2_STAP1 339 343 PF00017 0.482
LIG_SH2_STAT3 339 342 PF00017 0.544
LIG_SH2_STAT5 109 112 PF00017 0.497
LIG_SH2_STAT5 127 130 PF00017 0.332
LIG_SH2_STAT5 166 169 PF00017 0.465
LIG_SH2_STAT5 270 273 PF00017 0.394
LIG_SH2_STAT5 303 306 PF00017 0.455
LIG_SH2_STAT5 339 342 PF00017 0.532
LIG_SH2_STAT5 345 348 PF00017 0.538
LIG_SH3_1 444 450 PF00018 0.561
LIG_SH3_2 536 541 PF14604 0.585
LIG_SH3_2 593 598 PF14604 0.571
LIG_SH3_3 444 450 PF00018 0.651
LIG_SH3_3 479 485 PF00018 0.654
LIG_SH3_3 486 492 PF00018 0.713
LIG_SH3_3 506 512 PF00018 0.660
LIG_SH3_3 517 523 PF00018 0.589
LIG_SH3_3 533 539 PF00018 0.722
LIG_SH3_3 541 547 PF00018 0.758
LIG_SH3_3 573 579 PF00018 0.645
LIG_SH3_3 580 586 PF00018 0.676
LIG_SH3_3 588 594 PF00018 0.751
LIG_SH3_CIN85_PxpxPR_1 536 541 PF14604 0.537
LIG_SUMO_SIM_anti_2 361 367 PF11976 0.573
LIG_SUMO_SIM_anti_2 425 430 PF11976 0.407
LIG_SUMO_SIM_par_1 485 490 PF11976 0.606
LIG_SUMO_SIM_par_1 83 89 PF11976 0.449
LIG_TRAF2_1 407 410 PF00917 0.514
LIG_WRC_WIRS_1 373 378 PF05994 0.513
LIG_WRC_WIRS_1 66 71 PF05994 0.387
LIG_WW_3 538 542 PF00397 0.539
MOD_CDK_SPxxK_3 8 15 PF00069 0.530
MOD_CK1_1 142 148 PF00069 0.331
MOD_CK1_1 181 187 PF00069 0.450
MOD_CK1_1 193 199 PF00069 0.346
MOD_CK1_1 289 295 PF00069 0.451
MOD_CK1_1 41 47 PF00069 0.491
MOD_CK1_1 496 502 PF00069 0.709
MOD_CK1_1 510 516 PF00069 0.591
MOD_CK2_1 404 410 PF00069 0.506
MOD_CK2_1 468 474 PF00069 0.739
MOD_DYRK1A_RPxSP_1 8 12 PF00069 0.534
MOD_GlcNHglycan 102 105 PF01048 0.449
MOD_GlcNHglycan 123 126 PF01048 0.406
MOD_GlcNHglycan 178 181 PF01048 0.278
MOD_GlcNHglycan 192 195 PF01048 0.463
MOD_GlcNHglycan 206 209 PF01048 0.590
MOD_GlcNHglycan 210 213 PF01048 0.359
MOD_GlcNHglycan 221 224 PF01048 0.442
MOD_GlcNHglycan 225 228 PF01048 0.400
MOD_GlcNHglycan 263 266 PF01048 0.397
MOD_GlcNHglycan 291 294 PF01048 0.419
MOD_GlcNHglycan 306 309 PF01048 0.421
MOD_GlcNHglycan 366 369 PF01048 0.540
MOD_GlcNHglycan 441 444 PF01048 0.676
MOD_GlcNHglycan 457 460 PF01048 0.492
MOD_GlcNHglycan 466 469 PF01048 0.619
MOD_GlcNHglycan 494 498 PF01048 0.791
MOD_GlcNHglycan 516 519 PF01048 0.690
MOD_GlcNHglycan 533 536 PF01048 0.662
MOD_GlcNHglycan 551 554 PF01048 0.697
MOD_GlcNHglycan 609 613 PF01048 0.672
MOD_GSK3_1 117 124 PF00069 0.544
MOD_GSK3_1 138 145 PF00069 0.386
MOD_GSK3_1 17 24 PF00069 0.552
MOD_GSK3_1 178 185 PF00069 0.546
MOD_GSK3_1 204 211 PF00069 0.488
MOD_GSK3_1 215 222 PF00069 0.559
MOD_GSK3_1 306 313 PF00069 0.392
MOD_GSK3_1 37 44 PF00069 0.482
MOD_GSK3_1 372 379 PF00069 0.424
MOD_GSK3_1 405 412 PF00069 0.538
MOD_GSK3_1 434 441 PF00069 0.537
MOD_GSK3_1 462 469 PF00069 0.528
MOD_GSK3_1 493 500 PF00069 0.787
MOD_GSK3_1 503 510 PF00069 0.689
MOD_GSK3_1 527 534 PF00069 0.818
MOD_GSK3_1 560 567 PF00069 0.606
MOD_GSK3_1 613 620 PF00069 0.756
MOD_N-GLC_1 42 47 PF02516 0.462
MOD_NEK2_1 144 149 PF00069 0.417
MOD_NEK2_1 304 309 PF00069 0.426
MOD_NEK2_1 376 381 PF00069 0.431
MOD_NEK2_1 38 43 PF00069 0.427
MOD_NEK2_1 436 441 PF00069 0.436
MOD_NEK2_1 498 503 PF00069 0.772
MOD_NEK2_1 99 104 PF00069 0.382
MOD_NEK2_2 83 88 PF00069 0.352
MOD_PIKK_1 144 150 PF00454 0.392
MOD_PIKK_1 338 344 PF00454 0.548
MOD_PKA_2 204 210 PF00069 0.481
MOD_PKA_2 383 389 PF00069 0.478
MOD_PKA_2 420 426 PF00069 0.444
MOD_PKA_2 434 440 PF00069 0.404
MOD_PKA_2 510 516 PF00069 0.631
MOD_PKA_2 548 554 PF00069 0.729
MOD_Plk_1 142 148 PF00069 0.419
MOD_Plk_1 17 23 PF00069 0.627
MOD_Plk_1 181 187 PF00069 0.471
MOD_Plk_1 275 281 PF00069 0.481
MOD_Plk_1 310 316 PF00069 0.451
MOD_Plk_1 42 48 PF00069 0.458
MOD_Plk_1 493 499 PF00069 0.770
MOD_Plk_4 275 281 PF00069 0.481
MOD_Plk_4 42 48 PF00069 0.458
MOD_Plk_4 511 517 PF00069 0.759
MOD_Plk_4 83 89 PF00069 0.420
MOD_ProDKin_1 466 472 PF00069 0.528
MOD_ProDKin_1 487 493 PF00069 0.748
MOD_ProDKin_1 499 505 PF00069 0.751
MOD_ProDKin_1 521 527 PF00069 0.647
MOD_ProDKin_1 8 14 PF00069 0.646
MOD_SUMO_rev_2 24 29 PF00179 0.446
MOD_SUMO_rev_2 416 423 PF00179 0.441
TRG_DiLeu_BaEn_1 173 178 PF01217 0.551
TRG_DiLeu_BaEn_1 358 363 PF01217 0.473
TRG_DiLeu_BaLyEn_6 152 157 PF01217 0.286
TRG_ENDOCYTIC_2 200 203 PF00928 0.473
TRG_ENDOCYTIC_2 391 394 PF00928 0.454
TRG_ENDOCYTIC_2 568 571 PF00928 0.596
TRG_ENDOCYTIC_2 88 91 PF00928 0.490
TRG_ER_diArg_1 115 117 PF00400 0.346
TRG_ER_diArg_1 429 431 PF00400 0.452
TRG_ER_diArg_1 617 619 PF00400 0.703
TRG_ER_diArg_1 74 77 PF00400 0.609
TRG_Pf-PMV_PEXEL_1 168 173 PF00026 0.287
TRG_Pf-PMV_PEXEL_1 357 361 PF00026 0.530

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I367 Leptomonas seymouri 68% 91%
A0A1X0P0X2 Trypanosomatidae 39% 94%
A0A1X0P178 Trypanosomatidae 37% 100%
A0A3Q8IGU1 Leishmania donovani 99% 100%
A0A422N1N7 Trypanosoma rangeli 22% 72%
A4HLH8 Leishmania braziliensis 74% 98%
A4HLH9 Leishmania braziliensis 30% 100%
E9B3V7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 89% 99%
E9B3V8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 29% 71%
Q4Q466 Leishmania major 29% 73%
Q4Q467 Leishmania major 92% 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