LeishMANIAdb
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G protein-coupled receptor

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

Quick info

Protein:
G protein-coupled receptor
Gene product:
hypothetical protein, conserved
Species:
Leishmania braziliensis
UniProt:
A4HLQ6_LEIBR
TriTrypDb:
LbrM.33.2220 , LBRM2903_330029100 *
Length:
626

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: 18
NetGPI no yes: 0, no: 18
Cellular components
Term Name Level Count
GO:0016020 membrane 2 17
GO:0110165 cellular anatomical entity 1 17

Expansion

Sequence features

A4HLQ6
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HLQ6

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 4 8 PF00656 0.613
CLV_C14_Caspase3-7 413 417 PF00656 0.282
CLV_C14_Caspase3-7 60 64 PF00656 0.730
CLV_NRD_NRD_1 585 587 PF00675 0.707
CLV_NRD_NRD_1 8 10 PF00675 0.547
CLV_PCSK_FUR_1 334 338 PF00082 0.499
CLV_PCSK_KEX2_1 190 192 PF00082 0.400
CLV_PCSK_KEX2_1 336 338 PF00082 0.548
CLV_PCSK_PC1ET2_1 190 192 PF00082 0.297
CLV_PCSK_PC1ET2_1 336 338 PF00082 0.600
CLV_PCSK_SKI1_1 128 132 PF00082 0.389
CLV_PCSK_SKI1_1 337 341 PF00082 0.590
DEG_COP1_1 300 310 PF00400 0.457
DEG_MDM2_SWIB_1 271 279 PF02201 0.282
DEG_MDM2_SWIB_1 403 410 PF02201 0.327
DOC_ANK_TNKS_1 612 619 PF00023 0.380
DOC_CDC14_PxL_1 506 514 PF14671 0.186
DOC_MAPK_FxFP_2 359 362 PF00069 0.282
DOC_MAPK_gen_1 331 340 PF00069 0.343
DOC_MAPK_gen_1 382 391 PF00069 0.444
DOC_MAPK_HePTP_8 494 506 PF00069 0.210
DOC_MAPK_MEF2A_6 221 230 PF00069 0.564
DOC_MAPK_MEF2A_6 382 390 PF00069 0.444
DOC_MAPK_MEF2A_6 497 506 PF00069 0.354
DOC_MAPK_RevD_3 321 337 PF00069 0.448
DOC_PP1_RVXF_1 28 34 PF00149 0.576
DOC_PP1_RVXF_1 501 507 PF00149 0.300
DOC_PP1_RVXF_1 532 539 PF00149 0.623
DOC_PP1_RVXF_1 577 583 PF00149 0.377
DOC_PP2B_LxvP_1 305 308 PF13499 0.615
DOC_PP4_FxxP_1 15 18 PF00568 0.656
DOC_PP4_FxxP_1 174 177 PF00568 0.585
DOC_PP4_FxxP_1 359 362 PF00568 0.345
DOC_PP4_FxxP_1 591 594 PF00568 0.342
DOC_SPAK_OSR1_1 590 594 PF12202 0.339
DOC_USP7_MATH_1 102 106 PF00917 0.537
DOC_USP7_MATH_1 211 215 PF00917 0.522
DOC_USP7_MATH_1 605 609 PF00917 0.457
DOC_USP7_MATH_2 431 437 PF00917 0.251
DOC_WW_Pin1_4 160 165 PF00397 0.524
DOC_WW_Pin1_4 306 311 PF00397 0.513
DOC_WW_Pin1_4 574 579 PF00397 0.291
DOC_WW_Pin1_4 601 606 PF00397 0.379
LIG_14-3-3_CanoR_1 180 188 PF00244 0.606
LIG_14-3-3_CanoR_1 349 357 PF00244 0.341
LIG_14-3-3_CanoR_1 434 442 PF00244 0.291
LIG_14-3-3_CanoR_1 467 473 PF00244 0.504
LIG_14-3-3_CanoR_1 503 513 PF00244 0.391
LIG_14-3-3_CanoR_1 539 543 PF00244 0.451
LIG_14-3-3_CanoR_1 9 17 PF00244 0.793
LIG_Actin_WH2_2 174 192 PF00022 0.588
LIG_Actin_WH2_2 481 499 PF00022 0.210
LIG_APCC_ABBA_1 518 523 PF00400 0.222
LIG_BRCT_BRCA1_1 261 265 PF00533 0.338
LIG_BRCT_BRCA1_1 350 354 PF00533 0.221
LIG_BRCT_BRCA1_1 91 95 PF00533 0.612
LIG_Clathr_ClatBox_1 21 25 PF01394 0.635
LIG_CtBP_PxDLS_1 18 22 PF00389 0.651
LIG_deltaCOP1_diTrp_1 378 385 PF00928 0.513
LIG_EH1_1 124 132 PF00400 0.514
LIG_EH1_1 443 451 PF00400 0.186
LIG_eIF4E_1 263 269 PF01652 0.282
LIG_eIF4E_1 444 450 PF01652 0.186
LIG_eIF4E_1 552 558 PF01652 0.445
LIG_FHA_1 240 246 PF00498 0.411
LIG_FHA_1 265 271 PF00498 0.330
LIG_FHA_1 457 463 PF00498 0.410
LIG_FHA_1 499 505 PF00498 0.316
LIG_FHA_1 569 575 PF00498 0.477
LIG_FHA_2 133 139 PF00498 0.519
LIG_FHA_2 148 154 PF00498 0.546
LIG_FHA_2 286 292 PF00498 0.455
LIG_FHA_2 60 66 PF00498 0.712
LIG_GBD_Chelix_1 438 446 PF00786 0.282
LIG_GBD_Chelix_1 488 496 PF00786 0.271
LIG_LIR_Apic_2 12 18 PF02991 0.808
LIG_LIR_Apic_2 171 177 PF02991 0.549
LIG_LIR_Apic_2 588 594 PF02991 0.334
LIG_LIR_Gen_1 192 201 PF02991 0.495
LIG_LIR_Gen_1 301 312 PF02991 0.636
LIG_LIR_Gen_1 322 332 PF02991 0.386
LIG_LIR_Gen_1 352 362 PF02991 0.386
LIG_LIR_Gen_1 483 494 PF02991 0.307
LIG_LIR_Gen_1 505 514 PF02991 0.448
LIG_LIR_LC3C_4 20 23 PF02991 0.646
LIG_LIR_Nem_3 192 197 PF02991 0.528
LIG_LIR_Nem_3 262 268 PF02991 0.268
LIG_LIR_Nem_3 301 307 PF02991 0.644
LIG_LIR_Nem_3 309 314 PF02991 0.622
LIG_LIR_Nem_3 322 327 PF02991 0.177
LIG_LIR_Nem_3 351 357 PF02991 0.290
LIG_LIR_Nem_3 483 489 PF02991 0.308
LIG_LIR_Nem_3 505 509 PF02991 0.362
LIG_LIR_Nem_3 541 547 PF02991 0.461
LIG_LIR_Nem_3 548 552 PF02991 0.268
LIG_LIR_Nem_3 92 98 PF02991 0.567
LIG_NRBOX 553 559 PF00104 0.445
LIG_PCNA_PIPBox_1 148 157 PF02747 0.523
LIG_PCNA_yPIPBox_3 145 155 PF02747 0.564
LIG_Pex14_1 549 553 PF04695 0.426
LIG_Pex14_2 174 178 PF04695 0.549
LIG_Pex14_2 271 275 PF04695 0.282
LIG_Pex14_2 403 407 PF04695 0.387
LIG_Pex14_2 538 542 PF04695 0.626
LIG_PTB_Apo_2 224 231 PF02174 0.444
LIG_PTB_Apo_2 532 539 PF02174 0.560
LIG_Rb_pABgroove_1 195 203 PF01858 0.476
LIG_Rb_pABgroove_1 315 323 PF01858 0.186
LIG_REV1ctd_RIR_1 171 176 PF16727 0.470
LIG_SH2_CRK 186 190 PF00017 0.620
LIG_SH2_CRK 266 270 PF00017 0.330
LIG_SH2_CRK 355 359 PF00017 0.397
LIG_SH2_GRB2like 369 372 PF00017 0.570
LIG_SH2_NCK_1 355 359 PF00017 0.470
LIG_SH2_PTP2 196 199 PF00017 0.597
LIG_SH2_PTP2 311 314 PF00017 0.564
LIG_SH2_PTP2 387 390 PF00017 0.462
LIG_SH2_PTP2 486 489 PF00017 0.474
LIG_SH2_PTP2 491 494 PF00017 0.249
LIG_SH2_SRC 355 358 PF00017 0.421
LIG_SH2_STAP1 266 270 PF00017 0.308
LIG_SH2_STAP1 355 359 PF00017 0.186
LIG_SH2_STAP1 405 409 PF00017 0.391
LIG_SH2_STAT3 201 204 PF00017 0.499
LIG_SH2_STAT3 537 540 PF00017 0.446
LIG_SH2_STAT5 125 128 PF00017 0.510
LIG_SH2_STAT5 169 172 PF00017 0.504
LIG_SH2_STAT5 186 189 PF00017 0.517
LIG_SH2_STAT5 196 199 PF00017 0.596
LIG_SH2_STAT5 266 269 PF00017 0.320
LIG_SH2_STAT5 304 307 PF00017 0.508
LIG_SH2_STAT5 311 314 PF00017 0.512
LIG_SH2_STAT5 329 332 PF00017 0.290
LIG_SH2_STAT5 369 372 PF00017 0.510
LIG_SH2_STAT5 387 390 PF00017 0.405
LIG_SH2_STAT5 444 447 PF00017 0.361
LIG_SH2_STAT5 486 489 PF00017 0.421
LIG_SH2_STAT5 491 494 PF00017 0.400
LIG_SH2_STAT5 537 540 PF00017 0.560
LIG_SH2_STAT5 546 549 PF00017 0.264
LIG_SH2_STAT5 552 555 PF00017 0.224
LIG_SH2_STAT5 76 79 PF00017 0.653
LIG_SH3_3 20 26 PF00018 0.770
LIG_SH3_3 205 211 PF00018 0.576
LIG_SH3_3 304 310 PF00018 0.578
LIG_SH3_3 313 319 PF00018 0.293
LIG_SUMO_SIM_anti_2 20 25 PF11976 0.639
LIG_SUMO_SIM_anti_2 480 486 PF11976 0.396
LIG_SUMO_SIM_par_1 20 25 PF11976 0.639
LIG_SUMO_SIM_par_1 475 481 PF11976 0.404
LIG_SUMO_SIM_par_1 516 523 PF11976 0.406
LIG_SUMO_SIM_par_1 76 82 PF11976 0.646
LIG_TRFH_1 304 308 PF08558 0.433
LIG_TYR_ITIM 353 358 PF00017 0.186
LIG_TYR_ITIM 484 489 PF00017 0.258
LIG_UBA3_1 492 497 PF00899 0.210
LIG_UBA3_1 580 587 PF00899 0.392
LIG_WRC_WIRS_1 170 175 PF05994 0.469
MOD_CDK_SPK_2 574 579 PF00069 0.291
MOD_CK1_1 259 265 PF00069 0.320
MOD_CK1_1 348 354 PF00069 0.429
MOD_CK1_1 480 486 PF00069 0.276
MOD_CK1_1 609 615 PF00069 0.385
MOD_CK1_1 8 14 PF00069 0.784
MOD_CK1_1 89 95 PF00069 0.651
MOD_CK2_1 132 138 PF00069 0.513
MOD_CK2_1 147 153 PF00069 0.623
MOD_CK2_1 189 195 PF00069 0.484
MOD_CK2_1 290 296 PF00069 0.600
MOD_CK2_1 445 451 PF00069 0.466
MOD_GlcNHglycan 132 135 PF01048 0.344
MOD_GlcNHglycan 191 194 PF01048 0.331
MOD_GlcNHglycan 435 438 PF01048 0.507
MOD_GlcNHglycan 81 84 PF01048 0.401
MOD_GSK3_1 132 139 PF00069 0.627
MOD_GSK3_1 345 352 PF00069 0.295
MOD_GSK3_1 445 452 PF00069 0.449
MOD_GSK3_1 498 505 PF00069 0.336
MOD_GSK3_1 596 603 PF00069 0.416
MOD_GSK3_1 605 612 PF00069 0.389
MOD_N-GLC_1 217 222 PF02516 0.409
MOD_N-GLC_1 256 261 PF02516 0.612
MOD_N-GLC_1 51 56 PF02516 0.472
MOD_N-GLC_1 574 579 PF02516 0.491
MOD_N-GLC_1 606 611 PF02516 0.592
MOD_N-GLC_1 89 94 PF02516 0.270
MOD_NEK2_1 189 194 PF00069 0.554
MOD_NEK2_1 449 454 PF00069 0.301
MOD_NEK2_1 456 461 PF00069 0.334
MOD_NEK2_1 51 56 PF00069 0.791
MOD_NEK2_1 538 543 PF00069 0.605
MOD_NEK2_2 169 174 PF00069 0.503
MOD_PIKK_1 24 30 PF00454 0.562
MOD_PIKK_1 290 296 PF00454 0.479
MOD_PIKK_1 363 369 PF00454 0.320
MOD_PK_1 349 355 PF00069 0.186
MOD_PKA_1 586 592 PF00069 0.400
MOD_PKA_1 596 602 PF00069 0.394
MOD_PKA_2 179 185 PF00069 0.598
MOD_PKA_2 348 354 PF00069 0.435
MOD_PKA_2 433 439 PF00069 0.367
MOD_PKA_2 502 508 PF00069 0.400
MOD_PKA_2 538 544 PF00069 0.509
MOD_PKA_2 8 14 PF00069 0.769
MOD_Plk_1 290 296 PF00069 0.666
MOD_Plk_1 373 379 PF00069 0.649
MOD_Plk_1 497 503 PF00069 0.425
MOD_Plk_1 51 57 PF00069 0.750
MOD_Plk_2-3 132 138 PF00069 0.650
MOD_Plk_2-3 61 67 PF00069 0.736
MOD_Plk_4 169 175 PF00069 0.486
MOD_Plk_4 184 190 PF00069 0.441
MOD_Plk_4 211 217 PF00069 0.570
MOD_Plk_4 264 270 PF00069 0.390
MOD_Plk_4 349 355 PF00069 0.335
MOD_Plk_4 445 451 PF00069 0.352
MOD_Plk_4 51 57 PF00069 0.748
MOD_Plk_4 538 544 PF00069 0.563
MOD_ProDKin_1 160 166 PF00069 0.517
MOD_ProDKin_1 306 312 PF00069 0.513
MOD_ProDKin_1 574 580 PF00069 0.295
MOD_ProDKin_1 601 607 PF00069 0.382
TRG_DiLeu_BaEn_1 195 200 PF01217 0.477
TRG_DiLeu_BaEn_2 450 456 PF01217 0.426
TRG_DiLeu_BaLyEn_6 27 32 PF01217 0.711
TRG_DiLeu_BaLyEn_6 507 512 PF01217 0.327
TRG_DiLeu_BaLyEn_6 576 581 PF01217 0.371
TRG_ENDOCYTIC_2 167 170 PF00928 0.495
TRG_ENDOCYTIC_2 186 189 PF00928 0.539
TRG_ENDOCYTIC_2 196 199 PF00928 0.533
TRG_ENDOCYTIC_2 266 269 PF00928 0.335
TRG_ENDOCYTIC_2 304 307 PF00928 0.572
TRG_ENDOCYTIC_2 311 314 PF00928 0.489
TRG_ENDOCYTIC_2 355 358 PF00928 0.255
TRG_ENDOCYTIC_2 387 390 PF00928 0.372
TRG_ENDOCYTIC_2 405 408 PF00928 0.326
TRG_ENDOCYTIC_2 486 489 PF00928 0.447
TRG_ENDOCYTIC_2 491 494 PF00928 0.438
TRG_ENDOCYTIC_2 552 555 PF00928 0.303
TRG_ER_diArg_1 286 289 PF00400 0.608
TRG_ER_diArg_1 381 384 PF00400 0.544
TRG_Pf-PMV_PEXEL_1 128 132 PF00026 0.318
TRG_Pf-PMV_PEXEL_1 331 335 PF00026 0.494

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6A4 Leptomonas seymouri 23% 89%
A0A0S4IIV3 Bodo saltans 26% 82%
A0A1X0NUP0 Trypanosomatidae 21% 99%
A0A1X0P3P0 Trypanosomatidae 36% 91%
A0A3Q8IDV0 Leishmania donovani 77% 96%
A0A3R7R847 Trypanosoma rangeli 34% 94%
A0A3S7X5M8 Leishmania donovani 23% 100%
A0A422MY34 Trypanosoma rangeli 23% 99%
A4HKK2 Leishmania braziliensis 22% 100%
A4I834 Leishmania infantum 23% 100%
A4I956 Leishmania infantum 77% 96%
D0A6B6 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 31% 94%
E9B2Z2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 24% 100%
Q4Q3Z3 Leishmania major 76% 100%
Q4Q564 Leishmania major 23% 100%
V5B8R5 Trypanosoma cruzi 33% 95%
V5BBK9 Trypanosoma cruzi 24% 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