LeishMANIAdb
  • Home
  • Browse
  • Manual
  • FAQ
  • Download

G5-interacting protein

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

Quick info

Protein:
G5-interacting protein
Gene product:
G5-interacting protein, putative
Species:
Leishmania braziliensis
UniProt:
A4HKC5_LEIBR
TriTrypDb:
LbrM.32.1530 , LBRM2903_320021400 *
Length:
781

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
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

A4HKC5
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HKC5

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 664 668 PF00656 0.455
CLV_C14_Caspase3-7 766 770 PF00656 0.494
CLV_NRD_NRD_1 419 421 PF00675 0.297
CLV_NRD_NRD_1 739 741 PF00675 0.410
CLV_PCSK_KEX2_1 265 267 PF00082 0.537
CLV_PCSK_KEX2_1 458 460 PF00082 0.640
CLV_PCSK_KEX2_1 739 741 PF00082 0.410
CLV_PCSK_PC1ET2_1 265 267 PF00082 0.529
CLV_PCSK_PC1ET2_1 458 460 PF00082 0.520
CLV_PCSK_PC7_1 454 460 PF00082 0.466
CLV_PCSK_SKI1_1 312 316 PF00082 0.521
CLV_PCSK_SKI1_1 317 321 PF00082 0.549
CLV_PCSK_SKI1_1 458 462 PF00082 0.474
CLV_PCSK_SKI1_1 534 538 PF00082 0.497
DOC_CKS1_1 216 221 PF01111 0.526
DOC_CKS1_1 490 495 PF01111 0.321
DOC_CYCLIN_RxL_1 454 464 PF00134 0.488
DOC_CYCLIN_yClb5_NLxxxL_5 513 522 PF00134 0.473
DOC_MAPK_FxFP_2 646 649 PF00069 0.413
DOC_MAPK_gen_1 420 428 PF00069 0.407
DOC_MAPK_gen_1 653 660 PF00069 0.356
DOC_MAPK_gen_1 729 737 PF00069 0.534
DOC_MAPK_MEF2A_6 240 247 PF00069 0.315
DOC_MAPK_MEF2A_6 346 355 PF00069 0.265
DOC_MAPK_MEF2A_6 653 660 PF00069 0.356
DOC_MAPK_NFAT4_5 346 354 PF00069 0.341
DOC_PIKK_1 399 407 PF02985 0.405
DOC_PP1_RVXF_1 365 372 PF00149 0.533
DOC_PP2B_LxvP_1 226 229 PF13499 0.663
DOC_PP4_FxxP_1 630 633 PF00568 0.350
DOC_PP4_FxxP_1 646 649 PF00568 0.413
DOC_PP4_FxxP_1 756 759 PF00568 0.493
DOC_USP7_MATH_1 168 172 PF00917 0.680
DOC_USP7_MATH_1 181 185 PF00917 0.723
DOC_USP7_MATH_1 189 193 PF00917 0.632
DOC_USP7_MATH_1 285 289 PF00917 0.460
DOC_USP7_MATH_1 310 314 PF00917 0.405
DOC_USP7_MATH_1 452 456 PF00917 0.446
DOC_USP7_MATH_1 770 774 PF00917 0.301
DOC_USP7_UBL2_3 252 256 PF12436 0.515
DOC_USP7_UBL2_3 318 322 PF12436 0.473
DOC_USP7_UBL2_3 373 377 PF12436 0.468
DOC_USP7_UBL2_3 721 725 PF12436 0.620
DOC_USP7_UBL2_3 727 731 PF12436 0.585
DOC_WW_Pin1_4 185 190 PF00397 0.639
DOC_WW_Pin1_4 215 220 PF00397 0.753
DOC_WW_Pin1_4 239 244 PF00397 0.516
DOC_WW_Pin1_4 273 278 PF00397 0.463
DOC_WW_Pin1_4 300 305 PF00397 0.470
DOC_WW_Pin1_4 489 494 PF00397 0.321
DOC_WW_Pin1_4 74 79 PF00397 0.531
DOC_WW_Pin1_4 743 748 PF00397 0.521
LIG_14-3-3_CanoR_1 224 229 PF00244 0.677
LIG_14-3-3_CanoR_1 367 372 PF00244 0.529
LIG_BIR_II_1 1 5 PF00653 0.684
LIG_BRCT_BRCA1_1 590 594 PF00533 0.408
LIG_BRCT_BRCA1_2 590 596 PF00533 0.422
LIG_Clathr_ClatBox_1 553 557 PF01394 0.375
LIG_deltaCOP1_diTrp_1 667 672 PF00928 0.397
LIG_eIF4E_1 339 345 PF01652 0.455
LIG_FHA_1 240 246 PF00498 0.370
LIG_FHA_1 360 366 PF00498 0.322
LIG_FHA_1 490 496 PF00498 0.385
LIG_FHA_1 653 659 PF00498 0.418
LIG_FHA_1 704 710 PF00498 0.454
LIG_FHA_2 439 445 PF00498 0.479
LIG_FHA_2 464 470 PF00498 0.476
LIG_HP1_1 243 247 PF01393 0.359
LIG_LIR_Apic_2 429 435 PF02991 0.439
LIG_LIR_Apic_2 464 470 PF02991 0.445
LIG_LIR_Gen_1 100 109 PF02991 0.686
LIG_LIR_Gen_1 267 277 PF02991 0.504
LIG_LIR_Gen_1 475 483 PF02991 0.377
LIG_LIR_Gen_1 507 518 PF02991 0.375
LIG_LIR_Nem_3 100 105 PF02991 0.748
LIG_LIR_Nem_3 267 272 PF02991 0.441
LIG_LIR_Nem_3 475 479 PF02991 0.359
LIG_LIR_Nem_3 507 513 PF02991 0.370
LIG_LIR_Nem_3 514 519 PF02991 0.344
LIG_LIR_Nem_3 591 597 PF02991 0.473
LIG_LIR_Nem_3 619 624 PF02991 0.486
LIG_LIR_Nem_3 637 641 PF02991 0.488
LIG_LIR_Nem_3 671 675 PF02991 0.340
LIG_PTB_Apo_2 53 60 PF02174 0.736
LIG_PTB_Apo_2 642 649 PF02174 0.473
LIG_PTB_Phospho_1 53 59 PF10480 0.738
LIG_PTB_Phospho_1 642 648 PF10480 0.492
LIG_Rb_LxCxE_1 550 569 PF01857 0.387
LIG_RPA_C_Insects 571 586 PF08784 0.262
LIG_SH2_CRK 102 106 PF00017 0.743
LIG_SH2_CRK 129 133 PF00017 0.777
LIG_SH2_CRK 141 145 PF00017 0.634
LIG_SH2_CRK 516 520 PF00017 0.331
LIG_SH2_GRB2like 102 105 PF00017 0.746
LIG_SH2_GRB2like 54 57 PF00017 0.719
LIG_SH2_NCK_1 141 145 PF00017 0.629
LIG_SH2_NCK_1 467 471 PF00017 0.459
LIG_SH2_PTP2 271 274 PF00017 0.372
LIG_SH2_PTP2 510 513 PF00017 0.337
LIG_SH2_SRC 54 57 PF00017 0.663
LIG_SH2_STAP1 463 467 PF00017 0.586
LIG_SH2_STAP1 679 683 PF00017 0.538
LIG_SH2_STAT5 122 125 PF00017 0.656
LIG_SH2_STAT5 271 274 PF00017 0.372
LIG_SH2_STAT5 339 342 PF00017 0.332
LIG_SH2_STAT5 343 346 PF00017 0.356
LIG_SH2_STAT5 432 435 PF00017 0.419
LIG_SH2_STAT5 463 466 PF00017 0.573
LIG_SH2_STAT5 472 475 PF00017 0.330
LIG_SH2_STAT5 476 479 PF00017 0.289
LIG_SH2_STAT5 489 492 PF00017 0.253
LIG_SH2_STAT5 510 513 PF00017 0.315
LIG_SH2_STAT5 566 569 PF00017 0.358
LIG_SH2_STAT5 675 678 PF00017 0.426
LIG_SH3_1 432 438 PF00018 0.409
LIG_SH3_3 151 157 PF00018 0.724
LIG_SH3_3 209 215 PF00018 0.689
LIG_SH3_3 219 225 PF00018 0.666
LIG_SH3_3 3 9 PF00018 0.725
LIG_SH3_3 432 438 PF00018 0.399
LIG_SH3_3 542 548 PF00018 0.448
LIG_SH3_3 80 86 PF00018 0.680
LIG_SH3_3 92 98 PF00018 0.682
LIG_SH3_CIN85_PxpxPR_1 219 224 PF14604 0.613
LIG_SUMO_SIM_anti_2 393 401 PF11976 0.429
LIG_SUMO_SIM_anti_2 498 504 PF11976 0.300
LIG_SUMO_SIM_par_1 695 702 PF11976 0.486
LIG_TRAF2_1 528 531 PF00917 0.447
LIG_UBA3_1 518 523 PF00899 0.340
LIG_UBA3_1 532 537 PF00899 0.460
LIG_UBA3_1 570 575 PF00899 0.366
LIG_ULM_U2AF65_1 739 744 PF00076 0.466
LIG_WRC_WIRS_1 669 674 PF05994 0.465
LIG_WRC_WIRS_1 734 739 PF05994 0.416
MOD_CDK_SPK_2 239 244 PF00069 0.575
MOD_CDK_SPK_2 273 278 PF00069 0.319
MOD_CDK_SPxxK_3 217 224 PF00069 0.750
MOD_CDK_SPxxK_3 300 307 PF00069 0.481
MOD_CK1_1 185 191 PF00069 0.676
MOD_CK1_1 236 242 PF00069 0.632
MOD_CK1_1 599 605 PF00069 0.476
MOD_CK1_1 687 693 PF00069 0.516
MOD_CK1_1 763 769 PF00069 0.499
MOD_CK1_1 773 779 PF00069 0.541
MOD_CK2_1 285 291 PF00069 0.639
MOD_CK2_1 300 306 PF00069 0.523
MOD_CK2_1 360 366 PF00069 0.479
MOD_CK2_1 438 444 PF00069 0.526
MOD_CK2_1 463 469 PF00069 0.538
MOD_CK2_1 535 541 PF00069 0.448
MOD_Cter_Amidation 315 318 PF01082 0.308
MOD_GlcNHglycan 174 177 PF01048 0.665
MOD_GlcNHglycan 208 211 PF01048 0.781
MOD_GlcNHglycan 287 290 PF01048 0.581
MOD_GlcNHglycan 312 315 PF01048 0.369
MOD_GlcNHglycan 414 418 PF01048 0.467
MOD_GlcNHglycan 453 457 PF01048 0.442
MOD_GlcNHglycan 481 484 PF01048 0.483
MOD_GlcNHglycan 541 545 PF01048 0.504
MOD_GlcNHglycan 599 602 PF01048 0.496
MOD_GlcNHglycan 730 734 PF01048 0.426
MOD_GlcNHglycan 83 86 PF01048 0.810
MOD_GSK3_1 142 149 PF00069 0.644
MOD_GSK3_1 168 175 PF00069 0.700
MOD_GSK3_1 181 188 PF00069 0.533
MOD_GSK3_1 251 258 PF00069 0.511
MOD_GSK3_1 367 374 PF00069 0.616
MOD_GSK3_1 461 468 PF00069 0.445
MOD_GSK3_1 683 690 PF00069 0.475
MOD_GSK3_1 699 706 PF00069 0.307
MOD_GSK3_1 7 14 PF00069 0.763
MOD_GSK3_1 721 728 PF00069 0.569
MOD_GSK3_1 729 736 PF00069 0.406
MOD_GSK3_1 769 776 PF00069 0.520
MOD_N-GLC_1 182 187 PF02516 0.545
MOD_N-GLC_2 121 123 PF02516 0.656
MOD_NEK2_1 371 376 PF00069 0.571
MOD_NEK2_1 386 391 PF00069 0.359
MOD_NEK2_1 479 484 PF00069 0.416
MOD_NEK2_1 590 595 PF00069 0.500
MOD_NEK2_1 684 689 PF00069 0.490
MOD_NEK2_1 719 724 PF00069 0.524
MOD_NEK2_2 652 657 PF00069 0.265
MOD_PIKK_1 142 148 PF00454 0.642
MOD_PIKK_1 16 22 PF00454 0.529
MOD_PIKK_1 182 188 PF00454 0.541
MOD_PIKK_1 196 202 PF00454 0.698
MOD_PIKK_1 547 553 PF00454 0.427
MOD_PIKK_1 746 752 PF00454 0.472
MOD_PIKK_1 97 103 PF00454 0.696
MOD_PK_1 224 230 PF00069 0.666
MOD_PKA_1 317 323 PF00069 0.377
MOD_PKA_2 687 693 PF00069 0.521
MOD_Plk_1 359 365 PF00069 0.416
MOD_Plk_1 413 419 PF00069 0.386
MOD_Plk_1 452 458 PF00069 0.483
MOD_Plk_1 556 562 PF00069 0.361
MOD_Plk_1 729 735 PF00069 0.535
MOD_Plk_2-3 360 366 PF00069 0.443
MOD_Plk_4 233 239 PF00069 0.731
MOD_Plk_4 360 366 PF00069 0.500
MOD_Plk_4 498 504 PF00069 0.343
MOD_Plk_4 556 562 PF00069 0.380
MOD_Plk_4 763 769 PF00069 0.461
MOD_ProDKin_1 185 191 PF00069 0.639
MOD_ProDKin_1 215 221 PF00069 0.752
MOD_ProDKin_1 239 245 PF00069 0.500
MOD_ProDKin_1 273 279 PF00069 0.464
MOD_ProDKin_1 300 306 PF00069 0.469
MOD_ProDKin_1 489 495 PF00069 0.321
MOD_ProDKin_1 74 80 PF00069 0.532
MOD_ProDKin_1 743 749 PF00069 0.520
MOD_SUMO_for_1 264 267 PF00179 0.445
MOD_SUMO_for_1 402 405 PF00179 0.468
MOD_SUMO_for_1 536 539 PF00179 0.497
MOD_SUMO_rev_2 399 404 PF00179 0.474
MOD_SUMO_rev_2 607 616 PF00179 0.384
MOD_SUMO_rev_2 650 655 PF00179 0.451
TRG_DiLeu_BaEn_1 360 365 PF01217 0.432
TRG_DiLeu_BaEn_2 428 434 PF01217 0.422
TRG_DiLeu_BaLyEn_6 456 461 PF01217 0.318
TRG_DiLeu_BaLyEn_6 601 606 PF01217 0.462
TRG_ENDOCYTIC_2 102 105 PF00928 0.690
TRG_ENDOCYTIC_2 122 125 PF00928 0.656
TRG_ENDOCYTIC_2 129 132 PF00928 0.588
TRG_ENDOCYTIC_2 141 144 PF00928 0.540
TRG_ENDOCYTIC_2 271 274 PF00928 0.485
TRG_ENDOCYTIC_2 476 479 PF00928 0.357
TRG_ENDOCYTIC_2 510 513 PF00928 0.329
TRG_ENDOCYTIC_2 516 519 PF00928 0.361
TRG_ENDOCYTIC_2 621 624 PF00928 0.484
TRG_ER_diArg_1 656 659 PF00400 0.449
TRG_NLS_MonoExtC_3 533 539 PF00514 0.496

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P989 Leptomonas seymouri 58% 98%
A0A0S4IM67 Bodo saltans 23% 100%
A0A1X0NUG5 Trypanosomatidae 37% 100%
A0A3S7X5G1 Leishmania donovani 84% 99%
A0A422NI97 Trypanosoma rangeli 37% 100%
A4I7V2 Leishmania infantum 84% 99%
D0AA13 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 37% 100%
E9B2R2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 83% 98%
Q4Q5E5 Leishmania major 84% 99%

Download

Download
LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS