LeishMANIAdb
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Stealth_CR3 domain-containing protein

Quick info Annotations Function or PPIs Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Stealth_CR3 domain-containing protein
Gene product:
Protein of unknown function (DUF3184), putative
Species:
Leishmania mexicana
UniProt:
E9AQR2_LEIMU
TriTrypDb:
LmxM.16.1020
Length:
950

Annotations

LeishMANIAdb annotations

N-acetylglucosamine-1-phosphotransferase homologous protein. Assumed to be a type II TM protein like its distant relatives.. Signal-anchored glycan biogenesis protein essential for mannose 6-P generation (lysosomal signal for the Metazoan hosts). Family only expended in Leishmaniids.. Localization: Golgi (by homology)

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. yes yes: 120
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: 32
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 36
NetGPI no yes: 0, no: 36
Cellular components
Term Name Level Count
GO:0016020 membrane 2 20
GO:0110165 cellular anatomical entity 1 27
GO:0005794 Golgi apparatus 5 9
GO:0043226 organelle 2 9
GO:0043227 membrane-bounded organelle 3 9
GO:0043229 intracellular organelle 3 9
GO:0043231 intracellular membrane-bounded organelle 4 9

Expansion

Sequence features

E9AQR2
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AQR2

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 35
GO:0016740 transferase activity 2 35
GO:0016772 transferase activity, transferring phosphorus-containing groups 3 16

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 351 355 PF00656 0.467
CLV_C14_Caspase3-7 632 636 PF00656 0.370
CLV_C14_Caspase3-7 708 712 PF00656 0.437
CLV_MEL_PAP_1 172 178 PF00089 0.639
CLV_NRD_NRD_1 128 130 PF00675 0.674
CLV_NRD_NRD_1 164 166 PF00675 0.699
CLV_NRD_NRD_1 195 197 PF00675 0.618
CLV_NRD_NRD_1 310 312 PF00675 0.704
CLV_NRD_NRD_1 42 44 PF00675 0.570
CLV_NRD_NRD_1 46 48 PF00675 0.572
CLV_NRD_NRD_1 540 542 PF00675 0.686
CLV_NRD_NRD_1 543 545 PF00675 0.646
CLV_NRD_NRD_1 578 580 PF00675 0.611
CLV_NRD_NRD_1 616 618 PF00675 0.713
CLV_NRD_NRD_1 735 737 PF00675 0.532
CLV_NRD_NRD_1 829 831 PF00675 0.724
CLV_PCSK_FUR_1 43 47 PF00082 0.465
CLV_PCSK_FUR_1 541 545 PF00082 0.650
CLV_PCSK_FUR_1 614 618 PF00082 0.673
CLV_PCSK_KEX2_1 164 166 PF00082 0.689
CLV_PCSK_KEX2_1 310 312 PF00082 0.723
CLV_PCSK_KEX2_1 41 43 PF00082 0.588
CLV_PCSK_KEX2_1 45 47 PF00082 0.565
CLV_PCSK_KEX2_1 498 500 PF00082 0.617
CLV_PCSK_KEX2_1 540 542 PF00082 0.686
CLV_PCSK_KEX2_1 543 545 PF00082 0.604
CLV_PCSK_KEX2_1 616 618 PF00082 0.705
CLV_PCSK_KEX2_1 735 737 PF00082 0.532
CLV_PCSK_KEX2_1 829 831 PF00082 0.724
CLV_PCSK_KEX2_1 87 89 PF00082 0.731
CLV_PCSK_PC1ET2_1 45 47 PF00082 0.526
CLV_PCSK_PC1ET2_1 498 500 PF00082 0.610
CLV_PCSK_PC1ET2_1 87 89 PF00082 0.683
CLV_PCSK_PC7_1 38 44 PF00082 0.516
CLV_PCSK_SKI1_1 120 124 PF00082 0.678
CLV_PCSK_SKI1_1 165 169 PF00082 0.661
CLV_PCSK_SKI1_1 289 293 PF00082 0.609
CLV_PCSK_SKI1_1 357 361 PF00082 0.678
CLV_PCSK_SKI1_1 411 415 PF00082 0.586
CLV_PCSK_SKI1_1 465 469 PF00082 0.699
CLV_PCSK_SKI1_1 47 51 PF00082 0.303
CLV_PCSK_SKI1_1 544 548 PF00082 0.668
CLV_PCSK_SKI1_1 582 586 PF00082 0.562
CLV_PCSK_SKI1_1 694 698 PF00082 0.681
CLV_PCSK_SKI1_1 735 739 PF00082 0.657
CLV_PCSK_SKI1_1 791 795 PF00082 0.725
CLV_PCSK_SKI1_1 875 879 PF00082 0.697
DEG_APCC_DBOX_1 323 331 PF00400 0.447
DEG_APCC_DBOX_1 46 54 PF00400 0.534
DEG_SPOP_SBC_1 267 271 PF00917 0.493
DEG_SPOP_SBC_1 507 511 PF00917 0.380
DOC_CDC14_PxL_1 281 289 PF14671 0.394
DOC_CKS1_1 166 171 PF01111 0.330
DOC_CKS1_1 701 706 PF01111 0.490
DOC_CYCLIN_RxL_1 732 740 PF00134 0.333
DOC_CYCLIN_yCln2_LP_2 287 293 PF00134 0.378
DOC_CYCLIN_yCln2_LP_2 584 590 PF00134 0.361
DOC_MAPK_DCC_7 153 162 PF00069 0.368
DOC_MAPK_DCC_7 45 55 PF00069 0.462
DOC_MAPK_DCC_7 669 678 PF00069 0.427
DOC_MAPK_gen_1 373 381 PF00069 0.279
DOC_MAPK_gen_1 409 418 PF00069 0.386
DOC_MAPK_gen_1 41 50 PF00069 0.689
DOC_MAPK_gen_1 577 586 PF00069 0.472
DOC_MAPK_gen_1 669 678 PF00069 0.452
DOC_MAPK_HePTP_8 697 709 PF00069 0.488
DOC_MAPK_MEF2A_6 153 162 PF00069 0.388
DOC_MAPK_MEF2A_6 411 420 PF00069 0.386
DOC_MAPK_MEF2A_6 46 55 PF00069 0.472
DOC_MAPK_MEF2A_6 579 588 PF00069 0.472
DOC_MAPK_MEF2A_6 700 709 PF00069 0.488
DOC_MAPK_MEF2A_6 772 779 PF00069 0.527
DOC_PP1_RVXF_1 912 919 PF00149 0.400
DOC_PP2B_LxvP_1 48 51 PF13499 0.271
DOC_PP2B_LxvP_1 584 587 PF13499 0.472
DOC_PP2B_LxvP_1 878 881 PF13499 0.443
DOC_PP4_FxxP_1 701 704 PF00568 0.440
DOC_USP7_MATH_1 103 107 PF00917 0.500
DOC_USP7_MATH_1 224 228 PF00917 0.504
DOC_USP7_MATH_1 371 375 PF00917 0.415
DOC_USP7_MATH_1 489 493 PF00917 0.297
DOC_USP7_MATH_1 508 512 PF00917 0.428
DOC_USP7_MATH_1 533 537 PF00917 0.520
DOC_USP7_MATH_1 73 77 PF00917 0.447
DOC_USP7_MATH_1 867 871 PF00917 0.490
DOC_USP7_MATH_1 922 926 PF00917 0.511
DOC_USP7_UBL2_3 119 123 PF12436 0.475
DOC_USP7_UBL2_3 655 659 PF12436 0.297
DOC_WW_Pin1_4 165 170 PF00397 0.485
DOC_WW_Pin1_4 227 232 PF00397 0.594
DOC_WW_Pin1_4 236 241 PF00397 0.664
DOC_WW_Pin1_4 258 263 PF00397 0.491
DOC_WW_Pin1_4 273 278 PF00397 0.486
DOC_WW_Pin1_4 342 347 PF00397 0.361
DOC_WW_Pin1_4 599 604 PF00397 0.475
DOC_WW_Pin1_4 700 705 PF00397 0.489
DOC_WW_Pin1_4 89 94 PF00397 0.523
DOC_WW_Pin1_4 98 103 PF00397 0.514
LIG_14-3-3_CanoR_1 223 233 PF00244 0.448
LIG_14-3-3_CanoR_1 294 299 PF00244 0.376
LIG_14-3-3_CanoR_1 310 316 PF00244 0.496
LIG_14-3-3_CanoR_1 324 328 PF00244 0.424
LIG_14-3-3_CanoR_1 380 385 PF00244 0.379
LIG_14-3-3_CanoR_1 395 403 PF00244 0.320
LIG_14-3-3_CanoR_1 411 420 PF00244 0.361
LIG_14-3-3_CanoR_1 543 553 PF00244 0.347
LIG_14-3-3_CanoR_1 617 626 PF00244 0.484
LIG_14-3-3_CanoR_1 776 780 PF00244 0.520
LIG_14-3-3_CanoR_1 797 805 PF00244 0.458
LIG_14-3-3_CanoR_1 946 950 PF00244 0.517
LIG_14-3-3_CanoR_1 98 102 PF00244 0.500
LIG_Actin_WH2_2 274 291 PF00022 0.419
LIG_Actin_WH2_2 365 382 PF00022 0.474
LIG_Actin_WH2_2 483 500 PF00022 0.379
LIG_Actin_WH2_2 627 645 PF00022 0.329
LIG_APCC_ABBA_1 216 221 PF00400 0.375
LIG_BIR_III_2 622 626 PF00653 0.442
LIG_BIR_III_2 711 715 PF00653 0.438
LIG_BRCT_BRCA1_1 601 605 PF00533 0.390
LIG_eIF4E_1 485 491 PF01652 0.414
LIG_FHA_1 16 22 PF00498 0.684
LIG_FHA_1 203 209 PF00498 0.344
LIG_FHA_1 270 276 PF00498 0.472
LIG_FHA_1 318 324 PF00498 0.481
LIG_FHA_1 473 479 PF00498 0.388
LIG_FHA_1 625 631 PF00498 0.503
LIG_FHA_1 69 75 PF00498 0.473
LIG_FHA_1 808 814 PF00498 0.348
LIG_FHA_1 882 888 PF00498 0.430
LIG_FHA_1 928 934 PF00498 0.418
LIG_FHA_1 99 105 PF00498 0.544
LIG_FHA_2 166 172 PF00498 0.401
LIG_FHA_2 295 301 PF00498 0.428
LIG_FHA_2 349 355 PF00498 0.467
LIG_FHA_2 561 567 PF00498 0.308
LIG_FHA_2 784 790 PF00498 0.473
LIG_LIR_Apic_2 930 934 PF02991 0.400
LIG_LIR_Apic_2 944 950 PF02991 0.456
LIG_LIR_Gen_1 180 191 PF02991 0.410
LIG_LIR_Gen_1 214 222 PF02991 0.379
LIG_LIR_Gen_1 276 285 PF02991 0.403
LIG_LIR_Gen_1 297 305 PF02991 0.351
LIG_LIR_Gen_1 492 500 PF02991 0.355
LIG_LIR_Gen_1 703 714 PF02991 0.450
LIG_LIR_Gen_1 936 945 PF02991 0.509
LIG_LIR_LC3C_4 901 906 PF02991 0.484
LIG_LIR_Nem_3 180 186 PF02991 0.381
LIG_LIR_Nem_3 214 218 PF02991 0.355
LIG_LIR_Nem_3 276 281 PF02991 0.418
LIG_LIR_Nem_3 297 301 PF02991 0.336
LIG_LIR_Nem_3 433 439 PF02991 0.377
LIG_LIR_Nem_3 492 497 PF02991 0.388
LIG_LIR_Nem_3 555 561 PF02991 0.322
LIG_LIR_Nem_3 583 588 PF02991 0.350
LIG_LIR_Nem_3 602 608 PF02991 0.464
LIG_LIR_Nem_3 703 709 PF02991 0.483
LIG_LIR_Nem_3 888 893 PF02991 0.459
LIG_MAD2 797 805 PF02301 0.493
LIG_MYND_1 154 158 PF01753 0.484
LIG_PCNA_yPIPBox_3 196 208 PF02747 0.343
LIG_PTB_Apo_2 418 425 PF02174 0.361
LIG_PTB_Apo_2 671 678 PF02174 0.402
LIG_PTB_Phospho_1 418 424 PF10480 0.361
LIG_PTB_Phospho_1 671 677 PF10480 0.442
LIG_REV1ctd_RIR_1 558 568 PF16727 0.333
LIG_RPA_C_Fungi 903 915 PF08784 0.487
LIG_SH2_CRK 183 187 PF00017 0.490
LIG_SH2_CRK 195 199 PF00017 0.492
LIG_SH2_CRK 235 239 PF00017 0.544
LIG_SH2_GRB2like 235 238 PF00017 0.544
LIG_SH2_GRB2like 419 422 PF00017 0.564
LIG_SH2_GRB2like 677 680 PF00017 0.528
LIG_SH2_NCK_1 235 239 PF00017 0.543
LIG_SH2_PTP2 215 218 PF00017 0.396
LIG_SH2_SRC 233 236 PF00017 0.733
LIG_SH2_SRC 706 709 PF00017 0.583
LIG_SH2_SRC 752 755 PF00017 0.642
LIG_SH2_STAP1 298 302 PF00017 0.345
LIG_SH2_STAP1 545 549 PF00017 0.498
LIG_SH2_STAP1 565 569 PF00017 0.241
LIG_SH2_STAP1 809 813 PF00017 0.455
LIG_SH2_STAT3 665 668 PF00017 0.308
LIG_SH2_STAT3 809 812 PF00017 0.617
LIG_SH2_STAT5 215 218 PF00017 0.554
LIG_SH2_STAT5 233 236 PF00017 0.674
LIG_SH2_STAT5 424 427 PF00017 0.409
LIG_SH2_STAT5 485 488 PF00017 0.529
LIG_SH2_STAT5 553 556 PF00017 0.397
LIG_SH2_STAT5 608 611 PF00017 0.458
LIG_SH2_STAT5 665 668 PF00017 0.414
LIG_SH2_STAT5 677 680 PF00017 0.523
LIG_SH2_STAT5 706 709 PF00017 0.578
LIG_SH2_STAT5 809 812 PF00017 0.417
LIG_SH3_1 148 154 PF00018 0.443
LIG_SH3_3 106 112 PF00018 0.666
LIG_SH3_3 148 154 PF00018 0.623
LIG_SH3_3 163 169 PF00018 0.396
LIG_SH3_3 237 243 PF00018 0.813
LIG_SH3_3 509 515 PF00018 0.452
LIG_SH3_3 80 86 PF00018 0.610
LIG_SH3_3 836 842 PF00018 0.536
LIG_SH3_3 926 932 PF00018 0.500
LIG_SH3_3 99 105 PF00018 0.656
LIG_SH3_4 120 127 PF00018 0.569
LIG_SUMO_SIM_anti_2 477 484 PF11976 0.467
LIG_SUMO_SIM_anti_2 901 907 PF11976 0.543
LIG_SUMO_SIM_par_1 340 345 PF11976 0.444
LIG_SUMO_SIM_par_1 70 76 PF11976 0.554
LIG_SUMO_SIM_par_1 883 889 PF11976 0.538
LIG_SUMO_SIM_par_1 901 907 PF11976 0.356
LIG_SxIP_EBH_1 277 289 PF03271 0.446
LIG_SxIP_EBH_1 531 544 PF03271 0.417
LIG_TRAF2_1 751 754 PF00917 0.620
LIG_TYR_ITIM 181 186 PF00017 0.587
LIG_WRC_WIRS_1 182 187 PF05994 0.478
LIG_WW_2 102 105 PF00397 0.575
MOD_CDC14_SPxK_1 239 242 PF00782 0.548
MOD_CDC14_SPxK_1 92 95 PF00782 0.575
MOD_CDK_SPK_2 227 232 PF00069 0.569
MOD_CDK_SPK_2 599 604 PF00069 0.484
MOD_CDK_SPxK_1 236 242 PF00069 0.807
MOD_CDK_SPxK_1 89 95 PF00069 0.586
MOD_CK1_1 141 147 PF00069 0.503
MOD_CK1_1 214 220 PF00069 0.459
MOD_CK1_1 227 233 PF00069 0.562
MOD_CK1_1 236 242 PF00069 0.560
MOD_CK1_1 279 285 PF00069 0.627
MOD_CK1_1 326 332 PF00069 0.466
MOD_CK1_1 374 380 PF00069 0.513
MOD_CK1_1 459 465 PF00069 0.462
MOD_CK1_1 7 13 PF00069 0.643
MOD_CK1_1 814 820 PF00069 0.405
MOD_CK2_1 165 171 PF00069 0.496
MOD_CK2_1 294 300 PF00069 0.523
MOD_CK2_1 560 566 PF00069 0.335
MOD_CK2_1 73 79 PF00069 0.561
MOD_CK2_1 748 754 PF00069 0.471
MOD_CK2_1 783 789 PF00069 0.639
MOD_CK2_1 820 826 PF00069 0.614
MOD_Cter_Amidation 43 46 PF01082 0.699
MOD_DYRK1A_RPxSP_1 165 169 PF00069 0.382
MOD_DYRK1A_RPxSP_1 98 102 PF00069 0.595
MOD_GlcNHglycan 105 108 PF01048 0.659
MOD_GlcNHglycan 226 229 PF01048 0.592
MOD_GlcNHglycan 255 258 PF01048 0.600
MOD_GlcNHglycan 458 461 PF01048 0.574
MOD_GlcNHglycan 502 505 PF01048 0.676
MOD_GlcNHglycan 685 688 PF01048 0.564
MOD_GlcNHglycan 75 78 PF01048 0.811
MOD_GlcNHglycan 799 802 PF01048 0.566
MOD_GlcNHglycan 816 819 PF01048 0.553
MOD_GlcNHglycan 869 872 PF01048 0.622
MOD_GlcNHglycan 897 900 PF01048 0.418
MOD_GSK3_1 137 144 PF00069 0.560
MOD_GSK3_1 15 22 PF00069 0.582
MOD_GSK3_1 223 230 PF00069 0.614
MOD_GSK3_1 266 273 PF00069 0.655
MOD_GSK3_1 279 286 PF00069 0.509
MOD_GSK3_1 439 446 PF00069 0.456
MOD_GSK3_1 489 496 PF00069 0.392
MOD_GSK3_1 506 513 PF00069 0.430
MOD_GSK3_1 68 75 PF00069 0.565
MOD_GSK3_1 807 814 PF00069 0.433
MOD_LATS_1 378 384 PF00433 0.409
MOD_N-GLC_1 141 146 PF02516 0.516
MOD_N-GLC_1 186 191 PF02516 0.524
MOD_N-GLC_1 211 216 PF02516 0.571
MOD_N-GLC_1 236 241 PF02516 0.548
MOD_N-GLC_1 411 416 PF02516 0.409
MOD_N-GLC_1 500 505 PF02516 0.646
MOD_N-GLC_1 533 538 PF02516 0.384
MOD_N-GLC_2 201 203 PF02516 0.388
MOD_NEK2_1 323 328 PF00069 0.389
MOD_NEK2_1 379 384 PF00069 0.478
MOD_NEK2_1 493 498 PF00069 0.483
MOD_NEK2_1 560 565 PF00069 0.510
MOD_NEK2_1 569 574 PF00069 0.445
MOD_NEK2_1 612 617 PF00069 0.555
MOD_NEK2_1 759 764 PF00069 0.441
MOD_NEK2_1 927 932 PF00069 0.485
MOD_NEK2_2 29 34 PF00069 0.594
MOD_NEK2_2 783 788 PF00069 0.541
MOD_PIKK_1 467 473 PF00454 0.411
MOD_PIKK_1 624 630 PF00454 0.504
MOD_PIKK_1 646 652 PF00454 0.330
MOD_PK_1 311 317 PF00069 0.479
MOD_PK_1 820 826 PF00069 0.702
MOD_PKA_2 317 323 PF00069 0.430
MOD_PKA_2 374 380 PF00069 0.426
MOD_PKA_2 394 400 PF00069 0.393
MOD_PKA_2 68 74 PF00069 0.534
MOD_PKA_2 7 13 PF00069 0.767
MOD_PKA_2 775 781 PF00069 0.599
MOD_PKA_2 97 103 PF00069 0.592
MOD_PKB_1 409 417 PF00069 0.462
MOD_Plk_1 211 217 PF00069 0.516
MOD_Plk_1 411 417 PF00069 0.462
MOD_Plk_1 446 452 PF00069 0.366
MOD_Plk_1 533 539 PF00069 0.377
MOD_Plk_2-3 17 23 PF00069 0.551
MOD_Plk_2-3 317 323 PF00069 0.564
MOD_Plk_2-3 811 817 PF00069 0.629
MOD_Plk_4 181 187 PF00069 0.473
MOD_Plk_4 211 217 PF00069 0.496
MOD_Plk_4 283 289 PF00069 0.539
MOD_Plk_4 29 35 PF00069 0.592
MOD_Plk_4 348 354 PF00069 0.497
MOD_Plk_4 439 445 PF00069 0.456
MOD_Plk_4 489 495 PF00069 0.408
MOD_ProDKin_1 165 171 PF00069 0.578
MOD_ProDKin_1 227 233 PF00069 0.739
MOD_ProDKin_1 236 242 PF00069 0.833
MOD_ProDKin_1 258 264 PF00069 0.588
MOD_ProDKin_1 273 279 PF00069 0.579
MOD_ProDKin_1 342 348 PF00069 0.409
MOD_ProDKin_1 599 605 PF00069 0.566
MOD_ProDKin_1 700 706 PF00069 0.588
MOD_ProDKin_1 89 95 PF00069 0.641
MOD_ProDKin_1 98 104 PF00069 0.624
MOD_SUMO_for_1 208 211 PF00179 0.384
MOD_SUMO_for_1 86 89 PF00179 0.576
MOD_SUMO_rev_2 907 916 PF00179 0.676
TRG_DiLeu_BaEn_1 152 157 PF01217 0.586
TRG_DiLeu_BaEn_1 924 929 PF01217 0.501
TRG_DiLeu_BaLyEn_6 44 49 PF01217 0.668
TRG_ENDOCYTIC_2 183 186 PF00928 0.513
TRG_ENDOCYTIC_2 195 198 PF00928 0.628
TRG_ENDOCYTIC_2 215 218 PF00928 0.379
TRG_ENDOCYTIC_2 235 238 PF00928 0.531
TRG_ENDOCYTIC_2 298 301 PF00928 0.432
TRG_ENDOCYTIC_2 590 593 PF00928 0.414
TRG_ENDOCYTIC_2 677 680 PF00928 0.528
TRG_ENDOCYTIC_2 706 709 PF00928 0.599
TRG_ENDOCYTIC_2 938 941 PF00928 0.459
TRG_ER_diArg_1 126 129 PF00400 0.571
TRG_ER_diArg_1 133 136 PF00400 0.551
TRG_ER_diArg_1 164 166 PF00400 0.474
TRG_ER_diArg_1 338 341 PF00400 0.444
TRG_ER_diArg_1 372 375 PF00400 0.287
TRG_ER_diArg_1 408 411 PF00400 0.444
TRG_ER_diArg_1 41 43 PF00400 0.654
TRG_ER_diArg_1 46 48 PF00400 0.659
TRG_ER_diArg_1 539 541 PF00400 0.533
TRG_ER_diArg_1 542 544 PF00400 0.460
TRG_ER_diArg_1 574 577 PF00400 0.424
TRG_ER_diArg_1 614 617 PF00400 0.571
TRG_ER_diArg_1 734 736 PF00400 0.380
TRG_ER_diArg_1 852 855 PF00400 0.572
TRG_NLS_MonoExtN_4 42 49 PF00514 0.597
TRG_Pf-PMV_PEXEL_1 735 740 PF00026 0.428

Homologs

Protein Taxonomy Sequence identity Coverage
A0A1X0NYY7 Trypanosomatidae 44% 100%
A0A3Q8IAD3 Leishmania donovani 58% 97%
A0A3Q8IAF8 Leishmania donovani 82% 99%
A0A3Q8IAK8 Leishmania donovani 73% 98%
A0A3Q8IJ32 Leishmania donovani 72% 100%
A0A3S5H6Y1 Leishmania donovani 79% 100%
A0A3S7WTZ8 Leishmania donovani 58% 92%
A0A3S7WU13 Leishmania donovani 72% 100%
A0A422NAR5 Trypanosoma rangeli 45% 100%
A4H8M5 Leishmania braziliensis 71% 100%
A4H8M7 Leishmania braziliensis 67% 100%
A4H8N0 Leishmania braziliensis 47% 100%
A4H8N1 Leishmania braziliensis 50% 100%
A4HWZ5 Leishmania infantum 72% 100%
A4HWZ6 Leishmania infantum 76% 100%
A4HWZ8 Leishmania infantum 75% 100%
A4HX00 Leishmania infantum 58% 92%
A4HX01 Leishmania infantum 58% 100%
A4HX05 Leishmania infantum 83% 99%
E8NHI9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 97% 100%
E9AQQ9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 76% 100%
E9AQR0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 86% 100%
E9AQR1 Leishmania mexicana (strain MHOM/GT/2001/U1103) 72% 100%
E9AQR3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 63% 100%
E9AQR4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 58% 97%
Q4QER2 Leishmania major 56% 100%
Q4QER3 Leishmania major 57% 100%
Q4QER4 Leishmania major 85% 100%
Q4QER5 Leishmania major 70% 100%
Q4QER6 Leishmania major 70% 100%
Q4QER7 Leishmania major 77% 100%
Q4QER8 Leishmania major 76% 100%
Q4QER9 Leishmania major 78% 100%
Q4QES0 Leishmania major 70% 100%
V5ANJ8 Trypanosoma cruzi 46% 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