LeishMANIAdb
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WGS CADB00000000 data, contig 40

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

Quick info

Protein:
WGS CADB00000000 data, contig 40
Gene product:
hypothetical protein
Species:
Leishmania mexicana
UniProt:
E8NHI9_LEIMU
TriTrypDb:
LmxM.16.1010partial
Length:
934

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: 125
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: 37
NetGPI no yes: 0, no: 37
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

E8NHI9
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E8NHI9

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 36
GO:0016740 transferase activity 2 36
GO:0016772 transferase activity, transferring phosphorus-containing groups 3 16

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 335 339 PF00656 0.458
CLV_C14_Caspase3-7 616 620 PF00656 0.365
CLV_C14_Caspase3-7 692 696 PF00656 0.435
CLV_MEL_PAP_1 156 162 PF00089 0.632
CLV_NRD_NRD_1 112 114 PF00675 0.681
CLV_NRD_NRD_1 148 150 PF00675 0.699
CLV_NRD_NRD_1 179 181 PF00675 0.613
CLV_NRD_NRD_1 26 28 PF00675 0.587
CLV_NRD_NRD_1 294 296 PF00675 0.697
CLV_NRD_NRD_1 30 32 PF00675 0.539
CLV_NRD_NRD_1 524 526 PF00675 0.685
CLV_NRD_NRD_1 527 529 PF00675 0.645
CLV_NRD_NRD_1 562 564 PF00675 0.610
CLV_NRD_NRD_1 600 602 PF00675 0.713
CLV_NRD_NRD_1 719 721 PF00675 0.526
CLV_NRD_NRD_1 813 815 PF00675 0.716
CLV_PCSK_FUR_1 27 31 PF00082 0.256
CLV_PCSK_FUR_1 525 529 PF00082 0.646
CLV_PCSK_FUR_1 598 602 PF00082 0.670
CLV_PCSK_KEX2_1 148 150 PF00082 0.690
CLV_PCSK_KEX2_1 25 27 PF00082 0.587
CLV_PCSK_KEX2_1 29 31 PF00082 0.551
CLV_PCSK_KEX2_1 294 296 PF00082 0.716
CLV_PCSK_KEX2_1 482 484 PF00082 0.622
CLV_PCSK_KEX2_1 524 526 PF00082 0.685
CLV_PCSK_KEX2_1 527 529 PF00082 0.603
CLV_PCSK_KEX2_1 600 602 PF00082 0.701
CLV_PCSK_KEX2_1 71 73 PF00082 0.683
CLV_PCSK_KEX2_1 719 721 PF00082 0.526
CLV_PCSK_KEX2_1 813 815 PF00082 0.716
CLV_PCSK_PC1ET2_1 29 31 PF00082 0.549
CLV_PCSK_PC1ET2_1 482 484 PF00082 0.607
CLV_PCSK_PC1ET2_1 71 73 PF00082 0.683
CLV_PCSK_PC7_1 22 28 PF00082 0.546
CLV_PCSK_SKI1_1 104 108 PF00082 0.681
CLV_PCSK_SKI1_1 149 153 PF00082 0.654
CLV_PCSK_SKI1_1 273 277 PF00082 0.570
CLV_PCSK_SKI1_1 31 35 PF00082 0.306
CLV_PCSK_SKI1_1 341 345 PF00082 0.678
CLV_PCSK_SKI1_1 395 399 PF00082 0.584
CLV_PCSK_SKI1_1 449 453 PF00082 0.699
CLV_PCSK_SKI1_1 528 532 PF00082 0.666
CLV_PCSK_SKI1_1 566 570 PF00082 0.560
CLV_PCSK_SKI1_1 678 682 PF00082 0.678
CLV_PCSK_SKI1_1 719 723 PF00082 0.651
CLV_PCSK_SKI1_1 775 779 PF00082 0.718
CLV_PCSK_SKI1_1 859 863 PF00082 0.699
DEG_APCC_DBOX_1 30 38 PF00400 0.542
DEG_APCC_DBOX_1 307 315 PF00400 0.445
DEG_Nend_UBRbox_1 1 3 PF02207 0.650
DEG_SPOP_SBC_1 251 255 PF00917 0.483
DEG_SPOP_SBC_1 491 495 PF00917 0.379
DOC_CDC14_PxL_1 265 273 PF14671 0.336
DOC_CKS1_1 150 155 PF01111 0.331
DOC_CKS1_1 685 690 PF01111 0.483
DOC_CYCLIN_RxL_1 716 724 PF00134 0.326
DOC_CYCLIN_yCln2_LP_2 271 277 PF00134 0.330
DOC_CYCLIN_yCln2_LP_2 568 574 PF00134 0.359
DOC_MAPK_DCC_7 137 146 PF00069 0.367
DOC_MAPK_DCC_7 29 39 PF00069 0.269
DOC_MAPK_DCC_7 653 662 PF00069 0.428
DOC_MAPK_gen_1 25 34 PF00069 0.509
DOC_MAPK_gen_1 357 365 PF00069 0.277
DOC_MAPK_gen_1 393 402 PF00069 0.384
DOC_MAPK_gen_1 561 570 PF00069 0.463
DOC_MAPK_gen_1 653 662 PF00069 0.456
DOC_MAPK_HePTP_8 681 693 PF00069 0.482
DOC_MAPK_MEF2A_6 137 146 PF00069 0.386
DOC_MAPK_MEF2A_6 30 39 PF00069 0.280
DOC_MAPK_MEF2A_6 395 404 PF00069 0.384
DOC_MAPK_MEF2A_6 563 572 PF00069 0.463
DOC_MAPK_MEF2A_6 684 693 PF00069 0.482
DOC_MAPK_MEF2A_6 756 763 PF00069 0.518
DOC_PP1_RVXF_1 896 903 PF00149 0.403
DOC_PP2B_LxvP_1 32 35 PF13499 0.297
DOC_PP2B_LxvP_1 568 571 PF13499 0.463
DOC_PP2B_LxvP_1 862 865 PF13499 0.444
DOC_PP4_FxxP_1 6 9 PF00568 0.653
DOC_PP4_FxxP_1 685 688 PF00568 0.437
DOC_USP7_MATH_1 208 212 PF00917 0.515
DOC_USP7_MATH_1 355 359 PF00917 0.414
DOC_USP7_MATH_1 473 477 PF00917 0.297
DOC_USP7_MATH_1 492 496 PF00917 0.428
DOC_USP7_MATH_1 517 521 PF00917 0.520
DOC_USP7_MATH_1 57 61 PF00917 0.452
DOC_USP7_MATH_1 630 634 PF00917 0.430
DOC_USP7_MATH_1 851 855 PF00917 0.487
DOC_USP7_MATH_1 87 91 PF00917 0.493
DOC_USP7_MATH_1 906 910 PF00917 0.506
DOC_USP7_UBL2_3 103 107 PF12436 0.473
DOC_WW_Pin1_4 149 154 PF00397 0.483
DOC_WW_Pin1_4 211 216 PF00397 0.587
DOC_WW_Pin1_4 220 225 PF00397 0.650
DOC_WW_Pin1_4 242 247 PF00397 0.490
DOC_WW_Pin1_4 257 262 PF00397 0.448
DOC_WW_Pin1_4 326 331 PF00397 0.358
DOC_WW_Pin1_4 583 588 PF00397 0.474
DOC_WW_Pin1_4 684 689 PF00397 0.481
DOC_WW_Pin1_4 73 78 PF00397 0.526
DOC_WW_Pin1_4 82 87 PF00397 0.505
LIG_14-3-3_CanoR_1 207 217 PF00244 0.447
LIG_14-3-3_CanoR_1 278 283 PF00244 0.369
LIG_14-3-3_CanoR_1 294 300 PF00244 0.449
LIG_14-3-3_CanoR_1 308 312 PF00244 0.443
LIG_14-3-3_CanoR_1 364 369 PF00244 0.377
LIG_14-3-3_CanoR_1 379 383 PF00244 0.318
LIG_14-3-3_CanoR_1 395 404 PF00244 0.359
LIG_14-3-3_CanoR_1 527 537 PF00244 0.345
LIG_14-3-3_CanoR_1 601 610 PF00244 0.480
LIG_14-3-3_CanoR_1 760 764 PF00244 0.512
LIG_14-3-3_CanoR_1 781 789 PF00244 0.446
LIG_14-3-3_CanoR_1 82 86 PF00244 0.516
LIG_14-3-3_CanoR_1 930 934 PF00244 0.516
LIG_Actin_WH2_2 258 275 PF00022 0.368
LIG_Actin_WH2_2 349 366 PF00022 0.474
LIG_Actin_WH2_2 467 484 PF00022 0.378
LIG_APCC_ABBA_1 200 205 PF00400 0.371
LIG_BIR_III_2 606 610 PF00653 0.443
LIG_BIR_III_2 695 699 PF00653 0.439
LIG_BRCT_BRCA1_1 585 589 PF00533 0.389
LIG_eIF4E_1 469 475 PF01652 0.413
LIG_FHA_1 187 193 PF00498 0.324
LIG_FHA_1 254 260 PF00498 0.457
LIG_FHA_1 302 308 PF00498 0.480
LIG_FHA_1 457 463 PF00498 0.391
LIG_FHA_1 53 59 PF00498 0.474
LIG_FHA_1 609 615 PF00498 0.498
LIG_FHA_1 792 798 PF00498 0.346
LIG_FHA_1 83 89 PF00498 0.536
LIG_FHA_1 866 872 PF00498 0.430
LIG_FHA_1 912 918 PF00498 0.422
LIG_FHA_2 150 156 PF00498 0.399
LIG_FHA_2 279 285 PF00498 0.423
LIG_FHA_2 333 339 PF00498 0.458
LIG_FHA_2 545 551 PF00498 0.308
LIG_FHA_2 643 649 PF00498 0.415
LIG_FHA_2 768 774 PF00498 0.469
LIG_LIR_Apic_2 914 918 PF02991 0.402
LIG_LIR_Apic_2 928 934 PF02991 0.457
LIG_LIR_Gen_1 164 175 PF02991 0.408
LIG_LIR_Gen_1 198 206 PF02991 0.376
LIG_LIR_Gen_1 260 269 PF02991 0.353
LIG_LIR_Gen_1 281 289 PF02991 0.352
LIG_LIR_Gen_1 476 484 PF02991 0.352
LIG_LIR_Gen_1 687 698 PF02991 0.449
LIG_LIR_Gen_1 920 929 PF02991 0.504
LIG_LIR_LC3C_4 885 890 PF02991 0.478
LIG_LIR_Nem_3 164 170 PF02991 0.378
LIG_LIR_Nem_3 198 202 PF02991 0.347
LIG_LIR_Nem_3 260 265 PF02991 0.370
LIG_LIR_Nem_3 281 285 PF02991 0.340
LIG_LIR_Nem_3 417 423 PF02991 0.373
LIG_LIR_Nem_3 476 481 PF02991 0.384
LIG_LIR_Nem_3 539 545 PF02991 0.321
LIG_LIR_Nem_3 567 572 PF02991 0.348
LIG_LIR_Nem_3 586 592 PF02991 0.463
LIG_LIR_Nem_3 687 693 PF02991 0.477
LIG_LIR_Nem_3 872 877 PF02991 0.461
LIG_MAD2 781 789 PF02301 0.477
LIG_MYND_1 138 142 PF01753 0.479
LIG_PCNA_yPIPBox_3 180 192 PF02747 0.313
LIG_PTB_Apo_2 402 409 PF02174 0.359
LIG_PTB_Apo_2 655 662 PF02174 0.404
LIG_PTB_Phospho_1 402 408 PF10480 0.359
LIG_PTB_Phospho_1 655 661 PF10480 0.440
LIG_REV1ctd_RIR_1 542 552 PF16727 0.331
LIG_RPA_C_Fungi 887 899 PF08784 0.492
LIG_SH2_CRK 167 171 PF00017 0.487
LIG_SH2_CRK 179 183 PF00017 0.434
LIG_SH2_CRK 219 223 PF00017 0.534
LIG_SH2_GRB2like 219 222 PF00017 0.530
LIG_SH2_GRB2like 403 406 PF00017 0.551
LIG_SH2_GRB2like 661 664 PF00017 0.522
LIG_SH2_NCK_1 219 223 PF00017 0.532
LIG_SH2_PTP2 199 202 PF00017 0.386
LIG_SH2_SRC 217 220 PF00017 0.697
LIG_SH2_SRC 690 693 PF00017 0.577
LIG_SH2_SRC 736 739 PF00017 0.639
LIG_SH2_STAP1 282 286 PF00017 0.338
LIG_SH2_STAP1 529 533 PF00017 0.495
LIG_SH2_STAP1 549 553 PF00017 0.241
LIG_SH2_STAP1 793 797 PF00017 0.451
LIG_SH2_STAP1 922 926 PF00017 0.353
LIG_SH2_STAT3 793 796 PF00017 0.608
LIG_SH2_STAT5 199 202 PF00017 0.541
LIG_SH2_STAT5 217 220 PF00017 0.640
LIG_SH2_STAT5 408 411 PF00017 0.406
LIG_SH2_STAT5 469 472 PF00017 0.529
LIG_SH2_STAT5 537 540 PF00017 0.393
LIG_SH2_STAT5 592 595 PF00017 0.456
LIG_SH2_STAT5 661 664 PF00017 0.518
LIG_SH2_STAT5 690 693 PF00017 0.578
LIG_SH2_STAT5 793 796 PF00017 0.415
LIG_SH3_1 132 138 PF00018 0.446
LIG_SH3_3 132 138 PF00018 0.597
LIG_SH3_3 147 153 PF00018 0.417
LIG_SH3_3 221 227 PF00018 0.808
LIG_SH3_3 493 499 PF00018 0.446
LIG_SH3_3 64 70 PF00018 0.604
LIG_SH3_3 820 826 PF00018 0.534
LIG_SH3_3 83 89 PF00018 0.696
LIG_SH3_3 90 96 PF00018 0.685
LIG_SH3_3 910 916 PF00018 0.505
LIG_SH3_4 104 111 PF00018 0.564
LIG_SUMO_SIM_anti_2 461 468 PF11976 0.462
LIG_SUMO_SIM_anti_2 885 891 PF11976 0.543
LIG_SUMO_SIM_par_1 324 329 PF11976 0.440
LIG_SUMO_SIM_par_1 54 60 PF11976 0.544
LIG_SUMO_SIM_par_1 867 873 PF11976 0.537
LIG_SUMO_SIM_par_1 885 891 PF11976 0.357
LIG_SxIP_EBH_1 261 273 PF03271 0.372
LIG_SxIP_EBH_1 515 528 PF03271 0.417
LIG_TRAF2_1 735 738 PF00917 0.617
LIG_TYR_ITIM 165 170 PF00017 0.574
LIG_WRC_WIRS_1 166 171 PF05994 0.476
LIG_WW_2 86 89 PF00397 0.570
MOD_CDC14_SPxK_1 223 226 PF00782 0.523
MOD_CDC14_SPxK_1 76 79 PF00782 0.591
MOD_CDK_SPK_2 211 216 PF00069 0.562
MOD_CDK_SPK_2 583 588 PF00069 0.481
MOD_CDK_SPxK_1 220 226 PF00069 0.789
MOD_CDK_SPxK_1 73 79 PF00069 0.601
MOD_CK1_1 125 131 PF00069 0.507
MOD_CK1_1 198 204 PF00069 0.448
MOD_CK1_1 211 217 PF00069 0.560
MOD_CK1_1 220 226 PF00069 0.550
MOD_CK1_1 263 269 PF00069 0.551
MOD_CK1_1 310 316 PF00069 0.438
MOD_CK1_1 358 364 PF00069 0.510
MOD_CK1_1 443 449 PF00069 0.444
MOD_CK1_1 625 631 PF00069 0.455
MOD_CK1_1 798 804 PF00069 0.402
MOD_CK2_1 149 155 PF00069 0.492
MOD_CK2_1 278 284 PF00069 0.512
MOD_CK2_1 544 550 PF00069 0.334
MOD_CK2_1 57 63 PF00069 0.568
MOD_CK2_1 642 648 PF00069 0.506
MOD_CK2_1 732 738 PF00069 0.467
MOD_CK2_1 767 773 PF00069 0.632
MOD_CK2_1 804 810 PF00069 0.612
MOD_Cter_Amidation 27 30 PF01082 0.432
MOD_DYRK1A_RPxSP_1 149 153 PF00069 0.380
MOD_DYRK1A_RPxSP_1 82 86 PF00069 0.591
MOD_GlcNHglycan 210 213 PF01048 0.547
MOD_GlcNHglycan 239 242 PF01048 0.591
MOD_GlcNHglycan 442 445 PF01048 0.558
MOD_GlcNHglycan 486 489 PF01048 0.672
MOD_GlcNHglycan 59 62 PF01048 0.621
MOD_GlcNHglycan 627 630 PF01048 0.442
MOD_GlcNHglycan 669 672 PF01048 0.559
MOD_GlcNHglycan 783 786 PF01048 0.545
MOD_GlcNHglycan 800 803 PF01048 0.550
MOD_GlcNHglycan 853 856 PF01048 0.621
MOD_GlcNHglycan 881 884 PF01048 0.415
MOD_GlcNHglycan 89 92 PF01048 0.624
MOD_GSK3_1 121 128 PF00069 0.608
MOD_GSK3_1 207 214 PF00069 0.614
MOD_GSK3_1 250 257 PF00069 0.641
MOD_GSK3_1 263 270 PF00069 0.433
MOD_GSK3_1 423 430 PF00069 0.454
MOD_GSK3_1 473 480 PF00069 0.391
MOD_GSK3_1 490 497 PF00069 0.436
MOD_GSK3_1 52 59 PF00069 0.627
MOD_GSK3_1 791 798 PF00069 0.428
MOD_LATS_1 362 368 PF00433 0.406
MOD_N-GLC_1 125 130 PF02516 0.519
MOD_N-GLC_1 170 175 PF02516 0.519
MOD_N-GLC_1 195 200 PF02516 0.555
MOD_N-GLC_1 220 225 PF02516 0.532
MOD_N-GLC_1 395 400 PF02516 0.406
MOD_N-GLC_1 484 489 PF02516 0.644
MOD_N-GLC_1 517 522 PF02516 0.384
MOD_N-GLC_2 185 187 PF02516 0.361
MOD_NEK2_1 307 312 PF00069 0.409
MOD_NEK2_1 363 368 PF00069 0.468
MOD_NEK2_1 477 482 PF00069 0.479
MOD_NEK2_1 544 549 PF00069 0.508
MOD_NEK2_1 553 558 PF00069 0.441
MOD_NEK2_1 596 601 PF00069 0.555
MOD_NEK2_1 743 748 PF00069 0.440
MOD_NEK2_1 911 916 PF00069 0.495
MOD_NEK2_2 13 18 PF00069 0.617
MOD_NEK2_2 767 772 PF00069 0.533
MOD_PIKK_1 451 457 PF00454 0.409
MOD_PIKK_1 608 614 PF00454 0.500
MOD_PK_1 295 301 PF00069 0.472
MOD_PK_1 804 810 PF00069 0.703
MOD_PKA_2 301 307 PF00069 0.431
MOD_PKA_2 358 364 PF00069 0.422
MOD_PKA_2 378 384 PF00069 0.390
MOD_PKA_2 52 58 PF00069 0.594
MOD_PKA_2 759 765 PF00069 0.596
MOD_PKA_2 81 87 PF00069 0.599
MOD_PKB_1 393 401 PF00069 0.450
MOD_Plk_1 195 201 PF00069 0.497
MOD_Plk_1 395 401 PF00069 0.450
MOD_Plk_1 430 436 PF00069 0.368
MOD_Plk_1 517 523 PF00069 0.375
MOD_Plk_2-3 301 307 PF00069 0.548
MOD_Plk_2-3 795 801 PF00069 0.627
MOD_Plk_4 13 19 PF00069 0.603
MOD_Plk_4 165 171 PF00069 0.475
MOD_Plk_4 195 201 PF00069 0.477
MOD_Plk_4 267 273 PF00069 0.462
MOD_Plk_4 332 338 PF00069 0.494
MOD_Plk_4 423 429 PF00069 0.454
MOD_Plk_4 473 479 PF00069 0.403
MOD_Plk_4 622 628 PF00069 0.425
MOD_ProDKin_1 149 155 PF00069 0.576
MOD_ProDKin_1 211 217 PF00069 0.722
MOD_ProDKin_1 220 226 PF00069 0.815
MOD_ProDKin_1 242 248 PF00069 0.587
MOD_ProDKin_1 257 263 PF00069 0.525
MOD_ProDKin_1 326 332 PF00069 0.405
MOD_ProDKin_1 583 589 PF00069 0.565
MOD_ProDKin_1 684 690 PF00069 0.578
MOD_ProDKin_1 73 79 PF00069 0.645
MOD_ProDKin_1 82 88 PF00069 0.614
MOD_SUMO_for_1 192 195 PF00179 0.370
MOD_SUMO_for_1 70 73 PF00179 0.573
MOD_SUMO_rev_2 891 900 PF00179 0.684
TRG_DiLeu_BaEn_1 136 141 PF01217 0.579
TRG_DiLeu_BaEn_1 908 913 PF01217 0.505
TRG_DiLeu_BaLyEn_6 28 33 PF01217 0.346
TRG_ENDOCYTIC_2 167 170 PF00928 0.510
TRG_ENDOCYTIC_2 179 182 PF00928 0.437
TRG_ENDOCYTIC_2 199 202 PF00928 0.399
TRG_ENDOCYTIC_2 219 222 PF00928 0.517
TRG_ENDOCYTIC_2 282 285 PF00928 0.433
TRG_ENDOCYTIC_2 574 577 PF00928 0.411
TRG_ENDOCYTIC_2 637 640 PF00928 0.319
TRG_ENDOCYTIC_2 661 664 PF00928 0.522
TRG_ENDOCYTIC_2 690 693 PF00928 0.591
TRG_ENDOCYTIC_2 922 925 PF00928 0.459
TRG_ER_diArg_1 110 113 PF00400 0.581
TRG_ER_diArg_1 117 120 PF00400 0.562
TRG_ER_diArg_1 148 150 PF00400 0.479
TRG_ER_diArg_1 25 27 PF00400 0.670
TRG_ER_diArg_1 30 32 PF00400 0.505
TRG_ER_diArg_1 322 325 PF00400 0.440
TRG_ER_diArg_1 356 359 PF00400 0.285
TRG_ER_diArg_1 392 395 PF00400 0.443
TRG_ER_diArg_1 523 525 PF00400 0.527
TRG_ER_diArg_1 526 528 PF00400 0.461
TRG_ER_diArg_1 558 561 PF00400 0.421
TRG_ER_diArg_1 598 601 PF00400 0.567
TRG_ER_diArg_1 718 720 PF00400 0.367
TRG_ER_diArg_1 836 839 PF00400 0.562
TRG_NLS_MonoExtN_4 26 33 PF00514 0.365
TRG_Pf-PMV_PEXEL_1 719 724 PF00026 0.420

Homologs

Protein Taxonomy Sequence identity Coverage
A0A1X0NYY7 Trypanosomatidae 44% 100%
A0A3Q8IAD3 Leishmania donovani 59% 96%
A0A3Q8IAF8 Leishmania donovani 83% 97%
A0A3Q8IAK8 Leishmania donovani 74% 96%
A0A3Q8IJ32 Leishmania donovani 72% 100%
A0A3S5H6Y1 Leishmania donovani 80% 99%
A0A3S7WTZ8 Leishmania donovani 58% 91%
A0A3S7WU13 Leishmania donovani 72% 99%
A0A422NAR5 Trypanosoma rangeli 45% 100%
A4H8M5 Leishmania braziliensis 71% 100%
A4H8M7 Leishmania braziliensis 68% 100%
A4H8N0 Leishmania braziliensis 48% 100%
A4H8N1 Leishmania braziliensis 50% 100%
A4HWZ5 Leishmania infantum 72% 99%
A4HWZ6 Leishmania infantum 78% 100%
A4HWZ8 Leishmania infantum 77% 100%
A4HX00 Leishmania infantum 58% 91%
A4HX01 Leishmania infantum 59% 100%
A4HX05 Leishmania infantum 85% 97%
E9AGP0 Leishmania infantum 89% 100%
E9AQQ9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 77% 100%
E9AQR0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 87% 100%
E9AQR1 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
E9AQR2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 97% 98%
E9AQR3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 63% 100%
E9AQR4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 59% 95%
Q4QER2 Leishmania major 57% 100%
Q4QER3 Leishmania major 57% 100%
Q4QER4 Leishmania major 87% 100%
Q4QER5 Leishmania major 71% 100%
Q4QER6 Leishmania major 71% 100%
Q4QER7 Leishmania major 79% 100%
Q4QER8 Leishmania major 78% 100%
Q4QER9 Leishmania major 80% 100%
Q4QES0 Leishmania major 71% 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