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:
E9AQR3_LEIMU
TriTrypDb:
LmxM.16.1050
Length:
1018

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: 34
NetGPI no yes: 0, no: 34
Cellular components
Term Name Level Count
GO:0016020 membrane 2 19
GO:0110165 cellular anatomical entity 1 26
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

E9AQR3
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AQR3

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 33
GO:0016740 transferase activity 2 33
GO:0016772 transferase activity, transferring phosphorus-containing groups 3 14

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 338 342 PF00656 0.472
CLV_C14_Caspase3-7 776 780 PF00656 0.393
CLV_NRD_NRD_1 133 135 PF00675 0.662
CLV_NRD_NRD_1 222 224 PF00675 0.624
CLV_NRD_NRD_1 280 282 PF00675 0.568
CLV_NRD_NRD_1 30 32 PF00675 0.453
CLV_NRD_NRD_1 482 484 PF00675 0.597
CLV_NRD_NRD_1 516 518 PF00675 0.667
CLV_NRD_NRD_1 618 620 PF00675 0.546
CLV_NRD_NRD_1 732 734 PF00675 0.551
CLV_NRD_NRD_1 803 805 PF00675 0.542
CLV_NRD_NRD_1 87 89 PF00675 0.718
CLV_NRD_NRD_1 897 899 PF00675 0.730
CLV_PCSK_FUR_1 616 620 PF00082 0.477
CLV_PCSK_FUR_1 85 89 PF00082 0.680
CLV_PCSK_KEX2_1 10 12 PF00082 0.497
CLV_PCSK_KEX2_1 132 134 PF00082 0.655
CLV_PCSK_KEX2_1 282 284 PF00082 0.544
CLV_PCSK_KEX2_1 30 32 PF00082 0.466
CLV_PCSK_KEX2_1 482 484 PF00082 0.665
CLV_PCSK_KEX2_1 486 488 PF00082 0.700
CLV_PCSK_KEX2_1 515 517 PF00082 0.663
CLV_PCSK_KEX2_1 618 620 PF00082 0.504
CLV_PCSK_KEX2_1 732 734 PF00082 0.582
CLV_PCSK_KEX2_1 803 805 PF00082 0.542
CLV_PCSK_KEX2_1 87 89 PF00082 0.735
CLV_PCSK_KEX2_1 897 899 PF00082 0.730
CLV_PCSK_PC1ET2_1 10 12 PF00082 0.432
CLV_PCSK_PC1ET2_1 132 134 PF00082 0.655
CLV_PCSK_PC1ET2_1 282 284 PF00082 0.518
CLV_PCSK_PC1ET2_1 486 488 PF00082 0.696
CLV_PCSK_PC7_1 129 135 PF00082 0.624
CLV_PCSK_PC7_1 482 488 PF00082 0.601
CLV_PCSK_SKI1_1 129 133 PF00082 0.629
CLV_PCSK_SKI1_1 344 348 PF00082 0.662
CLV_PCSK_SKI1_1 398 402 PF00082 0.567
CLV_PCSK_SKI1_1 475 479 PF00082 0.561
CLV_PCSK_SKI1_1 482 486 PF00082 0.590
CLV_PCSK_SKI1_1 540 544 PF00082 0.556
CLV_PCSK_SKI1_1 621 625 PF00082 0.592
CLV_PCSK_SKI1_1 663 667 PF00082 0.588
CLV_PCSK_SKI1_1 7 11 PF00082 0.436
CLV_PCSK_SKI1_1 762 766 PF00082 0.729
CLV_PCSK_SKI1_1 803 807 PF00082 0.534
CLV_PCSK_SKI1_1 859 863 PF00082 0.725
CLV_PCSK_SKI1_1 943 947 PF00082 0.672
DEG_APCC_DBOX_1 310 318 PF00400 0.477
DEG_SPOP_SBC_1 552 556 PF00917 0.372
DOC_CKS1_1 510 515 PF01111 0.405
DOC_CKS1_1 565 570 PF01111 0.421
DOC_CKS1_1 769 774 PF01111 0.502
DOC_CYCLIN_RxL_1 469 480 PF00134 0.349
DOC_CYCLIN_RxL_1 800 808 PF00134 0.342
DOC_CYCLIN_yCln2_LP_2 562 568 PF00134 0.407
DOC_CYCLIN_yCln2_LP_2 623 629 PF00134 0.367
DOC_MAPK_gen_1 223 234 PF00069 0.317
DOC_MAPK_gen_1 281 290 PF00069 0.345
DOC_MAPK_gen_1 360 368 PF00069 0.285
DOC_MAPK_gen_1 396 405 PF00069 0.367
DOC_MAPK_gen_1 616 625 PF00069 0.477
DOC_MAPK_gen_1 669 677 PF00069 0.392
DOC_MAPK_HePTP_8 765 777 PF00069 0.498
DOC_MAPK_MEF2A_6 15 22 PF00069 0.612
DOC_MAPK_MEF2A_6 398 407 PF00069 0.367
DOC_MAPK_MEF2A_6 618 627 PF00069 0.477
DOC_MAPK_MEF2A_6 691 700 PF00069 0.355
DOC_MAPK_MEF2A_6 768 777 PF00069 0.499
DOC_MAPK_MEF2A_6 840 847 PF00069 0.530
DOC_PP1_RVXF_1 980 987 PF00149 0.407
DOC_PP1_RVXF_1 99 106 PF00149 0.402
DOC_PP2B_LxvP_1 623 626 PF13499 0.477
DOC_PP2B_LxvP_1 946 949 PF13499 0.491
DOC_PP4_FxxP_1 769 772 PF00568 0.525
DOC_USP7_MATH_1 16 20 PF00917 0.607
DOC_USP7_MATH_1 358 362 PF00917 0.477
DOC_USP7_MATH_1 552 556 PF00917 0.372
DOC_USP7_MATH_1 935 939 PF00917 0.511
DOC_USP7_MATH_1 990 994 PF00917 0.500
DOC_USP7_UBL2_3 577 581 PF12436 0.367
DOC_USP7_UBL2_3 6 10 PF12436 0.636
DOC_USP7_UBL2_3 687 691 PF12436 0.341
DOC_WW_Pin1_4 192 197 PF00397 0.494
DOC_WW_Pin1_4 250 255 PF00397 0.538
DOC_WW_Pin1_4 329 334 PF00397 0.367
DOC_WW_Pin1_4 509 514 PF00397 0.410
DOC_WW_Pin1_4 561 566 PF00397 0.429
DOC_WW_Pin1_4 638 643 PF00397 0.473
DOC_WW_Pin1_4 768 773 PF00397 0.499
DOC_WW_Pin1_4 79 84 PF00397 0.505
LIG_14-3-3_CanoR_1 1014 1018 PF00244 0.495
LIG_14-3-3_CanoR_1 11 18 PF00244 0.643
LIG_14-3-3_CanoR_1 186 191 PF00244 0.457
LIG_14-3-3_CanoR_1 227 235 PF00244 0.392
LIG_14-3-3_CanoR_1 274 280 PF00244 0.332
LIG_14-3-3_CanoR_1 311 315 PF00244 0.429
LIG_14-3-3_CanoR_1 367 372 PF00244 0.443
LIG_14-3-3_CanoR_1 382 386 PF00244 0.293
LIG_14-3-3_CanoR_1 398 407 PF00244 0.367
LIG_14-3-3_CanoR_1 497 503 PF00244 0.416
LIG_14-3-3_CanoR_1 598 603 PF00244 0.395
LIG_14-3-3_CanoR_1 844 848 PF00244 0.520
LIG_14-3-3_CanoR_1 865 873 PF00244 0.415
LIG_Actin_WH2_2 352 369 PF00022 0.477
LIG_AP2alpha_1 604 608 PF02296 0.282
LIG_APCC_ABBA_1 696 701 PF00400 0.340
LIG_BIR_III_2 779 783 PF00653 0.438
LIG_BRCT_BRCA1_1 101 105 PF00533 0.424
LIG_BRCT_BRCA1_1 600 604 PF00533 0.282
LIG_BRCT_BRCA1_1 640 644 PF00533 0.386
LIG_deltaCOP1_diTrp_1 679 685 PF00928 0.328
LIG_eIF4E_1 472 478 PF01652 0.414
LIG_FHA_1 138 144 PF00498 0.494
LIG_FHA_1 179 185 PF00498 0.417
LIG_FHA_1 295 301 PF00498 0.535
LIG_FHA_1 305 311 PF00498 0.468
LIG_FHA_1 66 72 PF00498 0.467
LIG_FHA_1 670 676 PF00498 0.441
LIG_FHA_1 693 699 PF00498 0.479
LIG_FHA_1 723 729 PF00498 0.367
LIG_FHA_1 876 882 PF00498 0.352
LIG_FHA_1 90 96 PF00498 0.450
LIG_FHA_1 950 956 PF00498 0.397
LIG_FHA_1 996 1002 PF00498 0.414
LIG_FHA_2 336 342 PF00498 0.472
LIG_FHA_2 852 858 PF00498 0.443
LIG_Integrin_RGD_1 443 445 PF01839 0.566
LIG_LIR_Apic_2 1012 1018 PF02991 0.436
LIG_LIR_Apic_2 710 715 PF02991 0.362
LIG_LIR_Apic_2 998 1002 PF02991 0.395
LIG_LIR_Gen_1 1004 1013 PF02991 0.509
LIG_LIR_Gen_1 171 179 PF02991 0.453
LIG_LIR_Gen_1 201 210 PF02991 0.381
LIG_LIR_Gen_1 606 613 PF02991 0.319
LIG_LIR_Gen_1 679 690 PF02991 0.320
LIG_LIR_Gen_1 771 782 PF02991 0.457
LIG_LIR_LC3C_4 969 974 PF02991 0.491
LIG_LIR_Nem_3 171 176 PF02991 0.454
LIG_LIR_Nem_3 198 203 PF02991 0.415
LIG_LIR_Nem_3 207 213 PF02991 0.379
LIG_LIR_Nem_3 261 265 PF02991 0.407
LIG_LIR_Nem_3 420 426 PF02991 0.382
LIG_LIR_Nem_3 457 463 PF02991 0.306
LIG_LIR_Nem_3 479 484 PF02991 0.433
LIG_LIR_Nem_3 606 611 PF02991 0.390
LIG_LIR_Nem_3 622 627 PF02991 0.420
LIG_LIR_Nem_3 641 647 PF02991 0.443
LIG_LIR_Nem_3 679 685 PF02991 0.328
LIG_LIR_Nem_3 742 748 PF02991 0.313
LIG_LIR_Nem_3 771 777 PF02991 0.494
LIG_LIR_Nem_3 956 961 PF02991 0.419
LIG_MAD2 865 873 PF02301 0.474
LIG_NRBOX 55 61 PF00104 0.348
LIG_PCNA_yPIPBox_3 281 291 PF02747 0.385
LIG_Pex14_1 498 502 PF04695 0.370
LIG_Pex14_1 600 604 PF04695 0.282
LIG_Pex14_2 604 608 PF04695 0.282
LIG_PTB_Apo_2 405 412 PF02174 0.367
LIG_PTB_Phospho_1 405 411 PF10480 0.367
LIG_RPA_C_Fungi 971 983 PF08784 0.533
LIG_SH2_CRK 173 177 PF00017 0.511
LIG_SH2_CRK 210 214 PF00017 0.487
LIG_SH2_CRK 276 280 PF00017 0.420
LIG_SH2_CRK 712 716 PF00017 0.430
LIG_SH2_GRB2like 406 409 PF00017 0.570
LIG_SH2_GRB2like 745 748 PF00017 0.550
LIG_SH2_PTP2 17 20 PF00017 0.465
LIG_SH2_SRC 774 777 PF00017 0.597
LIG_SH2_SRC 820 823 PF00017 0.621
LIG_SH2_STAP1 1006 1010 PF00017 0.349
LIG_SH2_STAP1 584 588 PF00017 0.570
LIG_SH2_STAP1 877 881 PF00017 0.461
LIG_SH2_STAT3 222 225 PF00017 0.412
LIG_SH2_STAT3 877 880 PF00017 0.624
LIG_SH2_STAT5 141 144 PF00017 0.551
LIG_SH2_STAT5 17 20 PF00017 0.485
LIG_SH2_STAT5 21 24 PF00017 0.453
LIG_SH2_STAT5 241 244 PF00017 0.524
LIG_SH2_STAT5 411 414 PF00017 0.415
LIG_SH2_STAT5 472 475 PF00017 0.573
LIG_SH2_STAT5 541 544 PF00017 0.380
LIG_SH2_STAT5 592 595 PF00017 0.402
LIG_SH2_STAT5 647 650 PF00017 0.473
LIG_SH2_STAT5 692 695 PF00017 0.365
LIG_SH2_STAT5 745 748 PF00017 0.545
LIG_SH2_STAT5 774 777 PF00017 0.612
LIG_SH2_STAT5 877 880 PF00017 0.424
LIG_SH3_3 173 179 PF00018 0.691
LIG_SH3_3 190 196 PF00018 0.410
LIG_SH3_3 562 568 PF00018 0.519
LIG_SH3_3 904 910 PF00018 0.545
LIG_SH3_3 994 1000 PF00018 0.471
LIG_SH3_CIN85_PxpxPR_1 255 260 PF14604 0.587
LIG_SUMO_SIM_anti_2 204 211 PF11976 0.343
LIG_SUMO_SIM_anti_2 969 975 PF11976 0.589
LIG_SUMO_SIM_par_1 233 238 PF11976 0.422
LIG_SUMO_SIM_par_1 327 332 PF11976 0.570
LIG_SUMO_SIM_par_1 647 653 PF11976 0.354
LIG_SUMO_SIM_par_1 73 79 PF11976 0.583
LIG_SUMO_SIM_par_1 951 957 PF11976 0.459
LIG_SUMO_SIM_par_1 969 975 PF11976 0.455
LIG_TRAF2_1 819 822 PF00917 0.625
LIG_TYR_ITIM 208 213 PF00017 0.582
LIG_UBA3_1 234 239 PF00899 0.401
LIG_UBA3_1 499 506 PF00899 0.457
LIG_WRC_WIRS_1 209 214 PF05994 0.475
LIG_WRC_WIRS_1 499 504 PF05994 0.423
MOD_CDC14_SPxK_1 82 85 PF00782 0.562
MOD_CDK_SPK_2 638 643 PF00069 0.443
MOD_CDK_SPxK_1 509 515 PF00069 0.463
MOD_CDK_SPxK_1 79 85 PF00069 0.569
MOD_CDK_SPxxK_3 509 516 PF00069 0.470
MOD_CK1_1 248 254 PF00069 0.606
MOD_CK1_1 294 300 PF00069 0.541
MOD_CK1_1 313 319 PF00069 0.502
MOD_CK1_1 361 367 PF00069 0.570
MOD_CK1_1 564 570 PF00069 0.498
MOD_CK1_1 79 85 PF00069 0.586
MOD_CK1_1 882 888 PF00069 0.410
MOD_CK1_1 99 105 PF00069 0.559
MOD_CK2_1 192 198 PF00069 0.520
MOD_CK2_1 250 256 PF00069 0.649
MOD_CK2_1 434 440 PF00069 0.472
MOD_CK2_1 446 452 PF00069 0.516
MOD_CK2_1 553 559 PF00069 0.433
MOD_CK2_1 750 756 PF00069 0.596
MOD_CK2_1 816 822 PF00069 0.526
MOD_CK2_1 851 857 PF00069 0.582
MOD_CK2_1 888 894 PF00069 0.531
MOD_Cter_Amidation 28 31 PF01082 0.479
MOD_Cter_Amidation 85 88 PF01082 0.568
MOD_DYRK1A_RPxSP_1 192 196 PF00069 0.406
MOD_GlcNHglycan 293 296 PF01048 0.520
MOD_GlcNHglycan 445 449 PF01048 0.599
MOD_GlcNHglycan 487 490 PF01048 0.660
MOD_GlcNHglycan 493 496 PF01048 0.615
MOD_GlcNHglycan 507 510 PF01048 0.458
MOD_GlcNHglycan 520 523 PF01048 0.518
MOD_GlcNHglycan 549 552 PF01048 0.382
MOD_GlcNHglycan 572 575 PF01048 0.427
MOD_GlcNHglycan 78 81 PF01048 0.597
MOD_GlcNHglycan 867 870 PF01048 0.506
MOD_GlcNHglycan 884 887 PF01048 0.523
MOD_GlcNHglycan 91 95 PF01048 0.560
MOD_GlcNHglycan 937 940 PF01048 0.637
MOD_GlcNHglycan 965 968 PF01048 0.425
MOD_GSK3_1 244 251 PF00069 0.617
MOD_GSK3_1 426 433 PF00069 0.485
MOD_GSK3_1 444 451 PF00069 0.542
MOD_GSK3_1 485 492 PF00069 0.508
MOD_GSK3_1 505 512 PF00069 0.445
MOD_GSK3_1 543 550 PF00069 0.422
MOD_GSK3_1 560 567 PF00069 0.507
MOD_GSK3_1 671 678 PF00069 0.499
MOD_GSK3_1 722 729 PF00069 0.354
MOD_GSK3_1 74 81 PF00069 0.610
MOD_GSK3_1 875 882 PF00069 0.436
MOD_LATS_1 365 371 PF00433 0.415
MOD_N-GLC_1 213 218 PF02516 0.521
MOD_N-GLC_1 398 403 PF02516 0.415
MOD_N-GLC_1 552 557 PF02516 0.419
MOD_N-GLC_1 726 731 PF02516 0.512
MOD_NEK2_1 152 157 PF00069 0.596
MOD_NEK2_1 226 231 PF00069 0.566
MOD_NEK2_1 275 280 PF00069 0.465
MOD_NEK2_1 291 296 PF00069 0.720
MOD_NEK2_1 310 315 PF00069 0.395
MOD_NEK2_1 366 371 PF00069 0.483
MOD_NEK2_1 477 482 PF00069 0.496
MOD_NEK2_1 722 727 PF00069 0.402
MOD_NEK2_1 76 81 PF00069 0.588
MOD_NEK2_1 827 832 PF00069 0.444
MOD_NEK2_1 995 1000 PF00069 0.458
MOD_NEK2_2 16 21 PF00069 0.468
MOD_NEK2_2 694 699 PF00069 0.382
MOD_PIKK_1 489 495 PF00454 0.483
MOD_PK_1 598 604 PF00069 0.300
MOD_PK_1 888 894 PF00069 0.694
MOD_PKA_1 10 16 PF00069 0.494
MOD_PKA_2 10 16 PF00069 0.570
MOD_PKA_2 152 158 PF00069 0.585
MOD_PKA_2 226 232 PF00069 0.388
MOD_PKA_2 304 310 PF00069 0.435
MOD_PKA_2 361 367 PF00069 0.431
MOD_PKA_2 381 387 PF00069 0.399
MOD_PKA_2 722 728 PF00069 0.396
MOD_PKA_2 843 849 PF00069 0.507
MOD_PKA_2 89 95 PF00069 0.645
MOD_PKB_1 396 404 PF00069 0.467
MOD_PKB_1 88 96 PF00069 0.536
MOD_Plk_1 137 143 PF00069 0.565
MOD_Plk_1 398 404 PF00069 0.467
MOD_Plk_1 552 558 PF00069 0.419
MOD_Plk_1 90 96 PF00069 0.603
MOD_Plk_2-3 304 310 PF00069 0.570
MOD_Plk_2-3 434 440 PF00069 0.426
MOD_Plk_2-3 879 885 PF00069 0.550
MOD_Plk_4 137 143 PF00069 0.557
MOD_Plk_4 16 22 PF00069 0.448
MOD_Plk_4 171 177 PF00069 0.537
MOD_Plk_4 186 192 PF00069 0.397
MOD_Plk_4 208 214 PF00069 0.471
MOD_Plk_4 275 281 PF00069 0.427
MOD_Plk_4 335 341 PF00069 0.562
MOD_Plk_4 426 432 PF00069 0.484
MOD_Plk_4 498 504 PF00069 0.450
MOD_Plk_4 553 559 PF00069 0.433
MOD_Plk_4 66 72 PF00069 0.513
MOD_Plk_4 694 700 PF00069 0.494
MOD_Plk_4 707 713 PF00069 0.463
MOD_ProDKin_1 192 198 PF00069 0.590
MOD_ProDKin_1 250 256 PF00069 0.657
MOD_ProDKin_1 329 335 PF00069 0.415
MOD_ProDKin_1 509 515 PF00069 0.480
MOD_ProDKin_1 561 567 PF00069 0.504
MOD_ProDKin_1 638 644 PF00069 0.563
MOD_ProDKin_1 768 774 PF00069 0.601
MOD_ProDKin_1 79 85 PF00069 0.610
MOD_SUMO_for_1 143 146 PF00179 0.562
MOD_SUMO_rev_2 656 665 PF00179 0.418
MOD_SUMO_rev_2 975 984 PF00179 0.545
TRG_DiLeu_BaEn_1 992 997 PF01217 0.464
TRG_DiLeu_BaEn_2 237 243 PF01217 0.413
TRG_DiLeu_BaLyEn_6 473 478 PF01217 0.393
TRG_DiLeu_BaLyEn_6 480 485 PF01217 0.416
TRG_DiLeu_LyEn_5 261 266 PF01217 0.426
TRG_ENDOCYTIC_2 1006 1009 PF00928 0.460
TRG_ENDOCYTIC_2 17 20 PF00928 0.472
TRG_ENDOCYTIC_2 173 176 PF00928 0.518
TRG_ENDOCYTIC_2 203 206 PF00928 0.440
TRG_ENDOCYTIC_2 210 213 PF00928 0.506
TRG_ENDOCYTIC_2 276 279 PF00928 0.443
TRG_ENDOCYTIC_2 629 632 PF00928 0.572
TRG_ENDOCYTIC_2 745 748 PF00928 0.550
TRG_ENDOCYTIC_2 774 777 PF00928 0.612
TRG_ER_diArg_1 133 136 PF00400 0.548
TRG_ER_diArg_1 280 283 PF00400 0.387
TRG_ER_diArg_1 30 32 PF00400 0.527
TRG_ER_diArg_1 325 328 PF00400 0.570
TRG_ER_diArg_1 359 362 PF00400 0.293
TRG_ER_diArg_1 395 398 PF00400 0.415
TRG_ER_diArg_1 481 483 PF00400 0.428
TRG_ER_diArg_1 515 517 PF00400 0.549
TRG_ER_diArg_1 618 621 PF00400 0.383
TRG_ER_diArg_1 802 804 PF00400 0.391
TRG_ER_diArg_1 85 88 PF00400 0.606
TRG_ER_diArg_1 920 923 PF00400 0.574
TRG_NLS_MonoExtC_3 131 136 PF00514 0.525
TRG_NLS_MonoExtC_3 280 286 PF00514 0.351
TRG_NLS_MonoExtN_4 129 136 PF00514 0.500
TRG_Pf-PMV_PEXEL_1 122 126 PF00026 0.520
TRG_Pf-PMV_PEXEL_1 475 479 PF00026 0.402
TRG_Pf-PMV_PEXEL_1 803 808 PF00026 0.373

Homologs

Protein Taxonomy Sequence identity Coverage
A0A1X0NYY7 Trypanosomatidae 37% 100%
A0A3Q8IAD3 Leishmania donovani 52% 100%
A0A3Q8IAF8 Leishmania donovani 59% 100%
A0A3Q8IAK8 Leishmania donovani 62% 100%
A0A3Q8IJ32 Leishmania donovani 60% 100%
A0A3S5H6Y1 Leishmania donovani 62% 100%
A0A3S7WTZ8 Leishmania donovani 89% 99%
A0A3S7WU13 Leishmania donovani 62% 100%
A4H8M5 Leishmania braziliensis 54% 100%
A4H8M7 Leishmania braziliensis 58% 100%
A4H8N0 Leishmania braziliensis 70% 100%
A4H8N1 Leishmania braziliensis 48% 100%
A4HWZ5 Leishmania infantum 62% 100%
A4HWZ6 Leishmania infantum 58% 100%
A4HWZ8 Leishmania infantum 62% 100%
A4HX00 Leishmania infantum 89% 99%
A4HX01 Leishmania infantum 53% 100%
A4HX05 Leishmania infantum 59% 100%
E8NHI9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 63% 100%
E9AQQ9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 65% 100%
E9AQR0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 64% 100%
E9AQR1 Leishmania mexicana (strain MHOM/GT/2001/U1103) 65% 100%
E9AQR2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 63% 100%
E9AQR4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 54% 100%
Q4QER2 Leishmania major 51% 100%
Q4QER3 Leishmania major 87% 100%
Q4QER4 Leishmania major 66% 100%
Q4QER5 Leishmania major 62% 100%
Q4QER6 Leishmania major 62% 100%
Q4QER7 Leishmania major 61% 100%
Q4QER8 Leishmania major 61% 100%
Q4QER9 Leishmania major 62% 100%
Q4QES0 Leishmania major 61% 96%

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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