LeishMANIAdb
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Putative arginine N-methyltransferase, type II

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

Quick info

Protein:
Putative arginine N-methyltransferase, type II
Gene product:
arginine N-methyltransferase, type II, putative
Species:
Leishmania braziliensis
UniProt:
A4HC16_LEIBR
TriTrypDb:
LbrM.21.1830 , LBRM2903_210022200 * , LBRM2903_210022300 *
Length:
1013

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: 6
NetGPI no yes: 0, no: 6
Cellular components
Term Name Level Count
GO:0005634 nucleus 5 1
GO:0005737 cytoplasm 2 1
GO:0005829 cytosol 2 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0043229 intracellular organelle 3 1
GO:0043231 intracellular membrane-bounded organelle 4 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A4HC16
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HC16

Function

Biological processes
Term Name Level Count
GO:0006479 protein methylation 4 7
GO:0006807 nitrogen compound metabolic process 2 7
GO:0008152 metabolic process 1 7
GO:0008213 protein alkylation 5 7
GO:0009987 cellular process 1 7
GO:0018193 peptidyl-amino acid modification 5 7
GO:0018195 peptidyl-arginine modification 6 7
GO:0018216 peptidyl-arginine methylation 5 7
GO:0019538 protein metabolic process 3 7
GO:0032259 methylation 2 7
GO:0036211 protein modification process 4 7
GO:0043170 macromolecule metabolic process 3 7
GO:0043412 macromolecule modification 4 7
GO:0043414 macromolecule methylation 3 7
GO:0044237 cellular metabolic process 2 7
GO:0044238 primary metabolic process 2 7
GO:0044260 obsolete cellular macromolecule metabolic process 3 7
GO:0071704 organic substance metabolic process 2 7
GO:1901564 organonitrogen compound metabolic process 3 7
GO:0006355 regulation of DNA-templated transcription 6 1
GO:0009889 regulation of biosynthetic process 4 1
GO:0010468 regulation of gene expression 5 1
GO:0010556 regulation of macromolecule biosynthetic process 5 1
GO:0016570 histone modification 5 1
GO:0016571 histone methylation 5 1
GO:0019219 regulation of nucleobase-containing compound metabolic process 5 1
GO:0019222 regulation of metabolic process 3 1
GO:0019918 peptidyl-arginine methylation, to symmetrical-dimethyl arginine 8 1
GO:0031323 regulation of cellular metabolic process 4 1
GO:0031326 regulation of cellular biosynthetic process 5 1
GO:0034969 histone arginine methylation 6 1
GO:0035246 peptidyl-arginine N-methylation 6 1
GO:0035247 peptidyl-arginine omega-N-methylation 7 1
GO:0050789 regulation of biological process 2 1
GO:0050794 regulation of cellular process 3 1
GO:0051171 regulation of nitrogen compound metabolic process 4 1
GO:0051252 regulation of RNA metabolic process 5 1
GO:0060255 regulation of macromolecule metabolic process 4 1
GO:0065007 biological regulation 1 1
GO:0080090 regulation of primary metabolic process 4 1
GO:1903506 regulation of nucleic acid-templated transcription 7 1
GO:2001141 regulation of RNA biosynthetic process 6 1
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 7
GO:0008168 methyltransferase activity 4 7
GO:0008170 N-methyltransferase activity 5 7
GO:0008276 protein methyltransferase activity 3 7
GO:0008757 S-adenosylmethionine-dependent methyltransferase activity 5 7
GO:0016273 arginine N-methyltransferase activity 6 7
GO:0016274 protein-arginine N-methyltransferase activity 4 7
GO:0016740 transferase activity 2 7
GO:0016741 transferase activity, transferring one-carbon groups 3 7
GO:0140096 catalytic activity, acting on a protein 2 7
GO:0008469 histone arginine N-methyltransferase activity 5 1
GO:0042054 histone methyltransferase activity 4 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 441 445 PF00656 0.580
CLV_C14_Caspase3-7 746 750 PF00656 0.491
CLV_NRD_NRD_1 289 291 PF00675 0.450
CLV_NRD_NRD_1 484 486 PF00675 0.556
CLV_NRD_NRD_1 529 531 PF00675 0.410
CLV_NRD_NRD_1 770 772 PF00675 0.305
CLV_NRD_NRD_1 962 964 PF00675 0.271
CLV_NRD_NRD_1 968 970 PF00675 0.272
CLV_PCSK_KEX2_1 484 486 PF00082 0.556
CLV_PCSK_KEX2_1 528 530 PF00082 0.394
CLV_PCSK_KEX2_1 633 635 PF00082 0.207
CLV_PCSK_KEX2_1 770 772 PF00082 0.305
CLV_PCSK_KEX2_1 859 861 PF00082 0.228
CLV_PCSK_KEX2_1 962 964 PF00082 0.289
CLV_PCSK_PC1ET2_1 633 635 PF00082 0.207
CLV_PCSK_PC1ET2_1 859 861 PF00082 0.228
CLV_PCSK_SKI1_1 349 353 PF00082 0.438
CLV_PCSK_SKI1_1 537 541 PF00082 0.457
CLV_PCSK_SKI1_1 559 563 PF00082 0.452
CLV_PCSK_SKI1_1 61 65 PF00082 0.535
CLV_PCSK_SKI1_1 808 812 PF00082 0.268
CLV_PCSK_SKI1_1 835 839 PF00082 0.268
CLV_Separin_Metazoa 525 529 PF03568 0.370
DEG_APCC_DBOX_1 271 279 PF00400 0.426
DEG_SPOP_SBC_1 319 323 PF00917 0.573
DOC_CKS1_1 300 305 PF01111 0.436
DOC_CKS1_1 422 427 PF01111 0.565
DOC_CYCLIN_yCln2_LP_2 569 575 PF00134 0.468
DOC_CYCLIN_yCln2_LP_2 727 733 PF00134 0.512
DOC_MAPK_gen_1 170 179 PF00069 0.394
DOC_MAPK_gen_1 528 534 PF00069 0.428
DOC_MAPK_MEF2A_6 186 194 PF00069 0.363
DOC_MAPK_MEF2A_6 866 873 PF00069 0.407
DOC_MAPK_MEF2A_6 951 960 PF00069 0.468
DOC_MAPK_RevD_3 515 530 PF00069 0.449
DOC_MAPK_RevD_3 956 970 PF00069 0.423
DOC_PP1_RVXF_1 769 776 PF00149 0.440
DOC_PP2B_LxvP_1 145 148 PF13499 0.482
DOC_PP2B_LxvP_1 569 572 PF13499 0.468
DOC_PP2B_LxvP_1 727 730 PF13499 0.512
DOC_PP2B_LxvP_1 810 813 PF13499 0.512
DOC_PP2B_LxvP_1 839 842 PF13499 0.468
DOC_PP4_FxxP_1 364 367 PF00568 0.443
DOC_PP4_FxxP_1 881 884 PF00568 0.468
DOC_USP7_MATH_1 109 113 PF00917 0.475
DOC_USP7_MATH_1 317 321 PF00917 0.728
DOC_USP7_MATH_1 333 337 PF00917 0.312
DOC_USP7_MATH_1 367 371 PF00917 0.373
DOC_USP7_MATH_1 457 461 PF00917 0.531
DOC_USP7_MATH_1 515 519 PF00917 0.480
DOC_USP7_MATH_1 636 640 PF00917 0.435
DOC_USP7_MATH_1 682 686 PF00917 0.412
DOC_USP7_MATH_1 792 796 PF00917 0.468
DOC_USP7_MATH_1 815 819 PF00917 0.407
DOC_USP7_MATH_1 989 993 PF00917 0.523
DOC_WW_Pin1_4 196 201 PF00397 0.422
DOC_WW_Pin1_4 299 304 PF00397 0.434
DOC_WW_Pin1_4 320 325 PF00397 0.580
DOC_WW_Pin1_4 41 46 PF00397 0.499
DOC_WW_Pin1_4 421 426 PF00397 0.689
DOC_WW_Pin1_4 465 470 PF00397 0.570
DOC_WW_Pin1_4 750 755 PF00397 0.468
DOC_WW_Pin1_4 911 916 PF00397 0.427
DOC_WW_Pin1_4 985 990 PF00397 0.565
LIG_14-3-3_CanoR_1 327 337 PF00244 0.358
LIG_14-3-3_CanoR_1 390 396 PF00244 0.508
LIG_14-3-3_CanoR_1 492 496 PF00244 0.575
LIG_14-3-3_CanoR_1 808 813 PF00244 0.407
LIG_14-3-3_CanoR_1 835 840 PF00244 0.468
LIG_14-3-3_CanoR_1 851 857 PF00244 0.468
LIG_14-3-3_CanoR_1 875 880 PF00244 0.512
LIG_14-3-3_CanoR_1 962 967 PF00244 0.444
LIG_BIR_II_1 1 5 PF00653 0.523
LIG_BIR_III_2 316 320 PF00653 0.549
LIG_BRCT_BRCA1_1 106 110 PF00533 0.569
LIG_BRCT_BRCA1_1 353 357 PF00533 0.478
LIG_BRCT_BRCA1_1 622 626 PF00533 0.407
LIG_BRCT_BRCA1_1 794 798 PF00533 0.512
LIG_BRCT_BRCA1_1 877 881 PF00533 0.512
LIG_BRCT_BRCA1_2 622 628 PF00533 0.407
LIG_CaM_IQ_9 955 971 PF13499 0.512
LIG_deltaCOP1_diTrp_1 694 704 PF00928 0.512
LIG_FHA_1 223 229 PF00498 0.480
LIG_FHA_1 291 297 PF00498 0.423
LIG_FHA_1 519 525 PF00498 0.371
LIG_FHA_1 556 562 PF00498 0.522
LIG_FHA_1 642 648 PF00498 0.492
LIG_FHA_1 705 711 PF00498 0.501
LIG_FHA_1 73 79 PF00498 0.395
LIG_FHA_1 785 791 PF00498 0.468
LIG_FHA_1 825 831 PF00498 0.512
LIG_FHA_2 392 398 PF00498 0.557
LIG_FHA_2 448 454 PF00498 0.670
LIG_FHA_2 536 542 PF00498 0.482
LIG_FHA_2 718 724 PF00498 0.575
LIG_FHA_2 976 982 PF00498 0.526
LIG_GBD_Chelix_1 739 747 PF00786 0.312
LIG_IBAR_NPY_1 776 778 PF08397 0.289
LIG_LIR_Apic_2 494 498 PF02991 0.541
LIG_LIR_Apic_2 787 792 PF02991 0.486
LIG_LIR_Apic_2 878 884 PF02991 0.474
LIG_LIR_Gen_1 103 113 PF02991 0.567
LIG_LIR_Gen_1 141 148 PF02991 0.541
LIG_LIR_Gen_1 444 454 PF02991 0.627
LIG_LIR_Gen_1 541 551 PF02991 0.326
LIG_LIR_Gen_1 560 569 PF02991 0.331
LIG_LIR_Gen_1 582 592 PF02991 0.468
LIG_LIR_Gen_1 600 611 PF02991 0.468
LIG_LIR_Gen_1 685 692 PF02991 0.476
LIG_LIR_Gen_1 694 704 PF02991 0.463
LIG_LIR_Gen_1 920 931 PF02991 0.468
LIG_LIR_Nem_3 103 108 PF02991 0.585
LIG_LIR_Nem_3 141 145 PF02991 0.532
LIG_LIR_Nem_3 444 449 PF02991 0.623
LIG_LIR_Nem_3 512 516 PF02991 0.474
LIG_LIR_Nem_3 538 543 PF02991 0.408
LIG_LIR_Nem_3 560 565 PF02991 0.448
LIG_LIR_Nem_3 582 588 PF02991 0.468
LIG_LIR_Nem_3 600 606 PF02991 0.468
LIG_LIR_Nem_3 694 700 PF02991 0.468
LIG_LIR_Nem_3 920 926 PF02991 0.576
LIG_LIR_Nem_3 976 982 PF02991 0.407
LIG_MLH1_MIPbox_1 622 626 PF16413 0.407
LIG_NRBOX 336 342 PF00104 0.413
LIG_OCRL_FandH_1 624 636 PF00620 0.512
LIG_PCNA_PIPBox_1 542 551 PF02747 0.402
LIG_PCNA_yPIPBox_3 170 183 PF02747 0.392
LIG_PCNA_yPIPBox_3 537 549 PF02747 0.468
LIG_Pex14_1 509 513 PF04695 0.371
LIG_Pex14_1 975 979 PF04695 0.468
LIG_Pex14_2 33 37 PF04695 0.469
LIG_Pex14_2 535 539 PF04695 0.430
LIG_Pex14_2 73 77 PF04695 0.416
LIG_Pex14_2 848 852 PF04695 0.468
LIG_Pex14_2 926 930 PF04695 0.468
LIG_PTB_Apo_2 407 414 PF02174 0.532
LIG_PTB_Phospho_1 407 413 PF10480 0.532
LIG_REV1ctd_RIR_1 623 632 PF16727 0.512
LIG_SH2_CRK 105 109 PF00017 0.574
LIG_SH2_CRK 446 450 PF00017 0.633
LIG_SH2_CRK 493 497 PF00017 0.568
LIG_SH2_CRK 543 547 PF00017 0.321
LIG_SH2_GRB2like 408 411 PF00017 0.536
LIG_SH2_NCK_1 446 450 PF00017 0.665
LIG_SH2_PTP2 495 498 PF00017 0.463
LIG_SH2_STAP1 493 497 PF00017 0.450
LIG_SH2_STAP1 786 790 PF00017 0.468
LIG_SH2_STAP1 973 977 PF00017 0.468
LIG_SH2_STAT3 273 276 PF00017 0.395
LIG_SH2_STAT3 406 409 PF00017 0.532
LIG_SH2_STAT5 25 28 PF00017 0.510
LIG_SH2_STAT5 493 496 PF00017 0.523
LIG_SH2_STAT5 548 551 PF00017 0.397
LIG_SH2_STAT5 605 608 PF00017 0.496
LIG_SH2_STAT5 702 705 PF00017 0.496
LIG_SH2_STAT5 778 781 PF00017 0.380
LIG_SH2_STAT5 786 789 PF00017 0.520
LIG_SH2_STAT5 895 898 PF00017 0.468
LIG_SH3_3 114 120 PF00018 0.549
LIG_SH3_3 185 191 PF00018 0.362
LIG_SH3_3 39 45 PF00018 0.532
LIG_SH3_3 551 557 PF00018 0.417
LIG_SH3_3 569 575 PF00018 0.468
LIG_SH3_3 632 638 PF00018 0.468
LIG_SH3_3 809 815 PF00018 0.468
LIG_SH3_3 838 844 PF00018 0.512
LIG_SUMO_SIM_anti_2 707 712 PF11976 0.468
LIG_SUMO_SIM_par_1 826 831 PF11976 0.512
LIG_SUMO_SIM_par_1 86 92 PF11976 0.508
LIG_SUMO_SIM_par_1 869 874 PF11976 0.455
LIG_TRAF2_1 20 23 PF00917 0.529
LIG_TRAF2_1 229 232 PF00917 0.476
LIG_TRAF2_1 382 385 PF00917 0.444
LIG_TRAF2_1 553 556 PF00917 0.301
LIG_TRAF2_1 720 723 PF00917 0.438
LIG_TRFH_1 930 934 PF08558 0.468
LIG_TYR_ITIM 977 982 PF00017 0.464
LIG_UBA3_1 545 552 PF00899 0.397
LIG_UBA3_1 59 64 PF00899 0.536
LIG_UBA3_1 674 679 PF00899 0.468
LIG_WRC_WIRS_1 248 253 PF05994 0.426
LIG_WRC_WIRS_1 562 567 PF05994 0.363
LIG_WW_3 883 887 PF00397 0.405
MOD_CDK_SPxxK_3 320 327 PF00069 0.454
MOD_CDK_SPxxK_3 911 918 PF00069 0.407
MOD_CK1_1 163 169 PF00069 0.480
MOD_CK1_1 224 230 PF00069 0.467
MOD_CK1_1 312 318 PF00069 0.546
MOD_CK1_1 320 326 PF00069 0.494
MOD_CK1_1 433 439 PF00069 0.655
MOD_CK1_1 44 50 PF00069 0.521
MOD_CK1_1 468 474 PF00069 0.606
MOD_CK1_1 518 524 PF00069 0.374
MOD_CK2_1 16 22 PF00069 0.537
MOD_CK2_1 204 210 PF00069 0.492
MOD_CK2_1 226 232 PF00069 0.580
MOD_CK2_1 391 397 PF00069 0.555
MOD_CK2_1 445 451 PF00069 0.621
MOD_CK2_1 472 478 PF00069 0.606
MOD_CK2_1 636 642 PF00069 0.468
MOD_CK2_1 717 723 PF00069 0.575
MOD_CK2_1 962 968 PF00069 0.445
MOD_CMANNOS 972 975 PF00535 0.268
MOD_GlcNHglycan 142 145 PF01048 0.473
MOD_GlcNHglycan 18 21 PF01048 0.581
MOD_GlcNHglycan 228 231 PF01048 0.444
MOD_GlcNHglycan 369 372 PF01048 0.374
MOD_GlcNHglycan 459 462 PF01048 0.631
MOD_GlcNHglycan 470 473 PF01048 0.613
MOD_GlcNHglycan 517 520 PF01048 0.369
MOD_GlcNHglycan 581 584 PF01048 0.312
MOD_GlcNHglycan 638 641 PF01048 0.207
MOD_GlcNHglycan 665 668 PF01048 0.314
MOD_GlcNHglycan 794 797 PF01048 0.268
MOD_GlcNHglycan 874 878 PF01048 0.223
MOD_GlcNHglycan 889 892 PF01048 0.318
MOD_GlcNHglycan 896 899 PF01048 0.289
MOD_GlcNHglycan 902 905 PF01048 0.304
MOD_GlcNHglycan 946 949 PF01048 0.210
MOD_GlcNHglycan 989 992 PF01048 0.588
MOD_GSK3_1 104 111 PF00069 0.495
MOD_GSK3_1 214 221 PF00069 0.563
MOD_GSK3_1 222 229 PF00069 0.472
MOD_GSK3_1 304 311 PF00069 0.418
MOD_GSK3_1 37 44 PF00069 0.403
MOD_GSK3_1 468 475 PF00069 0.597
MOD_GSK3_1 574 581 PF00069 0.468
MOD_GSK3_1 700 707 PF00069 0.482
MOD_GSK3_1 824 831 PF00069 0.468
MOD_GSK3_1 902 909 PF00069 0.512
MOD_GSK3_1 96 103 PF00069 0.653
MOD_GSK3_1 985 992 PF00069 0.534
MOD_LATS_1 388 394 PF00433 0.478
MOD_N-GLC_1 465 470 PF02516 0.518
MOD_N-GLC_1 723 728 PF02516 0.263
MOD_N-GLC_1 831 836 PF02516 0.275
MOD_N-GLC_2 24 26 PF02516 0.425
MOD_NEK2_1 104 109 PF00069 0.434
MOD_NEK2_1 309 314 PF00069 0.464
MOD_NEK2_1 341 346 PF00069 0.482
MOD_NEK2_1 391 396 PF00069 0.482
MOD_NEK2_1 535 540 PF00069 0.425
MOD_NEK2_1 59 64 PF00069 0.475
MOD_NEK2_1 69 74 PF00069 0.449
MOD_NEK2_1 700 705 PF00069 0.468
MOD_NEK2_1 743 748 PF00069 0.468
MOD_NEK2_1 824 829 PF00069 0.468
MOD_NEK2_1 873 878 PF00069 0.427
MOD_NEK2_1 900 905 PF00069 0.512
MOD_NEK2_2 1007 1012 PF00069 0.300
MOD_PIKK_1 222 228 PF00454 0.497
MOD_PIKK_1 433 439 PF00454 0.564
MOD_PIKK_1 574 580 PF00454 0.407
MOD_PIKK_1 695 701 PF00454 0.463
MOD_PIKK_1 96 102 PF00454 0.592
MOD_PKA_1 290 296 PF00069 0.398
MOD_PKA_1 962 968 PF00069 0.444
MOD_PKA_2 100 106 PF00069 0.523
MOD_PKA_2 221 227 PF00069 0.559
MOD_PKA_2 389 395 PF00069 0.502
MOD_PKA_2 483 489 PF00069 0.551
MOD_PKA_2 491 497 PF00069 0.521
MOD_PKA_2 850 856 PF00069 0.420
MOD_PKA_2 887 893 PF00069 0.405
MOD_PKA_2 962 968 PF00069 0.468
MOD_Plk_1 160 166 PF00069 0.450
MOD_Plk_1 438 444 PF00069 0.596
MOD_Plk_1 535 541 PF00069 0.481
MOD_Plk_1 641 647 PF00069 0.512
MOD_Plk_1 695 701 PF00069 0.463
MOD_Plk_1 723 729 PF00069 0.459
MOD_Plk_1 973 979 PF00069 0.468
MOD_Plk_2-3 205 211 PF00069 0.505
MOD_Plk_2-3 447 453 PF00069 0.668
MOD_Plk_4 100 106 PF00069 0.550
MOD_Plk_4 109 115 PF00069 0.530
MOD_Plk_4 247 253 PF00069 0.425
MOD_Plk_4 309 315 PF00069 0.592
MOD_Plk_4 333 339 PF00069 0.406
MOD_Plk_4 491 497 PF00069 0.583
MOD_Plk_4 518 524 PF00069 0.352
MOD_Plk_4 824 830 PF00069 0.563
MOD_Plk_4 875 881 PF00069 0.512
MOD_Plk_4 906 912 PF00069 0.551
MOD_Plk_4 921 927 PF00069 0.411
MOD_ProDKin_1 196 202 PF00069 0.424
MOD_ProDKin_1 299 305 PF00069 0.438
MOD_ProDKin_1 320 326 PF00069 0.576
MOD_ProDKin_1 41 47 PF00069 0.501
MOD_ProDKin_1 421 427 PF00069 0.688
MOD_ProDKin_1 465 471 PF00069 0.570
MOD_ProDKin_1 750 756 PF00069 0.468
MOD_ProDKin_1 911 917 PF00069 0.427
MOD_ProDKin_1 985 991 PF00069 0.573
MOD_SUMO_rev_2 947 953 PF00179 0.431
MOD_SUMO_rev_2 965 971 PF00179 0.386
TRG_DiLeu_BaEn_2 177 183 PF01217 0.369
TRG_DiLeu_BaEn_4 22 28 PF01217 0.521
TRG_DiLeu_BaEn_4 722 728 PF01217 0.407
TRG_DiLeu_BaLyEn_6 653 658 PF01217 0.468
TRG_ENDOCYTIC_2 105 108 PF00928 0.581
TRG_ENDOCYTIC_2 446 449 PF00928 0.607
TRG_ENDOCYTIC_2 493 496 PF00928 0.523
TRG_ENDOCYTIC_2 513 516 PF00928 0.302
TRG_ENDOCYTIC_2 543 546 PF00928 0.410
TRG_ENDOCYTIC_2 548 551 PF00928 0.389
TRG_ENDOCYTIC_2 585 588 PF00928 0.468
TRG_ENDOCYTIC_2 862 865 PF00928 0.407
TRG_ENDOCYTIC_2 923 926 PF00928 0.468
TRG_ENDOCYTIC_2 979 982 PF00928 0.310
TRG_ER_diArg_1 170 173 PF00400 0.404
TRG_ER_diArg_1 527 530 PF00400 0.384
TRG_ER_diArg_1 670 673 PF00400 0.468
TRG_ER_diArg_1 688 691 PF00400 0.516
TRG_ER_diArg_1 885 888 PF00400 0.405
TRG_NES_CRM1_1 699 714 PF08389 0.468
TRG_Pf-PMV_PEXEL_1 128 132 PF00026 0.431
TRG_Pf-PMV_PEXEL_1 61 65 PF00026 0.474

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1HT81 Leptomonas seymouri 56% 93%
A0A3S7WWP9 Leishmania donovani 77% 94%
A4HZE2 Leishmania infantum 77% 94%
E9AVC9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 78% 100%
Q4QC50 Leishmania major 79% 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