LeishMANIAdb
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TPR_REGION domain-containing protein

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

Quick info

Protein:
TPR_REGION domain-containing protein
Gene product:
TPR repeat, putative
Species:
Leishmania major
UniProt:
Q4QJG1_LEIMA
TriTrypDb:
LmjF.05.0410 , LMJLV39_050009000 , LMJSD75_050009000
Length:
920

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:0000151 ubiquitin ligase complex 3 2
GO:0000152 nuclear ubiquitin ligase complex 3 2
GO:0005680 anaphase-promoting complex 4 2
GO:0005737 cytoplasm 2 2
GO:0031461 cullin-RING ubiquitin ligase complex 4 2
GO:0032991 protein-containing complex 1 2
GO:0051286 cell tip 3 2
GO:0060187 cell pole 2 2
GO:0110165 cellular anatomical entity 1 2
GO:0140513 nuclear protein-containing complex 2 2
GO:0140535 intracellular protein-containing complex 2 2
GO:1902494 catalytic complex 2 2
GO:1990234 transferase complex 3 2

Expansion

Sequence features

Q4QJG1
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QJG1

Function

Biological processes
Term Name Level Count
GO:0006508 proteolysis 4 2
GO:0006511 ubiquitin-dependent protein catabolic process 7 2
GO:0006807 nitrogen compound metabolic process 2 2
GO:0007088 regulation of mitotic nuclear division 6 2
GO:0007091 metaphase/anaphase transition of mitotic cell cycle 5 2
GO:0007346 regulation of mitotic cell cycle 5 2
GO:0008152 metabolic process 1 2
GO:0009056 catabolic process 2 2
GO:0009057 macromolecule catabolic process 4 2
GO:0009987 cellular process 1 2
GO:0010498 proteasomal protein catabolic process 5 2
GO:0010564 regulation of cell cycle process 5 2
GO:0010638 positive regulation of organelle organization 6 2
GO:0010965 regulation of mitotic sister chromatid separation 6 2
GO:0016567 protein ubiquitination 7 2
GO:0019538 protein metabolic process 3 2
GO:0019941 modification-dependent protein catabolic process 6 2
GO:0022402 cell cycle process 2 2
GO:0030071 regulation of mitotic metaphase/anaphase transition 7 2
GO:0030163 protein catabolic process 4 2
GO:0031145 anaphase-promoting complex-dependent catabolic process 7 2
GO:0032446 protein modification by small protein conjugation 6 2
GO:0033043 regulation of organelle organization 5 2
GO:0033044 regulation of chromosome organization 6 2
GO:0033045 regulation of sister chromatid segregation 5 2
GO:0036211 protein modification process 4 2
GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process 6 2
GO:0043170 macromolecule metabolic process 3 2
GO:0043412 macromolecule modification 4 2
GO:0043632 modification-dependent macromolecule catabolic process 5 2
GO:0044237 cellular metabolic process 2 2
GO:0044238 primary metabolic process 2 2
GO:0044248 cellular catabolic process 3 2
GO:0044260 obsolete cellular macromolecule metabolic process 3 2
GO:0044265 obsolete cellular macromolecule catabolic process 4 2
GO:0044770 cell cycle phase transition 3 2
GO:0044772 mitotic cell cycle phase transition 4 2
GO:0044784 metaphase/anaphase transition of cell cycle 4 2
GO:0045787 positive regulation of cell cycle 5 2
GO:0045840 positive regulation of mitotic nuclear division 7 2
GO:0045842 positive regulation of mitotic metaphase/anaphase transition 8 2
GO:0045931 positive regulation of mitotic cell cycle 6 2
GO:0048518 positive regulation of biological process 3 2
GO:0048522 positive regulation of cellular process 4 2
GO:0050789 regulation of biological process 2 2
GO:0050794 regulation of cellular process 3 2
GO:0051128 regulation of cellular component organization 4 2
GO:0051130 positive regulation of cellular component organization 5 2
GO:0051301 cell division 2 2
GO:0051603 proteolysis involved in protein catabolic process 5 2
GO:0051726 regulation of cell cycle 4 2
GO:0051783 regulation of nuclear division 6 2
GO:0051785 positive regulation of nuclear division 7 2
GO:0051983 regulation of chromosome segregation 4 2
GO:0065007 biological regulation 1 2
GO:0070647 protein modification by small protein conjugation or removal 5 2
GO:0071704 organic substance metabolic process 2 2
GO:0090068 positive regulation of cell cycle process 6 2
GO:1901564 organonitrogen compound metabolic process 3 2
GO:1901565 organonitrogen compound catabolic process 4 2
GO:1901575 organic substance catabolic process 3 2
GO:1901970 positive regulation of mitotic sister chromatid separation 7 2
GO:1901987 regulation of cell cycle phase transition 6 2
GO:1901989 positive regulation of cell cycle phase transition 7 2
GO:1901990 regulation of mitotic cell cycle phase transition 6 2
GO:1901992 positive regulation of mitotic cell cycle phase transition 7 2
GO:1902099 regulation of metaphase/anaphase transition of cell cycle 6 2
GO:1902101 positive regulation of metaphase/anaphase transition of cell cycle 7 2
GO:1903047 mitotic cell cycle process 3 2
GO:1905818 regulation of chromosome separation 5 2
GO:1905820 positive regulation of chromosome separation 6 2
Could not find GO molecular_function term for this entry.

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 645 649 PF00656 0.447
CLV_NRD_NRD_1 225 227 PF00675 0.572
CLV_NRD_NRD_1 323 325 PF00675 0.467
CLV_NRD_NRD_1 396 398 PF00675 0.506
CLV_NRD_NRD_1 457 459 PF00675 0.640
CLV_NRD_NRD_1 530 532 PF00675 0.599
CLV_NRD_NRD_1 62 64 PF00675 0.816
CLV_NRD_NRD_1 839 841 PF00675 0.304
CLV_NRD_NRD_1 884 886 PF00675 0.569
CLV_NRD_NRD_1 902 904 PF00675 0.338
CLV_PCSK_KEX2_1 225 227 PF00082 0.599
CLV_PCSK_KEX2_1 322 324 PF00082 0.485
CLV_PCSK_KEX2_1 396 398 PF00082 0.506
CLV_PCSK_KEX2_1 457 459 PF00082 0.640
CLV_PCSK_KEX2_1 530 532 PF00082 0.591
CLV_PCSK_KEX2_1 62 64 PF00082 0.816
CLV_PCSK_KEX2_1 721 723 PF00082 0.376
CLV_PCSK_KEX2_1 839 841 PF00082 0.304
CLV_PCSK_KEX2_1 884 886 PF00082 0.396
CLV_PCSK_KEX2_1 902 904 PF00082 0.442
CLV_PCSK_PC1ET2_1 721 723 PF00082 0.376
CLV_PCSK_PC7_1 453 459 PF00082 0.637
CLV_PCSK_SKI1_1 460 464 PF00082 0.647
CLV_PCSK_SKI1_1 538 542 PF00082 0.591
CLV_PCSK_SKI1_1 714 718 PF00082 0.375
CLV_PCSK_SKI1_1 755 759 PF00082 0.317
CLV_PCSK_SKI1_1 803 807 PF00082 0.366
CLV_PCSK_SKI1_1 819 823 PF00082 0.398
CLV_PCSK_SKI1_1 860 864 PF00082 0.423
DEG_APCC_DBOX_1 321 329 PF00400 0.476
DEG_APCC_DBOX_1 713 721 PF00400 0.371
DEG_SPOP_SBC_1 314 318 PF00917 0.358
DEG_SPOP_SBC_1 597 601 PF00917 0.571
DEG_SPOP_SBC_1 621 625 PF00917 0.437
DOC_CKS1_1 104 109 PF01111 0.650
DOC_CYCLIN_yCln2_LP_2 661 667 PF00134 0.439
DOC_CYCLIN_yCln2_LP_2 849 855 PF00134 0.303
DOC_MAPK_gen_1 457 467 PF00069 0.649
DOC_MAPK_gen_1 711 720 PF00069 0.376
DOC_MAPK_gen_1 839 849 PF00069 0.304
DOC_MAPK_MEF2A_6 460 469 PF00069 0.644
DOC_MAPK_MEF2A_6 840 849 PF00069 0.304
DOC_MAPK_RevD_3 870 885 PF00069 0.354
DOC_MIT_MIM_1 149 157 PF04212 0.491
DOC_PP2B_LxvP_1 520 523 PF13499 0.580
DOC_USP7_MATH_1 108 112 PF00917 0.647
DOC_USP7_MATH_1 119 123 PF00917 0.497
DOC_USP7_MATH_1 201 205 PF00917 0.668
DOC_USP7_MATH_1 240 244 PF00917 0.594
DOC_USP7_MATH_1 369 373 PF00917 0.432
DOC_USP7_MATH_1 416 420 PF00917 0.545
DOC_USP7_MATH_1 489 493 PF00917 0.797
DOC_USP7_MATH_1 576 580 PF00917 0.594
DOC_USP7_MATH_1 620 624 PF00917 0.714
DOC_USP7_MATH_1 681 685 PF00917 0.371
DOC_USP7_MATH_1 82 86 PF00917 0.623
DOC_USP7_UBL2_3 789 793 PF12436 0.304
DOC_WW_Pin1_4 1 6 PF00397 0.608
DOC_WW_Pin1_4 114 119 PF00397 0.607
DOC_WW_Pin1_4 22 27 PF00397 0.693
DOC_WW_Pin1_4 46 51 PF00397 0.629
DOC_WW_Pin1_4 501 506 PF00397 0.644
DOC_WW_Pin1_4 579 584 PF00397 0.498
DOC_WW_Pin1_4 623 628 PF00397 0.440
DOC_WW_Pin1_4 794 799 PF00397 0.381
DOC_WW_Pin1_4 98 103 PF00397 0.700
LIG_14-3-3_CanoR_1 225 234 PF00244 0.580
LIG_14-3-3_CanoR_1 302 310 PF00244 0.349
LIG_14-3-3_CanoR_1 354 360 PF00244 0.462
LIG_14-3-3_CanoR_1 370 378 PF00244 0.371
LIG_14-3-3_CanoR_1 479 487 PF00244 0.675
LIG_14-3-3_CanoR_1 598 608 PF00244 0.616
LIG_14-3-3_CanoR_1 688 695 PF00244 0.415
LIG_14-3-3_CanoR_1 71 76 PF00244 0.640
LIG_14-3-3_CanoR_1 803 809 PF00244 0.367
LIG_14-3-3_CanoR_1 810 816 PF00244 0.428
LIG_APCC_ABBA_1 822 827 PF00400 0.304
LIG_BIR_II_1 1 5 PF00653 0.611
LIG_BIR_III_2 691 695 PF00653 0.426
LIG_BRCT_BRCA1_1 264 268 PF00533 0.608
LIG_Clathr_ClatBox_1 154 158 PF01394 0.434
LIG_Clathr_ClatBox_1 846 850 PF01394 0.304
LIG_eIF4E_1 161 167 PF01652 0.422
LIG_FHA_1 143 149 PF00498 0.483
LIG_FHA_1 247 253 PF00498 0.541
LIG_FHA_1 272 278 PF00498 0.490
LIG_FHA_1 315 321 PF00498 0.401
LIG_FHA_1 369 375 PF00498 0.487
LIG_FHA_1 429 435 PF00498 0.474
LIG_FHA_1 506 512 PF00498 0.621
LIG_FHA_1 697 703 PF00498 0.338
LIG_FHA_1 795 801 PF00498 0.371
LIG_FHA_1 824 830 PF00498 0.455
LIG_FHA_1 99 105 PF00498 0.705
LIG_FHA_2 262 268 PF00498 0.618
LIG_FHA_2 339 345 PF00498 0.609
LIG_FHA_2 688 694 PF00498 0.411
LIG_FHA_2 873 879 PF00498 0.338
LIG_LIR_Apic_2 549 553 PF02991 0.465
LIG_LIR_Gen_1 158 168 PF02991 0.452
LIG_LIR_Gen_1 269 277 PF02991 0.512
LIG_LIR_Gen_1 411 418 PF02991 0.528
LIG_LIR_Gen_1 648 658 PF02991 0.394
LIG_LIR_Nem_3 158 164 PF02991 0.447
LIG_LIR_Nem_3 179 184 PF02991 0.432
LIG_LIR_Nem_3 269 275 PF02991 0.541
LIG_LIR_Nem_3 407 412 PF02991 0.535
LIG_LIR_Nem_3 648 653 PF02991 0.395
LIG_LIR_Nem_3 74 78 PF02991 0.719
LIG_LIR_Nem_3 763 768 PF02991 0.304
LIG_LYPXL_yS_3 188 191 PF13949 0.667
LIG_NRBOX 303 309 PF00104 0.414
LIG_NRBOX 558 564 PF00104 0.452
LIG_NRBOX 858 864 PF00104 0.384
LIG_PCNA_PIPBox_1 136 145 PF02747 0.521
LIG_PCNA_yPIPBox_3 902 915 PF02747 0.404
LIG_Pex14_1 228 232 PF04695 0.645
LIG_Pex14_1 281 285 PF04695 0.357
LIG_PROFILIN_1 5 11 PF00235 0.548
LIG_RPA_C_Fungi 835 847 PF08784 0.369
LIG_SH2_CRK 181 185 PF00017 0.397
LIG_SH2_CRK 707 711 PF00017 0.377
LIG_SH2_CRK 75 79 PF00017 0.711
LIG_SH2_CRK 768 772 PF00017 0.304
LIG_SH2_NCK_1 272 276 PF00017 0.499
LIG_SH2_PTP2 412 415 PF00017 0.482
LIG_SH2_PTP2 873 876 PF00017 0.402
LIG_SH2_SRC 297 300 PF00017 0.406
LIG_SH2_SRC 732 735 PF00017 0.333
LIG_SH2_STAP1 144 148 PF00017 0.493
LIG_SH2_STAP1 669 673 PF00017 0.325
LIG_SH2_STAP1 732 736 PF00017 0.335
LIG_SH2_STAP1 825 829 PF00017 0.304
LIG_SH2_STAT3 292 295 PF00017 0.410
LIG_SH2_STAT3 808 811 PF00017 0.390
LIG_SH2_STAT5 142 145 PF00017 0.502
LIG_SH2_STAT5 171 174 PF00017 0.374
LIG_SH2_STAT5 285 288 PF00017 0.357
LIG_SH2_STAT5 309 312 PF00017 0.424
LIG_SH2_STAT5 399 402 PF00017 0.513
LIG_SH2_STAT5 412 415 PF00017 0.402
LIG_SH2_STAT5 56 59 PF00017 0.641
LIG_SH2_STAT5 765 768 PF00017 0.304
LIG_SH2_STAT5 825 828 PF00017 0.369
LIG_SH2_STAT5 873 876 PF00017 0.402
LIG_SH2_STAT5 906 909 PF00017 0.395
LIG_SH3_3 101 107 PF00018 0.654
LIG_SH3_3 192 198 PF00018 0.573
LIG_SH3_3 2 8 PF00018 0.596
LIG_SH3_3 397 403 PF00018 0.562
LIG_SH3_3 441 447 PF00018 0.679
LIG_SH3_3 861 867 PF00018 0.372
LIG_SUMO_SIM_anti_2 516 522 PF11976 0.513
LIG_SUMO_SIM_par_1 273 279 PF11976 0.499
LIG_SUMO_SIM_par_1 425 432 PF11976 0.512
LIG_TRAF2_1 134 137 PF00917 0.515
LIG_TRAF2_1 341 344 PF00917 0.607
LIG_TRAF2_1 408 411 PF00917 0.463
LIG_TRAF2_1 855 858 PF00917 0.304
LIG_TYR_ITIM 270 275 PF00017 0.583
LIG_TYR_ITIM 766 771 PF00017 0.304
LIG_TYR_ITIM 871 876 PF00017 0.402
LIG_Vh1_VBS_1 349 367 PF01044 0.452
LIG_WW_2 107 110 PF00397 0.648
MOD_CK1_1 111 117 PF00069 0.665
MOD_CK1_1 121 127 PF00069 0.461
MOD_CK1_1 13 19 PF00069 0.624
MOD_CK1_1 174 180 PF00069 0.403
MOD_CK1_1 25 31 PF00069 0.626
MOD_CK1_1 255 261 PF00069 0.697
MOD_CK1_1 339 345 PF00069 0.589
MOD_CK1_1 42 48 PF00069 0.533
MOD_CK1_1 49 55 PF00069 0.588
MOD_CK1_1 494 500 PF00069 0.699
MOD_CK1_1 516 522 PF00069 0.583
MOD_CK1_1 579 585 PF00069 0.615
MOD_CK1_1 58 64 PF00069 0.647
MOD_CK1_1 599 605 PF00069 0.612
MOD_CK1_1 623 629 PF00069 0.438
MOD_CK1_1 696 702 PF00069 0.342
MOD_CK1_1 93 99 PF00069 0.636
MOD_CK2_1 131 137 PF00069 0.520
MOD_CK2_1 254 260 PF00069 0.620
MOD_CK2_1 261 267 PF00069 0.566
MOD_CK2_1 338 344 PF00069 0.601
MOD_CK2_1 429 435 PF00069 0.522
MOD_CK2_1 687 693 PF00069 0.413
MOD_CK2_1 743 749 PF00069 0.325
MOD_CK2_1 872 878 PF00069 0.338
MOD_GlcNHglycan 1 4 PF01048 0.797
MOD_GlcNHglycan 110 113 PF01048 0.647
MOD_GlcNHglycan 139 142 PF01048 0.503
MOD_GlcNHglycan 173 176 PF01048 0.418
MOD_GlcNHglycan 205 208 PF01048 0.673
MOD_GlcNHglycan 216 219 PF01048 0.524
MOD_GlcNHglycan 242 245 PF01048 0.622
MOD_GlcNHglycan 246 249 PF01048 0.610
MOD_GlcNHglycan 254 257 PF01048 0.589
MOD_GlcNHglycan 45 48 PF01048 0.608
MOD_GlcNHglycan 482 485 PF01048 0.701
MOD_GlcNHglycan 491 494 PF01048 0.600
MOD_GlcNHglycan 498 501 PF01048 0.542
MOD_GlcNHglycan 515 518 PF01048 0.578
MOD_GlcNHglycan 57 60 PF01048 0.564
MOD_GlcNHglycan 578 581 PF01048 0.599
MOD_GlcNHglycan 590 593 PF01048 0.534
MOD_GlcNHglycan 603 606 PF01048 0.619
MOD_GlcNHglycan 614 617 PF01048 0.573
MOD_GlcNHglycan 645 648 PF01048 0.387
MOD_GlcNHglycan 679 682 PF01048 0.446
MOD_GlcNHglycan 695 698 PF01048 0.294
MOD_GlcNHglycan 95 98 PF01048 0.640
MOD_GSK3_1 110 117 PF00069 0.697
MOD_GSK3_1 118 125 PF00069 0.632
MOD_GSK3_1 127 134 PF00069 0.534
MOD_GSK3_1 193 200 PF00069 0.552
MOD_GSK3_1 224 231 PF00069 0.607
MOD_GSK3_1 240 247 PF00069 0.650
MOD_GSK3_1 250 257 PF00069 0.606
MOD_GSK3_1 312 319 PF00069 0.527
MOD_GSK3_1 35 42 PF00069 0.609
MOD_GSK3_1 364 371 PF00069 0.510
MOD_GSK3_1 45 52 PF00069 0.534
MOD_GSK3_1 501 508 PF00069 0.662
MOD_GSK3_1 54 61 PF00069 0.535
MOD_GSK3_1 584 591 PF00069 0.735
MOD_GSK3_1 596 603 PF00069 0.559
MOD_GSK3_1 677 684 PF00069 0.452
MOD_GSK3_1 9 16 PF00069 0.623
MOD_LATS_1 675 681 PF00433 0.455
MOD_N-GLC_1 13 18 PF02516 0.654
MOD_N-GLC_1 131 136 PF02516 0.496
MOD_N-GLC_1 261 266 PF02516 0.593
MOD_N-GLC_1 834 839 PF02516 0.304
MOD_NEK2_1 131 136 PF00069 0.472
MOD_NEK2_1 157 162 PF00069 0.427
MOD_NEK2_1 193 198 PF00069 0.564
MOD_NEK2_1 254 259 PF00069 0.600
MOD_NEK2_1 510 515 PF00069 0.558
MOD_NEK2_1 546 551 PF00069 0.493
MOD_NEK2_1 588 593 PF00069 0.649
MOD_NEK2_1 596 601 PF00069 0.562
MOD_NEK2_1 653 658 PF00069 0.432
MOD_NEK2_1 668 673 PF00069 0.298
MOD_NEK2_1 695 700 PF00069 0.429
MOD_NEK2_1 804 809 PF00069 0.359
MOD_PIKK_1 234 240 PF00454 0.548
MOD_PIKK_1 276 282 PF00454 0.518
MOD_PIKK_1 291 297 PF00454 0.321
MOD_PIKK_1 302 308 PF00454 0.411
MOD_PIKK_1 369 375 PF00454 0.422
MOD_PIKK_1 505 511 PF00454 0.790
MOD_PKA_1 902 908 PF00069 0.422
MOD_PKA_2 224 230 PF00069 0.599
MOD_PKA_2 353 359 PF00069 0.576
MOD_PKA_2 369 375 PF00069 0.335
MOD_PKA_2 523 529 PF00069 0.570
MOD_PKA_2 597 603 PF00069 0.620
MOD_PKA_2 687 693 PF00069 0.413
MOD_PKA_2 902 908 PF00069 0.422
MOD_PKB_1 458 466 PF00069 0.647
MOD_PKB_1 69 77 PF00069 0.636
MOD_Plk_1 131 137 PF00069 0.498
MOD_Plk_1 157 163 PF00069 0.415
MOD_Plk_1 760 766 PF00069 0.284
MOD_Plk_4 316 322 PF00069 0.518
MOD_Plk_4 422 428 PF00069 0.557
MOD_Plk_4 429 435 PF00069 0.537
MOD_Plk_4 516 522 PF00069 0.627
MOD_Plk_4 705 711 PF00069 0.366
MOD_Plk_4 760 766 PF00069 0.304
MOD_Plk_4 902 908 PF00069 0.422
MOD_ProDKin_1 1 7 PF00069 0.605
MOD_ProDKin_1 114 120 PF00069 0.605
MOD_ProDKin_1 22 28 PF00069 0.692
MOD_ProDKin_1 46 52 PF00069 0.631
MOD_ProDKin_1 501 507 PF00069 0.643
MOD_ProDKin_1 579 585 PF00069 0.501
MOD_ProDKin_1 623 629 PF00069 0.431
MOD_ProDKin_1 794 800 PF00069 0.377
MOD_ProDKin_1 98 104 PF00069 0.699
MOD_SUMO_for_1 676 679 PF00179 0.390
MOD_SUMO_rev_2 740 748 PF00179 0.369
MOD_SUMO_rev_2 749 757 PF00179 0.285
MOD_SUMO_rev_2 814 821 PF00179 0.399
MOD_SUMO_rev_2 857 862 PF00179 0.398
TRG_DiLeu_BaEn_1 858 863 PF01217 0.376
TRG_DiLeu_BaLyEn_6 179 184 PF01217 0.388
TRG_ENDOCYTIC_2 161 164 PF00928 0.428
TRG_ENDOCYTIC_2 181 184 PF00928 0.423
TRG_ENDOCYTIC_2 187 190 PF00928 0.524
TRG_ENDOCYTIC_2 272 275 PF00928 0.571
TRG_ENDOCYTIC_2 412 415 PF00928 0.530
TRG_ENDOCYTIC_2 707 710 PF00928 0.365
TRG_ENDOCYTIC_2 739 742 PF00928 0.304
TRG_ENDOCYTIC_2 75 78 PF00928 0.712
TRG_ENDOCYTIC_2 768 771 PF00928 0.304
TRG_ENDOCYTIC_2 873 876 PF00928 0.337
TRG_ER_diArg_1 321 324 PF00400 0.471
TRG_ER_diArg_1 395 397 PF00400 0.562
TRG_ER_diArg_1 451 454 PF00400 0.642
TRG_ER_diArg_1 457 460 PF00400 0.647
TRG_ER_diArg_1 69 72 PF00400 0.671
TRG_ER_diArg_1 839 842 PF00400 0.304
TRG_ER_diArg_1 883 885 PF00400 0.571
TRG_ER_diArg_1 901 903 PF00400 0.341
TRG_Pf-PMV_PEXEL_1 302 306 PF00026 0.349
TRG_Pf-PMV_PEXEL_1 323 327 PF00026 0.529

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1HU62 Leptomonas seymouri 56% 99%
A0A3S5H5H6 Leishmania donovani 93% 100%
A4H487 Leishmania braziliensis 81% 100%
A4HSG3 Leishmania infantum 93% 100%
E9AKE7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 91% 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