LeishMANIAdb
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Protein kinase domain-containing protein

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

Quick info

Protein:
Protein kinase domain-containing protein
Gene product:
protein lipid droplet kinase (LDK)
Species:
Leishmania major
UniProt:
Q4Q866_LEIMA
TriTrypDb:
LmjF.28.2000 , LMJLV39_280028000 , LMJSD75_280027600 *
Length:
877

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:0005811 lipid droplet 5 2
GO:0016020 membrane 2 2
GO:0043226 organelle 2 2
GO:0043228 non-membrane-bounded organelle 3 2
GO:0043229 intracellular organelle 3 2
GO:0043232 intracellular non-membrane-bounded organelle 4 2
GO:0110165 cellular anatomical entity 1 2

Expansion

Sequence features

Q4Q866
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q866

Function

Biological processes
Term Name Level Count
GO:0006468 protein phosphorylation 5 7
GO:0006793 phosphorus metabolic process 3 7
GO:0006796 phosphate-containing compound metabolic process 4 7
GO:0006807 nitrogen compound metabolic process 2 7
GO:0006996 organelle organization 4 2
GO:0007165 signal transduction 2 2
GO:0008152 metabolic process 1 7
GO:0009987 cellular process 1 7
GO:0016043 cellular component organization 3 2
GO:0016310 phosphorylation 5 7
GO:0019538 protein metabolic process 3 7
GO:0034389 lipid droplet organization 5 2
GO:0036211 protein modification process 4 7
GO:0042592 homeostatic process 3 2
GO:0043170 macromolecule metabolic process 3 7
GO:0043412 macromolecule modification 4 7
GO:0044237 cellular metabolic process 2 7
GO:0044238 primary metabolic process 2 7
GO:0046777 protein autophosphorylation 6 2
GO:0048878 chemical homeostasis 4 2
GO:0050789 regulation of biological process 2 2
GO:0050794 regulation of cellular process 3 2
GO:0055088 lipid homeostasis 5 2
GO:0065007 biological regulation 1 2
GO:0065008 regulation of biological quality 2 2
GO:0071704 organic substance metabolic process 2 7
GO:0071840 cellular component organization or biogenesis 2 2
GO:1901564 organonitrogen compound metabolic process 3 7
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 7
GO:0003824 catalytic activity 1 7
GO:0004672 protein kinase activity 3 7
GO:0004674 protein serine/threonine kinase activity 4 2
GO:0005488 binding 1 7
GO:0005524 ATP binding 5 7
GO:0016301 kinase activity 4 7
GO:0016740 transferase activity 2 7
GO:0016757 glycosyltransferase activity 3 5
GO:0016772 transferase activity, transferring phosphorus-containing groups 3 7
GO:0016773 phosphotransferase activity, alcohol group as acceptor 4 7
GO:0017076 purine nucleotide binding 4 7
GO:0030554 adenyl nucleotide binding 5 7
GO:0032553 ribonucleotide binding 3 7
GO:0032555 purine ribonucleotide binding 4 7
GO:0032559 adenyl ribonucleotide binding 5 7
GO:0035639 purine ribonucleoside triphosphate binding 4 7
GO:0036094 small molecule binding 2 7
GO:0043167 ion binding 2 7
GO:0043168 anion binding 3 7
GO:0097159 organic cyclic compound binding 2 7
GO:0097367 carbohydrate derivative binding 2 7
GO:0140096 catalytic activity, acting on a protein 2 7
GO:1901265 nucleoside phosphate binding 3 7
GO:1901363 heterocyclic compound binding 2 7
GO:0004645 1,4-alpha-oligoglucan phosphorylase activity 5 2
GO:0016758 hexosyltransferase activity 4 2
GO:0102250 linear malto-oligosaccharide phosphorylase activity 5 2
GO:0102499 SHG alpha-glucan phosphorylase activity 5 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 122 126 PF00656 0.516
CLV_C14_Caspase3-7 391 395 PF00656 0.699
CLV_C14_Caspase3-7 476 480 PF00656 0.628
CLV_NRD_NRD_1 106 108 PF00675 0.316
CLV_NRD_NRD_1 218 220 PF00675 0.269
CLV_NRD_NRD_1 396 398 PF00675 0.503
CLV_NRD_NRD_1 524 526 PF00675 0.222
CLV_NRD_NRD_1 585 587 PF00675 0.530
CLV_NRD_NRD_1 678 680 PF00675 0.531
CLV_NRD_NRD_1 707 709 PF00675 0.503
CLV_NRD_NRD_1 740 742 PF00675 0.487
CLV_NRD_NRD_1 771 773 PF00675 0.537
CLV_NRD_NRD_1 775 777 PF00675 0.502
CLV_PCSK_FUR_1 104 108 PF00082 0.316
CLV_PCSK_KEX2_1 106 108 PF00082 0.316
CLV_PCSK_KEX2_1 396 398 PF00082 0.508
CLV_PCSK_KEX2_1 524 526 PF00082 0.222
CLV_PCSK_KEX2_1 560 562 PF00082 0.380
CLV_PCSK_KEX2_1 585 587 PF00082 0.479
CLV_PCSK_KEX2_1 707 709 PF00082 0.518
CLV_PCSK_KEX2_1 739 741 PF00082 0.505
CLV_PCSK_KEX2_1 775 777 PF00082 0.504
CLV_PCSK_PC1ET2_1 560 562 PF00082 0.380
CLV_PCSK_PC1ET2_1 739 741 PF00082 0.505
CLV_PCSK_PC7_1 556 562 PF00082 0.448
CLV_PCSK_SKI1_1 145 149 PF00082 0.269
CLV_PCSK_SKI1_1 162 166 PF00082 0.269
CLV_PCSK_SKI1_1 177 181 PF00082 0.269
CLV_PCSK_SKI1_1 288 292 PF00082 0.269
CLV_PCSK_SKI1_1 400 404 PF00082 0.567
CLV_PCSK_SKI1_1 47 51 PF00082 0.284
CLV_PCSK_SKI1_1 556 560 PF00082 0.369
CLV_PCSK_SKI1_1 803 807 PF00082 0.499
DEG_APCC_DBOX_1 106 114 PF00400 0.460
DEG_SCF_FBW7_1 15 21 PF00400 0.500
DEG_SPOP_SBC_1 627 631 PF00917 0.616
DOC_CKS1_1 15 20 PF01111 0.500
DOC_CKS1_1 580 585 PF01111 0.627
DOC_CYCLIN_RxL_1 139 152 PF00134 0.469
DOC_CYCLIN_RxL_1 173 182 PF00134 0.484
DOC_CYCLIN_yCln2_LP_2 320 323 PF00134 0.636
DOC_MAPK_gen_1 162 171 PF00069 0.469
DOC_MAPK_gen_1 173 180 PF00069 0.469
DOC_MAPK_gen_1 396 407 PF00069 0.707
DOC_MAPK_gen_1 524 534 PF00069 0.466
DOC_MAPK_gen_1 560 568 PF00069 0.569
DOC_MAPK_gen_1 570 578 PF00069 0.565
DOC_MAPK_MEF2A_6 560 568 PF00069 0.583
DOC_MAPK_NFAT4_5 561 569 PF00069 0.547
DOC_MAPK_RevD_3 546 561 PF00069 0.284
DOC_PP2B_LxvP_1 320 323 PF13499 0.636
DOC_PP2B_LxvP_1 566 569 PF13499 0.572
DOC_PP2B_LxvP_1 731 734 PF13499 0.708
DOC_USP7_MATH_1 18 22 PF00917 0.500
DOC_USP7_MATH_1 186 190 PF00917 0.484
DOC_USP7_MATH_1 308 312 PF00917 0.697
DOC_USP7_MATH_1 323 327 PF00917 0.601
DOC_USP7_MATH_1 344 348 PF00917 0.703
DOC_USP7_MATH_1 429 433 PF00917 0.717
DOC_USP7_MATH_1 606 610 PF00917 0.674
DOC_USP7_MATH_1 692 696 PF00917 0.743
DOC_USP7_MATH_1 734 738 PF00917 0.822
DOC_USP7_MATH_1 784 788 PF00917 0.710
DOC_USP7_MATH_1 798 802 PF00917 0.638
DOC_USP7_MATH_1 811 815 PF00917 0.667
DOC_USP7_UBL2_3 42 46 PF12436 0.469
DOC_USP7_UBL2_3 80 84 PF12436 0.483
DOC_WW_Pin1_4 129 134 PF00397 0.500
DOC_WW_Pin1_4 14 19 PF00397 0.463
DOC_WW_Pin1_4 300 305 PF00397 0.684
DOC_WW_Pin1_4 405 410 PF00397 0.727
DOC_WW_Pin1_4 425 430 PF00397 0.627
DOC_WW_Pin1_4 579 584 PF00397 0.617
DOC_WW_Pin1_4 602 607 PF00397 0.638
DOC_WW_Pin1_4 628 633 PF00397 0.668
DOC_WW_Pin1_4 670 675 PF00397 0.652
DOC_WW_Pin1_4 68 73 PF00397 0.469
DOC_WW_Pin1_4 687 692 PF00397 0.831
DOC_WW_Pin1_4 746 751 PF00397 0.715
DOC_WW_Pin1_4 777 782 PF00397 0.730
DOC_WW_Pin1_4 807 812 PF00397 0.684
DOC_WW_Pin1_4 846 851 PF00397 0.677
LIG_14-3-3_CanoR_1 177 185 PF00244 0.469
LIG_14-3-3_CanoR_1 284 288 PF00244 0.469
LIG_14-3-3_CanoR_1 387 393 PF00244 0.721
LIG_14-3-3_CanoR_1 396 404 PF00244 0.658
LIG_14-3-3_CanoR_1 442 452 PF00244 0.624
LIG_14-3-3_CanoR_1 525 531 PF00244 0.364
LIG_14-3-3_CanoR_1 585 591 PF00244 0.670
LIG_14-3-3_CanoR_1 650 654 PF00244 0.625
LIG_14-3-3_CanoR_1 707 712 PF00244 0.719
LIG_14-3-3_CanoR_1 775 783 PF00244 0.698
LIG_14-3-3_CanoR_1 803 812 PF00244 0.679
LIG_Actin_WH2_2 569 587 PF00022 0.549
LIG_APCC_ABBAyCdc20_2 157 163 PF00400 0.516
LIG_BIR_II_1 1 5 PF00653 0.513
LIG_BRCT_BRCA1_1 20 24 PF00533 0.516
LIG_BRCT_BRCA1_1 431 435 PF00533 0.738
LIG_eIF4E_1 142 148 PF01652 0.514
LIG_eIF4E_1 204 210 PF01652 0.469
LIG_FHA_1 1 7 PF00498 0.580
LIG_FHA_1 174 180 PF00498 0.469
LIG_FHA_1 256 262 PF00498 0.582
LIG_FHA_1 36 42 PF00498 0.489
LIG_FHA_1 53 59 PF00498 0.429
LIG_FHA_1 628 634 PF00498 0.620
LIG_FHA_1 716 722 PF00498 0.634
LIG_FHA_1 73 79 PF00498 0.383
LIG_FHA_1 794 800 PF00498 0.726
LIG_FHA_2 295 301 PF00498 0.535
LIG_FHA_2 461 467 PF00498 0.654
LIG_FHA_2 96 102 PF00498 0.469
LIG_GBD_Chelix_1 551 559 PF00786 0.369
LIG_Integrin_RGD_1 244 246 PF01839 0.316
LIG_LIR_Apic_2 201 207 PF02991 0.469
LIG_LIR_Apic_2 256 262 PF02991 0.469
LIG_LIR_Gen_1 229 239 PF02991 0.469
LIG_LIR_Gen_1 357 368 PF02991 0.691
LIG_LIR_Gen_1 458 465 PF02991 0.617
LIG_LIR_Gen_1 484 495 PF02991 0.699
LIG_LIR_Gen_1 574 583 PF02991 0.605
LIG_LIR_Nem_3 132 137 PF02991 0.534
LIG_LIR_Nem_3 21 27 PF02991 0.516
LIG_LIR_Nem_3 229 234 PF02991 0.469
LIG_LIR_Nem_3 357 363 PF02991 0.755
LIG_LIR_Nem_3 458 462 PF02991 0.585
LIG_LIR_Nem_3 574 578 PF02991 0.609
LIG_LIR_Nem_3 866 871 PF02991 0.689
LIG_Pex14_2 24 28 PF04695 0.617
LIG_SH2_CRK 137 141 PF00017 0.469
LIG_SH2_CRK 231 235 PF00017 0.502
LIG_SH2_CRK 259 263 PF00017 0.484
LIG_SH2_CRK 360 364 PF00017 0.684
LIG_SH2_CRK 581 585 PF00017 0.647
LIG_SH2_SRC 840 843 PF00017 0.672
LIG_SH2_STAP1 39 43 PF00017 0.469
LIG_SH2_STAP1 722 726 PF00017 0.691
LIG_SH2_STAT3 143 146 PF00017 0.516
LIG_SH2_STAT5 143 146 PF00017 0.516
LIG_SH2_STAT5 204 207 PF00017 0.469
LIG_SH2_STAT5 510 513 PF00017 0.689
LIG_SH2_STAT5 575 578 PF00017 0.602
LIG_SH2_STAT5 581 584 PF00017 0.647
LIG_SH2_STAT5 73 76 PF00017 0.469
LIG_SH2_STAT5 840 843 PF00017 0.660
LIG_SH2_STAT5 88 91 PF00017 0.469
LIG_SH3_3 130 136 PF00018 0.472
LIG_SH3_3 316 322 PF00018 0.644
LIG_SH3_3 406 412 PF00018 0.692
LIG_SH3_3 688 694 PF00018 0.785
LIG_SH3_3 698 704 PF00018 0.674
LIG_SH3_3 778 784 PF00018 0.727
LIG_SH3_3 785 791 PF00018 0.718
LIG_SH3_3 847 853 PF00018 0.678
LIG_SH3_CIN85_PxpxPR_1 674 679 PF14604 0.700
LIG_SUMO_SIM_anti_2 98 105 PF11976 0.455
LIG_SUMO_SIM_par_1 147 152 PF11976 0.469
LIG_SUMO_SIM_par_1 248 258 PF11976 0.463
LIG_SUMO_SIM_par_1 403 408 PF11976 0.728
LIG_SxIP_EBH_1 626 639 PF03271 0.650
LIG_TRAF2_1 448 451 PF00917 0.704
LIG_UBA3_1 563 570 PF00899 0.531
LIG_WRC_WIRS_1 465 470 PF05994 0.603
LIG_WRC_WIRS_1 575 580 PF05994 0.585
MOD_CDK_SPxK_1 579 585 PF00069 0.615
MOD_CDK_SPxK_1 807 813 PF00069 0.704
MOD_CDK_SPxxK_3 579 586 PF00069 0.670
MOD_CK1_1 307 313 PF00069 0.679
MOD_CK1_1 31 37 PF00069 0.475
MOD_CK1_1 347 353 PF00069 0.691
MOD_CK1_1 370 376 PF00069 0.696
MOD_CK1_1 379 385 PF00069 0.718
MOD_CK1_1 395 401 PF00069 0.653
MOD_CK1_1 408 414 PF00069 0.634
MOD_CK1_1 443 449 PF00069 0.718
MOD_CK1_1 461 467 PF00069 0.551
MOD_CK1_1 508 514 PF00069 0.654
MOD_CK1_1 605 611 PF00069 0.681
MOD_CK1_1 686 692 PF00069 0.822
MOD_CK1_1 695 701 PF00069 0.688
MOD_CK1_1 767 773 PF00069 0.808
MOD_CK1_1 777 783 PF00069 0.679
MOD_CK1_1 793 799 PF00069 0.657
MOD_CK1_1 801 807 PF00069 0.765
MOD_CK1_1 830 836 PF00069 0.688
MOD_CK2_1 294 300 PF00069 0.597
MOD_CK2_1 323 329 PF00069 0.654
MOD_CK2_1 395 401 PF00069 0.698
MOD_CK2_1 444 450 PF00069 0.663
MOD_CK2_1 460 466 PF00069 0.588
MOD_CK2_1 468 474 PF00069 0.625
MOD_CK2_1 477 483 PF00069 0.629
MOD_CK2_1 714 720 PF00069 0.703
MOD_Cter_Amidation 217 220 PF01082 0.295
MOD_Cter_Amidation 522 525 PF01082 0.396
MOD_GlcNHglycan 129 132 PF01048 0.290
MOD_GlcNHglycan 151 154 PF01048 0.284
MOD_GlcNHglycan 20 23 PF01048 0.376
MOD_GlcNHglycan 304 307 PF01048 0.497
MOD_GlcNHglycan 310 313 PF01048 0.481
MOD_GlcNHglycan 315 318 PF01048 0.433
MOD_GlcNHglycan 325 328 PF01048 0.413
MOD_GlcNHglycan 34 37 PF01048 0.260
MOD_GlcNHglycan 373 376 PF01048 0.489
MOD_GlcNHglycan 446 449 PF01048 0.454
MOD_GlcNHglycan 521 524 PF01048 0.462
MOD_GlcNHglycan 591 594 PF01048 0.494
MOD_GlcNHglycan 608 611 PF01048 0.482
MOD_GlcNHglycan 621 625 PF01048 0.596
MOD_GlcNHglycan 635 638 PF01048 0.435
MOD_GlcNHglycan 727 731 PF01048 0.543
MOD_GlcNHglycan 792 795 PF01048 0.465
MOD_GlcNHglycan 806 809 PF01048 0.514
MOD_GlcNHglycan 832 835 PF01048 0.491
MOD_GlcNHglycan 836 840 PF01048 0.488
MOD_GSK3_1 115 122 PF00069 0.509
MOD_GSK3_1 123 130 PF00069 0.469
MOD_GSK3_1 14 21 PF00069 0.564
MOD_GSK3_1 279 286 PF00069 0.422
MOD_GSK3_1 28 35 PF00069 0.407
MOD_GSK3_1 300 307 PF00069 0.649
MOD_GSK3_1 323 330 PF00069 0.823
MOD_GSK3_1 332 339 PF00069 0.736
MOD_GSK3_1 366 373 PF00069 0.696
MOD_GSK3_1 375 382 PF00069 0.745
MOD_GSK3_1 388 395 PF00069 0.661
MOD_GSK3_1 425 432 PF00069 0.755
MOD_GSK3_1 440 447 PF00069 0.621
MOD_GSK3_1 457 464 PF00069 0.567
MOD_GSK3_1 477 484 PF00069 0.667
MOD_GSK3_1 501 508 PF00069 0.669
MOD_GSK3_1 594 601 PF00069 0.640
MOD_GSK3_1 602 609 PF00069 0.679
MOD_GSK3_1 679 686 PF00069 0.823
MOD_GSK3_1 68 75 PF00069 0.469
MOD_GSK3_1 695 702 PF00069 0.651
MOD_GSK3_1 703 710 PF00069 0.669
MOD_GSK3_1 793 800 PF00069 0.731
MOD_GSK3_1 803 810 PF00069 0.786
MOD_LATS_1 681 687 PF00433 0.713
MOD_N-GLC_1 376 381 PF02516 0.530
MOD_N-GLC_1 501 506 PF02516 0.507
MOD_NEK2_1 113 118 PF00069 0.463
MOD_NEK2_1 127 132 PF00069 0.489
MOD_NEK2_1 149 154 PF00069 0.469
MOD_NEK2_1 359 364 PF00069 0.636
MOD_NEK2_1 368 373 PF00069 0.679
MOD_NEK2_1 376 381 PF00069 0.696
MOD_NEK2_1 392 397 PF00069 0.632
MOD_NEK2_1 505 510 PF00069 0.658
MOD_NEK2_1 532 537 PF00069 0.455
MOD_NEK2_1 584 589 PF00069 0.619
MOD_NEK2_1 598 603 PF00069 0.783
MOD_NEK2_1 649 654 PF00069 0.671
MOD_NEK2_1 835 840 PF00069 0.695
MOD_NEK2_2 198 203 PF00069 0.469
MOD_NEK2_2 226 231 PF00069 0.504
MOD_NEK2_2 798 803 PF00069 0.700
MOD_PIKK_1 279 285 PF00454 0.422
MOD_PIKK_1 380 386 PF00454 0.773
MOD_PIKK_1 699 705 PF00454 0.819
MOD_PIKK_1 817 823 PF00454 0.703
MOD_PKA_1 679 685 PF00069 0.715
MOD_PKA_1 707 713 PF00069 0.720
MOD_PKA_1 775 781 PF00069 0.686
MOD_PKA_2 240 246 PF00069 0.455
MOD_PKA_2 28 34 PF00069 0.516
MOD_PKA_2 283 289 PF00069 0.469
MOD_PKA_2 388 394 PF00069 0.722
MOD_PKA_2 395 401 PF00069 0.668
MOD_PKA_2 441 447 PF00069 0.705
MOD_PKA_2 526 532 PF00069 0.364
MOD_PKA_2 584 590 PF00069 0.603
MOD_PKA_2 649 655 PF00069 0.664
MOD_PKA_2 707 713 PF00069 0.720
MOD_PKA_2 774 780 PF00069 0.708
MOD_PKB_1 762 770 PF00069 0.794
MOD_Plk_1 254 260 PF00069 0.516
MOD_Plk_1 376 382 PF00069 0.721
MOD_Plk_1 457 463 PF00069 0.626
MOD_Plk_1 481 487 PF00069 0.666
MOD_Plk_1 501 507 PF00069 0.614
MOD_Plk_1 683 689 PF00069 0.741
MOD_Plk_1 726 732 PF00069 0.682
MOD_Plk_1 767 773 PF00069 0.758
MOD_Plk_1 835 841 PF00069 0.656
MOD_Plk_2-3 212 218 PF00069 0.516
MOD_Plk_2-3 336 342 PF00069 0.680
MOD_Plk_2-3 95 101 PF00069 0.469
MOD_Plk_4 119 125 PF00069 0.484
MOD_Plk_4 186 192 PF00069 0.467
MOD_Plk_4 23 29 PF00069 0.504
MOD_Plk_4 344 350 PF00069 0.644
MOD_Plk_4 464 470 PF00069 0.591
MOD_Plk_4 649 655 PF00069 0.671
MOD_Plk_4 95 101 PF00069 0.469
MOD_ProDKin_1 129 135 PF00069 0.500
MOD_ProDKin_1 14 20 PF00069 0.463
MOD_ProDKin_1 300 306 PF00069 0.685
MOD_ProDKin_1 405 411 PF00069 0.726
MOD_ProDKin_1 425 431 PF00069 0.627
MOD_ProDKin_1 579 585 PF00069 0.621
MOD_ProDKin_1 602 608 PF00069 0.637
MOD_ProDKin_1 628 634 PF00069 0.666
MOD_ProDKin_1 670 676 PF00069 0.650
MOD_ProDKin_1 68 74 PF00069 0.469
MOD_ProDKin_1 687 693 PF00069 0.831
MOD_ProDKin_1 746 752 PF00069 0.716
MOD_ProDKin_1 777 783 PF00069 0.729
MOD_ProDKin_1 807 813 PF00069 0.686
MOD_ProDKin_1 846 852 PF00069 0.677
MOD_SUMO_for_1 164 167 PF00179 0.469
MOD_SUMO_for_1 448 451 PF00179 0.673
TRG_DiLeu_BaEn_1 95 100 PF01217 0.469
TRG_DiLeu_BaLyEn_6 174 179 PF01217 0.484
TRG_ENDOCYTIC_2 137 140 PF00928 0.578
TRG_ENDOCYTIC_2 231 234 PF00928 0.469
TRG_ENDOCYTIC_2 360 363 PF00928 0.757
TRG_ENDOCYTIC_2 575 578 PF00928 0.602
TRG_ENDOCYTIC_2 581 584 PF00928 0.647
TRG_ENDOCYTIC_2 87 90 PF00928 0.478
TRG_ER_diArg_1 139 142 PF00400 0.484
TRG_ER_diArg_1 175 178 PF00400 0.472
TRG_ER_diArg_1 386 389 PF00400 0.740
TRG_ER_diArg_1 439 442 PF00400 0.649
TRG_ER_diArg_1 524 527 PF00400 0.469
TRG_ER_diArg_1 584 586 PF00400 0.685
TRG_Pf-PMV_PEXEL_1 177 182 PF00026 0.284
TRG_Pf-PMV_PEXEL_1 561 565 PF00026 0.370

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1PD19 Leptomonas seymouri 43% 98%
A0A3Q8IE08 Leishmania donovani 90% 100%
A4HGQ4 Leishmania braziliensis 67% 100%
A4I3S8 Leishmania infantum 91% 100%
E9B020 Leishmania mexicana (strain MHOM/GT/2001/U1103) 83% 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