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 kinase, putative
Species:
Leishmania braziliensis
UniProt:
A4H7R1_LEIBR
TriTrypDb:
LbrM.14.1060 , LBRM2903_140016300
Length:
1027

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: 10
NetGPI no yes: 0, no: 10
Cellular components
Term Name Level Count
GO:0005737 cytoplasm 2 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A4H7R1
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4H7R1

Function

Biological processes
Term Name Level Count
GO:0006468 protein phosphorylation 5 11
GO:0006793 phosphorus metabolic process 3 11
GO:0006796 phosphate-containing compound metabolic process 4 11
GO:0006807 nitrogen compound metabolic process 2 11
GO:0008152 metabolic process 1 11
GO:0009987 cellular process 1 11
GO:0016310 phosphorylation 5 11
GO:0019538 protein metabolic process 3 11
GO:0036211 protein modification process 4 11
GO:0043170 macromolecule metabolic process 3 11
GO:0043412 macromolecule modification 4 11
GO:0044237 cellular metabolic process 2 11
GO:0044238 primary metabolic process 2 11
GO:0071704 organic substance metabolic process 2 11
GO:1901564 organonitrogen compound metabolic process 3 11
GO:0018105 peptidyl-serine phosphorylation 6 1
GO:0018107 peptidyl-threonine phosphorylation 6 1
GO:0018193 peptidyl-amino acid modification 5 1
GO:0018209 peptidyl-serine modification 6 1
GO:0018210 peptidyl-threonine modification 6 1
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 11
GO:0003824 catalytic activity 1 11
GO:0004672 protein kinase activity 3 11
GO:0005488 binding 1 11
GO:0005524 ATP binding 5 11
GO:0016301 kinase activity 4 11
GO:0016740 transferase activity 2 11
GO:0016772 transferase activity, transferring phosphorus-containing groups 3 11
GO:0016773 phosphotransferase activity, alcohol group as acceptor 4 11
GO:0017076 purine nucleotide binding 4 11
GO:0030554 adenyl nucleotide binding 5 11
GO:0032553 ribonucleotide binding 3 11
GO:0032555 purine ribonucleotide binding 4 11
GO:0032559 adenyl ribonucleotide binding 5 11
GO:0035639 purine ribonucleoside triphosphate binding 4 11
GO:0036094 small molecule binding 2 11
GO:0043167 ion binding 2 11
GO:0043168 anion binding 3 11
GO:0097159 organic cyclic compound binding 2 11
GO:0097367 carbohydrate derivative binding 2 11
GO:0140096 catalytic activity, acting on a protein 2 11
GO:1901265 nucleoside phosphate binding 3 11
GO:1901363 heterocyclic compound binding 2 11
GO:0004674 protein serine/threonine kinase activity 4 1
GO:0004713 protein tyrosine kinase activity 4 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 166 170 PF00656 0.798
CLV_C14_Caspase3-7 37 41 PF00656 0.659
CLV_C14_Caspase3-7 398 402 PF00656 0.783
CLV_C14_Caspase3-7 61 65 PF00656 0.707
CLV_C14_Caspase3-7 622 626 PF00656 0.671
CLV_C14_Caspase3-7 629 633 PF00656 0.718
CLV_NRD_NRD_1 133 135 PF00675 0.636
CLV_NRD_NRD_1 322 324 PF00675 0.815
CLV_NRD_NRD_1 375 377 PF00675 0.725
CLV_NRD_NRD_1 534 536 PF00675 0.572
CLV_NRD_NRD_1 671 673 PF00675 0.765
CLV_NRD_NRD_1 686 688 PF00675 0.610
CLV_NRD_NRD_1 897 899 PF00675 0.355
CLV_NRD_NRD_1 959 961 PF00675 0.441
CLV_PCSK_KEX2_1 1009 1011 PF00082 0.355
CLV_PCSK_KEX2_1 132 134 PF00082 0.639
CLV_PCSK_KEX2_1 20 22 PF00082 0.711
CLV_PCSK_KEX2_1 321 323 PF00082 0.823
CLV_PCSK_KEX2_1 375 377 PF00082 0.725
CLV_PCSK_KEX2_1 484 486 PF00082 0.725
CLV_PCSK_KEX2_1 534 536 PF00082 0.569
CLV_PCSK_KEX2_1 669 671 PF00082 0.746
CLV_PCSK_KEX2_1 688 690 PF00082 0.519
CLV_PCSK_KEX2_1 897 899 PF00082 0.355
CLV_PCSK_PC1ET2_1 1009 1011 PF00082 0.355
CLV_PCSK_PC1ET2_1 20 22 PF00082 0.664
CLV_PCSK_PC1ET2_1 484 486 PF00082 0.715
CLV_PCSK_PC1ET2_1 669 671 PF00082 0.746
CLV_PCSK_PC1ET2_1 688 690 PF00082 0.519
CLV_PCSK_SKI1_1 1023 1027 PF00082 0.428
CLV_PCSK_SKI1_1 122 126 PF00082 0.537
CLV_PCSK_SKI1_1 168 172 PF00082 0.686
CLV_PCSK_SKI1_1 24 28 PF00082 0.688
CLV_PCSK_SKI1_1 502 506 PF00082 0.741
CLV_PCSK_SKI1_1 521 525 PF00082 0.460
CLV_PCSK_SKI1_1 689 693 PF00082 0.539
CLV_PCSK_SKI1_1 706 710 PF00082 0.209
CLV_PCSK_SKI1_1 717 721 PF00082 0.324
CLV_PCSK_SKI1_1 779 783 PF00082 0.389
CLV_PCSK_SKI1_1 897 901 PF00082 0.335
CLV_Separin_Metazoa 751 755 PF03568 0.447
DEG_COP1_1 876 883 PF00400 0.335
DEG_SCF_FBW7_1 944 950 PF00400 0.447
DEG_SPOP_SBC_1 159 163 PF00917 0.631
DEG_SPOP_SBC_1 32 36 PF00917 0.721
DEG_SPOP_SBC_1 651 655 PF00917 0.512
DEG_SPOP_SBC_1 661 665 PF00917 0.480
DOC_CDC14_PxL_1 772 780 PF14671 0.355
DOC_CKS1_1 944 949 PF01111 0.335
DOC_MAPK_gen_1 839 848 PF00069 0.335
DOC_MAPK_HePTP_8 836 848 PF00069 0.335
DOC_MAPK_MEF2A_6 839 848 PF00069 0.335
DOC_PP1_RVXF_1 519 526 PF00149 0.596
DOC_PP1_RVXF_1 816 823 PF00149 0.335
DOC_PP4_FxxP_1 773 776 PF00568 0.355
DOC_USP7_MATH_1 157 161 PF00917 0.638
DOC_USP7_MATH_1 263 267 PF00917 0.700
DOC_USP7_MATH_1 28 32 PF00917 0.581
DOC_USP7_MATH_1 33 37 PF00917 0.588
DOC_USP7_MATH_1 379 383 PF00917 0.711
DOC_USP7_MATH_1 49 53 PF00917 0.680
DOC_USP7_MATH_1 496 500 PF00917 0.716
DOC_USP7_MATH_1 527 531 PF00917 0.449
DOC_USP7_MATH_1 651 655 PF00917 0.767
DOC_USP7_MATH_1 7 11 PF00917 0.611
DOC_USP7_MATH_1 87 91 PF00917 0.698
DOC_USP7_MATH_1 959 963 PF00917 0.358
DOC_USP7_UBL2_3 118 122 PF12436 0.545
DOC_USP7_UBL2_3 239 243 PF12436 0.690
DOC_USP7_UBL2_3 669 673 PF12436 0.773
DOC_WW_Pin1_4 192 197 PF00397 0.530
DOC_WW_Pin1_4 218 223 PF00397 0.771
DOC_WW_Pin1_4 321 326 PF00397 0.567
DOC_WW_Pin1_4 399 404 PF00397 0.803
DOC_WW_Pin1_4 508 513 PF00397 0.592
DOC_WW_Pin1_4 890 895 PF00397 0.447
DOC_WW_Pin1_4 943 948 PF00397 0.335
DOC_WW_Pin1_4 955 960 PF00397 0.327
DOC_WW_Pin1_4 964 969 PF00397 0.183
LIG_14-3-3_CanoR_1 1010 1017 PF00244 0.447
LIG_14-3-3_CanoR_1 141 145 PF00244 0.664
LIG_14-3-3_CanoR_1 30 38 PF00244 0.687
LIG_14-3-3_CanoR_1 392 399 PF00244 0.571
LIG_14-3-3_CanoR_1 546 552 PF00244 0.664
LIG_14-3-3_CanoR_1 717 722 PF00244 0.355
LIG_14-3-3_CanoR_1 904 913 PF00244 0.335
LIG_AP2alpha_2 561 563 PF02296 0.655
LIG_BIR_II_1 1 5 PF00653 0.737
LIG_BRCT_BRCA1_1 823 827 PF00533 0.335
LIG_EH1_1 584 592 PF00400 0.416
LIG_FHA_1 108 114 PF00498 0.547
LIG_FHA_1 133 139 PF00498 0.629
LIG_FHA_1 324 330 PF00498 0.819
LIG_FHA_1 33 39 PF00498 0.652
LIG_FHA_1 346 352 PF00498 0.635
LIG_FHA_1 372 378 PF00498 0.699
LIG_FHA_1 475 481 PF00498 0.515
LIG_FHA_1 551 557 PF00498 0.620
LIG_FHA_1 678 684 PF00498 0.492
LIG_FHA_1 748 754 PF00498 0.333
LIG_FHA_1 780 786 PF00498 0.381
LIG_FHA_1 868 874 PF00498 0.335
LIG_FHA_2 1010 1016 PF00498 0.451
LIG_FHA_2 161 167 PF00498 0.801
LIG_FHA_2 325 331 PF00498 0.730
LIG_FHA_2 35 41 PF00498 0.660
LIG_FHA_2 481 487 PF00498 0.597
LIG_FHA_2 563 569 PF00498 0.534
LIG_FHA_2 754 760 PF00498 0.447
LIG_FHA_2 877 883 PF00498 0.335
LIG_LIR_Apic_2 770 776 PF02991 0.355
LIG_LIR_Apic_2 838 844 PF02991 0.335
LIG_LIR_Gen_1 143 151 PF02991 0.601
LIG_LIR_Gen_1 489 500 PF02991 0.721
LIG_LIR_Gen_1 511 519 PF02991 0.582
LIG_LIR_Gen_1 522 532 PF02991 0.564
LIG_LIR_Gen_1 975 986 PF02991 0.370
LIG_LIR_Gen_1 992 1003 PF02991 0.239
LIG_LIR_Nem_3 143 147 PF02991 0.594
LIG_LIR_Nem_3 489 495 PF02991 0.631
LIG_LIR_Nem_3 511 516 PF02991 0.589
LIG_LIR_Nem_3 522 528 PF02991 0.587
LIG_LIR_Nem_3 570 576 PF02991 0.537
LIG_LIR_Nem_3 759 763 PF02991 0.335
LIG_LIR_Nem_3 769 775 PF02991 0.335
LIG_LIR_Nem_3 939 945 PF02991 0.338
LIG_LIR_Nem_3 975 981 PF02991 0.351
LIG_LIR_Nem_3 992 998 PF02991 0.271
LIG_MAD2 886 894 PF02301 0.335
LIG_NRBOX 717 723 PF00104 0.447
LIG_PDZ_Class_2 1022 1027 PF00595 0.610
LIG_Pex14_2 563 567 PF04695 0.644
LIG_Rb_pABgroove_1 456 464 PF01858 0.447
LIG_SH2_CRK 343 347 PF00017 0.637
LIG_SH2_CRK 439 443 PF00017 0.509
LIG_SH2_CRK 694 698 PF00017 0.447
LIG_SH2_CRK 945 949 PF00017 0.335
LIG_SH2_CRK 978 982 PF00017 0.335
LIG_SH2_GRB2like 909 912 PF00017 0.447
LIG_SH2_NCK_1 492 496 PF00017 0.726
LIG_SH2_NCK_1 585 589 PF00017 0.517
LIG_SH2_SRC 492 495 PF00017 0.701
LIG_SH2_SRC 585 588 PF00017 0.397
LIG_SH2_SRC 758 761 PF00017 0.335
LIG_SH2_SRC 791 794 PF00017 0.335
LIG_SH2_SRC 917 920 PF00017 0.447
LIG_SH2_STAP1 144 148 PF00017 0.626
LIG_SH2_STAP1 513 517 PF00017 0.667
LIG_SH2_STAP1 620 624 PF00017 0.769
LIG_SH2_STAP1 812 816 PF00017 0.447
LIG_SH2_STAT3 603 606 PF00017 0.539
LIG_SH2_STAT5 16 19 PF00017 0.530
LIG_SH2_STAT5 177 180 PF00017 0.542
LIG_SH2_STAT5 772 775 PF00017 0.335
LIG_SH2_STAT5 791 794 PF00017 0.335
LIG_SH2_STAT5 835 838 PF00017 0.335
LIG_SH2_STAT5 889 892 PF00017 0.335
LIG_SH2_STAT5 909 912 PF00017 0.422
LIG_SH2_STAT5 942 945 PF00017 0.339
LIG_SH3_1 400 406 PF00018 0.798
LIG_SH3_1 439 445 PF00018 0.518
LIG_SH3_1 571 577 PF00018 0.610
LIG_SH3_3 190 196 PF00018 0.542
LIG_SH3_3 400 406 PF00018 0.798
LIG_SH3_3 439 445 PF00018 0.565
LIG_SH3_3 506 512 PF00018 0.590
LIG_SH3_3 57 63 PF00018 0.552
LIG_SH3_3 571 577 PF00018 0.610
LIG_SH3_3 965 971 PF00018 0.459
LIG_SUMO_SIM_anti_2 309 315 PF11976 0.540
LIG_SUMO_SIM_anti_2 744 751 PF11976 0.447
LIG_SUMO_SIM_par_1 477 483 PF11976 0.505
LIG_SUMO_SIM_par_1 514 520 PF11976 0.560
LIG_TRAF2_1 294 297 PF00917 0.562
LIG_TRAF2_1 530 533 PF00917 0.546
LIG_TYR_ITIM 692 697 PF00017 0.474
LIG_UBA3_1 587 593 PF00899 0.448
LIG_UBA3_1 718 726 PF00899 0.324
LIG_WRC_WIRS_1 504 509 PF05994 0.601
LIG_WRC_WIRS_1 551 556 PF05994 0.522
LIG_WW_3 969 973 PF00397 0.480
MOD_CDC14_SPxK_1 958 961 PF00782 0.227
MOD_CDK_SPK_2 955 960 PF00069 0.227
MOD_CDK_SPxK_1 955 961 PF00069 0.227
MOD_CDK_SPxxK_3 890 897 PF00069 0.447
MOD_CK1_1 10 16 PF00069 0.641
MOD_CK1_1 100 106 PF00069 0.720
MOD_CK1_1 160 166 PF00069 0.783
MOD_CK1_1 19 25 PF00069 0.525
MOD_CK1_1 221 227 PF00069 0.776
MOD_CK1_1 3 9 PF00069 0.616
MOD_CK1_1 31 37 PF00069 0.549
MOD_CK1_1 390 396 PF00069 0.776
MOD_CK1_1 474 480 PF00069 0.683
MOD_CK1_1 52 58 PF00069 0.728
MOD_CK2_1 1009 1015 PF00069 0.431
MOD_CK2_1 109 115 PF00069 0.559
MOD_CK2_1 120 126 PF00069 0.536
MOD_CK2_1 133 139 PF00069 0.671
MOD_CK2_1 160 166 PF00069 0.786
MOD_CK2_1 197 203 PF00069 0.737
MOD_CK2_1 324 330 PF00069 0.566
MOD_CK2_1 392 398 PF00069 0.717
MOD_CK2_1 508 514 PF00069 0.624
MOD_CK2_1 527 533 PF00069 0.576
MOD_CK2_1 562 568 PF00069 0.526
MOD_CK2_1 652 658 PF00069 0.534
MOD_CK2_1 678 684 PF00069 0.492
MOD_CK2_1 709 715 PF00069 0.335
MOD_CK2_1 75 81 PF00069 0.602
MOD_CK2_1 87 93 PF00069 0.785
MOD_CK2_1 876 882 PF00069 0.321
MOD_GlcNHglycan 1012 1015 PF01048 0.480
MOD_GlcNHglycan 102 105 PF01048 0.736
MOD_GlcNHglycan 12 15 PF01048 0.785
MOD_GlcNHglycan 205 208 PF01048 0.625
MOD_GlcNHglycan 21 24 PF01048 0.720
MOD_GlcNHglycan 223 226 PF01048 0.779
MOD_GlcNHglycan 30 33 PF01048 0.571
MOD_GlcNHglycan 377 380 PF01048 0.740
MOD_GlcNHglycan 381 384 PF01048 0.819
MOD_GlcNHglycan 394 397 PF01048 0.605
MOD_GlcNHglycan 407 410 PF01048 0.579
MOD_GlcNHglycan 498 501 PF01048 0.636
MOD_GlcNHglycan 632 635 PF01048 0.746
MOD_GlcNHglycan 77 80 PF01048 0.815
MOD_GSK3_1 102 109 PF00069 0.563
MOD_GSK3_1 157 164 PF00069 0.706
MOD_GSK3_1 171 178 PF00069 0.560
MOD_GSK3_1 28 35 PF00069 0.738
MOD_GSK3_1 3 10 PF00069 0.690
MOD_GSK3_1 36 43 PF00069 0.644
MOD_GSK3_1 371 378 PF00069 0.635
MOD_GSK3_1 390 397 PF00069 0.680
MOD_GSK3_1 470 477 PF00069 0.690
MOD_GSK3_1 49 56 PF00069 0.729
MOD_GSK3_1 630 637 PF00069 0.749
MOD_GSK3_1 64 71 PF00069 0.740
MOD_GSK3_1 646 653 PF00069 0.632
MOD_GSK3_1 660 667 PF00069 0.776
MOD_GSK3_1 674 681 PF00069 0.669
MOD_GSK3_1 787 794 PF00069 0.447
MOD_GSK3_1 822 829 PF00069 0.335
MOD_GSK3_1 83 90 PF00069 0.746
MOD_GSK3_1 831 838 PF00069 0.335
MOD_GSK3_1 93 100 PF00069 0.814
MOD_GSK3_1 943 950 PF00069 0.442
MOD_GSK3_1 955 962 PF00069 0.447
MOD_GSK3_1 972 979 PF00069 0.426
MOD_LATS_1 1007 1013 PF00433 0.447
MOD_N-GLC_1 3 8 PF02516 0.547
MOD_N-GLC_1 390 395 PF02516 0.779
MOD_N-GLC_1 474 479 PF02516 0.536
MOD_N-GLC_1 665 670 PF02516 0.757
MOD_N-GLC_1 68 73 PF02516 0.779
MOD_N-GLC_1 702 707 PF02516 0.335
MOD_N-GLC_1 87 92 PF02516 0.584
MOD_NEK2_1 120 125 PF00069 0.600
MOD_NEK2_1 753 758 PF00069 0.410
MOD_NEK2_1 771 776 PF00069 0.150
MOD_NEK2_1 808 813 PF00069 0.335
MOD_NEK2_1 822 827 PF00069 0.335
MOD_PIKK_1 197 203 PF00454 0.737
MOD_PIKK_1 227 233 PF00454 0.788
MOD_PIKK_1 264 270 PF00454 0.725
MOD_PIKK_1 312 318 PF00454 0.787
MOD_PIKK_1 345 351 PF00454 0.654
MOD_PIKK_1 49 55 PF00454 0.543
MOD_PK_1 134 140 PF00069 0.686
MOD_PKA_1 1009 1015 PF00069 0.447
MOD_PKA_1 132 138 PF00069 0.633
MOD_PKA_1 375 381 PF00069 0.520
MOD_PKA_2 1009 1015 PF00069 0.447
MOD_PKA_2 132 138 PF00069 0.633
MOD_PKA_2 140 146 PF00069 0.613
MOD_PKA_2 203 209 PF00069 0.641
MOD_PKA_2 375 381 PF00069 0.685
MOD_PKA_2 58 64 PF00069 0.708
MOD_PKA_2 753 759 PF00069 0.447
MOD_PKA_2 903 909 PF00069 0.335
MOD_PKA_2 959 965 PF00069 0.444
MOD_PKB_1 132 140 PF00069 0.687
MOD_PKB_1 321 329 PF00069 0.567
MOD_PKB_1 392 400 PF00069 0.805
MOD_PKB_1 777 785 PF00069 0.447
MOD_Plk_1 168 174 PF00069 0.761
MOD_Plk_1 253 259 PF00069 0.561
MOD_Plk_1 502 508 PF00069 0.687
MOD_Plk_1 709 715 PF00069 0.335
MOD_Plk_2-3 619 625 PF00069 0.714
MOD_Plk_4 109 115 PF00069 0.549
MOD_Plk_4 120 126 PF00069 0.515
MOD_Plk_4 576 582 PF00069 0.458
MOD_Plk_4 717 723 PF00069 0.334
MOD_Plk_4 753 759 PF00069 0.398
MOD_Plk_4 787 793 PF00069 0.447
MOD_Plk_4 831 837 PF00069 0.335
MOD_Plk_4 976 982 PF00069 0.360
MOD_ProDKin_1 192 198 PF00069 0.531
MOD_ProDKin_1 218 224 PF00069 0.774
MOD_ProDKin_1 321 327 PF00069 0.567
MOD_ProDKin_1 399 405 PF00069 0.806
MOD_ProDKin_1 508 514 PF00069 0.582
MOD_ProDKin_1 890 896 PF00069 0.447
MOD_ProDKin_1 943 949 PF00069 0.335
MOD_ProDKin_1 955 961 PF00069 0.327
MOD_ProDKin_1 964 970 PF00069 0.183
MOD_SUMO_for_1 802 805 PF00179 0.335
MOD_SUMO_rev_2 1018 1027 PF00179 0.593
MOD_SUMO_rev_2 111 120 PF00179 0.540
MOD_SUMO_rev_2 160 170 PF00179 0.762
MOD_SUMO_rev_2 393 402 PF00179 0.788
MOD_SUMO_rev_2 568 573 PF00179 0.509
MOD_SUMO_rev_2 90 96 PF00179 0.778
TRG_DiLeu_BaEn_1 744 749 PF01217 0.335
TRG_DiLeu_BaEn_2 804 810 PF01217 0.335
TRG_DiLeu_BaEn_2 993 999 PF01217 0.349
TRG_DiLeu_BaEn_4 115 121 PF01217 0.524
TRG_DiLeu_BaEn_4 939 945 PF01217 0.447
TRG_DiLeu_BaLyEn_6 453 458 PF01217 0.448
TRG_DiLeu_BaLyEn_6 714 719 PF01217 0.335
TRG_DiLeu_BaLyEn_6 732 737 PF01217 0.335
TRG_DiLeu_BaLyEn_6 776 781 PF01217 0.227
TRG_ENDOCYTIC_2 144 147 PF00928 0.589
TRG_ENDOCYTIC_2 343 346 PF00928 0.637
TRG_ENDOCYTIC_2 360 363 PF00928 0.602
TRG_ENDOCYTIC_2 492 495 PF00928 0.724
TRG_ENDOCYTIC_2 513 516 PF00928 0.668
TRG_ENDOCYTIC_2 585 588 PF00928 0.397
TRG_ENDOCYTIC_2 694 697 PF00928 0.388
TRG_ENDOCYTIC_2 772 775 PF00928 0.335
TRG_ENDOCYTIC_2 945 948 PF00928 0.350
TRG_ENDOCYTIC_2 978 981 PF00928 0.335
TRG_ER_diArg_1 132 134 PF00400 0.641
TRG_ER_diArg_1 320 323 PF00400 0.565
TRG_ER_diArg_1 375 377 PF00400 0.658
TRG_ER_diArg_1 534 537 PF00400 0.594
TRG_ER_diArg_1 776 779 PF00400 0.336
TRG_ER_diArg_1 896 898 PF00400 0.355
TRG_NES_CRM1_1 787 801 PF08389 0.335
TRG_NES_CRM1_1 994 1006 PF08389 0.447
TRG_NLS_Bipartite_1 672 692 PF00514 0.607
TRG_NLS_MonoExtC_3 668 673 PF00514 0.701
TRG_NLS_MonoExtN_4 687 692 PF00514 0.500
TRG_NLS_MonoExtN_4 959 964 PF00514 0.349
TRG_Pf-PMV_PEXEL_1 539 544 PF00026 0.570
TRG_Pf-PMV_PEXEL_1 557 561 PF00026 0.499
TRG_Pf-PMV_PEXEL_1 779 784 PF00026 0.350
TRG_Pf-PMV_PEXEL_1 898 902 PF00026 0.355

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P4G9 Leptomonas seymouri 72% 100%
A0A1X0NNI0 Trypanosomatidae 52% 100%
A0A3Q8IIF0 Leishmania donovani 79% 99%
A0A422MWR8 Trypanosoma rangeli 47% 100%
A4HW49 Leishmania infantum 81% 100%
C9ZSX0 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 48% 100%
E9APV3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 78% 100%
Q4QFM8 Leishmania major 80% 99%
V5AZ01 Trypanosoma cruzi 47% 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