LeishMANIAdb
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ATPase_AAA_core domain-containing protein

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

Quick info

Protein:
ATPase_AAA_core domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania mexicana
UniProt:
E9B0S7_LEIMU
TriTrypDb:
LmxM.29.1530
Length:
1052

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 7
GO:0043226 organelle 2 7
GO:0043227 membrane-bounded organelle 3 7
GO:0043229 intracellular organelle 3 7
GO:0043231 intracellular membrane-bounded organelle 4 7
GO:0110165 cellular anatomical entity 1 7

Expansion

Sequence features

E9B0S7
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9B0S7

Function

Biological processes
Term Name Level Count
GO:0006139 nucleobase-containing compound metabolic process 3 7
GO:0006259 DNA metabolic process 4 7
GO:0006281 DNA repair 5 7
GO:0006725 cellular aromatic compound metabolic process 3 7
GO:0006807 nitrogen compound metabolic process 2 7
GO:0006950 response to stress 2 7
GO:0006974 DNA damage response 4 7
GO:0008152 metabolic process 1 7
GO:0009987 cellular process 1 7
GO:0033554 cellular response to stress 3 7
GO:0034641 cellular nitrogen compound metabolic process 3 7
GO:0043170 macromolecule metabolic process 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:0046483 heterocycle metabolic process 3 7
GO:0050896 response to stimulus 1 7
GO:0051716 cellular response to stimulus 2 7
GO:0071704 organic substance metabolic process 2 7
GO:0090304 nucleic acid metabolic process 4 7
GO:1901360 organic cyclic compound metabolic process 3 7
GO:0000075 cell cycle checkpoint signaling 4 1
GO:0000076 DNA replication checkpoint signaling 6 1
GO:0000077 DNA damage checkpoint signaling 5 1
GO:0007093 mitotic cell cycle checkpoint signaling 4 1
GO:0007165 signal transduction 2 1
GO:0007346 regulation of mitotic cell cycle 5 1
GO:0010389 regulation of G2/M transition of mitotic cell cycle 7 1
GO:0010564 regulation of cell cycle process 5 1
GO:0010948 negative regulation of cell cycle process 6 1
GO:0010972 negative regulation of G2/M transition of mitotic cell cycle 8 1
GO:0022402 cell cycle process 2 1
GO:0031570 DNA integrity checkpoint signaling 5 1
GO:0033314 mitotic DNA replication checkpoint signaling 6 1
GO:0035556 intracellular signal transduction 3 1
GO:0042770 signal transduction in response to DNA damage 4 1
GO:0044774 mitotic DNA integrity checkpoint signaling 5 1
GO:0044818 mitotic G2/M transition checkpoint 5 1
GO:0045786 negative regulation of cell cycle 5 1
GO:0045930 negative regulation of mitotic cell cycle 6 1
GO:0048519 negative regulation of biological process 3 1
GO:0048523 negative regulation of cellular process 4 1
GO:0050789 regulation of biological process 2 1
GO:0050794 regulation of cellular process 3 1
GO:0051726 regulation of cell cycle 4 1
GO:0065007 biological regulation 1 1
GO:1901987 regulation of cell cycle phase transition 6 1
GO:1901988 negative regulation of cell cycle phase transition 7 1
GO:1901990 regulation of mitotic cell cycle phase transition 6 1
GO:1901991 negative regulation of mitotic cell cycle phase transition 7 1
GO:1902749 regulation of cell cycle G2/M phase transition 7 1
GO:1902750 negative regulation of cell cycle G2/M phase transition 8 1
GO:1903047 mitotic cell cycle process 3 1
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 7
GO:0005488 binding 1 7
GO:0005524 ATP binding 5 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:1901265 nucleoside phosphate binding 3 7
GO:1901363 heterocyclic compound binding 2 7
GO:0003682 chromatin binding 2 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 153 157 PF00656 0.578
CLV_C14_Caspase3-7 510 514 PF00656 0.611
CLV_C14_Caspase3-7 568 572 PF00656 0.599
CLV_C14_Caspase3-7 682 686 PF00656 0.533
CLV_NRD_NRD_1 227 229 PF00675 0.639
CLV_NRD_NRD_1 236 238 PF00675 0.451
CLV_NRD_NRD_1 283 285 PF00675 0.578
CLV_NRD_NRD_1 302 304 PF00675 0.404
CLV_NRD_NRD_1 335 337 PF00675 0.716
CLV_NRD_NRD_1 341 343 PF00675 0.688
CLV_NRD_NRD_1 551 553 PF00675 0.669
CLV_NRD_NRD_1 588 590 PF00675 0.644
CLV_NRD_NRD_1 651 653 PF00675 0.501
CLV_NRD_NRD_1 708 710 PF00675 0.591
CLV_NRD_NRD_1 782 784 PF00675 0.707
CLV_NRD_NRD_1 830 832 PF00675 0.628
CLV_NRD_NRD_1 956 958 PF00675 0.628
CLV_PCSK_FUR_1 333 337 PF00082 0.620
CLV_PCSK_FUR_1 706 710 PF00082 0.587
CLV_PCSK_KEX2_1 227 229 PF00082 0.639
CLV_PCSK_KEX2_1 236 238 PF00082 0.451
CLV_PCSK_KEX2_1 285 287 PF00082 0.491
CLV_PCSK_KEX2_1 301 303 PF00082 0.522
CLV_PCSK_KEX2_1 335 337 PF00082 0.755
CLV_PCSK_KEX2_1 341 343 PF00082 0.693
CLV_PCSK_KEX2_1 553 555 PF00082 0.671
CLV_PCSK_KEX2_1 587 589 PF00082 0.638
CLV_PCSK_KEX2_1 708 710 PF00082 0.591
CLV_PCSK_KEX2_1 782 784 PF00082 0.707
CLV_PCSK_KEX2_1 830 832 PF00082 0.638
CLV_PCSK_KEX2_1 956 958 PF00082 0.628
CLV_PCSK_PC1ET2_1 285 287 PF00082 0.491
CLV_PCSK_PC1ET2_1 301 303 PF00082 0.522
CLV_PCSK_PC1ET2_1 341 343 PF00082 0.740
CLV_PCSK_PC1ET2_1 553 555 PF00082 0.671
CLV_PCSK_PC7_1 297 303 PF00082 0.544
CLV_PCSK_SKI1_1 20 24 PF00082 0.419
CLV_PCSK_SKI1_1 336 340 PF00082 0.546
CLV_PCSK_SKI1_1 381 385 PF00082 0.502
CLV_PCSK_SKI1_1 61 65 PF00082 0.600
CLV_PCSK_SKI1_1 613 617 PF00082 0.612
CLV_PCSK_SKI1_1 632 636 PF00082 0.490
CLV_PCSK_SKI1_1 652 656 PF00082 0.494
CLV_PCSK_SKI1_1 957 961 PF00082 0.618
DEG_APCC_DBOX_1 1010 1018 PF00400 0.568
DEG_APCC_DBOX_1 191 199 PF00400 0.500
DEG_APCC_DBOX_1 283 291 PF00400 0.626
DEG_APCC_DBOX_1 380 388 PF00400 0.495
DEG_APCC_DBOX_1 651 659 PF00400 0.492
DEG_APCC_DBOX_1 860 868 PF00400 0.560
DEG_COP1_1 69 78 PF00400 0.481
DEG_Kelch_Keap1_1 511 516 PF01344 0.584
DEG_Nend_Nbox_1 1 3 PF02207 0.494
DEG_SPOP_SBC_1 319 323 PF00917 0.502
DEG_SPOP_SBC_1 354 358 PF00917 0.531
DEG_SPOP_SBC_1 78 82 PF00917 0.563
DEG_SPOP_SBC_1 941 945 PF00917 0.579
DOC_CKS1_1 344 349 PF01111 0.584
DOC_CKS1_1 990 995 PF01111 0.571
DOC_CYCLIN_RxL_1 234 245 PF00134 0.546
DOC_CYCLIN_RxL_1 56 67 PF00134 0.542
DOC_CYCLIN_yClb5_NLxxxL_5 236 243 PF00134 0.547
DOC_CYCLIN_yClb5_NLxxxL_5 278 287 PF00134 0.489
DOC_CYCLIN_yCln2_LP_2 895 898 PF00134 0.497
DOC_MAPK_gen_1 236 242 PF00069 0.494
DOC_MAPK_gen_1 284 293 PF00069 0.591
DOC_MAPK_HePTP_8 283 295 PF00069 0.520
DOC_MAPK_MEF2A_6 286 295 PF00069 0.523
DOC_MAPK_MEF2A_6 56 64 PF00069 0.452
DOC_MAPK_MEF2A_6 726 735 PF00069 0.527
DOC_MAPK_MEF2A_6 799 806 PF00069 0.416
DOC_MAPK_MEF2A_6 989 998 PF00069 0.562
DOC_PP1_RVXF_1 235 242 PF00149 0.545
DOC_PP2B_LxvP_1 133 136 PF13499 0.645
DOC_PP2B_LxvP_1 647 650 PF13499 0.578
DOC_PP2B_LxvP_1 895 898 PF13499 0.497
DOC_USP7_MATH_1 1030 1034 PF00917 0.694
DOC_USP7_MATH_1 319 323 PF00917 0.588
DOC_USP7_MATH_1 395 399 PF00917 0.635
DOC_USP7_MATH_1 403 407 PF00917 0.614
DOC_USP7_MATH_1 466 470 PF00917 0.704
DOC_USP7_MATH_1 471 475 PF00917 0.649
DOC_USP7_MATH_1 555 559 PF00917 0.691
DOC_USP7_MATH_1 607 611 PF00917 0.682
DOC_USP7_MATH_1 717 721 PF00917 0.539
DOC_USP7_MATH_1 813 817 PF00917 0.620
DOC_USP7_MATH_1 911 915 PF00917 0.665
DOC_USP7_MATH_1 941 945 PF00917 0.633
DOC_USP7_MATH_1 963 967 PF00917 0.613
DOC_USP7_UBL2_3 339 343 PF12436 0.681
DOC_USP7_UBL2_3 541 545 PF12436 0.724
DOC_WW_Pin1_4 138 143 PF00397 0.591
DOC_WW_Pin1_4 264 269 PF00397 0.548
DOC_WW_Pin1_4 273 278 PF00397 0.513
DOC_WW_Pin1_4 327 332 PF00397 0.539
DOC_WW_Pin1_4 343 348 PF00397 0.678
DOC_WW_Pin1_4 355 360 PF00397 0.522
DOC_WW_Pin1_4 467 472 PF00397 0.703
DOC_WW_Pin1_4 474 479 PF00397 0.606
DOC_WW_Pin1_4 529 534 PF00397 0.577
DOC_WW_Pin1_4 557 562 PF00397 0.727
DOC_WW_Pin1_4 846 851 PF00397 0.654
DOC_WW_Pin1_4 925 930 PF00397 0.689
DOC_WW_Pin1_4 989 994 PF00397 0.637
LIG_14-3-3_CanoR_1 18 23 PF00244 0.443
LIG_14-3-3_CanoR_1 192 196 PF00244 0.422
LIG_14-3-3_CanoR_1 34 39 PF00244 0.634
LIG_14-3-3_CanoR_1 450 455 PF00244 0.646
LIG_14-3-3_CanoR_1 554 564 PF00244 0.692
LIG_14-3-3_CanoR_1 632 640 PF00244 0.481
LIG_14-3-3_CanoR_1 688 696 PF00244 0.576
LIG_14-3-3_CanoR_1 714 721 PF00244 0.602
LIG_14-3-3_CanoR_1 741 751 PF00244 0.676
LIG_14-3-3_CanoR_1 851 860 PF00244 0.772
LIG_14-3-3_CanoR_1 870 879 PF00244 0.453
LIG_14-3-3_CanoR_1 905 915 PF00244 0.570
LIG_14-3-3_CanoR_1 956 960 PF00244 0.622
LIG_Actin_WH2_2 191 207 PF00022 0.422
LIG_APCC_ABBA_1 1039 1044 PF00400 0.609
LIG_BRCT_BRCA1_1 1011 1015 PF00533 0.650
LIG_BRCT_BRCA1_1 692 696 PF00533 0.672
LIG_BRCT_BRCA1_1 96 100 PF00533 0.415
LIG_EH1_1 627 635 PF00400 0.575
LIG_EVH1_2 749 753 PF00568 0.705
LIG_FHA_1 1005 1011 PF00498 0.571
LIG_FHA_1 19 25 PF00498 0.477
LIG_FHA_1 267 273 PF00498 0.365
LIG_FHA_1 421 427 PF00498 0.422
LIG_FHA_1 455 461 PF00498 0.627
LIG_FHA_1 468 474 PF00498 0.595
LIG_FHA_1 475 481 PF00498 0.527
LIG_FHA_1 57 63 PF00498 0.586
LIG_FHA_1 644 650 PF00498 0.582
LIG_FHA_1 722 728 PF00498 0.487
LIG_FHA_1 737 743 PF00498 0.481
LIG_FHA_1 79 85 PF00498 0.673
LIG_FHA_1 847 853 PF00498 0.715
LIG_FHA_1 872 878 PF00498 0.610
LIG_FHA_1 977 983 PF00498 0.506
LIG_FHA_2 243 249 PF00498 0.513
LIG_FHA_2 617 623 PF00498 0.604
LIG_FHA_2 67 73 PF00498 0.473
LIG_FHA_2 714 720 PF00498 0.605
LIG_FHA_2 8 14 PF00498 0.507
LIG_GBD_Chelix_1 727 735 PF00786 0.416
LIG_LIR_Gen_1 200 208 PF02991 0.537
LIG_LIR_Gen_1 423 433 PF02991 0.507
LIG_LIR_Gen_1 798 809 PF02991 0.422
LIG_LIR_Gen_1 97 108 PF02991 0.552
LIG_LIR_Nem_3 200 204 PF02991 0.521
LIG_LIR_Nem_3 423 428 PF02991 0.504
LIG_LIR_Nem_3 621 626 PF02991 0.559
LIG_LIR_Nem_3 739 743 PF02991 0.610
LIG_LIR_Nem_3 798 804 PF02991 0.425
LIG_LIR_Nem_3 880 884 PF02991 0.616
LIG_LIR_Nem_3 97 103 PF02991 0.546
LIG_LRP6_Inhibitor_1 658 664 PF00058 0.526
LIG_LYPXL_yS_3 766 769 PF13949 0.579
LIG_MYND_1 894 898 PF01753 0.492
LIG_MYND_1 986 990 PF01753 0.614
LIG_NRBOX 59 65 PF00104 0.446
LIG_Pex14_1 92 96 PF04695 0.446
LIG_RPA_C_Fungi 298 310 PF08784 0.480
LIG_SH2_CRK 49 53 PF00017 0.498
LIG_SH2_CRK 740 744 PF00017 0.642
LIG_SH2_NCK_1 882 886 PF00017 0.529
LIG_SH2_PTP2 887 890 PF00017 0.552
LIG_SH2_SRC 116 119 PF00017 0.535
LIG_SH2_STAP1 113 117 PF00017 0.409
LIG_SH2_STAP1 674 678 PF00017 0.589
LIG_SH2_STAP1 96 100 PF00017 0.509
LIG_SH2_STAT5 116 119 PF00017 0.418
LIG_SH2_STAT5 123 126 PF00017 0.436
LIG_SH2_STAT5 623 626 PF00017 0.536
LIG_SH2_STAT5 638 641 PF00017 0.664
LIG_SH2_STAT5 657 660 PF00017 0.379
LIG_SH2_STAT5 665 668 PF00017 0.515
LIG_SH2_STAT5 761 764 PF00017 0.673
LIG_SH2_STAT5 795 798 PF00017 0.587
LIG_SH2_STAT5 887 890 PF00017 0.552
LIG_SH3_1 932 938 PF00018 0.529
LIG_SH3_3 1035 1041 PF00018 0.731
LIG_SH3_3 2 8 PF00018 0.504
LIG_SH3_3 214 220 PF00018 0.468
LIG_SH3_3 341 347 PF00018 0.616
LIG_SH3_3 527 533 PF00018 0.539
LIG_SH3_3 68 74 PF00018 0.588
LIG_SH3_3 744 750 PF00018 0.682
LIG_SH3_3 891 897 PF00018 0.656
LIG_SH3_3 932 938 PF00018 0.639
LIG_SH3_3 987 993 PF00018 0.627
LIG_SH3_CIN85_PxpxPR_1 951 956 PF14604 0.522
LIG_SUMO_SIM_anti_2 360 365 PF11976 0.558
LIG_SUMO_SIM_anti_2 854 862 PF11976 0.564
LIG_SUMO_SIM_par_1 20 26 PF11976 0.549
LIG_SUMO_SIM_par_1 450 455 PF11976 0.635
LIG_SUMO_SIM_par_1 565 572 PF11976 0.574
LIG_TRFH_1 882 886 PF08558 0.529
LIG_TYR_ITIM 738 743 PF00017 0.632
LIG_TYR_ITIM 764 769 PF00017 0.591
LIG_TYR_ITIM 879 884 PF00017 0.617
LIG_WW_1 758 761 PF00397 0.685
LIG_WW_3 649 653 PF00397 0.583
MOD_CDC14_SPxK_1 330 333 PF00782 0.535
MOD_CDK_SPK_2 846 851 PF00069 0.634
MOD_CDK_SPxK_1 327 333 PF00069 0.534
MOD_CDK_SPxxK_3 474 481 PF00069 0.586
MOD_CDK_SPxxK_3 529 536 PF00069 0.589
MOD_CDK_SPxxK_3 925 932 PF00069 0.556
MOD_CK1_1 119 125 PF00069 0.509
MOD_CK1_1 141 147 PF00069 0.713
MOD_CK1_1 148 154 PF00069 0.642
MOD_CK1_1 165 171 PF00069 0.592
MOD_CK1_1 259 265 PF00069 0.658
MOD_CK1_1 317 323 PF00069 0.738
MOD_CK1_1 406 412 PF00069 0.623
MOD_CK1_1 455 461 PF00069 0.592
MOD_CK1_1 467 473 PF00069 0.623
MOD_CK1_1 474 480 PF00069 0.597
MOD_CK1_1 511 517 PF00069 0.679
MOD_CK1_1 524 530 PF00069 0.585
MOD_CK1_1 532 538 PF00069 0.620
MOD_CK1_1 690 696 PF00069 0.671
MOD_CK1_1 820 826 PF00069 0.702
MOD_CK1_1 844 850 PF00069 0.734
MOD_CK1_1 939 945 PF00069 0.678
MOD_CK1_1 965 971 PF00069 0.678
MOD_CK1_1 978 984 PF00069 0.573
MOD_CK2_1 1030 1036 PF00069 0.646
MOD_CK2_1 134 140 PF00069 0.600
MOD_CK2_1 496 502 PF00069 0.687
MOD_CK2_1 519 525 PF00069 0.774
MOD_CK2_1 569 575 PF00069 0.678
MOD_CK2_1 616 622 PF00069 0.604
MOD_CK2_1 66 72 PF00069 0.460
MOD_CK2_1 713 719 PF00069 0.603
MOD_CK2_1 794 800 PF00069 0.549
MOD_CK2_1 813 819 PF00069 0.597
MOD_Cter_Amidation 225 228 PF01082 0.594
MOD_DYRK1A_RPxSP_1 989 993 PF00069 0.577
MOD_GlcNHglycan 1032 1035 PF01048 0.672
MOD_GlcNHglycan 153 156 PF01048 0.658
MOD_GlcNHglycan 164 167 PF01048 0.573
MOD_GlcNHglycan 327 330 PF01048 0.807
MOD_GlcNHglycan 348 351 PF01048 0.560
MOD_GlcNHglycan 39 42 PF01048 0.505
MOD_GlcNHglycan 405 408 PF01048 0.615
MOD_GlcNHglycan 454 457 PF01048 0.668
MOD_GlcNHglycan 473 476 PF01048 0.586
MOD_GlcNHglycan 482 485 PF01048 0.742
MOD_GlcNHglycan 513 516 PF01048 0.714
MOD_GlcNHglycan 691 695 PF01048 0.639
MOD_GlcNHglycan 791 794 PF01048 0.573
MOD_GlcNHglycan 815 818 PF01048 0.640
MOD_GlcNHglycan 819 823 PF01048 0.679
MOD_GlcNHglycan 899 902 PF01048 0.638
MOD_GlcNHglycan 908 911 PF01048 0.726
MOD_GlcNHglycan 944 947 PF01048 0.576
MOD_GlcNHglycan 967 970 PF01048 0.623
MOD_GSK3_1 102 109 PF00069 0.455
MOD_GSK3_1 134 141 PF00069 0.590
MOD_GSK3_1 14 21 PF00069 0.432
MOD_GSK3_1 144 151 PF00069 0.652
MOD_GSK3_1 162 169 PF00069 0.555
MOD_GSK3_1 242 249 PF00069 0.507
MOD_GSK3_1 255 262 PF00069 0.564
MOD_GSK3_1 314 321 PF00069 0.614
MOD_GSK3_1 325 332 PF00069 0.577
MOD_GSK3_1 346 353 PF00069 0.675
MOD_GSK3_1 450 457 PF00069 0.593
MOD_GSK3_1 460 467 PF00069 0.623
MOD_GSK3_1 496 503 PF00069 0.742
MOD_GSK3_1 507 514 PF00069 0.634
MOD_GSK3_1 520 527 PF00069 0.569
MOD_GSK3_1 565 572 PF00069 0.676
MOD_GSK3_1 607 614 PF00069 0.656
MOD_GSK3_1 713 720 PF00069 0.756
MOD_GSK3_1 74 81 PF00069 0.665
MOD_GSK3_1 813 820 PF00069 0.622
MOD_GSK3_1 840 847 PF00069 0.701
MOD_GSK3_1 921 928 PF00069 0.707
MOD_GSK3_1 936 943 PF00069 0.578
MOD_GSK3_1 945 952 PF00069 0.647
MOD_GSK3_1 961 968 PF00069 0.686
MOD_N-GLC_1 256 261 PF02516 0.485
MOD_N-GLC_1 539 544 PF02516 0.550
MOD_NEK2_1 162 167 PF00069 0.673
MOD_NEK2_1 204 209 PF00069 0.369
MOD_NEK2_1 242 247 PF00069 0.488
MOD_NEK2_1 256 261 PF00069 0.536
MOD_NEK2_1 314 319 PF00069 0.675
MOD_NEK2_1 452 457 PF00069 0.657
MOD_NEK2_1 480 485 PF00069 0.607
MOD_NEK2_1 569 574 PF00069 0.587
MOD_NEK2_1 624 629 PF00069 0.534
MOD_NEK2_1 692 697 PF00069 0.588
MOD_NEK2_1 721 726 PF00069 0.660
MOD_NEK2_1 727 732 PF00069 0.567
MOD_NEK2_1 777 782 PF00069 0.548
MOD_NEK2_1 962 967 PF00069 0.641
MOD_NEK2_2 955 960 PF00069 0.622
MOD_NEK2_2 96 101 PF00069 0.343
MOD_PIKK_1 373 379 PF00454 0.499
MOD_PIKK_1 395 401 PF00454 0.503
MOD_PIKK_1 569 575 PF00454 0.591
MOD_PIKK_1 607 613 PF00454 0.722
MOD_PIKK_1 632 638 PF00454 0.489
MOD_PIKK_1 87 93 PF00454 0.536
MOD_PK_1 286 292 PF00069 0.576
MOD_PK_1 808 814 PF00069 0.650
MOD_PKA_1 588 594 PF00069 0.588
MOD_PKA_2 148 154 PF00069 0.624
MOD_PKA_2 191 197 PF00069 0.410
MOD_PKA_2 204 210 PF00069 0.478
MOD_PKA_2 334 340 PF00069 0.727
MOD_PKA_2 480 486 PF00069 0.533
MOD_PKA_2 500 506 PF00069 0.741
MOD_PKA_2 555 561 PF00069 0.705
MOD_PKA_2 588 594 PF00069 0.593
MOD_PKA_2 687 693 PF00069 0.571
MOD_PKA_2 713 719 PF00069 0.603
MOD_PKA_2 817 823 PF00069 0.675
MOD_PKA_2 955 961 PF00069 0.621
MOD_PKB_1 284 292 PF00069 0.577
MOD_PKB_1 32 40 PF00069 0.439
MOD_PKB_1 554 562 PF00069 0.688
MOD_Plk_1 106 112 PF00069 0.437
MOD_Plk_1 256 262 PF00069 0.439
MOD_Plk_1 524 530 PF00069 0.682
MOD_Plk_1 66 72 PF00069 0.605
MOD_Plk_2-3 496 502 PF00069 0.743
MOD_Plk_2-3 66 72 PF00069 0.418
MOD_Plk_2-3 679 685 PF00069 0.613
MOD_Plk_4 116 122 PF00069 0.498
MOD_Plk_4 191 197 PF00069 0.497
MOD_Plk_4 23 29 PF00069 0.403
MOD_Plk_4 260 266 PF00069 0.550
MOD_Plk_4 286 292 PF00069 0.520
MOD_Plk_4 420 426 PF00069 0.484
MOD_Plk_4 565 571 PF00069 0.572
MOD_Plk_4 66 72 PF00069 0.474
MOD_ProDKin_1 138 144 PF00069 0.592
MOD_ProDKin_1 264 270 PF00069 0.547
MOD_ProDKin_1 273 279 PF00069 0.511
MOD_ProDKin_1 327 333 PF00069 0.541
MOD_ProDKin_1 343 349 PF00069 0.678
MOD_ProDKin_1 355 361 PF00069 0.513
MOD_ProDKin_1 467 473 PF00069 0.705
MOD_ProDKin_1 474 480 PF00069 0.609
MOD_ProDKin_1 529 535 PF00069 0.577
MOD_ProDKin_1 557 563 PF00069 0.723
MOD_ProDKin_1 846 852 PF00069 0.650
MOD_ProDKin_1 925 931 PF00069 0.690
MOD_ProDKin_1 989 995 PF00069 0.633
MOD_SUMO_rev_2 535 542 PF00179 0.608
TRG_DiLeu_BaEn_1 66 71 PF01217 0.496
TRG_DiLeu_BaEn_2 213 219 PF01217 0.462
TRG_DiLeu_BaLyEn_6 1035 1040 PF01217 0.732
TRG_DiLeu_BaLyEn_6 629 634 PF01217 0.495
TRG_DiLeu_BaLyEn_6 891 896 PF01217 0.480
TRG_ENDOCYTIC_2 201 204 PF00928 0.433
TRG_ENDOCYTIC_2 623 626 PF00928 0.548
TRG_ENDOCYTIC_2 740 743 PF00928 0.653
TRG_ENDOCYTIC_2 761 764 PF00928 0.637
TRG_ENDOCYTIC_2 766 769 PF00928 0.565
TRG_ENDOCYTIC_2 881 884 PF00928 0.556
TRG_ENDOCYTIC_2 887 890 PF00928 0.524
TRG_ER_diArg_1 235 237 PF00400 0.436
TRG_ER_diArg_1 283 286 PF00400 0.577
TRG_ER_diArg_1 302 304 PF00400 0.405
TRG_ER_diArg_1 333 336 PF00400 0.544
TRG_ER_diArg_1 552 555 PF00400 0.702
TRG_ER_diArg_1 587 589 PF00400 0.601
TRG_ER_diArg_1 767 770 PF00400 0.550
TRG_ER_diArg_1 781 783 PF00400 0.664
TRG_ER_diArg_1 830 833 PF00400 0.639
TRG_ER_diArg_1 955 957 PF00400 0.629
TRG_NLS_Bipartite_1 284 305 PF00514 0.535
TRG_NLS_MonoCore_2 552 557 PF00514 0.701
TRG_NLS_MonoExtC_3 340 345 PF00514 0.532
TRG_NLS_MonoExtC_3 551 556 PF00514 0.699
TRG_NLS_MonoExtN_4 339 345 PF00514 0.730
TRG_NLS_MonoExtN_4 552 557 PF00514 0.714
TRG_Pf-PMV_PEXEL_1 632 636 PF00026 0.479
TRG_Pf-PMV_PEXEL_1 652 656 PF00026 0.581
TRG_Pf-PMV_PEXEL_1 709 713 PF00026 0.584

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P8V0 Leptomonas seymouri 42% 100%
A0A3Q8IRX6 Leishmania donovani 86% 100%
A4HI98 Leishmania braziliensis 72% 100%
A4I5I2 Leishmania infantum 87% 100%
Q4Q7F1 Leishmania major 86% 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