LeishMANIAdb
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Kinesin-like protein

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

Quick info

Protein:
Kinesin-like protein
Gene product:
OSM3-like kinesin - putative
Species:
Leishmania infantum
UniProt:
A4HXF7_LEIIN
TriTrypDb:
LINF_170015000
Length:
940

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) yes yes: 3
Silverman et al. no yes: 0
Pissara et al. yes yes: 16
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: 7
NetGPI no yes: 0, no: 7
Cellular components
Term Name Level Count
GO:0005874 microtubule 6 7
GO:0099080 supramolecular complex 2 7
GO:0099081 supramolecular polymer 3 7
GO:0099512 supramolecular fiber 4 7
GO:0099513 polymeric cytoskeletal fiber 5 7
GO:0110165 cellular anatomical entity 1 7
GO:0005737 cytoplasm 2 1
GO:0005871 kinesin complex 3 1
GO:0005875 microtubule associated complex 2 1
GO:0005929 cilium 4 1
GO:0032991 protein-containing complex 1 1
GO:0042995 cell projection 2 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0120025 plasma membrane bounded cell projection 3 1

Expansion

Sequence features

A4HXF7
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HXF7

Function

Biological processes
Term Name Level Count
GO:0007017 microtubule-based process 2 8
GO:0007018 microtubule-based movement 3 8
GO:0009987 cellular process 1 8
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 8
GO:0003774 cytoskeletal motor activity 1 8
GO:0003777 microtubule motor activity 2 8
GO:0005488 binding 1 8
GO:0005515 protein binding 2 8
GO:0005524 ATP binding 5 8
GO:0008017 microtubule binding 5 8
GO:0008092 cytoskeletal protein binding 3 8
GO:0015631 tubulin binding 4 8
GO:0017076 purine nucleotide binding 4 8
GO:0030554 adenyl nucleotide binding 5 8
GO:0032553 ribonucleotide binding 3 8
GO:0032555 purine ribonucleotide binding 4 8
GO:0032559 adenyl ribonucleotide binding 5 8
GO:0035639 purine ribonucleoside triphosphate binding 4 8
GO:0036094 small molecule binding 2 8
GO:0043167 ion binding 2 8
GO:0043168 anion binding 3 8
GO:0097159 organic cyclic compound binding 2 8
GO:0097367 carbohydrate derivative binding 2 8
GO:0140657 ATP-dependent activity 1 8
GO:1901265 nucleoside phosphate binding 3 8
GO:1901363 heterocyclic compound binding 2 8
GO:0003824 catalytic activity 1 1
GO:0016462 pyrophosphatase activity 5 1
GO:0016787 hydrolase activity 2 1
GO:0016817 hydrolase activity, acting on acid anhydrides 3 1
GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides 4 1
GO:0016887 ATP hydrolysis activity 7 1
GO:0017111 ribonucleoside triphosphate phosphatase activity 6 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 565 569 PF00656 0.575
CLV_C14_Caspase3-7 799 803 PF00656 0.575
CLV_NRD_NRD_1 203 205 PF00675 0.344
CLV_NRD_NRD_1 613 615 PF00675 0.588
CLV_NRD_NRD_1 862 864 PF00675 0.552
CLV_NRD_NRD_1 878 880 PF00675 0.547
CLV_NRD_NRD_1 908 910 PF00675 0.532
CLV_NRD_NRD_1 927 929 PF00675 0.798
CLV_PCSK_KEX2_1 202 204 PF00082 0.345
CLV_PCSK_KEX2_1 556 558 PF00082 0.618
CLV_PCSK_KEX2_1 613 615 PF00082 0.584
CLV_PCSK_KEX2_1 811 813 PF00082 0.575
CLV_PCSK_KEX2_1 878 880 PF00082 0.547
CLV_PCSK_KEX2_1 907 909 PF00082 0.533
CLV_PCSK_KEX2_1 927 929 PF00082 0.746
CLV_PCSK_PC1ET2_1 556 558 PF00082 0.618
CLV_PCSK_PC1ET2_1 811 813 PF00082 0.575
CLV_PCSK_SKI1_1 120 124 PF00082 0.469
CLV_PCSK_SKI1_1 156 160 PF00082 0.403
CLV_PCSK_SKI1_1 339 343 PF00082 0.343
CLV_PCSK_SKI1_1 369 373 PF00082 0.603
CLV_PCSK_SKI1_1 495 499 PF00082 0.587
CLV_PCSK_SKI1_1 532 536 PF00082 0.647
CLV_PCSK_SKI1_1 756 760 PF00082 0.465
CLV_PCSK_SKI1_1 832 836 PF00082 0.518
CLV_PCSK_SKI1_1 863 867 PF00082 0.557
CLV_PCSK_SKI1_1 920 924 PF00082 0.668
CLV_Separin_Metazoa 492 496 PF03568 0.653
DEG_APCC_DBOX_1 699 707 PF00400 0.531
DEG_APCC_KENBOX_2 24 28 PF00400 0.366
DEG_SPOP_SBC_1 136 140 PF00917 0.366
DOC_CKS1_1 470 475 PF01111 0.671
DOC_CYCLIN_RxL_1 753 760 PF00134 0.472
DOC_MAPK_gen_1 781 790 PF00069 0.594
DOC_MAPK_gen_1 869 876 PF00069 0.550
DOC_MAPK_MEF2A_6 161 168 PF00069 0.343
DOC_MAPK_MEF2A_6 265 274 PF00069 0.343
DOC_MAPK_MEF2A_6 32 39 PF00069 0.343
DOC_MAPK_MEF2A_6 342 349 PF00069 0.460
DOC_MAPK_MEF2A_6 391 399 PF00069 0.580
DOC_PP1_RVXF_1 309 316 PF00149 0.343
DOC_PP4_FxxP_1 470 473 PF00568 0.670
DOC_PP4_FxxP_1 75 78 PF00568 0.343
DOC_USP7_MATH_1 212 216 PF00917 0.335
DOC_USP7_MATH_1 238 242 PF00917 0.403
DOC_USP7_MATH_1 292 296 PF00917 0.362
DOC_USP7_MATH_1 402 406 PF00917 0.566
DOC_USP7_MATH_1 454 458 PF00917 0.581
DOC_USP7_MATH_1 562 566 PF00917 0.668
DOC_USP7_MATH_1 618 622 PF00917 0.700
DOC_USP7_MATH_1 645 649 PF00917 0.581
DOC_USP7_MATH_1 667 671 PF00917 0.593
DOC_USP7_MATH_1 731 735 PF00917 0.561
DOC_USP7_MATH_2 651 657 PF00917 0.655
DOC_USP7_UBL2_3 531 535 PF12436 0.683
DOC_USP7_UBL2_3 768 772 PF12436 0.461
DOC_USP7_UBL2_3 832 836 PF12436 0.523
DOC_WW_Pin1_4 293 298 PF00397 0.362
DOC_WW_Pin1_4 469 474 PF00397 0.674
LIG_14-3-3_CanoR_1 20 29 PF00244 0.461
LIG_14-3-3_CanoR_1 216 221 PF00244 0.403
LIG_14-3-3_CanoR_1 237 246 PF00244 0.420
LIG_14-3-3_CanoR_1 323 332 PF00244 0.403
LIG_14-3-3_CanoR_1 424 428 PF00244 0.517
LIG_14-3-3_CanoR_1 430 435 PF00244 0.511
LIG_14-3-3_CanoR_1 55 59 PF00244 0.343
LIG_14-3-3_CanoR_1 557 561 PF00244 0.619
LIG_14-3-3_CanoR_1 625 633 PF00244 0.685
LIG_14-3-3_CanoR_1 920 926 PF00244 0.686
LIG_14-3-3_CanoR_1 927 933 PF00244 0.682
LIG_Actin_WH2_2 506 523 PF00022 0.572
LIG_Actin_WH2_2 849 865 PF00022 0.546
LIG_APCC_ABBAyCdc20_2 689 695 PF00400 0.620
LIG_Clathr_ClatBox_1 431 435 PF01394 0.629
LIG_Clathr_ClatBox_1 787 791 PF01394 0.535
LIG_deltaCOP1_diTrp_1 461 470 PF00928 0.658
LIG_deltaCOP1_diTrp_1 54 58 PF00928 0.403
LIG_FHA_1 173 179 PF00498 0.409
LIG_FHA_1 226 232 PF00498 0.432
LIG_FHA_1 234 240 PF00498 0.352
LIG_FHA_1 297 303 PF00498 0.343
LIG_FHA_1 358 364 PF00498 0.497
LIG_FHA_1 376 382 PF00498 0.543
LIG_FHA_1 41 47 PF00498 0.403
LIG_FHA_1 427 433 PF00498 0.515
LIG_FHA_1 515 521 PF00498 0.693
LIG_FHA_1 625 631 PF00498 0.726
LIG_FHA_1 71 77 PF00498 0.355
LIG_FHA_1 78 84 PF00498 0.351
LIG_FHA_1 782 788 PF00498 0.542
LIG_FHA_2 228 234 PF00498 0.403
LIG_FHA_2 261 267 PF00498 0.343
LIG_FHA_2 277 283 PF00498 0.343
LIG_FHA_2 470 476 PF00498 0.583
LIG_FHA_2 487 493 PF00498 0.458
LIG_FHA_2 528 534 PF00498 0.627
LIG_FHA_2 580 586 PF00498 0.617
LIG_FHA_2 730 736 PF00498 0.680
LIG_FHA_2 737 743 PF00498 0.543
LIG_GBD_Chelix_1 362 370 PF00786 0.532
LIG_IRF3_LxIS_1 441 448 PF10401 0.660
LIG_LIR_Apic_2 73 78 PF02991 0.343
LIG_LIR_Gen_1 142 151 PF02991 0.395
LIG_LIR_Gen_1 219 225 PF02991 0.343
LIG_LIR_Gen_1 312 320 PF02991 0.343
LIG_LIR_Gen_1 464 473 PF02991 0.662
LIG_LIR_Gen_1 487 497 PF02991 0.445
LIG_LIR_Gen_1 57 66 PF02991 0.349
LIG_LIR_Gen_1 69 79 PF02991 0.343
LIG_LIR_Gen_1 690 698 PF02991 0.544
LIG_LIR_Nem_3 142 147 PF02991 0.395
LIG_LIR_Nem_3 219 224 PF02991 0.343
LIG_LIR_Nem_3 312 318 PF02991 0.343
LIG_LIR_Nem_3 464 470 PF02991 0.717
LIG_LIR_Nem_3 487 493 PF02991 0.447
LIG_LIR_Nem_3 57 61 PF02991 0.349
LIG_LIR_Nem_3 69 75 PF02991 0.362
LIG_LIR_Nem_3 690 696 PF02991 0.663
LIG_LIR_Nem_3 774 778 PF02991 0.608
LIG_PCNA_yPIPBox_3 111 123 PF02747 0.397
LIG_PCNA_yPIPBox_3 152 161 PF02747 0.343
LIG_Pex14_1 463 467 PF04695 0.651
LIG_Pex14_1 848 852 PF04695 0.548
LIG_PTB_Apo_2 60 67 PF02174 0.343
LIG_Rb_LxCxE_1 222 240 PF01857 0.403
LIG_REV1ctd_RIR_1 174 183 PF16727 0.397
LIG_SH2_GRB2like 373 376 PF00017 0.550
LIG_SH2_STAP1 724 728 PF00017 0.522
LIG_SH2_STAT3 581 584 PF00017 0.572
LIG_SH2_STAT5 144 147 PF00017 0.343
LIG_SH2_STAT5 469 472 PF00017 0.552
LIG_SH2_STAT5 581 584 PF00017 0.637
LIG_SH2_STAT5 775 778 PF00017 0.488
LIG_SH3_3 183 189 PF00018 0.359
LIG_SH3_3 627 633 PF00018 0.749
LIG_SUMO_SIM_par_1 42 48 PF11976 0.412
LIG_SUMO_SIM_par_1 650 659 PF11976 0.677
LIG_SUMO_SIM_par_1 784 791 PF11976 0.534
LIG_TRAF2_1 489 492 PF00917 0.599
LIG_TRAF2_1 508 511 PF00917 0.574
LIG_TRAF2_1 582 585 PF00917 0.572
LIG_TRAF2_1 865 868 PF00917 0.491
LIG_TRAF2_1 903 906 PF00917 0.577
LIG_TRFH_1 469 473 PF08558 0.672
LIG_UBA3_1 588 593 PF00899 0.641
LIG_WRC_WIRS_1 144 149 PF05994 0.343
MOD_CDK_SPxxK_3 469 476 PF00069 0.673
MOD_CK1_1 214 220 PF00069 0.357
MOD_CK1_1 260 266 PF00069 0.403
MOD_CK1_1 296 302 PF00069 0.362
MOD_CK1_1 448 454 PF00069 0.588
MOD_CK1_1 656 662 PF00069 0.636
MOD_CK1_1 688 694 PF00069 0.671
MOD_CK1_1 921 927 PF00069 0.721
MOD_CK1_1 99 105 PF00069 0.333
MOD_CK2_1 109 115 PF00069 0.397
MOD_CK2_1 143 149 PF00069 0.343
MOD_CK2_1 20 26 PF00069 0.403
MOD_CK2_1 260 266 PF00069 0.343
MOD_CK2_1 469 475 PF00069 0.582
MOD_CK2_1 486 492 PF00069 0.459
MOD_CK2_1 505 511 PF00069 0.615
MOD_CK2_1 520 526 PF00069 0.609
MOD_CK2_1 527 533 PF00069 0.556
MOD_CK2_1 579 585 PF00069 0.627
MOD_CK2_1 729 735 PF00069 0.595
MOD_CK2_1 736 742 PF00069 0.557
MOD_CK2_1 776 782 PF00069 0.511
MOD_CK2_1 880 886 PF00069 0.582
MOD_Cter_Amidation 1 4 PF01082 0.630
MOD_GlcNHglycan 259 262 PF01048 0.391
MOD_GlcNHglycan 274 277 PF01048 0.318
MOD_GlcNHglycan 449 453 PF01048 0.649
MOD_GlcNHglycan 620 623 PF01048 0.693
MOD_GlcNHglycan 636 639 PF01048 0.677
MOD_GlcNHglycan 647 650 PF01048 0.671
MOD_GlcNHglycan 658 661 PF01048 0.572
MOD_GlcNHglycan 820 823 PF01048 0.566
MOD_GlcNHglycan 920 923 PF01048 0.702
MOD_GlcNHglycan 96 99 PF01048 0.339
MOD_GSK3_1 135 142 PF00069 0.329
MOD_GSK3_1 212 219 PF00069 0.356
MOD_GSK3_1 233 240 PF00069 0.356
MOD_GSK3_1 272 279 PF00069 0.343
MOD_GSK3_1 292 299 PF00069 0.350
MOD_GSK3_1 323 330 PF00069 0.354
MOD_GSK3_1 412 419 PF00069 0.568
MOD_GSK3_1 426 433 PF00069 0.605
MOD_GSK3_1 634 641 PF00069 0.804
MOD_GSK3_1 736 743 PF00069 0.609
MOD_GSK3_1 814 821 PF00069 0.544
MOD_GSK3_1 927 934 PF00069 0.673
MOD_GSK3_1 99 106 PF00069 0.359
MOD_N-GLC_1 110 115 PF02516 0.397
MOD_N-GLC_1 270 275 PF02516 0.343
MOD_N-GLC_1 323 328 PF02516 0.357
MOD_N-GLC_1 400 405 PF02516 0.563
MOD_N-GLC_1 62 67 PF02516 0.341
MOD_N-GLC_1 87 92 PF02516 0.343
MOD_NEK2_1 109 114 PF00069 0.461
MOD_NEK2_1 143 148 PF00069 0.348
MOD_NEK2_1 272 277 PF00069 0.374
MOD_NEK2_1 302 307 PF00069 0.344
MOD_NEK2_1 325 330 PF00069 0.314
MOD_NEK2_1 484 489 PF00069 0.729
MOD_NEK2_1 520 525 PF00069 0.652
MOD_NEK2_1 534 539 PF00069 0.431
MOD_NEK2_1 654 659 PF00069 0.683
MOD_NEK2_1 706 711 PF00069 0.473
MOD_NEK2_1 776 781 PF00069 0.533
MOD_NEK2_1 79 84 PF00069 0.343
MOD_NEK2_1 87 92 PF00069 0.343
MOD_PIKK_1 436 442 PF00454 0.662
MOD_PIKK_1 454 460 PF00454 0.497
MOD_PIKK_1 520 526 PF00454 0.656
MOD_PIKK_1 64 70 PF00454 0.343
MOD_PK_1 216 222 PF00069 0.343
MOD_PK_1 556 562 PF00069 0.622
MOD_PK_1 636 642 PF00069 0.587
MOD_PKA_1 556 562 PF00069 0.638
MOD_PKA_1 927 933 PF00069 0.691
MOD_PKA_2 423 429 PF00069 0.575
MOD_PKA_2 54 60 PF00069 0.343
MOD_PKA_2 556 562 PF00069 0.731
MOD_PKA_2 624 630 PF00069 0.605
MOD_PKA_2 688 694 PF00069 0.555
MOD_PKA_2 926 932 PF00069 0.753
MOD_PKB_1 18 26 PF00069 0.403
MOD_PKB_1 202 210 PF00069 0.343
MOD_PKB_1 744 752 PF00069 0.559
MOD_Plk_1 110 116 PF00069 0.397
MOD_Plk_1 172 178 PF00069 0.403
MOD_Plk_1 270 276 PF00069 0.343
MOD_Plk_1 436 442 PF00069 0.617
MOD_Plk_1 505 511 PF00069 0.611
MOD_Plk_1 579 585 PF00069 0.714
MOD_Plk_1 62 68 PF00069 0.321
MOD_Plk_1 706 712 PF00069 0.536
MOD_Plk_1 736 742 PF00069 0.610
MOD_Plk_1 825 831 PF00069 0.559
MOD_Plk_1 87 93 PF00069 0.355
MOD_Plk_2-3 54 60 PF00069 0.343
MOD_Plk_4 139 145 PF00069 0.374
MOD_Plk_4 172 178 PF00069 0.345
MOD_Plk_4 216 222 PF00069 0.343
MOD_Plk_4 276 282 PF00069 0.343
MOD_Plk_4 296 302 PF00069 0.343
MOD_Plk_4 309 315 PF00069 0.343
MOD_Plk_4 45 51 PF00069 0.420
MOD_Plk_4 688 694 PF00069 0.555
MOD_Plk_4 79 85 PF00069 0.346
MOD_Plk_4 87 93 PF00069 0.343
MOD_Plk_4 921 927 PF00069 0.652
MOD_ProDKin_1 293 299 PF00069 0.362
MOD_ProDKin_1 469 475 PF00069 0.672
MOD_SUMO_for_1 371 374 PF00179 0.578
MOD_SUMO_for_1 548 551 PF00179 0.586
MOD_SUMO_for_1 680 683 PF00179 0.534
MOD_SUMO_for_1 704 707 PF00179 0.610
MOD_SUMO_for_1 903 906 PF00179 0.577
MOD_SUMO_rev_2 350 357 PF00179 0.493
MOD_SUMO_rev_2 515 523 PF00179 0.597
MOD_SUMO_rev_2 550 558 PF00179 0.666
MOD_SUMO_rev_2 580 589 PF00179 0.588
MOD_SUMO_rev_2 674 680 PF00179 0.546
MOD_SUMO_rev_2 723 729 PF00179 0.542
MOD_SUMO_rev_2 796 803 PF00179 0.574
MOD_SUMO_rev_2 849 856 PF00179 0.499
MOD_SUMO_rev_2 861 871 PF00179 0.523
TRG_DiLeu_BaEn_1 872 877 PF01217 0.544
TRG_DiLeu_BaEn_4 383 389 PF01217 0.550
TRG_DiLeu_BaEn_4 607 613 PF01217 0.595
TRG_DiLeu_BaLyEn_6 427 432 PF01217 0.631
TRG_DiLeu_LyEn_5 872 877 PF01217 0.544
TRG_ENDOCYTIC_2 144 147 PF00928 0.343
TRG_ENDOCYTIC_2 467 470 PF00928 0.679
TRG_ENDOCYTIC_2 693 696 PF00928 0.542
TRG_ENDOCYTIC_2 775 778 PF00928 0.606
TRG_ER_diArg_1 17 20 PF00400 0.344
TRG_ER_diArg_1 202 204 PF00400 0.344
TRG_ER_diArg_1 612 614 PF00400 0.577
TRG_ER_diArg_1 877 879 PF00400 0.528
TRG_ER_diArg_1 907 909 PF00400 0.678
TRG_ER_diArg_1 926 928 PF00400 0.587
TRG_NES_CRM1_1 387 400 PF08389 0.507
TRG_NES_CRM1_1 436 449 PF08389 0.575
TRG_NLS_MonoExtC_3 831 836 PF00514 0.510
TRG_NLS_MonoExtN_4 830 836 PF00514 0.513
TRG_Pf-PMV_PEXEL_1 194 198 PF00026 0.461
TRG_Pf-PMV_PEXEL_1 364 368 PF00026 0.579
TRG_Pf-PMV_PEXEL_1 430 435 PF00026 0.629
TRG_Pf-PMV_PEXEL_1 543 547 PF00026 0.655
TRG_Pf-PMV_PEXEL_1 603 607 PF00026 0.651
TRG_Pf-PMV_PEXEL_1 756 760 PF00026 0.465
TRG_Pf-PMV_PEXEL_1 864 868 PF00026 0.544

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P5L3 Leptomonas seymouri 68% 100%
A0A3Q8I9R7 Leishmania donovani 100% 100%
A0A3R7MU74 Trypanosoma rangeli 26% 84%
A4H925 Leishmania braziliensis 83% 99%
E9AR52 Leishmania mexicana (strain MHOM/GT/2001/U1103) 94% 100%
Q0DV28 Oryza sativa subsp. japonica 30% 99%
Q4QEB1 Leishmania major 97% 100%
Q5W7C6 Oryza sativa subsp. japonica 32% 89%
V5B325 Trypanosoma cruzi 30% 100%
V5BFF1 Trypanosoma cruzi 56% 85%

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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