LeishMANIAdb
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Kinesin-like protein

Quick info Annotations Function or PPIs Localization Phosphorylation Abundance Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Kinesin-like protein
Gene product:
Kinesin-13 5 - putative
Species:
Leishmania infantum
UniProt:
A4HVT9_LEIIN
TriTrypDb:
LINF_130021600
Length:
728

Annotations

Annotations by Jardim et al.

Structural Proteins, Kinesin-like

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) yes yes: 2
Forrest at al. (procyclic) yes yes: 2
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: 6
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 6
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 16
NetGPI no yes: 0, no: 16
Cellular components
Term Name Level Count
GO:0005874 microtubule 6 17
GO:0099080 supramolecular complex 2 17
GO:0099081 supramolecular polymer 3 17
GO:0099512 supramolecular fiber 4 17
GO:0099513 polymeric cytoskeletal fiber 5 17
GO:0110165 cellular anatomical entity 1 17
GO:0000922 spindle pole 2 1
GO:0005634 nucleus 5 1
GO:0005819 spindle 5 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0043228 non-membrane-bounded organelle 3 1
GO:0043229 intracellular organelle 3 1
GO:0043231 intracellular membrane-bounded organelle 4 1
GO:0043232 intracellular non-membrane-bounded organelle 4 1

Phosphorylation

Amastigote: 169
Promastigote: 174, 645, 650
Promastigote/Amastigote: 139, 165, 175, 177, 601

Abundance

Amastigote (protein)
Source Evidence on protein Close homologs
Pescher et al. (upgregulation) no yes: 0
Promastigote and amastigote
Source Evidence on protein Close homologs
Lahav et al.
- mRNA
- Protein

Expansion

Sequence features

A4HVT9
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HVT9

Function

Biological processes
Term Name Level Count
GO:0007017 microtubule-based process 2 17
GO:0007018 microtubule-based movement 3 17
GO:0009987 cellular process 1 17
GO:0000226 microtubule cytoskeleton organization 3 2
GO:0006996 organelle organization 4 2
GO:0007010 cytoskeleton organization 5 2
GO:0007019 microtubule depolymerization 5 2
GO:0007051 spindle organization 3 1
GO:0007052 mitotic spindle organization 4 1
GO:0016043 cellular component organization 3 2
GO:0022402 cell cycle process 2 1
GO:0022411 cellular component disassembly 4 2
GO:0031109 microtubule polymerization or depolymerization 4 2
GO:0032984 protein-containing complex disassembly 5 2
GO:0043933 protein-containing complex organization 4 2
GO:0050789 regulation of biological process 2 1
GO:0050794 regulation of cellular process 3 1
GO:0051261 protein depolymerization 6 2
GO:0051983 regulation of chromosome segregation 4 1
GO:0065007 biological regulation 1 1
GO:0071840 cellular component organization or biogenesis 2 2
GO:0097435 supramolecular fiber organization 4 2
GO:1902850 microtubule cytoskeleton organization involved in mitosis 4 1
GO:1903047 mitotic cell cycle process 3 1
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 17
GO:0003774 cytoskeletal motor activity 1 17
GO:0003777 microtubule motor activity 2 17
GO:0005488 binding 1 17
GO:0005515 protein binding 2 17
GO:0005524 ATP binding 5 17
GO:0008017 microtubule binding 5 17
GO:0008092 cytoskeletal protein binding 3 17
GO:0015631 tubulin binding 4 17
GO:0017076 purine nucleotide binding 4 17
GO:0030554 adenyl nucleotide binding 5 17
GO:0032553 ribonucleotide binding 3 17
GO:0032555 purine ribonucleotide binding 4 17
GO:0032559 adenyl ribonucleotide binding 5 17
GO:0035639 purine ribonucleoside triphosphate binding 4 17
GO:0036094 small molecule binding 2 17
GO:0043167 ion binding 2 17
GO:0043168 anion binding 3 17
GO:0097159 organic cyclic compound binding 2 17
GO:0097367 carbohydrate derivative binding 2 17
GO:0140657 ATP-dependent activity 1 17
GO:1901265 nucleoside phosphate binding 3 17
GO:1901363 heterocyclic compound binding 2 17

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 211 215 PF00656 0.282
CLV_C14_Caspase3-7 222 226 PF00656 0.298
CLV_C14_Caspase3-7 431 435 PF00656 0.230
CLV_C14_Caspase3-7 590 594 PF00656 0.658
CLV_C14_Caspase3-7 646 650 PF00656 0.590
CLV_NRD_NRD_1 115 117 PF00675 0.575
CLV_NRD_NRD_1 125 127 PF00675 0.664
CLV_NRD_NRD_1 142 144 PF00675 0.456
CLV_NRD_NRD_1 181 183 PF00675 0.604
CLV_NRD_NRD_1 193 195 PF00675 0.618
CLV_NRD_NRD_1 202 204 PF00675 0.296
CLV_NRD_NRD_1 258 260 PF00675 0.257
CLV_NRD_NRD_1 51 53 PF00675 0.324
CLV_NRD_NRD_1 552 554 PF00675 0.577
CLV_NRD_NRD_1 695 697 PF00675 0.525
CLV_NRD_NRD_1 706 708 PF00675 0.478
CLV_NRD_NRD_1 712 714 PF00675 0.474
CLV_PCSK_KEX2_1 115 117 PF00082 0.602
CLV_PCSK_KEX2_1 125 127 PF00082 0.664
CLV_PCSK_KEX2_1 142 144 PF00082 0.456
CLV_PCSK_KEX2_1 181 183 PF00082 0.611
CLV_PCSK_KEX2_1 192 194 PF00082 0.583
CLV_PCSK_KEX2_1 204 206 PF00082 0.276
CLV_PCSK_KEX2_1 51 53 PF00082 0.336
CLV_PCSK_KEX2_1 552 554 PF00082 0.577
CLV_PCSK_KEX2_1 62 64 PF00082 0.455
CLV_PCSK_KEX2_1 695 697 PF00082 0.523
CLV_PCSK_KEX2_1 706 708 PF00082 0.477
CLV_PCSK_KEX2_1 712 714 PF00082 0.472
CLV_PCSK_PC1ET2_1 204 206 PF00082 0.303
CLV_PCSK_PC1ET2_1 62 64 PF00082 0.431
CLV_PCSK_SKI1_1 115 119 PF00082 0.688
CLV_PCSK_SKI1_1 181 185 PF00082 0.657
CLV_PCSK_SKI1_1 33 37 PF00082 0.406
CLV_PCSK_SKI1_1 448 452 PF00082 0.273
CLV_PCSK_SKI1_1 515 519 PF00082 0.469
CLV_PCSK_SKI1_1 52 56 PF00082 0.332
CLV_PCSK_SKI1_1 552 556 PF00082 0.678
CLV_PCSK_SKI1_1 557 561 PF00082 0.685
CLV_PCSK_SKI1_1 6 10 PF00082 0.387
CLV_PCSK_SKI1_1 605 609 PF00082 0.565
DEG_APCC_DBOX_1 50 58 PF00400 0.317
DEG_Nend_UBRbox_2 1 3 PF02207 0.346
DEG_SCF_FBW7_1 620 625 PF00400 0.610
DEG_SPOP_SBC_1 558 562 PF00917 0.625
DEG_SPOP_SBC_1 606 610 PF00917 0.638
DOC_AGCK_PIF_1 415 420 PF00069 0.230
DOC_ANK_TNKS_1 181 188 PF00023 0.700
DOC_CKS1_1 110 115 PF01111 0.677
DOC_CKS1_1 573 578 PF01111 0.563
DOC_CKS1_1 635 640 PF01111 0.679
DOC_CYCLIN_RxL_1 445 455 PF00134 0.273
DOC_MAPK_gen_1 192 202 PF00069 0.453
DOC_MAPK_gen_1 302 310 PF00069 0.365
DOC_MAPK_gen_1 319 328 PF00069 0.444
DOC_MAPK_gen_1 51 60 PF00069 0.411
DOC_MAPK_HePTP_8 316 328 PF00069 0.248
DOC_MAPK_MEF2A_6 193 202 PF00069 0.441
DOC_MAPK_MEF2A_6 319 328 PF00069 0.254
DOC_MAPK_MEF2A_6 398 407 PF00069 0.273
DOC_USP7_MATH_1 386 390 PF00917 0.263
DOC_USP7_MATH_1 394 398 PF00917 0.270
DOC_USP7_MATH_1 497 501 PF00917 0.230
DOC_USP7_MATH_1 606 610 PF00917 0.702
DOC_USP7_MATH_1 622 626 PF00917 0.611
DOC_USP7_MATH_1 66 70 PF00917 0.554
DOC_USP7_MATH_1 686 690 PF00917 0.438
DOC_USP7_MATH_1 78 82 PF00917 0.528
DOC_USP7_UBL2_3 515 519 PF12436 0.397
DOC_WW_Pin1_4 109 114 PF00397 0.602
DOC_WW_Pin1_4 115 120 PF00397 0.666
DOC_WW_Pin1_4 172 177 PF00397 0.591
DOC_WW_Pin1_4 492 497 PF00397 0.280
DOC_WW_Pin1_4 572 577 PF00397 0.588
DOC_WW_Pin1_4 608 613 PF00397 0.596
DOC_WW_Pin1_4 618 623 PF00397 0.509
DOC_WW_Pin1_4 634 639 PF00397 0.574
DOC_WW_Pin1_4 71 76 PF00397 0.593
DOC_WW_Pin1_4 83 88 PF00397 0.549
LIG_14-3-3_CanoR_1 136 145 PF00244 0.637
LIG_14-3-3_CanoR_1 170 176 PF00244 0.616
LIG_14-3-3_CanoR_1 197 201 PF00244 0.376
LIG_14-3-3_CanoR_1 249 253 PF00244 0.261
LIG_14-3-3_CanoR_1 417 421 PF00244 0.255
LIG_14-3-3_CanoR_1 597 603 PF00244 0.666
LIG_14-3-3_CanoR_1 605 612 PF00244 0.672
LIG_BRCT_BRCA1_1 545 549 PF00533 0.554
LIG_EH1_1 40 48 PF00400 0.483
LIG_EH1_1 663 671 PF00400 0.488
LIG_FHA_1 197 203 PF00498 0.397
LIG_FHA_1 240 246 PF00498 0.254
LIG_FHA_1 369 375 PF00498 0.231
LIG_FHA_1 436 442 PF00498 0.248
LIG_FHA_1 473 479 PF00498 0.273
LIG_FHA_1 486 492 PF00498 0.273
LIG_FHA_1 535 541 PF00498 0.581
LIG_FHA_2 116 122 PF00498 0.579
LIG_FHA_2 220 226 PF00498 0.230
LIG_FHA_2 229 235 PF00498 0.230
LIG_FHA_2 259 265 PF00498 0.317
LIG_FHA_2 274 280 PF00498 0.244
LIG_FHA_2 34 40 PF00498 0.393
LIG_FHA_2 417 423 PF00498 0.282
LIG_FHA_2 437 443 PF00498 0.273
LIG_LIR_Apic_2 616 620 PF02991 0.559
LIG_LIR_Gen_1 214 224 PF02991 0.286
LIG_LIR_Gen_1 251 256 PF02991 0.234
LIG_LIR_Gen_1 296 303 PF02991 0.230
LIG_LIR_Gen_1 315 324 PF02991 0.281
LIG_LIR_Gen_1 39 48 PF02991 0.350
LIG_LIR_Gen_1 419 424 PF02991 0.264
LIG_LIR_Nem_3 214 220 PF02991 0.289
LIG_LIR_Nem_3 251 255 PF02991 0.256
LIG_LIR_Nem_3 296 300 PF02991 0.230
LIG_LIR_Nem_3 315 320 PF02991 0.281
LIG_LIR_Nem_3 329 334 PF02991 0.308
LIG_LIR_Nem_3 39 43 PF02991 0.383
LIG_LIR_Nem_3 419 423 PF02991 0.264
LIG_NRBOX 337 343 PF00104 0.273
LIG_NRBOX 4 10 PF00104 0.360
LIG_NRP_CendR_1 727 728 PF00754 0.560
LIG_Pex14_2 414 418 PF04695 0.230
LIG_Rb_LxCxE_1 344 365 PF01857 0.230
LIG_REV1ctd_RIR_1 412 421 PF16727 0.230
LIG_SH2_CRK 217 221 PF00017 0.230
LIG_SH2_CRK 252 256 PF00017 0.230
LIG_SH2_CRK 297 301 PF00017 0.248
LIG_SH2_CRK 339 343 PF00017 0.379
LIG_SH2_CRK 40 44 PF00017 0.343
LIG_SH2_CRK 617 621 PF00017 0.652
LIG_SH2_SRC 266 269 PF00017 0.364
LIG_SH2_STAP1 217 221 PF00017 0.230
LIG_SH2_STAP1 252 256 PF00017 0.230
LIG_SH2_STAP1 510 514 PF00017 0.273
LIG_SH2_STAP1 718 722 PF00017 0.526
LIG_SH2_STAT5 244 247 PF00017 0.273
LIG_SH2_STAT5 297 300 PF00017 0.268
LIG_SH2_STAT5 309 312 PF00017 0.224
LIG_SH2_STAT5 693 696 PF00017 0.372
LIG_SH2_STAT5 718 721 PF00017 0.459
LIG_SH3_2 104 109 PF14604 0.643
LIG_SH3_3 101 107 PF00018 0.597
LIG_SH3_3 157 163 PF00018 0.642
LIG_SH3_3 570 576 PF00018 0.602
LIG_SH3_3 72 78 PF00018 0.622
LIG_SH3_3 81 87 PF00018 0.602
LIG_SUMO_SIM_anti_2 196 202 PF11976 0.374
LIG_SUMO_SIM_par_1 228 234 PF11976 0.274
LIG_TRAF2_1 526 529 PF00917 0.497
LIG_TRAF2_2 235 240 PF00917 0.230
LIG_UBA3_1 229 238 PF00899 0.257
LIG_UBA3_1 450 454 PF00899 0.273
LIG_UBA3_1 54 62 PF00899 0.336
LIG_UBA3_1 669 674 PF00899 0.357
LIG_WRC_WIRS_1 581 586 PF05994 0.655
MOD_CDC14_SPxK_1 611 614 PF00782 0.687
MOD_CDK_SPxK_1 109 115 PF00069 0.635
MOD_CDK_SPxK_1 608 614 PF00069 0.679
MOD_CDK_SPxxK_3 109 116 PF00069 0.607
MOD_CDK_SPxxK_3 174 181 PF00069 0.602
MOD_CDK_SPxxK_3 572 579 PF00069 0.549
MOD_CDK_SPxxK_3 608 615 PF00069 0.682
MOD_CK1_1 174 180 PF00069 0.586
MOD_CK1_1 196 202 PF00069 0.484
MOD_CK1_1 293 299 PF00069 0.273
MOD_CK1_1 318 324 PF00069 0.285
MOD_CK1_1 396 402 PF00069 0.255
MOD_CK1_1 435 441 PF00069 0.248
MOD_CK1_1 472 478 PF00069 0.273
MOD_CK1_1 495 501 PF00069 0.230
MOD_CK1_1 522 528 PF00069 0.625
MOD_CK1_1 561 567 PF00069 0.583
MOD_CK1_1 592 598 PF00069 0.666
MOD_CK1_1 601 607 PF00069 0.570
MOD_CK1_1 629 635 PF00069 0.588
MOD_CK1_1 647 653 PF00069 0.515
MOD_CK2_1 115 121 PF00069 0.581
MOD_CK2_1 228 234 PF00069 0.401
MOD_CK2_1 273 279 PF00069 0.229
MOD_CK2_1 326 332 PF00069 0.292
MOD_CK2_1 436 442 PF00069 0.273
MOD_CK2_1 522 528 PF00069 0.585
MOD_Cter_Amidation 179 182 PF01082 0.716
MOD_Cter_Amidation 725 728 PF01082 0.497
MOD_GlcNHglycan 138 141 PF01048 0.632
MOD_GlcNHglycan 292 295 PF01048 0.275
MOD_GlcNHglycan 497 500 PF01048 0.230
MOD_GlcNHglycan 524 527 PF01048 0.586
MOD_GlcNHglycan 545 548 PF01048 0.577
MOD_GlcNHglycan 628 631 PF01048 0.653
MOD_GlcNHglycan 632 635 PF01048 0.631
MOD_GlcNHglycan 646 649 PF01048 0.504
MOD_GlcNHglycan 68 71 PF01048 0.582
MOD_GlcNHglycan 690 693 PF01048 0.403
MOD_GSK3_1 162 169 PF00069 0.563
MOD_GSK3_1 432 439 PF00069 0.230
MOD_GSK3_1 497 504 PF00069 0.252
MOD_GSK3_1 539 546 PF00069 0.557
MOD_GSK3_1 557 564 PF00069 0.581
MOD_GSK3_1 588 595 PF00069 0.708
MOD_GSK3_1 601 608 PF00069 0.587
MOD_GSK3_1 618 625 PF00069 0.592
MOD_GSK3_1 626 633 PF00069 0.618
MOD_GSK3_1 640 647 PF00069 0.637
MOD_GSK3_1 79 86 PF00069 0.647
MOD_GSK3_1 88 95 PF00069 0.700
MOD_LATS_1 624 630 PF00433 0.578
MOD_N-GLC_1 207 212 PF02516 0.269
MOD_N-GLC_1 326 331 PF02516 0.364
MOD_N-GLC_1 446 451 PF02516 0.273
MOD_N-GLC_1 492 497 PF02516 0.230
MOD_N-GLC_1 598 603 PF02516 0.557
MOD_N-GLC_1 66 71 PF02516 0.553
MOD_N-GLC_2 359 361 PF02516 0.234
MOD_NEK2_1 14 19 PF00069 0.429
MOD_NEK2_1 273 278 PF00069 0.300
MOD_NEK2_1 403 408 PF00069 0.230
MOD_NEK2_1 469 474 PF00069 0.282
MOD_NEK2_1 483 488 PF00069 0.297
MOD_NEK2_1 580 585 PF00069 0.638
MOD_NEK2_2 281 286 PF00069 0.298
MOD_NEK2_2 380 385 PF00069 0.230
MOD_PIKK_1 563 569 PF00454 0.573
MOD_PIKK_1 675 681 PF00454 0.522
MOD_PIKK_1 700 706 PF00454 0.438
MOD_PKA_1 181 187 PF00069 0.701
MOD_PKA_1 193 199 PF00069 0.435
MOD_PKA_2 181 187 PF00069 0.711
MOD_PKA_2 193 199 PF00069 0.390
MOD_PKA_2 248 254 PF00069 0.252
MOD_PKA_2 258 264 PF00069 0.248
MOD_PKA_2 318 324 PF00069 0.406
MOD_PKA_2 416 422 PF00069 0.262
MOD_PKA_2 436 442 PF00069 0.273
MOD_PKA_2 469 475 PF00069 0.273
MOD_PKA_2 562 568 PF00069 0.565
MOD_Plk_1 14 20 PF00069 0.367
MOD_Plk_1 239 245 PF00069 0.360
MOD_Plk_1 326 332 PF00069 0.364
MOD_Plk_1 446 452 PF00069 0.278
MOD_Plk_1 501 507 PF00069 0.273
MOD_Plk_1 592 598 PF00069 0.682
MOD_Plk_1 640 646 PF00069 0.659
MOD_Plk_1 675 681 PF00069 0.483
MOD_Plk_1 686 692 PF00069 0.539
MOD_Plk_2-3 144 150 PF00069 0.758
MOD_Plk_4 273 279 PF00069 0.273
MOD_Plk_4 295 301 PF00069 0.288
MOD_Plk_4 326 332 PF00069 0.287
MOD_Plk_4 446 452 PF00069 0.273
MOD_ProDKin_1 109 115 PF00069 0.605
MOD_ProDKin_1 172 178 PF00069 0.595
MOD_ProDKin_1 492 498 PF00069 0.280
MOD_ProDKin_1 572 578 PF00069 0.586
MOD_ProDKin_1 608 614 PF00069 0.600
MOD_ProDKin_1 618 624 PF00069 0.509
MOD_ProDKin_1 634 640 PF00069 0.571
MOD_ProDKin_1 71 77 PF00069 0.592
MOD_ProDKin_1 83 89 PF00069 0.547
MOD_SUMO_for_1 673 676 PF00179 0.414
MOD_SUMO_rev_2 253 261 PF00179 0.275
TRG_DiLeu_BaEn_1 306 311 PF01217 0.230
TRG_DiLeu_BaEn_1 654 659 PF01217 0.516
TRG_DiLeu_BaEn_2 55 61 PF01217 0.472
TRG_DiLeu_BaEn_3 654 660 PF01217 0.426
TRG_DiLeu_BaLyEn_6 269 274 PF01217 0.273
TRG_ENDOCYTIC_2 217 220 PF00928 0.230
TRG_ENDOCYTIC_2 252 255 PF00928 0.262
TRG_ENDOCYTIC_2 297 300 PF00928 0.274
TRG_ENDOCYTIC_2 339 342 PF00928 0.379
TRG_ENDOCYTIC_2 40 43 PF00928 0.374
TRG_ER_diArg_1 114 116 PF00400 0.668
TRG_ER_diArg_1 192 194 PF00400 0.581
TRG_ER_diArg_1 202 205 PF00400 0.255
TRG_ER_diArg_1 695 697 PF00400 0.563
TRG_ER_diArg_1 705 707 PF00400 0.508
TRG_ER_diArg_1 711 713 PF00400 0.414
TRG_NLS_Bipartite_1 192 207 PF00514 0.427
TRG_Pf-PMV_PEXEL_1 271 275 PF00026 0.299
TRG_Pf-PMV_PEXEL_1 458 462 PF00026 0.273
TRG_Pf-PMV_PEXEL_1 52 56 PF00026 0.332
TRG_Pf-PMV_PEXEL_1 706 710 PF00026 0.521
TRG_Pf-PMV_PEXEL_1 713 717 PF00026 0.549

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6P6 Leptomonas seymouri 47% 100%
A0A0N1PAZ2 Leptomonas seymouri 82% 97%
A0A0N1PDD6 Leptomonas seymouri 28% 96%
A0A1X0NL76 Trypanosomatidae 65% 100%
A0A3S5H4S8 Leishmania donovani 46% 100%
A0A3S7WST0 Leishmania donovani 100% 100%
A0A422P4C5 Trypanosoma rangeli 64% 100%
A4H337 Leishmania braziliensis 46% 100%
A4H7F1 Leishmania braziliensis 93% 100%
A4H8S6 Leishmania braziliensis 30% 70%
A4HAQ7 Leishmania braziliensis 27% 100%
A4HRC5 Leishmania infantum 46% 100%
A4HSA6 Leishmania infantum 30% 100%
A4I9W6 Leishmania infantum 27% 68%
B9EY52 Oryza sativa subsp. japonica 42% 100%
B9FMJ3 Oryza sativa subsp. japonica 38% 89%
C9ZXH0 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 39% 100%
D0A6E6 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 64% 100%
E9ABZ2 Leishmania major 46% 100%
E9AJ89 Leishmania mexicana (strain MHOM/GT/2001/U1103) 46% 100%
E9API5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 98% 99%
E9B4X8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 26% 67%
Q4QFZ3 Leishmania major 98% 100%
Q940B8 Arabidopsis thaliana 40% 92%
Q940Y8 Arabidopsis thaliana 42% 100%
V5BHI2 Trypanosoma cruzi 65% 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