LeishMANIAdb
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Heat shock 70 protein-like protein (Chaperone protein-like protein)

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

Quick info

Protein:
Heat shock 70 protein-like protein (Chaperone protein-like protein)
Gene product:
heat shock 70 protein-like protein
Species:
Leishmania mexicana
UniProt:
E9AY68_LEIMU
TriTrypDb:
LmxM.26.0900
Length:
944

Localization

Secreted promastigote
Source Evidence on protein Close homologs
Cuervo et al. no yes: 1
Hassani et al. no yes: 0
Forrest at al. (metacyclic) no yes: 4
Forrest at al. (procyclic) no yes: 4
Silverman et al. no yes: 4
Pissara et al. no yes: 14
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: 8
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 12
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 17
NetGPI no yes: 0, no: 17
Cellular components
Term Name Level Count
GO:0043226 organelle 2 18
GO:0110165 cellular anatomical entity 1 18
GO:0005737 cytoplasm 2 3
GO:0016020 membrane 2 1

Expansion

Sequence features

E9AY68
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AY68

Function

Biological processes
Term Name Level Count
GO:0006457 protein folding 2 3
GO:0006458 'de novo' protein folding 3 3
GO:0006950 response to stress 2 3
GO:0006986 response to unfolded protein 4 3
GO:0009987 cellular process 1 3
GO:0010033 response to organic substance 3 3
GO:0033554 cellular response to stress 3 3
GO:0034620 cellular response to unfolded protein 5 3
GO:0035966 response to topologically incorrect protein 3 3
GO:0035967 cellular response to topologically incorrect protein 4 3
GO:0042026 protein refolding 3 3
GO:0042221 response to chemical 2 3
GO:0050896 response to stimulus 1 3
GO:0051084 'de novo' post-translational protein folding 4 3
GO:0051085 chaperone cofactor-dependent protein refolding 4 3
GO:0051716 cellular response to stimulus 2 3
GO:0061077 chaperone-mediated protein folding 3 3
GO:0070887 cellular response to chemical stimulus 3 3
GO:0071310 cellular response to organic substance 4 3
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 18
GO:0005488 binding 1 18
GO:0005524 ATP binding 5 18
GO:0017076 purine nucleotide binding 4 18
GO:0030554 adenyl nucleotide binding 5 18
GO:0032553 ribonucleotide binding 3 18
GO:0032555 purine ribonucleotide binding 4 18
GO:0032559 adenyl ribonucleotide binding 5 18
GO:0035639 purine ribonucleoside triphosphate binding 4 18
GO:0036094 small molecule binding 2 18
GO:0043167 ion binding 2 18
GO:0043168 anion binding 3 18
GO:0044183 protein folding chaperone 1 18
GO:0097159 organic cyclic compound binding 2 18
GO:0097367 carbohydrate derivative binding 2 18
GO:0140657 ATP-dependent activity 1 18
GO:0140662 ATP-dependent protein folding chaperone 2 18
GO:1901265 nucleoside phosphate binding 3 18
GO:1901363 heterocyclic compound binding 2 18
GO:0003824 catalytic activity 1 3
GO:0005515 protein binding 2 3
GO:0016462 pyrophosphatase activity 5 3
GO:0016787 hydrolase activity 2 3
GO:0016817 hydrolase activity, acting on acid anhydrides 3 3
GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides 4 3
GO:0016887 ATP hydrolysis activity 7 3
GO:0017111 ribonucleoside triphosphate phosphatase activity 6 3
GO:0031072 heat shock protein binding 3 3
GO:0051082 unfolded protein binding 3 3
GO:0051787 misfolded protein binding 3 3

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 280 284 PF00656 0.369
CLV_NRD_NRD_1 113 115 PF00675 0.211
CLV_NRD_NRD_1 286 288 PF00675 0.518
CLV_NRD_NRD_1 569 571 PF00675 0.452
CLV_NRD_NRD_1 619 621 PF00675 0.437
CLV_NRD_NRD_1 635 637 PF00675 0.413
CLV_NRD_NRD_1 642 644 PF00675 0.460
CLV_NRD_NRD_1 66 68 PF00675 0.502
CLV_NRD_NRD_1 7 9 PF00675 0.630
CLV_NRD_NRD_1 775 777 PF00675 0.550
CLV_PCSK_KEX2_1 113 115 PF00082 0.314
CLV_PCSK_KEX2_1 162 164 PF00082 0.332
CLV_PCSK_KEX2_1 278 280 PF00082 0.404
CLV_PCSK_KEX2_1 286 288 PF00082 0.517
CLV_PCSK_KEX2_1 333 335 PF00082 0.391
CLV_PCSK_KEX2_1 569 571 PF00082 0.530
CLV_PCSK_KEX2_1 619 621 PF00082 0.437
CLV_PCSK_KEX2_1 635 637 PF00082 0.413
CLV_PCSK_KEX2_1 65 67 PF00082 0.485
CLV_PCSK_KEX2_1 650 652 PF00082 0.408
CLV_PCSK_KEX2_1 7 9 PF00082 0.630
CLV_PCSK_KEX2_1 774 776 PF00082 0.551
CLV_PCSK_KEX2_1 87 89 PF00082 0.564
CLV_PCSK_KEX2_1 887 889 PF00082 0.498
CLV_PCSK_PC1ET2_1 162 164 PF00082 0.332
CLV_PCSK_PC1ET2_1 278 280 PF00082 0.359
CLV_PCSK_PC1ET2_1 333 335 PF00082 0.391
CLV_PCSK_PC1ET2_1 650 652 PF00082 0.428
CLV_PCSK_PC1ET2_1 87 89 PF00082 0.564
CLV_PCSK_PC1ET2_1 887 889 PF00082 0.498
CLV_PCSK_PC7_1 282 288 PF00082 0.368
CLV_PCSK_PC7_1 3 9 PF00082 0.494
CLV_PCSK_SKI1_1 213 217 PF00082 0.277
CLV_PCSK_SKI1_1 243 247 PF00082 0.255
CLV_PCSK_SKI1_1 3 7 PF00082 0.617
CLV_PCSK_SKI1_1 359 363 PF00082 0.211
CLV_PCSK_SKI1_1 478 482 PF00082 0.208
CLV_PCSK_SKI1_1 506 510 PF00082 0.228
CLV_PCSK_SKI1_1 573 577 PF00082 0.464
CLV_PCSK_SKI1_1 619 623 PF00082 0.432
CLV_PCSK_SKI1_1 635 639 PF00082 0.451
CLV_PCSK_SKI1_1 678 682 PF00082 0.454
CLV_PCSK_SKI1_1 855 859 PF00082 0.467
CLV_PCSK_SKI1_1 867 871 PF00082 0.437
CLV_Separin_Metazoa 675 679 PF03568 0.400
DEG_APCC_DBOX_1 854 862 PF00400 0.544
DEG_SPOP_SBC_1 318 322 PF00917 0.551
DOC_CKS1_1 15 20 PF01111 0.459
DOC_CKS1_1 237 242 PF01111 0.228
DOC_CYCLIN_RxL_1 333 342 PF00134 0.228
DOC_CYCLIN_RxL_1 410 420 PF00134 0.228
DOC_CYCLIN_RxL_1 501 511 PF00134 0.337
DOC_CYCLIN_RxL_1 569 581 PF00134 0.462
DOC_CYCLIN_RxL_1 616 627 PF00134 0.466
DOC_CYCLIN_yCln2_LP_2 464 470 PF00134 0.251
DOC_CYCLIN_yCln2_LP_2 857 863 PF00134 0.508
DOC_MAPK_gen_1 333 341 PF00069 0.277
DOC_MAPK_gen_1 445 452 PF00069 0.247
DOC_MAPK_gen_1 569 577 PF00069 0.459
DOC_MAPK_gen_1 887 894 PF00069 0.493
DOC_MAPK_MEF2A_6 190 197 PF00069 0.315
DOC_MAPK_MEF2A_6 887 894 PF00069 0.521
DOC_PP1_RVXF_1 335 342 PF00149 0.228
DOC_PP1_RVXF_1 421 427 PF00149 0.228
DOC_USP7_MATH_1 121 125 PF00917 0.222
DOC_USP7_MATH_1 150 154 PF00917 0.337
DOC_USP7_MATH_1 230 234 PF00917 0.337
DOC_USP7_MATH_1 304 308 PF00917 0.674
DOC_USP7_MATH_1 317 321 PF00917 0.555
DOC_USP7_MATH_1 35 39 PF00917 0.654
DOC_USP7_MATH_1 780 784 PF00917 0.509
DOC_USP7_MATH_1 808 812 PF00917 0.518
DOC_USP7_MATH_2 829 835 PF00917 0.458
DOC_USP7_UBL2_3 744 748 PF12436 0.492
DOC_WW_Pin1_4 117 122 PF00397 0.307
DOC_WW_Pin1_4 14 19 PF00397 0.473
DOC_WW_Pin1_4 236 241 PF00397 0.228
DOC_WW_Pin1_4 288 293 PF00397 0.479
DOC_WW_Pin1_4 321 326 PF00397 0.603
LIG_14-3-3_CanoR_1 151 158 PF00244 0.228
LIG_14-3-3_CanoR_1 200 205 PF00244 0.213
LIG_14-3-3_CanoR_1 213 223 PF00244 0.213
LIG_14-3-3_CanoR_1 334 340 PF00244 0.277
LIG_14-3-3_CanoR_1 48 54 PF00244 0.533
LIG_14-3-3_CanoR_1 7 15 PF00244 0.592
LIG_14-3-3_CanoR_1 809 813 PF00244 0.511
LIG_14-3-3_CanoR_1 859 864 PF00244 0.456
LIG_APCC_ABBA_1 139 144 PF00400 0.228
LIG_BIR_III_4 328 332 PF00653 0.383
LIG_BRCT_BRCA1_1 337 341 PF00533 0.230
LIG_BRCT_BRCA1_1 382 386 PF00533 0.236
LIG_BRCT_BRCA1_2 382 388 PF00533 0.337
LIG_Clathr_ClatBox_1 610 614 PF01394 0.440
LIG_EH1_1 201 209 PF00400 0.228
LIG_EH1_1 254 262 PF00400 0.326
LIG_FHA_1 180 186 PF00498 0.228
LIG_FHA_1 199 205 PF00498 0.228
LIG_FHA_1 463 469 PF00498 0.247
LIG_FHA_1 549 555 PF00498 0.487
LIG_FHA_1 577 583 PF00498 0.668
LIG_FHA_1 693 699 PF00498 0.531
LIG_FHA_1 8 14 PF00498 0.738
LIG_FHA_1 894 900 PF00498 0.508
LIG_FHA_2 184 190 PF00498 0.323
LIG_FHA_2 270 276 PF00498 0.291
LIG_FHA_2 365 371 PF00498 0.333
LIG_FHA_2 455 461 PF00498 0.228
LIG_FHA_2 484 490 PF00498 0.248
LIG_FHA_2 731 737 PF00498 0.654
LIG_FHA_2 860 866 PF00498 0.456
LIG_FHA_2 896 902 PF00498 0.595
LIG_FHA_2 917 923 PF00498 0.485
LIG_GBD_Chelix_1 204 212 PF00786 0.247
LIG_GBD_Chelix_1 567 575 PF00786 0.435
LIG_GBD_Chelix_1 679 687 PF00786 0.475
LIG_LIR_Apic_2 122 128 PF02991 0.228
LIG_LIR_Apic_2 391 397 PF02991 0.228
LIG_LIR_Apic_2 819 825 PF02991 0.520
LIG_LIR_Gen_1 201 210 PF02991 0.247
LIG_LIR_Gen_1 377 386 PF02991 0.296
LIG_LIR_Gen_1 459 468 PF02991 0.274
LIG_LIR_Gen_1 834 842 PF02991 0.394
LIG_LIR_Nem_3 201 205 PF02991 0.247
LIG_LIR_Nem_3 377 381 PF02991 0.296
LIG_LIR_Nem_3 430 436 PF02991 0.368
LIG_LIR_Nem_3 459 464 PF02991 0.274
LIG_LIR_Nem_3 543 547 PF02991 0.474
LIG_LIR_Nem_3 75 80 PF02991 0.522
LIG_LIR_Nem_3 834 838 PF02991 0.402
LIG_LRP6_Inhibitor_1 582 594 PF00058 0.495
LIG_MAD2 516 524 PF02301 0.230
LIG_NRP_CendR_1 941 944 PF00754 0.581
LIG_PCNA_TLS_4 506 513 PF02747 0.230
LIG_Pex14_2 386 390 PF04695 0.317
LIG_PTB_Apo_2 329 336 PF02174 0.347
LIG_PTB_Phospho_1 329 335 PF10480 0.359
LIG_SH2_CRK 202 206 PF00017 0.247
LIG_SH2_GRB2like 55 58 PF00017 0.603
LIG_SH2_NCK_1 436 440 PF00017 0.228
LIG_SH2_NCK_1 485 489 PF00017 0.211
LIG_SH2_PTP2 461 464 PF00017 0.208
LIG_SH2_SRC 55 58 PF00017 0.497
LIG_SH2_STAP1 527 531 PF00017 0.228
LIG_SH2_STAP1 606 610 PF00017 0.441
LIG_SH2_STAT5 107 110 PF00017 0.228
LIG_SH2_STAT5 202 205 PF00017 0.234
LIG_SH2_STAT5 214 217 PF00017 0.356
LIG_SH2_STAT5 237 240 PF00017 0.343
LIG_SH2_STAT5 271 274 PF00017 0.288
LIG_SH2_STAT5 335 338 PF00017 0.398
LIG_SH2_STAT5 461 464 PF00017 0.228
LIG_SH2_STAT5 485 488 PF00017 0.201
LIG_SH2_STAT5 512 515 PF00017 0.228
LIG_SH2_STAT5 574 577 PF00017 0.421
LIG_SH2_STAT5 78 81 PF00017 0.549
LIG_SH3_2 46 51 PF14604 0.537
LIG_SH3_3 21 27 PF00018 0.625
LIG_SH3_3 229 235 PF00018 0.320
LIG_SH3_3 287 293 PF00018 0.423
LIG_SH3_3 43 49 PF00018 0.551
LIG_SH3_3 743 749 PF00018 0.611
LIG_SH3_3 822 828 PF00018 0.516
LIG_SH3_3 845 851 PF00018 0.458
LIG_SH3_3 873 879 PF00018 0.627
LIG_SUMO_SIM_anti_2 256 263 PF11976 0.234
LIG_SUMO_SIM_anti_2 491 497 PF11976 0.331
LIG_SUMO_SIM_par_1 182 189 PF11976 0.239
LIG_SUMO_SIM_par_1 256 263 PF11976 0.228
LIG_TRAF2_1 397 400 PF00917 0.337
LIG_TRAF2_1 457 460 PF00917 0.228
LIG_TRAF2_1 785 788 PF00917 0.467
LIG_TRAF2_1 924 927 PF00917 0.651
LIG_TYR_ITIM 269 274 PF00017 0.314
LIG_UBA3_1 652 660 PF00899 0.483
LIG_UBA3_1 863 867 PF00899 0.448
MOD_CDK_SPxxK_3 236 243 PF00069 0.228
MOD_CK1_1 177 183 PF00069 0.230
MOD_CK1_1 320 326 PF00069 0.474
MOD_CK1_1 429 435 PF00069 0.430
MOD_CK2_1 183 189 PF00069 0.238
MOD_CK2_1 214 220 PF00069 0.264
MOD_CK2_1 269 275 PF00069 0.247
MOD_CK2_1 320 326 PF00069 0.601
MOD_CK2_1 454 460 PF00069 0.228
MOD_CK2_1 540 546 PF00069 0.459
MOD_CK2_1 557 563 PF00069 0.429
MOD_CK2_1 596 602 PF00069 0.570
MOD_CK2_1 831 837 PF00069 0.432
MOD_CK2_1 859 865 PF00069 0.466
MOD_CK2_1 895 901 PF00069 0.600
MOD_CK2_1 916 922 PF00069 0.411
MOD_Cter_Amidation 160 163 PF01082 0.313
MOD_Cter_Amidation 513 516 PF01082 0.337
MOD_GlcNHglycan 152 155 PF01048 0.228
MOD_GlcNHglycan 159 162 PF01048 0.228
MOD_GlcNHglycan 262 267 PF01048 0.231
MOD_GlcNHglycan 294 297 PF01048 0.607
MOD_GlcNHglycan 301 304 PF01048 0.645
MOD_GlcNHglycan 308 311 PF01048 0.639
MOD_GlcNHglycan 554 557 PF01048 0.482
MOD_GlcNHglycan 720 723 PF01048 0.598
MOD_GlcNHglycan 749 752 PF01048 0.815
MOD_GlcNHglycan 759 762 PF01048 0.642
MOD_GlcNHglycan 783 786 PF01048 0.563
MOD_GlcNHglycan 806 809 PF01048 0.545
MOD_GlcNHglycan 880 883 PF01048 0.487
MOD_GlcNHglycan 937 941 PF01048 0.430
MOD_GSK3_1 117 124 PF00069 0.228
MOD_GSK3_1 150 157 PF00069 0.228
MOD_GSK3_1 179 186 PF00069 0.218
MOD_GSK3_1 288 295 PF00069 0.576
MOD_GSK3_1 317 324 PF00069 0.558
MOD_GSK3_1 35 42 PF00069 0.637
MOD_GSK3_1 548 555 PF00069 0.447
MOD_GSK3_1 699 706 PF00069 0.488
MOD_GSK3_1 709 716 PF00069 0.503
MOD_GSK3_1 731 738 PF00069 0.574
MOD_GSK3_1 804 811 PF00069 0.511
MOD_GSK3_1 893 900 PF00069 0.489
MOD_N-GLC_1 177 182 PF02516 0.211
MOD_N-GLC_1 35 40 PF02516 0.553
MOD_N-GLC_1 730 735 PF02516 0.652
MOD_N-GLC_2 102 104 PF02516 0.228
MOD_NEK2_1 179 184 PF00069 0.305
MOD_NEK2_1 198 203 PF00069 0.235
MOD_NEK2_1 269 274 PF00069 0.228
MOD_NEK2_1 364 369 PF00069 0.258
MOD_NEK2_1 452 457 PF00069 0.313
MOD_NEK2_1 480 485 PF00069 0.259
MOD_NEK2_1 540 545 PF00069 0.426
MOD_NEK2_1 577 582 PF00069 0.586
MOD_NEK2_1 6 11 PF00069 0.588
MOD_NEK2_1 613 618 PF00069 0.545
MOD_NEK2_1 709 714 PF00069 0.653
MOD_NEK2_1 98 103 PF00069 0.325
MOD_PIKK_1 380 386 PF00454 0.228
MOD_PIKK_1 754 760 PF00454 0.654
MOD_PKA_1 635 641 PF00069 0.421
MOD_PKA_1 7 13 PF00069 0.502
MOD_PKA_2 150 156 PF00069 0.228
MOD_PKA_2 6 12 PF00069 0.590
MOD_PKA_2 635 641 PF00069 0.441
MOD_PKA_2 752 758 PF00069 0.543
MOD_PKA_2 808 814 PF00069 0.510
MOD_Plk_1 35 41 PF00069 0.535
MOD_Plk_1 452 458 PF00069 0.228
MOD_Plk_1 81 87 PF00069 0.404
MOD_Plk_2-3 831 837 PF00069 0.432
MOD_Plk_4 121 127 PF00069 0.315
MOD_Plk_4 200 206 PF00069 0.339
MOD_Plk_4 269 275 PF00069 0.228
MOD_Plk_4 377 383 PF00069 0.364
MOD_Plk_4 429 435 PF00069 0.337
MOD_Plk_4 808 814 PF00069 0.510
MOD_Plk_4 859 865 PF00069 0.452
MOD_ProDKin_1 117 123 PF00069 0.307
MOD_ProDKin_1 14 20 PF00069 0.476
MOD_ProDKin_1 236 242 PF00069 0.228
MOD_ProDKin_1 288 294 PF00069 0.481
MOD_ProDKin_1 321 327 PF00069 0.598
MOD_SUMO_for_1 215 218 PF00179 0.228
MOD_SUMO_for_1 277 280 PF00179 0.346
MOD_SUMO_for_1 59 62 PF00179 0.477
MOD_SUMO_for_1 924 927 PF00179 0.589
MOD_SUMO_rev_2 831 841 PF00179 0.412
TRG_DiLeu_BaEn_1 926 931 PF01217 0.380
TRG_DiLeu_BaEn_2 217 223 PF01217 0.247
TRG_DiLeu_BaEn_4 459 465 PF01217 0.251
TRG_DiLeu_BaLyEn_6 160 165 PF01217 0.315
TRG_DiLeu_BaLyEn_6 617 622 PF01217 0.434
TRG_ENDOCYTIC_2 202 205 PF00928 0.247
TRG_ENDOCYTIC_2 271 274 PF00928 0.288
TRG_ENDOCYTIC_2 358 361 PF00928 0.211
TRG_ENDOCYTIC_2 461 464 PF00928 0.228
TRG_ENDOCYTIC_2 574 577 PF00928 0.421
TRG_ENDOCYTIC_2 77 80 PF00928 0.548
TRG_ER_diArg_1 113 115 PF00400 0.211
TRG_ER_diArg_1 468 471 PF00400 0.293
TRG_ER_diArg_1 568 570 PF00400 0.452
TRG_ER_diArg_1 591 594 PF00400 0.497
TRG_ER_diArg_1 6 8 PF00400 0.631
TRG_ER_diArg_1 619 621 PF00400 0.437
TRG_ER_diArg_1 634 636 PF00400 0.415
TRG_ER_diArg_1 65 67 PF00400 0.484
TRG_ER_diArg_1 74 77 PF00400 0.488
TRG_ER_diArg_1 773 776 PF00400 0.550
TRG_Pf-PMV_PEXEL_1 213 218 PF00026 0.228
TRG_Pf-PMV_PEXEL_1 221 225 PF00026 0.228
TRG_Pf-PMV_PEXEL_1 337 342 PF00026 0.228
TRG_Pf-PMV_PEXEL_1 413 418 PF00026 0.228
TRG_Pf-PMV_PEXEL_1 506 510 PF00026 0.280
TRG_Pf-PMV_PEXEL_1 608 612 PF00026 0.436
TRG_Pf-PMV_PEXEL_1 619 624 PF00026 0.423
TRG_Pf-PMV_PEXEL_1 67 71 PF00026 0.578
TRG_Pf-PMV_PEXEL_1 681 685 PF00026 0.407

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1PEK8 Leptomonas seymouri 76% 100%
A0A1X0NSC2 Trypanosomatidae 63% 100%
A0A3Q8IB80 Leishmania donovani 30% 100%
A0A3Q8ICR2 Leishmania donovani 94% 100%
A0A3Q8IQX0 Leishmania donovani 30% 100%
A0A3S7WZX1 Leishmania donovani 28% 100%
A0A3S7X1F5 Leishmania donovani 27% 100%
A0A3S7X203 Leishmania donovani 26% 100%
A4HEU5 Leishmania braziliensis 88% 99%
A4HEX9 Leishmania braziliensis 27% 100%
A4HGG7 Leishmania braziliensis 27% 100%
A4HGY1 Leishmania braziliensis 29% 100%
A4HGY5 Leishmania braziliensis 26% 100%
A4I219 Leishmania infantum 96% 100%
A4I253 Leishmania infantum 28% 100%
A4I3J9 Leishmania infantum 27% 100%
A4I412 Leishmania infantum 30% 100%
A4I417 Leishmania infantum 26% 100%
A6T226 Janthinobacterium sp. (strain Marseille) 28% 100%
B0U3J8 Xylella fastidiosa (strain M12) 27% 100%
B2I6F6 Xylella fastidiosa (strain M23) 27% 100%
C9ZRY8 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 64% 100%
E9AYA3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 28% 100%
E9AZT9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 27% 100%
E9B099 Leishmania mexicana (strain MHOM/GT/2001/U1103) 30% 100%
E9B0A4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 26% 100%
Q4Q7Y0 Leishmania major 26% 100%
Q4Q7Y4 Leishmania major 30% 100%
Q4Q8E6 Leishmania major 27% 100%
Q4Q970 Leishmania major 28% 100%
Q4Q9A4 Leishmania major 94% 100%
Q87BS8 Xylella fastidiosa (strain Temecula1 / ATCC 700964) 27% 100%
Q9PB05 Xylella fastidiosa (strain 9a5c) 27% 100%
V5BUG8 Trypanosoma cruzi 63% 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