LeishMANIAdb
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DNA mismatch repair protein MSH2, putative

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

Quick info

Protein:
DNA mismatch repair protein MSH2, putative
Gene product:
DNA mismatch repair protein MSH2, putative
Species:
Leishmania donovani
UniProt:
A0A3Q8IGP6_LEIDO
TriTrypDb:
LdBPK_330420.1 , LdCL_330009600 , LDHU3_33.0630
Length:
939

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: 11
NetGPI no yes: 0, no: 11
Cellular components
Term Name Level Count
GO:0005634 nucleus 5 12
GO:0032300 mismatch repair complex 2 12
GO:0032991 protein-containing complex 1 12
GO:0043226 organelle 2 12
GO:0043227 membrane-bounded organelle 3 12
GO:0043229 intracellular organelle 3 12
GO:0043231 intracellular membrane-bounded organelle 4 12
GO:0110165 cellular anatomical entity 1 12
GO:0005737 cytoplasm 2 1
GO:0032301 MutSalpha complex 3 1
GO:0140513 nuclear protein-containing complex 2 1

Expansion

Sequence features

A0A3Q8IGP6
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3Q8IGP6

Function

Biological processes
Term Name Level Count
GO:0006139 nucleobase-containing compound metabolic process 3 12
GO:0006259 DNA metabolic process 4 12
GO:0006281 DNA repair 5 12
GO:0006298 mismatch repair 6 12
GO:0006725 cellular aromatic compound metabolic process 3 12
GO:0006807 nitrogen compound metabolic process 2 12
GO:0006950 response to stress 2 12
GO:0006974 DNA damage response 4 12
GO:0008152 metabolic process 1 12
GO:0009987 cellular process 1 12
GO:0033554 cellular response to stress 3 12
GO:0034641 cellular nitrogen compound metabolic process 3 12
GO:0043170 macromolecule metabolic process 3 12
GO:0044237 cellular metabolic process 2 12
GO:0044238 primary metabolic process 2 12
GO:0044260 obsolete cellular macromolecule metabolic process 3 12
GO:0046483 heterocycle metabolic process 3 12
GO:0050896 response to stimulus 1 12
GO:0051716 cellular response to stimulus 2 12
GO:0071704 organic substance metabolic process 2 12
GO:0090304 nucleic acid metabolic process 4 12
GO:1901360 organic cyclic compound metabolic process 3 12
GO:0006310 DNA recombination 5 1
GO:0006312 mitotic recombination 6 1
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 12
GO:0003676 nucleic acid binding 3 12
GO:0003677 DNA binding 4 12
GO:0003690 double-stranded DNA binding 5 12
GO:0003824 catalytic activity 1 12
GO:0005488 binding 1 12
GO:0005524 ATP binding 5 12
GO:0008094 ATP-dependent activity, acting on DNA 2 12
GO:0017076 purine nucleotide binding 4 12
GO:0030554 adenyl nucleotide binding 5 12
GO:0030983 mismatched DNA binding 6 12
GO:0032553 ribonucleotide binding 3 12
GO:0032555 purine ribonucleotide binding 4 12
GO:0032559 adenyl ribonucleotide binding 5 12
GO:0035639 purine ribonucleoside triphosphate binding 4 12
GO:0036094 small molecule binding 2 12
GO:0043167 ion binding 2 12
GO:0043168 anion binding 3 12
GO:0097159 organic cyclic compound binding 2 12
GO:0097367 carbohydrate derivative binding 2 12
GO:0140097 catalytic activity, acting on DNA 3 12
GO:0140299 small molecule sensor activity 1 12
GO:0140612 DNA damage sensor activity 2 12
GO:0140640 catalytic activity, acting on a nucleic acid 2 12
GO:0140657 ATP-dependent activity 1 12
GO:0140664 ATP-dependent DNA damage sensor activity 3 12
GO:1901265 nucleoside phosphate binding 3 12
GO:1901363 heterocyclic compound binding 2 12

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 176 180 PF00656 0.423
CLV_C14_Caspase3-7 3 7 PF00656 0.536
CLV_C14_Caspase3-7 545 549 PF00656 0.450
CLV_MEL_PAP_1 725 731 PF00089 0.250
CLV_NRD_NRD_1 217 219 PF00675 0.480
CLV_NRD_NRD_1 289 291 PF00675 0.562
CLV_NRD_NRD_1 295 297 PF00675 0.522
CLV_NRD_NRD_1 395 397 PF00675 0.271
CLV_NRD_NRD_1 400 402 PF00675 0.280
CLV_NRD_NRD_1 527 529 PF00675 0.250
CLV_NRD_NRD_1 565 567 PF00675 0.279
CLV_NRD_NRD_1 579 581 PF00675 0.261
CLV_NRD_NRD_1 89 91 PF00675 0.450
CLV_NRD_NRD_1 892 894 PF00675 0.586
CLV_PCSK_KEX2_1 217 219 PF00082 0.480
CLV_PCSK_KEX2_1 289 291 PF00082 0.562
CLV_PCSK_KEX2_1 295 297 PF00082 0.522
CLV_PCSK_KEX2_1 386 388 PF00082 0.257
CLV_PCSK_KEX2_1 400 402 PF00082 0.229
CLV_PCSK_KEX2_1 565 567 PF00082 0.336
CLV_PCSK_KEX2_1 579 581 PF00082 0.336
CLV_PCSK_KEX2_1 654 656 PF00082 0.503
CLV_PCSK_KEX2_1 89 91 PF00082 0.449
CLV_PCSK_KEX2_1 900 902 PF00082 0.501
CLV_PCSK_PC1ET2_1 386 388 PF00082 0.336
CLV_PCSK_PC1ET2_1 579 581 PF00082 0.355
CLV_PCSK_PC1ET2_1 654 656 PF00082 0.316
CLV_PCSK_PC1ET2_1 900 902 PF00082 0.501
CLV_PCSK_PC7_1 396 402 PF00082 0.261
CLV_PCSK_SKI1_1 162 166 PF00082 0.291
CLV_PCSK_SKI1_1 188 192 PF00082 0.409
CLV_PCSK_SKI1_1 289 293 PF00082 0.557
CLV_PCSK_SKI1_1 377 381 PF00082 0.274
CLV_PCSK_SKI1_1 434 438 PF00082 0.336
CLV_PCSK_SKI1_1 510 514 PF00082 0.274
CLV_Separin_Metazoa 253 257 PF03568 0.510
DEG_APCC_DBOX_1 656 664 PF00400 0.382
DEG_APCC_DBOX_1 931 939 PF00400 0.589
DOC_CYCLIN_RxL_1 159 170 PF00134 0.522
DOC_CYCLIN_RxL_1 396 408 PF00134 0.536
DOC_CYCLIN_yClb5_NLxxxL_5 182 191 PF00134 0.410
DOC_MAPK_gen_1 396 405 PF00069 0.450
DOC_MAPK_gen_1 535 543 PF00069 0.453
DOC_MAPK_gen_1 654 663 PF00069 0.516
DOC_MAPK_gen_1 790 797 PF00069 0.490
DOC_MAPK_HePTP_8 651 663 PF00069 0.511
DOC_MAPK_MEF2A_6 222 229 PF00069 0.508
DOC_MAPK_MEF2A_6 363 371 PF00069 0.461
DOC_MAPK_MEF2A_6 654 663 PF00069 0.516
DOC_MAPK_MEF2A_6 697 705 PF00069 0.450
DOC_PP1_RVXF_1 160 167 PF00149 0.468
DOC_PP2B_LxvP_1 255 258 PF13499 0.391
DOC_USP7_MATH_1 102 106 PF00917 0.520
DOC_USP7_MATH_1 136 140 PF00917 0.462
DOC_USP7_MATH_1 18 22 PF00917 0.455
DOC_USP7_MATH_1 197 201 PF00917 0.677
DOC_USP7_MATH_1 878 882 PF00917 0.688
DOC_USP7_MATH_2 258 264 PF00917 0.472
DOC_USP7_UBL2_3 47 51 PF12436 0.483
DOC_WW_Pin1_4 110 115 PF00397 0.393
DOC_WW_Pin1_4 169 174 PF00397 0.476
DOC_WW_Pin1_4 193 198 PF00397 0.577
LIG_14-3-3_CanoR_1 162 167 PF00244 0.377
LIG_14-3-3_CanoR_1 212 219 PF00244 0.490
LIG_14-3-3_CanoR_1 261 265 PF00244 0.469
LIG_14-3-3_CanoR_1 295 299 PF00244 0.468
LIG_14-3-3_CanoR_1 363 367 PF00244 0.450
LIG_14-3-3_CanoR_1 400 404 PF00244 0.503
LIG_14-3-3_CanoR_1 532 541 PF00244 0.531
LIG_14-3-3_CanoR_1 551 560 PF00244 0.343
LIG_14-3-3_CanoR_1 769 775 PF00244 0.450
LIG_14-3-3_CanoR_1 790 796 PF00244 0.536
LIG_14-3-3_CanoR_1 831 837 PF00244 0.461
LIG_14-3-3_CanoR_1 89 95 PF00244 0.400
LIG_14-3-3_CanoR_1 893 902 PF00244 0.512
LIG_Actin_WH2_2 391 408 PF00022 0.510
LIG_Actin_WH2_2 519 537 PF00022 0.536
LIG_Actin_WH2_2 75 91 PF00022 0.393
LIG_Actin_WH2_2 816 833 PF00022 0.461
LIG_APCC_ABBA_1 367 372 PF00400 0.536
LIG_BIR_III_2 646 650 PF00653 0.521
LIG_BRCT_BRCA1_1 138 142 PF00533 0.491
LIG_BRCT_BRCA1_1 20 24 PF00533 0.498
LIG_BRCT_BRCA1_1 797 801 PF00533 0.444
LIG_CaM_IQ_9 232 248 PF13499 0.547
LIG_CaM_IQ_9 379 395 PF13499 0.453
LIG_Clathr_ClatBox_1 124 128 PF01394 0.470
LIG_CtBP_PxDLS_1 686 692 PF00389 0.450
LIG_deltaCOP1_diTrp_1 869 873 PF00928 0.586
LIG_FHA_1 170 176 PF00498 0.369
LIG_FHA_1 379 385 PF00498 0.512
LIG_FHA_1 51 57 PF00498 0.414
LIG_FHA_1 535 541 PF00498 0.561
LIG_FHA_1 600 606 PF00498 0.536
LIG_FHA_1 629 635 PF00498 0.679
LIG_FHA_1 677 683 PF00498 0.418
LIG_FHA_1 730 736 PF00498 0.450
LIG_FHA_1 739 745 PF00498 0.450
LIG_FHA_1 758 764 PF00498 0.450
LIG_FHA_2 116 122 PF00498 0.455
LIG_FHA_2 163 169 PF00498 0.355
LIG_FHA_2 174 180 PF00498 0.417
LIG_FHA_2 204 210 PF00498 0.594
LIG_FHA_2 363 369 PF00498 0.510
LIG_FHA_2 454 460 PF00498 0.498
LIG_FHA_2 543 549 PF00498 0.485
LIG_GBD_Chelix_1 582 590 PF00786 0.355
LIG_LIR_Apic_2 427 431 PF02991 0.519
LIG_LIR_Apic_2 438 443 PF02991 0.416
LIG_LIR_Gen_1 300 310 PF02991 0.372
LIG_LIR_Gen_1 408 419 PF02991 0.512
LIG_LIR_Gen_1 798 808 PF02991 0.450
LIG_LIR_Gen_1 869 878 PF02991 0.595
LIG_LIR_Nem_3 165 169 PF02991 0.355
LIG_LIR_Nem_3 21 27 PF02991 0.481
LIG_LIR_Nem_3 300 305 PF02991 0.389
LIG_LIR_Nem_3 328 334 PF02991 0.450
LIG_LIR_Nem_3 408 414 PF02991 0.512
LIG_LIR_Nem_3 495 501 PF02991 0.536
LIG_LIR_Nem_3 519 523 PF02991 0.452
LIG_LIR_Nem_3 561 567 PF02991 0.474
LIG_LIR_Nem_3 588 592 PF02991 0.450
LIG_LIR_Nem_3 652 656 PF02991 0.490
LIG_LIR_Nem_3 771 777 PF02991 0.450
LIG_LIR_Nem_3 798 804 PF02991 0.536
LIG_LIR_Nem_3 844 848 PF02991 0.450
LIG_LIR_Nem_3 869 873 PF02991 0.572
LIG_NRBOX 186 192 PF00104 0.406
LIG_PCNA_yPIPBox_3 373 387 PF02747 0.536
LIG_PDZ_Class_3 934 939 PF00595 0.581
LIG_Pex14_2 777 781 PF04695 0.450
LIG_Pex14_2 797 801 PF04695 0.319
LIG_PTB_Apo_2 813 820 PF02174 0.450
LIG_SH2_CRK 428 432 PF00017 0.555
LIG_SH2_CRK 498 502 PF00017 0.499
LIG_SH2_CRK 520 524 PF00017 0.450
LIG_SH2_CRK 564 568 PF00017 0.474
LIG_SH2_PTP2 440 443 PF00017 0.458
LIG_SH2_SRC 589 592 PF00017 0.474
LIG_SH2_STAP1 898 902 PF00017 0.442
LIG_SH2_STAT3 834 837 PF00017 0.492
LIG_SH2_STAT5 106 109 PF00017 0.436
LIG_SH2_STAT5 169 172 PF00017 0.419
LIG_SH2_STAT5 293 296 PF00017 0.406
LIG_SH2_STAT5 36 39 PF00017 0.355
LIG_SH2_STAT5 428 431 PF00017 0.499
LIG_SH2_STAT5 440 443 PF00017 0.405
LIG_SH2_STAT5 49 52 PF00017 0.342
LIG_SH2_STAT5 522 525 PF00017 0.450
LIG_SH2_STAT5 589 592 PF00017 0.450
LIG_SH2_STAT5 834 837 PF00017 0.522
LIG_SH2_STAT5 848 851 PF00017 0.390
LIG_SH2_STAT5 934 937 PF00017 0.612
LIG_SH3_3 191 197 PF00018 0.529
LIG_SH3_3 280 286 PF00018 0.551
LIG_SH3_3 368 374 PF00018 0.461
LIG_SUMO_SIM_anti_2 631 636 PF11976 0.727
LIG_SUMO_SIM_anti_2 70 76 PF11976 0.400
LIG_SUMO_SIM_anti_2 759 766 PF11976 0.449
LIG_SUMO_SIM_par_1 539 546 PF11976 0.474
LIG_SUMO_SIM_par_1 70 76 PF11976 0.411
LIG_SUMO_SIM_par_1 759 766 PF11976 0.490
LIG_TRFH_1 834 838 PF08558 0.450
LIG_Vh1_VBS_1 746 764 PF01044 0.510
LIG_WRC_WIRS_1 650 655 PF05994 0.490
LIG_WRC_WIRS_1 739 744 PF05994 0.450
MOD_CK1_1 228 234 PF00069 0.552
MOD_CK1_1 28 34 PF00069 0.442
MOD_CK1_1 329 335 PF00069 0.471
MOD_CK1_1 61 67 PF00069 0.598
MOD_CK1_1 751 757 PF00069 0.516
MOD_CK1_1 826 832 PF00069 0.499
MOD_CK1_1 879 885 PF00069 0.561
MOD_CK2_1 115 121 PF00069 0.441
MOD_CK2_1 162 168 PF00069 0.382
MOD_CK2_1 228 234 PF00069 0.476
MOD_CK2_1 362 368 PF00069 0.461
MOD_CK2_1 453 459 PF00069 0.520
MOD_CK2_1 524 530 PF00069 0.467
MOD_CK2_1 533 539 PF00069 0.451
MOD_GlcNHglycan 136 139 PF01048 0.446
MOD_GlcNHglycan 199 202 PF01048 0.613
MOD_GlcNHglycan 306 309 PF01048 0.467
MOD_GlcNHglycan 60 63 PF01048 0.511
MOD_GlcNHglycan 640 643 PF01048 0.673
MOD_GlcNHglycan 65 68 PF01048 0.555
MOD_GlcNHglycan 748 751 PF01048 0.250
MOD_GlcNHglycan 811 814 PF01048 0.344
MOD_GlcNHglycan 824 828 PF01048 0.281
MOD_GlcNHglycan 881 884 PF01048 0.683
MOD_GlcNHglycan 895 898 PF01048 0.375
MOD_GSK3_1 169 176 PF00069 0.479
MOD_GSK3_1 193 200 PF00069 0.563
MOD_GSK3_1 294 301 PF00069 0.421
MOD_GSK3_1 322 329 PF00069 0.461
MOD_GSK3_1 426 433 PF00069 0.504
MOD_GSK3_1 458 465 PF00069 0.452
MOD_GSK3_1 539 546 PF00069 0.459
MOD_GSK3_1 57 64 PF00069 0.541
MOD_GSK3_1 691 698 PF00069 0.450
MOD_GSK3_1 791 798 PF00069 0.515
MOD_GSK3_1 826 833 PF00069 0.474
MOD_GSK3_1 98 105 PF00069 0.555
MOD_N-GLC_1 115 120 PF02516 0.457
MOD_N-GLC_1 157 162 PF02516 0.384
MOD_N-GLC_1 62 67 PF02516 0.452
MOD_N-GLC_2 335 337 PF02516 0.250
MOD_NEK2_1 120 125 PF00069 0.440
MOD_NEK2_1 134 139 PF00069 0.369
MOD_NEK2_1 157 162 PF00069 0.384
MOD_NEK2_1 294 299 PF00069 0.453
MOD_NEK2_1 379 384 PF00069 0.502
MOD_NEK2_1 405 410 PF00069 0.478
MOD_NEK2_1 487 492 PF00069 0.536
MOD_NEK2_1 524 529 PF00069 0.461
MOD_NEK2_1 582 587 PF00069 0.452
MOD_NEK2_1 673 678 PF00069 0.460
MOD_NEK2_1 682 687 PF00069 0.424
MOD_NEK2_1 746 751 PF00069 0.450
MOD_NEK2_1 795 800 PF00069 0.452
MOD_NEK2_1 830 835 PF00069 0.447
MOD_NEK2_2 649 654 PF00069 0.520
MOD_PIKK_1 142 148 PF00454 0.439
MOD_PIKK_1 18 24 PF00454 0.434
MOD_PIKK_1 379 385 PF00454 0.428
MOD_PIKK_1 405 411 PF00454 0.536
MOD_PIKK_1 487 493 PF00454 0.555
MOD_PIKK_1 674 680 PF00454 0.369
MOD_PIKK_1 754 760 PF00454 0.498
MOD_PIKK_1 802 808 PF00454 0.461
MOD_PK_1 90 96 PF00069 0.389
MOD_PKA_1 565 571 PF00069 0.555
MOD_PKA_1 57 63 PF00069 0.496
MOD_PKA_1 893 899 PF00069 0.574
MOD_PKA_2 211 217 PF00069 0.548
MOD_PKA_2 260 266 PF00069 0.474
MOD_PKA_2 28 34 PF00069 0.480
MOD_PKA_2 294 300 PF00069 0.466
MOD_PKA_2 322 328 PF00069 0.461
MOD_PKA_2 362 368 PF00069 0.450
MOD_PKA_2 399 405 PF00069 0.461
MOD_PKA_2 524 530 PF00069 0.455
MOD_PKA_2 534 540 PF00069 0.440
MOD_PKA_2 565 571 PF00069 0.536
MOD_PKA_2 768 774 PF00069 0.462
MOD_PKA_2 791 797 PF00069 0.533
MOD_PKA_2 830 836 PF00069 0.461
MOD_PKA_2 98 104 PF00069 0.501
MOD_Plk_1 120 126 PF00069 0.449
MOD_Plk_1 157 163 PF00069 0.370
MOD_Plk_1 203 209 PF00069 0.650
MOD_Plk_1 458 464 PF00069 0.467
MOD_Plk_1 802 808 PF00069 0.461
MOD_Plk_2-3 260 266 PF00069 0.474
MOD_Plk_2-3 869 875 PF00069 0.561
MOD_Plk_4 102 108 PF00069 0.590
MOD_Plk_4 120 126 PF00069 0.340
MOD_Plk_4 136 142 PF00069 0.300
MOD_Plk_4 298 304 PF00069 0.396
MOD_Plk_4 326 332 PF00069 0.450
MOD_Plk_4 362 368 PF00069 0.450
MOD_Plk_4 40 46 PF00069 0.427
MOD_Plk_4 453 459 PF00069 0.555
MOD_Plk_4 585 591 PF00069 0.458
MOD_Plk_4 691 697 PF00069 0.450
MOD_Plk_4 738 744 PF00069 0.450
MOD_Plk_4 748 754 PF00069 0.450
MOD_Plk_4 791 797 PF00069 0.510
MOD_Plk_4 855 861 PF00069 0.524
MOD_ProDKin_1 110 116 PF00069 0.393
MOD_ProDKin_1 169 175 PF00069 0.470
MOD_ProDKin_1 193 199 PF00069 0.591
MOD_SUMO_for_1 436 439 PF00179 0.536
MOD_SUMO_for_1 512 515 PF00179 0.450
MOD_SUMO_for_1 635 638 PF00179 0.706
MOD_SUMO_for_1 921 924 PF00179 0.538
MOD_SUMO_rev_2 594 599 PF00179 0.450
TRG_DiLeu_BaEn_1 311 316 PF01217 0.536
TRG_DiLeu_BaEn_4 259 265 PF01217 0.490
TRG_ENDOCYTIC_2 302 305 PF00928 0.473
TRG_ENDOCYTIC_2 498 501 PF00928 0.536
TRG_ENDOCYTIC_2 520 523 PF00928 0.450
TRG_ENDOCYTIC_2 564 567 PF00928 0.474
TRG_ENDOCYTIC_2 589 592 PF00928 0.450
TRG_ENDOCYTIC_2 774 777 PF00928 0.450
TRG_ER_diArg_1 216 218 PF00400 0.478
TRG_ER_diArg_1 294 296 PF00400 0.525
TRG_ER_diArg_1 564 566 PF00400 0.536
TRG_ER_diArg_1 789 792 PF00400 0.527
TRG_ER_diArg_1 88 90 PF00400 0.447
TRG_NES_CRM1_1 358 372 PF08389 0.461
TRG_NES_CRM1_1 733 748 PF08389 0.450
TRG_NLS_Bipartite_1 565 583 PF00514 0.536
TRG_NLS_MonoExtC_3 578 584 PF00514 0.510
TRG_Pf-PMV_PEXEL_1 217 221 PF00026 0.409
TRG_Pf-PMV_PEXEL_1 230 234 PF00026 0.463
TRG_Pf-PMV_PEXEL_1 455 459 PF00026 0.290
TRG_Pf-PMV_PEXEL_1 565 569 PF00026 0.330
TRG_Pf-PMV_PEXEL_1 580 584 PF00026 0.348
TRG_Pf-PMV_PEXEL_1 903 907 PF00026 0.558

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I6N3 Leptomonas seymouri 80% 99%
A0A0S4J224 Bodo saltans 50% 100%
A0A1X0P1A3 Trypanosomatidae 59% 98%
A0A3R7KEP9 Trypanosoma rangeli 59% 98%
A1R0M2 Borrelia turicatae (strain 91E135) 29% 100%
A4HL76 Leishmania braziliensis 88% 100%
A4I8Q5 Leishmania infantum 100% 100%
A6LLR1 Thermosipho melanesiensis (strain DSM 12029 / CIP 104789 / BI429) 26% 100%
A7HMG4 Fervidobacterium nodosum (strain ATCC 35602 / DSM 5306 / Rt17-B1) 28% 100%
A9NGL6 Acholeplasma laidlawii (strain PG-8A) 27% 100%
A9WFZ9 Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl) 31% 97%
B0B918 Chlamydia trachomatis serovar L2 (strain 434/Bu / ATCC VR-902B) 27% 100%
B0BAP7 Chlamydia trachomatis serovar L2b (strain UCH-1/proctitis) 27% 100%
B0VAU7 Acinetobacter baumannii (strain AYE) 29% 100%
B2HX50 Acinetobacter baumannii (strain ACICU) 29% 100%
B3E6P2 Trichlorobacter lovleyi (strain ATCC BAA-1151 / DSM 17278 / SZ) 31% 100%
B3EEE1 Chlorobium limicola (strain DSM 245 / NBRC 103803 / 6330) 31% 100%
B7GW85 Acinetobacter baumannii (strain AB307-0294) 29% 100%
B7IBV9 Acinetobacter baumannii (strain AB0057) 29% 100%
B9LB04 Chloroflexus aurantiacus (strain ATCC 29364 / DSM 637 / Y-400-fl) 31% 97%
C5D9H5 Geobacillus sp. (strain WCH70) 31% 100%
D0A4P2 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 57% 99%
E9B3L9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 96% 100%
O13396 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) 31% 100%
O24617 Arabidopsis thaliana 33% 100%
O74502 Schizosaccharomyces pombe (strain 972 / ATCC 24843) 26% 75%
O74773 Schizosaccharomyces pombe (strain 972 / ATCC 24843) 32% 96%
P25847 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 30% 97%
P43246 Homo sapiens 33% 100%
P43247 Mus musculus 33% 100%
P43248 Drosophila melanogaster 31% 100%
P54275 Rattus norvegicus 33% 100%
P61672 Treponema denticola (strain ATCC 35405 / DSM 14222 / CIP 103919 / JCM 8153 / KCTC 15104) 29% 100%
Q03R33 Levilactobacillus brevis (strain ATCC 367 / BCRC 12310 / CIP 105137 / JCM 1170 / LMG 11437 / NCIMB 947 / NCTC 947) 30% 100%
Q07V29 Rhodopseudomonas palustris (strain BisA53) 30% 100%
Q1WT15 Ligilactobacillus salivarius (strain UCC118) 30% 100%
Q24X61 Desulfitobacterium hafniense (strain Y51) 31% 100%
Q2JT35 Synechococcus sp. (strain JA-3-3Ab) 30% 100%
Q3JYM3 Streptococcus agalactiae serotype Ia (strain ATCC 27591 / A909 / CDC SS700) 28% 100%
Q3M892 Trichormus variabilis (strain ATCC 29413 / PCC 7937) 28% 100%
Q3MHE4 Bos taurus 33% 100%
Q49X88 Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) 29% 100%
Q4Q4J6 Leishmania major 96% 100%
Q553L4 Dictyostelium discoideum 33% 100%
Q5NYP9 Aromatoleum aromaticum (strain EbN1) 31% 100%
Q5UZG9 Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) 27% 100%
Q5XXB5 Chlorocebus aethiops 33% 100%
Q60BA1 Methylococcus capsulatus (strain ATCC 33009 / NCIMB 11132 / Bath) 30% 100%
Q65JE2 Bacillus licheniformis (strain ATCC 14580 / DSM 13 / JCM 2505 / CCUG 7422 / NBRC 12200 / NCIMB 9375 / NCTC 10341 / NRRL NRS-1264 / Gibson 46) 31% 100%
Q6G542 Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) 28% 100%
Q8DWW1 Streptococcus agalactiae serotype V (strain ATCC BAA-611 / 2603 V/R) 28% 100%
Q8E2R3 Streptococcus agalactiae serotype III (strain NEM316) 28% 100%
Q9XGC9 Zea mays 31% 100%
V5BB82 Trypanosoma cruzi 58% 98%
V5BK71 Trypanosoma cruzi 28% 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