LeishMANIAdb
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V-type proton ATPase subunit a

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

Quick info

Protein:
V-type proton ATPase subunit a
Gene product:
vacuolar proton-ATPase-like protein, putative
Species:
Leishmania major
UniProt:
Q4Q5J0_LEIMA
TriTrypDb:
LmjF.32.0920 , LMJLV39_320014900 * , LMJSD75_320014900 *
Length:
893

Annotations

LeishMANIAdb annotations

Homologous to animal V-type proton pumps, vacuolar or lysosomal. For some reason, this family expanded in kinetoplastids. Localization: Endosomal (by homology) / Lysosomal (by homology)

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: 18
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 21
NetGPI no yes: 0, no: 21
Cellular components
Term Name Level Count
GO:0000220 vacuolar proton-transporting V-type ATPase, V0 domain 5 22
GO:0016020 membrane 2 22
GO:0016469 proton-transporting two-sector ATPase complex 3 3
GO:0016471 vacuolar proton-transporting V-type ATPase complex 5 3
GO:0032991 protein-containing complex 1 22
GO:0033176 proton-transporting V-type ATPase complex 4 3
GO:0033177 proton-transporting two-sector ATPase complex, proton-transporting domain 3 22
GO:0033179 proton-transporting V-type ATPase, V0 domain 4 22
GO:0098796 membrane protein complex 2 22
GO:0110165 cellular anatomical entity 1 22
GO:0000323 lytic vacuole 6 1
GO:0005764 lysosome 7 1
GO:0005773 vacuole 5 1
GO:0005794 Golgi apparatus 5 1
GO:0020022 acidocalcisome 5 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0043229 intracellular organelle 3 1
GO:0043231 intracellular membrane-bounded organelle 4 1

Expansion

Sequence features

Q4Q5J0
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q5J0

Function

Biological processes
Term Name Level Count
GO:0006873 intracellular monoatomic ion homeostasis 4 3
GO:0006885 regulation of pH 8 3
GO:0007035 vacuolar acidification 10 3
GO:0009987 cellular process 1 3
GO:0019725 cellular homeostasis 2 3
GO:0030003 intracellular monoatomic cation homeostasis 5 3
GO:0030004 obsolete cellular monovalent inorganic cation homeostasis 6 3
GO:0030641 regulation of cellular pH 7 3
GO:0042592 homeostatic process 3 3
GO:0048878 chemical homeostasis 4 3
GO:0050801 monoatomic ion homeostasis 5 3
GO:0051452 intracellular pH reduction 9 3
GO:0051453 regulation of intracellular pH 8 3
GO:0055067 obsolete monovalent inorganic cation homeostasis 7 3
GO:0055080 monoatomic cation homeostasis 6 3
GO:0055082 intracellular chemical homeostasis 3 3
GO:0065007 biological regulation 1 3
GO:0065008 regulation of biological quality 2 3
GO:0098771 inorganic ion homeostasis 6 3
Molecular functions
Term Name Level Count
GO:0005215 transporter activity 1 22
GO:0005488 binding 1 3
GO:0005515 protein binding 2 3
GO:0008324 monoatomic cation transmembrane transporter activity 4 22
GO:0009678 pyrophosphate hydrolysis-driven proton transmembrane transporter activity 5 22
GO:0015075 monoatomic ion transmembrane transporter activity 3 22
GO:0015078 proton transmembrane transporter activity 5 22
GO:0015318 inorganic molecular entity transmembrane transporter activity 3 22
GO:0015399 primary active transmembrane transporter activity 4 22
GO:0019829 ATPase-coupled monoatomic cation transmembrane transporter activity 3 22
GO:0019899 enzyme binding 3 3
GO:0022804 active transmembrane transporter activity 3 22
GO:0022853 active monoatomic ion transmembrane transporter activity 4 22
GO:0022857 transmembrane transporter activity 2 22
GO:0022890 inorganic cation transmembrane transporter activity 4 22
GO:0042625 ATPase-coupled ion transmembrane transporter activity 3 22
GO:0042626 ATPase-coupled transmembrane transporter activity 2 22
GO:0044769 ATPase activity, coupled to transmembrane movement of ions, rotational mechanism 4 22
GO:0046961 proton-transporting ATPase activity, rotational mechanism 4 22
GO:0051117 ATPase binding 4 3
GO:0140657 ATP-dependent activity 1 22
GO:0003824 catalytic activity 1 2
GO:0016787 hydrolase activity 2 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 696 700 PF00656 0.368
CLV_NRD_NRD_1 292 294 PF00675 0.479
CLV_NRD_NRD_1 347 349 PF00675 0.491
CLV_NRD_NRD_1 63 65 PF00675 0.448
CLV_NRD_NRD_1 671 673 PF00675 0.241
CLV_NRD_NRD_1 679 681 PF00675 0.251
CLV_NRD_NRD_1 69 71 PF00675 0.444
CLV_PCSK_FUR_1 292 296 PF00082 0.410
CLV_PCSK_KEX2_1 292 294 PF00082 0.522
CLV_PCSK_KEX2_1 347 349 PF00082 0.512
CLV_PCSK_KEX2_1 63 65 PF00082 0.448
CLV_PCSK_KEX2_1 666 668 PF00082 0.267
CLV_PCSK_KEX2_1 670 672 PF00082 0.250
CLV_PCSK_KEX2_1 678 680 PF00082 0.232
CLV_PCSK_PC1ET2_1 294 296 PF00082 0.523
CLV_PCSK_PC1ET2_1 666 668 PF00082 0.273
CLV_PCSK_PC7_1 667 673 PF00082 0.309
CLV_PCSK_SKI1_1 26 30 PF00082 0.525
CLV_PCSK_SKI1_1 295 299 PF00082 0.458
CLV_PCSK_SKI1_1 316 320 PF00082 0.466
CLV_PCSK_SKI1_1 347 351 PF00082 0.440
CLV_PCSK_SKI1_1 459 463 PF00082 0.297
CLV_PCSK_SKI1_1 56 60 PF00082 0.542
CLV_PCSK_SKI1_1 573 577 PF00082 0.267
DEG_APCC_DBOX_1 458 466 PF00400 0.304
DEG_SCF_TRCP1_1 716 721 PF00400 0.354
DOC_CKS1_1 156 161 PF01111 0.238
DOC_CKS1_1 505 510 PF01111 0.334
DOC_CYCLIN_RxL_1 64 78 PF00134 0.321
DOC_CYCLIN_yClb1_LxF_4 532 537 PF00134 0.266
DOC_MAPK_gen_1 205 215 PF00069 0.279
DOC_MAPK_gen_1 249 257 PF00069 0.296
DOC_MAPK_gen_1 292 300 PF00069 0.286
DOC_MAPK_gen_1 306 314 PF00069 0.266
DOC_MAPK_gen_1 515 524 PF00069 0.154
DOC_MAPK_gen_1 542 551 PF00069 0.246
DOC_MAPK_gen_1 683 692 PF00069 0.518
DOC_MAPK_MEF2A_6 13 22 PF00069 0.331
DOC_MAPK_MEF2A_6 249 257 PF00069 0.293
DOC_MAPK_MEF2A_6 542 551 PF00069 0.252
DOC_PP1_RVXF_1 532 538 PF00149 0.279
DOC_PP1_RVXF_1 571 577 PF00149 0.517
DOC_PP1_RVXF_1 68 75 PF00149 0.317
DOC_PP1_RVXF_1 861 867 PF00149 0.446
DOC_PP2B_LxvP_1 577 580 PF13499 0.348
DOC_PP2B_LxvP_1 655 658 PF13499 0.319
DOC_PP4_FxxP_1 54 57 PF00568 0.266
DOC_PP4_FxxP_1 621 624 PF00568 0.246
DOC_PP4_FxxP_1 745 748 PF00568 0.354
DOC_USP7_MATH_1 164 168 PF00917 0.319
DOC_USP7_MATH_1 174 178 PF00917 0.306
DOC_USP7_MATH_1 233 237 PF00917 0.316
DOC_USP7_MATH_1 353 357 PF00917 0.311
DOC_USP7_MATH_1 705 709 PF00917 0.470
DOC_USP7_MATH_1 748 752 PF00917 0.381
DOC_USP7_UBL2_3 309 313 PF12436 0.332
DOC_USP7_UBL2_3 569 573 PF12436 0.532
DOC_WW_Pin1_4 155 160 PF00397 0.332
DOC_WW_Pin1_4 240 245 PF00397 0.261
DOC_WW_Pin1_4 504 509 PF00397 0.247
LIG_14-3-3_CanoR_1 103 107 PF00244 0.295
LIG_14-3-3_CanoR_1 183 188 PF00244 0.309
LIG_14-3-3_CanoR_1 306 312 PF00244 0.294
LIG_14-3-3_CanoR_1 382 390 PF00244 0.332
LIG_14-3-3_CanoR_1 683 692 PF00244 0.438
LIG_APCC_ABBA_1 365 370 PF00400 0.238
LIG_BRCT_BRCA1_1 177 181 PF00533 0.290
LIG_BRCT_BRCA1_1 811 815 PF00533 0.306
LIG_BRCT_BRCA1_1 828 832 PF00533 0.252
LIG_Clathr_ClatBox_1 849 853 PF01394 0.297
LIG_CSL_BTD_1 336 339 PF09270 0.252
LIG_CtBP_PxDLS_1 883 887 PF00389 0.516
LIG_deltaCOP1_diTrp_1 568 578 PF00928 0.487
LIG_EH1_1 770 778 PF00400 0.532
LIG_eIF4E_1 149 155 PF01652 0.238
LIG_eIF4E_1 572 578 PF01652 0.438
LIG_EVH1_2 374 378 PF00568 0.266
LIG_FHA_1 124 130 PF00498 0.287
LIG_FHA_1 443 449 PF00498 0.438
LIG_FHA_1 57 63 PF00498 0.262
LIG_FHA_1 685 691 PF00498 0.479
LIG_FHA_1 731 737 PF00498 0.557
LIG_FHA_1 755 761 PF00498 0.438
LIG_FHA_1 821 827 PF00498 0.258
LIG_FHA_1 843 849 PF00498 0.289
LIG_FHA_2 119 125 PF00498 0.329
LIG_FHA_2 128 134 PF00498 0.272
LIG_FHA_2 156 162 PF00498 0.210
LIG_FHA_2 261 267 PF00498 0.285
LIG_FHA_2 30 36 PF00498 0.283
LIG_FHA_2 374 380 PF00498 0.249
LIG_FHA_2 757 763 PF00498 0.519
LIG_FHA_2 96 102 PF00498 0.295
LIG_LIR_Apic_2 52 57 PF02991 0.268
LIG_LIR_Apic_2 618 624 PF02991 0.250
LIG_LIR_Gen_1 178 188 PF02991 0.334
LIG_LIR_Gen_1 235 244 PF02991 0.283
LIG_LIR_Gen_1 310 319 PF02991 0.258
LIG_LIR_Gen_1 536 546 PF02991 0.246
LIG_LIR_Gen_1 581 589 PF02991 0.302
LIG_LIR_Gen_1 766 776 PF02991 0.476
LIG_LIR_Gen_1 795 806 PF02991 0.446
LIG_LIR_Nem_3 178 184 PF02991 0.311
LIG_LIR_Nem_3 186 191 PF02991 0.278
LIG_LIR_Nem_3 235 240 PF02991 0.281
LIG_LIR_Nem_3 310 314 PF02991 0.262
LIG_LIR_Nem_3 335 340 PF02991 0.323
LIG_LIR_Nem_3 384 390 PF02991 0.248
LIG_LIR_Nem_3 411 415 PF02991 0.255
LIG_LIR_Nem_3 466 471 PF02991 0.364
LIG_LIR_Nem_3 478 482 PF02991 0.187
LIG_LIR_Nem_3 492 496 PF02991 0.214
LIG_LIR_Nem_3 536 541 PF02991 0.246
LIG_LIR_Nem_3 568 574 PF02991 0.485
LIG_LIR_Nem_3 581 585 PF02991 0.294
LIG_LIR_Nem_3 588 594 PF02991 0.286
LIG_LIR_Nem_3 766 771 PF02991 0.459
LIG_LIR_Nem_3 795 801 PF02991 0.446
LIG_LIR_Nem_3 812 818 PF02991 0.297
LIG_PCNA_PIPBox_1 852 861 PF02747 0.446
LIG_Pex14_2 383 387 PF04695 0.255
LIG_Pex14_2 412 416 PF04695 0.246
LIG_Pex14_2 427 431 PF04695 0.297
LIG_Pex14_2 54 58 PF04695 0.283
LIG_Pex14_2 555 559 PF04695 0.365
LIG_Pex14_2 578 582 PF04695 0.378
LIG_Pex14_2 869 873 PF04695 0.446
LIG_PTB_Apo_2 474 481 PF02174 0.297
LIG_PTB_Apo_2 561 568 PF02174 0.306
LIG_PTB_Apo_2 626 633 PF02174 0.238
LIG_PTB_Apo_2 691 698 PF02174 0.382
LIG_PTB_Apo_2 868 875 PF02174 0.451
LIG_PTB_Phospho_1 561 567 PF10480 0.306
LIG_PTB_Phospho_1 691 697 PF10480 0.354
LIG_PTB_Phospho_1 868 874 PF10480 0.451
LIG_REV1ctd_RIR_1 433 443 PF16727 0.285
LIG_SH2_CRK 152 156 PF00017 0.238
LIG_SH2_CRK 471 475 PF00017 0.441
LIG_SH2_CRK 538 542 PF00017 0.246
LIG_SH2_CRK 591 595 PF00017 0.297
LIG_SH2_NCK_1 697 701 PF00017 0.410
LIG_SH2_SRC 169 172 PF00017 0.349
LIG_SH2_SRC 302 305 PF00017 0.324
LIG_SH2_SRC 780 783 PF00017 0.466
LIG_SH2_STAP1 567 571 PF00017 0.532
LIG_SH2_STAP1 697 701 PF00017 0.410
LIG_SH2_STAT5 262 265 PF00017 0.341
LIG_SH2_STAT5 311 314 PF00017 0.294
LIG_SH2_STAT5 414 417 PF00017 0.297
LIG_SH2_STAT5 460 463 PF00017 0.291
LIG_SH2_STAT5 491 494 PF00017 0.283
LIG_SH2_STAT5 659 662 PF00017 0.545
LIG_SH2_STAT5 697 700 PF00017 0.410
LIG_SH2_STAT5 780 783 PF00017 0.447
LIG_SH2_STAT5 787 790 PF00017 0.445
LIG_SH2_STAT5 798 801 PF00017 0.433
LIG_SH3_3 153 159 PF00018 0.365
LIG_SH3_3 502 508 PF00018 0.278
LIG_SH3_3 511 517 PF00018 0.278
LIG_SH3_3 624 630 PF00018 0.236
LIG_SUMO_SIM_anti_2 593 598 PF11976 0.348
LIG_SUMO_SIM_anti_2 612 618 PF11976 0.120
LIG_SUMO_SIM_par_1 211 216 PF11976 0.267
LIG_SUMO_SIM_par_1 460 466 PF11976 0.285
LIG_SUMO_SIM_par_1 612 618 PF11976 0.332
LIG_SUMO_SIM_par_1 687 693 PF11976 0.528
LIG_SUMO_SIM_par_1 822 827 PF11976 0.326
LIG_SUMO_SIM_par_1 882 887 PF11976 0.396
LIG_TRAF2_1 751 754 PF00917 0.507
LIG_TRAF2_1 98 101 PF00917 0.332
LIG_TRFH_1 620 624 PF08558 0.297
LIG_TYR_ITIM 418 423 PF00017 0.315
LIG_UBA3_1 187 194 PF00899 0.404
LIG_UBA3_1 246 252 PF00899 0.417
LIG_UBA3_1 430 439 PF00899 0.313
LIG_UBA3_1 594 599 PF00899 0.265
LIG_WRC_WIRS_1 586 591 PF05994 0.279
LIG_WRC_WIRS_1 815 820 PF05994 0.353
LIG_WW_3 515 519 PF00397 0.168
MOD_CK1_1 165 171 PF00069 0.320
MOD_CK1_1 193 199 PF00069 0.369
MOD_CK1_1 328 334 PF00069 0.311
MOD_CK1_1 360 366 PF00069 0.357
MOD_CK1_1 489 495 PF00069 0.331
MOD_CK1_1 688 694 PF00069 0.356
MOD_CK1_1 695 701 PF00069 0.358
MOD_CK1_1 756 762 PF00069 0.426
MOD_CK1_1 790 796 PF00069 0.455
MOD_CK1_1 809 815 PF00069 0.294
MOD_CK2_1 118 124 PF00069 0.311
MOD_CK2_1 127 133 PF00069 0.253
MOD_CK2_1 260 266 PF00069 0.359
MOD_CK2_1 29 35 PF00069 0.397
MOD_CK2_1 373 379 PF00069 0.342
MOD_CK2_1 562 568 PF00069 0.285
MOD_CK2_1 609 615 PF00069 0.314
MOD_CK2_1 714 720 PF00069 0.265
MOD_CK2_1 748 754 PF00069 0.448
MOD_CK2_1 756 762 PF00069 0.421
MOD_CK2_1 95 101 PF00069 0.363
MOD_GlcNHglycan 327 330 PF01048 0.309
MOD_GlcNHglycan 334 337 PF01048 0.301
MOD_GlcNHglycan 355 358 PF01048 0.327
MOD_GlcNHglycan 488 491 PF01048 0.305
MOD_GlcNHglycan 704 708 PF01048 0.389
MOD_GlcNHglycan 716 719 PF01048 0.400
MOD_GlcNHglycan 720 723 PF01048 0.423
MOD_GlcNHglycan 8 11 PF01048 0.465
MOD_GlcNHglycan 829 832 PF01048 0.319
MOD_GlcNHglycan 855 858 PF01048 0.302
MOD_GlcNHglycan 95 98 PF01048 0.368
MOD_GSK3_1 123 130 PF00069 0.429
MOD_GSK3_1 175 182 PF00069 0.394
MOD_GSK3_1 272 279 PF00069 0.323
MOD_GSK3_1 317 324 PF00069 0.318
MOD_GSK3_1 328 335 PF00069 0.294
MOD_GSK3_1 353 360 PF00069 0.334
MOD_GSK3_1 373 380 PF00069 0.266
MOD_GSK3_1 485 492 PF00069 0.382
MOD_GSK3_1 499 506 PF00069 0.359
MOD_GSK3_1 558 565 PF00069 0.285
MOD_GSK3_1 600 607 PF00069 0.330
MOD_GSK3_1 684 691 PF00069 0.386
MOD_GSK3_1 714 721 PF00069 0.427
MOD_GSK3_1 749 756 PF00069 0.422
MOD_GSK3_1 788 795 PF00069 0.301
MOD_GSK3_1 802 809 PF00069 0.287
MOD_GSK3_1 816 823 PF00069 0.351
MOD_GSK3_1 884 891 PF00069 0.550
MOD_N-GLC_1 165 170 PF02516 0.283
MOD_N-GLC_1 357 362 PF02516 0.417
MOD_N-GLC_1 562 567 PF02516 0.276
MOD_N-GLC_1 827 832 PF02516 0.422
MOD_N-GLC_2 323 325 PF02516 0.324
MOD_NEK2_1 102 107 PF00069 0.369
MOD_NEK2_1 162 167 PF00069 0.373
MOD_NEK2_1 190 195 PF00069 0.438
MOD_NEK2_1 274 279 PF00069 0.342
MOD_NEK2_1 29 34 PF00069 0.345
MOD_NEK2_1 307 312 PF00069 0.375
MOD_NEK2_1 327 332 PF00069 0.275
MOD_NEK2_1 377 382 PF00069 0.342
MOD_NEK2_1 383 388 PF00069 0.329
MOD_NEK2_1 463 468 PF00069 0.346
MOD_NEK2_1 480 485 PF00069 0.182
MOD_NEK2_1 486 491 PF00069 0.345
MOD_NEK2_1 537 542 PF00069 0.313
MOD_NEK2_1 558 563 PF00069 0.361
MOD_NEK2_1 585 590 PF00069 0.298
MOD_NEK2_1 685 690 PF00069 0.354
MOD_NEK2_1 806 811 PF00069 0.326
MOD_NEK2_1 816 821 PF00069 0.307
MOD_NEK2_1 884 889 PF00069 0.524
MOD_OFUCOSY 325 332 PF10250 0.325
MOD_PIKK_1 806 812 PF00454 0.307
MOD_PK_1 609 615 PF00069 0.285
MOD_PKA_2 102 108 PF00069 0.281
MOD_PKA_2 204 210 PF00069 0.303
MOD_PKA_2 381 387 PF00069 0.372
MOD_PKA_2 685 691 PF00069 0.296
MOD_PKA_2 711 717 PF00069 0.342
MOD_Plk_1 118 124 PF00069 0.341
MOD_Plk_1 165 171 PF00069 0.354
MOD_Plk_1 283 289 PF00069 0.435
MOD_Plk_1 342 348 PF00069 0.404
MOD_Plk_1 562 568 PF00069 0.276
MOD_Plk_1 75 81 PF00069 0.372
MOD_Plk_2-3 260 266 PF00069 0.226
MOD_Plk_4 102 108 PF00069 0.316
MOD_Plk_4 183 189 PF00069 0.417
MOD_Plk_4 233 239 PF00069 0.376
MOD_Plk_4 242 248 PF00069 0.317
MOD_Plk_4 29 35 PF00069 0.334
MOD_Plk_4 296 302 PF00069 0.291
MOD_Plk_4 307 313 PF00069 0.341
MOD_Plk_4 360 366 PF00069 0.306
MOD_Plk_4 373 379 PF00069 0.266
MOD_Plk_4 463 469 PF00069 0.380
MOD_Plk_4 562 568 PF00069 0.340
MOD_Plk_4 590 596 PF00069 0.344
MOD_Plk_4 609 615 PF00069 0.256
MOD_Plk_4 685 691 PF00069 0.383
MOD_Plk_4 756 762 PF00069 0.427
MOD_Plk_4 794 800 PF00069 0.297
MOD_ProDKin_1 155 161 PF00069 0.417
MOD_ProDKin_1 240 246 PF00069 0.318
MOD_ProDKin_1 504 510 PF00069 0.298
MOD_SUMO_for_1 312 315 PF00179 0.417
MOD_SUMO_rev_2 186 196 PF00179 0.246
MOD_SUMO_rev_2 497 502 PF00179 0.246
MOD_SUMO_rev_2 530 535 PF00179 0.298
TRG_DiLeu_BaEn_1 581 586 PF01217 0.348
TRG_DiLeu_BaEn_2 217 223 PF01217 0.285
TRG_DiLeu_BaEn_4 197 203 PF01217 0.417
TRG_DiLeu_BaLyEn_6 150 155 PF01217 0.246
TRG_ENDOCYTIC_2 152 155 PF00928 0.417
TRG_ENDOCYTIC_2 311 314 PF00928 0.317
TRG_ENDOCYTIC_2 399 402 PF00928 0.239
TRG_ENDOCYTIC_2 420 423 PF00928 0.295
TRG_ENDOCYTIC_2 460 463 PF00928 0.297
TRG_ENDOCYTIC_2 471 474 PF00928 0.297
TRG_ENDOCYTIC_2 476 479 PF00928 0.297
TRG_ENDOCYTIC_2 538 541 PF00928 0.297
TRG_ENDOCYTIC_2 591 594 PF00928 0.297
TRG_ENDOCYTIC_2 659 662 PF00928 0.431
TRG_ENDOCYTIC_2 798 801 PF00928 0.297
TRG_ER_diArg_1 292 295 PF00400 0.353
TRG_ER_diArg_1 346 348 PF00400 0.422
TRG_ER_diArg_1 62 64 PF00400 0.306
TRG_ER_diArg_1 670 672 PF00400 0.278
TRG_ER_diArg_1 678 680 PF00400 0.310
TRG_NES_CRM1_1 853 868 PF08389 0.297
TRG_Pf-PMV_PEXEL_1 153 157 PF00026 0.447
TRG_Pf-PMV_PEXEL_1 348 352 PF00026 0.359
TRG_Pf-PMV_PEXEL_1 724 729 PF00026 0.285

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P622 Leptomonas seymouri 41% 100%
A0A0N1PFQ1 Leptomonas seymouri 70% 97%
A0A0S4JG87 Bodo saltans 37% 99%
A0A0S4JMR5 Bodo saltans 43% 100%
A0A1X0NV83 Trypanosomatidae 50% 100%
A0A1X0NWN0 Trypanosomatidae 43% 100%
A0A3Q8IB62 Leishmania donovani 43% 100%
A0A3Q8IGN1 Leishmania donovani 95% 100%
A0A3R7KUW1 Trypanosoma rangeli 48% 100%
A0A422NJD7 Trypanosoma rangeli 42% 100%
A1A5G6 Xenopus tropicalis 33% 100%
A4HD35 Leishmania braziliensis 41% 100%
A4HK73 Leishmania braziliensis 85% 100%
A4I0M2 Leishmania infantum 42% 100%
A4I7Q8 Leishmania infantum 95% 100%
B2MZD0 Caenorhabditis elegans 30% 74%
C9ZNR3 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 43% 100%
E9AWI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 42% 100%
E9B2L6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 92% 100%
G5EEK9 Caenorhabditis elegans 31% 100%
G5EGP4 Caenorhabditis elegans 27% 100%
O13742 Schizosaccharomyces pombe (strain 972 / ATCC 24843) 30% 100%
O97681 Bos taurus 31% 100%
P15920 Mus musculus 31% 100%
P25286 Rattus norvegicus 32% 100%
P30628 Caenorhabditis elegans 30% 99%
P32563 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 30% 100%
P37296 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 30% 100%
Q01290 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) 32% 100%
Q13488 Homo sapiens 31% 100%
Q29466 Bos taurus 33% 100%
Q4QAY7 Leishmania major 42% 100%
Q54E04 Dictyostelium discoideum 34% 100%
Q5R422 Pongo abelii 32% 100%
Q8AVM5 Xenopus laevis 33% 100%
Q8RWZ7 Arabidopsis thaliana 31% 100%
Q8W4S4 Arabidopsis thaliana 34% 100%
Q920R6 Mus musculus 32% 100%
Q93050 Homo sapiens 33% 100%
Q9HBG4 Homo sapiens 33% 100%
Q9I8D0 Gallus gallus 30% 100%
Q9SJT7 Arabidopsis thaliana 32% 100%
Q9Y487 Homo sapiens 31% 100%
Q9Z1G4 Mus musculus 32% 100%
V5BQN9 Trypanosoma cruzi 51% 100%
V5D763 Trypanosoma cruzi 42% 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