LeishMANIAdb
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AAA domain-containing protein

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

Quick info

Protein:
AAA domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania mexicana
UniProt:
E9AXH2_LEIMU
TriTrypDb:
LmxM.25.0940
Length:
683

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: 5
NetGPI no yes: 0, no: 5
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

E9AXH2
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AXH2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 138 142 PF00656 0.764
CLV_C14_Caspase3-7 218 222 PF00656 0.602
CLV_C14_Caspase3-7 224 228 PF00656 0.614
CLV_C14_Caspase3-7 490 494 PF00656 0.531
CLV_NRD_NRD_1 189 191 PF00675 0.682
CLV_NRD_NRD_1 237 239 PF00675 0.653
CLV_NRD_NRD_1 256 258 PF00675 0.531
CLV_NRD_NRD_1 275 277 PF00675 0.580
CLV_NRD_NRD_1 453 455 PF00675 0.533
CLV_NRD_NRD_1 460 462 PF00675 0.490
CLV_NRD_NRD_1 472 474 PF00675 0.473
CLV_NRD_NRD_1 486 488 PF00675 0.563
CLV_NRD_NRD_1 561 563 PF00675 0.691
CLV_NRD_NRD_1 565 567 PF00675 0.671
CLV_NRD_NRD_1 640 642 PF00675 0.541
CLV_PCSK_FUR_1 557 561 PF00082 0.667
CLV_PCSK_KEX2_1 178 180 PF00082 0.666
CLV_PCSK_KEX2_1 237 239 PF00082 0.694
CLV_PCSK_KEX2_1 256 258 PF00082 0.531
CLV_PCSK_KEX2_1 275 277 PF00082 0.580
CLV_PCSK_KEX2_1 453 455 PF00082 0.533
CLV_PCSK_KEX2_1 462 464 PF00082 0.485
CLV_PCSK_KEX2_1 485 487 PF00082 0.701
CLV_PCSK_KEX2_1 559 561 PF00082 0.675
CLV_PCSK_KEX2_1 565 567 PF00082 0.652
CLV_PCSK_KEX2_1 677 679 PF00082 0.583
CLV_PCSK_PC1ET2_1 178 180 PF00082 0.666
CLV_PCSK_PC1ET2_1 462 464 PF00082 0.569
CLV_PCSK_PC1ET2_1 559 561 PF00082 0.675
CLV_PCSK_PC1ET2_1 677 679 PF00082 0.583
CLV_PCSK_PC7_1 174 180 PF00082 0.659
CLV_PCSK_PC7_1 557 563 PF00082 0.675
CLV_PCSK_PC7_1 673 679 PF00082 0.552
CLV_PCSK_SKI1_1 179 183 PF00082 0.661
CLV_PCSK_SKI1_1 394 398 PF00082 0.595
CLV_Separin_Metazoa 367 371 PF03568 0.522
DEG_APCC_DBOX_1 356 364 PF00400 0.502
DEG_COP1_1 601 608 PF00400 0.667
DEG_SCF_FBW7_1 408 413 PF00400 0.646
DEG_SPOP_SBC_1 577 581 PF00917 0.555
DOC_ANK_TNKS_1 485 492 PF00023 0.654
DOC_CKS1_1 314 319 PF01111 0.664
DOC_CKS1_1 635 640 PF01111 0.551
DOC_CYCLIN_yCln2_LP_2 60 63 PF00134 0.516
DOC_MAPK_gen_1 354 363 PF00069 0.513
DOC_MAPK_HePTP_8 416 428 PF00069 0.489
DOC_MAPK_MEF2A_6 419 428 PF00069 0.532
DOC_PP1_RVXF_1 368 375 PF00149 0.395
DOC_PP1_RVXF_1 671 677 PF00149 0.531
DOC_PP2B_LxvP_1 510 513 PF13499 0.687
DOC_PP2B_LxvP_1 60 63 PF13499 0.497
DOC_USP7_MATH_1 144 148 PF00917 0.693
DOC_USP7_MATH_1 160 164 PF00917 0.585
DOC_USP7_MATH_1 249 253 PF00917 0.550
DOC_USP7_MATH_1 302 306 PF00917 0.626
DOC_USP7_MATH_1 323 327 PF00917 0.810
DOC_USP7_MATH_1 410 414 PF00917 0.553
DOC_USP7_MATH_1 577 581 PF00917 0.629
DOC_USP7_MATH_1 593 597 PF00917 0.639
DOC_USP7_MATH_1 599 603 PF00917 0.618
DOC_USP7_MATH_1 69 73 PF00917 0.523
DOC_USP7_UBL2_3 470 474 PF12436 0.642
DOC_WW_Pin1_4 139 144 PF00397 0.613
DOC_WW_Pin1_4 150 155 PF00397 0.691
DOC_WW_Pin1_4 29 34 PF00397 0.474
DOC_WW_Pin1_4 313 318 PF00397 0.770
DOC_WW_Pin1_4 326 331 PF00397 0.590
DOC_WW_Pin1_4 406 411 PF00397 0.825
DOC_WW_Pin1_4 418 423 PF00397 0.559
DOC_WW_Pin1_4 48 53 PF00397 0.547
DOC_WW_Pin1_4 570 575 PF00397 0.670
DOC_WW_Pin1_4 61 66 PF00397 0.608
DOC_WW_Pin1_4 631 636 PF00397 0.578
DOC_WW_Pin1_4 99 104 PF00397 0.572
LIG_14-3-3_CanoR_1 179 184 PF00244 0.656
LIG_14-3-3_CanoR_1 256 266 PF00244 0.555
LIG_14-3-3_CanoR_1 306 314 PF00244 0.709
LIG_14-3-3_CanoR_1 357 361 PF00244 0.512
LIG_14-3-3_CanoR_1 453 459 PF00244 0.516
LIG_14-3-3_CanoR_1 463 469 PF00244 0.523
LIG_14-3-3_CanoR_1 560 569 PF00244 0.650
LIG_14-3-3_CanoR_1 578 586 PF00244 0.577
LIG_14-3-3_CanoR_1 646 654 PF00244 0.576
LIG_14-3-3_CanoR_1 73 78 PF00244 0.632
LIG_Actin_WH2_2 342 359 PF00022 0.551
LIG_deltaCOP1_diTrp_1 514 524 PF00928 0.686
LIG_EH1_1 54 62 PF00400 0.491
LIG_eIF4E_1 25 31 PF01652 0.475
LIG_FHA_1 180 186 PF00498 0.539
LIG_FHA_1 314 320 PF00498 0.711
LIG_FHA_1 45 51 PF00498 0.567
LIG_FHA_2 216 222 PF00498 0.556
LIG_FHA_2 635 641 PF00498 0.547
LIG_LIR_Apic_2 43 49 PF02991 0.477
LIG_LIR_Gen_1 514 524 PF02991 0.565
LIG_LIR_Gen_1 660 669 PF02991 0.522
LIG_LIR_Nem_3 514 520 PF02991 0.567
LIG_LIR_Nem_3 660 665 PF02991 0.535
LIG_Rb_LxCxE_1 607 622 PF01857 0.614
LIG_SH2_CRK 46 50 PF00017 0.476
LIG_SH2_CRK 662 666 PF00017 0.517
LIG_SH2_SRC 438 441 PF00017 0.496
LIG_SH2_STAP1 446 450 PF00017 0.514
LIG_SH2_STAP1 644 648 PF00017 0.552
LIG_SH2_STAP1 662 666 PF00017 0.350
LIG_SH2_STAT5 438 441 PF00017 0.549
LIG_SH2_STAT5 46 49 PF00017 0.476
LIG_SH2_STAT5 647 650 PF00017 0.550
LIG_SH3_1 397 403 PF00018 0.590
LIG_SH3_1 46 52 PF00018 0.471
LIG_SH3_3 263 269 PF00018 0.580
LIG_SH3_3 3 9 PF00018 0.500
LIG_SH3_3 311 317 PF00018 0.664
LIG_SH3_3 360 366 PF00018 0.489
LIG_SH3_3 397 403 PF00018 0.634
LIG_SH3_3 421 427 PF00018 0.569
LIG_SH3_3 46 52 PF00018 0.487
LIG_SH3_3 515 521 PF00018 0.683
LIG_SH3_3 59 65 PF00018 0.481
LIG_SH3_3 611 617 PF00018 0.632
LIG_SH3_3 629 635 PF00018 0.450
LIG_Sin3_3 629 636 PF02671 0.605
LIG_TRAF2_1 143 146 PF00917 0.544
LIG_TRAF2_1 196 199 PF00917 0.666
LIG_TRAF2_1 269 272 PF00917 0.549
LIG_TRAF2_1 333 336 PF00917 0.621
LIG_TRAF2_1 637 640 PF00917 0.550
LIG_TRFH_1 29 33 PF08558 0.467
LIG_UBA3_1 425 430 PF00899 0.547
MOD_CDK_SPK_2 29 34 PF00069 0.468
MOD_CDK_SPxxK_3 634 641 PF00069 0.555
MOD_CK1_1 147 153 PF00069 0.622
MOD_CK1_1 155 161 PF00069 0.655
MOD_CK1_1 230 236 PF00069 0.550
MOD_CK1_1 252 258 PF00069 0.546
MOD_CK1_1 304 310 PF00069 0.712
MOD_CK1_1 324 330 PF00069 0.651
MOD_CK1_1 414 420 PF00069 0.554
MOD_CK1_1 478 484 PF00069 0.682
MOD_CK1_1 573 579 PF00069 0.656
MOD_CK1_1 592 598 PF00069 0.572
MOD_CK1_1 634 640 PF00069 0.450
MOD_CK1_1 99 105 PF00069 0.598
MOD_CK2_1 139 145 PF00069 0.705
MOD_CK2_1 219 225 PF00069 0.677
MOD_CK2_1 282 288 PF00069 0.701
MOD_CK2_1 634 640 PF00069 0.566
MOD_CK2_1 88 94 PF00069 0.537
MOD_CMANNOS 550 553 PF00535 0.647
MOD_Cter_Amidation 188 191 PF01082 0.682
MOD_Cter_Amidation 471 474 PF01082 0.644
MOD_GlcNHglycan 107 110 PF01048 0.664
MOD_GlcNHglycan 145 149 PF01048 0.616
MOD_GlcNHglycan 162 165 PF01048 0.618
MOD_GlcNHglycan 209 212 PF01048 0.574
MOD_GlcNHglycan 323 326 PF01048 0.825
MOD_GlcNHglycan 385 388 PF01048 0.579
MOD_GlcNHglycan 477 480 PF01048 0.649
MOD_GlcNHglycan 533 536 PF01048 0.669
MOD_GlcNHglycan 541 544 PF01048 0.574
MOD_GlcNHglycan 575 578 PF01048 0.680
MOD_GlcNHglycan 583 586 PF01048 0.624
MOD_GlcNHglycan 591 594 PF01048 0.554
MOD_GlcNHglycan 601 604 PF01048 0.588
MOD_GlcNHglycan 627 630 PF01048 0.664
MOD_GlcNHglycan 650 653 PF01048 0.589
MOD_GSK3_1 144 151 PF00069 0.702
MOD_GSK3_1 15 22 PF00069 0.500
MOD_GSK3_1 152 159 PF00069 0.657
MOD_GSK3_1 160 167 PF00069 0.605
MOD_GSK3_1 194 201 PF00069 0.651
MOD_GSK3_1 213 220 PF00069 0.589
MOD_GSK3_1 223 230 PF00069 0.629
MOD_GSK3_1 302 309 PF00069 0.805
MOD_GSK3_1 40 47 PF00069 0.521
MOD_GSK3_1 406 413 PF00069 0.664
MOD_GSK3_1 414 421 PF00069 0.553
MOD_GSK3_1 474 481 PF00069 0.624
MOD_GSK3_1 561 568 PF00069 0.692
MOD_GSK3_1 573 580 PF00069 0.604
MOD_GSK3_1 589 596 PF00069 0.668
MOD_GSK3_1 604 611 PF00069 0.527
MOD_GSK3_1 69 76 PF00069 0.502
MOD_GSK3_1 84 91 PF00069 0.700
MOD_LATS_1 71 77 PF00433 0.504
MOD_NEK2_1 126 131 PF00069 0.523
MOD_NEK2_1 356 361 PF00069 0.554
MOD_NEK2_1 664 669 PF00069 0.515
MOD_PIKK_1 219 225 PF00454 0.611
MOD_PIKK_1 398 404 PF00454 0.688
MOD_PIKK_1 452 458 PF00454 0.493
MOD_PKA_1 473 479 PF00069 0.616
MOD_PKA_1 560 566 PF00069 0.691
MOD_PKA_2 302 308 PF00069 0.725
MOD_PKA_2 356 362 PF00069 0.512
MOD_PKA_2 452 458 PF00069 0.560
MOD_PKA_2 464 470 PF00069 0.518
MOD_PKA_2 560 566 PF00069 0.691
MOD_PKA_2 577 583 PF00069 0.546
MOD_PKA_2 96 102 PF00069 0.635
MOD_PKB_1 306 314 PF00069 0.709
MOD_Plk_1 126 132 PF00069 0.515
MOD_Plk_1 197 203 PF00069 0.717
MOD_Plk_1 69 75 PF00069 0.502
MOD_Plk_1 82 88 PF00069 0.526
MOD_Plk_4 198 204 PF00069 0.716
MOD_Plk_4 249 255 PF00069 0.551
MOD_Plk_4 315 321 PF00069 0.673
MOD_Plk_4 356 362 PF00069 0.556
MOD_ProDKin_1 139 145 PF00069 0.615
MOD_ProDKin_1 150 156 PF00069 0.693
MOD_ProDKin_1 29 35 PF00069 0.472
MOD_ProDKin_1 313 319 PF00069 0.771
MOD_ProDKin_1 326 332 PF00069 0.584
MOD_ProDKin_1 406 412 PF00069 0.823
MOD_ProDKin_1 418 424 PF00069 0.549
MOD_ProDKin_1 48 54 PF00069 0.547
MOD_ProDKin_1 570 576 PF00069 0.669
MOD_ProDKin_1 61 67 PF00069 0.607
MOD_ProDKin_1 631 637 PF00069 0.571
MOD_ProDKin_1 99 105 PF00069 0.569
MOD_SUMO_for_1 258 261 PF00179 0.580
MOD_SUMO_for_1 333 336 PF00179 0.566
MOD_SUMO_rev_2 495 505 PF00179 0.627
TRG_DiLeu_BaEn_1 198 203 PF01217 0.716
TRG_DiLeu_BaLyEn_6 421 426 PF01217 0.567
TRG_DiLeu_BaLyEn_6 62 67 PF01217 0.513
TRG_ENDOCYTIC_2 662 665 PF00928 0.520
TRG_ER_diArg_1 256 258 PF00400 0.548
TRG_ER_diArg_1 274 276 PF00400 0.574
TRG_ER_diArg_1 452 454 PF00400 0.539
TRG_ER_diArg_1 463 466 PF00400 0.479
TRG_ER_diArg_1 485 487 PF00400 0.660
TRG_ER_diArg_1 560 562 PF00400 0.681
TRG_ER_diArg_1 565 567 PF00400 0.661
TRG_NLS_Bipartite_1 176 194 PF00514 0.668
TRG_NLS_MonoCore_2 175 180 PF00514 0.660
TRG_NLS_MonoExtC_3 189 194 PF00514 0.679
TRG_NLS_MonoExtC_3 460 465 PF00514 0.566
TRG_NLS_MonoExtN_4 174 181 PF00514 0.658
TRG_NLS_MonoExtN_4 461 466 PF00514 0.575
TRG_Pf-PMV_PEXEL_1 376 381 PF00026 0.551
TRG_Pf-PMV_PEXEL_1 430 434 PF00026 0.519

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8INB5 Leishmania donovani 81% 100%
A4HE29 Leishmania braziliensis 69% 99%
A4I1D5 Leishmania infantum 81% 100%
Q4QA00 Leishmania major 79% 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