LeishMANIAdb
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Inositol-1,4,5-trisphosphate (IP3) 5-phosphatase,putative

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

Quick info

Protein:
Inositol-1,4,5-trisphosphate (IP3) 5-phosphatase,putative
Gene product:
inositol-1,4,5-trisphosphate (IP3) 5-phosphatase, putative
Species:
Leishmania mexicana
UniProt:
E9ANP5_LEIMU
TriTrypDb:
LmxM.11.1010
Length:
687

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: 6
NetGPI no yes: 0, no: 6
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

E9ANP5
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9ANP5

Function

Biological processes
Term Name Level Count
GO:0005975 carbohydrate metabolic process 3 1
GO:0006066 alcohol metabolic process 3 1
GO:0006793 phosphorus metabolic process 3 1
GO:0006796 phosphate-containing compound metabolic process 4 1
GO:0007165 signal transduction 2 1
GO:0008152 metabolic process 1 1
GO:0009056 catabolic process 2 1
GO:0009987 cellular process 1 1
GO:0016311 dephosphorylation 5 1
GO:0019637 organophosphate metabolic process 3 1
GO:0019751 polyol metabolic process 4 1
GO:0019932 second-messenger-mediated signaling 4 1
GO:0035556 intracellular signal transduction 3 1
GO:0043647 inositol phosphate metabolic process 4 1
GO:0044237 cellular metabolic process 2 1
GO:0044238 primary metabolic process 2 1
GO:0044262 obsolete cellular carbohydrate metabolic process 3 1
GO:0044281 small molecule metabolic process 2 1
GO:0044282 small molecule catabolic process 3 1
GO:0046164 alcohol catabolic process 4 1
GO:0046174 polyol catabolic process 5 1
GO:0046434 organophosphate catabolic process 4 1
GO:0046838 obsolete phosphorylated carbohydrate dephosphorylation 4 1
GO:0046855 obsolete inositol phosphate dephosphorylation 5 1
GO:0048016 inositol phosphate-mediated signaling 5 1
GO:0050789 regulation of biological process 2 1
GO:0050794 regulation of cellular process 3 1
GO:0065007 biological regulation 1 1
GO:0071545 inositol phosphate catabolic process 5 1
GO:0071704 organic substance metabolic process 2 1
GO:1901575 organic substance catabolic process 3 1
GO:1901615 organic hydroxy compound metabolic process 3 1
GO:1901616 organic hydroxy compound catabolic process 4 1
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 7
GO:0004445 inositol-polyphosphate 5-phosphatase activity 8 7
GO:0016787 hydrolase activity 2 7
GO:0016788 hydrolase activity, acting on ester bonds 3 7
GO:0016791 phosphatase activity 5 7
GO:0042578 phosphoric ester hydrolase activity 4 7
GO:0046030 inositol trisphosphate phosphatase activity 7 7
GO:0052658 inositol-1,4,5-trisphosphate 5-phosphatase activity 8 6
GO:0052659 inositol-1,3,4,5-tetrakisphosphate 5-phosphatase activity 8 6
GO:0052743 inositol tetrakisphosphate phosphatase activity 7 6
GO:0052745 inositol phosphate phosphatase activity 6 7

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 28 32 PF00656 0.610
CLV_C14_Caspase3-7 96 100 PF00656 0.670
CLV_NRD_NRD_1 262 264 PF00675 0.752
CLV_NRD_NRD_1 366 368 PF00675 0.487
CLV_NRD_NRD_1 409 411 PF00675 0.500
CLV_PCSK_KEX2_1 262 264 PF00082 0.831
CLV_PCSK_KEX2_1 409 411 PF00082 0.500
CLV_PCSK_KEX2_1 463 465 PF00082 0.637
CLV_PCSK_PC1ET2_1 463 465 PF00082 0.637
CLV_PCSK_PC7_1 459 465 PF00082 0.643
CLV_PCSK_SKI1_1 368 372 PF00082 0.531
CLV_PCSK_SKI1_1 396 400 PF00082 0.505
CLV_PCSK_SKI1_1 412 416 PF00082 0.479
CLV_PCSK_SKI1_1 616 620 PF00082 0.423
DEG_APCC_DBOX_1 187 195 PF00400 0.644
DEG_SCF_FBW7_2 64 70 PF00400 0.565
DEG_SPOP_SBC_1 140 144 PF00917 0.476
DEG_SPOP_SBC_1 154 158 PF00917 0.510
DEG_SPOP_SBC_1 243 247 PF00917 0.608
DEG_SPOP_SBC_1 582 586 PF00917 0.515
DOC_AGCK_PIF_3 684 687 PF00069 0.649
DOC_CKS1_1 64 69 PF01111 0.565
DOC_CYCLIN_yCln2_LP_2 427 433 PF00134 0.550
DOC_MAPK_gen_1 365 375 PF00069 0.568
DOC_MAPK_JIP1_4 33 39 PF00069 0.610
DOC_MAPK_MEF2A_6 188 196 PF00069 0.465
DOC_MAPK_MEF2A_6 29 38 PF00069 0.642
DOC_MAPK_MEF2A_6 367 375 PF00069 0.553
DOC_MAPK_NFAT4_5 368 376 PF00069 0.554
DOC_PP1_RVXF_1 614 620 PF00149 0.468
DOC_PP2B_LxvP_1 330 333 PF13499 0.491
DOC_PP2B_PxIxI_1 189 195 PF00149 0.455
DOC_PP4_FxxP_1 318 321 PF00568 0.508
DOC_PP4_FxxP_1 475 478 PF00568 0.546
DOC_PP4_FxxP_1 86 89 PF00568 0.729
DOC_SPAK_OSR1_1 20 24 PF12202 0.666
DOC_USP7_MATH_1 136 140 PF00917 0.659
DOC_USP7_MATH_1 155 159 PF00917 0.681
DOC_USP7_MATH_1 172 176 PF00917 0.557
DOC_USP7_MATH_1 243 247 PF00917 0.549
DOC_USP7_MATH_1 312 316 PF00917 0.463
DOC_USP7_MATH_1 363 367 PF00917 0.510
DOC_USP7_MATH_1 398 402 PF00917 0.613
DOC_USP7_MATH_1 419 423 PF00917 0.495
DOC_USP7_MATH_1 587 591 PF00917 0.629
DOC_USP7_MATH_1 641 645 PF00917 0.825
DOC_USP7_MATH_1 78 82 PF00917 0.745
DOC_USP7_MATH_1 9 13 PF00917 0.690
DOC_USP7_UBL2_3 205 209 PF12436 0.627
DOC_WW_Pin1_4 102 107 PF00397 0.605
DOC_WW_Pin1_4 159 164 PF00397 0.806
DOC_WW_Pin1_4 165 170 PF00397 0.769
DOC_WW_Pin1_4 2 7 PF00397 0.704
DOC_WW_Pin1_4 237 242 PF00397 0.491
DOC_WW_Pin1_4 267 272 PF00397 0.564
DOC_WW_Pin1_4 317 322 PF00397 0.504
DOC_WW_Pin1_4 399 404 PF00397 0.518
DOC_WW_Pin1_4 537 542 PF00397 0.697
DOC_WW_Pin1_4 583 588 PF00397 0.783
DOC_WW_Pin1_4 596 601 PF00397 0.578
DOC_WW_Pin1_4 63 68 PF00397 0.707
LIG_14-3-3_CanoR_1 109 119 PF00244 0.339
LIG_14-3-3_CanoR_1 125 129 PF00244 0.542
LIG_14-3-3_CanoR_1 181 186 PF00244 0.550
LIG_14-3-3_CanoR_1 20 24 PF00244 0.666
LIG_14-3-3_CanoR_1 220 224 PF00244 0.574
LIG_14-3-3_CanoR_1 251 258 PF00244 0.768
LIG_14-3-3_CanoR_1 262 267 PF00244 0.686
LIG_14-3-3_CanoR_1 631 636 PF00244 0.740
LIG_14-3-3_CanoR_1 661 670 PF00244 0.591
LIG_APCC_ABBA_1 387 392 PF00400 0.562
LIG_APCC_ABBA_1 431 436 PF00400 0.436
LIG_BIR_II_1 1 5 PF00653 0.711
LIG_BRCT_BRCA1_1 21 25 PF00533 0.598
LIG_BRCT_BRCA1_1 314 318 PF00533 0.468
LIG_BRCT_BRCA1_1 356 360 PF00533 0.498
LIG_BRCT_BRCA1_1 75 79 PF00533 0.700
LIG_deltaCOP1_diTrp_1 469 475 PF00928 0.527
LIG_FHA_1 111 117 PF00498 0.339
LIG_FHA_1 182 188 PF00498 0.668
LIG_FHA_1 219 225 PF00498 0.627
LIG_FHA_1 228 234 PF00498 0.407
LIG_FHA_1 297 303 PF00498 0.761
LIG_FHA_1 3 9 PF00498 0.754
LIG_FHA_1 38 44 PF00498 0.538
LIG_FHA_1 409 415 PF00498 0.394
LIG_FHA_1 566 572 PF00498 0.696
LIG_FHA_1 583 589 PF00498 0.507
LIG_FHA_2 262 268 PF00498 0.797
LIG_FHA_2 415 421 PF00498 0.369
LIG_FHA_2 478 484 PF00498 0.632
LIG_FHA_2 547 553 PF00498 0.754
LIG_FHA_2 57 63 PF00498 0.732
LIG_FHA_2 676 682 PF00498 0.569
LIG_GSK3_LRP6_1 163 168 PF00069 0.772
LIG_LIR_Apic_2 315 321 PF02991 0.489
LIG_LIR_Apic_2 473 478 PF02991 0.544
LIG_LIR_Apic_2 84 89 PF02991 0.721
LIG_LIR_Gen_1 307 318 PF02991 0.506
LIG_LIR_Gen_1 469 478 PF02991 0.538
LIG_LIR_Gen_1 517 523 PF02991 0.571
LIG_LIR_Gen_1 681 687 PF02991 0.569
LIG_LIR_Gen_1 76 86 PF02991 0.738
LIG_LIR_Gen_1 90 98 PF02991 0.700
LIG_LIR_Nem_3 307 313 PF02991 0.533
LIG_LIR_Nem_3 336 340 PF02991 0.491
LIG_LIR_Nem_3 469 475 PF02991 0.527
LIG_LIR_Nem_3 517 521 PF02991 0.662
LIG_LIR_Nem_3 665 670 PF02991 0.667
LIG_LIR_Nem_3 681 687 PF02991 0.456
LIG_LIR_Nem_3 90 94 PF02991 0.716
LIG_Pex14_2 21 25 PF04695 0.598
LIG_Pex14_2 211 215 PF04695 0.496
LIG_Pex14_2 471 475 PF04695 0.586
LIG_PTB_Apo_2 205 212 PF02174 0.550
LIG_Rb_LxCxE_1 461 483 PF01857 0.639
LIG_SH2_CRK 518 522 PF00017 0.626
LIG_SH2_NCK_1 518 522 PF00017 0.626
LIG_SH2_NCK_1 670 674 PF00017 0.587
LIG_SH2_PTP2 337 340 PF00017 0.513
LIG_SH2_PTP2 91 94 PF00017 0.667
LIG_SH2_SRC 337 340 PF00017 0.513
LIG_SH2_SRC 668 671 PF00017 0.622
LIG_SH2_SRC 91 94 PF00017 0.714
LIG_SH2_STAP1 183 187 PF00017 0.442
LIG_SH2_STAP1 518 522 PF00017 0.588
LIG_SH2_STAP1 668 672 PF00017 0.622
LIG_SH2_STAT5 183 186 PF00017 0.586
LIG_SH2_STAT5 214 217 PF00017 0.453
LIG_SH2_STAT5 309 312 PF00017 0.499
LIG_SH2_STAT5 337 340 PF00017 0.479
LIG_SH2_STAT5 406 409 PF00017 0.495
LIG_SH2_STAT5 91 94 PF00017 0.724
LIG_SH3_1 633 639 PF00018 0.753
LIG_SH3_3 158 164 PF00018 0.720
LIG_SH3_3 184 190 PF00018 0.641
LIG_SH3_3 279 285 PF00018 0.544
LIG_SH3_3 3 9 PF00018 0.754
LIG_SH3_3 338 344 PF00018 0.655
LIG_SH3_3 570 576 PF00018 0.627
LIG_SH3_3 58 64 PF00018 0.793
LIG_SH3_3 633 639 PF00018 0.706
LIG_SUMO_SIM_anti_2 193 198 PF11976 0.420
LIG_SUMO_SIM_anti_2 35 40 PF11976 0.534
LIG_SUMO_SIM_anti_2 497 504 PF11976 0.611
LIG_SUMO_SIM_par_1 35 40 PF11976 0.534
LIG_SUMO_SIM_par_1 422 429 PF11976 0.576
LIG_TRAF2_1 480 483 PF00917 0.581
LIG_WW_2 6 9 PF00397 0.750
MOD_CDC14_SPxK_1 599 602 PF00782 0.664
MOD_CDK_SPK_2 317 322 PF00069 0.504
MOD_CDK_SPxK_1 596 602 PF00069 0.668
MOD_CDK_SPxxK_3 102 109 PF00069 0.592
MOD_CK1_1 127 133 PF00069 0.520
MOD_CK1_1 139 145 PF00069 0.475
MOD_CK1_1 156 162 PF00069 0.551
MOD_CK1_1 2 8 PF00069 0.645
MOD_CK1_1 293 299 PF00069 0.719
MOD_CK1_1 32 38 PF00069 0.567
MOD_CK1_1 328 334 PF00069 0.492
MOD_CK1_1 401 407 PF00069 0.521
MOD_CK1_1 643 649 PF00069 0.647
MOD_CK1_1 662 668 PF00069 0.584
MOD_CK1_1 81 87 PF00069 0.627
MOD_CK2_1 261 267 PF00069 0.772
MOD_CK2_1 414 420 PF00069 0.368
MOD_CK2_1 477 483 PF00069 0.563
MOD_CK2_1 500 506 PF00069 0.519
MOD_CK2_1 56 62 PF00069 0.784
MOD_Cter_Amidation 407 410 PF01082 0.571
MOD_DYRK1A_RPxSP_1 63 67 PF00069 0.696
MOD_GlcNHglycan 129 132 PF01048 0.608
MOD_GlcNHglycan 137 141 PF01048 0.561
MOD_GlcNHglycan 143 146 PF01048 0.690
MOD_GlcNHglycan 148 151 PF01048 0.680
MOD_GlcNHglycan 15 18 PF01048 0.483
MOD_GlcNHglycan 158 161 PF01048 0.562
MOD_GlcNHglycan 2 5 PF01048 0.815
MOD_GlcNHglycan 230 233 PF01048 0.676
MOD_GlcNHglycan 278 281 PF01048 0.733
MOD_GlcNHglycan 356 359 PF01048 0.507
MOD_GlcNHglycan 420 424 PF01048 0.486
MOD_GlcNHglycan 552 556 PF01048 0.581
MOD_GlcNHglycan 627 630 PF01048 0.573
MOD_GlcNHglycan 633 636 PF01048 0.709
MOD_GlcNHglycan 645 648 PF01048 0.752
MOD_GlcNHglycan 650 653 PF01048 0.669
MOD_GlcNHglycan 661 664 PF01048 0.579
MOD_GlcNHglycan 74 78 PF01048 0.764
MOD_GSK3_1 136 143 PF00069 0.676
MOD_GSK3_1 155 162 PF00069 0.692
MOD_GSK3_1 179 186 PF00069 0.686
MOD_GSK3_1 25 32 PF00069 0.472
MOD_GSK3_1 286 293 PF00069 0.749
MOD_GSK3_1 308 315 PF00069 0.554
MOD_GSK3_1 404 411 PF00069 0.407
MOD_GSK3_1 473 480 PF00069 0.603
MOD_GSK3_1 524 531 PF00069 0.704
MOD_GSK3_1 547 554 PF00069 0.784
MOD_GSK3_1 583 590 PF00069 0.702
MOD_GSK3_1 625 632 PF00069 0.582
MOD_GSK3_1 641 648 PF00069 0.645
MOD_GSK3_1 9 16 PF00069 0.720
MOD_N-GLC_1 276 281 PF02516 0.749
MOD_N-GLC_1 293 298 PF02516 0.786
MOD_N-GLC_2 383 385 PF02516 0.442
MOD_N-GLC_2 604 606 PF02516 0.709
MOD_NEK2_1 244 249 PF00069 0.836
MOD_NEK2_1 261 266 PF00069 0.550
MOD_NEK2_1 354 359 PF00069 0.482
MOD_NEK2_1 37 42 PF00069 0.596
MOD_NEK2_1 371 376 PF00069 0.453
MOD_NEK2_1 454 459 PF00069 0.629
MOD_NEK2_1 56 61 PF00069 0.543
MOD_NEK2_2 183 188 PF00069 0.437
MOD_PIKK_1 37 43 PF00454 0.523
MOD_PIKK_1 477 483 PF00454 0.652
MOD_PKA_1 262 268 PF00069 0.834
MOD_PKA_2 124 130 PF00069 0.539
MOD_PKA_2 19 25 PF00069 0.661
MOD_PKA_2 219 225 PF00069 0.576
MOD_PKA_2 261 267 PF00069 0.751
MOD_PKA_2 286 292 PF00069 0.730
MOD_PKA_2 408 414 PF00069 0.398
MOD_PKB_1 251 259 PF00069 0.755
MOD_Plk_1 419 425 PF00069 0.483
MOD_Plk_4 124 130 PF00069 0.539
MOD_Plk_4 219 225 PF00069 0.529
MOD_Plk_4 312 318 PF00069 0.481
MOD_Plk_4 32 38 PF00069 0.567
MOD_Plk_4 401 407 PF00069 0.504
MOD_Plk_4 81 87 PF00069 0.611
MOD_ProDKin_1 102 108 PF00069 0.598
MOD_ProDKin_1 159 165 PF00069 0.807
MOD_ProDKin_1 2 8 PF00069 0.703
MOD_ProDKin_1 237 243 PF00069 0.499
MOD_ProDKin_1 267 273 PF00069 0.565
MOD_ProDKin_1 317 323 PF00069 0.506
MOD_ProDKin_1 399 405 PF00069 0.521
MOD_ProDKin_1 537 543 PF00069 0.695
MOD_ProDKin_1 583 589 PF00069 0.782
MOD_ProDKin_1 596 602 PF00069 0.576
MOD_ProDKin_1 63 69 PF00069 0.704
MOD_SUMO_rev_2 26 35 PF00179 0.660
MOD_SUMO_rev_2 436 446 PF00179 0.445
MOD_SUMO_rev_2 448 454 PF00179 0.611
TRG_DiLeu_BaEn_1 491 496 PF01217 0.489
TRG_DiLeu_BaLyEn_6 187 192 PF01217 0.590
TRG_DiLeu_BaLyEn_6 573 578 PF01217 0.527
TRG_ENDOCYTIC_2 337 340 PF00928 0.513
TRG_ENDOCYTIC_2 518 521 PF00928 0.573
TRG_ENDOCYTIC_2 670 673 PF00928 0.581
TRG_ENDOCYTIC_2 91 94 PF00928 0.714
TRG_ER_diArg_1 261 263 PF00400 0.795
TRG_ER_diArg_1 409 412 PF00400 0.441
TRG_ER_diArg_1 484 487 PF00400 0.554
TRG_ER_diArg_1 523 526 PF00400 0.665
TRG_ER_diArg_1 571 574 PF00400 0.828
TRG_NLS_MonoExtN_4 460 467 PF00514 0.534
TRG_Pf-PMV_PEXEL_1 412 416 PF00026 0.517

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P2E4 Leptomonas seymouri 51% 100%
A0A3S5H6J4 Leishmania donovani 89% 100%
A4H6M7 Leishmania braziliensis 72% 100%
A4HV10 Leishmania infantum 88% 100%
Q4QGX8 Leishmania major 87% 99%

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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