LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein - conserved
Species:
Leishmania infantum
UniProt:
A4HY81_LEIIN
TriTrypDb:
LINF_190010900
Length:
777

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

A4HY81
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HY81

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 197 201 PF00656 0.565
CLV_C14_Caspase3-7 685 689 PF00656 0.535
CLV_NRD_NRD_1 282 284 PF00675 0.660
CLV_NRD_NRD_1 399 401 PF00675 0.686
CLV_NRD_NRD_1 456 458 PF00675 0.452
CLV_NRD_NRD_1 488 490 PF00675 0.514
CLV_NRD_NRD_1 69 71 PF00675 0.649
CLV_PCSK_FUR_1 472 476 PF00082 0.476
CLV_PCSK_KEX2_1 282 284 PF00082 0.621
CLV_PCSK_KEX2_1 474 476 PF00082 0.526
CLV_PCSK_KEX2_1 488 490 PF00082 0.514
CLV_PCSK_PC1ET2_1 474 476 PF00082 0.526
CLV_PCSK_SKI1_1 481 485 PF00082 0.446
CLV_PCSK_SKI1_1 498 502 PF00082 0.496
CLV_PCSK_SKI1_1 535 539 PF00082 0.613
DEG_SPOP_SBC_1 212 216 PF00917 0.621
DEG_SPOP_SBC_1 37 41 PF00917 0.637
DOC_ANK_TNKS_1 335 342 PF00023 0.616
DOC_CKS1_1 204 209 PF01111 0.621
DOC_CKS1_1 743 748 PF01111 0.656
DOC_MAPK_MEF2A_6 619 627 PF00069 0.524
DOC_PP1_RVXF_1 708 715 PF00149 0.585
DOC_PP2B_LxvP_1 108 111 PF13499 0.566
DOC_PP2B_LxvP_1 83 86 PF13499 0.587
DOC_PP2B_PxIxI_1 206 212 PF00149 0.599
DOC_USP7_MATH_1 100 104 PF00917 0.628
DOC_USP7_MATH_1 129 133 PF00917 0.641
DOC_USP7_MATH_1 162 166 PF00917 0.662
DOC_USP7_MATH_1 168 172 PF00917 0.617
DOC_USP7_MATH_1 183 187 PF00917 0.543
DOC_USP7_MATH_1 189 193 PF00917 0.578
DOC_USP7_MATH_1 199 203 PF00917 0.528
DOC_USP7_MATH_1 212 216 PF00917 0.580
DOC_USP7_MATH_1 250 254 PF00917 0.653
DOC_USP7_MATH_1 266 270 PF00917 0.516
DOC_USP7_MATH_1 292 296 PF00917 0.609
DOC_USP7_MATH_1 37 41 PF00917 0.660
DOC_USP7_MATH_1 386 390 PF00917 0.712
DOC_USP7_MATH_1 50 54 PF00917 0.576
DOC_USP7_MATH_1 526 530 PF00917 0.594
DOC_USP7_MATH_1 548 552 PF00917 0.534
DOC_USP7_MATH_1 574 578 PF00917 0.558
DOC_USP7_MATH_1 635 639 PF00917 0.589
DOC_USP7_MATH_1 683 687 PF00917 0.559
DOC_WW_Pin1_4 103 108 PF00397 0.678
DOC_WW_Pin1_4 146 151 PF00397 0.636
DOC_WW_Pin1_4 164 169 PF00397 0.547
DOC_WW_Pin1_4 175 180 PF00397 0.609
DOC_WW_Pin1_4 191 196 PF00397 0.590
DOC_WW_Pin1_4 203 208 PF00397 0.539
DOC_WW_Pin1_4 360 365 PF00397 0.658
DOC_WW_Pin1_4 408 413 PF00397 0.623
DOC_WW_Pin1_4 596 601 PF00397 0.578
DOC_WW_Pin1_4 742 747 PF00397 0.732
DOC_WW_Pin1_4 78 83 PF00397 0.695
LIG_14-3-3_CanoR_1 131 138 PF00244 0.687
LIG_14-3-3_CanoR_1 265 271 PF00244 0.657
LIG_14-3-3_CanoR_1 282 291 PF00244 0.510
LIG_14-3-3_CanoR_1 429 437 PF00244 0.658
LIG_14-3-3_CanoR_1 640 649 PF00244 0.612
LIG_14-3-3_CanoR_1 70 74 PF00244 0.685
LIG_Actin_WH2_2 332 348 PF00022 0.597
LIG_Actin_WH2_2 597 613 PF00022 0.498
LIG_BIR_III_2 20 24 PF00653 0.646
LIG_eIF4E_1 649 655 PF01652 0.498
LIG_EVH1_1 757 761 PF00568 0.603
LIG_EVH1_2 109 113 PF00568 0.639
LIG_FHA_1 186 192 PF00498 0.644
LIG_FHA_1 204 210 PF00498 0.497
LIG_FHA_1 351 357 PF00498 0.631
LIG_FHA_1 388 394 PF00498 0.691
LIG_FHA_2 673 679 PF00498 0.575
LIG_LIR_Apic_2 232 236 PF02991 0.638
LIG_LIR_Apic_2 631 637 PF02991 0.588
LIG_LIR_Nem_3 446 452 PF02991 0.554
LIG_LIR_Nem_3 454 459 PF02991 0.417
LIG_LIR_Nem_3 706 712 PF02991 0.637
LIG_SH2_CRK 233 237 PF00017 0.643
LIG_SH2_CRK 449 453 PF00017 0.506
LIG_SH2_CRK 709 713 PF00017 0.637
LIG_SH2_STAT3 138 141 PF00017 0.705
LIG_SH2_STAT5 114 117 PF00017 0.579
LIG_SH2_STAT5 451 454 PF00017 0.630
LIG_SH2_STAT5 663 666 PF00017 0.590
LIG_SH3_3 104 110 PF00018 0.675
LIG_SH3_3 201 207 PF00018 0.663
LIG_SH3_3 301 307 PF00018 0.601
LIG_SH3_3 358 364 PF00018 0.652
LIG_SH3_3 434 440 PF00018 0.646
LIG_SH3_3 573 579 PF00018 0.655
LIG_SH3_3 583 589 PF00018 0.541
LIG_SH3_3 620 626 PF00018 0.619
LIG_SH3_3 713 719 PF00018 0.630
LIG_SH3_3 752 758 PF00018 0.703
LIG_SH3_3 764 770 PF00018 0.603
LIG_SUMO_SIM_par_1 599 606 PF11976 0.517
LIG_TRAF2_1 494 497 PF00917 0.463
LIG_WW_2 755 758 PF00397 0.596
MOD_CDC14_SPxK_1 149 152 PF00782 0.582
MOD_CDK_SPxK_1 146 152 PF00069 0.584
MOD_CDK_SPxxK_3 191 198 PF00069 0.647
MOD_CK1_1 103 109 PF00069 0.681
MOD_CK1_1 132 138 PF00069 0.662
MOD_CK1_1 166 172 PF00069 0.670
MOD_CK1_1 194 200 PF00069 0.674
MOD_CK1_1 216 222 PF00069 0.563
MOD_CK1_1 258 264 PF00069 0.658
MOD_CK1_1 40 46 PF00069 0.672
MOD_CK1_1 430 436 PF00069 0.609
MOD_CK1_1 53 59 PF00069 0.586
MOD_CK1_1 686 692 PF00069 0.651
MOD_CK1_1 727 733 PF00069 0.687
MOD_CK2_1 490 496 PF00069 0.415
MOD_CK2_1 600 606 PF00069 0.512
MOD_GlcNHglycan 127 130 PF01048 0.686
MOD_GlcNHglycan 170 173 PF01048 0.640
MOD_GlcNHglycan 185 188 PF01048 0.550
MOD_GlcNHglycan 200 204 PF01048 0.528
MOD_GlcNHglycan 223 226 PF01048 0.648
MOD_GlcNHglycan 266 269 PF01048 0.596
MOD_GlcNHglycan 270 273 PF01048 0.608
MOD_GlcNHglycan 358 361 PF01048 0.640
MOD_GlcNHglycan 384 387 PF01048 0.718
MOD_GlcNHglycan 40 43 PF01048 0.578
MOD_GlcNHglycan 405 408 PF01048 0.657
MOD_GlcNHglycan 432 435 PF01048 0.581
MOD_GlcNHglycan 459 462 PF01048 0.380
MOD_GlcNHglycan 492 495 PF01048 0.461
MOD_GlcNHglycan 528 531 PF01048 0.615
MOD_GlcNHglycan 550 553 PF01048 0.640
MOD_GlcNHglycan 56 59 PF01048 0.615
MOD_GlcNHglycan 596 599 PF01048 0.653
MOD_GlcNHglycan 63 66 PF01048 0.664
MOD_GlcNHglycan 726 729 PF01048 0.617
MOD_GlcNHglycan 89 92 PF01048 0.661
MOD_GSK3_1 121 128 PF00069 0.683
MOD_GSK3_1 129 136 PF00069 0.619
MOD_GSK3_1 162 169 PF00069 0.675
MOD_GSK3_1 181 188 PF00069 0.520
MOD_GSK3_1 190 197 PF00069 0.591
MOD_GSK3_1 199 206 PF00069 0.517
MOD_GSK3_1 212 219 PF00069 0.526
MOD_GSK3_1 250 257 PF00069 0.649
MOD_GSK3_1 264 271 PF00069 0.540
MOD_GSK3_1 274 281 PF00069 0.555
MOD_GSK3_1 292 299 PF00069 0.521
MOD_GSK3_1 341 348 PF00069 0.641
MOD_GSK3_1 356 363 PF00069 0.552
MOD_GSK3_1 36 43 PF00069 0.665
MOD_GSK3_1 382 389 PF00069 0.709
MOD_GSK3_1 50 57 PF00069 0.570
MOD_GSK3_1 574 581 PF00069 0.633
MOD_GSK3_1 590 597 PF00069 0.595
MOD_GSK3_1 668 675 PF00069 0.518
MOD_GSK3_1 682 689 PF00069 0.525
MOD_GSK3_1 69 76 PF00069 0.558
MOD_GSK3_1 737 744 PF00069 0.665
MOD_LATS_1 196 202 PF00433 0.679
MOD_N-GLC_1 255 260 PF02516 0.635
MOD_N-GLC_1 278 283 PF02516 0.573
MOD_NEK2_1 125 130 PF00069 0.700
MOD_NEK2_1 244 249 PF00069 0.577
MOD_NEK2_1 270 275 PF00069 0.622
MOD_NEK2_1 287 292 PF00069 0.509
MOD_NEK2_1 324 329 PF00069 0.628
MOD_NEK2_1 345 350 PF00069 0.614
MOD_NEK2_1 590 595 PF00069 0.559
MOD_NEK2_2 341 346 PF00069 0.613
MOD_PIKK_1 375 381 PF00454 0.655
MOD_PIKK_1 683 689 PF00454 0.604
MOD_PIKK_1 73 79 PF00454 0.708
MOD_PIKK_1 749 755 PF00454 0.660
MOD_PIKK_1 8 14 PF00454 0.661
MOD_PKA_1 282 288 PF00069 0.608
MOD_PKA_1 457 463 PF00069 0.456
MOD_PKA_2 130 136 PF00069 0.686
MOD_PKA_2 264 270 PF00069 0.555
MOD_PKA_2 281 287 PF00069 0.554
MOD_PKA_2 387 393 PF00069 0.634
MOD_PKA_2 641 647 PF00069 0.617
MOD_PKA_2 69 75 PF00069 0.703
MOD_PKB_1 640 648 PF00069 0.548
MOD_Plk_1 199 205 PF00069 0.626
MOD_Plk_1 255 261 PF00069 0.628
MOD_Plk_1 630 636 PF00069 0.680
MOD_Plk_2-3 422 428 PF00069 0.637
MOD_Plk_2-3 630 636 PF00069 0.636
MOD_Plk_4 270 276 PF00069 0.661
MOD_Plk_4 351 357 PF00069 0.629
MOD_Plk_4 669 675 PF00069 0.517
MOD_ProDKin_1 103 109 PF00069 0.676
MOD_ProDKin_1 146 152 PF00069 0.638
MOD_ProDKin_1 164 170 PF00069 0.547
MOD_ProDKin_1 175 181 PF00069 0.607
MOD_ProDKin_1 191 197 PF00069 0.589
MOD_ProDKin_1 203 209 PF00069 0.540
MOD_ProDKin_1 360 366 PF00069 0.660
MOD_ProDKin_1 408 414 PF00069 0.622
MOD_ProDKin_1 596 602 PF00069 0.569
MOD_ProDKin_1 742 748 PF00069 0.733
MOD_ProDKin_1 78 84 PF00069 0.693
MOD_SUMO_for_1 473 476 PF00179 0.620
TRG_DiLeu_BaEn_1 497 502 PF01217 0.525
TRG_DiLeu_BaEn_1 650 655 PF01217 0.471
TRG_DiLeu_BaLyEn_6 597 602 PF01217 0.564
TRG_ENDOCYTIC_2 239 242 PF00928 0.640
TRG_ENDOCYTIC_2 449 452 PF00928 0.618
TRG_ENDOCYTIC_2 453 456 PF00928 0.582
TRG_ENDOCYTIC_2 709 712 PF00928 0.636
TRG_ER_diArg_1 3 6 PF00400 0.677
TRG_ER_diArg_1 487 489 PF00400 0.514
TRG_Pf-PMV_PEXEL_1 450 454 PF00026 0.500

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IEG9 Leishmania donovani 99% 100%
A4HA18 Leishmania braziliensis 55% 96%
E9AS12 Leishmania mexicana (strain MHOM/GT/2001/U1103) 78% 95%
Q4QDG1 Leishmania major 84% 98%

Download

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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