LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein - conserved
Species:
Leishmania infantum
UniProt:
A4IBW2_LEIIN
TriTrypDb:
LINF_350048000
Length:
600

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.

Phosphorylation

Amastigote: 358, 364, 366

Expansion

Sequence features

A4IBW2
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4IBW2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 229 233 PF00656 0.668
CLV_NRD_NRD_1 273 275 PF00675 0.689
CLV_NRD_NRD_1 36 38 PF00675 0.728
CLV_NRD_NRD_1 579 581 PF00675 0.732
CLV_NRD_NRD_1 592 594 PF00675 0.558
CLV_PCSK_KEX2_1 216 218 PF00082 0.782
CLV_PCSK_KEX2_1 36 38 PF00082 0.728
CLV_PCSK_KEX2_1 587 589 PF00082 0.712
CLV_PCSK_KEX2_1 591 593 PF00082 0.692
CLV_PCSK_PC1ET2_1 216 218 PF00082 0.782
CLV_PCSK_PC1ET2_1 587 589 PF00082 0.642
CLV_PCSK_PC7_1 588 594 PF00082 0.696
CLV_PCSK_SKI1_1 216 220 PF00082 0.794
CLV_PCSK_SKI1_1 24 28 PF00082 0.649
CLV_PCSK_SKI1_1 388 392 PF00082 0.701
CLV_PCSK_SKI1_1 498 502 PF00082 0.605
DEG_SPOP_SBC_1 160 164 PF00917 0.616
DEG_SPOP_SBC_1 321 325 PF00917 0.651
DEG_SPOP_SBC_1 436 440 PF00917 0.687
DOC_CKS1_1 125 130 PF01111 0.647
DOC_CYCLIN_yCln2_LP_2 250 256 PF00134 0.741
DOC_CYCLIN_yCln2_LP_2 273 279 PF00134 0.669
DOC_MAPK_MEF2A_6 326 334 PF00069 0.583
DOC_MAPK_MEF2A_6 75 84 PF00069 0.663
DOC_PP2B_LxvP_1 250 253 PF13499 0.738
DOC_USP7_MATH_1 111 115 PF00917 0.810
DOC_USP7_MATH_1 118 122 PF00917 0.741
DOC_USP7_MATH_1 138 142 PF00917 0.541
DOC_USP7_MATH_1 206 210 PF00917 0.698
DOC_USP7_MATH_1 226 230 PF00917 0.782
DOC_USP7_MATH_1 231 235 PF00917 0.711
DOC_USP7_MATH_1 254 258 PF00917 0.758
DOC_USP7_MATH_1 321 325 PF00917 0.754
DOC_USP7_MATH_1 338 342 PF00917 0.505
DOC_USP7_MATH_1 349 353 PF00917 0.589
DOC_USP7_MATH_1 361 365 PF00917 0.836
DOC_USP7_MATH_1 374 378 PF00917 0.620
DOC_USP7_MATH_1 397 401 PF00917 0.739
DOC_USP7_MATH_1 436 440 PF00917 0.667
DOC_USP7_MATH_1 511 515 PF00917 0.643
DOC_USP7_MATH_1 551 555 PF00917 0.661
DOC_USP7_UBL2_3 30 34 PF12436 0.644
DOC_WW_Pin1_4 120 125 PF00397 0.738
DOC_WW_Pin1_4 278 283 PF00397 0.729
DOC_WW_Pin1_4 49 54 PF00397 0.743
DOC_WW_Pin1_4 92 97 PF00397 0.712
LIG_14-3-3_CanoR_1 161 169 PF00244 0.714
LIG_14-3-3_CanoR_1 220 228 PF00244 0.704
LIG_14-3-3_CanoR_1 267 276 PF00244 0.690
LIG_14-3-3_CanoR_1 363 370 PF00244 0.766
LIG_14-3-3_CanoR_1 382 387 PF00244 0.509
LIG_14-3-3_CanoR_1 512 522 PF00244 0.698
LIG_14-3-3_CanoR_1 523 528 PF00244 0.690
LIG_Actin_WH2_2 465 482 PF00022 0.614
LIG_BIR_II_1 1 5 PF00653 0.714
LIG_BRCT_BRCA1_1 569 573 PF00533 0.615
LIG_FHA_1 125 131 PF00498 0.701
LIG_FHA_1 135 141 PF00498 0.664
LIG_FHA_1 268 274 PF00498 0.594
LIG_FHA_1 425 431 PF00498 0.736
LIG_FHA_1 457 463 PF00498 0.633
LIG_FHA_1 481 487 PF00498 0.733
LIG_FHA_2 233 239 PF00498 0.757
LIG_FHA_2 593 599 PF00498 0.724
LIG_LIR_Apic_2 19 23 PF02991 0.605
LIG_LIR_Gen_1 439 449 PF02991 0.721
LIG_LIR_Gen_1 595 600 PF02991 0.730
LIG_LIR_Nem_3 403 409 PF02991 0.702
LIG_LIR_Nem_3 439 445 PF02991 0.716
LIG_LIR_Nem_3 448 452 PF02991 0.604
LIG_LIR_Nem_3 595 600 PF02991 0.730
LIG_MYND_1 124 128 PF01753 0.600
LIG_PDZ_Class_3 595 600 PF00595 0.730
LIG_SH2_CRK 442 446 PF00017 0.727
LIG_SH2_SRC 20 23 PF00017 0.662
LIG_SH2_SRC 404 407 PF00017 0.649
LIG_SH2_SRC 452 455 PF00017 0.625
LIG_SH2_STAP1 449 453 PF00017 0.637
LIG_SH2_STAT5 20 23 PF00017 0.662
LIG_SH3_2 211 216 PF14604 0.722
LIG_SH3_3 122 128 PF00018 0.665
LIG_SH3_3 208 214 PF00018 0.727
LIG_SH3_3 299 305 PF00018 0.694
LIG_SH3_3 315 321 PF00018 0.534
LIG_SH3_3 324 330 PF00018 0.597
LIG_SH3_3 350 356 PF00018 0.752
LIG_SH3_3 484 490 PF00018 0.789
LIG_SH3_3 502 508 PF00018 0.567
LIG_SH3_3 91 97 PF00018 0.707
LIG_SH3_3 98 104 PF00018 0.740
LIG_WW_3 152 156 PF00397 0.607
LIG_WW_3 509 513 PF00397 0.664
MOD_CDK_SPK_2 49 54 PF00069 0.749
MOD_CK1_1 129 135 PF00069 0.628
MOD_CK1_1 163 169 PF00069 0.737
MOD_CK1_1 194 200 PF00069 0.743
MOD_CK1_1 209 215 PF00069 0.585
MOD_CK1_1 224 230 PF00069 0.664
MOD_CK1_1 234 240 PF00069 0.690
MOD_CK1_1 257 263 PF00069 0.584
MOD_CK1_1 278 284 PF00069 0.726
MOD_CK1_1 291 297 PF00069 0.658
MOD_CK1_1 378 384 PF00069 0.684
MOD_CK1_1 435 441 PF00069 0.677
MOD_CK1_1 471 477 PF00069 0.698
MOD_CK1_1 516 522 PF00069 0.747
MOD_CK1_1 545 551 PF00069 0.666
MOD_CK1_1 92 98 PF00069 0.743
MOD_CK2_1 232 238 PF00069 0.759
MOD_CK2_1 239 245 PF00069 0.666
MOD_CK2_1 392 398 PF00069 0.667
MOD_CK2_1 551 557 PF00069 0.714
MOD_GlcNHglycan 109 112 PF01048 0.793
MOD_GlcNHglycan 120 123 PF01048 0.646
MOD_GlcNHglycan 140 143 PF01048 0.642
MOD_GlcNHglycan 157 160 PF01048 0.763
MOD_GlcNHglycan 163 166 PF01048 0.735
MOD_GlcNHglycan 189 192 PF01048 0.707
MOD_GlcNHglycan 229 232 PF01048 0.734
MOD_GlcNHglycan 24 27 PF01048 0.436
MOD_GlcNHglycan 250 253 PF01048 0.728
MOD_GlcNHglycan 277 280 PF01048 0.744
MOD_GlcNHglycan 299 302 PF01048 0.818
MOD_GlcNHglycan 400 403 PF01048 0.701
MOD_GlcNHglycan 434 437 PF01048 0.665
MOD_GlcNHglycan 473 476 PF01048 0.748
MOD_GlcNHglycan 49 52 PF01048 0.625
MOD_GlcNHglycan 492 495 PF01048 0.736
MOD_GlcNHglycan 501 504 PF01048 0.656
MOD_GlcNHglycan 515 518 PF01048 0.629
MOD_GlcNHglycan 547 550 PF01048 0.621
MOD_GlcNHglycan 8 11 PF01048 0.761
MOD_GSK3_1 107 114 PF00069 0.716
MOD_GSK3_1 116 123 PF00069 0.636
MOD_GSK3_1 129 136 PF00069 0.623
MOD_GSK3_1 155 162 PF00069 0.726
MOD_GSK3_1 181 188 PF00069 0.803
MOD_GSK3_1 220 227 PF00069 0.756
MOD_GSK3_1 234 241 PF00069 0.582
MOD_GSK3_1 293 300 PF00069 0.798
MOD_GSK3_1 355 362 PF00069 0.735
MOD_GSK3_1 372 379 PF00069 0.623
MOD_GSK3_1 382 389 PF00069 0.626
MOD_GSK3_1 420 427 PF00069 0.784
MOD_GSK3_1 428 435 PF00069 0.656
MOD_GSK3_1 436 443 PF00069 0.565
MOD_GSK3_1 45 52 PF00069 0.708
MOD_GSK3_1 467 474 PF00069 0.736
MOD_GSK3_1 521 528 PF00069 0.684
MOD_GSK3_1 538 545 PF00069 0.526
MOD_GSK3_1 85 92 PF00069 0.725
MOD_N-GLC_1 111 116 PF02516 0.692
MOD_N-GLC_1 338 343 PF02516 0.578
MOD_N-GLC_1 567 572 PF02516 0.589
MOD_NEK2_1 219 224 PF00069 0.749
MOD_NEK2_1 386 391 PF00069 0.596
MOD_NEK2_1 424 429 PF00069 0.753
MOD_NEK2_1 479 484 PF00069 0.610
MOD_NEK2_1 536 541 PF00069 0.698
MOD_NEK2_2 239 244 PF00069 0.695
MOD_NEK2_2 330 335 PF00069 0.685
MOD_PIKK_1 116 122 PF00454 0.697
MOD_PIKK_1 424 430 PF00454 0.752
MOD_PIKK_1 99 105 PF00454 0.652
MOD_PK_1 376 382 PF00069 0.688
MOD_PK_1 542 548 PF00069 0.586
MOD_PKA_1 44 50 PF00069 0.629
MOD_PKA_1 592 598 PF00069 0.720
MOD_PKA_2 144 150 PF00069 0.811
MOD_PKA_2 154 160 PF00069 0.668
MOD_PKA_2 219 225 PF00069 0.770
MOD_PKA_2 297 303 PF00069 0.744
MOD_PKA_2 344 350 PF00069 0.801
MOD_PKA_2 362 368 PF00069 0.765
MOD_PKA_2 372 378 PF00069 0.633
MOD_PKA_2 381 387 PF00069 0.538
MOD_PKA_2 445 451 PF00069 0.692
MOD_PKA_2 479 485 PF00069 0.782
MOD_PKA_2 511 517 PF00069 0.664
MOD_PKA_2 592 598 PF00069 0.663
MOD_Plk_1 239 245 PF00069 0.709
MOD_Plk_1 330 336 PF00069 0.581
MOD_Plk_1 440 446 PF00069 0.721
MOD_Plk_1 45 51 PF00069 0.658
MOD_Plk_4 440 446 PF00069 0.661
MOD_ProDKin_1 120 126 PF00069 0.738
MOD_ProDKin_1 278 284 PF00069 0.727
MOD_ProDKin_1 49 55 PF00069 0.740
MOD_ProDKin_1 92 98 PF00069 0.716
MOD_SUMO_for_1 393 396 PF00179 0.724
MOD_SUMO_for_1 559 562 PF00179 0.777
TRG_DiLeu_BaLyEn_6 458 463 PF01217 0.586
TRG_ENDOCYTIC_2 406 409 PF00928 0.699
TRG_ENDOCYTIC_2 442 445 PF00928 0.723
TRG_ER_diArg_1 35 37 PF00400 0.732
TRG_ER_diArg_1 370 373 PF00400 0.608
TRG_ER_diArg_1 591 593 PF00400 0.716

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IJF9 Leishmania donovani 99% 100%
A4HN92 Leishmania braziliensis 54% 100%
E9AFP9 Leishmania major 85% 100%
E9B6V2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 77% 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