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:
A4I344_LEIIN
TriTrypDb:
LINF_270032500
Length:
570

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

A4I344
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4I344

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 114 118 PF00656 0.581
CLV_NRD_NRD_1 147 149 PF00675 0.626
CLV_NRD_NRD_1 186 188 PF00675 0.733
CLV_NRD_NRD_1 206 208 PF00675 0.411
CLV_NRD_NRD_1 404 406 PF00675 0.778
CLV_NRD_NRD_1 555 557 PF00675 0.836
CLV_NRD_NRD_1 60 62 PF00675 0.685
CLV_PCSK_KEX2_1 146 148 PF00082 0.617
CLV_PCSK_KEX2_1 186 188 PF00082 0.733
CLV_PCSK_KEX2_1 206 208 PF00082 0.411
CLV_PCSK_KEX2_1 336 338 PF00082 0.789
CLV_PCSK_KEX2_1 380 382 PF00082 0.735
CLV_PCSK_KEX2_1 555 557 PF00082 0.836
CLV_PCSK_KEX2_1 60 62 PF00082 0.685
CLV_PCSK_PC1ET2_1 336 338 PF00082 0.789
CLV_PCSK_PC1ET2_1 380 382 PF00082 0.735
CLV_PCSK_SKI1_1 129 133 PF00082 0.599
CLV_PCSK_SKI1_1 248 252 PF00082 0.559
CLV_PCSK_SKI1_1 356 360 PF00082 0.767
CLV_PCSK_SKI1_1 95 99 PF00082 0.688
DEG_SIAH_1 319 327 PF03145 0.744
DEG_SPOP_SBC_1 109 113 PF00917 0.639
DEG_SPOP_SBC_1 130 134 PF00917 0.592
DEG_SPOP_SBC_1 416 420 PF00917 0.672
DEG_SPOP_SBC_1 560 564 PF00917 0.843
DOC_CKS1_1 192 197 PF01111 0.578
DOC_CKS1_1 463 468 PF01111 0.755
DOC_CYCLIN_yClb3_PxF_3 507 513 PF00134 0.681
DOC_PP2B_LxvP_1 250 253 PF13499 0.730
DOC_PP2B_LxvP_1 506 509 PF13499 0.696
DOC_USP7_MATH_1 109 113 PF00917 0.751
DOC_USP7_MATH_1 257 261 PF00917 0.766
DOC_USP7_MATH_1 281 285 PF00917 0.768
DOC_USP7_MATH_1 291 295 PF00917 0.686
DOC_USP7_MATH_1 313 317 PF00917 0.734
DOC_USP7_MATH_1 318 322 PF00917 0.735
DOC_USP7_MATH_1 327 331 PF00917 0.594
DOC_USP7_MATH_1 386 390 PF00917 0.787
DOC_USP7_MATH_1 426 430 PF00917 0.842
DOC_USP7_MATH_1 497 501 PF00917 0.820
DOC_USP7_MATH_1 72 76 PF00917 0.638
DOC_WW_Pin1_4 123 128 PF00397 0.728
DOC_WW_Pin1_4 178 183 PF00397 0.726
DOC_WW_Pin1_4 191 196 PF00397 0.456
DOC_WW_Pin1_4 219 224 PF00397 0.778
DOC_WW_Pin1_4 316 321 PF00397 0.810
DOC_WW_Pin1_4 322 327 PF00397 0.720
DOC_WW_Pin1_4 328 333 PF00397 0.612
DOC_WW_Pin1_4 382 387 PF00397 0.772
DOC_WW_Pin1_4 408 413 PF00397 0.815
DOC_WW_Pin1_4 418 423 PF00397 0.662
DOC_WW_Pin1_4 439 444 PF00397 0.818
DOC_WW_Pin1_4 448 453 PF00397 0.693
DOC_WW_Pin1_4 456 461 PF00397 0.578
DOC_WW_Pin1_4 462 467 PF00397 0.620
DOC_WW_Pin1_4 484 489 PF00397 0.699
DOC_WW_Pin1_4 539 544 PF00397 0.723
LIG_14-3-3_CanoR_1 25 29 PF00244 0.607
LIG_14-3-3_CanoR_1 280 286 PF00244 0.701
LIG_14-3-3_CanoR_1 344 350 PF00244 0.820
LIG_14-3-3_CanoR_1 367 372 PF00244 0.691
LIG_14-3-3_CanoR_1 54 62 PF00244 0.675
LIG_14-3-3_CanoR_1 68 76 PF00244 0.527
LIG_BIR_II_1 1 5 PF00653 0.582
LIG_EVH1_1 506 510 PF00568 0.695
LIG_EVH1_2 509 513 PF00568 0.762
LIG_FHA_1 130 136 PF00498 0.587
LIG_FHA_1 267 273 PF00498 0.744
LIG_FHA_1 457 463 PF00498 0.630
LIG_FHA_1 47 53 PF00498 0.663
LIG_FHA_1 96 102 PF00498 0.668
LIG_FHA_2 137 143 PF00498 0.663
LIG_FHA_2 32 38 PF00498 0.667
LIG_FHA_2 385 391 PF00498 0.750
LIG_FHA_2 561 567 PF00498 0.834
LIG_LIR_Gen_1 151 160 PF02991 0.608
LIG_LIR_Gen_1 19 28 PF02991 0.662
LIG_LIR_Nem_3 19 24 PF02991 0.653
LIG_PROFILIN_1 466 472 PF00235 0.740
LIG_PROFILIN_1 490 496 PF00235 0.688
LIG_SH2_CRK 481 485 PF00017 0.742
LIG_SH2_NCK_1 481 485 PF00017 0.742
LIG_SH2_SRC 481 484 PF00017 0.646
LIG_SH2_SRC 8 11 PF00017 0.558
LIG_SH2_STAP1 199 203 PF00017 0.682
LIG_SH2_STAT5 152 155 PF00017 0.683
LIG_SH2_STAT5 8 11 PF00017 0.558
LIG_SH3_1 449 455 PF00018 0.656
LIG_SH3_2 551 556 PF14604 0.820
LIG_SH3_3 162 168 PF00018 0.731
LIG_SH3_3 246 252 PF00018 0.710
LIG_SH3_3 258 264 PF00018 0.539
LIG_SH3_3 269 275 PF00018 0.638
LIG_SH3_3 282 288 PF00018 0.579
LIG_SH3_3 407 413 PF00018 0.729
LIG_SH3_3 449 455 PF00018 0.720
LIG_SH3_3 457 463 PF00018 0.662
LIG_SH3_3 464 470 PF00018 0.669
LIG_SH3_3 482 488 PF00018 0.547
LIG_SH3_3 489 495 PF00018 0.670
LIG_SH3_3 502 508 PF00018 0.551
LIG_SH3_3 532 538 PF00018 0.645
LIG_SH3_3 548 554 PF00018 0.634
LIG_TRAF2_1 112 115 PF00917 0.706
LIG_WW_3 421 425 PF00397 0.803
LIG_WW_3 552 556 PF00397 0.701
MOD_CDC14_SPxK_1 126 129 PF00782 0.679
MOD_CDC14_SPxK_1 421 424 PF00782 0.764
MOD_CDK_SPxK_1 123 129 PF00069 0.673
MOD_CDK_SPxK_1 418 424 PF00069 0.804
MOD_CDK_SPxxK_3 322 329 PF00069 0.747
MOD_CDK_SPxxK_3 539 546 PF00069 0.618
MOD_CK1_1 121 127 PF00069 0.805
MOD_CK1_1 134 140 PF00069 0.559
MOD_CK1_1 3 9 PF00069 0.607
MOD_CK1_1 307 313 PF00069 0.815
MOD_CK1_1 316 322 PF00069 0.666
MOD_CK1_1 361 367 PF00069 0.814
MOD_CK1_1 370 376 PF00069 0.659
MOD_CK1_1 385 391 PF00069 0.588
MOD_CK1_1 394 400 PF00069 0.674
MOD_CK1_1 427 433 PF00069 0.732
MOD_CK1_1 437 443 PF00069 0.675
MOD_CK1_1 454 460 PF00069 0.550
MOD_CK1_1 55 61 PF00069 0.675
MOD_CK1_1 562 568 PF00069 0.831
MOD_CK2_1 108 114 PF00069 0.754
MOD_CK2_1 136 142 PF00069 0.675
MOD_CK2_1 156 162 PF00069 0.602
MOD_CK2_1 31 37 PF00069 0.539
MOD_GlcNHglycan 243 246 PF01048 0.749
MOD_GlcNHglycan 253 256 PF01048 0.630
MOD_GlcNHglycan 293 296 PF01048 0.635
MOD_GlcNHglycan 311 314 PF01048 0.707
MOD_GlcNHglycan 315 318 PF01048 0.742
MOD_GlcNHglycan 320 323 PF01048 0.670
MOD_GlcNHglycan 347 350 PF01048 0.818
MOD_GlcNHglycan 372 375 PF01048 0.813
MOD_GlcNHglycan 426 429 PF01048 0.804
MOD_GlcNHglycan 436 439 PF01048 0.708
MOD_GlcNHglycan 474 477 PF01048 0.758
MOD_GlcNHglycan 499 502 PF01048 0.748
MOD_GlcNHglycan 518 521 PF01048 0.503
MOD_GlcNHglycan 539 542 PF01048 0.727
MOD_GlcNHglycan 54 57 PF01048 0.455
MOD_GSK3_1 117 124 PF00069 0.739
MOD_GSK3_1 129 136 PF00069 0.606
MOD_GSK3_1 237 244 PF00069 0.722
MOD_GSK3_1 287 294 PF00069 0.624
MOD_GSK3_1 304 311 PF00069 0.713
MOD_GSK3_1 312 319 PF00069 0.680
MOD_GSK3_1 328 335 PF00069 0.560
MOD_GSK3_1 358 365 PF00069 0.815
MOD_GSK3_1 382 389 PF00069 0.737
MOD_GSK3_1 390 397 PF00069 0.701
MOD_GSK3_1 426 433 PF00069 0.794
MOD_GSK3_1 447 454 PF00069 0.639
MOD_GSK3_1 533 540 PF00069 0.749
MOD_GSK3_1 63 70 PF00069 0.545
MOD_NEK2_1 131 136 PF00069 0.721
MOD_NEK2_1 24 29 PF00069 0.570
MOD_NEK2_1 243 248 PF00069 0.569
MOD_NEK2_1 305 310 PF00069 0.813
MOD_NEK2_1 358 363 PF00069 0.818
MOD_NEK2_1 415 420 PF00069 0.783
MOD_NEK2_1 514 519 PF00069 0.808
MOD_PIKK_1 430 436 PF00454 0.718
MOD_PIKK_1 63 69 PF00454 0.670
MOD_PIKK_1 84 90 PF00454 0.654
MOD_PK_1 367 373 PF00069 0.692
MOD_PKA_2 24 30 PF00069 0.604
MOD_PKA_2 67 73 PF00069 0.663
MOD_Plk_1 3 9 PF00069 0.601
MOD_Plk_4 281 287 PF00069 0.696
MOD_Plk_4 3 9 PF00069 0.562
MOD_Plk_4 442 448 PF00069 0.614
MOD_ProDKin_1 123 129 PF00069 0.732
MOD_ProDKin_1 178 184 PF00069 0.726
MOD_ProDKin_1 191 197 PF00069 0.447
MOD_ProDKin_1 219 225 PF00069 0.777
MOD_ProDKin_1 316 322 PF00069 0.811
MOD_ProDKin_1 328 334 PF00069 0.612
MOD_ProDKin_1 382 388 PF00069 0.775
MOD_ProDKin_1 408 414 PF00069 0.818
MOD_ProDKin_1 418 424 PF00069 0.665
MOD_ProDKin_1 439 445 PF00069 0.819
MOD_ProDKin_1 448 454 PF00069 0.693
MOD_ProDKin_1 456 462 PF00069 0.576
MOD_ProDKin_1 484 490 PF00069 0.696
MOD_ProDKin_1 539 545 PF00069 0.728
MOD_SUMO_for_1 297 300 PF00179 0.728
TRG_DiLeu_BaEn_4 12 18 PF01217 0.684
TRG_ENDOCYTIC_2 152 155 PF00928 0.605
TRG_ER_diArg_1 145 148 PF00400 0.618
TRG_ER_diArg_1 186 188 PF00400 0.733
TRG_ER_diArg_1 554 556 PF00400 0.823
TRG_ER_diArg_1 60 62 PF00400 0.685

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3S7X110 Leishmania donovani 99% 100%
A4HG23 Leishmania braziliensis 69% 100%
E9ACW3 Leishmania major 90% 100%
E9AZF2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 87% 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