LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania major
UniProt:
Q4Q064_LEIMA
TriTrypDb:
LmjF.36.6900 , LMJLV39_360084400 * , LMJSD75_360084200
Length:
707

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
Cellular components
Term Name Level Count
GO:0000164 protein phosphatase type 1 complex 5 2
GO:0005929 cilium 4 7
GO:0008287 protein serine/threonine phosphatase complex 4 2
GO:0032991 protein-containing complex 1 2
GO:0042995 cell projection 2 7
GO:0043226 organelle 2 7
GO:0043227 membrane-bounded organelle 3 7
GO:0110165 cellular anatomical entity 1 7
GO:0120025 plasma membrane bounded cell projection 3 7
GO:1902494 catalytic complex 2 2
GO:1903293 phosphatase complex 3 2

Expansion

Sequence features

Q4Q064
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q064

Function

Biological processes
Term Name Level Count
GO:0009893 positive regulation of metabolic process 4 2
GO:0010562 positive regulation of phosphorus metabolic process 6 2
GO:0010604 positive regulation of macromolecule metabolic process 5 2
GO:0019220 regulation of phosphate metabolic process 6 2
GO:0019222 regulation of metabolic process 3 2
GO:0031323 regulation of cellular metabolic process 4 2
GO:0031325 positive regulation of cellular metabolic process 5 2
GO:0031399 regulation of protein modification process 6 2
GO:0031401 positive regulation of protein modification process 7 2
GO:0035303 regulation of dephosphorylation 7 2
GO:0035304 regulation of protein dephosphorylation 7 2
GO:0035306 positive regulation of dephosphorylation 8 2
GO:0035307 positive regulation of protein dephosphorylation 8 2
GO:0045937 positive regulation of phosphate metabolic process 7 2
GO:0048518 positive regulation of biological process 3 2
GO:0048522 positive regulation of cellular process 4 2
GO:0050789 regulation of biological process 2 2
GO:0050794 regulation of cellular process 3 2
GO:0051171 regulation of nitrogen compound metabolic process 4 2
GO:0051173 positive regulation of nitrogen compound metabolic process 5 2
GO:0051174 regulation of phosphorus metabolic process 5 2
GO:0051246 regulation of protein metabolic process 5 2
GO:0051247 positive regulation of protein metabolic process 6 2
GO:0060255 regulation of macromolecule metabolic process 4 2
GO:0065007 biological regulation 1 2
GO:0080090 regulation of primary metabolic process 4 2
Molecular functions
Term Name Level Count
GO:0004857 enzyme inhibitor activity 3 2
GO:0004864 protein phosphatase inhibitor activity 5 2
GO:0004865 protein serine/threonine phosphatase inhibitor activity 6 2
GO:0019208 phosphatase regulator activity 3 2
GO:0019212 phosphatase inhibitor activity 4 2
GO:0019888 protein phosphatase regulator activity 4 2
GO:0030234 enzyme regulator activity 2 2
GO:0098772 molecular function regulator activity 1 2
GO:0140678 molecular function inhibitor activity 2 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 100 104 PF00656 0.410
CLV_C14_Caspase3-7 241 245 PF00656 0.478
CLV_C14_Caspase3-7 435 439 PF00656 0.606
CLV_C14_Caspase3-7 681 685 PF00656 0.633
CLV_C14_Caspase3-7 701 705 PF00656 0.515
CLV_NRD_NRD_1 150 152 PF00675 0.509
CLV_NRD_NRD_1 153 155 PF00675 0.565
CLV_NRD_NRD_1 204 206 PF00675 0.419
CLV_NRD_NRD_1 21 23 PF00675 0.482
CLV_NRD_NRD_1 372 374 PF00675 0.599
CLV_NRD_NRD_1 468 470 PF00675 0.631
CLV_NRD_NRD_1 595 597 PF00675 0.662
CLV_NRD_NRD_1 652 654 PF00675 0.600
CLV_PCSK_FUR_1 151 155 PF00082 0.432
CLV_PCSK_KEX2_1 120 122 PF00082 0.385
CLV_PCSK_KEX2_1 150 152 PF00082 0.519
CLV_PCSK_KEX2_1 153 155 PF00082 0.579
CLV_PCSK_KEX2_1 158 160 PF00082 0.413
CLV_PCSK_KEX2_1 204 206 PF00082 0.419
CLV_PCSK_KEX2_1 371 373 PF00082 0.601
CLV_PCSK_KEX2_1 652 654 PF00082 0.600
CLV_PCSK_PC1ET2_1 120 122 PF00082 0.385
CLV_PCSK_PC1ET2_1 158 160 PF00082 0.468
CLV_PCSK_PC7_1 154 160 PF00082 0.417
CLV_PCSK_SKI1_1 121 125 PF00082 0.344
CLV_PCSK_SKI1_1 169 173 PF00082 0.538
CLV_PCSK_SKI1_1 197 201 PF00082 0.413
CLV_PCSK_SKI1_1 314 318 PF00082 0.488
CLV_PCSK_SKI1_1 343 347 PF00082 0.385
CLV_PCSK_SKI1_1 376 380 PF00082 0.565
CLV_PCSK_SKI1_1 63 67 PF00082 0.360
CLV_PCSK_SKI1_1 695 699 PF00082 0.576
DEG_APCC_DBOX_1 296 304 PF00400 0.388
DEG_Nend_UBRbox_2 1 3 PF02207 0.422
DEG_SCF_FBW7_1 378 383 PF00400 0.520
DEG_SCF_FBW7_1 415 422 PF00400 0.603
DEG_SPOP_SBC_1 214 218 PF00917 0.436
DEG_SPOP_SBC_1 414 418 PF00917 0.644
DOC_CDC14_PxL_1 332 340 PF14671 0.363
DOC_CDC14_PxL_1 567 575 PF14671 0.595
DOC_CKS1_1 635 640 PF01111 0.542
DOC_CYCLIN_RxL_1 309 322 PF00134 0.392
DOC_CYCLIN_RxL_1 340 349 PF00134 0.328
DOC_CYCLIN_RxL_1 692 702 PF00134 0.615
DOC_CYCLIN_yCln2_LP_2 224 227 PF00134 0.632
DOC_MAPK_DCC_7 309 318 PF00069 0.382
DOC_MAPK_DCC_7 584 593 PF00069 0.557
DOC_MAPK_gen_1 120 126 PF00069 0.352
DOC_MAPK_gen_1 201 209 PF00069 0.355
DOC_MAPK_gen_1 22 30 PF00069 0.445
DOC_MAPK_gen_1 297 305 PF00069 0.550
DOC_MAPK_gen_1 309 318 PF00069 0.351
DOC_MAPK_gen_1 584 593 PF00069 0.574
DOC_MAPK_gen_1 652 663 PF00069 0.607
DOC_MAPK_MEF2A_6 23 32 PF00069 0.434
DOC_MAPK_MEF2A_6 297 305 PF00069 0.580
DOC_MAPK_MEF2A_6 351 358 PF00069 0.480
DOC_MAPK_MEF2A_6 88 97 PF00069 0.327
DOC_PP2B_LxvP_1 224 227 PF13499 0.632
DOC_PP2B_LxvP_1 591 594 PF13499 0.639
DOC_USP7_MATH_1 106 110 PF00917 0.373
DOC_USP7_MATH_1 136 140 PF00917 0.433
DOC_USP7_MATH_1 214 218 PF00917 0.499
DOC_USP7_MATH_1 384 388 PF00917 0.689
DOC_USP7_MATH_1 395 399 PF00917 0.538
DOC_USP7_MATH_1 414 418 PF00917 0.736
DOC_USP7_MATH_1 419 423 PF00917 0.584
DOC_USP7_MATH_1 456 460 PF00917 0.581
DOC_USP7_MATH_1 519 523 PF00917 0.653
DOC_USP7_MATH_1 529 533 PF00917 0.679
DOC_USP7_MATH_1 582 586 PF00917 0.620
DOC_USP7_MATH_1 605 609 PF00917 0.633
DOC_USP7_MATH_1 678 682 PF00917 0.707
DOC_USP7_MATH_1 688 692 PF00917 0.587
DOC_USP7_UBL2_3 116 120 PF12436 0.429
DOC_USP7_UBL2_3 466 470 PF12436 0.611
DOC_WW_Pin1_4 371 376 PF00397 0.656
DOC_WW_Pin1_4 380 385 PF00397 0.568
DOC_WW_Pin1_4 406 411 PF00397 0.685
DOC_WW_Pin1_4 415 420 PF00397 0.613
DOC_WW_Pin1_4 634 639 PF00397 0.615
LIG_14-3-3_CanoR_1 137 145 PF00244 0.366
LIG_14-3-3_CanoR_1 164 169 PF00244 0.439
LIG_14-3-3_CanoR_1 182 192 PF00244 0.448
LIG_14-3-3_CanoR_1 314 319 PF00244 0.394
LIG_14-3-3_CanoR_1 426 434 PF00244 0.548
LIG_14-3-3_CanoR_1 458 465 PF00244 0.606
LIG_14-3-3_CanoR_1 549 557 PF00244 0.629
LIG_14-3-3_CanoR_1 602 612 PF00244 0.620
LIG_14-3-3_CanoR_1 658 664 PF00244 0.551
LIG_14-3-3_CanoR_1 67 72 PF00244 0.414
LIG_14-3-3_CanoR_1 693 698 PF00244 0.630
LIG_BIR_III_4 322 326 PF00653 0.437
LIG_BRCT_BRCA1_1 386 390 PF00533 0.577
LIG_BRCT_BRCA1_1 490 494 PF00533 0.610
LIG_BRCT_BRCA1_1 645 649 PF00533 0.650
LIG_BRCT_BRCA1_1 659 663 PF00533 0.581
LIG_BRCT_BRCA1_1 690 694 PF00533 0.639
LIG_BRCT_BRCA1_2 386 392 PF00533 0.512
LIG_CaM_IQ_9 187 203 PF13499 0.527
LIG_Clathr_ClatBox_1 252 256 PF01394 0.345
LIG_deltaCOP1_diTrp_1 536 540 PF00928 0.536
LIG_DLG_GKlike_1 58 65 PF00625 0.410
LIG_DLG_GKlike_1 67 74 PF00625 0.320
LIG_eIF4E_1 3 9 PF01652 0.359
LIG_eIF4E_1 342 348 PF01652 0.368
LIG_eIF4E_1 87 93 PF01652 0.322
LIG_FHA_1 201 207 PF00498 0.475
LIG_FHA_1 325 331 PF00498 0.412
LIG_FHA_1 604 610 PF00498 0.677
LIG_FHA_2 106 112 PF00498 0.396
LIG_FHA_2 136 142 PF00498 0.383
LIG_FHA_2 184 190 PF00498 0.542
LIG_FHA_2 191 197 PF00498 0.433
LIG_FHA_2 36 42 PF00498 0.414
LIG_FHA_2 399 405 PF00498 0.668
LIG_FHA_2 531 537 PF00498 0.547
LIG_FHA_2 628 634 PF00498 0.580
LIG_LIR_Gen_1 139 149 PF02991 0.406
LIG_LIR_Gen_1 2 9 PF02991 0.366
LIG_LIR_Gen_1 25 32 PF02991 0.449
LIG_LIR_Gen_1 276 284 PF02991 0.449
LIG_LIR_Gen_1 329 340 PF02991 0.365
LIG_LIR_Gen_1 38 48 PF02991 0.276
LIG_LIR_Gen_1 534 543 PF02991 0.543
LIG_LIR_Nem_3 127 131 PF02991 0.396
LIG_LIR_Nem_3 139 145 PF02991 0.427
LIG_LIR_Nem_3 147 152 PF02991 0.276
LIG_LIR_Nem_3 2 6 PF02991 0.379
LIG_LIR_Nem_3 25 30 PF02991 0.396
LIG_LIR_Nem_3 276 280 PF02991 0.476
LIG_LIR_Nem_3 329 335 PF02991 0.375
LIG_LIR_Nem_3 38 43 PF02991 0.267
LIG_LIR_Nem_3 534 540 PF02991 0.540
LIG_LIR_Nem_3 60 65 PF02991 0.411
LIG_LIR_Nem_3 691 697 PF02991 0.663
LIG_MYND_1 223 227 PF01753 0.567
LIG_MYND_1 571 575 PF01753 0.613
LIG_NRBOX 88 94 PF00104 0.320
LIG_PTB_Apo_2 36 43 PF02174 0.279
LIG_SH2_CRK 142 146 PF00017 0.366
LIG_SH2_CRK 342 346 PF00017 0.340
LIG_SH2_STAP1 142 146 PF00017 0.383
LIG_SH2_STAT5 463 466 PF00017 0.531
LIG_SH2_STAT5 48 51 PF00017 0.357
LIG_SH3_1 569 575 PF00018 0.618
LIG_SH3_3 220 226 PF00018 0.554
LIG_SH3_3 349 355 PF00018 0.409
LIG_SH3_3 552 558 PF00018 0.571
LIG_SH3_3 565 571 PF00018 0.605
LIG_SH3_3 621 627 PF00018 0.602
LIG_SUMO_SIM_anti_2 251 256 PF11976 0.409
LIG_TRAF2_1 108 111 PF00917 0.387
LIG_TRAF2_1 550 553 PF00917 0.612
LIG_TYR_ITIM 126 131 PF00017 0.343
LIG_WRC_WIRS_1 385 390 PF05994 0.601
LIG_WRC_WIRS_1 59 64 PF05994 0.356
LIG_WW_3 593 597 PF00397 0.610
MOD_CDK_SPK_2 371 376 PF00069 0.612
MOD_CDK_SPK_2 406 411 PF00069 0.523
MOD_CK1_1 163 169 PF00069 0.350
MOD_CK1_1 293 299 PF00069 0.470
MOD_CK1_1 383 389 PF00069 0.633
MOD_CK1_1 398 404 PF00069 0.545
MOD_CK1_1 417 423 PF00069 0.570
MOD_CK1_1 451 457 PF00069 0.565
MOD_CK1_1 506 512 PF00069 0.618
MOD_CK1_1 532 538 PF00069 0.576
MOD_CK1_1 548 554 PF00069 0.656
MOD_CK1_1 604 610 PF00069 0.621
MOD_CK1_1 631 637 PF00069 0.646
MOD_CK1_1 642 648 PF00069 0.585
MOD_CK1_1 659 665 PF00069 0.523
MOD_CK1_1 70 76 PF00069 0.406
MOD_CK2_1 105 111 PF00069 0.400
MOD_CK2_1 135 141 PF00069 0.391
MOD_CK2_1 183 189 PF00069 0.544
MOD_CK2_1 190 196 PF00069 0.441
MOD_CK2_1 245 251 PF00069 0.445
MOD_CK2_1 35 41 PF00069 0.405
MOD_CK2_1 388 394 PF00069 0.593
MOD_CK2_1 398 404 PF00069 0.581
MOD_CK2_1 530 536 PF00069 0.588
MOD_CK2_1 539 545 PF00069 0.550
MOD_CK2_1 627 633 PF00069 0.547
MOD_Cter_Amidation 118 121 PF01082 0.389
MOD_Cter_Amidation 650 653 PF01082 0.611
MOD_GlcNHglycan 138 141 PF01048 0.410
MOD_GlcNHglycan 217 220 PF01048 0.546
MOD_GlcNHglycan 247 250 PF01048 0.459
MOD_GlcNHglycan 348 351 PF01048 0.418
MOD_GlcNHglycan 368 371 PF01048 0.467
MOD_GlcNHglycan 380 383 PF01048 0.595
MOD_GlcNHglycan 419 422 PF01048 0.605
MOD_GlcNHglycan 428 431 PF01048 0.535
MOD_GlcNHglycan 446 449 PF01048 0.673
MOD_GlcNHglycan 450 453 PF01048 0.603
MOD_GlcNHglycan 495 499 PF01048 0.596
MOD_GlcNHglycan 603 606 PF01048 0.635
MOD_GlcNHglycan 609 612 PF01048 0.594
MOD_GlcNHglycan 615 618 PF01048 0.544
MOD_GlcNHglycan 669 672 PF01048 0.762
MOD_GlcNHglycan 680 683 PF01048 0.616
MOD_GlcNHglycan 684 687 PF01048 0.573
MOD_GSK3_1 160 167 PF00069 0.454
MOD_GSK3_1 376 383 PF00069 0.785
MOD_GSK3_1 384 391 PF00069 0.581
MOD_GSK3_1 395 402 PF00069 0.509
MOD_GSK3_1 413 420 PF00069 0.515
MOD_GSK3_1 444 451 PF00069 0.703
MOD_GSK3_1 541 548 PF00069 0.671
MOD_GSK3_1 600 607 PF00069 0.632
MOD_GSK3_1 627 634 PF00069 0.659
MOD_GSK3_1 63 70 PF00069 0.377
MOD_GSK3_1 639 646 PF00069 0.545
MOD_GSK3_1 659 666 PF00069 0.531
MOD_GSK3_1 667 674 PF00069 0.554
MOD_GSK3_1 678 685 PF00069 0.621
MOD_GSK3_1 689 696 PF00069 0.583
MOD_GSK3_1 698 705 PF00069 0.517
MOD_LATS_1 312 318 PF00433 0.377
MOD_LATS_1 56 62 PF00433 0.340
MOD_N-GLC_1 175 180 PF02516 0.414
MOD_N-GLC_1 183 188 PF02516 0.479
MOD_N-GLC_1 438 443 PF02516 0.594
MOD_N-GLC_1 576 581 PF02516 0.549
MOD_N-GLC_1 627 632 PF02516 0.754
MOD_N-GLC_1 671 676 PF02516 0.548
MOD_NEK2_1 124 129 PF00069 0.337
MOD_NEK2_1 175 180 PF00069 0.521
MOD_NEK2_1 213 218 PF00069 0.562
MOD_NEK2_1 346 351 PF00069 0.417
MOD_NEK2_1 388 393 PF00069 0.560
MOD_NEK2_1 42 47 PF00069 0.424
MOD_NEK2_1 494 499 PF00069 0.612
MOD_NEK2_1 530 535 PF00069 0.564
MOD_NEK2_1 663 668 PF00069 0.691
MOD_PIKK_1 106 112 PF00454 0.338
MOD_PIKK_1 157 163 PF00454 0.521
MOD_PIKK_1 175 181 PF00454 0.359
MOD_PIKK_1 595 601 PF00454 0.608
MOD_PIKK_1 639 645 PF00454 0.626
MOD_PK_1 164 170 PF00069 0.389
MOD_PKA_2 136 142 PF00069 0.367
MOD_PKA_2 163 169 PF00069 0.378
MOD_PKA_2 200 206 PF00069 0.447
MOD_PKA_2 35 41 PF00069 0.383
MOD_PKA_2 468 474 PF00069 0.726
MOD_PKA_2 548 554 PF00069 0.626
MOD_PKA_2 595 601 PF00069 0.600
MOD_PKA_2 657 663 PF00069 0.583
MOD_PKA_2 678 684 PF00069 0.624
MOD_Plk_1 195 201 PF00069 0.486
MOD_Plk_1 627 633 PF00069 0.758
MOD_Plk_4 256 262 PF00069 0.480
MOD_Plk_4 290 296 PF00069 0.418
MOD_Plk_4 354 360 PF00069 0.607
MOD_Plk_4 643 649 PF00069 0.637
MOD_Plk_4 663 669 PF00069 0.497
MOD_ProDKin_1 371 377 PF00069 0.657
MOD_ProDKin_1 380 386 PF00069 0.569
MOD_ProDKin_1 406 412 PF00069 0.692
MOD_ProDKin_1 415 421 PF00069 0.611
MOD_ProDKin_1 634 640 PF00069 0.614
MOD_SUMO_rev_2 155 160 PF00179 0.455
TRG_DiLeu_BaEn_4 523 529 PF01217 0.522
TRG_DiLeu_BaLyEn_6 220 225 PF01217 0.601
TRG_DiLeu_BaLyEn_6 333 338 PF01217 0.437
TRG_ENDOCYTIC_2 128 131 PF00928 0.396
TRG_ENDOCYTIC_2 142 145 PF00928 0.419
TRG_ENDOCYTIC_2 3 6 PF00928 0.370
TRG_ENDOCYTIC_2 342 345 PF00928 0.339
TRG_ENDOCYTIC_2 86 89 PF00928 0.385
TRG_ER_diArg_1 149 151 PF00400 0.508
TRG_ER_diArg_1 152 154 PF00400 0.575
TRG_ER_diArg_1 204 206 PF00400 0.419
TRG_ER_diArg_1 297 300 PF00400 0.499
TRG_ER_diArg_1 308 311 PF00400 0.347
TRG_ER_diArg_1 34 37 PF00400 0.394
TRG_ER_diArg_1 371 373 PF00400 0.596
TRG_NLS_MonoExtN_4 466 473 PF00514 0.544
TRG_Pf-PMV_PEXEL_1 150 155 PF00026 0.551
TRG_Pf-PMV_PEXEL_1 63 68 PF00026 0.370
TRG_Pf-PMV_PEXEL_1 695 700 PF00026 0.617
TRG_Pf-PMV_PEXEL_1 72 77 PF00026 0.359

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I0K7 Leptomonas seymouri 50% 100%
A0A3S7XCG9 Leishmania donovani 87% 100%
A4HQL1 Leishmania braziliensis 59% 97%
A4ICD1 Leishmania infantum 87% 100%
E9AUC6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 81% 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