LeishMANIAdb
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SET domain-containing protein

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

Quick info

Protein:
SET domain-containing protein
Gene product:
SET domain containing protein, putative
Species:
Leishmania major
UniProt:
Q4Q4F8_LEIMA
TriTrypDb:
LmjF.33.0510 * , LMJLV39_330011400 * , LMJSD75_330011400 *
Length:
887

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
Cellular components
Term Name Level Count
GO:0005634 nucleus 5 2
GO:0043226 organelle 2 2
GO:0043227 membrane-bounded organelle 3 2
GO:0043229 intracellular organelle 3 2
GO:0043231 intracellular membrane-bounded organelle 4 2
GO:0110165 cellular anatomical entity 1 2

Expansion

Sequence features

Q4Q4F8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q4F8

Function

Biological processes
Term Name Level Count
GO:0006479 protein methylation 4 2
GO:0006807 nitrogen compound metabolic process 2 2
GO:0008152 metabolic process 1 2
GO:0008213 protein alkylation 5 2
GO:0009987 cellular process 1 2
GO:0016570 histone modification 5 2
GO:0016571 histone methylation 5 2
GO:0018022 peptidyl-lysine methylation 5 2
GO:0018193 peptidyl-amino acid modification 5 2
GO:0018205 peptidyl-lysine modification 6 2
GO:0019538 protein metabolic process 3 2
GO:0032259 methylation 2 2
GO:0034968 histone lysine methylation 6 2
GO:0036211 protein modification process 4 2
GO:0043170 macromolecule metabolic process 3 2
GO:0043412 macromolecule modification 4 2
GO:0043414 macromolecule methylation 3 2
GO:0044237 cellular metabolic process 2 2
GO:0044238 primary metabolic process 2 2
GO:0044260 obsolete cellular macromolecule metabolic process 3 2
GO:0071704 organic substance metabolic process 2 2
GO:1901564 organonitrogen compound metabolic process 3 2
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 2
GO:0008168 methyltransferase activity 4 2
GO:0008170 N-methyltransferase activity 5 2
GO:0008276 protein methyltransferase activity 3 2
GO:0008757 S-adenosylmethionine-dependent methyltransferase activity 5 2
GO:0016278 lysine N-methyltransferase activity 6 2
GO:0016279 protein-lysine N-methyltransferase activity 4 2
GO:0016740 transferase activity 2 2
GO:0016741 transferase activity, transferring one-carbon groups 3 2
GO:0018024 obsolete histone lysine N-methyltransferase activity 5 2
GO:0042054 histone methyltransferase activity 4 2
GO:0140096 catalytic activity, acting on a protein 2 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 287 291 PF00656 0.500
CLV_C14_Caspase3-7 485 489 PF00656 0.439
CLV_NRD_NRD_1 316 318 PF00675 0.647
CLV_NRD_NRD_1 341 343 PF00675 0.649
CLV_NRD_NRD_1 429 431 PF00675 0.650
CLV_NRD_NRD_1 469 471 PF00675 0.533
CLV_NRD_NRD_1 536 538 PF00675 0.239
CLV_NRD_NRD_1 647 649 PF00675 0.575
CLV_NRD_NRD_1 821 823 PF00675 0.411
CLV_PCSK_KEX2_1 316 318 PF00082 0.647
CLV_PCSK_KEX2_1 429 431 PF00082 0.650
CLV_PCSK_KEX2_1 469 471 PF00082 0.560
CLV_PCSK_KEX2_1 536 538 PF00082 0.239
CLV_PCSK_KEX2_1 632 634 PF00082 0.574
CLV_PCSK_KEX2_1 646 648 PF00082 0.464
CLV_PCSK_KEX2_1 821 823 PF00082 0.411
CLV_PCSK_PC1ET2_1 632 634 PF00082 0.561
CLV_PCSK_SKI1_1 118 122 PF00082 0.504
CLV_PCSK_SKI1_1 140 144 PF00082 0.444
CLV_PCSK_SKI1_1 160 164 PF00082 0.427
CLV_PCSK_SKI1_1 217 221 PF00082 0.485
CLV_PCSK_SKI1_1 385 389 PF00082 0.578
CLV_PCSK_SKI1_1 403 407 PF00082 0.533
CLV_PCSK_SKI1_1 507 511 PF00082 0.332
CLV_PCSK_SKI1_1 57 61 PF00082 0.608
CLV_PCSK_SKI1_1 586 590 PF00082 0.439
CLV_PCSK_SKI1_1 593 597 PF00082 0.458
CLV_PCSK_SKI1_1 632 636 PF00082 0.603
CLV_PCSK_SKI1_1 676 680 PF00082 0.529
CLV_PCSK_SKI1_1 710 714 PF00082 0.499
CLV_PCSK_SKI1_1 77 81 PF00082 0.421
DEG_APCC_DBOX_1 216 224 PF00400 0.498
DEG_APCC_DBOX_1 56 64 PF00400 0.578
DEG_APCC_DBOX_1 76 84 PF00400 0.389
DEG_SPOP_SBC_1 228 232 PF00917 0.492
DOC_CDC14_PxL_1 443 451 PF14671 0.631
DOC_CYCLIN_RxL_1 583 591 PF00134 0.396
DOC_CYCLIN_RxL_1 707 715 PF00134 0.466
DOC_CYCLIN_yCln2_LP_2 158 164 PF00134 0.402
DOC_MAPK_gen_1 118 126 PF00069 0.517
DOC_MAPK_gen_1 215 223 PF00069 0.501
DOC_MAPK_MEF2A_6 127 134 PF00069 0.467
DOC_MAPK_MEF2A_6 215 223 PF00069 0.501
DOC_MAPK_MEF2A_6 668 677 PF00069 0.412
DOC_MAPK_MEF2A_6 77 85 PF00069 0.553
DOC_USP7_MATH_1 128 132 PF00917 0.612
DOC_USP7_MATH_1 147 151 PF00917 0.318
DOC_USP7_MATH_1 228 232 PF00917 0.554
DOC_USP7_MATH_1 248 252 PF00917 0.537
DOC_USP7_MATH_1 389 393 PF00917 0.624
DOC_USP7_MATH_1 431 435 PF00917 0.584
DOC_USP7_MATH_1 497 501 PF00917 0.523
DOC_USP7_MATH_1 552 556 PF00917 0.454
DOC_USP7_MATH_1 620 624 PF00917 0.584
DOC_USP7_MATH_1 628 632 PF00917 0.448
DOC_USP7_MATH_1 90 94 PF00917 0.600
DOC_WW_Pin1_4 12 17 PF00397 0.646
DOC_WW_Pin1_4 126 131 PF00397 0.556
DOC_WW_Pin1_4 224 229 PF00397 0.483
DOC_WW_Pin1_4 305 310 PF00397 0.633
DOC_WW_Pin1_4 413 418 PF00397 0.635
DOC_WW_Pin1_4 47 52 PF00397 0.493
DOC_WW_Pin1_4 495 500 PF00397 0.439
DOC_WW_Pin1_4 528 533 PF00397 0.532
LIG_14-3-3_CanoR_1 160 168 PF00244 0.569
LIG_14-3-3_CanoR_1 197 207 PF00244 0.555
LIG_14-3-3_CanoR_1 215 220 PF00244 0.330
LIG_14-3-3_CanoR_1 316 326 PF00244 0.600
LIG_14-3-3_CanoR_1 43 48 PF00244 0.606
LIG_14-3-3_CanoR_1 57 66 PF00244 0.493
LIG_14-3-3_CanoR_1 633 637 PF00244 0.562
LIG_14-3-3_CanoR_1 858 862 PF00244 0.442
LIG_Actin_WH2_2 357 375 PF00022 0.572
LIG_Actin_WH2_2 521 538 PF00022 0.439
LIG_APCC_ABBA_1 14 19 PF00400 0.631
LIG_APCC_ABBA_1 143 148 PF00400 0.485
LIG_APCC_ABBA_1 238 243 PF00400 0.429
LIG_BIR_III_4 100 104 PF00653 0.599
LIG_Clathr_ClatBox_1 701 705 PF01394 0.426
LIG_EVH1_1 48 52 PF00568 0.623
LIG_EVH1_2 10 14 PF00568 0.550
LIG_FHA_1 216 222 PF00498 0.482
LIG_FHA_1 292 298 PF00498 0.574
LIG_FHA_1 34 40 PF00498 0.641
LIG_FHA_1 565 571 PF00498 0.489
LIG_FHA_1 573 579 PF00498 0.408
LIG_FHA_1 59 65 PF00498 0.597
LIG_FHA_1 713 719 PF00498 0.446
LIG_FHA_2 114 120 PF00498 0.530
LIG_FHA_2 209 215 PF00498 0.389
LIG_FHA_2 260 266 PF00498 0.434
LIG_FHA_2 483 489 PF00498 0.439
LIG_FHA_2 749 755 PF00498 0.443
LIG_FHA_2 792 798 PF00498 0.406
LIG_FHA_2 867 873 PF00498 0.450
LIG_Integrin_RGD_1 288 290 PF01839 0.491
LIG_Integrin_RGD_1 486 488 PF01839 0.301
LIG_LIR_Gen_1 715 724 PF02991 0.428
LIG_LIR_Gen_1 830 840 PF02991 0.479
LIG_LIR_Nem_3 114 120 PF02991 0.557
LIG_LIR_Nem_3 27 33 PF02991 0.623
LIG_LIR_Nem_3 715 720 PF02991 0.436
LIG_LIR_Nem_3 830 835 PF02991 0.447
LIG_LYPXL_SIV_4 728 736 PF13949 0.456
LIG_NRBOX 219 225 PF00104 0.499
LIG_NRBOX 360 366 PF00104 0.587
LIG_PCNA_yPIPBox_3 667 679 PF02747 0.420
LIG_PDZ_Class_3 882 887 PF00595 0.507
LIG_PTAP_UEV_1 1 6 PF05743 0.628
LIG_PTAP_UEV_1 443 448 PF05743 0.586
LIG_Rb_LxCxE_1 872 887 PF01857 0.505
LIG_SH2_CRK 729 733 PF00017 0.439
LIG_SH2_NCK_1 146 150 PF00017 0.481
LIG_SH2_NCK_1 729 733 PF00017 0.439
LIG_SH2_PTP2 832 835 PF00017 0.462
LIG_SH2_SRC 146 149 PF00017 0.481
LIG_SH2_SRC 237 240 PF00017 0.578
LIG_SH2_SRC 563 566 PF00017 0.484
LIG_SH2_SRC 610 613 PF00017 0.548
LIG_SH2_STAP1 729 733 PF00017 0.439
LIG_SH2_STAP1 859 863 PF00017 0.434
LIG_SH2_STAT5 237 240 PF00017 0.435
LIG_SH2_STAT5 563 566 PF00017 0.484
LIG_SH2_STAT5 772 775 PF00017 0.409
LIG_SH2_STAT5 832 835 PF00017 0.462
LIG_SH3_3 441 447 PF00018 0.656
LIG_SH3_3 46 52 PF00018 0.629
LIG_SH3_3 687 693 PF00018 0.427
LIG_SH3_3 7 13 PF00018 0.632
LIG_SH3_3 812 818 PF00018 0.430
LIG_SUMO_SIM_anti_2 155 160 PF11976 0.440
LIG_SUMO_SIM_par_1 256 262 PF11976 0.411
LIG_SUMO_SIM_par_1 35 41 PF11976 0.643
LIG_SUMO_SIM_par_1 524 529 PF11976 0.532
LIG_SUMO_SIM_par_1 61 67 PF11976 0.572
LIG_SUMO_SIM_par_1 700 705 PF11976 0.430
LIG_TRAF2_1 25 28 PF00917 0.605
LIG_TRAF2_1 555 558 PF00917 0.532
LIG_TRAF2_1 751 754 PF00917 0.444
LIG_TRFH_1 236 240 PF08558 0.432
LIG_WRC_WIRS_1 852 857 PF05994 0.452
LIG_WW_3 463 467 PF00397 0.624
MOD_CDK_SPxxK_3 305 312 PF00069 0.635
MOD_CK1_1 205 211 PF00069 0.516
MOD_CK1_1 227 233 PF00069 0.578
MOD_CK1_1 291 297 PF00069 0.564
MOD_CK1_1 502 508 PF00069 0.287
MOD_CK1_1 58 64 PF00069 0.554
MOD_CK1_1 738 744 PF00069 0.454
MOD_CK2_1 113 119 PF00069 0.434
MOD_CK2_1 259 265 PF00069 0.420
MOD_CK2_1 552 558 PF00069 0.456
MOD_CK2_1 570 576 PF00069 0.585
MOD_CK2_1 747 753 PF00069 0.432
MOD_CK2_1 791 797 PF00069 0.400
MOD_CK2_1 866 872 PF00069 0.445
MOD_CK2_1 875 881 PF00069 0.403
MOD_GlcNHglycan 106 110 PF01048 0.474
MOD_GlcNHglycan 2 5 PF01048 0.667
MOD_GlcNHglycan 294 297 PF01048 0.608
MOD_GlcNHglycan 320 323 PF01048 0.627
MOD_GlcNHglycan 344 347 PF01048 0.746
MOD_GlcNHglycan 354 358 PF01048 0.587
MOD_GlcNHglycan 391 394 PF01048 0.585
MOD_GlcNHglycan 444 447 PF01048 0.580
MOD_GlcNHglycan 499 502 PF01048 0.368
MOD_GlcNHglycan 537 540 PF01048 0.382
MOD_GlcNHglycan 554 557 PF01048 0.407
MOD_GlcNHglycan 57 60 PF01048 0.569
MOD_GlcNHglycan 660 663 PF01048 0.579
MOD_GlcNHglycan 71 74 PF01048 0.462
MOD_GlcNHglycan 740 743 PF01048 0.447
MOD_GSK3_1 128 135 PF00069 0.581
MOD_GSK3_1 198 205 PF00069 0.508
MOD_GSK3_1 224 231 PF00069 0.556
MOD_GSK3_1 242 249 PF00069 0.315
MOD_GSK3_1 274 281 PF00069 0.466
MOD_GSK3_1 284 291 PF00069 0.496
MOD_GSK3_1 413 420 PF00069 0.666
MOD_GSK3_1 43 50 PF00069 0.533
MOD_GSK3_1 495 502 PF00069 0.317
MOD_GSK3_1 564 571 PF00069 0.485
MOD_GSK3_1 628 635 PF00069 0.589
MOD_GSK3_1 653 660 PF00069 0.528
MOD_GSK3_1 708 715 PF00069 0.463
MOD_N-GLC_1 420 425 PF02516 0.650
MOD_NEK2_1 113 118 PF00069 0.499
MOD_NEK2_1 229 234 PF00069 0.533
MOD_NEK2_1 304 309 PF00069 0.545
MOD_NEK2_1 32 37 PF00069 0.612
MOD_NEK2_1 55 60 PF00069 0.558
MOD_NEK2_1 570 575 PF00069 0.499
MOD_NEK2_1 577 582 PF00069 0.407
MOD_NEK2_1 588 593 PF00069 0.317
MOD_NEK2_1 727 732 PF00069 0.435
MOD_NEK2_1 736 741 PF00069 0.371
MOD_NEK2_1 747 752 PF00069 0.238
MOD_NEK2_1 773 778 PF00069 0.414
MOD_PIKK_1 570 576 PF00454 0.487
MOD_PIKK_1 588 594 PF00454 0.437
MOD_PKA_1 342 348 PF00069 0.597
MOD_PKA_1 632 638 PF00069 0.546
MOD_PKA_2 196 202 PF00069 0.484
MOD_PKA_2 42 48 PF00069 0.643
MOD_PKA_2 431 437 PF00069 0.553
MOD_PKA_2 535 541 PF00069 0.254
MOD_PKA_2 632 638 PF00069 0.546
MOD_PKA_2 857 863 PF00069 0.443
MOD_Plk_1 105 111 PF00069 0.537
MOD_Plk_1 147 153 PF00069 0.480
MOD_Plk_1 208 214 PF00069 0.447
MOD_Plk_1 242 248 PF00069 0.484
MOD_Plk_1 26 32 PF00069 0.654
MOD_Plk_1 502 508 PF00069 0.476
MOD_Plk_1 557 563 PF00069 0.385
MOD_Plk_4 208 214 PF00069 0.392
MOD_Plk_4 360 366 PF00069 0.601
MOD_Plk_4 43 49 PF00069 0.641
MOD_Plk_4 543 549 PF00069 0.385
MOD_Plk_4 559 565 PF00069 0.385
MOD_Plk_4 632 638 PF00069 0.609
MOD_Plk_4 848 854 PF00069 0.446
MOD_ProDKin_1 12 18 PF00069 0.648
MOD_ProDKin_1 126 132 PF00069 0.551
MOD_ProDKin_1 224 230 PF00069 0.491
MOD_ProDKin_1 305 311 PF00069 0.635
MOD_ProDKin_1 413 419 PF00069 0.636
MOD_ProDKin_1 47 53 PF00069 0.496
MOD_ProDKin_1 495 501 PF00069 0.254
MOD_ProDKin_1 528 534 PF00069 0.385
MOD_SUMO_for_1 678 681 PF00179 0.557
MOD_SUMO_rev_2 114 122 PF00179 0.520
MOD_SUMO_rev_2 651 661 PF00179 0.546
TRG_DiLeu_BaEn_1 604 609 PF01217 0.491
TRG_DiLeu_BaEn_1 754 759 PF01217 0.482
TRG_DiLeu_BaEn_1 805 810 PF01217 0.480
TRG_DiLeu_BaEn_1 848 853 PF01217 0.423
TRG_DiLeu_BaEn_1 872 877 PF01217 0.465
TRG_DiLeu_BaEn_4 27 33 PF01217 0.544
TRG_DiLeu_BaLyEn_6 344 349 PF01217 0.602
TRG_DiLeu_BaLyEn_6 761 766 PF01217 0.457
TRG_ENDOCYTIC_2 729 732 PF00928 0.443
TRG_ENDOCYTIC_2 772 775 PF00928 0.409
TRG_ENDOCYTIC_2 832 835 PF00928 0.462
TRG_ER_diArg_1 315 317 PF00400 0.637
TRG_ER_diArg_1 428 430 PF00400 0.656
TRG_ER_diArg_1 468 470 PF00400 0.512
TRG_ER_diArg_1 535 537 PF00400 0.254
TRG_ER_diArg_1 583 586 PF00400 0.399
TRG_ER_diArg_1 646 648 PF00400 0.564
TRG_ER_diArg_1 718 721 PF00400 0.380
TRG_ER_diArg_1 820 822 PF00400 0.408
TRG_Pf-PMV_PEXEL_1 668 672 PF00026 0.418
TRG_Pf-PMV_PEXEL_1 699 703 PF00026 0.441

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3S7X6B7 Leishmania donovani 90% 88%
A4HL86 Leishmania braziliensis 70% 100%
A4I8R4 Leishmania infantum 89% 88%
E9B3M9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 85% 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