LeishMANIAdb
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Mak10 subunit, NatC N-terminal acetyltransferase-domain-containing protein

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

Quick info

Protein:
Mak10 subunit, NatC N-terminal acetyltransferase-domain-containing protein
Gene product:
Mak10 subunit, NatC N(alpha)-terminal acetyltransferase, putative
Species:
Leishmania major
UniProt:
Q4QE93_LEIMA
TriTrypDb:
LmjF.17.0980 , LMJLV39_170016900 * , LMJSD75_170016500 *
Length:
741

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. yes yes: 20
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: 11
NetGPI no yes: 0, no: 11
Cellular components
Term Name Level Count
GO:0005737 cytoplasm 2 2
GO:0031248 protein acetyltransferase complex 3 12
GO:0031414 N-terminal protein acetyltransferase complex 4 12
GO:0031417 NatC complex 5 12
GO:0032991 protein-containing complex 1 12
GO:0110165 cellular anatomical entity 1 2
GO:0140535 intracellular protein-containing complex 2 12
GO:1902493 acetyltransferase complex 4 12
GO:1902494 catalytic complex 2 12
GO:1990234 transferase complex 3 12

Expansion

Sequence features

Q4QE93
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QE93

Function

Biological processes
Term Name Level Count
GO:0006473 protein acetylation 6 12
GO:0006474 N-terminal protein amino acid acetylation 5 12
GO:0006807 nitrogen compound metabolic process 2 12
GO:0008152 metabolic process 1 12
GO:0017196 N-terminal peptidyl-methionine acetylation 6 12
GO:0018193 peptidyl-amino acid modification 5 12
GO:0018206 peptidyl-methionine modification 6 12
GO:0019538 protein metabolic process 3 12
GO:0031365 N-terminal protein amino acid modification 5 12
GO:0036211 protein modification process 4 12
GO:0043170 macromolecule metabolic process 3 12
GO:0043412 macromolecule modification 4 12
GO:0043543 protein acylation 5 12
GO:0044238 primary metabolic process 2 12
GO:0051604 protein maturation 4 12
GO:0071704 organic substance metabolic process 2 12
GO:1901564 organonitrogen compound metabolic process 3 12
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 2
GO:0016740 transferase activity 2 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 576 580 PF00656 0.466
CLV_NRD_NRD_1 201 203 PF00675 0.368
CLV_NRD_NRD_1 346 348 PF00675 0.534
CLV_NRD_NRD_1 406 408 PF00675 0.483
CLV_NRD_NRD_1 432 434 PF00675 0.405
CLV_NRD_NRD_1 589 591 PF00675 0.488
CLV_NRD_NRD_1 676 678 PF00675 0.460
CLV_NRD_NRD_1 682 684 PF00675 0.503
CLV_NRD_NRD_1 732 734 PF00675 0.479
CLV_PCSK_KEX2_1 217 219 PF00082 0.549
CLV_PCSK_KEX2_1 284 286 PF00082 0.408
CLV_PCSK_KEX2_1 346 348 PF00082 0.544
CLV_PCSK_KEX2_1 354 356 PF00082 0.443
CLV_PCSK_KEX2_1 406 408 PF00082 0.483
CLV_PCSK_KEX2_1 432 434 PF00082 0.404
CLV_PCSK_KEX2_1 544 546 PF00082 0.498
CLV_PCSK_KEX2_1 682 684 PF00082 0.535
CLV_PCSK_KEX2_1 734 736 PF00082 0.577
CLV_PCSK_PC1ET2_1 217 219 PF00082 0.549
CLV_PCSK_PC1ET2_1 284 286 PF00082 0.402
CLV_PCSK_PC1ET2_1 354 356 PF00082 0.434
CLV_PCSK_PC1ET2_1 544 546 PF00082 0.605
CLV_PCSK_PC1ET2_1 734 736 PF00082 0.556
CLV_PCSK_SKI1_1 137 141 PF00082 0.448
CLV_PCSK_SKI1_1 203 207 PF00082 0.373
CLV_PCSK_SKI1_1 284 288 PF00082 0.388
CLV_PCSK_SKI1_1 346 350 PF00082 0.562
CLV_PCSK_SKI1_1 394 398 PF00082 0.533
CLV_PCSK_SKI1_1 407 411 PF00082 0.485
CLV_PCSK_SKI1_1 614 618 PF00082 0.566
CLV_PCSK_SKI1_1 665 669 PF00082 0.358
CLV_PCSK_SKI1_1 99 103 PF00082 0.366
DEG_APCC_DBOX_1 136 144 PF00400 0.431
DEG_APCC_DBOX_1 345 353 PF00400 0.488
DEG_APCC_DBOX_1 589 597 PF00400 0.498
DEG_APCC_KENBOX_2 522 526 PF00400 0.511
DEG_Nend_UBRbox_3 1 3 PF02207 0.693
DEG_SPOP_SBC_1 150 154 PF00917 0.546
DEG_SPOP_SBC_1 188 192 PF00917 0.554
DEG_SPOP_SBC_1 667 671 PF00917 0.484
DOC_ANK_TNKS_1 681 688 PF00023 0.553
DOC_CKS1_1 264 269 PF01111 0.613
DOC_CYCLIN_yCln2_LP_2 114 120 PF00134 0.532
DOC_CYCLIN_yCln2_LP_2 163 166 PF00134 0.626
DOC_CYCLIN_yCln2_LP_2 508 514 PF00134 0.372
DOC_MAPK_gen_1 544 550 PF00069 0.471
DOC_MAPK_gen_1 590 596 PF00069 0.531
DOC_MAPK_RevD_3 418 433 PF00069 0.431
DOC_MAPK_RevD_3 638 652 PF00069 0.468
DOC_PP1_RVXF_1 196 202 PF00149 0.369
DOC_PP2B_LxvP_1 163 166 PF13499 0.626
DOC_PP2B_LxvP_1 46 49 PF13499 0.349
DOC_PP4_MxPP_1 1 4 PF00568 0.741
DOC_USP7_MATH_1 172 176 PF00917 0.634
DOC_USP7_MATH_1 187 191 PF00917 0.490
DOC_USP7_MATH_1 272 276 PF00917 0.570
DOC_USP7_MATH_1 320 324 PF00917 0.411
DOC_USP7_MATH_1 334 338 PF00917 0.409
DOC_USP7_MATH_1 461 465 PF00917 0.561
DOC_USP7_MATH_1 573 577 PF00917 0.488
DOC_USP7_MATH_1 600 604 PF00917 0.481
DOC_USP7_MATH_1 626 630 PF00917 0.559
DOC_USP7_MATH_1 636 640 PF00917 0.538
DOC_USP7_MATH_1 81 85 PF00917 0.603
DOC_WD40_RPTOR_TOS_1 496 501 PF00400 0.505
DOC_WW_Pin1_4 189 194 PF00397 0.481
DOC_WW_Pin1_4 263 268 PF00397 0.507
DOC_WW_Pin1_4 387 392 PF00397 0.497
DOC_WW_Pin1_4 643 648 PF00397 0.381
LIG_14-3-3_CanoR_1 242 246 PF00244 0.564
LIG_14-3-3_CanoR_1 379 385 PF00244 0.469
LIG_14-3-3_CanoR_1 406 416 PF00244 0.368
LIG_14-3-3_CanoR_1 433 439 PF00244 0.542
LIG_14-3-3_CanoR_1 473 478 PF00244 0.510
LIG_14-3-3_CanoR_1 632 640 PF00244 0.573
LIG_Actin_WH2_2 373 390 PF00022 0.549
LIG_BRCT_BRCA1_1 532 536 PF00533 0.568
LIG_Clathr_ClatBox_1 296 300 PF01394 0.526
LIG_Clathr_ClatBox_1 417 421 PF01394 0.391
LIG_Clathr_ClatBox_1 604 608 PF01394 0.480
LIG_deltaCOP1_diTrp_1 13 22 PF00928 0.512
LIG_eIF4E_1 582 588 PF01652 0.491
LIG_eIF4E_1 66 72 PF01652 0.578
LIG_FHA_1 266 272 PF00498 0.514
LIG_FHA_1 448 454 PF00498 0.505
LIG_FHA_1 532 538 PF00498 0.561
LIG_FHA_1 689 695 PF00498 0.520
LIG_FHA_1 72 78 PF00498 0.594
LIG_FHA_2 12 18 PF00498 0.501
LIG_FHA_2 435 441 PF00498 0.555
LIG_FHA_2 502 508 PF00498 0.413
LIG_FXI_DFP_1 113 117 PF00024 0.385
LIG_LIR_Apic_2 337 343 PF02991 0.481
LIG_LIR_Apic_2 353 359 PF02991 0.450
LIG_LIR_Gen_1 110 120 PF02991 0.526
LIG_LIR_Gen_1 13 22 PF02991 0.595
LIG_LIR_Gen_1 158 168 PF02991 0.615
LIG_LIR_Gen_1 413 424 PF02991 0.475
LIG_LIR_Gen_1 440 449 PF02991 0.506
LIG_LIR_Gen_1 714 724 PF02991 0.347
LIG_LIR_Gen_1 94 103 PF02991 0.589
LIG_LIR_Nem_3 110 116 PF02991 0.526
LIG_LIR_Nem_3 13 18 PF02991 0.617
LIG_LIR_Nem_3 158 164 PF02991 0.580
LIG_LIR_Nem_3 281 286 PF02991 0.461
LIG_LIR_Nem_3 292 296 PF02991 0.400
LIG_LIR_Nem_3 310 315 PF02991 0.217
LIG_LIR_Nem_3 413 419 PF02991 0.486
LIG_LIR_Nem_3 440 444 PF02991 0.507
LIG_LIR_Nem_3 714 719 PF02991 0.358
LIG_LIR_Nem_3 94 98 PF02991 0.590
LIG_NRBOX 208 214 PF00104 0.505
LIG_NRBOX 67 73 PF00104 0.501
LIG_PDZ_Class_1 736 741 PF00595 0.698
LIG_Pex14_1 513 517 PF04695 0.384
LIG_Pex14_2 201 205 PF04695 0.458
LIG_Pex14_2 308 312 PF04695 0.482
LIG_SH2_CRK 283 287 PF00017 0.458
LIG_SH2_CRK 340 344 PF00017 0.500
LIG_SH2_CRK 356 360 PF00017 0.437
LIG_SH2_CRK 361 365 PF00017 0.439
LIG_SH2_CRK 619 623 PF00017 0.552
LIG_SH2_GRB2like 514 517 PF00017 0.402
LIG_SH2_NCK_1 716 720 PF00017 0.350
LIG_SH2_PTP2 95 98 PF00017 0.585
LIG_SH2_SRC 95 98 PF00017 0.585
LIG_SH2_STAP1 449 453 PF00017 0.479
LIG_SH2_STAP1 630 634 PF00017 0.469
LIG_SH2_STAP1 649 653 PF00017 0.456
LIG_SH2_STAT5 103 106 PF00017 0.488
LIG_SH2_STAT5 113 116 PF00017 0.440
LIG_SH2_STAT5 118 121 PF00017 0.475
LIG_SH2_STAT5 135 138 PF00017 0.354
LIG_SH2_STAT5 240 243 PF00017 0.553
LIG_SH2_STAT5 416 419 PF00017 0.380
LIG_SH2_STAT5 449 452 PF00017 0.478
LIG_SH2_STAT5 514 517 PF00017 0.435
LIG_SH2_STAT5 582 585 PF00017 0.495
LIG_SH2_STAT5 95 98 PF00017 0.531
LIG_SH3_2 317 322 PF14604 0.390
LIG_SH3_3 1 7 PF00018 0.772
LIG_SH3_3 261 267 PF00018 0.480
LIG_SH3_3 314 320 PF00018 0.416
LIG_SH3_3 716 722 PF00018 0.433
LIG_SUMO_SIM_anti_2 230 238 PF11976 0.478
LIG_SUMO_SIM_anti_2 499 504 PF11976 0.525
LIG_SUMO_SIM_par_1 475 482 PF11976 0.464
LIG_SUMO_SIM_par_1 592 598 PF11976 0.453
LIG_SUMO_SIM_par_1 603 608 PF11976 0.456
LIG_SUMO_SIM_par_1 88 94 PF11976 0.507
LIG_SxIP_EBH_1 544 554 PF03271 0.556
LIG_TRAF2_1 157 160 PF00917 0.518
LIG_TRFH_1 161 165 PF08558 0.605
LIG_TYR_ITIM 617 622 PF00017 0.546
LIG_UBA3_1 286 294 PF00899 0.404
LIG_UBA3_1 348 354 PF00899 0.503
LIG_UBA3_1 593 601 PF00899 0.462
LIG_WRC_WIRS_1 290 295 PF05994 0.511
LIG_WRC_WIRS_1 493 498 PF05994 0.475
MOD_CDK_SPxK_1 263 269 PF00069 0.494
MOD_CDK_SPxxK_3 387 394 PF00069 0.570
MOD_CK1_1 263 269 PF00069 0.494
MOD_CK1_1 292 298 PF00069 0.470
MOD_CK1_1 30 36 PF00069 0.583
MOD_CK1_1 448 454 PF00069 0.439
MOD_CK1_1 578 584 PF00069 0.487
MOD_CK1_1 603 609 PF00069 0.425
MOD_CK1_1 79 85 PF00069 0.379
MOD_CK2_1 154 160 PF00069 0.485
MOD_CK2_1 172 178 PF00069 0.587
MOD_CK2_1 216 222 PF00069 0.506
MOD_CK2_1 44 50 PF00069 0.343
MOD_CK2_1 501 507 PF00069 0.388
MOD_GlcNHglycan 280 283 PF01048 0.503
MOD_GlcNHglycan 46 49 PF01048 0.349
MOD_GlcNHglycan 57 60 PF01048 0.352
MOD_GlcNHglycan 583 586 PF01048 0.465
MOD_GlcNHglycan 597 600 PF01048 0.424
MOD_GlcNHglycan 634 637 PF01048 0.513
MOD_GlcNHglycan 670 673 PF01048 0.606
MOD_GlcNHglycan 702 705 PF01048 0.558
MOD_GlcNHglycan 725 728 PF01048 0.554
MOD_GlcNHglycan 78 81 PF01048 0.348
MOD_GSK3_1 105 112 PF00069 0.468
MOD_GSK3_1 150 157 PF00069 0.436
MOD_GSK3_1 212 219 PF00069 0.536
MOD_GSK3_1 447 454 PF00069 0.458
MOD_GSK3_1 472 479 PF00069 0.440
MOD_GSK3_1 553 560 PF00069 0.474
MOD_GSK3_1 632 639 PF00069 0.543
MOD_LATS_1 97 103 PF00433 0.468
MOD_N-GLC_1 11 16 PF02516 0.596
MOD_N-GLC_1 128 133 PF02516 0.469
MOD_N-GLC_1 154 159 PF02516 0.584
MOD_N-GLC_1 334 339 PF02516 0.550
MOD_N-GLC_1 524 529 PF02516 0.432
MOD_N-GLC_2 23 25 PF02516 0.456
MOD_N-GLC_2 483 485 PF02516 0.295
MOD_NEK2_1 109 114 PF00069 0.376
MOD_NEK2_1 151 156 PF00069 0.550
MOD_NEK2_1 212 217 PF00069 0.480
MOD_NEK2_1 348 353 PF00069 0.443
MOD_NEK2_1 419 424 PF00069 0.457
MOD_NEK2_1 434 439 PF00069 0.459
MOD_NEK2_1 531 536 PF00069 0.565
MOD_NEK2_1 553 558 PF00069 0.411
MOD_NEK2_1 668 673 PF00069 0.525
MOD_NEK2_1 688 693 PF00069 0.429
MOD_NEK2_1 728 733 PF00069 0.487
MOD_PIKK_1 107 113 PF00454 0.452
MOD_PIKK_1 501 507 PF00454 0.403
MOD_PKA_1 216 222 PF00069 0.544
MOD_PKA_1 735 741 PF00069 0.626
MOD_PKA_2 241 247 PF00069 0.476
MOD_PKA_2 472 478 PF00069 0.476
MOD_PKA_2 557 563 PF00069 0.551
MOD_PKB_1 733 741 PF00069 0.602
MOD_Plk_1 11 17 PF00069 0.534
MOD_Plk_1 128 134 PF00069 0.406
MOD_Plk_1 172 178 PF00069 0.594
MOD_Plk_1 28 34 PF00069 0.574
MOD_Plk_1 334 340 PF00069 0.548
MOD_Plk_1 445 451 PF00069 0.403
MOD_Plk_1 524 530 PF00069 0.525
MOD_Plk_1 578 584 PF00069 0.516
MOD_Plk_1 99 105 PF00069 0.456
MOD_Plk_4 109 115 PF00069 0.463
MOD_Plk_4 207 213 PF00069 0.439
MOD_Plk_4 260 266 PF00069 0.578
MOD_Plk_4 292 298 PF00069 0.479
MOD_Plk_4 334 340 PF00069 0.464
MOD_Plk_4 419 425 PF00069 0.442
MOD_Plk_4 451 457 PF00069 0.436
MOD_Plk_4 473 479 PF00069 0.459
MOD_Plk_4 537 543 PF00069 0.535
MOD_Plk_4 578 584 PF00069 0.508
MOD_Plk_4 600 606 PF00069 0.474
MOD_Plk_4 99 105 PF00069 0.468
MOD_ProDKin_1 189 195 PF00069 0.473
MOD_ProDKin_1 263 269 PF00069 0.509
MOD_ProDKin_1 387 393 PF00069 0.496
MOD_ProDKin_1 643 649 PF00069 0.378
MOD_SUMO_for_1 26 29 PF00179 0.575
MOD_SUMO_for_1 72 75 PF00179 0.353
MOD_SUMO_rev_2 243 253 PF00179 0.563
MOD_SUMO_rev_2 47 56 PF00179 0.334
MOD_SUMO_rev_2 584 593 PF00179 0.481
TRG_DiLeu_BaEn_1 159 164 PF01217 0.616
TRG_DiLeu_BaEn_1 230 235 PF01217 0.405
TRG_DiLeu_BaEn_1 392 397 PF01217 0.454
TRG_DiLeu_BaEn_1 589 594 PF01217 0.419
TRG_DiLeu_BaEn_4 63 69 PF01217 0.452
TRG_DiLeu_BaLyEn_6 282 287 PF01217 0.385
TRG_DiLeu_BaLyEn_6 314 319 PF01217 0.386
TRG_DiLeu_BaLyEn_6 611 616 PF01217 0.516
TRG_ENDOCYTIC_2 113 116 PF00928 0.295
TRG_ENDOCYTIC_2 283 286 PF00928 0.389
TRG_ENDOCYTIC_2 345 348 PF00928 0.480
TRG_ENDOCYTIC_2 361 364 PF00928 0.362
TRG_ENDOCYTIC_2 416 419 PF00928 0.471
TRG_ENDOCYTIC_2 514 517 PF00928 0.382
TRG_ENDOCYTIC_2 619 622 PF00928 0.542
TRG_ENDOCYTIC_2 716 719 PF00928 0.353
TRG_ENDOCYTIC_2 95 98 PF00928 0.472
TRG_ER_diArg_1 198 201 PF00400 0.372
TRG_ER_diArg_1 345 347 PF00400 0.507
TRG_ER_diArg_1 405 407 PF00400 0.485
TRG_ER_diArg_1 432 434 PF00400 0.404
TRG_ER_diArg_1 681 683 PF00400 0.550
TRG_ER_diArg_1 732 735 PF00400 0.585
TRG_NES_CRM1_1 230 245 PF08389 0.460
TRG_NES_CRM1_1 288 300 PF08389 0.518
TRG_NES_CRM1_1 491 505 PF08389 0.432
TRG_Pf-PMV_PEXEL_1 285 289 PF00026 0.396
TRG_Pf-PMV_PEXEL_1 394 399 PF00026 0.474

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P4Y3 Leptomonas seymouri 79% 100%
A0A0S4IMZ6 Bodo saltans 32% 100%
A0A1X0NSS7 Trypanosomatidae 52% 100%
A0A3R7M3C6 Trypanosoma rangeli 49% 100%
A0A3S7WUK2 Leishmania donovani 98% 100%
A4H953 Leishmania braziliensis 90% 100%
A4HXH5 Leishmania infantum 98% 100%
C9ZP62 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 47% 100%
E9AR70 Leishmania mexicana (strain MHOM/GT/2001/U1103) 94% 100%
V5D6H5 Trypanosoma cruzi 48% 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