LeishMANIAdb
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Putative glutaminyl cyclase

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

Quick info

Protein:
Putative glutaminyl cyclase
Gene product:
glutaminyl cyclase, putative
Species:
Leishmania major
UniProt:
Q4QJA7_LEIMA
TriTrypDb:
LmjF.05.0950 , LMJLV39_050014400 * , LMJSD75_050014700
Length:
907

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:0016020 membrane 2 6
GO:0110165 cellular anatomical entity 1 6

Expansion

Sequence features

Q4QJA7
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QJA7

Function

Biological processes
Term Name Level Count
GO:0006807 nitrogen compound metabolic process 2 2
GO:0008152 metabolic process 1 2
GO:0017186 peptidyl-pyroglutamic acid biosynthetic process, using glutaminyl-peptide cyclotransferase 7 2
GO:0018193 peptidyl-amino acid modification 5 2
GO:0018199 peptidyl-glutamine modification 6 2
GO:0019538 protein metabolic process 3 2
GO:0036211 protein modification process 4 2
GO:0043170 macromolecule metabolic process 3 2
GO:0043412 macromolecule modification 4 2
GO:0044238 primary metabolic process 2 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 7
GO:0005488 binding 1 2
GO:0008270 zinc ion binding 6 2
GO:0016603 glutaminyl-peptide cyclotransferase activity 4 5
GO:0016740 transferase activity 2 7
GO:0016746 acyltransferase activity 3 7
GO:0016755 aminoacyltransferase activity 3 5
GO:0043167 ion binding 2 2
GO:0043169 cation binding 3 2
GO:0046872 metal ion binding 4 2
GO:0046914 transition metal ion binding 5 2
GO:0140096 catalytic activity, acting on a protein 2 5

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 183 187 PF00656 0.516
CLV_C14_Caspase3-7 228 232 PF00656 0.502
CLV_C14_Caspase3-7 275 279 PF00656 0.494
CLV_C14_Caspase3-7 872 876 PF00656 0.223
CLV_NRD_NRD_1 10 12 PF00675 0.479
CLV_NRD_NRD_1 125 127 PF00675 0.673
CLV_NRD_NRD_1 13 15 PF00675 0.453
CLV_NRD_NRD_1 142 144 PF00675 0.588
CLV_NRD_NRD_1 161 163 PF00675 0.571
CLV_NRD_NRD_1 17 19 PF00675 0.421
CLV_NRD_NRD_1 245 247 PF00675 0.715
CLV_NRD_NRD_1 336 338 PF00675 0.632
CLV_NRD_NRD_1 365 367 PF00675 0.705
CLV_NRD_NRD_1 371 373 PF00675 0.709
CLV_NRD_NRD_1 49 51 PF00675 0.273
CLV_NRD_NRD_1 747 749 PF00675 0.673
CLV_NRD_NRD_1 837 839 PF00675 0.468
CLV_NRD_NRD_1 904 906 PF00675 0.664
CLV_PCSK_FUR_1 11 15 PF00082 0.474
CLV_PCSK_FUR_1 47 51 PF00082 0.389
CLV_PCSK_KEX2_1 13 15 PF00082 0.450
CLV_PCSK_KEX2_1 142 144 PF00082 0.697
CLV_PCSK_KEX2_1 150 152 PF00082 0.633
CLV_PCSK_KEX2_1 161 163 PF00082 0.570
CLV_PCSK_KEX2_1 17 19 PF00082 0.417
CLV_PCSK_KEX2_1 229 231 PF00082 0.656
CLV_PCSK_KEX2_1 244 246 PF00082 0.672
CLV_PCSK_KEX2_1 29 31 PF00082 0.312
CLV_PCSK_KEX2_1 336 338 PF00082 0.632
CLV_PCSK_KEX2_1 364 366 PF00082 0.705
CLV_PCSK_KEX2_1 49 51 PF00082 0.273
CLV_PCSK_KEX2_1 747 749 PF00082 0.672
CLV_PCSK_KEX2_1 837 839 PF00082 0.468
CLV_PCSK_KEX2_1 9 11 PF00082 0.485
CLV_PCSK_PC1ET2_1 150 152 PF00082 0.654
CLV_PCSK_PC1ET2_1 229 231 PF00082 0.656
CLV_PCSK_PC1ET2_1 29 31 PF00082 0.439
CLV_PCSK_PC7_1 9 15 PF00082 0.468
CLV_PCSK_SKI1_1 150 154 PF00082 0.681
CLV_PCSK_SKI1_1 230 234 PF00082 0.773
CLV_PCSK_SKI1_1 266 270 PF00082 0.695
CLV_PCSK_SKI1_1 351 355 PF00082 0.711
CLV_PCSK_SKI1_1 373 377 PF00082 0.730
CLV_PCSK_SKI1_1 409 413 PF00082 0.725
CLV_PCSK_SKI1_1 420 424 PF00082 0.710
CLV_PCSK_SKI1_1 485 489 PF00082 0.468
CLV_PCSK_SKI1_1 49 53 PF00082 0.271
CLV_PCSK_SKI1_1 528 532 PF00082 0.657
CLV_PCSK_SKI1_1 747 751 PF00082 0.677
CLV_PCSK_SKI1_1 840 844 PF00082 0.488
DEG_APCC_DBOX_1 141 149 PF00400 0.491
DEG_APCC_DBOX_1 48 56 PF00400 0.471
DEG_APCC_DBOX_1 536 544 PF00400 0.403
DEG_APCC_DBOX_1 586 594 PF00400 0.349
DEG_APCC_KENBOX_2 128 132 PF00400 0.396
DEG_Nend_UBRbox_3 1 3 PF02207 0.677
DOC_CDC14_PxL_1 465 473 PF14671 0.288
DOC_CYCLIN_RxL_1 260 270 PF00134 0.484
DOC_CYCLIN_yCln2_LP_2 543 549 PF00134 0.392
DOC_MAPK_DCC_7 29 37 PF00069 0.600
DOC_MAPK_DCC_7 857 866 PF00069 0.312
DOC_MAPK_FxFP_2 200 203 PF00069 0.446
DOC_MAPK_FxFP_2 327 330 PF00069 0.358
DOC_MAPK_gen_1 29 37 PF00069 0.600
DOC_MAPK_gen_1 47 57 PF00069 0.507
DOC_MAPK_gen_1 720 729 PF00069 0.449
DOC_MAPK_gen_1 837 844 PF00069 0.288
DOC_MAPK_MEF2A_6 29 37 PF00069 0.600
DOC_MAPK_MEF2A_6 49 57 PF00069 0.471
DOC_MAPK_MEF2A_6 720 729 PF00069 0.437
DOC_MAPK_MEF2A_6 857 866 PF00069 0.312
DOC_MAPK_MEF2A_6 96 103 PF00069 0.485
DOC_MAPK_RevD_3 232 246 PF00069 0.479
DOC_PP2B_LxvP_1 201 204 PF13499 0.444
DOC_PP2B_LxvP_1 438 441 PF13499 0.440
DOC_PP2B_PxIxI_1 596 602 PF00149 0.346
DOC_PP4_FxxP_1 200 203 PF00568 0.446
DOC_PP4_FxxP_1 327 330 PF00568 0.362
DOC_PP4_FxxP_1 557 560 PF00568 0.390
DOC_PP4_FxxP_1 827 830 PF00568 0.268
DOC_USP7_MATH_1 152 156 PF00917 0.467
DOC_USP7_MATH_1 163 167 PF00917 0.437
DOC_USP7_MATH_1 272 276 PF00917 0.464
DOC_USP7_MATH_1 341 345 PF00917 0.466
DOC_USP7_MATH_1 473 477 PF00917 0.268
DOC_USP7_MATH_1 506 510 PF00917 0.448
DOC_USP7_MATH_1 672 676 PF00917 0.410
DOC_USP7_MATH_1 737 741 PF00917 0.466
DOC_USP7_MATH_1 808 812 PF00917 0.351
DOC_USP7_MATH_1 88 92 PF00917 0.541
DOC_WW_Pin1_4 259 264 PF00397 0.586
DOC_WW_Pin1_4 421 426 PF00397 0.470
DOC_WW_Pin1_4 542 547 PF00397 0.404
DOC_WW_Pin1_4 629 634 PF00397 0.422
DOC_WW_Pin1_4 730 735 PF00397 0.558
DOC_WW_Pin1_4 768 773 PF00397 0.540
DOC_WW_Pin1_4 79 84 PF00397 0.497
DOC_WW_Pin1_4 826 831 PF00397 0.411
LIG_14-3-3_CanoR_1 142 146 PF00244 0.496
LIG_14-3-3_CanoR_1 162 172 PF00244 0.379
LIG_14-3-3_CanoR_1 298 304 PF00244 0.358
LIG_14-3-3_CanoR_1 38 43 PF00244 0.663
LIG_14-3-3_CanoR_1 528 536 PF00244 0.421
LIG_14-3-3_CanoR_1 539 544 PF00244 0.402
LIG_14-3-3_CanoR_1 628 633 PF00244 0.416
LIG_14-3-3_CanoR_1 637 647 PF00244 0.395
LIG_14-3-3_CanoR_1 783 791 PF00244 0.265
LIG_Actin_RPEL_3 749 768 PF02755 0.468
LIG_AP2alpha_2 105 107 PF02296 0.464
LIG_AP2alpha_2 724 726 PF02296 0.457
LIG_BIR_III_4 426 430 PF00653 0.516
LIG_BRCT_BRCA1_1 196 200 PF00533 0.484
LIG_BRCT_BRCA1_1 461 465 PF00533 0.312
LIG_BRCT_BRCA1_1 674 678 PF00533 0.397
LIG_deltaCOP1_diTrp_1 294 303 PF00928 0.428
LIG_EH1_1 64 72 PF00400 0.239
LIG_eIF4E_1 648 654 PF01652 0.358
LIG_FHA_1 305 311 PF00498 0.385
LIG_FHA_1 417 423 PF00498 0.522
LIG_FHA_1 46 52 PF00498 0.636
LIG_FHA_1 59 65 PF00498 0.227
LIG_FHA_1 630 636 PF00498 0.523
LIG_FHA_1 744 750 PF00498 0.417
LIG_FHA_1 783 789 PF00498 0.288
LIG_FHA_1 853 859 PF00498 0.333
LIG_FHA_2 134 140 PF00498 0.443
LIG_FHA_2 166 172 PF00498 0.508
LIG_FHA_2 226 232 PF00498 0.459
LIG_FHA_2 365 371 PF00498 0.529
LIG_FHA_2 530 536 PF00498 0.553
LIG_FHA_2 578 584 PF00498 0.459
LIG_FHA_2 586 592 PF00498 0.332
LIG_FHA_2 782 788 PF00498 0.406
LIG_FHA_2 80 86 PF00498 0.496
LIG_FHA_2 870 876 PF00498 0.324
LIG_FHA_2 882 888 PF00498 0.226
LIG_FHA_2 893 899 PF00498 0.319
LIG_LIR_Apic_2 197 203 PF02991 0.495
LIG_LIR_Gen_1 193 203 PF02991 0.486
LIG_LIR_Gen_1 21 32 PF02991 0.618
LIG_LIR_Gen_1 300 311 PF02991 0.345
LIG_LIR_Gen_1 462 473 PF02991 0.312
LIG_LIR_Gen_1 646 656 PF02991 0.319
LIG_LIR_Gen_1 724 734 PF02991 0.464
LIG_LIR_Gen_1 792 800 PF02991 0.304
LIG_LIR_Nem_3 136 140 PF02991 0.445
LIG_LIR_Nem_3 193 198 PF02991 0.450
LIG_LIR_Nem_3 21 27 PF02991 0.617
LIG_LIR_Nem_3 300 306 PF02991 0.345
LIG_LIR_Nem_3 462 468 PF02991 0.277
LIG_LIR_Nem_3 646 651 PF02991 0.333
LIG_LIR_Nem_3 652 657 PF02991 0.295
LIG_LIR_Nem_3 724 729 PF02991 0.474
LIG_LIR_Nem_3 765 769 PF02991 0.407
LIG_LIR_Nem_3 792 797 PF02991 0.304
LIG_MAD2 857 865 PF02301 0.268
LIG_MLH1_MIPbox_1 461 465 PF16413 0.312
LIG_MYND_1 259 263 PF01753 0.522
LIG_NRBOX 539 545 PF00104 0.398
LIG_NRBOX 65 71 PF00104 0.320
LIG_NRBOX 887 893 PF00104 0.312
LIG_Pex14_1 460 464 PF04695 0.312
LIG_Pex14_2 790 794 PF04695 0.288
LIG_Pex14_2 866 870 PF04695 0.268
LIG_PTB_Apo_2 321 328 PF02174 0.391
LIG_Rb_pABgroove_1 651 659 PF01858 0.295
LIG_REV1ctd_RIR_1 554 559 PF16727 0.420
LIG_SH2_CRK 679 683 PF00017 0.344
LIG_SH2_CRK 769 773 PF00017 0.398
LIG_SH2_GRB2like 818 821 PF00017 0.296
LIG_SH2_NCK_1 648 652 PF00017 0.365
LIG_SH2_NCK_1 708 712 PF00017 0.359
LIG_SH2_SRC 708 711 PF00017 0.359
LIG_SH2_STAP1 745 749 PF00017 0.444
LIG_SH2_STAT3 671 674 PF00017 0.386
LIG_SH2_STAT5 391 394 PF00017 0.397
LIG_SH2_STAT5 464 467 PF00017 0.392
LIG_SH2_STAT5 555 558 PF00017 0.370
LIG_SH2_STAT5 745 748 PF00017 0.568
LIG_SH2_STAT5 818 821 PF00017 0.312
LIG_SH3_1 30 36 PF00018 0.560
LIG_SH3_2 33 38 PF14604 0.572
LIG_SH3_3 100 106 PF00018 0.469
LIG_SH3_3 253 259 PF00018 0.533
LIG_SH3_3 274 280 PF00018 0.474
LIG_SH3_3 30 36 PF00018 0.560
LIG_SH3_3 402 408 PF00018 0.502
LIG_SH3_3 419 425 PF00018 0.414
LIG_SH3_3 430 436 PF00018 0.462
LIG_SH3_3 80 86 PF00018 0.503
LIG_SH3_3 92 98 PF00018 0.439
LIG_SUMO_SIM_anti_2 113 118 PF11976 0.450
LIG_SUMO_SIM_par_1 774 780 PF11976 0.433
LIG_SUMO_SIM_par_1 894 901 PF11976 0.371
LIG_TRAF2_1 831 834 PF00917 0.296
LIG_TRAF2_2 830 835 PF00917 0.288
LIG_TYR_ITIM 677 682 PF00017 0.409
LIG_UBA3_1 483 488 PF00899 0.302
LIG_UBA3_1 69 76 PF00899 0.421
LIG_UBA3_1 861 868 PF00899 0.262
MOD_CDK_SPK_2 259 264 PF00069 0.657
MOD_CDK_SPxxK_3 259 266 PF00069 0.613
MOD_CDK_SPxxK_3 421 428 PF00069 0.651
MOD_CK1_1 542 548 PF00069 0.548
MOD_CK1_1 631 637 PF00069 0.565
MOD_CK1_1 638 644 PF00069 0.528
MOD_CK1_1 698 704 PF00069 0.492
MOD_CK1_1 755 761 PF00069 0.498
MOD_CK1_1 77 83 PF00069 0.605
MOD_CK1_1 869 875 PF00069 0.363
MOD_CK2_1 133 139 PF00069 0.611
MOD_CK2_1 152 158 PF00069 0.423
MOD_CK2_1 315 321 PF00069 0.509
MOD_CK2_1 529 535 PF00069 0.527
MOD_CK2_1 577 583 PF00069 0.587
MOD_CK2_1 680 686 PF00069 0.439
MOD_CK2_1 730 736 PF00069 0.536
MOD_CK2_1 768 774 PF00069 0.506
MOD_CK2_1 79 85 PF00069 0.618
MOD_CK2_1 828 834 PF00069 0.341
MOD_CK2_1 892 898 PF00069 0.371
MOD_CK2_1 901 907 PF00069 0.489
MOD_CMANNOS 589 592 PF00535 0.405
MOD_Cter_Amidation 11 14 PF01082 0.548
MOD_Cter_Amidation 159 162 PF01082 0.577
MOD_Cter_Amidation 242 245 PF01082 0.636
MOD_DYRK1A_RPxSP_1 79 83 PF00069 0.562
MOD_GlcNHglycan 165 168 PF01048 0.673
MOD_GlcNHglycan 20 23 PF01048 0.491
MOD_GlcNHglycan 343 346 PF01048 0.589
MOD_GlcNHglycan 438 441 PF01048 0.667
MOD_GlcNHglycan 475 478 PF01048 0.302
MOD_GlcNHglycan 507 511 PF01048 0.588
MOD_GlcNHglycan 515 519 PF01048 0.536
MOD_GlcNHglycan 613 616 PF01048 0.472
MOD_GlcNHglycan 674 677 PF01048 0.429
MOD_GlcNHglycan 697 700 PF01048 0.557
MOD_GSK3_1 341 348 PF00069 0.587
MOD_GSK3_1 38 45 PF00069 0.567
MOD_GSK3_1 631 638 PF00069 0.500
MOD_GSK3_1 643 650 PF00069 0.432
MOD_GSK3_1 694 701 PF00069 0.497
MOD_GSK3_1 758 765 PF00069 0.580
MOD_GSK3_1 777 784 PF00069 0.272
MOD_N-GLC_1 304 309 PF02516 0.399
MOD_N-GLC_1 528 533 PF02516 0.591
MOD_N-GLC_1 752 757 PF02516 0.595
MOD_N-GLC_1 77 82 PF02516 0.527
MOD_N-GLC_1 875 880 PF02516 0.239
MOD_NEK2_1 194 199 PF00069 0.629
MOD_NEK2_1 23 28 PF00069 0.429
MOD_NEK2_1 483 488 PF00069 0.334
MOD_NEK2_1 500 505 PF00069 0.520
MOD_NEK2_1 523 528 PF00069 0.525
MOD_NEK2_1 59 64 PF00069 0.306
MOD_NEK2_1 694 699 PF00069 0.507
MOD_NEK2_1 891 896 PF00069 0.374
MOD_NEK2_2 663 668 PF00069 0.389
MOD_PIKK_1 389 395 PF00454 0.575
MOD_PIKK_1 444 450 PF00454 0.591
MOD_PIKK_1 670 676 PF00454 0.447
MOD_PIKK_1 680 686 PF00454 0.411
MOD_PIKK_1 828 834 PF00454 0.329
MOD_PIKK_1 852 858 PF00454 0.302
MOD_PK_1 38 44 PF00069 0.524
MOD_PK_1 559 565 PF00069 0.588
MOD_PKA_1 364 370 PF00069 0.671
MOD_PKA_2 133 139 PF00069 0.651
MOD_PKA_2 141 147 PF00069 0.545
MOD_PKA_2 297 303 PF00069 0.452
MOD_PKA_2 364 370 PF00069 0.633
MOD_PKA_2 638 644 PF00069 0.489
MOD_PKA_2 755 761 PF00069 0.523
MOD_PKA_2 782 788 PF00069 0.298
MOD_PKB_1 537 545 PF00069 0.552
MOD_Plk_1 616 622 PF00069 0.375
MOD_Plk_1 709 715 PF00069 0.614
MOD_Plk_1 809 815 PF00069 0.329
MOD_Plk_2-3 585 591 PF00069 0.465
MOD_Plk_4 133 139 PF00069 0.549
MOD_Plk_4 152 158 PF00069 0.533
MOD_Plk_4 23 29 PF00069 0.433
MOD_Plk_4 386 392 PF00069 0.555
MOD_Plk_4 539 545 PF00069 0.546
MOD_Plk_4 59 65 PF00069 0.306
MOD_Plk_4 631 637 PF00069 0.581
MOD_Plk_4 643 649 PF00069 0.381
MOD_Plk_4 892 898 PF00069 0.371
MOD_ProDKin_1 259 265 PF00069 0.739
MOD_ProDKin_1 421 427 PF00069 0.583
MOD_ProDKin_1 542 548 PF00069 0.486
MOD_ProDKin_1 629 635 PF00069 0.529
MOD_ProDKin_1 730 736 PF00069 0.708
MOD_ProDKin_1 768 774 PF00069 0.686
MOD_ProDKin_1 79 85 PF00069 0.628
MOD_ProDKin_1 826 832 PF00069 0.502
MOD_SUMO_rev_2 370 375 PF00179 0.665
MOD_SUMO_rev_2 424 430 PF00179 0.614
TRG_DiLeu_BaEn_1 321 326 PF01217 0.468
TRG_DiLeu_BaEn_2 565 571 PF01217 0.509
TRG_DiLeu_BaLyEn_6 725 730 PF01217 0.586
TRG_DiLeu_BaLyEn_6 745 750 PF01217 0.406
TRG_ENDOCYTIC_2 137 140 PF00928 0.548
TRG_ENDOCYTIC_2 553 556 PF00928 0.516
TRG_ENDOCYTIC_2 648 651 PF00928 0.427
TRG_ENDOCYTIC_2 657 660 PF00928 0.289
TRG_ENDOCYTIC_2 679 682 PF00928 0.404
TRG_ENDOCYTIC_2 800 803 PF00928 0.380
TRG_ER_diArg_1 117 120 PF00400 0.548
TRG_ER_diArg_1 13 15 PF00400 0.560
TRG_ER_diArg_1 244 246 PF00400 0.650
TRG_ER_diArg_1 335 337 PF00400 0.506
TRG_ER_diArg_1 364 366 PF00400 0.678
TRG_ER_diArg_1 47 50 PF00400 0.508
TRG_ER_diArg_1 636 639 PF00400 0.587
TRG_ER_diArg_1 689 692 PF00400 0.528
TRG_ER_diArg_1 747 749 PF00400 0.586
TRG_ER_diArg_1 836 838 PF00400 0.302
TRG_ER_diArg_1 9 11 PF00400 0.600
TRG_NES_CRM1_1 645 658 PF08389 0.365
TRG_Pf-PMV_PEXEL_1 266 270 PF00026 0.594
TRG_Pf-PMV_PEXEL_1 623 627 PF00026 0.405

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1PBR2 Leptomonas seymouri 51% 99%
A0A3S7WP80 Leishmania donovani 95% 100%
A4H4D8 Leishmania braziliensis 80% 100%
A4HSL7 Leishmania infantum 95% 100%
E9AKK1 Leishmania mexicana (strain MHOM/GT/2001/U1103) 90% 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