LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase 5

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

Quick info

Protein:
Phosphoglycan beta 1,3 galactosyltransferase 5
Gene product:
phosphoglycan beta 1 -3 galactosyltransferase 5
Species:
Leishmania infantum
UniProt:
A4I7B5_LEIIN
TriTrypDb:
LINF_310039800 *
Length:
1130

Annotations

Annotations by Jardim et al.

Glycosylation, Phosphoglycan beta 1,3 galactosyltransferase 5 SCG5

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) yes yes: 2
Forrest at al. (procyclic) yes yes: 2
Silverman et al. no yes: 0
Pissara et al. yes yes: 12
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: 6
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 12
NetGPI no yes: 0, no: 12
Cellular components
Term Name Level Count
GO:0005737 cytoplasm 2 1
GO:0032838 plasma membrane bounded cell projection cytoplasm 4 1
GO:0097014 ciliary plasm 5 1
GO:0099568 cytoplasmic region 3 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A4I7B5
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4I7B5

Function

Biological processes
Term Name Level Count
GO:0006508 proteolysis 4 12
GO:0006807 nitrogen compound metabolic process 2 12
GO:0008152 metabolic process 1 12
GO:0019538 protein metabolic process 3 12
GO:0043170 macromolecule metabolic process 3 12
GO:0044238 primary metabolic process 2 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 12
GO:0004175 endopeptidase activity 4 12
GO:0004222 metalloendopeptidase activity 5 12
GO:0005488 binding 1 13
GO:0008233 peptidase activity 3 12
GO:0008237 metallopeptidase activity 4 12
GO:0016740 transferase activity 2 6
GO:0016757 glycosyltransferase activity 3 6
GO:0016787 hydrolase activity 2 12
GO:0043167 ion binding 2 13
GO:0043169 cation binding 3 13
GO:0046872 metal ion binding 4 13
GO:0140096 catalytic activity, acting on a protein 2 12

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 1099 1103 PF00656 0.667
CLV_C14_Caspase3-7 156 160 PF00656 0.497
CLV_C14_Caspase3-7 378 382 PF00656 0.408
CLV_C14_Caspase3-7 430 434 PF00656 0.576
CLV_NRD_NRD_1 1067 1069 PF00675 0.542
CLV_NRD_NRD_1 236 238 PF00675 0.642
CLV_NRD_NRD_1 631 633 PF00675 0.393
CLV_NRD_NRD_1 717 719 PF00675 0.543
CLV_PCSK_KEX2_1 1067 1069 PF00082 0.542
CLV_PCSK_KEX2_1 236 238 PF00082 0.648
CLV_PCSK_KEX2_1 359 361 PF00082 0.401
CLV_PCSK_KEX2_1 979 981 PF00082 0.533
CLV_PCSK_KEX2_1 998 1000 PF00082 0.479
CLV_PCSK_PC1ET2_1 359 361 PF00082 0.460
CLV_PCSK_PC1ET2_1 979 981 PF00082 0.503
CLV_PCSK_PC1ET2_1 998 1000 PF00082 0.283
CLV_PCSK_SKI1_1 392 396 PF00082 0.502
CLV_PCSK_SKI1_1 419 423 PF00082 0.566
CLV_PCSK_SKI1_1 426 430 PF00082 0.546
CLV_PCSK_SKI1_1 476 480 PF00082 0.554
CLV_PCSK_SKI1_1 642 646 PF00082 0.443
CLV_PCSK_SKI1_1 761 765 PF00082 0.501
CLV_PCSK_SKI1_1 815 819 PF00082 0.559
CLV_PCSK_SKI1_1 915 919 PF00082 0.506
DEG_APCC_DBOX_1 1067 1075 PF00400 0.623
DEG_APCC_DBOX_1 391 399 PF00400 0.502
DEG_APCC_DBOX_1 914 922 PF00400 0.479
DOC_CKS1_1 477 482 PF01111 0.469
DOC_CKS1_1 58 63 PF01111 0.444
DOC_CYCLIN_yCln2_LP_2 101 107 PF00134 0.495
DOC_CYCLIN_yCln2_LP_2 549 555 PF00134 0.584
DOC_CYCLIN_yCln2_LP_2 829 835 PF00134 0.567
DOC_MAPK_gen_1 419 429 PF00069 0.509
DOC_MAPK_gen_1 718 725 PF00069 0.537
DOC_MIT_MIM_1 816 825 PF04212 0.359
DOC_PP1_RVXF_1 166 173 PF00149 0.372
DOC_PP1_RVXF_1 319 325 PF00149 0.388
DOC_PP1_RVXF_1 424 430 PF00149 0.504
DOC_PP1_RVXF_1 952 959 PF00149 0.392
DOC_PP2B_LxvP_1 1095 1098 PF13499 0.544
DOC_PP2B_LxvP_1 549 552 PF13499 0.605
DOC_PP2B_LxvP_1 595 598 PF13499 0.397
DOC_PP2B_LxvP_1 829 832 PF13499 0.482
DOC_PP2B_LxvP_1 866 869 PF13499 0.566
DOC_PP4_FxxP_1 173 176 PF00568 0.372
DOC_PP4_FxxP_1 212 215 PF00568 0.460
DOC_USP7_MATH_1 1070 1074 PF00917 0.611
DOC_USP7_MATH_1 174 178 PF00917 0.455
DOC_USP7_MATH_1 189 193 PF00917 0.262
DOC_USP7_MATH_1 21 25 PF00917 0.576
DOC_USP7_MATH_1 304 308 PF00917 0.460
DOC_USP7_MATH_1 50 54 PF00917 0.534
DOC_USP7_MATH_1 507 511 PF00917 0.730
DOC_USP7_MATH_1 537 541 PF00917 0.783
DOC_USP7_MATH_1 596 600 PF00917 0.523
DOC_USP7_MATH_1 652 656 PF00917 0.425
DOC_USP7_MATH_1 776 780 PF00917 0.472
DOC_USP7_MATH_1 855 859 PF00917 0.581
DOC_USP7_MATH_1 924 928 PF00917 0.571
DOC_WW_Pin1_4 172 177 PF00397 0.503
DOC_WW_Pin1_4 325 330 PF00397 0.474
DOC_WW_Pin1_4 333 338 PF00397 0.439
DOC_WW_Pin1_4 433 438 PF00397 0.387
DOC_WW_Pin1_4 476 481 PF00397 0.481
DOC_WW_Pin1_4 498 503 PF00397 0.689
DOC_WW_Pin1_4 57 62 PF00397 0.455
DOC_WW_Pin1_4 621 626 PF00397 0.450
DOC_WW_Pin1_4 648 653 PF00397 0.397
DOC_WW_Pin1_4 654 659 PF00397 0.397
DOC_WW_Pin1_4 691 696 PF00397 0.303
DOC_WW_Pin1_4 887 892 PF00397 0.456
LIG_14-3-3_CanoR_1 22 28 PF00244 0.591
LIG_14-3-3_CanoR_1 289 293 PF00244 0.474
LIG_14-3-3_CanoR_1 327 337 PF00244 0.475
LIG_14-3-3_CanoR_1 582 587 PF00244 0.464
LIG_14-3-3_CanoR_1 718 724 PF00244 0.485
LIG_14-3-3_CanoR_1 765 769 PF00244 0.530
LIG_Actin_WH2_2 381 398 PF00022 0.480
LIG_Actin_WH2_2 822 838 PF00022 0.612
LIG_BIR_II_1 1 5 PF00653 0.576
LIG_BIR_III_3 1 5 PF00653 0.576
LIG_BIR_III_4 1083 1087 PF00653 0.721
LIG_BRCT_BRCA1_1 174 178 PF00533 0.390
LIG_BRCT_BRCA1_1 904 908 PF00533 0.424
LIG_CtBP_PxDLS_1 592 596 PF00389 0.502
LIG_EH_1 600 604 PF12763 0.397
LIG_eIF4E_1 793 799 PF01652 0.534
LIG_FAT_LD_1 822 830 PF03623 0.551
LIG_FHA_1 1090 1096 PF00498 0.721
LIG_FHA_1 13 19 PF00498 0.462
LIG_FHA_1 257 263 PF00498 0.474
LIG_FHA_1 349 355 PF00498 0.448
LIG_FHA_1 362 368 PF00498 0.332
LIG_FHA_1 383 389 PF00498 0.530
LIG_FHA_1 570 576 PF00498 0.475
LIG_FHA_1 58 64 PF00498 0.458
LIG_FHA_1 686 692 PF00498 0.451
LIG_FHA_1 765 771 PF00498 0.530
LIG_FHA_1 826 832 PF00498 0.574
LIG_FHA_1 888 894 PF00498 0.446
LIG_FHA_2 1022 1028 PF00498 0.550
LIG_FHA_2 1097 1103 PF00498 0.619
LIG_FHA_2 227 233 PF00498 0.488
LIG_FHA_2 449 455 PF00498 0.532
LIG_FHA_2 499 505 PF00498 0.748
LIG_FHA_2 528 534 PF00498 0.872
LIG_FHA_2 727 733 PF00498 0.464
LIG_GBD_Chelix_1 818 826 PF00786 0.386
LIG_LIR_Apic_2 171 176 PF02991 0.372
LIG_LIR_Apic_2 211 215 PF02991 0.477
LIG_LIR_Gen_1 1001 1010 PF02991 0.565
LIG_LIR_Gen_1 128 138 PF02991 0.460
LIG_LIR_Gen_1 167 176 PF02991 0.372
LIG_LIR_Gen_1 27 34 PF02991 0.585
LIG_LIR_Gen_1 307 314 PF02991 0.461
LIG_LIR_Gen_1 374 384 PF02991 0.466
LIG_LIR_Gen_1 545 555 PF02991 0.472
LIG_LIR_Gen_1 580 591 PF02991 0.390
LIG_LIR_Gen_1 711 721 PF02991 0.416
LIG_LIR_Gen_1 784 794 PF02991 0.580
LIG_LIR_Gen_1 862 870 PF02991 0.551
LIG_LIR_Gen_1 906 917 PF02991 0.440
LIG_LIR_Nem_3 1001 1007 PF02991 0.554
LIG_LIR_Nem_3 128 134 PF02991 0.372
LIG_LIR_Nem_3 151 157 PF02991 0.372
LIG_LIR_Nem_3 167 172 PF02991 0.372
LIG_LIR_Nem_3 200 205 PF02991 0.432
LIG_LIR_Nem_3 27 31 PF02991 0.587
LIG_LIR_Nem_3 307 311 PF02991 0.461
LIG_LIR_Nem_3 374 380 PF02991 0.468
LIG_LIR_Nem_3 399 405 PF02991 0.368
LIG_LIR_Nem_3 545 551 PF02991 0.479
LIG_LIR_Nem_3 580 586 PF02991 0.390
LIG_LIR_Nem_3 606 611 PF02991 0.373
LIG_LIR_Nem_3 711 717 PF02991 0.405
LIG_LIR_Nem_3 731 736 PF02991 0.198
LIG_LIR_Nem_3 767 771 PF02991 0.357
LIG_LIR_Nem_3 782 786 PF02991 0.542
LIG_LIR_Nem_3 862 866 PF02991 0.472
LIG_LIR_Nem_3 905 911 PF02991 0.436
LIG_MLH1_MIPbox_1 905 909 PF16413 0.435
LIG_NRBOX 821 827 PF00104 0.395
LIG_PCNA_yPIPBox_3 1009 1021 PF02747 0.492
LIG_Pex14_2 169 173 PF04695 0.372
LIG_PTB_Apo_2 1031 1038 PF02174 0.358
LIG_REV1ctd_RIR_1 1034 1044 PF16727 0.512
LIG_RPA_C_Fungi 1035 1047 PF08784 0.581
LIG_SH2_CRK 402 406 PF00017 0.397
LIG_SH2_CRK 570 574 PF00017 0.530
LIG_SH2_CRK 663 667 PF00017 0.383
LIG_SH2_CRK 681 685 PF00017 0.382
LIG_SH2_CRK 753 757 PF00017 0.502
LIG_SH2_PTP2 1004 1007 PF00017 0.371
LIG_SH2_SRC 1118 1121 PF00017 0.559
LIG_SH2_SRC 793 796 PF00017 0.543
LIG_SH2_STAP1 1112 1116 PF00017 0.606
LIG_SH2_STAP1 663 667 PF00017 0.416
LIG_SH2_STAP1 681 685 PF00017 0.311
LIG_SH2_STAP1 710 714 PF00017 0.500
LIG_SH2_STAP1 733 737 PF00017 0.423
LIG_SH2_STAT3 474 477 PF00017 0.483
LIG_SH2_STAT5 1004 1007 PF00017 0.508
LIG_SH2_STAT5 1035 1038 PF00017 0.484
LIG_SH2_STAT5 154 157 PF00017 0.474
LIG_SH2_STAT5 253 256 PF00017 0.372
LIG_SH2_STAT5 340 343 PF00017 0.388
LIG_SH2_STAT5 474 477 PF00017 0.523
LIG_SH2_STAT5 630 633 PF00017 0.453
LIG_SH2_STAT5 663 666 PF00017 0.432
LIG_SH2_STAT5 71 74 PF00017 0.480
LIG_SH2_STAT5 736 739 PF00017 0.448
LIG_SH2_STAT5 769 772 PF00017 0.412
LIG_SH2_STAT5 786 789 PF00017 0.447
LIG_SH2_STAT5 793 796 PF00017 0.384
LIG_SH2_STAT5 920 923 PF00017 0.436
LIG_SH2_STAT5 930 933 PF00017 0.407
LIG_SH2_STAT5 950 953 PF00017 0.301
LIG_SH3_3 102 108 PF00018 0.485
LIG_SH3_3 1066 1072 PF00018 0.514
LIG_SH3_3 2 8 PF00018 0.506
LIG_SH3_3 212 218 PF00018 0.360
LIG_SH3_3 323 329 PF00018 0.425
LIG_SH3_3 570 576 PF00018 0.490
LIG_SH3_3 587 593 PF00018 0.280
LIG_SH3_3 646 652 PF00018 0.502
LIG_SH3_3 699 705 PF00018 0.404
LIG_SH3_3 867 873 PF00018 0.545
LIG_SUMO_SIM_anti_2 259 264 PF11976 0.465
LIG_SUMO_SIM_anti_2 269 276 PF11976 0.470
LIG_SUMO_SIM_par_1 1019 1024 PF11976 0.491
LIG_SUMO_SIM_par_1 1089 1099 PF11976 0.740
LIG_SUMO_SIM_par_1 258 264 PF11976 0.479
LIG_SUMO_SIM_par_1 269 276 PF11976 0.425
LIG_SUMO_SIM_par_1 383 389 PF11976 0.467
LIG_SUMO_SIM_par_1 807 813 PF11976 0.286
LIG_TRAF2_1 1076 1079 PF00917 0.758
LIG_TRAF2_1 525 528 PF00917 0.796
LIG_TRAF2_1 530 533 PF00917 0.811
LIG_TRAF2_1 543 546 PF00917 0.659
LIG_TRAF2_1 614 617 PF00917 0.460
LIG_TRAF2_1 729 732 PF00917 0.530
LIG_TRAF2_1 971 974 PF00917 0.587
LIG_TYR_ITIM 152 157 PF00017 0.460
LIG_TYR_ITIM 400 405 PF00017 0.416
LIG_UBA3_1 117 124 PF00899 0.388
LIG_UBA3_1 982 988 PF00899 0.579
LIG_WRC_WIRS_1 1097 1102 PF05994 0.652
LIG_WRC_WIRS_1 11 16 PF05994 0.486
LIG_WRC_WIRS_1 131 136 PF05994 0.460
LIG_WRC_WIRS_1 245 250 PF05994 0.485
LIG_WRC_WIRS_1 786 791 PF05994 0.536
LIG_WRC_WIRS_1 860 865 PF05994 0.579
MOD_CDK_SPK_2 887 892 PF00069 0.589
MOD_CDK_SPxxK_3 654 661 PF00069 0.439
MOD_CK1_1 1073 1079 PF00069 0.699
MOD_CK1_1 1089 1095 PF00069 0.731
MOD_CK1_1 1101 1107 PF00069 0.526
MOD_CK1_1 1111 1117 PF00069 0.567
MOD_CK1_1 133 139 PF00069 0.460
MOD_CK1_1 158 164 PF00069 0.545
MOD_CK1_1 24 30 PF00069 0.540
MOD_CK1_1 244 250 PF00069 0.366
MOD_CK1_1 264 270 PF00069 0.240
MOD_CK1_1 328 334 PF00069 0.398
MOD_CK1_1 540 546 PF00069 0.668
MOD_CK1_1 560 566 PF00069 0.524
MOD_CK1_1 585 591 PF00069 0.425
MOD_CK1_1 779 785 PF00069 0.549
MOD_CK2_1 1005 1011 PF00069 0.585
MOD_CK2_1 1073 1079 PF00069 0.764
MOD_CK2_1 1102 1108 PF00069 0.545
MOD_CK2_1 1111 1117 PF00069 0.447
MOD_CK2_1 189 195 PF00069 0.369
MOD_CK2_1 264 270 PF00069 0.487
MOD_CK2_1 288 294 PF00069 0.540
MOD_CK2_1 448 454 PF00069 0.523
MOD_CK2_1 498 504 PF00069 0.714
MOD_CK2_1 522 528 PF00069 0.818
MOD_CK2_1 540 546 PF00069 0.452
MOD_CK2_1 726 732 PF00069 0.476
MOD_CK2_1 957 963 PF00069 0.563
MOD_CK2_1 968 974 PF00069 0.413
MOD_GlcNHglycan 1113 1116 PF01048 0.613
MOD_GlcNHglycan 138 141 PF01048 0.497
MOD_GlcNHglycan 266 269 PF01048 0.366
MOD_GlcNHglycan 301 304 PF01048 0.452
MOD_GlcNHglycan 330 333 PF01048 0.421
MOD_GlcNHglycan 337 340 PF01048 0.402
MOD_GlcNHglycan 524 527 PF01048 0.848
MOD_GlcNHglycan 542 545 PF01048 0.453
MOD_GlcNHglycan 587 590 PF01048 0.493
MOD_GlcNHglycan 654 657 PF01048 0.425
MOD_GlcNHglycan 68 71 PF01048 0.438
MOD_GlcNHglycan 778 781 PF01048 0.545
MOD_GlcNHglycan 795 798 PF01048 0.448
MOD_GlcNHglycan 940 943 PF01048 0.431
MOD_GlcNHglycan 959 962 PF01048 0.403
MOD_GlcNHglycan 970 973 PF01048 0.508
MOD_GSK3_1 1005 1012 PF00069 0.605
MOD_GSK3_1 1089 1096 PF00069 0.734
MOD_GSK3_1 1098 1105 PF00069 0.527
MOD_GSK3_1 1107 1114 PF00069 0.412
MOD_GSK3_1 12 19 PF00069 0.506
MOD_GSK3_1 139 146 PF00069 0.394
MOD_GSK3_1 172 179 PF00069 0.359
MOD_GSK3_1 20 27 PF00069 0.547
MOD_GSK3_1 306 313 PF00069 0.444
MOD_GSK3_1 328 335 PF00069 0.424
MOD_GSK3_1 380 387 PF00069 0.470
MOD_GSK3_1 527 534 PF00069 0.881
MOD_GSK3_1 648 655 PF00069 0.451
MOD_GSK3_1 669 676 PF00069 0.494
MOD_GSK3_1 732 739 PF00069 0.451
MOD_GSK3_1 855 862 PF00069 0.627
MOD_GSK3_1 864 871 PF00069 0.562
MOD_N-GLC_1 1038 1043 PF02516 0.443
MOD_N-GLC_1 225 230 PF02516 0.466
MOD_N-GLC_1 448 453 PF02516 0.469
MOD_N-GLC_1 540 545 PF02516 0.727
MOD_N-GLC_1 560 565 PF02516 0.198
MOD_N-GLC_1 855 860 PF02516 0.653
MOD_N-GLC_2 439 441 PF02516 0.508
MOD_NEK2_1 12 17 PF00069 0.530
MOD_NEK2_1 299 304 PF00069 0.460
MOD_NEK2_1 367 372 PF00069 0.527
MOD_NEK2_1 380 385 PF00069 0.477
MOD_NEK2_1 40 45 PF00069 0.509
MOD_NEK2_1 547 552 PF00069 0.501
MOD_NEK2_1 569 574 PF00069 0.429
MOD_NEK2_1 683 688 PF00069 0.458
MOD_NEK2_1 756 761 PF00069 0.507
MOD_NEK2_1 825 830 PF00069 0.608
MOD_NEK2_1 835 840 PF00069 0.553
MOD_NEK2_1 896 901 PF00069 0.434
MOD_NEK2_1 903 908 PF00069 0.394
MOD_NEK2_1 923 928 PF00069 0.244
MOD_PIKK_1 29 35 PF00454 0.582
MOD_PIKK_1 520 526 PF00454 0.785
MOD_PIKK_1 703 709 PF00454 0.473
MOD_PIKK_1 756 762 PF00454 0.474
MOD_PKA_1 761 767 PF00069 0.425
MOD_PKA_2 21 27 PF00069 0.580
MOD_PKA_2 241 247 PF00069 0.338
MOD_PKA_2 288 294 PF00069 0.509
MOD_PKA_2 557 563 PF00069 0.495
MOD_PKA_2 764 770 PF00069 0.514
MOD_PKA_2 842 848 PF00069 0.506
MOD_Plk_1 1107 1113 PF00069 0.545
MOD_Plk_1 225 231 PF00069 0.517
MOD_Plk_1 349 355 PF00069 0.388
MOD_Plk_1 380 386 PF00069 0.391
MOD_Plk_1 560 566 PF00069 0.435
MOD_Plk_1 606 612 PF00069 0.382
MOD_Plk_1 855 861 PF00069 0.643
MOD_Plk_1 924 930 PF00069 0.432
MOD_Plk_2-3 270 276 PF00069 0.390
MOD_Plk_2-3 732 738 PF00069 0.513
MOD_Plk_4 130 136 PF00069 0.425
MOD_Plk_4 148 154 PF00069 0.252
MOD_Plk_4 256 262 PF00069 0.431
MOD_Plk_4 270 276 PF00069 0.373
MOD_Plk_4 349 355 PF00069 0.400
MOD_Plk_4 582 588 PF00069 0.513
MOD_Plk_4 626 632 PF00069 0.390
MOD_Plk_4 732 738 PF00069 0.455
MOD_Plk_4 764 770 PF00069 0.425
MOD_Plk_4 785 791 PF00069 0.537
MOD_Plk_4 855 861 PF00069 0.617
MOD_Plk_4 904 910 PF00069 0.440
MOD_ProDKin_1 172 178 PF00069 0.503
MOD_ProDKin_1 325 331 PF00069 0.474
MOD_ProDKin_1 333 339 PF00069 0.439
MOD_ProDKin_1 433 439 PF00069 0.392
MOD_ProDKin_1 476 482 PF00069 0.478
MOD_ProDKin_1 498 504 PF00069 0.698
MOD_ProDKin_1 57 63 PF00069 0.452
MOD_ProDKin_1 621 627 PF00069 0.450
MOD_ProDKin_1 648 654 PF00069 0.397
MOD_ProDKin_1 691 697 PF00069 0.303
MOD_ProDKin_1 887 893 PF00069 0.455
MOD_SUMO_for_1 421 424 PF00179 0.478
MOD_SUMO_rev_2 1026 1030 PF00179 0.528
MOD_SUMO_rev_2 991 1000 PF00179 0.374
TRG_DiLeu_BaEn_1 270 275 PF01217 0.497
TRG_DiLeu_BaEn_1 795 800 PF01217 0.537
TRG_DiLeu_BaEn_2 114 120 PF01217 0.388
TRG_DiLeu_BaEn_2 129 135 PF01217 0.388
TRG_ENDOCYTIC_2 1004 1007 PF00928 0.549
TRG_ENDOCYTIC_2 154 157 PF00928 0.372
TRG_ENDOCYTIC_2 202 205 PF00928 0.460
TRG_ENDOCYTIC_2 402 405 PF00928 0.397
TRG_ENDOCYTIC_2 418 421 PF00928 0.459
TRG_ENDOCYTIC_2 570 573 PF00928 0.502
TRG_ENDOCYTIC_2 663 666 PF00928 0.381
TRG_ENDOCYTIC_2 680 683 PF00928 0.303
TRG_ENDOCYTIC_2 710 713 PF00928 0.500
TRG_ENDOCYTIC_2 753 756 PF00928 0.464
TRG_ENDOCYTIC_2 768 771 PF00928 0.391
TRG_ENDOCYTIC_2 786 789 PF00928 0.412
TRG_ENDOCYTIC_2 920 923 PF00928 0.470
TRG_ER_diArg_1 1067 1069 PF00400 0.541
TRG_ER_diArg_1 1074 1077 PF00400 0.591
TRG_ER_diArg_1 218 221 PF00400 0.506
TRG_ER_diArg_1 840 843 PF00400 0.621
TRG_ER_diArg_1 912 915 PF00400 0.475
TRG_Pf-PMV_PEXEL_1 476 481 PF00026 0.555
TRG_Pf-PMV_PEXEL_1 567 571 PF00026 0.390
TRG_Pf-PMV_PEXEL_1 754 758 PF00026 0.507

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P423 Leptomonas seymouri 66% 100%
A0A0S4JGH1 Bodo saltans 34% 97%
A0A1X0NIF3 Trypanosomatidae 43% 100%
A0A3R7LVD3 Trypanosoma rangeli 44% 100%
A0A3S7X521 Leishmania donovani 100% 100%
A4HJU8 Leishmania braziliensis 80% 100%
A4HJV3 Leishmania braziliensis 83% 100%
C9ZWJ2 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 44% 100%
E9B2A8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 92% 100%
F4HNU6 Arabidopsis thaliana 27% 100%
Q4Q5U8 Leishmania major 93% 100%
V5BDV9 Trypanosoma cruzi 46% 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