LeishMANIAdb
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B30.2/SPRY domain-containing protein

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

Quick info

Protein:
B30.2/SPRY domain-containing protein
Gene product:
hypothetical protein - conserved
Species:
Leishmania infantum
UniProt:
A4HX50_LEIIN
TriTrypDb:
LINF_160021300
Length:
1150

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: 9
NetGPI no yes: 0, no: 9
Cellular components
Term Name Level Count
GO:0031298 replication fork protection complex 3 1
GO:0032991 protein-containing complex 1 1
GO:0140513 nuclear protein-containing complex 2 1

Expansion

Sequence features

A4HX50
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HX50

Function

Biological processes
Term Name Level Count
GO:0000075 cell cycle checkpoint signaling 4 1
GO:0000076 DNA replication checkpoint signaling 6 1
GO:0006139 nucleobase-containing compound metabolic process 3 1
GO:0006259 DNA metabolic process 4 1
GO:0006275 regulation of DNA replication 6 1
GO:0006281 DNA repair 5 1
GO:0006725 cellular aromatic compound metabolic process 3 1
GO:0006807 nitrogen compound metabolic process 2 1
GO:0006950 response to stress 2 1
GO:0006974 DNA damage response 4 1
GO:0007165 signal transduction 2 1
GO:0008152 metabolic process 1 1
GO:0008156 negative regulation of DNA replication 7 1
GO:0009892 negative regulation of metabolic process 4 1
GO:0009987 cellular process 1 1
GO:0010564 regulation of cell cycle process 5 1
GO:0010605 negative regulation of macromolecule metabolic process 5 1
GO:0010948 negative regulation of cell cycle process 6 1
GO:0019219 regulation of nucleobase-containing compound metabolic process 5 1
GO:0019222 regulation of metabolic process 3 1
GO:0031323 regulation of cellular metabolic process 4 1
GO:0031324 negative regulation of cellular metabolic process 5 1
GO:0031570 DNA integrity checkpoint signaling 5 1
GO:0033554 cellular response to stress 3 1
GO:0034641 cellular nitrogen compound metabolic process 3 1
GO:0035556 intracellular signal transduction 3 1
GO:0043111 replication fork arrest 6 1
GO:0043170 macromolecule metabolic process 3 1
GO:0044237 cellular metabolic process 2 1
GO:0044238 primary metabolic process 2 1
GO:0044260 obsolete cellular macromolecule metabolic process 3 1
GO:0045005 DNA-templated DNA replication maintenance of fidelity 5 1
GO:0045786 negative regulation of cell cycle 5 1
GO:0045934 negative regulation of nucleobase-containing compound metabolic process 6 1
GO:0046483 heterocycle metabolic process 3 1
GO:0048478 obsolete replication fork protection 6 1
GO:0048519 negative regulation of biological process 3 1
GO:0048523 negative regulation of cellular process 4 1
GO:0050789 regulation of biological process 2 1
GO:0050794 regulation of cellular process 3 1
GO:0050896 response to stimulus 1 1
GO:0051052 regulation of DNA metabolic process 5 1
GO:0051053 negative regulation of DNA metabolic process 6 1
GO:0051171 regulation of nitrogen compound metabolic process 4 1
GO:0051172 negative regulation of nitrogen compound metabolic process 5 1
GO:0051716 cellular response to stimulus 2 1
GO:0051726 regulation of cell cycle 4 1
GO:0060255 regulation of macromolecule metabolic process 4 1
GO:0065007 biological regulation 1 1
GO:0071704 organic substance metabolic process 2 1
GO:0080090 regulation of primary metabolic process 4 1
GO:0090304 nucleic acid metabolic process 4 1
GO:0090329 regulation of DNA-templated DNA replication 7 1
GO:1901360 organic cyclic compound metabolic process 3 1
GO:1901987 regulation of cell cycle phase transition 6 1
GO:1901988 negative regulation of cell cycle phase transition 7 1
GO:2000104 negative regulation of DNA-templated DNA replication 8 1
Molecular functions
Term Name Level Count
GO:0003676 nucleic acid binding 3 1
GO:0003677 DNA binding 4 1
GO:0005488 binding 1 1
GO:0097159 organic cyclic compound binding 2 1
GO:1901363 heterocyclic compound binding 2 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 1038 1042 PF00656 0.694
CLV_C14_Caspase3-7 1105 1109 PF00656 0.569
CLV_C14_Caspase3-7 728 732 PF00656 0.629
CLV_NRD_NRD_1 1025 1027 PF00675 0.597
CLV_NRD_NRD_1 1028 1030 PF00675 0.604
CLV_NRD_NRD_1 1077 1079 PF00675 0.715
CLV_NRD_NRD_1 1089 1091 PF00675 0.807
CLV_NRD_NRD_1 256 258 PF00675 0.520
CLV_NRD_NRD_1 429 431 PF00675 0.635
CLV_NRD_NRD_1 442 444 PF00675 0.452
CLV_NRD_NRD_1 604 606 PF00675 0.339
CLV_NRD_NRD_1 666 668 PF00675 0.424
CLV_NRD_NRD_1 671 673 PF00675 0.331
CLV_PCSK_FUR_1 1023 1027 PF00082 0.596
CLV_PCSK_KEX2_1 1003 1005 PF00082 0.608
CLV_PCSK_KEX2_1 1025 1027 PF00082 0.582
CLV_PCSK_KEX2_1 1028 1030 PF00082 0.587
CLV_PCSK_KEX2_1 1076 1078 PF00082 0.715
CLV_PCSK_KEX2_1 1087 1089 PF00082 0.752
CLV_PCSK_KEX2_1 176 178 PF00082 0.369
CLV_PCSK_KEX2_1 429 431 PF00082 0.651
CLV_PCSK_KEX2_1 444 446 PF00082 0.456
CLV_PCSK_KEX2_1 603 605 PF00082 0.329
CLV_PCSK_KEX2_1 666 668 PF00082 0.399
CLV_PCSK_KEX2_1 7 9 PF00082 0.433
CLV_PCSK_KEX2_1 701 703 PF00082 0.515
CLV_PCSK_KEX2_1 808 810 PF00082 0.537
CLV_PCSK_PC1ET2_1 1003 1005 PF00082 0.608
CLV_PCSK_PC1ET2_1 1076 1078 PF00082 0.715
CLV_PCSK_PC1ET2_1 1087 1089 PF00082 0.752
CLV_PCSK_PC1ET2_1 176 178 PF00082 0.369
CLV_PCSK_PC1ET2_1 444 446 PF00082 0.515
CLV_PCSK_PC1ET2_1 7 9 PF00082 0.433
CLV_PCSK_PC1ET2_1 701 703 PF00082 0.550
CLV_PCSK_PC1ET2_1 808 810 PF00082 0.537
CLV_PCSK_PC7_1 1073 1079 PF00082 0.586
CLV_PCSK_SKI1_1 1029 1033 PF00082 0.621
CLV_PCSK_SKI1_1 1055 1059 PF00082 0.761
CLV_PCSK_SKI1_1 147 151 PF00082 0.421
CLV_PCSK_SKI1_1 447 451 PF00082 0.492
CLV_PCSK_SKI1_1 546 550 PF00082 0.488
CLV_PCSK_SKI1_1 553 557 PF00082 0.524
CLV_PCSK_SKI1_1 594 598 PF00082 0.306
CLV_PCSK_SKI1_1 655 659 PF00082 0.387
CLV_PCSK_SKI1_1 8 12 PF00082 0.379
CLV_PCSK_SKI1_1 808 812 PF00082 0.757
CLV_PCSK_SKI1_1 824 828 PF00082 0.608
CLV_PCSK_SKI1_1 898 902 PF00082 0.368
CLV_PCSK_SKI1_1 965 969 PF00082 0.431
CLV_Separin_Metazoa 741 745 PF03568 0.556
DEG_APCC_DBOX_1 545 553 PF00400 0.417
DEG_APCC_DBOX_1 7 15 PF00400 0.410
DEG_APCC_DBOX_1 823 831 PF00400 0.651
DOC_AGCK_PIF_1 677 682 PF00069 0.408
DOC_CDC14_PxL_1 21 29 PF14671 0.327
DOC_CYCLIN_RxL_1 962 972 PF00134 0.443
DOC_CYCLIN_yCln2_LP_2 105 111 PF00134 0.425
DOC_MAPK_gen_1 560 570 PF00069 0.411
DOC_MAPK_gen_1 600 610 PF00069 0.405
DOC_MAPK_gen_1 7 14 PF00069 0.410
DOC_MAPK_MEF2A_6 104 111 PF00069 0.378
DOC_MAPK_MEF2A_6 127 136 PF00069 0.328
DOC_MAPK_MEF2A_6 184 192 PF00069 0.330
DOC_MAPK_MEF2A_6 217 225 PF00069 0.326
DOC_MAPK_MEF2A_6 264 273 PF00069 0.735
DOC_MAPK_MEF2A_6 603 612 PF00069 0.440
DOC_MAPK_MEF2A_6 7 14 PF00069 0.410
DOC_MAPK_MEF2A_6 934 943 PF00069 0.500
DOC_MAPK_NFAT4_5 7 15 PF00069 0.413
DOC_MAPK_RevD_3 163 177 PF00069 0.334
DOC_PP2B_LxvP_1 105 108 PF13499 0.422
DOC_PP2B_LxvP_1 134 137 PF13499 0.385
DOC_PP2B_LxvP_1 697 700 PF13499 0.501
DOC_PP4_FxxP_1 922 925 PF00568 0.358
DOC_USP7_MATH_1 241 245 PF00917 0.603
DOC_USP7_MATH_1 299 303 PF00917 0.543
DOC_USP7_MATH_1 338 342 PF00917 0.430
DOC_USP7_MATH_1 398 402 PF00917 0.528
DOC_USP7_MATH_1 499 503 PF00917 0.308
DOC_USP7_MATH_1 642 646 PF00917 0.351
DOC_USP7_MATH_1 700 704 PF00917 0.526
DOC_USP7_MATH_1 792 796 PF00917 0.510
DOC_USP7_UBL2_3 383 387 PF12436 0.555
DOC_USP7_UBL2_3 690 694 PF12436 0.424
DOC_USP7_UBL2_3 704 708 PF12436 0.516
DOC_WW_Pin1_4 1016 1021 PF00397 0.611
DOC_WW_Pin1_4 1056 1061 PF00397 0.561
DOC_WW_Pin1_4 361 366 PF00397 0.691
DOC_WW_Pin1_4 454 459 PF00397 0.522
DOC_WW_Pin1_4 522 527 PF00397 0.534
DOC_WW_Pin1_4 844 849 PF00397 0.477
LIG_14-3-3_CanoR_1 138 145 PF00244 0.438
LIG_14-3-3_CanoR_1 367 373 PF00244 0.603
LIG_14-3-3_CanoR_1 407 413 PF00244 0.593
LIG_14-3-3_CanoR_1 809 816 PF00244 0.567
LIG_14-3-3_CanoR_1 934 939 PF00244 0.567
LIG_Actin_WH2_2 535 552 PF00022 0.300
LIG_APCC_ABBAyCdc20_2 277 283 PF00400 0.582
LIG_BIR_II_1 1 5 PF00653 0.413
LIG_BIR_III_4 1103 1107 PF00653 0.535
LIG_BRCT_BRCA1_1 27 31 PF00533 0.384
LIG_BRCT_BRCA1_1 478 482 PF00533 0.438
LIG_BRCT_BRCA1_1 838 842 PF00533 0.469
LIG_BRCT_BRCA1_1 885 889 PF00533 0.476
LIG_Clathr_ClatBox_1 11 15 PF01394 0.408
LIG_deltaCOP1_diTrp_1 325 331 PF00928 0.368
LIG_deltaCOP1_diTrp_1 386 390 PF00928 0.528
LIG_deltaCOP1_diTrp_1 756 764 PF00928 0.574
LIG_EH1_1 218 226 PF00400 0.441
LIG_EH1_1 873 881 PF00400 0.429
LIG_eIF4E_1 614 620 PF01652 0.405
LIG_eIF4E_1 693 699 PF01652 0.443
LIG_FHA_1 1116 1122 PF00498 0.595
LIG_FHA_1 177 183 PF00498 0.522
LIG_FHA_1 196 202 PF00498 0.329
LIG_FHA_1 206 212 PF00498 0.486
LIG_FHA_1 264 270 PF00498 0.704
LIG_FHA_1 47 53 PF00498 0.424
LIG_FHA_1 518 524 PF00498 0.565
LIG_FHA_1 554 560 PF00498 0.380
LIG_FHA_1 679 685 PF00498 0.410
LIG_FHA_1 89 95 PF00498 0.410
LIG_FHA_1 962 968 PF00498 0.474
LIG_FHA_2 1114 1120 PF00498 0.623
LIG_FHA_2 176 182 PF00498 0.480
LIG_FHA_2 204 210 PF00498 0.331
LIG_FHA_2 65 71 PF00498 0.469
LIG_FHA_2 974 980 PF00498 0.482
LIG_IRF3_LxIS_1 14 20 PF10401 0.407
LIG_KLC1_Yacidic_2 974 979 PF13176 0.476
LIG_LIR_Apic_2 341 347 PF02991 0.395
LIG_LIR_Apic_2 921 925 PF02991 0.377
LIG_LIR_Gen_1 1005 1015 PF02991 0.708
LIG_LIR_Gen_1 1092 1099 PF02991 0.525
LIG_LIR_Gen_1 160 171 PF02991 0.329
LIG_LIR_Gen_1 421 428 PF02991 0.536
LIG_LIR_Gen_1 475 485 PF02991 0.353
LIG_LIR_Gen_1 489 498 PF02991 0.352
LIG_LIR_Gen_1 529 539 PF02991 0.400
LIG_LIR_Gen_1 565 571 PF02991 0.609
LIG_LIR_Gen_1 582 593 PF02991 0.344
LIG_LIR_Gen_1 681 688 PF02991 0.414
LIG_LIR_Gen_1 839 848 PF02991 0.474
LIG_LIR_Gen_1 852 863 PF02991 0.460
LIG_LIR_Gen_1 91 101 PF02991 0.392
LIG_LIR_Gen_1 972 983 PF02991 0.427
LIG_LIR_Gen_1 988 994 PF02991 0.525
LIG_LIR_LC3C_4 103 107 PF02991 0.434
LIG_LIR_LC3C_4 222 227 PF02991 0.380
LIG_LIR_LC3C_4 565 569 PF02991 0.365
LIG_LIR_Nem_3 1005 1010 PF02991 0.685
LIG_LIR_Nem_3 1092 1097 PF02991 0.527
LIG_LIR_Nem_3 159 165 PF02991 0.324
LIG_LIR_Nem_3 385 391 PF02991 0.475
LIG_LIR_Nem_3 421 426 PF02991 0.566
LIG_LIR_Nem_3 475 480 PF02991 0.338
LIG_LIR_Nem_3 489 493 PF02991 0.315
LIG_LIR_Nem_3 529 535 PF02991 0.477
LIG_LIR_Nem_3 565 569 PF02991 0.615
LIG_LIR_Nem_3 582 588 PF02991 0.299
LIG_LIR_Nem_3 681 685 PF02991 0.411
LIG_LIR_Nem_3 787 793 PF02991 0.676
LIG_LIR_Nem_3 839 845 PF02991 0.417
LIG_LIR_Nem_3 852 858 PF02991 0.386
LIG_LIR_Nem_3 885 891 PF02991 0.473
LIG_LIR_Nem_3 953 957 PF02991 0.397
LIG_LIR_Nem_3 972 978 PF02991 0.331
LIG_LIR_Nem_3 988 992 PF02991 0.520
LIG_MAD2 917 925 PF02301 0.467
LIG_MLH1_MIPbox_1 838 842 PF16413 0.469
LIG_MLH1_MIPbox_1 885 889 PF16413 0.405
LIG_NRBOX 124 130 PF00104 0.323
LIG_NRBOX 368 374 PF00104 0.592
LIG_NRBOX 621 627 PF00104 0.432
LIG_Pex14_1 760 764 PF04695 0.573
LIG_Pex14_2 566 570 PF04695 0.407
LIG_Pex14_2 889 893 PF04695 0.358
LIG_Pex14_2 923 927 PF04695 0.443
LIG_PTB_Apo_2 226 233 PF02174 0.332
LIG_PTB_Apo_2 887 894 PF02174 0.375
LIG_PTB_Apo_2 921 928 PF02174 0.393
LIG_PTB_Phospho_1 226 232 PF10480 0.325
LIG_REV1ctd_RIR_1 839 847 PF16727 0.413
LIG_SH2_CRK 1094 1098 PF00017 0.527
LIG_SH2_CRK 232 236 PF00017 0.436
LIG_SH2_CRK 532 536 PF00017 0.453
LIG_SH2_CRK 541 545 PF00017 0.405
LIG_SH2_CRK 855 859 PF00017 0.462
LIG_SH2_CRK 989 993 PF00017 0.564
LIG_SH2_GRB2like 532 535 PF00017 0.485
LIG_SH2_GRB2like 74 77 PF00017 0.665
LIG_SH2_NCK_1 1094 1098 PF00017 0.527
LIG_SH2_NCK_1 989 993 PF00017 0.564
LIG_SH2_PTP2 551 554 PF00017 0.359
LIG_SH2_PTP2 585 588 PF00017 0.247
LIG_SH2_STAP1 1094 1098 PF00017 0.527
LIG_SH2_STAP1 664 668 PF00017 0.453
LIG_SH2_STAT5 199 202 PF00017 0.440
LIG_SH2_STAT5 551 554 PF00017 0.376
LIG_SH2_STAT5 585 588 PF00017 0.357
LIG_SH2_STAT5 614 617 PF00017 0.286
LIG_SH2_STAT5 954 957 PF00017 0.513
LIG_SH2_STAT5 975 978 PF00017 0.542
LIG_SH2_STAT5 989 992 PF00017 0.628
LIG_SH3_3 1054 1060 PF00018 0.634
LIG_SH3_3 1129 1135 PF00018 0.617
LIG_SH3_3 520 526 PF00018 0.477
LIG_SH3_3 565 571 PF00018 0.452
LIG_SUMO_SIM_anti_2 185 191 PF11976 0.319
LIG_SUMO_SIM_anti_2 222 228 PF11976 0.434
LIG_SUMO_SIM_anti_2 483 489 PF11976 0.347
LIG_SUMO_SIM_anti_2 617 624 PF11976 0.346
LIG_SUMO_SIM_par_1 10 15 PF11976 0.402
LIG_SUMO_SIM_par_1 185 191 PF11976 0.343
LIG_SUMO_SIM_par_1 192 198 PF11976 0.327
LIG_SUMO_SIM_par_1 483 489 PF11976 0.407
LIG_SUMO_SIM_par_1 519 525 PF11976 0.529
LIG_SUMO_SIM_par_1 578 584 PF11976 0.340
LIG_SUMO_SIM_par_1 617 624 PF11976 0.324
LIG_TRAF2_1 347 350 PF00917 0.485
LIG_TYR_ITIM 539 544 PF00017 0.329
LIG_TYR_ITIM 549 554 PF00017 0.349
LIG_TYR_ITIM 583 588 PF00017 0.374
LIG_TYR_ITIM 853 858 PF00017 0.448
LIG_TYR_ITIM 973 978 PF00017 0.481
LIG_UBA3_1 121 127 PF00899 0.327
LIG_UBA3_1 149 154 PF00899 0.398
LIG_WRC_WIRS_1 477 482 PF05994 0.431
LIG_WRC_WIRS_1 487 492 PF05994 0.369
LIG_WRC_WIRS_1 593 598 PF05994 0.425
LIG_WRC_WIRS_1 679 684 PF05994 0.410
MOD_CDC14_SPxK_1 364 367 PF00782 0.512
MOD_CDK_SPK_2 454 459 PF00069 0.364
MOD_CDK_SPK_2 844 849 PF00069 0.477
MOD_CDK_SPxK_1 361 367 PF00069 0.515
MOD_CDK_SPxxK_3 1016 1023 PF00069 0.602
MOD_CK1_1 1016 1022 PF00069 0.702
MOD_CK1_1 244 250 PF00069 0.583
MOD_CK1_1 26 32 PF00069 0.385
MOD_CK1_1 267 273 PF00069 0.506
MOD_CK1_1 300 306 PF00069 0.566
MOD_CK1_1 361 367 PF00069 0.637
MOD_CK1_1 409 415 PF00069 0.697
MOD_CK1_1 486 492 PF00069 0.430
MOD_CK1_1 517 523 PF00069 0.525
MOD_CK1_1 662 668 PF00069 0.446
MOD_CK1_1 729 735 PF00069 0.680
MOD_CK1_1 767 773 PF00069 0.666
MOD_CK1_1 795 801 PF00069 0.505
MOD_CK1_1 818 824 PF00069 0.575
MOD_CK1_1 828 834 PF00069 0.489
MOD_CK2_1 1044 1050 PF00069 0.672
MOD_CK2_1 1113 1119 PF00069 0.680
MOD_CK2_1 1141 1147 PF00069 0.537
MOD_CK2_1 137 143 PF00069 0.428
MOD_CK2_1 175 181 PF00069 0.430
MOD_CK2_1 203 209 PF00069 0.411
MOD_CK2_1 243 249 PF00069 0.530
MOD_CK2_1 26 32 PF00069 0.422
MOD_CK2_1 64 70 PF00069 0.512
MOD_CK2_1 829 835 PF00069 0.475
MOD_CK2_1 86 92 PF00069 0.565
MOD_CK2_1 973 979 PF00069 0.449
MOD_Cter_Amidation 255 258 PF01082 0.518
MOD_GlcNHglycan 1 4 PF01048 0.588
MOD_GlcNHglycan 1032 1035 PF01048 0.772
MOD_GlcNHglycan 1101 1107 PF01048 0.756
MOD_GlcNHglycan 1110 1113 PF01048 0.672
MOD_GlcNHglycan 139 142 PF01048 0.395
MOD_GlcNHglycan 265 269 PF01048 0.704
MOD_GlcNHglycan 409 412 PF01048 0.654
MOD_GlcNHglycan 474 477 PF01048 0.333
MOD_GlcNHglycan 501 504 PF01048 0.377
MOD_GlcNHglycan 516 519 PF01048 0.435
MOD_GlcNHglycan 577 580 PF01048 0.483
MOD_GlcNHglycan 731 734 PF01048 0.675
MOD_GlcNHglycan 779 782 PF01048 0.696
MOD_GlcNHglycan 795 798 PF01048 0.515
MOD_GlcNHglycan 838 841 PF01048 0.567
MOD_GlcNHglycan 948 951 PF01048 0.502
MOD_GSK3_1 1030 1037 PF00069 0.798
MOD_GSK3_1 1040 1047 PF00069 0.645
MOD_GSK3_1 1102 1109 PF00069 0.678
MOD_GSK3_1 113 120 PF00069 0.301
MOD_GSK3_1 152 159 PF00069 0.550
MOD_GSK3_1 263 270 PF00069 0.617
MOD_GSK3_1 293 300 PF00069 0.579
MOD_GSK3_1 357 364 PF00069 0.575
MOD_GSK3_1 407 414 PF00069 0.733
MOD_GSK3_1 468 475 PF00069 0.559
MOD_GSK3_1 517 524 PF00069 0.485
MOD_GSK3_1 558 565 PF00069 0.483
MOD_GSK3_1 575 582 PF00069 0.270
MOD_GSK3_1 588 595 PF00069 0.292
MOD_GSK3_1 764 771 PF00069 0.668
MOD_GSK3_1 804 811 PF00069 0.636
MOD_GSK3_1 814 821 PF00069 0.546
MOD_GSK3_1 822 829 PF00069 0.455
MOD_GSK3_1 849 856 PF00069 0.456
MOD_GSK3_1 946 953 PF00069 0.569
MOD_GSK3_1 957 964 PF00069 0.441
MOD_GSK3_1 969 976 PF00069 0.477
MOD_LATS_1 262 268 PF00433 0.587
MOD_N-GLC_1 230 235 PF02516 0.427
MOD_N-GLC_1 64 69 PF02516 0.452
MOD_N-GLC_1 726 731 PF02516 0.673
MOD_N-GLC_1 849 854 PF02516 0.452
MOD_N-GLC_1 968 973 PF02516 0.465
MOD_N-GLC_1 997 1002 PF02516 0.614
MOD_NEK2_1 117 122 PF00069 0.371
MOD_NEK2_1 488 493 PF00069 0.337
MOD_NEK2_1 588 593 PF00069 0.406
MOD_NEK2_1 621 626 PF00069 0.326
MOD_NEK2_1 643 648 PF00069 0.316
MOD_NEK2_1 680 685 PF00069 0.316
MOD_NEK2_1 764 769 PF00069 0.772
MOD_NEK2_1 853 858 PF00069 0.356
MOD_NEK2_1 875 880 PF00069 0.314
MOD_NEK2_1 957 962 PF00069 0.435
MOD_NEK2_1 968 973 PF00069 0.458
MOD_NEK2_1 987 992 PF00069 0.475
MOD_NEK2_2 418 423 PF00069 0.564
MOD_PIKK_1 1035 1041 PF00454 0.641
MOD_PIKK_1 809 815 PF00454 0.617
MOD_PK_1 1141 1147 PF00069 0.488
MOD_PK_1 815 821 PF00069 0.680
MOD_PK_1 934 940 PF00069 0.478
MOD_PKA_1 176 182 PF00069 0.406
MOD_PKA_1 382 388 PF00069 0.569
MOD_PKA_1 808 814 PF00069 0.537
MOD_PKA_2 1027 1033 PF00069 0.642
MOD_PKA_2 1106 1112 PF00069 0.546
MOD_PKA_2 137 143 PF00069 0.428
MOD_PKA_2 176 182 PF00069 0.406
MOD_PKA_2 263 269 PF00069 0.523
MOD_PKA_2 300 306 PF00069 0.615
MOD_PKA_2 406 412 PF00069 0.561
MOD_PKA_2 808 814 PF00069 0.694
MOD_PKA_2 961 967 PF00069 0.462
MOD_Plk_1 1005 1011 PF00069 0.718
MOD_Plk_1 230 236 PF00069 0.472
MOD_Plk_1 293 299 PF00069 0.594
MOD_Plk_1 46 52 PF00069 0.498
MOD_Plk_1 606 612 PF00069 0.376
MOD_Plk_1 726 732 PF00069 0.668
MOD_Plk_1 756 762 PF00069 0.566
MOD_Plk_1 764 770 PF00069 0.561
MOD_Plk_1 822 828 PF00069 0.631
MOD_Plk_1 849 855 PF00069 0.422
MOD_Plk_1 957 963 PF00069 0.403
MOD_Plk_1 968 974 PF00069 0.418
MOD_Plk_2-3 726 732 PF00069 0.691
MOD_Plk_2-3 736 742 PF00069 0.665
MOD_Plk_4 117 123 PF00069 0.360
MOD_Plk_4 192 198 PF00069 0.333
MOD_Plk_4 26 32 PF00069 0.388
MOD_Plk_4 338 344 PF00069 0.430
MOD_Plk_4 352 358 PF00069 0.511
MOD_Plk_4 368 374 PF00069 0.579
MOD_Plk_4 418 424 PF00069 0.539
MOD_Plk_4 483 489 PF00069 0.326
MOD_Plk_4 562 568 PF00069 0.490
MOD_Plk_4 621 627 PF00069 0.293
MOD_Plk_4 643 649 PF00069 0.314
MOD_Plk_4 870 876 PF00069 0.411
MOD_Plk_4 883 889 PF00069 0.353
MOD_Plk_4 934 940 PF00069 0.584
MOD_Plk_4 950 956 PF00069 0.322
MOD_Plk_4 973 979 PF00069 0.454
MOD_ProDKin_1 1016 1022 PF00069 0.611
MOD_ProDKin_1 1056 1062 PF00069 0.560
MOD_ProDKin_1 361 367 PF00069 0.689
MOD_ProDKin_1 454 460 PF00069 0.512
MOD_ProDKin_1 522 528 PF00069 0.533
MOD_ProDKin_1 844 850 PF00069 0.471
MOD_SUMO_for_1 1002 1005 PF00179 0.687
MOD_SUMO_for_1 559 562 PF00179 0.453
MOD_SUMO_rev_2 1065 1071 PF00179 0.560
MOD_SUMO_rev_2 501 510 PF00179 0.503
MOD_SUMO_rev_2 595 602 PF00179 0.412
MOD_SUMO_rev_2 770 779 PF00179 0.673
MOD_SUMO_rev_2 974 983 PF00179 0.423
TRG_DiLeu_BaEn_1 161 166 PF01217 0.338
TRG_DiLeu_BaEn_1 617 622 PF01217 0.320
TRG_DiLeu_BaEn_2 561 567 PF01217 0.508
TRG_DiLeu_BaEn_4 349 355 PF01217 0.485
TRG_DiLeu_BaLyEn_6 105 110 PF01217 0.326
TRG_DiLeu_BaLyEn_6 40 45 PF01217 0.386
TRG_DiLeu_BaLyEn_6 550 555 PF01217 0.258
TRG_ENDOCYTIC_2 1094 1097 PF00928 0.529
TRG_ENDOCYTIC_2 232 235 PF00928 0.424
TRG_ENDOCYTIC_2 453 456 PF00928 0.538
TRG_ENDOCYTIC_2 532 535 PF00928 0.361
TRG_ENDOCYTIC_2 541 544 PF00928 0.264
TRG_ENDOCYTIC_2 551 554 PF00928 0.219
TRG_ENDOCYTIC_2 585 588 PF00928 0.357
TRG_ENDOCYTIC_2 855 858 PF00928 0.455
TRG_ENDOCYTIC_2 920 923 PF00928 0.361
TRG_ENDOCYTIC_2 954 957 PF00928 0.513
TRG_ENDOCYTIC_2 975 978 PF00928 0.418
TRG_ENDOCYTIC_2 989 992 PF00928 0.535
TRG_ER_diArg_1 1023 1026 PF00400 0.597
TRG_ER_diArg_1 1077 1080 PF00400 0.621
TRG_ER_diArg_1 1088 1090 PF00400 0.585
TRG_ER_diArg_1 40 43 PF00400 0.347
TRG_ER_diArg_1 428 430 PF00400 0.650
TRG_ER_diArg_1 442 445 PF00400 0.459
TRG_ER_diArg_1 48 51 PF00400 0.389
TRG_ER_diArg_1 602 605 PF00400 0.336
TRG_ER_diArg_1 666 668 PF00400 0.399
TRG_NES_CRM1_1 9 22 PF08389 0.300
TRG_NLS_Bipartite_1 1076 1091 PF00514 0.717
TRG_NLS_Bipartite_1 429 448 PF00514 0.597
TRG_NLS_MonoCore_2 1086 1091 PF00514 0.707
TRG_NLS_MonoExtC_3 1075 1080 PF00514 0.701
TRG_NLS_MonoExtC_3 1086 1092 PF00514 0.791
TRG_NLS_MonoExtC_3 442 447 PF00514 0.494
TRG_NLS_MonoExtN_4 1073 1080 PF00514 0.709
TRG_NLS_MonoExtN_4 1086 1091 PF00514 0.807
TRG_NLS_MonoExtN_4 443 448 PF00514 0.495
TRG_NLS_MonoExtN_4 700 705 PF00514 0.531
TRG_Pf-PMV_PEXEL_1 308 312 PF00026 0.519
TRG_Pf-PMV_PEXEL_1 43 47 PF00026 0.360
TRG_Pf-PMV_PEXEL_1 553 557 PF00026 0.445

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1PC20 Leptomonas seymouri 65% 100%
A0A3S7WU73 Leishmania donovani 99% 100%
A0A422N424 Trypanosoma rangeli 41% 100%
A4H8T1 Leishmania braziliensis 75% 100%
C9ZVU2 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 40% 100%
E9AQW5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 91% 100%
Q4QEL3 Leishmania major 90% 100%
V5BS96 Trypanosoma cruzi 41% 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