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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H6C9
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0007096 | regulation of exit from mitosis | 7 | 7 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010564 | regulation of cell cycle process | 5 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 7 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 7 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0032465 | regulation of cytokinesis | 5 | 1 |
GO:0032467 | positive regulation of cytokinesis | 6 | 1 |
GO:0045787 | positive regulation of cell cycle | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0051302 | regulation of cell division | 4 | 1 |
GO:0051781 | positive regulation of cell division | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090068 | positive regulation of cell cycle process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 7 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 5 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 669 | 675 | PF00089 | 0.719 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.830 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.777 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 838 | 840 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 849 | 851 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 908 | 910 | PF00675 | 0.716 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.823 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 718 | 720 | PF00082 | 0.820 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 848 | 850 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 867 | 869 | PF00082 | 0.829 |
CLV_PCSK_KEX2_1 | 907 | 909 | PF00082 | 0.694 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.823 |
CLV_PCSK_PC1ET2_1 | 718 | 720 | PF00082 | 0.820 |
CLV_PCSK_PC1ET2_1 | 867 | 869 | PF00082 | 0.840 |
CLV_PCSK_PC7_1 | 375 | 381 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.845 |
CLV_PCSK_SKI1_1 | 840 | 844 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 999 | 1003 | PF00082 | 0.813 |
CLV_Separin_Metazoa | 757 | 761 | PF03568 | 0.626 |
CLV_Separin_Metazoa | 83 | 87 | PF03568 | 0.567 |
DEG_APCC_KENBOX_2 | 13 | 17 | PF00400 | 0.462 |
DEG_SCF_FBW7_1 | 889 | 896 | PF00400 | 0.618 |
DEG_SCF_TRCP1_1 | 624 | 629 | PF00400 | 0.600 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.766 |
DEG_SPOP_SBC_1 | 539 | 543 | PF00917 | 0.705 |
DEG_SPOP_SBC_1 | 763 | 767 | PF00917 | 0.748 |
DOC_CKS1_1 | 948 | 953 | PF01111 | 0.652 |
DOC_CYCLIN_yCln2_LP_2 | 58 | 64 | PF00134 | 0.597 |
DOC_MAPK_gen_1 | 282 | 291 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 530 | 539 | PF00069 | 0.586 |
DOC_MAPK_HePTP_8 | 279 | 291 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 282 | 291 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 450 | 459 | PF00069 | 0.437 |
DOC_PP1_RVXF_1 | 914 | 920 | PF00149 | 0.747 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.674 |
DOC_PP2B_LxvP_1 | 987 | 990 | PF13499 | 0.729 |
DOC_PP4_FxxP_1 | 241 | 244 | PF00568 | 0.566 |
DOC_PP4_FxxP_1 | 525 | 528 | PF00568 | 0.634 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.836 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 769 | 773 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 856 | 860 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 879 | 883 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 957 | 961 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 990 | 994 | PF00917 | 0.775 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 703 | 708 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 733 | 738 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 889 | 894 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 902 | 907 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 947 | 952 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 975 | 980 | PF00397 | 0.743 |
LIG_14-3-3_CanoR_1 | 169 | 176 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 375 | 383 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 530 | 540 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 587 | 595 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 634 | 643 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 672 | 681 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 719 | 728 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 787 | 794 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 807 | 815 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 849 | 858 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 959 | 963 | PF00244 | 0.785 |
LIG_14-3-3_CanoR_1 | 984 | 988 | PF00244 | 0.679 |
LIG_Actin_WH2_2 | 292 | 309 | PF00022 | 0.572 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.491 |
LIG_BIR_III_2 | 571 | 575 | PF00653 | 0.716 |
LIG_BIR_III_2 | 604 | 608 | PF00653 | 0.712 |
LIG_BRCT_BRCA1_1 | 534 | 538 | PF00533 | 0.483 |
LIG_BRCT_BRCA1_1 | 745 | 749 | PF00533 | 0.688 |
LIG_CtBP_PxDLS_1 | 68 | 72 | PF00389 | 0.425 |
LIG_deltaCOP1_diTrp_1 | 253 | 262 | PF00928 | 0.452 |
LIG_eIF4E_1 | 300 | 306 | PF01652 | 0.570 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.608 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.465 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.574 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.461 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.557 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.784 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.663 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.773 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.766 |
LIG_FHA_1 | 676 | 682 | PF00498 | 0.780 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.656 |
LIG_FHA_1 | 745 | 751 | PF00498 | 0.746 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.642 |
LIG_FHA_1 | 841 | 847 | PF00498 | 0.766 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.646 |
LIG_FHA_2 | 791 | 797 | PF00498 | 0.728 |
LIG_FHA_2 | 869 | 875 | PF00498 | 0.753 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.602 |
LIG_FHA_2 | 968 | 974 | PF00498 | 0.756 |
LIG_GBD_Chelix_1 | 291 | 299 | PF00786 | 0.434 |
LIG_LIR_Apic_2 | 240 | 244 | PF02991 | 0.542 |
LIG_LIR_Apic_2 | 253 | 259 | PF02991 | 0.356 |
LIG_LIR_Apic_2 | 350 | 355 | PF02991 | 0.661 |
LIG_LIR_Gen_1 | 253 | 262 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 399 | 409 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 45 | 56 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 746 | 755 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 645 | 649 | PF02991 | 0.788 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.195 |
LIG_LYPXL_S_1 | 199 | 203 | PF13949 | 0.346 |
LIG_MLH1_MIPbox_1 | 745 | 749 | PF16413 | 0.688 |
LIG_MYND_1 | 381 | 385 | PF01753 | 0.619 |
LIG_NRBOX | 80 | 86 | PF00104 | 0.445 |
LIG_PCNA_PIPBox_1 | 5 | 14 | PF02747 | 0.578 |
LIG_Pex14_1 | 192 | 196 | PF04695 | 0.546 |
LIG_Pex14_2 | 13 | 17 | PF04695 | 0.476 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.421 |
LIG_PTAP_UEV_1 | 405 | 410 | PF05743 | 0.710 |
LIG_PTAP_UEV_1 | 953 | 958 | PF05743 | 0.756 |
LIG_RPA_C_Fungi | 629 | 641 | PF08784 | 0.591 |
LIG_SH2_CRK | 516 | 520 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 852 | 856 | PF00017 | 0.748 |
LIG_SH2_SRC | 252 | 255 | PF00017 | 0.394 |
LIG_SH2_SRC | 317 | 320 | PF00017 | 0.495 |
LIG_SH2_SRC | 489 | 492 | PF00017 | 0.611 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 744 | 748 | PF00017 | 0.690 |
LIG_SH2_STAP1 | 794 | 798 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 852 | 856 | PF00017 | 0.825 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 748 | 751 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 852 | 855 | PF00017 | 0.823 |
LIG_SH3_2 | 954 | 959 | PF14604 | 0.768 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.576 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.721 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.745 |
LIG_SH3_3 | 948 | 954 | PF00018 | 0.709 |
LIG_SH3_3 | 973 | 979 | PF00018 | 0.787 |
LIG_Sin3_3 | 467 | 474 | PF02671 | 0.461 |
LIG_SUMO_SIM_anti_2 | 691 | 697 | PF11976 | 0.633 |
LIG_SUMO_SIM_par_1 | 216 | 222 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 344 | 350 | PF11976 | 0.651 |
LIG_SUMO_SIM_par_1 | 676 | 685 | PF11976 | 0.793 |
LIG_SUMO_SIM_par_1 | 978 | 983 | PF11976 | 0.709 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.575 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.510 |
LIG_TRAF2_1 | 685 | 688 | PF00917 | 0.594 |
LIG_WRC_WIRS_1 | 238 | 243 | PF05994 | 0.572 |
LIG_WRC_WIRS_1 | 643 | 648 | PF05994 | 0.787 |
LIG_WRPW_2 | 59 | 62 | PF00400 | 0.497 |
MOD_CDC14_SPxK_1 | 905 | 908 | PF00782 | 0.629 |
MOD_CDK_SPK_2 | 733 | 738 | PF00069 | 0.810 |
MOD_CDK_SPK_2 | 902 | 907 | PF00069 | 0.803 |
MOD_CDK_SPxK_1 | 902 | 908 | PF00069 | 0.630 |
MOD_CDK_SPxxK_3 | 300 | 307 | PF00069 | 0.577 |
MOD_CDK_SPxxK_3 | 703 | 710 | PF00069 | 0.782 |
MOD_CDK_SPxxK_3 | 902 | 909 | PF00069 | 0.727 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.735 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.714 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.648 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.535 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.695 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.764 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.609 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.731 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.539 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.739 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.700 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.688 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.802 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.710 |
MOD_CK1_1 | 811 | 817 | PF00069 | 0.743 |
MOD_CK1_1 | 831 | 837 | PF00069 | 0.644 |
MOD_CK1_1 | 896 | 902 | PF00069 | 0.797 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.750 |
MOD_CK1_1 | 983 | 989 | PF00069 | 0.822 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.651 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.594 |
MOD_CK2_1 | 790 | 796 | PF00069 | 0.731 |
MOD_CK2_1 | 868 | 874 | PF00069 | 0.755 |
MOD_CK2_1 | 967 | 973 | PF00069 | 0.756 |
MOD_Cter_Amidation | 521 | 524 | PF01082 | 0.707 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.562 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.735 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.751 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.480 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.513 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.626 |
MOD_GlcNHglycan | 270 | 275 | PF01048 | 0.536 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.616 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.770 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.628 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.572 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.726 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.731 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.699 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.710 |
MOD_GlcNHglycan | 623 | 627 | PF01048 | 0.760 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.796 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.810 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.643 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.707 |
MOD_GlcNHglycan | 771 | 774 | PF01048 | 0.679 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.767 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.811 |
MOD_GlcNHglycan | 954 | 957 | PF01048 | 0.759 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.741 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.698 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.648 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.360 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.411 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.628 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.681 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.784 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.691 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.497 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.756 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.722 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.500 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.614 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.708 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.708 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.745 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.698 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.733 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.747 |
MOD_GSK3_1 | 879 | 886 | PF00069 | 0.747 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.675 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.779 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.821 |
MOD_N-GLC_1 | 674 | 679 | PF02516 | 0.754 |
MOD_N-GLC_1 | 708 | 713 | PF02516 | 0.831 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.467 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.591 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.411 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.443 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.501 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.668 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.436 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.503 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.728 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.726 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.708 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.417 |
MOD_NEK2_1 | 958 | 963 | PF00069 | 0.794 |
MOD_NEK2_1 | 980 | 985 | PF00069 | 0.746 |
MOD_NEK2_2 | 713 | 718 | PF00069 | 0.759 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.513 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.742 |
MOD_PIKK_1 | 899 | 905 | PF00454 | 0.730 |
MOD_PK_1 | 478 | 484 | PF00069 | 0.457 |
MOD_PKA_1 | 27 | 33 | PF00069 | 0.591 |
MOD_PKA_1 | 671 | 677 | PF00069 | 0.691 |
MOD_PKA_1 | 718 | 724 | PF00069 | 0.735 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.686 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.793 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.756 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.654 |
MOD_PKA_2 | 671 | 677 | PF00069 | 0.685 |
MOD_PKA_2 | 718 | 724 | PF00069 | 0.715 |
MOD_PKA_2 | 799 | 805 | PF00069 | 0.763 |
MOD_PKA_2 | 808 | 814 | PF00069 | 0.690 |
MOD_PKA_2 | 958 | 964 | PF00069 | 0.846 |
MOD_PKA_2 | 983 | 989 | PF00069 | 0.655 |
MOD_PKB_1 | 531 | 539 | PF00069 | 0.682 |
MOD_PKB_1 | 848 | 856 | PF00069 | 0.819 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.429 |
MOD_Plk_1 | 811 | 817 | PF00069 | 0.743 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.513 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.513 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.492 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.670 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.433 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.709 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.731 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.664 |
MOD_Plk_4 | 744 | 750 | PF00069 | 0.689 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.678 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.460 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.477 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.800 |
MOD_ProDKin_1 | 703 | 709 | PF00069 | 0.779 |
MOD_ProDKin_1 | 733 | 739 | PF00069 | 0.783 |
MOD_ProDKin_1 | 889 | 895 | PF00069 | 0.761 |
MOD_ProDKin_1 | 902 | 908 | PF00069 | 0.805 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.646 |
MOD_ProDKin_1 | 947 | 953 | PF00069 | 0.814 |
MOD_ProDKin_1 | 975 | 981 | PF00069 | 0.744 |
MOD_SUMO_rev_2 | 266 | 274 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 736 | 745 | PF00179 | 0.658 |
MOD_SUMO_rev_2 | 941 | 948 | PF00179 | 0.649 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.576 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 516 | 519 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.497 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.777 |
TRG_ER_diArg_1 | 495 | 498 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 523 | 525 | PF00400 | 0.702 |
TRG_ER_diArg_1 | 530 | 533 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 620 | 622 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 807 | 810 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 836 | 839 | PF00400 | 0.796 |
TRG_ER_diArg_1 | 848 | 850 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 906 | 909 | PF00400 | 0.765 |
TRG_ER_diArg_1 | 914 | 917 | PF00400 | 0.528 |
TRG_NES_CRM1_1 | 691 | 704 | PF08389 | 0.738 |
TRG_NLS_MonoExtN_4 | 117 | 124 | PF00514 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4R5 | Leptomonas seymouri | 44% | 89% |
A4H5L8 | Leishmania braziliensis | 69% | 100% |
A4HTV6 | Leishmania infantum | 100% | 100% |
E9AMP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
Q4QHY2 | Leishmania major | 89% | 99% |