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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X3B4
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 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:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0035329 | hippo signaling | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003712 | transcription coregulator activity | 2 | 1 |
GO:0003713 | transcription coactivator activity | 3 | 1 |
GO:0140110 | transcription regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 535 | 539 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 579 | 583 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 605 | 609 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 675 | 679 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 920 | 924 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 884 | 886 | PF00675 | 0.494 |
CLV_PCSK_FUR_1 | 646 | 650 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 884 | 886 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 901 | 903 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 648 | 650 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 901 | 903 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 884 | 888 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 946 | 950 | PF00082 | 0.492 |
CLV_Separin_Metazoa | 643 | 647 | PF03568 | 0.627 |
DEG_APCC_DBOX_1 | 475 | 483 | PF00400 | 0.560 |
DEG_APCC_DBOX_1 | 6 | 14 | PF00400 | 0.726 |
DEG_APCC_DBOX_1 | 945 | 953 | PF00400 | 0.564 |
DEG_SCF_FBW7_1 | 949 | 954 | PF00400 | 0.593 |
DEG_SCF_TRCP1_1 | 538 | 543 | PF00400 | 0.615 |
DEG_SPOP_SBC_1 | 301 | 305 | PF00917 | 0.573 |
DEG_SPOP_SBC_1 | 833 | 837 | PF00917 | 0.644 |
DEG_SPOP_SBC_1 | 907 | 911 | PF00917 | 0.701 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.523 |
DOC_CKS1_1 | 285 | 290 | PF01111 | 0.593 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.563 |
DOC_CKS1_1 | 766 | 771 | PF01111 | 0.592 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 332 | 341 | PF00134 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 424 | 430 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 913 | 919 | PF00134 | 0.550 |
DOC_MAPK_DCC_7 | 463 | 472 | PF00069 | 0.533 |
DOC_MAPK_FxFP_2 | 238 | 241 | PF00069 | 0.610 |
DOC_MAPK_FxFP_2 | 513 | 516 | PF00069 | 0.627 |
DOC_MAPK_gen_1 | 450 | 459 | PF00069 | 0.591 |
DOC_MAPK_gen_1 | 463 | 472 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 450 | 459 | PF00069 | 0.597 |
DOC_MAPK_MEF2A_6 | 463 | 472 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 908 | 917 | PF00069 | 0.582 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.578 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 600 | 603 | PF13499 | 0.719 |
DOC_PP2B_LxvP_1 | 913 | 916 | PF13499 | 0.698 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.610 |
DOC_PP4_FxxP_1 | 513 | 516 | PF00568 | 0.627 |
DOC_PP4_MxPP_1 | 412 | 415 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 833 | 837 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 841 | 845 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 907 | 911 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 919 | 923 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 964 | 968 | PF00917 | 0.638 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 710 | 715 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 765 | 770 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 821 | 826 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 908 | 913 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 937 | 942 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 947 | 952 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 229 | 239 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 469 | 473 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 512 | 516 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 554 | 558 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 737 | 741 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 902 | 912 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.518 |
LIG_Actin_WH2_2 | 922 | 937 | PF00022 | 0.499 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_BIR_III_2 | 193 | 197 | PF00653 | 0.590 |
LIG_BIR_III_2 | 678 | 682 | PF00653 | 0.676 |
LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.691 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.586 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.389 |
LIG_Clathr_ClatBox_1 | 12 | 16 | PF01394 | 0.725 |
LIG_EH1_1 | 148 | 156 | PF00400 | 0.410 |
LIG_EH1_1 | 60 | 68 | PF00400 | 0.559 |
LIG_eIF4E_1 | 61 | 67 | PF01652 | 0.555 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.544 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.776 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.427 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.732 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.546 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.450 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.467 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.532 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.571 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.705 |
LIG_FHA_1 | 761 | 767 | PF00498 | 0.787 |
LIG_FHA_1 | 948 | 954 | PF00498 | 0.650 |
LIG_FHA_1 | 963 | 969 | PF00498 | 0.639 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.474 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.507 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.339 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.614 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.542 |
LIG_GSK3_LRP6_1 | 284 | 289 | PF00069 | 0.594 |
LIG_LIR_Apic_2 | 16 | 20 | PF02991 | 0.597 |
LIG_LIR_Apic_2 | 235 | 241 | PF02991 | 0.628 |
LIG_LIR_Apic_2 | 505 | 511 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 254 | 265 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 401 | 412 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 877 | 887 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 36 | 40 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 877 | 882 | PF02991 | 0.500 |
LIG_MAD2 | 624 | 632 | PF02301 | 0.561 |
LIG_Pex14_1 | 486 | 490 | PF04695 | 0.335 |
LIG_Pex14_2 | 430 | 434 | PF04695 | 0.491 |
LIG_PTAP_UEV_1 | 195 | 200 | PF05743 | 0.659 |
LIG_PTB_Apo_2 | 628 | 635 | PF02174 | 0.541 |
LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.543 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.651 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.466 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.538 |
LIG_SH2_CRK | 794 | 798 | PF00017 | 0.602 |
LIG_SH2_GRB2like | 17 | 20 | PF00017 | 0.649 |
LIG_SH2_GRB2like | 794 | 797 | PF00017 | 0.583 |
LIG_SH2_NCK_1 | 17 | 21 | PF00017 | 0.597 |
LIG_SH2_NCK_1 | 442 | 446 | PF00017 | 0.538 |
LIG_SH2_SRC | 794 | 797 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 794 | 798 | PF00017 | 0.595 |
LIG_SH2_STAT3 | 638 | 641 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.335 |
LIG_SH3_2 | 196 | 201 | PF14604 | 0.663 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.717 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.670 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.616 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.588 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.563 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.552 |
LIG_SH3_CIN85_PxpxPR_1 | 196 | 201 | PF14604 | 0.663 |
LIG_Sin3_3 | 276 | 283 | PF02671 | 0.573 |
LIG_Sin3_3 | 665 | 672 | PF02671 | 0.575 |
LIG_SUMO_SIM_anti_2 | 120 | 126 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 261 | 270 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 11 | 16 | PF11976 | 0.726 |
LIG_SUMO_SIM_par_1 | 261 | 270 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 454 | 460 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 613 | 619 | PF11976 | 0.563 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.504 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.460 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.608 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.335 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.559 |
LIG_TRAF2_2 | 703 | 708 | PF00917 | 0.607 |
LIG_UBA3_1 | 154 | 162 | PF00899 | 0.486 |
LIG_UBA3_1 | 268 | 274 | PF00899 | 0.440 |
LIG_WW_3 | 198 | 202 | PF00397 | 0.698 |
MOD_CDK_SPxK_1 | 712 | 718 | PF00069 | 0.658 |
MOD_CDK_SPxxK_3 | 544 | 551 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 821 | 828 | PF00069 | 0.655 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.737 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.716 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.587 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.612 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.535 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.405 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.586 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.669 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.392 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.609 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.823 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.614 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.696 |
MOD_CK1_1 | 712 | 718 | PF00069 | 0.657 |
MOD_CK1_1 | 809 | 815 | PF00069 | 0.722 |
MOD_CK1_1 | 816 | 822 | PF00069 | 0.599 |
MOD_CK1_1 | 850 | 856 | PF00069 | 0.718 |
MOD_CK1_1 | 911 | 917 | PF00069 | 0.781 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.472 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.516 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.594 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.335 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.563 |
MOD_CK2_1 | 758 | 764 | PF00069 | 0.660 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.591 |
MOD_CK2_1 | 784 | 790 | PF00069 | 0.723 |
MOD_CK2_1 | 812 | 818 | PF00069 | 0.657 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.516 |
MOD_Cter_Amidation | 493 | 496 | PF01082 | 0.335 |
MOD_DYRK1A_RPxSP_1 | 544 | 548 | PF00069 | 0.649 |
MOD_DYRK1A_RPxSP_1 | 908 | 912 | PF00069 | 0.674 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.738 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.594 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.601 |
MOD_GlcNHglycan | 297 | 301 | PF01048 | 0.683 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.417 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.449 |
MOD_GlcNHglycan | 42 | 46 | PF01048 | 0.629 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.557 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.652 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.674 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.776 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.697 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.670 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.639 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.603 |
MOD_GlcNHglycan | 728 | 734 | PF01048 | 0.668 |
MOD_GlcNHglycan | 757 | 763 | PF01048 | 0.742 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.744 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.705 |
MOD_GlcNHglycan | 807 | 811 | PF01048 | 0.737 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.631 |
MOD_GlcNHglycan | 941 | 944 | PF01048 | 0.662 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.738 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.534 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.628 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.636 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.662 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.602 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.465 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.577 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.518 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.624 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.588 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.354 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.646 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.693 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.646 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.670 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.634 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.654 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.715 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.742 |
MOD_GSK3_1 | 806 | 813 | PF00069 | 0.653 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.671 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.770 |
MOD_GSK3_1 | 902 | 909 | PF00069 | 0.644 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.665 |
MOD_GSK3_1 | 956 | 963 | PF00069 | 0.643 |
MOD_LATS_1 | 227 | 233 | PF00433 | 0.607 |
MOD_LATS_1 | 92 | 98 | PF00433 | 0.539 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.472 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.565 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.423 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.604 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.472 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.643 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.392 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.446 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.461 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.471 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.479 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.482 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.457 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.509 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.627 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.347 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.682 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.543 |
MOD_NEK2_1 | 709 | 714 | PF00069 | 0.584 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.495 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.512 |
MOD_PIKK_1 | 500 | 506 | PF00454 | 0.313 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.719 |
MOD_PIKK_1 | 701 | 707 | PF00454 | 0.605 |
MOD_PIKK_1 | 778 | 784 | PF00454 | 0.651 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.541 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.564 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.734 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.587 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.547 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.672 |
MOD_PKA_2 | 907 | 913 | PF00069 | 0.691 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.473 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.390 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.427 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.582 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.529 |
MOD_Plk_1 | 729 | 735 | PF00069 | 0.601 |
MOD_Plk_1 | 817 | 823 | PF00069 | 0.610 |
MOD_Plk_1 | 877 | 883 | PF00069 | 0.468 |
MOD_Plk_2-3 | 215 | 221 | PF00069 | 0.630 |
MOD_Plk_2-3 | 261 | 267 | PF00069 | 0.427 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.538 |
MOD_Plk_2-3 | 748 | 754 | PF00069 | 0.614 |
MOD_Plk_2-3 | 871 | 877 | PF00069 | 0.533 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.584 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.552 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.595 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.530 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.427 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.497 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.457 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.454 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.467 |
MOD_Plk_4 | 847 | 853 | PF00069 | 0.647 |
MOD_Plk_4 | 871 | 877 | PF00069 | 0.533 |
MOD_Plk_4 | 964 | 970 | PF00069 | 0.657 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.515 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.670 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.536 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.594 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.599 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.572 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.534 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.647 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.670 |
MOD_ProDKin_1 | 710 | 716 | PF00069 | 0.633 |
MOD_ProDKin_1 | 765 | 771 | PF00069 | 0.602 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.563 |
MOD_ProDKin_1 | 821 | 827 | PF00069 | 0.685 |
MOD_ProDKin_1 | 908 | 914 | PF00069 | 0.681 |
MOD_ProDKin_1 | 937 | 943 | PF00069 | 0.520 |
MOD_ProDKin_1 | 947 | 953 | PF00069 | 0.511 |
MOD_SUMO_for_1 | 740 | 743 | PF00179 | 0.670 |
MOD_SUMO_rev_2 | 895 | 903 | PF00179 | 0.496 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.476 |
TRG_DiLeu_BaEn_4 | 142 | 148 | PF01217 | 0.392 |
TRG_DiLeu_BaEn_4 | 42 | 48 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_4 | 729 | 735 | PF01217 | 0.621 |
TRG_DiLeu_BaLyEn_6 | 154 | 159 | PF01217 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 341 | 346 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.710 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 794 | 797 | PF00928 | 0.601 |
TRG_ER_diArg_1 | 462 | 465 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 622 | 625 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 883 | 885 | PF00400 | 0.549 |
TRG_NLS_Bipartite_1 | 648 | 665 | PF00514 | 0.438 |
TRG_NLS_Bipartite_1 | 884 | 905 | PF00514 | 0.629 |
TRG_NLS_MonoCore_2 | 900 | 905 | PF00514 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 650 | 654 | PF00026 | 0.609 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA79 | Leptomonas seymouri | 62% | 74% |
A4HI63 | Leishmania braziliensis | 73% | 99% |
A4I5E0 | Leishmania infantum | 99% | 100% |
E9B0N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4Q7J4 | Leishmania major | 92% | 100% |