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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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: A0A3S7X053
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 1 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 1 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 1 |
GO:0033314 | mitotic DNA replication checkpoint signaling | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 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:0051726 | regulation of cell cycle | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 1 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003688 | DNA replication origin binding | 7 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 658 | 662 | PF00656 | 0.617 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.457 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.657 |
CLV_PCSK_FUR_1 | 250 | 254 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 640 | 642 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 852 | 854 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 411 | 413 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 640 | 642 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 747 | 749 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 852 | 854 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.443 |
CLV_Separin_Metazoa | 876 | 880 | PF03568 | 0.447 |
DEG_SCF_FBW7_1 | 153 | 160 | PF00400 | 0.704 |
DEG_SCF_FBW7_1 | 181 | 186 | PF00400 | 0.678 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.602 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.594 |
DEG_SPOP_SBC_1 | 403 | 407 | PF00917 | 0.618 |
DEG_SPOP_SBC_1 | 599 | 603 | PF00917 | 0.576 |
DEG_SPOP_SBC_1 | 646 | 650 | PF00917 | 0.531 |
DEG_SPOP_SBC_1 | 656 | 660 | PF00917 | 0.644 |
DEG_SPOP_SBC_1 | 692 | 696 | PF00917 | 0.608 |
DOC_CKS1_1 | 154 | 159 | PF01111 | 0.679 |
DOC_CYCLIN_RxL_1 | 147 | 158 | PF00134 | 0.664 |
DOC_CYCLIN_RxL_1 | 554 | 563 | PF00134 | 0.464 |
DOC_MAPK_DCC_7 | 411 | 421 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 537 | 546 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 556 | 562 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 412 | 421 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 777 | 786 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 797 | 803 | PF00149 | 0.515 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.445 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.301 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.525 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 695 | 700 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 764 | 769 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 101 | 109 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 147 | 154 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 203 | 209 | PF00244 | 0.753 |
LIG_14-3-3_CanoR_1 | 323 | 331 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 530 | 538 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 540 | 548 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 575 | 584 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 618 | 623 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 657 | 665 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 833 | 838 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 861 | 869 | PF00244 | 0.579 |
LIG_Actin_WH2_2 | 415 | 433 | PF00022 | 0.459 |
LIG_Actin_WH2_2 | 816 | 831 | PF00022 | 0.483 |
LIG_APCC_ABBA_1 | 476 | 481 | PF00400 | 0.457 |
LIG_BIR_III_2 | 111 | 115 | PF00653 | 0.483 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.684 |
LIG_BIR_III_4 | 661 | 665 | PF00653 | 0.622 |
LIG_BRCT_BRCA1_1 | 648 | 652 | PF00533 | 0.607 |
LIG_BRCT_BRCA1_1 | 669 | 673 | PF00533 | 0.571 |
LIG_EH1_1 | 44 | 52 | PF00400 | 0.544 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.774 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.679 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.377 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.662 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.560 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.401 |
LIG_FHA_1 | 779 | 785 | PF00498 | 0.473 |
LIG_FHA_1 | 829 | 835 | PF00498 | 0.457 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.412 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.371 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.629 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.573 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.688 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.711 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.637 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.564 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.499 |
LIG_FHA_2 | 726 | 732 | PF00498 | 0.455 |
LIG_LIR_Apic_2 | 443 | 449 | PF02991 | 0.391 |
LIG_LIR_Apic_2 | 840 | 844 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 871 | 882 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 630 | 636 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 819 | 823 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 871 | 877 | PF02991 | 0.466 |
LIG_LYPXL_yS_3 | 313 | 316 | PF13949 | 0.458 |
LIG_PCNA_PIPBox_1 | 786 | 795 | PF02747 | 0.472 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.449 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.430 |
LIG_SH2_CRK | 793 | 797 | PF00017 | 0.395 |
LIG_SH2_GRB2like | 343 | 346 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 304 | 308 | PF00017 | 0.489 |
LIG_SH2_NCK_1 | 479 | 483 | PF00017 | 0.423 |
LIG_SH2_SRC | 551 | 554 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 793 | 797 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 735 | 738 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 793 | 796 | PF00017 | 0.400 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.612 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.423 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.404 |
LIG_SUMO_SIM_anti_2 | 738 | 744 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 350 | 356 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 420 | 426 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 738 | 744 | PF11976 | 0.416 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.708 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.710 |
LIG_UBA3_1 | 376 | 385 | PF00899 | 0.458 |
LIG_WW_3 | 295 | 299 | PF00397 | 0.609 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.682 |
MOD_CDK_SPK_2 | 6 | 11 | PF00069 | 0.618 |
MOD_CDK_SPK_2 | 652 | 657 | PF00069 | 0.622 |
MOD_CDK_SPxxK_3 | 19 | 26 | PF00069 | 0.606 |
MOD_CDK_SPxxK_3 | 243 | 250 | PF00069 | 0.570 |
MOD_CDK_SPxxK_3 | 509 | 516 | PF00069 | 0.558 |
MOD_CDK_SPxxK_3 | 6 | 13 | PF00069 | 0.675 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.670 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.650 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.658 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.649 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.719 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.718 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.634 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.649 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.592 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.545 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.650 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.606 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.681 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.534 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.617 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.636 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.803 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.622 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.563 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.501 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.572 |
MOD_CK2_1 | 725 | 731 | PF00069 | 0.465 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.470 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.614 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.595 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.748 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.622 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.716 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.620 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.806 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.710 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.553 |
MOD_GlcNHglycan | 348 | 352 | PF01048 | 0.422 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.453 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.578 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.614 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.608 |
MOD_GlcNHglycan | 561 | 565 | PF01048 | 0.410 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.384 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.767 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.654 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.547 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.774 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.653 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.793 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.655 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.599 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.833 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.512 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.749 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.781 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.692 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.617 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.606 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.387 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.432 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.685 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.667 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.664 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.645 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.613 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.594 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.597 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.432 |
MOD_GSK3_1 | 749 | 756 | PF00069 | 0.487 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.423 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.686 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.607 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.445 |
MOD_N-GLC_1 | 837 | 842 | PF02516 | 0.437 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.682 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.529 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.471 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.437 |
MOD_NEK2_2 | 307 | 312 | PF00069 | 0.454 |
MOD_NEK2_2 | 730 | 735 | PF00069 | 0.443 |
MOD_NEK2_2 | 780 | 785 | PF00069 | 0.506 |
MOD_OFUCOSY | 359 | 366 | PF10250 | 0.443 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.511 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.674 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.555 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.485 |
MOD_PK_1 | 36 | 42 | PF00069 | 0.552 |
MOD_PK_1 | 618 | 624 | PF00069 | 0.552 |
MOD_PKA_1 | 272 | 278 | PF00069 | 0.597 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.407 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.749 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.687 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.724 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.667 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.726 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.601 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.478 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.592 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.696 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.458 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.558 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.634 |
MOD_PKA_2 | 671 | 677 | PF00069 | 0.572 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.525 |
MOD_PKA_2 | 828 | 834 | PF00069 | 0.506 |
MOD_PKA_2 | 860 | 866 | PF00069 | 0.538 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.647 |
MOD_Plk_1 | 618 | 624 | PF00069 | 0.578 |
MOD_Plk_1 | 730 | 736 | PF00069 | 0.437 |
MOD_Plk_1 | 749 | 755 | PF00069 | 0.481 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.442 |
MOD_Plk_2-3 | 634 | 640 | PF00069 | 0.500 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.671 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.447 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.571 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.501 |
MOD_Plk_4 | 730 | 736 | PF00069 | 0.437 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.318 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.736 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.590 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.589 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.776 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.581 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.717 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.703 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.673 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.546 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.556 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.696 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.633 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.622 |
MOD_ProDKin_1 | 695 | 701 | PF00069 | 0.608 |
MOD_ProDKin_1 | 764 | 770 | PF00069 | 0.655 |
MOD_SUMO_rev_2 | 267 | 275 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 531 | 539 | PF00179 | 0.640 |
TRG_DiLeu_BaEn_1 | 880 | 885 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 793 | 796 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 546 | 549 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 745 | 748 | PF00400 | 0.353 |
TRG_NLS_MonoExtN_4 | 250 | 256 | PF00514 | 0.655 |
TRG_NLS_MonoExtN_4 | 410 | 415 | PF00514 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 165 | 170 | PF00026 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 557 | 561 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 72 | 77 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIL4 | Leptomonas seymouri | 54% | 100% |
A4HF65 | Leishmania braziliensis | 76% | 100% |
A4I2E8 | Leishmania infantum | 99% | 100% |
C9ZX58 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AYK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q8X1 | Leishmania major | 91% | 98% |