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: A4HF65
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 | 174 | 178 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.522 |
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.502 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.759 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 743 | 745 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 850 | 852 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 850 | 852 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.434 |
CLV_Separin_Metazoa | 874 | 878 | PF03568 | 0.415 |
DEG_SCF_FBW7_1 | 157 | 164 | PF00400 | 0.654 |
DEG_SCF_FBW7_1 | 181 | 186 | PF00400 | 0.669 |
DEG_SCF_FBW7_1 | 403 | 410 | PF00400 | 0.418 |
DEG_SPOP_SBC_1 | 156 | 160 | PF00917 | 0.512 |
DEG_SPOP_SBC_1 | 183 | 187 | PF00917 | 0.532 |
DEG_SPOP_SBC_1 | 649 | 653 | PF00917 | 0.716 |
DEG_SPOP_SBC_1 | 691 | 695 | PF00917 | 0.625 |
DOC_CKS1_1 | 36 | 41 | PF01111 | 0.552 |
DOC_CYCLIN_RxL_1 | 148 | 158 | PF00134 | 0.635 |
DOC_CYCLIN_RxL_1 | 554 | 563 | PF00134 | 0.435 |
DOC_CYCLIN_RxL_1 | 69 | 78 | PF00134 | 0.318 |
DOC_MAPK_DCC_7 | 412 | 421 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 412 | 421 | PF00069 | 0.301 |
DOC_MAPK_gen_1 | 556 | 562 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 607 | 615 | PF00069 | 0.506 |
DOC_MAPK_HePTP_8 | 409 | 421 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 412 | 421 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 775 | 784 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 795 | 801 | PF00149 | 0.472 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.436 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.465 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 762 | 767 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 101 | 109 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 195 | 199 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 26 | 36 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 272 | 277 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 525 | 529 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 540 | 548 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 575 | 580 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 607 | 615 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 655 | 663 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 831 | 836 | PF00244 | 0.437 |
LIG_Actin_WH2_2 | 417 | 433 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 814 | 829 | PF00022 | 0.450 |
LIG_APCC_ABBA_1 | 476 | 481 | PF00400 | 0.434 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.674 |
LIG_BRCT_BRCA1_1 | 667 | 671 | PF00533 | 0.568 |
LIG_eIF4E_1 | 69 | 75 | PF01652 | 0.310 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.622 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.757 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.714 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.558 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.362 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.444 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.667 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.551 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.642 |
LIG_FHA_1 | 729 | 735 | PF00498 | 0.372 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.444 |
LIG_FHA_1 | 827 | 833 | PF00498 | 0.426 |
LIG_FHA_1 | 836 | 842 | PF00498 | 0.374 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.375 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.636 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.680 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.672 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.353 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.570 |
LIG_LIR_Apic_2 | 443 | 449 | PF02991 | 0.386 |
LIG_LIR_Apic_2 | 838 | 842 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 462 | 471 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 578 | 589 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 869 | 880 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 462 | 466 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 509 | 515 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 817 | 821 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 869 | 875 | PF02991 | 0.429 |
LIG_LYPXL_yS_3 | 313 | 316 | PF13949 | 0.438 |
LIG_PCNA_PIPBox_1 | 784 | 793 | PF02747 | 0.446 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.400 |
LIG_SH2_CRK | 791 | 795 | PF00017 | 0.363 |
LIG_SH2_GRB2like | 343 | 346 | PF00017 | 0.345 |
LIG_SH2_SRC | 551 | 554 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 791 | 795 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 733 | 736 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 791 | 794 | PF00017 | 0.369 |
LIG_SH3_1 | 33 | 39 | PF00018 | 0.522 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.721 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.595 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.490 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.394 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.383 |
LIG_SH3_3 | 684 | 690 | PF00018 | 0.609 |
LIG_SUMO_SIM_anti_2 | 736 | 742 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 350 | 356 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 420 | 426 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 611 | 618 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 736 | 742 | PF11976 | 0.389 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.734 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.685 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.296 |
LIG_UBA3_1 | 376 | 385 | PF00899 | 0.440 |
MOD_CDC14_SPxK_1 | 246 | 249 | PF00782 | 0.530 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.660 |
MOD_CDK_SPxK_1 | 243 | 249 | PF00069 | 0.534 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.569 |
MOD_CDK_SPxxK_3 | 7 | 14 | PF00069 | 0.664 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.671 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.696 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.758 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.667 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.694 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.633 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.474 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.544 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.471 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.664 |
MOD_CK1_1 | 693 | 699 | PF00069 | 0.681 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.651 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.548 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.783 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.567 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.558 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.468 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.511 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.478 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.770 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.638 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.653 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.691 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.541 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.615 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.544 |
MOD_GlcNHglycan | 348 | 352 | PF01048 | 0.392 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.378 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.781 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.431 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.573 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.604 |
MOD_GlcNHglycan | 561 | 565 | PF01048 | 0.403 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.548 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.680 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.655 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.645 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.541 |
MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.480 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.609 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.788 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.717 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.561 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.656 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.588 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.711 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.774 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.739 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.650 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.366 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.377 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.599 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.381 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.556 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.597 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.684 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.633 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.526 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.612 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.605 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.607 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.478 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.599 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.391 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.435 |
MOD_GSK3_1 | 831 | 838 | PF00069 | 0.391 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.462 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.311 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.371 |
MOD_N-GLC_1 | 608 | 613 | PF02516 | 0.590 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.427 |
MOD_N-GLC_1 | 835 | 840 | PF02516 | 0.399 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.676 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.312 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.486 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.513 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.416 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.362 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.399 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.546 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.537 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.467 |
MOD_NEK2_2 | 728 | 733 | PF00069 | 0.410 |
MOD_NEK2_2 | 778 | 783 | PF00069 | 0.478 |
MOD_OFUCOSY | 359 | 366 | PF10250 | 0.422 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.629 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.465 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.468 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.360 |
MOD_PK_1 | 575 | 581 | PF00069 | 0.384 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.550 |
MOD_PKA_1 | 285 | 291 | PF00069 | 0.520 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.667 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.616 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.519 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.655 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.707 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.474 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.492 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.453 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.545 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.543 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.422 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.626 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.543 |
MOD_PKA_2 | 654 | 660 | PF00069 | 0.636 |
MOD_PKA_2 | 669 | 675 | PF00069 | 0.573 |
MOD_PKA_2 | 826 | 832 | PF00069 | 0.475 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.536 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.522 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.470 |
MOD_Plk_1 | 608 | 614 | PF00069 | 0.578 |
MOD_Plk_1 | 728 | 734 | PF00069 | 0.405 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.424 |
MOD_Plk_2-3 | 302 | 308 | PF00069 | 0.354 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.538 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.656 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.461 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.434 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.567 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.506 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.472 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.405 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.328 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.654 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.592 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.684 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.682 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.691 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.609 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.574 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.595 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.558 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.503 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.678 |
MOD_ProDKin_1 | 762 | 768 | PF00069 | 0.636 |
MOD_SUMO_for_1 | 587 | 590 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 542 | 548 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 583 | 589 | PF00179 | 0.362 |
TRG_DiLeu_BaEn_1 | 878 | 883 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 70 | 75 | PF01217 | 0.343 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 791 | 794 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.426 |
TRG_NLS_MonoExtN_4 | 249 | 256 | PF00514 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 557 | 561 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 72 | 77 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIL4 | Leptomonas seymouri | 56% | 100% |
A0A3S7X053 | Leishmania donovani | 76% | 100% |
A4I2E8 | Leishmania infantum | 76% | 100% |
C9ZX58 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AYK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q8X1 | Leishmania major | 76% | 98% |