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 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q8X1
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 2 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 2 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 2 |
GO:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0010948 | negative regulation of cell cycle process | 6 | 2 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 2 |
GO:0033314 | mitotic DNA replication checkpoint signaling | 6 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 2 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 2 |
GO:0045786 | negative regulation of cell cycle | 5 | 2 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 2 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 2 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 2 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 2 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 2 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003688 | DNA replication origin binding | 7 | 2 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0043565 | sequence-specific DNA binding | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 642 | 646 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 729 | 731 | PF00675 | 0.357 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 836 | 838 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 411 | 413 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 520 | 522 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 836 | 838 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.349 |
CLV_PCSK_PC7_1 | 115 | 121 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.424 |
CLV_Separin_Metazoa | 860 | 864 | PF03568 | 0.370 |
DEG_COP1_1 | 35 | 43 | PF00400 | 0.488 |
DEG_SCF_FBW7_1 | 153 | 160 | PF00400 | 0.591 |
DEG_SCF_FBW7_1 | 181 | 186 | PF00400 | 0.602 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.519 |
DEG_SPOP_SBC_1 | 403 | 407 | PF00917 | 0.541 |
DEG_SPOP_SBC_1 | 582 | 586 | PF00917 | 0.479 |
DOC_ANK_TNKS_1 | 389 | 396 | PF00023 | 0.451 |
DOC_CDC14_PxL_1 | 463 | 471 | PF14671 | 0.290 |
DOC_CKS1_1 | 154 | 159 | PF01111 | 0.569 |
DOC_CYCLIN_RxL_1 | 148 | 158 | PF00134 | 0.591 |
DOC_CYCLIN_RxL_1 | 537 | 546 | PF00134 | 0.350 |
DOC_MAPK_DCC_7 | 411 | 421 | PF00069 | 0.435 |
DOC_MAPK_DCC_7 | 461 | 471 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 520 | 529 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 539 | 545 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 412 | 421 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 761 | 770 | PF00069 | 0.440 |
DOC_PP1_RVXF_1 | 781 | 787 | PF00149 | 0.416 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.371 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 738 | 742 | PF00917 | 0.469 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 748 | 753 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 101 | 109 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 120 | 124 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 203 | 209 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 521 | 531 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 558 | 563 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 602 | 607 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 817 | 822 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 845 | 853 | PF00244 | 0.454 |
LIG_Actin_WH2_2 | 415 | 433 | PF00022 | 0.380 |
LIG_Actin_WH2_2 | 800 | 815 | PF00022 | 0.375 |
LIG_APCC_ABBA_1 | 476 | 481 | PF00400 | 0.341 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.593 |
LIG_BIR_III_4 | 645 | 649 | PF00653 | 0.583 |
LIG_BRCT_BRCA1_1 | 632 | 636 | PF00533 | 0.552 |
LIG_EH1_1 | 44 | 52 | PF00400 | 0.480 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.695 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.545 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.339 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.571 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.508 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.299 |
LIG_FHA_1 | 763 | 769 | PF00498 | 0.425 |
LIG_FHA_1 | 813 | 819 | PF00498 | 0.388 |
LIG_FHA_1 | 822 | 828 | PF00498 | 0.386 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.334 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.558 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.541 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.618 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.609 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.529 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.471 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.364 |
LIG_FHA_2 | 710 | 716 | PF00498 | 0.347 |
LIG_LIR_Apic_2 | 824 | 828 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 855 | 866 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 803 | 807 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 855 | 861 | PF02991 | 0.391 |
LIG_LYPXL_yS_3 | 313 | 316 | PF13949 | 0.369 |
LIG_NRBOX | 470 | 476 | PF00104 | 0.262 |
LIG_PCNA_PIPBox_1 | 770 | 779 | PF02747 | 0.387 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.376 |
LIG_SH2_CRK | 534 | 538 | PF00017 | 0.313 |
LIG_SH2_CRK | 777 | 781 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 343 | 346 | PF00017 | 0.326 |
LIG_SH2_NCK_1 | 304 | 308 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 479 | 483 | PF00017 | 0.346 |
LIG_SH2_SRC | 534 | 537 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 777 | 781 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 719 | 722 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 777 | 780 | PF00017 | 0.348 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.357 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.354 |
LIG_SUMO_SIM_anti_2 | 722 | 728 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 350 | 356 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 420 | 426 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 722 | 728 | PF11976 | 0.309 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.632 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.633 |
LIG_UBA3_1 | 376 | 385 | PF00899 | 0.378 |
LIG_WW_3 | 295 | 299 | PF00397 | 0.524 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.575 |
MOD_CDK_SPK_2 | 6 | 11 | PF00069 | 0.583 |
MOD_CDK_SPxxK_3 | 19 | 26 | PF00069 | 0.565 |
MOD_CDK_SPxxK_3 | 6 | 13 | PF00069 | 0.617 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.575 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.594 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.571 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.566 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.579 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.587 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.504 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.589 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.520 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.484 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.546 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.552 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.548 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.574 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.535 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.586 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.351 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.527 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.556 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.546 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.586 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.526 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.464 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.368 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.478 |
MOD_CK2_1 | 709 | 715 | PF00069 | 0.354 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.409 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.548 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.544 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.523 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.647 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.489 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.533 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.770 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.604 |
MOD_GlcNHglycan | 348 | 352 | PF01048 | 0.330 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.510 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.416 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.505 |
MOD_GlcNHglycan | 544 | 548 | PF01048 | 0.361 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.688 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.565 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.465 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.637 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.531 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.597 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.734 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.571 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.562 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.766 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.489 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.531 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.626 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.544 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.496 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.479 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.349 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.373 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.690 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.483 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.594 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.611 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.765 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.573 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.535 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.534 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.344 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.414 |
MOD_GSK3_1 | 733 | 740 | PF00069 | 0.422 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.376 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.587 |
MOD_N-GLC_1 | 602 | 607 | PF02516 | 0.550 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.368 |
MOD_N-GLC_1 | 821 | 826 | PF02516 | 0.384 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.594 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.541 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.397 |
MOD_NEK2_1 | 821 | 826 | PF00069 | 0.384 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.528 |
MOD_NEK2_2 | 307 | 312 | PF00069 | 0.400 |
MOD_NEK2_2 | 714 | 719 | PF00069 | 0.332 |
MOD_NEK2_2 | 764 | 769 | PF00069 | 0.409 |
MOD_OFUCOSY | 126 | 131 | PF10250 | 0.511 |
MOD_OFUCOSY | 359 | 366 | PF10250 | 0.353 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.607 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.466 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.379 |
MOD_PIKK_1 | 627 | 633 | PF00454 | 0.483 |
MOD_PIKK_1 | 637 | 643 | PF00454 | 0.486 |
MOD_PK_1 | 558 | 564 | PF00069 | 0.304 |
MOD_PK_1 | 602 | 608 | PF00069 | 0.513 |
MOD_PKA_1 | 119 | 125 | PF00069 | 0.464 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.356 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.477 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.575 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.616 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.583 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.640 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.383 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.509 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.389 |
MOD_PKA_2 | 601 | 607 | PF00069 | 0.574 |
MOD_PKA_2 | 655 | 661 | PF00069 | 0.510 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.428 |
MOD_PKA_2 | 812 | 818 | PF00069 | 0.399 |
MOD_PKA_2 | 844 | 850 | PF00069 | 0.438 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.592 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.460 |
MOD_Plk_1 | 602 | 608 | PF00069 | 0.530 |
MOD_Plk_1 | 714 | 720 | PF00069 | 0.327 |
MOD_Plk_1 | 733 | 739 | PF00069 | 0.426 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.366 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.576 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.322 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.464 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.359 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.327 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.296 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.585 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.548 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.557 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.664 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.556 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.599 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.600 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.549 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.443 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.532 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.597 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.534 |
MOD_ProDKin_1 | 748 | 754 | PF00069 | 0.591 |
MOD_SUMO_for_1 | 570 | 573 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 525 | 531 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 566 | 572 | PF00179 | 0.339 |
TRG_DiLeu_BaEn_1 | 864 | 869 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 777 | 780 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.353 |
TRG_NLS_Bipartite_1 | 508 | 524 | PF00514 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 106 | 111 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 165 | 170 | PF00026 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 540 | 544 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 72 | 77 | PF00026 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIL4 | Leptomonas seymouri | 54% | 99% |
A0A3S7X053 | Leishmania donovani | 91% | 98% |
A4HF65 | Leishmania braziliensis | 76% | 98% |
A4I2E8 | Leishmania infantum | 91% | 98% |
E9AYK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 98% |