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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0042555 | MCM complex | 2 | 12 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4QI01
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 2 |
GO:0000725 | recombinational repair | 6 | 2 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006268 | DNA unwinding involved in DNA replication | 9 | 2 |
GO:0006270 | DNA replication initiation | 5 | 12 |
GO:0006271 | DNA strand elongation involved in DNA replication | 6 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022616 | DNA strand elongation | 5 | 2 |
GO:0032392 | DNA geometric change | 7 | 2 |
GO:0032508 | DNA duplex unwinding | 8 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051276 | chromosome organization | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071103 | DNA conformation change | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1902292 | cell cycle DNA replication initiation | 3 | 2 |
GO:1902315 | nuclear cell cycle DNA replication initiation | 4 | 2 |
GO:1902975 | mitotic DNA replication initiation | 4 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 3 | 12 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.430 |
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.293 |
CLV_C14_Caspase3-7 | 671 | 675 | PF00656 | 0.594 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 627 | 629 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 821 | 823 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 829 | 831 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 627 | 629 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 782 | 784 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 821 | 823 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 828 | 830 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.229 |
CLV_PCSK_PC1ET2_1 | 782 | 784 | PF00082 | 0.278 |
CLV_PCSK_PC1ET2_1 | 828 | 830 | PF00082 | 0.477 |
CLV_PCSK_PC7_1 | 22 | 28 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 791 | 795 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 845 | 849 | PF00082 | 0.371 |
CLV_Separin_Metazoa | 313 | 317 | PF03568 | 0.523 |
CLV_Separin_Metazoa | 81 | 85 | PF03568 | 0.412 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 435 | 443 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 577 | 585 | PF00400 | 0.411 |
DEG_Kelch_Keap1_1 | 485 | 490 | PF01344 | 0.411 |
DEG_Kelch_Keap1_1 | 637 | 642 | PF01344 | 0.512 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.488 |
DEG_SPOP_SBC_1 | 425 | 429 | PF00917 | 0.542 |
DOC_CKS1_1 | 342 | 347 | PF01111 | 0.637 |
DOC_MAPK_DCC_7 | 181 | 191 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 181 | 191 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 766 | 775 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 102 | 109 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 184 | 191 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 436 | 443 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 578 | 586 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 90 | 97 | PF00069 | 0.423 |
DOC_MAPK_RevD_3 | 582 | 596 | PF00069 | 0.478 |
DOC_PP2B_PxIxI_1 | 186 | 192 | PF00149 | 0.421 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 740 | 744 | PF00917 | 0.443 |
DOC_USP7_UBL2_3 | 240 | 244 | PF12436 | 0.513 |
DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.513 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 57 | 61 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 650 | 658 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 759 | 767 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 836 | 842 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 90 | 94 | PF00244 | 0.479 |
LIG_Actin_WH2_2 | 122 | 139 | PF00022 | 0.463 |
LIG_AP2alpha_1 | 21 | 25 | PF02296 | 0.391 |
LIG_APCC_ABBA_1 | 18 | 23 | PF00400 | 0.440 |
LIG_APCC_ABBA_1 | 234 | 239 | PF00400 | 0.411 |
LIG_APCC_ABBA_1 | 602 | 607 | PF00400 | 0.411 |
LIG_APCC_ABBA_1 | 685 | 690 | PF00400 | 0.465 |
LIG_APCC_ABBAyCdc20_2 | 412 | 418 | PF00400 | 0.513 |
LIG_BIR_III_4 | 664 | 668 | PF00653 | 0.782 |
LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.513 |
LIG_CaM_IQ_9 | 196 | 212 | PF13499 | 0.435 |
LIG_Clathr_ClatBox_1 | 800 | 804 | PF01394 | 0.491 |
LIG_eIF4E_1 | 130 | 136 | PF01652 | 0.463 |
LIG_eIF4E_1 | 237 | 243 | PF01652 | 0.513 |
LIG_eIF4E_1 | 77 | 83 | PF01652 | 0.470 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.516 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.453 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.368 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.657 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.541 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.411 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.411 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.411 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.411 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.411 |
LIG_FHA_1 | 795 | 801 | PF00498 | 0.457 |
LIG_FHA_1 | 836 | 842 | PF00498 | 0.449 |
LIG_FHA_1 | 882 | 888 | PF00498 | 0.475 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.521 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.304 |
LIG_FHA_2 | 669 | 675 | PF00498 | 0.651 |
LIG_LIR_Gen_1 | 369 | 378 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 379 | 389 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 5 | 16 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 509 | 517 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 577 | 586 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 708 | 718 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 866 | 871 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 94 | 105 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 379 | 384 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 577 | 582 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 708 | 713 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 716 | 722 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 866 | 870 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.463 |
LIG_NRBOX | 438 | 444 | PF00104 | 0.513 |
LIG_NRBOX | 580 | 586 | PF00104 | 0.411 |
LIG_NRBOX | 78 | 84 | PF00104 | 0.412 |
LIG_NRBOX | 822 | 828 | PF00104 | 0.441 |
LIG_Pex14_1 | 197 | 201 | PF04695 | 0.513 |
LIG_Pex14_2 | 21 | 25 | PF04695 | 0.247 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.411 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.409 |
LIG_SH2_PTP2 | 710 | 713 | PF00017 | 0.435 |
LIG_SH2_PTP2 | 734 | 737 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 71 | 74 | PF00017 | 0.467 |
LIG_SH2_STAT3 | 831 | 834 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 734 | 737 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 831 | 834 | PF00017 | 0.446 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.480 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.706 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.541 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.411 |
LIG_SH3_3 | 694 | 700 | PF00018 | 0.416 |
LIG_SH3_3 | 855 | 861 | PF00018 | 0.556 |
LIG_SUMO_SIM_anti_2 | 132 | 137 | PF11976 | 0.547 |
LIG_SUMO_SIM_anti_2 | 866 | 872 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 837 | 843 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 91 | 96 | PF11976 | 0.437 |
LIG_TRAF2_1 | 640 | 643 | PF00917 | 0.606 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.495 |
LIG_UBA3_1 | 172 | 176 | PF00899 | 0.513 |
LIG_WRC_WIRS_1 | 29 | 34 | PF05994 | 0.468 |
LIG_WRC_WIRS_1 | 385 | 390 | PF05994 | 0.411 |
LIG_WRC_WIRS_1 | 877 | 882 | PF05994 | 0.379 |
MOD_CDK_SPK_2 | 611 | 616 | PF00069 | 0.489 |
MOD_CDK_SPxK_1 | 285 | 291 | PF00069 | 0.513 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.422 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.713 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.463 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.489 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.499 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.610 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.207 |
MOD_CK1_1 | 743 | 749 | PF00069 | 0.463 |
MOD_CK1_1 | 771 | 777 | PF00069 | 0.513 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.434 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.711 |
MOD_CK2_1 | 837 | 843 | PF00069 | 0.353 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.435 |
MOD_Cter_Amidation | 625 | 628 | PF01082 | 0.731 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.318 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.324 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.505 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.262 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.314 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.230 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.240 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.601 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.705 |
MOD_GlcNHglycan | 637 | 642 | PF01048 | 0.700 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.246 |
MOD_GlcNHglycan | 785 | 788 | PF01048 | 0.218 |
MOD_GlcNHglycan | 852 | 855 | PF01048 | 0.598 |
MOD_GlcNHglycan | 871 | 874 | PF01048 | 0.299 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.583 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.353 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.411 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.513 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.440 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.513 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.411 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.411 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.519 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.737 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.736 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.692 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.437 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.427 |
MOD_GSK3_1 | 876 | 883 | PF00069 | 0.376 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.227 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.725 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.679 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.546 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.450 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.357 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.411 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.584 |
MOD_NEK2_1 | 880 | 885 | PF00069 | 0.410 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.513 |
MOD_NEK2_2 | 714 | 719 | PF00069 | 0.421 |
MOD_PIKK_1 | 449 | 455 | PF00454 | 0.411 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.432 |
MOD_PIKK_1 | 644 | 650 | PF00454 | 0.649 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.411 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.536 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.425 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.440 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.516 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.719 |
MOD_PKA_2 | 714 | 720 | PF00069 | 0.425 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.435 |
MOD_PKA_2 | 758 | 764 | PF00069 | 0.435 |
MOD_PKA_2 | 835 | 841 | PF00069 | 0.406 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.455 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.489 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.427 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.401 |
MOD_Plk_1 | 644 | 650 | PF00069 | 0.649 |
MOD_Plk_1 | 771 | 777 | PF00069 | 0.453 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.469 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.529 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.421 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.490 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.510 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.513 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.425 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.414 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.401 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.411 |
MOD_Plk_4 | 702 | 708 | PF00069 | 0.528 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.494 |
MOD_Plk_4 | 753 | 759 | PF00069 | 0.411 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.503 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.439 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.383 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.513 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.659 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.696 |
MOD_SUMO_rev_2 | 235 | 242 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 774 | 784 | PF00179 | 0.418 |
TRG_DiLeu_BaEn_1 | 238 | 243 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_1 | 438 | 443 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_1 | 494 | 499 | PF01217 | 0.427 |
TRG_DiLeu_BaEn_1 | 866 | 871 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 710 | 713 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 734 | 737 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.500 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 595 | 597 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 627 | 629 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 820 | 822 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 829 | 831 | PF00400 | 0.379 |
TRG_NES_CRM1_1 | 562 | 572 | PF08389 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 821 | 825 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 830 | 834 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P860 | Leptomonas seymouri | 31% | 90% |
A0A0N1I383 | Leptomonas seymouri | 77% | 88% |
A0A0S4IW18 | Bodo saltans | 56% | 100% |
A0A1X0NNF6 | Trypanosomatidae | 58% | 98% |
A0A1X0NZT6 | Trypanosomatidae | 30% | 95% |
A0A3R7K9K0 | Trypanosoma rangeli | 30% | 100% |
A0A3R7NBN0 | Trypanosoma rangeli | 30% | 94% |
A0A3S7WQI8 | Leishmania donovani | 97% | 100% |
A0A3S7WY81 | Leishmania donovani | 30% | 100% |
A0A422NDD9 | Trypanosoma rangeli | 59% | 100% |
A4FUD9 | Bos taurus | 33% | 100% |
A4H5K0 | Leishmania braziliensis | 87% | 97% |
A4HDE7 | Leishmania braziliensis | 29% | 100% |
A4HGC9 | Leishmania braziliensis | 30% | 92% |
A4HTX2 | Leishmania infantum | 97% | 100% |
A4I0T0 | Leishmania infantum | 30% | 100% |
B8AZ14 | Oryza sativa subsp. indica | 31% | 100% |
B8AZ99 | Oryza sativa subsp. indica | 30% | 100% |
B8BKI8 | Oryza sativa subsp. indica | 29% | 93% |
B9FKM7 | Oryza sativa subsp. japonica | 31% | 100% |
D0A7X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 94% |
D0A999 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
D3ZVK1 | Rattus norvegicus | 30% | 100% |
E1BPX4 | Bos taurus | 30% | 100% |
E9AMM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B059 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
I0IUP3 | Gallus gallus | 30% | 100% |
P24279 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 92% |
P25205 | Homo sapiens | 33% | 100% |
P25206 | Mus musculus | 32% | 100% |
P29458 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 41% | 96% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P30664 | Xenopus laevis | 43% | 100% |
P30665 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 96% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
P33991 | Homo sapiens | 43% | 100% |
P49717 | Mus musculus | 43% | 100% |
P49739 | Xenopus laevis | 32% | 100% |
Q0DHC4 | Oryza sativa subsp. japonica | 30% | 100% |
Q0V9Q6 | Xenopus tropicalis | 30% | 100% |
Q21902 | Caenorhabditis elegans | 28% | 100% |
Q26454 | Drosophila melanogaster | 41% | 100% |
Q28BS0 | Xenopus tropicalis | 31% | 100% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 32% | 100% |
Q2R482 | Oryza sativa subsp. japonica | 29% | 93% |
Q43704 | Zea mays | 30% | 100% |
Q498J7 | Xenopus laevis | 31% | 100% |
Q4Q826 | Leishmania major | 30% | 100% |
Q4Q8I2 | Leishmania major | 31% | 92% |
Q4QAP2 | Leishmania major | 30% | 100% |
Q5F310 | Xenopus laevis | 29% | 100% |
Q5JKB0 | Oryza sativa subsp. japonica | 42% | 100% |
Q5R8G6 | Pongo abelii | 33% | 100% |
Q5XK83 | Xenopus laevis | 43% | 100% |
Q5ZMN2 | Gallus gallus | 32% | 100% |
Q6GL41 | Xenopus tropicalis | 43% | 100% |
Q7Q0Q1 | Anopheles gambiae | 32% | 100% |
Q7ZXZ0 | Xenopus laevis | 31% | 100% |
Q86B14 | Dictyostelium discoideum | 27% | 100% |
Q95XQ8 | Caenorhabditis elegans | 41% | 100% |
Q9CWV1 | Mus musculus | 31% | 100% |
Q9FL33 | Arabidopsis thaliana | 30% | 100% |
Q9LPD9 | Arabidopsis thaliana | 28% | 96% |
Q9SF37 | Arabidopsis thaliana | 29% | 100% |
Q9SX03 | Zea mays | 30% | 100% |
Q9SX04 | Zea mays | 30% | 100% |
Q9UJA3 | Homo sapiens | 29% | 100% |
Q9V461 | Drosophila melanogaster | 33% | 100% |
Q9VF30 | Drosophila melanogaster | 25% | 100% |
Q9XYU1 | Drosophila melanogaster | 31% | 100% |
V5BAH7 | Trypanosoma cruzi | 30% | 100% |
V5BQA9 | Trypanosoma cruzi | 30% | 100% |
V5BSG2 | Trypanosoma cruzi | 58% | 100% |