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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HJJ5
Term | Name | Level | Count |
---|---|---|---|
GO:0000394 | RNA splicing, via endonucleolytic cleavage and ligation | 8 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006388 | tRNA splicing, via endonucleolytic cleavage and ligation | 9 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006399 | tRNA metabolic process | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008033 | tRNA processing | 8 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0008380 | RNA splicing | 7 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046939 | obsolete nucleotide phosphorylation | 6 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003972 | RNA ligase (ATP) activity | 5 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008452 | RNA ligase activity | 4 | 10 |
GO:0016874 | ligase activity | 2 | 10 |
GO:0016886 | ligase activity, forming phosphoric ester bonds | 3 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016791 | phosphatase activity | 5 | 1 |
GO:0019205 | nucleobase-containing compound kinase activity | 5 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0046403 | polynucleotide 3'-phosphatase activity | 6 | 1 |
GO:0046404 | polydeoxyribonucleotide 5'-hydroxyl-kinase activity | 7 | 1 |
GO:0051731 | polynucleotide 5'-hydroxyl-kinase activity | 5 | 1 |
GO:0051733 | polydeoxyribonucleotide kinase activity | 6 | 1 |
GO:0051734 | polynucleotide kinase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.328 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.680 |
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.376 |
CLV_C14_Caspase3-7 | 531 | 535 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 694 | 696 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 870 | 872 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 894 | 896 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.284 |
CLV_PCSK_FUR_1 | 50 | 54 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 694 | 696 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 894 | 896 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.284 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 894 | 896 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.274 |
DOC_ANK_TNKS_1 | 210 | 217 | PF00023 | 0.402 |
DOC_CKS1_1 | 719 | 724 | PF01111 | 0.288 |
DOC_CYCLIN_yClb1_LxF_4 | 315 | 320 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 88 | PF00134 | 0.503 |
DOC_MAPK_DCC_7 | 76 | 86 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 317 | 325 | PF00069 | 0.266 |
DOC_MAPK_gen_1 | 49 | 59 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 894 | 900 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 369 | 377 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 708 | 717 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 315 | 321 | PF00149 | 0.364 |
DOC_PP2B_LxvP_1 | 373 | 376 | PF13499 | 0.418 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.460 |
DOC_PP2B_PxIxI_1 | 863 | 869 | PF00149 | 0.308 |
DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.454 |
DOC_SPAK_OSR1_1 | 211 | 215 | PF12202 | 0.331 |
DOC_SPAK_OSR1_1 | 92 | 96 | PF12202 | 0.260 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.537 |
DOC_USP7_MATH_2 | 550 | 556 | PF00917 | 0.390 |
DOC_USP7_UBL2_3 | 149 | 153 | PF12436 | 0.466 |
DOC_USP7_UBL2_3 | 327 | 331 | PF12436 | 0.310 |
DOC_USP7_UBL2_3 | 614 | 618 | PF12436 | 0.362 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 881 | 886 | PF00397 | 0.360 |
LIG_14-3-3_CanoR_1 | 242 | 249 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 413 | 417 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 434 | 443 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 52 | 58 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 521 | 526 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 786 | 791 | PF00244 | 0.324 |
LIG_APCC_ABBA_1 | 848 | 853 | PF00400 | 0.203 |
LIG_BIR_III_4 | 427 | 431 | PF00653 | 0.512 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 906 | 910 | PF00533 | 0.317 |
LIG_CtBP_PxDLS_1 | 475 | 479 | PF00389 | 0.331 |
LIG_CtBP_PxDLS_1 | 641 | 645 | PF00389 | 0.457 |
LIG_CtBP_PxDLS_1 | 710 | 714 | PF00389 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 293 | 299 | PF00928 | 0.254 |
LIG_deltaCOP1_diTrp_1 | 484 | 492 | PF00928 | 0.377 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.443 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.546 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.417 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.421 |
LIG_FHA_1 | 831 | 837 | PF00498 | 0.465 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.484 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.538 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.307 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.466 |
LIG_FHA_2 | 744 | 750 | PF00498 | 0.463 |
LIG_LIR_Apic_2 | 154 | 160 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 180 | 185 | PF02991 | 0.423 |
LIG_LIR_Apic_2 | 397 | 403 | PF02991 | 0.465 |
LIG_LIR_Apic_2 | 645 | 651 | PF02991 | 0.375 |
LIG_LIR_Apic_2 | 78 | 83 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 381 | 391 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 520 | 529 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 636 | 644 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 757 | 768 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 520 | 525 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 636 | 640 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 757 | 763 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 809 | 815 | PF02991 | 0.295 |
LIG_MYND_1 | 276 | 280 | PF01753 | 0.351 |
LIG_MYND_1 | 679 | 683 | PF01753 | 0.448 |
LIG_NRBOX | 462 | 468 | PF00104 | 0.309 |
LIG_NRBOX | 579 | 585 | PF00104 | 0.347 |
LIG_NRBOX | 823 | 829 | PF00104 | 0.470 |
LIG_Pex14_1 | 295 | 299 | PF04695 | 0.437 |
LIG_Pex14_1 | 492 | 496 | PF04695 | 0.429 |
LIG_Pex14_2 | 299 | 303 | PF04695 | 0.467 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.584 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.465 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.418 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.270 |
LIG_SH2_CRK | 637 | 641 | PF00017 | 0.516 |
LIG_SH2_CRK | 773 | 777 | PF00017 | 0.328 |
LIG_SH2_GRB2like | 637 | 640 | PF00017 | 0.520 |
LIG_SH2_GRB2like | 878 | 881 | PF00017 | 0.284 |
LIG_SH2_NCK_1 | 138 | 142 | PF00017 | 0.582 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 400 | 404 | PF00017 | 0.575 |
LIG_SH2_NCK_1 | 773 | 777 | PF00017 | 0.352 |
LIG_SH2_PTP2 | 405 | 408 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 760 | 764 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 878 | 882 | PF00017 | 0.284 |
LIG_SH2_STAT3 | 367 | 370 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 811 | 814 | PF00017 | 0.466 |
LIG_SH3_2 | 889 | 894 | PF14604 | 0.360 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.327 |
LIG_SH3_3 | 704 | 710 | PF00018 | 0.553 |
LIG_SH3_3 | 765 | 771 | PF00018 | 0.519 |
LIG_SH3_3 | 812 | 818 | PF00018 | 0.280 |
LIG_SH3_3 | 837 | 843 | PF00018 | 0.330 |
LIG_SH3_3 | 886 | 892 | PF00018 | 0.358 |
LIG_SH3_3 | 895 | 901 | PF00018 | 0.272 |
LIG_SUFU_1 | 175 | 182 | PF12470 | 0.245 |
LIG_SUMO_SIM_anti_2 | 559 | 564 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 640 | 645 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 712 | 718 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 831 | 838 | PF11976 | 0.416 |
LIG_TRAF2_1 | 353 | 356 | PF00917 | 0.532 |
LIG_TRAF2_1 | 682 | 685 | PF00917 | 0.578 |
LIG_TYR_ITIM | 136 | 141 | PF00017 | 0.301 |
LIG_WRC_WIRS_1 | 2 | 7 | PF05994 | 0.517 |
LIG_WRC_WIRS_1 | 760 | 765 | PF05994 | 0.392 |
LIG_WW_1 | 875 | 878 | PF00397 | 0.400 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.743 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.532 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.396 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.398 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.502 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.404 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.724 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.492 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.321 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.456 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.491 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.394 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.558 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.587 |
MOD_GlcNHglycan | 311 | 315 | PF01048 | 0.535 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.628 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.585 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.621 |
MOD_GlcNHglycan | 906 | 909 | PF01048 | 0.273 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.675 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.501 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.758 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.554 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.646 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.411 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.567 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.354 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.541 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.399 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.407 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.523 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.500 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.360 |
MOD_GSK3_1 | 828 | 835 | PF00069 | 0.312 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.300 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.536 |
MOD_N-GLC_1 | 902 | 907 | PF02516 | 0.446 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.733 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.344 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.356 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.424 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.371 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.324 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.397 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.474 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.492 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.546 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.450 |
MOD_NEK2_1 | 717 | 722 | PF00069 | 0.477 |
MOD_NEK2_1 | 805 | 810 | PF00069 | 0.331 |
MOD_NEK2_1 | 828 | 833 | PF00069 | 0.404 |
MOD_NEK2_2 | 667 | 672 | PF00069 | 0.469 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.354 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.528 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.237 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.316 |
MOD_PK_1 | 786 | 792 | PF00069 | 0.359 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.263 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.407 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.737 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.347 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.437 |
MOD_PKA_2 | 667 | 673 | PF00069 | 0.390 |
MOD_PKB_1 | 519 | 527 | PF00069 | 0.382 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.485 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.460 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.298 |
MOD_Plk_1 | 902 | 908 | PF00069 | 0.477 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.381 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.449 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.412 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.390 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.412 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.283 |
MOD_Plk_4 | 759 | 765 | PF00069 | 0.310 |
MOD_Plk_4 | 786 | 792 | PF00069 | 0.310 |
MOD_Plk_4 | 835 | 841 | PF00069 | 0.350 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.359 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.497 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.751 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.537 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.363 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.541 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.529 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.557 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.528 |
MOD_ProDKin_1 | 881 | 887 | PF00069 | 0.360 |
MOD_SUMO_rev_2 | 534 | 539 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 597 | 605 | PF00179 | 0.398 |
TRG_DiLeu_BaEn_1 | 404 | 409 | PF01217 | 0.322 |
TRG_DiLeu_BaEn_1 | 462 | 467 | PF01217 | 0.306 |
TRG_DiLeu_BaLyEn_6 | 783 | 788 | PF01217 | 0.273 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 760 | 763 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 773 | 776 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 504 | 506 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 693 | 695 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 727 | 729 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.530 |
TRG_NES_CRM1_1 | 823 | 837 | PF08389 | 0.293 |
TRG_NLS_MonoExtN_4 | 892 | 898 | PF00514 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.286 |
TRG_Pf-PMV_PEXEL_1 | 673 | 678 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 728 | 732 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 92 | 97 | PF00026 | 0.259 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6S2 | Leptomonas seymouri | 60% | 100% |
A0A0S4J4W5 | Bodo saltans | 33% | 100% |
A0A1X0NHZ8 | Trypanosomatidae | 34% | 100% |
A0A3R7M5Z2 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X4Q3 | Leishmania donovani | 70% | 98% |
A4I6Z2 | Leishmania infantum | 70% | 98% |
E9B213 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 98% |
Q4Q648 | Leishmania major | 70% | 100% |