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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005657 | replication fork | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IGY7
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006310 | DNA recombination | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0032200 | telomere organization | 6 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051276 | chromosome organization | 5 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003678 | DNA helicase activity | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004386 | helicase activity | 2 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0000287 | magnesium ion binding | 5 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.269 |
CLV_C14_Caspase3-7 | 619 | 623 | PF00656 | 0.734 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 774 | 776 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 875 | 877 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 894 | 896 | PF00675 | 0.432 |
CLV_PCSK_FUR_1 | 672 | 676 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 894 | 896 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 671 | 673 | PF00082 | 0.602 |
CLV_PCSK_PC7_1 | 152 | 158 | PF00082 | 0.494 |
CLV_PCSK_PC7_1 | 223 | 229 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 674 | 678 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 781 | 785 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 895 | 899 | PF00082 | 0.431 |
DEG_APCC_DBOX_1 | 544 | 552 | PF00400 | 0.420 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.579 |
DEG_SPOP_SBC_1 | 107 | 111 | PF00917 | 0.414 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.579 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.601 |
DOC_CKS1_1 | 439 | 444 | PF01111 | 0.347 |
DOC_CKS1_1 | 509 | 514 | PF01111 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 270 | 276 | PF00134 | 0.595 |
DOC_CYCLIN_yCln2_LP_2 | 439 | 445 | PF00134 | 0.347 |
DOC_CYCLIN_yCln2_LP_2 | 471 | 477 | PF00134 | 0.466 |
DOC_CYCLIN_yCln2_LP_2 | 830 | 836 | PF00134 | 0.369 |
DOC_MAPK_DCC_7 | 791 | 801 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 662 | 668 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 736 | 745 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 774 | 784 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 874 | 883 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 894 | 900 | PF00069 | 0.223 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.228 |
DOC_MAPK_MEF2A_6 | 401 | 410 | PF00069 | 0.240 |
DOC_MAPK_MEF2A_6 | 432 | 439 | PF00069 | 0.270 |
DOC_MAPK_RevD_3 | 881 | 895 | PF00069 | 0.376 |
DOC_PP1_RVXF_1 | 779 | 785 | PF00149 | 0.432 |
DOC_PP2B_LxvP_1 | 830 | 833 | PF13499 | 0.372 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.540 |
DOC_PP4_FxxP_1 | 350 | 353 | PF00568 | 0.269 |
DOC_PP4_FxxP_1 | 764 | 767 | PF00568 | 0.353 |
DOC_PP4_FxxP_1 | 98 | 101 | PF00568 | 0.341 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 907 | 911 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 919 | 923 | PF00917 | 0.482 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.216 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 912 | 917 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 108 | 118 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 193 | 202 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 44 | 48 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 631 | 636 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 647 | 656 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 674 | 679 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 699 | 704 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 774 | 782 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 894 | 900 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 921 | 925 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 926 | 933 | PF00244 | 0.485 |
LIG_Actin_WH2_2 | 247 | 264 | PF00022 | 0.428 |
LIG_Actin_WH2_2 | 314 | 329 | PF00022 | 0.269 |
LIG_Actin_WH2_2 | 544 | 562 | PF00022 | 0.368 |
LIG_Actin_WH2_2 | 725 | 740 | PF00022 | 0.501 |
LIG_BIR_III_4 | 534 | 538 | PF00653 | 0.517 |
LIG_BRCT_BRCA1_1 | 427 | 431 | PF00533 | 0.269 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.553 |
LIG_EH_1 | 99 | 103 | PF12763 | 0.361 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.518 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.269 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.281 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.531 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.454 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.609 |
LIG_FHA_1 | 829 | 835 | PF00498 | 0.372 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.588 |
LIG_FHA_1 | 851 | 857 | PF00498 | 0.314 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.407 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.494 |
LIG_FHA_2 | 681 | 687 | PF00498 | 0.384 |
LIG_FHA_2 | 700 | 706 | PF00498 | 0.498 |
LIG_FHA_2 | 717 | 723 | PF00498 | 0.493 |
LIG_Integrin_isoDGR_2 | 103 | 105 | PF01839 | 0.563 |
LIG_LIR_Apic_2 | 483 | 487 | PF02991 | 0.355 |
LIG_LIR_Apic_2 | 762 | 767 | PF02991 | 0.354 |
LIG_LIR_Apic_2 | 96 | 101 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 245 | 254 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 413 | 421 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 466 | 476 | PF02991 | 0.503 |
LIG_LIR_LC3C_4 | 879 | 883 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 413 | 417 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 466 | 471 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.670 |
LIG_PCNA_yPIPBox_3 | 251 | 262 | PF02747 | 0.543 |
LIG_PCNA_yPIPBox_3 | 791 | 802 | PF02747 | 0.397 |
LIG_PDZ_Class_2 | 932 | 937 | PF00595 | 0.543 |
LIG_Pex14_2 | 118 | 122 | PF04695 | 0.509 |
LIG_Pex14_2 | 346 | 350 | PF04695 | 0.269 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.395 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.531 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.550 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.575 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.482 |
LIG_SH2_GRB2like | 249 | 252 | PF00017 | 0.543 |
LIG_SH2_NCK_1 | 426 | 430 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 426 | 430 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 838 | 842 | PF00017 | 0.432 |
LIG_SH2_STAT3 | 884 | 887 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 823 | 826 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 869 | 872 | PF00017 | 0.291 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.434 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.674 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.665 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.539 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.432 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.389 |
LIG_SH3_3 | 804 | 810 | PF00018 | 0.346 |
LIG_SH3_CIN85_PxpxPR_1 | 22 | 27 | PF14604 | 0.571 |
LIG_SUMO_SIM_anti_2 | 376 | 382 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 581 | 586 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 664 | 670 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 712 | 717 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 852 | 857 | PF11976 | 0.306 |
MOD_CDK_SPxK_1 | 438 | 444 | PF00069 | 0.347 |
MOD_CDK_SPxK_1 | 508 | 514 | PF00069 | 0.463 |
MOD_CDK_SPxK_1 | 730 | 736 | PF00069 | 0.434 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.577 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.371 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.311 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.686 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.563 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.721 |
MOD_CK1_1 | 754 | 760 | PF00069 | 0.355 |
MOD_CK1_1 | 922 | 928 | PF00069 | 0.454 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.502 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.301 |
MOD_CK2_1 | 678 | 684 | PF00069 | 0.481 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.538 |
MOD_CK2_1 | 893 | 899 | PF00069 | 0.361 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.410 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.628 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.564 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.611 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.304 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.254 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.479 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.725 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.520 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.741 |
MOD_GlcNHglycan | 895 | 898 | PF01048 | 0.342 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.522 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.729 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.595 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.609 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.670 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.316 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.502 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.571 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.672 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.488 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.671 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.630 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.430 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.605 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.598 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.421 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.332 |
MOD_N-GLC_1 | 477 | 482 | PF02516 | 0.477 |
MOD_N-GLC_1 | 747 | 752 | PF02516 | 0.410 |
MOD_N-GLC_1 | 754 | 759 | PF02516 | 0.356 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.420 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.520 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.269 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.335 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.582 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.431 |
MOD_NEK2_1 | 714 | 719 | PF00069 | 0.510 |
MOD_NEK2_1 | 749 | 754 | PF00069 | 0.422 |
MOD_NEK2_1 | 816 | 821 | PF00069 | 0.443 |
MOD_NEK2_1 | 850 | 855 | PF00069 | 0.317 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.507 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.287 |
MOD_NEK2_2 | 657 | 662 | PF00069 | 0.535 |
MOD_NEK2_2 | 767 | 772 | PF00069 | 0.438 |
MOD_NEK2_2 | 838 | 843 | PF00069 | 0.310 |
MOD_OFUCOSY | 48 | 54 | PF10250 | 0.495 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.554 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.447 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.427 |
MOD_PKA_1 | 674 | 680 | PF00069 | 0.476 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.408 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.548 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.596 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.659 |
MOD_PKA_2 | 630 | 636 | PF00069 | 0.707 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.592 |
MOD_PKA_2 | 773 | 779 | PF00069 | 0.615 |
MOD_PKA_2 | 893 | 899 | PF00069 | 0.420 |
MOD_PKA_2 | 907 | 913 | PF00069 | 0.432 |
MOD_PKA_2 | 920 | 926 | PF00069 | 0.356 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.495 |
MOD_PKB_1 | 672 | 680 | PF00069 | 0.496 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.269 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.314 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.429 |
MOD_Plk_1 | 767 | 773 | PF00069 | 0.500 |
MOD_Plk_2-3 | 376 | 382 | PF00069 | 0.269 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.402 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.309 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.269 |
MOD_Plk_4 | 699 | 705 | PF00069 | 0.456 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.455 |
MOD_Plk_4 | 767 | 773 | PF00069 | 0.472 |
MOD_Plk_4 | 819 | 825 | PF00069 | 0.408 |
MOD_Plk_4 | 850 | 856 | PF00069 | 0.313 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.456 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.498 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.521 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.216 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.347 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.409 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.679 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.412 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.626 |
MOD_ProDKin_1 | 912 | 918 | PF00069 | 0.552 |
MOD_SUMO_rev_2 | 491 | 500 | PF00179 | 0.362 |
TRG_DiLeu_BaEn_3 | 706 | 712 | PF01217 | 0.424 |
TRG_DiLeu_BaEn_4 | 554 | 560 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 350 | 355 | PF01217 | 0.217 |
TRG_DiLeu_BaLyEn_6 | 544 | 549 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 797 | 802 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.561 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 487 | 490 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 599 | 602 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 672 | 675 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 773 | 775 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 893 | 895 | PF00400 | 0.573 |
TRG_NLS_MonoExtC_3 | 184 | 190 | PF00514 | 0.546 |
TRG_NLS_MonoExtC_3 | 670 | 675 | PF00514 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 319 | 323 | PF00026 | 0.243 |
TRG_Pf-PMV_PEXEL_1 | 781 | 785 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 800 | 805 | PF00026 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 876 | 880 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCJ6 | Leptomonas seymouri | 59% | 84% |
A0A1X0NSB2 | Trypanosomatidae | 51% | 100% |
A0A422NKI2 | Trypanosoma rangeli | 50% | 100% |
A4HGV5 | Leishmania braziliensis | 80% | 100% |
A4I3Y5 | Leishmania infantum | 100% | 100% |
D0A956 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9B075 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q383A1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 47% | 100% |
Q4Q810 | Leishmania major | 92% | 100% |
V5BL79 | Trypanosoma cruzi | 50% | 100% |