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:0005657 | replication fork | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q810
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:0006260 | DNA replication | 5 | 2 |
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:0032392 | DNA geometric change | 7 | 2 |
GO:0032508 | DNA duplex unwinding | 8 | 2 |
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:0071103 | DNA conformation change | 6 | 2 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0000287 | magnesium ion binding | 5 | 2 |
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:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 378 | 382 | PF00656 | 0.327 |
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.330 |
CLV_C14_Caspase3-7 | 621 | 625 | PF00656 | 0.789 |
CLV_C14_Caspase3-7 | 71 | 75 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 723 | 727 | PF00656 | 0.466 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 773 | 775 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 874 | 876 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 893 | 895 | PF00675 | 0.489 |
CLV_PCSK_FUR_1 | 671 | 675 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 773 | 775 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 784 | 786 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 893 | 895 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 670 | 672 | PF00082 | 0.741 |
CLV_PCSK_PC1ET2_1 | 784 | 786 | PF00082 | 0.366 |
CLV_PCSK_PC7_1 | 152 | 158 | PF00082 | 0.622 |
CLV_PCSK_PC7_1 | 223 | 229 | PF00082 | 0.574 |
CLV_PCSK_PC7_1 | 780 | 786 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 780 | 784 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 894 | 898 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 523 | 531 | PF00400 | 0.415 |
DEG_APCC_DBOX_1 | 543 | 551 | PF00400 | 0.522 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.679 |
DEG_SPOP_SBC_1 | 107 | 111 | PF00917 | 0.539 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.680 |
DOC_ANK_TNKS_1 | 612 | 619 | PF00023 | 0.594 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.634 |
DOC_CKS1_1 | 438 | 443 | PF01111 | 0.408 |
DOC_CKS1_1 | 508 | 513 | PF01111 | 0.494 |
DOC_CKS1_1 | 58 | 63 | PF01111 | 0.551 |
DOC_CYCLIN_yCln2_LP_2 | 270 | 276 | PF00134 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 438 | 444 | PF00134 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 470 | 476 | PF00134 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 660 | 666 | PF00134 | 0.525 |
DOC_CYCLIN_yCln2_LP_2 | 829 | 835 | PF00134 | 0.516 |
DOC_MAPK_DCC_7 | 790 | 800 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 661 | 667 | PF00069 | 0.684 |
DOC_MAPK_gen_1 | 735 | 744 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 773 | 783 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 873 | 882 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 893 | 899 | PF00069 | 0.219 |
DOC_MAPK_MEF2A_6 | 431 | 438 | PF00069 | 0.336 |
DOC_MAPK_RevD_3 | 880 | 894 | PF00069 | 0.438 |
DOC_PP1_RVXF_1 | 778 | 784 | PF00149 | 0.553 |
DOC_PP2B_LxvP_1 | 829 | 832 | PF13499 | 0.518 |
DOC_PP4_FxxP_1 | 34 | 37 | PF00568 | 0.616 |
DOC_PP4_FxxP_1 | 350 | 353 | PF00568 | 0.335 |
DOC_PP4_FxxP_1 | 763 | 766 | PF00568 | 0.418 |
DOC_PP4_FxxP_1 | 98 | 101 | PF00568 | 0.409 |
DOC_SPAK_OSR1_1 | 461 | 465 | PF12202 | 0.357 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 766 | 770 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 772 | 776 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 906 | 910 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 918 | 922 | PF00917 | 0.536 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 729 | 734 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 911 | 916 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 108 | 113 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 193 | 202 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 44 | 48 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 673 | 678 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 698 | 703 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 773 | 781 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 893 | 899 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 920 | 924 | PF00244 | 0.449 |
LIG_Actin_WH2_2 | 247 | 264 | PF00022 | 0.538 |
LIG_Actin_WH2_2 | 314 | 329 | PF00022 | 0.335 |
LIG_BIR_III_4 | 533 | 537 | PF00653 | 0.673 |
LIG_BRCT_BRCA1_1 | 426 | 430 | PF00533 | 0.335 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.605 |
LIG_EH_1 | 99 | 103 | PF12763 | 0.427 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.448 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.553 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.584 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.329 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.335 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.570 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.539 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.706 |
LIG_FHA_1 | 828 | 834 | PF00498 | 0.519 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.654 |
LIG_FHA_1 | 850 | 856 | PF00498 | 0.376 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.546 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.571 |
LIG_FHA_2 | 699 | 705 | PF00498 | 0.547 |
LIG_FHA_2 | 716 | 722 | PF00498 | 0.540 |
LIG_Integrin_isoDGR_2 | 103 | 105 | PF01839 | 0.593 |
LIG_LIR_Apic_2 | 263 | 268 | PF02991 | 0.459 |
LIG_LIR_Apic_2 | 33 | 37 | PF02991 | 0.604 |
LIG_LIR_Apic_2 | 482 | 486 | PF02991 | 0.425 |
LIG_LIR_Apic_2 | 55 | 61 | PF02991 | 0.543 |
LIG_LIR_Apic_2 | 761 | 766 | PF02991 | 0.417 |
LIG_LIR_Apic_2 | 96 | 101 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 245 | 254 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 412 | 420 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 465 | 475 | PF02991 | 0.514 |
LIG_LIR_LC3C_4 | 878 | 882 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 412 | 416 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 683 | 687 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.631 |
LIG_PCNA_yPIPBox_3 | 251 | 262 | PF02747 | 0.570 |
LIG_PCNA_yPIPBox_3 | 790 | 801 | PF02747 | 0.522 |
LIG_PDZ_Class_2 | 931 | 936 | PF00595 | 0.652 |
LIG_Pex14_2 | 118 | 122 | PF04695 | 0.505 |
LIG_Pex14_2 | 346 | 350 | PF04695 | 0.319 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.472 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.558 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.584 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.628 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.708 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.616 |
LIG_SH2_GRB2like | 249 | 252 | PF00017 | 0.563 |
LIG_SH2_NCK_1 | 425 | 429 | PF00017 | 0.440 |
LIG_SH2_NCK_1 | 58 | 62 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 837 | 841 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 883 | 886 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 822 | 825 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 868 | 871 | PF00017 | 0.354 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.503 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.741 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.761 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.673 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.620 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.467 |
LIG_SH3_3 | 672 | 678 | PF00018 | 0.500 |
LIG_SH3_3 | 803 | 809 | PF00018 | 0.412 |
LIG_SH3_CIN85_PxpxPR_1 | 22 | 27 | PF14604 | 0.694 |
LIG_SUMO_SIM_anti_2 | 370 | 376 | PF11976 | 0.331 |
LIG_SUMO_SIM_anti_2 | 580 | 585 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 281 | 286 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 370 | 376 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 663 | 669 | PF11976 | 0.696 |
LIG_SUMO_SIM_par_1 | 851 | 856 | PF11976 | 0.368 |
MOD_CDK_SPxK_1 | 437 | 443 | PF00069 | 0.408 |
MOD_CDK_SPxK_1 | 507 | 513 | PF00069 | 0.522 |
MOD_CDK_SPxK_1 | 729 | 735 | PF00069 | 0.499 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.691 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.378 |
MOD_CK1_1 | 628 | 634 | PF00069 | 0.747 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.767 |
MOD_CK1_1 | 753 | 759 | PF00069 | 0.404 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.541 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.567 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.533 |
MOD_CK2_1 | 698 | 704 | PF00069 | 0.574 |
MOD_CK2_1 | 892 | 898 | PF00069 | 0.424 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.730 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.673 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.758 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.371 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.528 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.763 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.730 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.726 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.565 |
MOD_GlcNHglycan | 894 | 897 | PF01048 | 0.404 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.608 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.710 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.732 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.660 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.747 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.382 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.542 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.542 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.727 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.515 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.699 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.705 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.600 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.645 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.462 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.451 |
MOD_GSK3_1 | 845 | 852 | PF00069 | 0.396 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.456 |
MOD_N-GLC_1 | 476 | 481 | PF02516 | 0.536 |
MOD_N-GLC_1 | 746 | 751 | PF02516 | 0.469 |
MOD_N-GLC_1 | 753 | 758 | PF02516 | 0.419 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.464 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.558 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.324 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.320 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.733 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.474 |
MOD_NEK2_1 | 748 | 753 | PF00069 | 0.451 |
MOD_NEK2_1 | 815 | 820 | PF00069 | 0.600 |
MOD_NEK2_1 | 849 | 854 | PF00069 | 0.380 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.549 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.354 |
MOD_NEK2_2 | 656 | 661 | PF00069 | 0.691 |
MOD_NEK2_2 | 766 | 771 | PF00069 | 0.514 |
MOD_NEK2_2 | 837 | 842 | PF00069 | 0.373 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.602 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.599 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.554 |
MOD_PKA_1 | 673 | 679 | PF00069 | 0.629 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.481 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.656 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.729 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.740 |
MOD_PKA_2 | 629 | 635 | PF00069 | 0.768 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.594 |
MOD_PKA_2 | 772 | 778 | PF00069 | 0.649 |
MOD_PKA_2 | 892 | 898 | PF00069 | 0.477 |
MOD_PKA_2 | 906 | 912 | PF00069 | 0.525 |
MOD_PKA_2 | 919 | 925 | PF00069 | 0.403 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.551 |
MOD_PKB_1 | 671 | 679 | PF00069 | 0.616 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.335 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.381 |
MOD_Plk_1 | 476 | 482 | PF00069 | 0.488 |
MOD_Plk_1 | 766 | 772 | PF00069 | 0.544 |
MOD_Plk_2-3 | 375 | 381 | PF00069 | 0.335 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.370 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.324 |
MOD_Plk_4 | 766 | 772 | PF00069 | 0.529 |
MOD_Plk_4 | 818 | 824 | PF00069 | 0.479 |
MOD_Plk_4 | 849 | 855 | PF00069 | 0.376 |
MOD_Plk_4 | 919 | 925 | PF00069 | 0.407 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.499 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.541 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.575 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.373 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.398 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.475 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.733 |
MOD_ProDKin_1 | 729 | 735 | PF00069 | 0.481 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.543 |
MOD_ProDKin_1 | 911 | 917 | PF00069 | 0.620 |
MOD_SUMO_rev_2 | 490 | 499 | PF00179 | 0.428 |
TRG_DiLeu_BaLyEn_6 | 543 | 548 | PF01217 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 796 | 801 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 486 | 489 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 598 | 601 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 671 | 674 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 772 | 774 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 892 | 894 | PF00400 | 0.572 |
TRG_NLS_MonoExtC_3 | 669 | 674 | PF00514 | 0.740 |
TRG_Pf-PMV_PEXEL_1 | 799 | 804 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 875 | 879 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCJ6 | Leptomonas seymouri | 59% | 84% |
A0A1X0NSB2 | Trypanosomatidae | 51% | 100% |
A0A3Q8IGY7 | Leishmania donovani | 92% | 100% |
A0A422NKI2 | Trypanosoma rangeli | 50% | 100% |
A4HGV5 | Leishmania braziliensis | 79% | 100% |
A4I3Y5 | Leishmania infantum | 92% | 100% |
D0A956 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9B075 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q383A1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 48% | 100% |
V5BL79 | Trypanosoma cruzi | 50% | 100% |