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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9B2T5
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 9 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006259 | DNA metabolic process | 4 | 9 |
GO:0006281 | DNA repair | 5 | 9 |
GO:0006310 | DNA recombination | 5 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0006950 | response to stress | 2 | 9 |
GO:0006974 | DNA damage response | 4 | 9 |
GO:0006996 | organelle organization | 4 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016043 | cellular component organization | 3 | 9 |
GO:0032200 | telomere organization | 6 | 9 |
GO:0033554 | cellular response to stress | 3 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0050896 | response to stimulus | 1 | 9 |
GO:0051276 | chromosome organization | 5 | 9 |
GO:0051716 | cellular response to stimulus | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003678 | DNA helicase activity | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004386 | helicase activity | 2 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 9 |
GO:0016462 | pyrophosphatase activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 9 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 9 |
GO:0016887 | ATP hydrolysis activity | 7 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
GO:0140657 | ATP-dependent activity | 1 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 522 | 526 | PF00656 | 0.376 |
CLV_MEL_PAP_1 | 331 | 337 | PF00089 | 0.412 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.781 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 696 | 698 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 873 | 875 | PF00675 | 0.478 |
CLV_PCSK_FUR_1 | 337 | 341 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.787 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 696 | 698 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 719 | 721 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.820 |
CLV_PCSK_PC1ET2_1 | 719 | 721 | PF00082 | 0.401 |
CLV_PCSK_PC7_1 | 297 | 303 | PF00082 | 0.203 |
CLV_PCSK_PC7_1 | 334 | 340 | PF00082 | 0.448 |
CLV_PCSK_PC7_1 | 692 | 698 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.455 |
CLV_Separin_Metazoa | 682 | 686 | PF03568 | 0.608 |
DEG_APCC_DBOX_1 | 572 | 580 | PF00400 | 0.577 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.609 |
DEG_SCF_FBW7_1 | 323 | 330 | PF00400 | 0.473 |
DEG_SCF_FBW7_2 | 15 | 20 | PF00400 | 0.579 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.513 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.621 |
DOC_ANK_TNKS_1 | 796 | 803 | PF00023 | 0.457 |
DOC_CKS1_1 | 205 | 210 | PF01111 | 0.669 |
DOC_CKS1_1 | 324 | 329 | PF01111 | 0.437 |
DOC_CKS1_1 | 831 | 836 | PF01111 | 0.435 |
DOC_CYCLIN_RxL_1 | 258 | 270 | PF00134 | 0.672 |
DOC_CYCLIN_yClb1_LxF_4 | 262 | 267 | PF00134 | 0.601 |
DOC_CYCLIN_yCln2_LP_2 | 604 | 610 | PF00134 | 0.636 |
DOC_MAPK_DCC_7 | 667 | 677 | PF00069 | 0.368 |
DOC_MAPK_DCC_7 | 803 | 812 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 719 | 729 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 872 | 881 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 671 | 679 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 803 | 812 | PF00069 | 0.372 |
DOC_PP1_RVXF_1 | 261 | 268 | PF00149 | 0.659 |
DOC_PP2B_LxvP_1 | 925 | 928 | PF13499 | 0.540 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.337 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 559 | 562 | PF00568 | 0.483 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 914 | 918 | PF00917 | 0.535 |
DOC_USP7_UBL2_3 | 496 | 500 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 764 | 769 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 830 | 835 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 882 | 887 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 915 | 920 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 932 | 937 | PF00397 | 0.522 |
LIG_14-3-3_CanoR_1 | 114 | 123 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 178 | 187 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 26 | 36 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 632 | 637 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 731 | 736 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 749 | 758 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 887 | 892 | PF00244 | 0.468 |
LIG_Actin_WH2_2 | 691 | 709 | PF00022 | 0.626 |
LIG_BIR_III_4 | 799 | 803 | PF00653 | 0.507 |
LIG_BRCT_BRCA1_1 | 307 | 311 | PF00533 | 0.420 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.293 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_1 | 436 | 440 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 894 | 898 | PF00533 | 0.503 |
LIG_CaM_NSCaTE_8 | 821 | 828 | PF13499 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 426 | 435 | PF00928 | 0.598 |
LIG_deltaCOP1_diTrp_1 | 436 | 440 | PF00928 | 0.456 |
LIG_deltaCOP1_diTrp_1 | 820 | 823 | PF00928 | 0.585 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.679 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.362 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.635 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.552 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.756 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.682 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.418 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.488 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.656 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.580 |
LIG_FHA_1 | 809 | 815 | PF00498 | 0.540 |
LIG_FHA_1 | 897 | 903 | PF00498 | 0.485 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.731 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.496 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.620 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.639 |
LIG_FHA_2 | 532 | 538 | PF00498 | 0.565 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.316 |
LIG_FHA_2 | 815 | 821 | PF00498 | 0.534 |
LIG_Integrin_RGD_1 | 424 | 426 | PF01839 | 0.465 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.338 |
LIG_LIR_Apic_2 | 257 | 262 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 319 | 329 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.200 |
LIG_LIR_Nem_3 | 437 | 443 | PF02991 | 0.558 |
LIG_MAD2 | 355 | 363 | PF02301 | 0.353 |
LIG_MYND_1 | 42 | 46 | PF01753 | 0.585 |
LIG_PCNA_yPIPBox_3 | 739 | 749 | PF02747 | 0.461 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.337 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.532 |
LIG_SH2_CRK | 602 | 606 | PF00017 | 0.535 |
LIG_SH2_GRB2like | 737 | 740 | PF00017 | 0.425 |
LIG_SH2_SRC | 737 | 740 | PF00017 | 0.425 |
LIG_SH2_SRC | 926 | 929 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 610 | 614 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 665 | 669 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 836 | 840 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 737 | 740 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 926 | 929 | PF00017 | 0.621 |
LIG_SH3_2 | 42 | 47 | PF14604 | 0.673 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.739 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.381 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.644 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.673 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.782 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.454 |
LIG_SH3_3 | 674 | 680 | PF00018 | 0.361 |
LIG_SH3_3 | 788 | 794 | PF00018 | 0.530 |
LIG_SH3_3 | 802 | 808 | PF00018 | 0.356 |
LIG_SH3_3 | 828 | 834 | PF00018 | 0.383 |
LIG_SH3_3 | 888 | 894 | PF00018 | 0.498 |
LIG_SUMO_SIM_anti_2 | 275 | 280 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 221 | 229 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 277 | 283 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 506 | 511 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 811 | 817 | PF11976 | 0.508 |
LIG_TRAF2_1 | 587 | 590 | PF00917 | 0.311 |
LIG_UBA3_1 | 164 | 171 | PF00899 | 0.413 |
LIG_UBA3_1 | 211 | 217 | PF00899 | 0.641 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.473 |
LIG_WRC_WIRS_1 | 748 | 753 | PF05994 | 0.472 |
LIG_WW_2 | 42 | 45 | PF00397 | 0.585 |
LIG_WW_3 | 44 | 48 | PF00397 | 0.685 |
MOD_CDC14_SPxK_1 | 561 | 564 | PF00782 | 0.424 |
MOD_CDK_SPK_2 | 882 | 887 | PF00069 | 0.471 |
MOD_CDK_SPK_2 | 915 | 920 | PF00069 | 0.378 |
MOD_CDK_SPK_2 | 932 | 937 | PF00069 | 0.458 |
MOD_CDK_SPxK_1 | 558 | 564 | PF00069 | 0.405 |
MOD_CDK_SPxxK_3 | 129 | 136 | PF00069 | 0.429 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.376 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.675 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.716 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.729 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.641 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.802 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.616 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.594 |
MOD_CK1_1 | 741 | 747 | PF00069 | 0.299 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.773 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.722 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.750 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.429 |
MOD_Cter_Amidation | 335 | 338 | PF01082 | 0.713 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.362 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.556 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.674 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.628 |
MOD_GlcNHglycan | 416 | 420 | PF01048 | 0.685 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.678 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.441 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.640 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.557 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.609 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.634 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.568 |
MOD_GlcNHglycan | 781 | 784 | PF01048 | 0.556 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.557 |
MOD_GlcNHglycan | 920 | 923 | PF01048 | 0.651 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.705 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.369 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.768 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.407 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.723 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.756 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.477 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.749 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.668 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.557 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.700 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.761 |
MOD_GSK3_1 | 808 | 815 | PF00069 | 0.586 |
MOD_GSK3_1 | 892 | 899 | PF00069 | 0.468 |
MOD_GSK3_1 | 914 | 921 | PF00069 | 0.566 |
MOD_N-GLC_1 | 731 | 736 | PF02516 | 0.472 |
MOD_N-GLC_1 | 738 | 743 | PF02516 | 0.400 |
MOD_N-GLC_1 | 882 | 887 | PF02516 | 0.427 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.596 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.362 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.583 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.462 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.434 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.563 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.567 |
MOD_NEK2_1 | 779 | 784 | PF00069 | 0.503 |
MOD_NEK2_1 | 896 | 901 | PF00069 | 0.450 |
MOD_NEK2_2 | 193 | 198 | PF00069 | 0.362 |
MOD_NEK2_2 | 382 | 387 | PF00069 | 0.661 |
MOD_NEK2_2 | 821 | 826 | PF00069 | 0.534 |
MOD_NEK2_2 | 836 | 841 | PF00069 | 0.343 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.538 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.729 |
MOD_PIKK_1 | 896 | 902 | PF00454 | 0.514 |
MOD_PK_1 | 2 | 8 | PF00069 | 0.559 |
MOD_PK_1 | 528 | 534 | PF00069 | 0.477 |
MOD_PK_1 | 887 | 893 | PF00069 | 0.506 |
MOD_PK_1 | 901 | 907 | PF00069 | 0.518 |
MOD_PKA_1 | 409 | 415 | PF00069 | 0.801 |
MOD_PKA_1 | 632 | 638 | PF00069 | 0.492 |
MOD_PKA_1 | 711 | 717 | PF00069 | 0.574 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.586 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.801 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.449 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.493 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.563 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.564 |
MOD_PKB_1 | 558 | 566 | PF00069 | 0.408 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.698 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.337 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.630 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.558 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.453 |
MOD_Plk_1 | 731 | 737 | PF00069 | 0.482 |
MOD_Plk_2-3 | 112 | 118 | PF00069 | 0.439 |
MOD_Plk_2-3 | 137 | 143 | PF00069 | 0.473 |
MOD_Plk_2-3 | 97 | 103 | PF00069 | 0.519 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.308 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.318 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.504 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.514 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.569 |
MOD_Plk_4 | 741 | 747 | PF00069 | 0.301 |
MOD_Plk_4 | 892 | 898 | PF00069 | 0.482 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.434 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.671 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.405 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.437 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.652 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.675 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.581 |
MOD_ProDKin_1 | 764 | 770 | PF00069 | 0.648 |
MOD_ProDKin_1 | 830 | 836 | PF00069 | 0.433 |
MOD_ProDKin_1 | 882 | 888 | PF00069 | 0.417 |
MOD_ProDKin_1 | 915 | 921 | PF00069 | 0.524 |
MOD_SUMO_rev_2 | 756 | 764 | PF00179 | 0.635 |
MOD_SUMO_rev_2 | 799 | 805 | PF00179 | 0.382 |
TRG_DiLeu_BaLyEn_6 | 488 | 493 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.687 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.741 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 573 | 576 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 695 | 697 | PF00400 | 0.542 |
TRG_NLS_MonoCore_2 | 406 | 411 | PF00514 | 0.609 |
TRG_NLS_MonoExtN_4 | 404 | 411 | PF00514 | 0.817 |
TRG_Pf-PMV_PEXEL_1 | 166 | 170 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 586 | 590 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 731 | 736 | PF00026 | 0.471 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAU3 | Leptomonas seymouri | 49% | 100% |
A0A1X0NW19 | Trypanosomatidae | 32% | 100% |
A0A3R7LZC1 | Trypanosoma rangeli | 38% | 100% |
A0A3S7X5K3 | Leishmania donovani | 84% | 100% |
A4HKE6 | Leishmania braziliensis | 66% | 100% |
A4I7X4 | Leishmania infantum | 85% | 86% |
D0AA39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q381V6 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 33% | 100% |