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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005657 | replication fork | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: Q4QH48
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 8 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006260 | DNA replication | 5 | 2 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006310 | DNA recombination | 5 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0006996 | organelle organization | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016043 | cellular component organization | 3 | 8 |
GO:0032200 | telomere organization | 6 | 8 |
GO:0032392 | DNA geometric change | 7 | 2 |
GO:0032508 | DNA duplex unwinding | 8 | 2 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051276 | chromosome organization | 5 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0071103 | DNA conformation change | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0071840 | cellular component organization or biogenesis | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003678 | DNA helicase activity | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004386 | helicase activity | 2 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 8 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0016887 | ATP hydrolysis activity | 7 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.634 |
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.791 |
CLV_C14_Caspase3-7 | 766 | 770 | PF00656 | 0.453 |
CLV_C14_Caspase3-7 | 913 | 917 | PF00656 | 0.661 |
CLV_NRD_NRD_1 | 1147 | 1149 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 1152 | 1154 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 1158 | 1160 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 1168 | 1170 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 1204 | 1206 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 1207 | 1209 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 812 | 814 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 982 | 984 | PF00675 | 0.512 |
CLV_PCSK_FUR_1 | 1205 | 1209 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 1147 | 1149 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 1152 | 1154 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 1160 | 1162 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 1167 | 1169 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 1206 | 1208 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 735 | 737 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 812 | 814 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 839 | 841 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.747 |
CLV_PCSK_PC1ET2_1 | 1160 | 1162 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 1167 | 1169 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 1206 | 1208 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.736 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.674 |
CLV_PCSK_PC7_1 | 1148 | 1154 | PF00082 | 0.569 |
CLV_PCSK_PC7_1 | 86 | 92 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 1155 | 1159 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 1192 | 1196 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 922 | 926 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 960 | 964 | PF00082 | 0.413 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.503 |
DEG_SCF_FBW7_2 | 300 | 306 | PF00400 | 0.596 |
DEG_SPOP_SBC_1 | 690 | 694 | PF00917 | 0.564 |
DEG_SPOP_SBC_1 | 845 | 849 | PF00917 | 0.714 |
DOC_CDC14_PxL_1 | 773 | 781 | PF14671 | 0.480 |
DOC_CKS1_1 | 300 | 305 | PF01111 | 0.593 |
DOC_CKS1_1 | 945 | 950 | PF01111 | 0.614 |
DOC_CYCLIN_RxL_1 | 90 | 101 | PF00134 | 0.714 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 373 | 379 | PF00134 | 0.623 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 962 | 971 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 779 | 782 | PF00134 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 949 | 955 | PF00134 | 0.515 |
DOC_MAPK_DCC_7 | 795 | 804 | PF00069 | 0.598 |
DOC_MAPK_DCC_7 | 871 | 880 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 1099 | 1108 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 337 | 347 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 430 | 437 | PF00069 | 0.693 |
DOC_MAPK_gen_1 | 621 | 629 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 649 | 657 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 90 | 97 | PF00069 | 0.707 |
DOC_MAPK_JIP1_4 | 951 | 957 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 348 | 357 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 430 | 437 | PF00069 | 0.693 |
DOC_MAPK_MEF2A_6 | 515 | 522 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 621 | 629 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 649 | 657 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 795 | 804 | PF00069 | 0.627 |
DOC_MAPK_RevD_3 | 800 | 813 | PF00069 | 0.567 |
DOC_PP1_RVXF_1 | 381 | 387 | PF00149 | 0.518 |
DOC_PP1_RVXF_1 | 657 | 664 | PF00149 | 0.626 |
DOC_PP2B_LxvP_1 | 655 | 658 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 779 | 782 | PF13499 | 0.603 |
DOC_PP4_FxxP_1 | 1017 | 1020 | PF00568 | 0.518 |
DOC_PP4_FxxP_1 | 312 | 315 | PF00568 | 0.723 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 844 | 848 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 851 | 855 | PF00917 | 0.673 |
DOC_USP7_MATH_2 | 411 | 417 | PF00917 | 0.550 |
DOC_USP7_UBL2_3 | 801 | 805 | PF12436 | 0.580 |
DOC_WW_Pin1_4 | 1207 | 1212 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 1217 | 1222 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 723 | 728 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 944 | 949 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 1152 | 1158 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 1205 | 1211 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 144 | 152 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 250 | 257 | PF00244 | 0.832 |
LIG_14-3-3_CanoR_1 | 383 | 387 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 401 | 408 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 718 | 727 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 824 | 829 | PF00244 | 0.714 |
LIG_Actin_WH2_2 | 567 | 585 | PF00022 | 0.375 |
LIG_APCC_ABBA_1 | 700 | 705 | PF00400 | 0.744 |
LIG_APCC_ABBA_1 | 924 | 929 | PF00400 | 0.661 |
LIG_BIR_III_2 | 154 | 158 | PF00653 | 0.569 |
LIG_BRCT_BRCA1_1 | 599 | 603 | PF00533 | 0.410 |
LIG_BRCT_BRCA1_1 | 616 | 620 | PF00533 | 0.290 |
LIG_BRCT_BRCA1_1 | 659 | 663 | PF00533 | 0.631 |
LIG_BRCT_BRCA1_1 | 853 | 857 | PF00533 | 0.768 |
LIG_CSL_BTD_1 | 787 | 790 | PF09270 | 0.548 |
LIG_CtBP_PxDLS_1 | 1058 | 1062 | PF00389 | 0.467 |
LIG_CtBP_PxDLS_1 | 781 | 785 | PF00389 | 0.609 |
LIG_FHA_1 | 1036 | 1042 | PF00498 | 0.448 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.657 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.685 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.679 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.738 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.474 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.467 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.614 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.340 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.482 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.545 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.766 |
LIG_FHA_1 | 723 | 729 | PF00498 | 0.805 |
LIG_FHA_1 | 760 | 766 | PF00498 | 0.625 |
LIG_FHA_1 | 789 | 795 | PF00498 | 0.412 |
LIG_FHA_1 | 804 | 810 | PF00498 | 0.476 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.676 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.602 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.608 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.794 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.606 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.562 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.754 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.525 |
LIG_FHA_2 | 751 | 757 | PF00498 | 0.514 |
LIG_FHA_2 | 758 | 764 | PF00498 | 0.548 |
LIG_FHA_2 | 931 | 937 | PF00498 | 0.504 |
LIG_Integrin_isoDGR_2 | 1028 | 1030 | PF01839 | 0.570 |
LIG_IRF3_LxIS_1 | 538 | 545 | PF10401 | 0.499 |
LIG_LIR_Apic_2 | 1014 | 1020 | PF02991 | 0.525 |
LIG_LIR_Apic_2 | 309 | 315 | PF02991 | 0.764 |
LIG_LIR_Gen_1 | 208 | 217 | PF02991 | 0.739 |
LIG_LIR_Gen_1 | 557 | 567 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 573 | 582 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 600 | 611 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 1009 | 1013 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.740 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 573 | 578 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 600 | 606 | PF02991 | 0.384 |
LIG_LYPXL_S_1 | 875 | 879 | PF13949 | 0.592 |
LIG_MYND_1 | 777 | 781 | PF01753 | 0.596 |
LIG_PCNA_yPIPBox_3 | 680 | 691 | PF02747 | 0.626 |
LIG_PCNA_yPIPBox_3 | 973 | 984 | PF02747 | 0.463 |
LIG_Pex14_1 | 788 | 792 | PF04695 | 0.465 |
LIG_Pex14_2 | 620 | 624 | PF04695 | 0.413 |
LIG_PTB_Apo_2 | 1043 | 1050 | PF02174 | 0.521 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.581 |
LIG_SH2_CRK | 559 | 563 | PF00017 | 0.375 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.669 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.670 |
LIG_SH2_STAP1 | 1007 | 1011 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 1063 | 1067 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.675 |
LIG_SH2_STAP1 | 559 | 563 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 1010 | 1013 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 1094 | 1097 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 1165 | 1168 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 792 | 795 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 819 | 822 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 904 | 907 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 943 | 946 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 993 | 996 | PF00017 | 0.529 |
LIG_SH3_3 | 1017 | 1023 | PF00018 | 0.432 |
LIG_SH3_3 | 1030 | 1036 | PF00018 | 0.369 |
LIG_SH3_3 | 1097 | 1103 | PF00018 | 0.410 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.582 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.650 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.665 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.781 |
LIG_SH3_3 | 871 | 877 | PF00018 | 0.516 |
LIG_SH3_3 | 884 | 890 | PF00018 | 0.337 |
LIG_SUMO_SIM_anti_2 | 349 | 354 | PF11976 | 0.546 |
LIG_SUMO_SIM_anti_2 | 560 | 566 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 560 | 566 | PF11976 | 0.340 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.666 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.712 |
LIG_UBA3_1 | 461 | 468 | PF00899 | 0.710 |
LIG_UBA3_1 | 505 | 510 | PF00899 | 0.429 |
LIG_WRC_WIRS_1 | 1108 | 1113 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 772 | 777 | PF05994 | 0.521 |
LIG_WRC_WIRS_1 | 804 | 809 | PF05994 | 0.604 |
MOD_CDK_SPxK_1 | 1207 | 1213 | PF00069 | 0.675 |
MOD_CDK_SPxK_1 | 723 | 729 | PF00069 | 0.566 |
MOD_CDK_SPxxK_3 | 944 | 951 | PF00069 | 0.621 |
MOD_CK1_1 | 1107 | 1113 | PF00069 | 0.529 |
MOD_CK1_1 | 1175 | 1181 | PF00069 | 0.662 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.738 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.583 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.501 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.363 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.543 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.661 |
MOD_CK1_1 | 716 | 722 | PF00069 | 0.804 |
MOD_CK1_1 | 827 | 833 | PF00069 | 0.740 |
MOD_CK1_1 | 847 | 853 | PF00069 | 0.458 |
MOD_CK1_1 | 869 | 875 | PF00069 | 0.567 |
MOD_CK1_1 | 975 | 981 | PF00069 | 0.448 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.688 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.765 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.699 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.725 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.617 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.549 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.726 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.779 |
MOD_CK2_1 | 750 | 756 | PF00069 | 0.469 |
MOD_CK2_1 | 757 | 763 | PF00069 | 0.478 |
MOD_CK2_1 | 835 | 841 | PF00069 | 0.528 |
MOD_CK2_1 | 864 | 870 | PF00069 | 0.637 |
MOD_GlcNHglycan | 1200 | 1203 | PF01048 | 0.740 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.683 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.688 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.700 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.807 |
MOD_GlcNHglycan | 30 | 34 | PF01048 | 0.757 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.689 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.590 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.771 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.429 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.792 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.770 |
MOD_GlcNHglycan | 853 | 856 | PF01048 | 0.438 |
MOD_GSK3_1 | 1044 | 1051 | PF00069 | 0.511 |
MOD_GSK3_1 | 1107 | 1114 | PF00069 | 0.478 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.641 |
MOD_GSK3_1 | 1142 | 1149 | PF00069 | 0.546 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.627 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.787 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.693 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.795 |
MOD_GSK3_1 | 718 | 725 | PF00069 | 0.586 |
MOD_GSK3_1 | 780 | 787 | PF00069 | 0.499 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.625 |
MOD_GSK3_1 | 831 | 838 | PF00069 | 0.616 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.695 |
MOD_LATS_1 | 1204 | 1210 | PF00433 | 0.670 |
MOD_LATS_1 | 626 | 632 | PF00433 | 0.388 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.553 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.561 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.566 |
MOD_N-GLC_1 | 585 | 590 | PF02516 | 0.258 |
MOD_N-GLC_1 | 855 | 860 | PF02516 | 0.715 |
MOD_N-GLC_1 | 972 | 977 | PF02516 | 0.454 |
MOD_NEK2_1 | 1081 | 1086 | PF00069 | 0.413 |
MOD_NEK2_1 | 1106 | 1111 | PF00069 | 0.426 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.719 |
MOD_NEK2_1 | 1125 | 1130 | PF00069 | 0.406 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.607 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.427 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.583 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.588 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.584 |
MOD_NEK2_1 | 938 | 943 | PF00069 | 0.580 |
MOD_NEK2_1 | 962 | 967 | PF00069 | 0.494 |
MOD_NEK2_2 | 1063 | 1068 | PF00069 | 0.389 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.582 |
MOD_NEK2_2 | 534 | 539 | PF00069 | 0.375 |
MOD_NEK2_2 | 713 | 718 | PF00069 | 0.808 |
MOD_PIKK_1 | 1130 | 1136 | PF00454 | 0.597 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.706 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.413 |
MOD_PIKK_1 | 716 | 722 | PF00454 | 0.760 |
MOD_PIKK_1 | 824 | 830 | PF00454 | 0.679 |
MOD_PIKK_1 | 938 | 944 | PF00454 | 0.462 |
MOD_PK_1 | 1000 | 1006 | PF00069 | 0.594 |
MOD_PK_1 | 736 | 742 | PF00069 | 0.650 |
MOD_PKA_1 | 1147 | 1153 | PF00069 | 0.563 |
MOD_PKA_1 | 1206 | 1212 | PF00069 | 0.709 |
MOD_PKA_1 | 736 | 742 | PF00069 | 0.650 |
MOD_PKA_2 | 1146 | 1152 | PF00069 | 0.670 |
MOD_PKA_2 | 1198 | 1204 | PF00069 | 0.727 |
MOD_PKA_2 | 1206 | 1212 | PF00069 | 0.531 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.794 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.602 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.545 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.551 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.688 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.731 |
MOD_PKA_2 | 823 | 829 | PF00069 | 0.746 |
MOD_PKA_2 | 831 | 837 | PF00069 | 0.641 |
MOD_Plk_1 | 1000 | 1006 | PF00069 | 0.577 |
MOD_Plk_1 | 1081 | 1087 | PF00069 | 0.418 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.688 |
MOD_Plk_1 | 1125 | 1131 | PF00069 | 0.441 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.669 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.787 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.556 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.666 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.557 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.552 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.380 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.290 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.543 |
MOD_Plk_1 | 713 | 719 | PF00069 | 0.805 |
MOD_Plk_1 | 869 | 875 | PF00069 | 0.543 |
MOD_Plk_1 | 936 | 942 | PF00069 | 0.552 |
MOD_Plk_2-3 | 197 | 203 | PF00069 | 0.775 |
MOD_Plk_2-3 | 249 | 255 | PF00069 | 0.716 |
MOD_Plk_2-3 | 555 | 561 | PF00069 | 0.429 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.705 |
MOD_Plk_4 | 1000 | 1006 | PF00069 | 0.568 |
MOD_Plk_4 | 1071 | 1077 | PF00069 | 0.437 |
MOD_Plk_4 | 1111 | 1117 | PF00069 | 0.468 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.667 |
MOD_Plk_4 | 1153 | 1159 | PF00069 | 0.630 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.718 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.358 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.311 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.340 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.476 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.447 |
MOD_Plk_4 | 780 | 786 | PF00069 | 0.498 |
MOD_Plk_4 | 788 | 794 | PF00069 | 0.384 |
MOD_Plk_4 | 975 | 981 | PF00069 | 0.448 |
MOD_ProDKin_1 | 1207 | 1213 | PF00069 | 0.719 |
MOD_ProDKin_1 | 1217 | 1223 | PF00069 | 0.641 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.728 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.754 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.499 |
MOD_ProDKin_1 | 723 | 729 | PF00069 | 0.798 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.486 |
MOD_ProDKin_1 | 944 | 950 | PF00069 | 0.609 |
MOD_SUMO_for_1 | 1011 | 1014 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 1185 | 1194 | PF00179 | 0.648 |
MOD_SUMO_rev_2 | 460 | 470 | PF00179 | 0.682 |
MOD_SUMO_rev_2 | 58 | 64 | PF00179 | 0.545 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.600 |
TRG_DiLeu_BaEn_3 | 896 | 902 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_4 | 196 | 202 | PF01217 | 0.717 |
TRG_DiLeu_BaLyEn_6 | 1184 | 1189 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 610 | 615 | PF01217 | 0.518 |
TRG_ENDOCYTIC_2 | 1094 | 1097 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.670 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.718 |
TRG_ENDOCYTIC_2 | 559 | 562 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 876 | 879 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 1146 | 1148 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 1158 | 1161 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 1205 | 1208 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 582 | 584 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 620 | 622 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 648 | 650 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 734 | 737 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 811 | 813 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 885 | 888 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 919 | 922 | PF00400 | 0.552 |
TRG_NES_CRM1_1 | 1071 | 1082 | PF08389 | 0.419 |
TRG_NLS_Bipartite_1 | 1152 | 1171 | PF00514 | 0.611 |
TRG_NLS_Bipartite_1 | 218 | 232 | PF00514 | 0.814 |
TRG_NLS_MonoCore_2 | 1204 | 1209 | PF00514 | 0.669 |
TRG_NLS_MonoExtC_3 | 227 | 232 | PF00514 | 0.784 |
TRG_NLS_MonoExtN_4 | 1152 | 1157 | PF00514 | 0.634 |
TRG_NLS_MonoExtN_4 | 1205 | 1210 | PF00514 | 0.712 |
TRG_NLS_MonoExtN_4 | 225 | 232 | PF00514 | 0.827 |
TRG_Pf-PMV_PEXEL_1 | 1187 | 1191 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.758 |
TRG_Pf-PMV_PEXEL_1 | 25 | 30 | PF00026 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 373 | 378 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 401 | 405 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 507 | 511 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 572 | 576 | PF00026 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 93 | 98 | PF00026 | 0.716 |
TRG_Pf-PMV_PEXEL_1 | 983 | 988 | PF00026 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIS5 | Leptomonas seymouri | 63% | 90% |
A0A3R7MZY3 | Trypanosoma rangeli | 43% | 100% |
A0A3S7WRJ2 | Leishmania donovani | 93% | 100% |
A4H6E9 | Leishmania braziliensis | 79% | 100% |
A4HUU3 | Leishmania infantum | 93% | 81% |
E9ANH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |