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:0005737 | cytoplasm | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005657 | replication fork | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7WRJ2
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: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: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: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 |
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 | 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 | 290 | 294 | PF00656 | 0.816 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.652 |
CLV_C14_Caspase3-7 | 912 | 916 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 1146 | 1148 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 1151 | 1153 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 1157 | 1159 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 1203 | 1205 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 1206 | 1208 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 620 | 622 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 648 | 650 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 735 | 737 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 811 | 813 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 838 | 840 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 981 | 983 | PF00675 | 0.509 |
CLV_PCSK_FUR_1 | 1204 | 1208 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 1146 | 1148 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 1151 | 1153 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 1159 | 1161 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 1167 | 1169 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 1205 | 1207 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.788 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 648 | 650 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 811 | 813 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 838 | 840 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.759 |
CLV_PCSK_PC1ET2_1 | 1159 | 1161 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 1167 | 1169 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 1205 | 1207 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.786 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.746 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.686 |
CLV_PCSK_PC7_1 | 1147 | 1153 | PF00082 | 0.592 |
CLV_PCSK_PC7_1 | 86 | 92 | PF00082 | 0.733 |
CLV_PCSK_SKI1_1 | 1154 | 1158 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 1191 | 1195 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.755 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 921 | 925 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 959 | 963 | PF00082 | 0.446 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.569 |
DEG_SPOP_SBC_1 | 844 | 848 | PF00917 | 0.717 |
DOC_CDC14_PxL_1 | 772 | 780 | PF14671 | 0.477 |
DOC_CKS1_1 | 944 | 949 | PF01111 | 0.631 |
DOC_CYCLIN_RxL_1 | 90 | 101 | PF00134 | 0.712 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 373 | 379 | PF00134 | 0.618 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 961 | 970 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 778 | 781 | PF00134 | 0.597 |
DOC_CYCLIN_yCln2_LP_2 | 948 | 954 | PF00134 | 0.518 |
DOC_MAPK_DCC_7 | 794 | 803 | PF00069 | 0.574 |
DOC_MAPK_DCC_7 | 870 | 879 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 1098 | 1107 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 337 | 347 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 582 | 589 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 620 | 628 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 648 | 656 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 90 | 97 | PF00069 | 0.715 |
DOC_MAPK_HePTP_8 | 579 | 591 | PF00069 | 0.411 |
DOC_MAPK_JIP1_4 | 950 | 956 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 348 | 357 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 514 | 521 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 582 | 591 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 620 | 628 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 648 | 656 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 794 | 803 | PF00069 | 0.603 |
DOC_MAPK_RevD_3 | 799 | 812 | PF00069 | 0.551 |
DOC_PP1_RVXF_1 | 381 | 387 | PF00149 | 0.500 |
DOC_PP1_RVXF_1 | 634 | 641 | PF00149 | 0.534 |
DOC_PP1_RVXF_1 | 656 | 663 | PF00149 | 0.622 |
DOC_PP2B_LxvP_1 | 300 | 303 | PF13499 | 0.598 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 654 | 657 | PF13499 | 0.528 |
DOC_PP2B_LxvP_1 | 778 | 781 | PF13499 | 0.597 |
DOC_PP4_FxxP_1 | 1016 | 1019 | PF00568 | 0.514 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.835 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 712 | 716 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 843 | 847 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 850 | 854 | PF00917 | 0.687 |
DOC_USP7_MATH_2 | 411 | 417 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 800 | 804 | PF12436 | 0.559 |
DOC_WW_Pin1_4 | 1206 | 1211 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 1216 | 1221 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 722 | 727 | PF00397 | 0.796 |
DOC_WW_Pin1_4 | 785 | 790 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 943 | 948 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 1146 | 1150 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 1151 | 1157 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 1204 | 1210 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 144 | 152 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 250 | 257 | PF00244 | 0.846 |
LIG_14-3-3_CanoR_1 | 383 | 387 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 401 | 408 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 717 | 726 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 823 | 828 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 831 | 837 | PF00244 | 0.657 |
LIG_Actin_WH2_2 | 566 | 584 | PF00022 | 0.375 |
LIG_APCC_ABBA_1 | 699 | 704 | PF00400 | 0.753 |
LIG_APCC_ABBA_1 | 923 | 928 | PF00400 | 0.650 |
LIG_BIR_III_2 | 71 | 75 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 598 | 602 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_1 | 615 | 619 | PF00533 | 0.326 |
LIG_BRCT_BRCA1_1 | 658 | 662 | PF00533 | 0.627 |
LIG_BRCT_BRCA1_1 | 852 | 856 | PF00533 | 0.767 |
LIG_CSL_BTD_1 | 786 | 789 | PF09270 | 0.528 |
LIG_CtBP_PxDLS_1 | 1057 | 1061 | PF00389 | 0.464 |
LIG_CtBP_PxDLS_1 | 780 | 784 | PF00389 | 0.601 |
LIG_FHA_1 | 1035 | 1041 | PF00498 | 0.467 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.678 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.653 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.695 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.618 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.491 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.512 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.609 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.375 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.552 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.803 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.625 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.429 |
LIG_FHA_1 | 803 | 809 | PF00498 | 0.482 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.685 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.805 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.553 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.549 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.755 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.532 |
LIG_FHA_2 | 750 | 756 | PF00498 | 0.522 |
LIG_FHA_2 | 757 | 763 | PF00498 | 0.505 |
LIG_FHA_2 | 930 | 936 | PF00498 | 0.500 |
LIG_Integrin_isoDGR_2 | 1027 | 1029 | PF01839 | 0.572 |
LIG_IRF3_LxIS_1 | 537 | 544 | PF10401 | 0.499 |
LIG_LIR_Apic_2 | 1013 | 1019 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 208 | 217 | PF02991 | 0.751 |
LIG_LIR_Gen_1 | 556 | 566 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 572 | 581 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 599 | 610 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 1008 | 1012 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.753 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.725 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 599 | 605 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 728 | 733 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 899 | 903 | PF02991 | 0.527 |
LIG_LYPXL_S_1 | 874 | 878 | PF13949 | 0.585 |
LIG_MYND_1 | 776 | 780 | PF01753 | 0.591 |
LIG_PCNA_yPIPBox_3 | 679 | 690 | PF02747 | 0.627 |
LIG_PCNA_yPIPBox_3 | 972 | 983 | PF02747 | 0.488 |
LIG_Pex14_1 | 787 | 791 | PF04695 | 0.448 |
LIG_Pex14_2 | 619 | 623 | PF04695 | 0.455 |
LIG_PTB_Apo_2 | 1042 | 1049 | PF02174 | 0.516 |
LIG_SH2_CRK | 558 | 562 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.679 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.682 |
LIG_SH2_STAP1 | 1006 | 1010 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 1062 | 1066 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.634 |
LIG_SH2_STAP1 | 558 | 562 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 1009 | 1012 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 1093 | 1096 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 1164 | 1167 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.193 |
LIG_SH2_STAT5 | 791 | 794 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 813 | 816 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 818 | 821 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 903 | 906 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 992 | 995 | PF00017 | 0.501 |
LIG_SH3_3 | 1016 | 1022 | PF00018 | 0.477 |
LIG_SH3_3 | 1029 | 1035 | PF00018 | 0.385 |
LIG_SH3_3 | 1096 | 1102 | PF00018 | 0.444 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.762 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.517 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.641 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.682 |
LIG_SH3_3 | 723 | 729 | PF00018 | 0.777 |
LIG_SH3_3 | 870 | 876 | PF00018 | 0.539 |
LIG_SH3_3 | 883 | 889 | PF00018 | 0.362 |
LIG_SUMO_SIM_anti_2 | 349 | 354 | PF11976 | 0.538 |
LIG_SUMO_SIM_anti_2 | 559 | 565 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 465 | 473 | PF11976 | 0.609 |
LIG_SUMO_SIM_par_1 | 559 | 565 | PF11976 | 0.375 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.678 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.702 |
LIG_UBA3_1 | 460 | 467 | PF00899 | 0.709 |
LIG_UBA3_1 | 504 | 509 | PF00899 | 0.429 |
LIG_WRC_WIRS_1 | 1107 | 1112 | PF05994 | 0.534 |
LIG_WRC_WIRS_1 | 771 | 776 | PF05994 | 0.520 |
LIG_WRC_WIRS_1 | 803 | 808 | PF05994 | 0.588 |
MOD_CDK_SPxK_1 | 1206 | 1212 | PF00069 | 0.672 |
MOD_CDK_SPxxK_3 | 943 | 950 | PF00069 | 0.625 |
MOD_CK1_1 | 1106 | 1112 | PF00069 | 0.599 |
MOD_CK1_1 | 1174 | 1180 | PF00069 | 0.651 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.751 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.543 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.556 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.719 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.410 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.662 |
MOD_CK1_1 | 715 | 721 | PF00069 | 0.808 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.751 |
MOD_CK1_1 | 846 | 852 | PF00069 | 0.459 |
MOD_CK1_1 | 868 | 874 | PF00069 | 0.570 |
MOD_CK1_1 | 974 | 980 | PF00069 | 0.499 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.751 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.709 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.739 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.498 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.720 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.780 |
MOD_CK2_1 | 749 | 755 | PF00069 | 0.494 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.477 |
MOD_CK2_1 | 863 | 869 | PF00069 | 0.651 |
MOD_GlcNHglycan | 1199 | 1202 | PF01048 | 0.718 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.663 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.716 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.744 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.837 |
MOD_GlcNHglycan | 30 | 34 | PF01048 | 0.759 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.698 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.689 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.587 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.802 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.429 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.792 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.790 |
MOD_GlcNHglycan | 852 | 855 | PF01048 | 0.439 |
MOD_GSK3_1 | 1043 | 1050 | PF00069 | 0.576 |
MOD_GSK3_1 | 1106 | 1113 | PF00069 | 0.532 |
MOD_GSK3_1 | 1141 | 1148 | PF00069 | 0.598 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.785 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.692 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.808 |
MOD_GSK3_1 | 717 | 724 | PF00069 | 0.587 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.537 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.598 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.695 |
MOD_LATS_1 | 1203 | 1209 | PF00433 | 0.658 |
MOD_N-GLC_1 | 854 | 859 | PF02516 | 0.718 |
MOD_N-GLC_1 | 971 | 976 | PF02516 | 0.481 |
MOD_NEK2_1 | 1080 | 1085 | PF00069 | 0.448 |
MOD_NEK2_1 | 1105 | 1110 | PF00069 | 0.461 |
MOD_NEK2_1 | 1124 | 1129 | PF00069 | 0.443 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.669 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.671 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.523 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.470 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.601 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.565 |
MOD_NEK2_1 | 937 | 942 | PF00069 | 0.586 |
MOD_NEK2_1 | 961 | 966 | PF00069 | 0.489 |
MOD_NEK2_2 | 1062 | 1067 | PF00069 | 0.422 |
MOD_NEK2_2 | 238 | 243 | PF00069 | 0.619 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.587 |
MOD_NEK2_2 | 533 | 538 | PF00069 | 0.429 |
MOD_NEK2_2 | 712 | 717 | PF00069 | 0.812 |
MOD_PIKK_1 | 1129 | 1135 | PF00454 | 0.602 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.741 |
MOD_PIKK_1 | 527 | 533 | PF00454 | 0.429 |
MOD_PIKK_1 | 715 | 721 | PF00454 | 0.765 |
MOD_PIKK_1 | 823 | 829 | PF00454 | 0.692 |
MOD_PIKK_1 | 937 | 943 | PF00454 | 0.464 |
MOD_PK_1 | 735 | 741 | PF00069 | 0.658 |
MOD_PK_1 | 999 | 1005 | PF00069 | 0.585 |
MOD_PKA_1 | 1152 | 1158 | PF00069 | 0.630 |
MOD_PKA_1 | 1205 | 1211 | PF00069 | 0.708 |
MOD_PKA_1 | 316 | 322 | PF00069 | 0.713 |
MOD_PKA_1 | 735 | 741 | PF00069 | 0.658 |
MOD_PKA_2 | 1145 | 1151 | PF00069 | 0.697 |
MOD_PKA_2 | 1197 | 1203 | PF00069 | 0.708 |
MOD_PKA_2 | 1205 | 1211 | PF00069 | 0.645 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.808 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.713 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.597 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.528 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.547 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.739 |
MOD_PKA_2 | 822 | 828 | PF00069 | 0.756 |
MOD_PKA_2 | 830 | 836 | PF00069 | 0.657 |
MOD_Plk_1 | 1080 | 1086 | PF00069 | 0.419 |
MOD_Plk_1 | 1124 | 1130 | PF00069 | 0.440 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.796 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.556 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.402 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.334 |
MOD_Plk_1 | 712 | 718 | PF00069 | 0.811 |
MOD_Plk_1 | 868 | 874 | PF00069 | 0.546 |
MOD_Plk_1 | 935 | 941 | PF00069 | 0.557 |
MOD_Plk_1 | 999 | 1005 | PF00069 | 0.569 |
MOD_Plk_2-3 | 197 | 203 | PF00069 | 0.785 |
MOD_Plk_2-3 | 249 | 255 | PF00069 | 0.729 |
MOD_Plk_2-3 | 267 | 273 | PF00069 | 0.637 |
MOD_Plk_2-3 | 554 | 560 | PF00069 | 0.429 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.713 |
MOD_Plk_4 | 1070 | 1076 | PF00069 | 0.468 |
MOD_Plk_4 | 1110 | 1116 | PF00069 | 0.521 |
MOD_Plk_4 | 1152 | 1158 | PF00069 | 0.656 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.720 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.375 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.375 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.375 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.542 |
MOD_Plk_4 | 779 | 785 | PF00069 | 0.522 |
MOD_Plk_4 | 787 | 793 | PF00069 | 0.402 |
MOD_Plk_4 | 974 | 980 | PF00069 | 0.499 |
MOD_Plk_4 | 999 | 1005 | PF00069 | 0.585 |
MOD_ProDKin_1 | 1206 | 1212 | PF00069 | 0.726 |
MOD_ProDKin_1 | 1216 | 1222 | PF00069 | 0.673 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.746 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.734 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.499 |
MOD_ProDKin_1 | 722 | 728 | PF00069 | 0.796 |
MOD_ProDKin_1 | 785 | 791 | PF00069 | 0.456 |
MOD_ProDKin_1 | 943 | 949 | PF00069 | 0.555 |
MOD_SUMO_for_1 | 1010 | 1013 | PF00179 | 0.515 |
MOD_SUMO_rev_2 | 1184 | 1193 | PF00179 | 0.642 |
MOD_SUMO_rev_2 | 459 | 469 | PF00179 | 0.702 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.610 |
TRG_DiLeu_BaEn_3 | 895 | 901 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_4 | 196 | 202 | PF01217 | 0.726 |
TRG_DiLeu_BaLyEn_6 | 1183 | 1188 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 609 | 614 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 1093 | 1096 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.682 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.725 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 875 | 878 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 1145 | 1147 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 1157 | 1160 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 1204 | 1207 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 619 | 621 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 647 | 649 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 733 | 736 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 810 | 812 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 837 | 839 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 884 | 887 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 918 | 921 | PF00400 | 0.535 |
TRG_NES_CRM1_1 | 1070 | 1081 | PF08389 | 0.452 |
TRG_NLS_Bipartite_1 | 1151 | 1170 | PF00514 | 0.616 |
TRG_NLS_Bipartite_1 | 218 | 235 | PF00514 | 0.821 |
TRG_NLS_MonoCore_2 | 1203 | 1208 | PF00514 | 0.656 |
TRG_NLS_MonoExtC_3 | 227 | 232 | PF00514 | 0.828 |
TRG_NLS_MonoExtN_4 | 1151 | 1156 | PF00514 | 0.655 |
TRG_NLS_MonoExtN_4 | 1204 | 1209 | PF00514 | 0.703 |
TRG_NLS_MonoExtN_4 | 225 | 232 | PF00514 | 0.829 |
TRG_Pf-PMV_PEXEL_1 | 1186 | 1190 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.767 |
TRG_Pf-PMV_PEXEL_1 | 373 | 378 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 401 | 405 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 571 | 575 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 93 | 98 | PF00026 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 982 | 987 | PF00026 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIS5 | Leptomonas seymouri | 63% | 89% |
A0A3R7MZY3 | Trypanosoma rangeli | 44% | 100% |
A4H6E9 | Leishmania braziliensis | 79% | 97% |
A4HUU3 | Leishmania infantum | 99% | 100% |
E9ANH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QH48 | Leishmania major | 93% | 100% |