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: A4HGV5
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 | 298 | 302 | PF00656 | 0.335 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 593 | 595 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 794 | 796 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 813 | 815 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.404 |
CLV_PCSK_FUR_1 | 591 | 595 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 593 | 595 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 813 | 815 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 590 | 592 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 700 | 704 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 814 | 818 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 852 | 856 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.747 |
DEG_APCC_DBOX_1 | 463 | 471 | PF00400 | 0.527 |
DEG_Kelch_Keap1_1 | 539 | 544 | PF01344 | 0.530 |
DEG_ODPH_VHL_1 | 492 | 504 | PF01847 | 0.372 |
DEG_ODPH_VHL_1 | 651 | 664 | PF01847 | 0.432 |
DEG_SCF_TRCP1_1 | 541 | 547 | PF00400 | 0.529 |
DOC_CKS1_1 | 190 | 195 | PF01111 | 0.628 |
DOC_CKS1_1 | 358 | 363 | PF01111 | 0.510 |
DOC_CKS1_1 | 99 | 104 | PF01111 | 0.488 |
DOC_CYCLIN_RxL_1 | 91 | 104 | PF00134 | 0.459 |
DOC_CYCLIN_yCln2_LP_2 | 358 | 364 | PF00134 | 0.510 |
DOC_CYCLIN_yCln2_LP_2 | 390 | 396 | PF00134 | 0.586 |
DOC_CYCLIN_yCln2_LP_2 | 749 | 755 | PF00134 | 0.515 |
DOC_MAPK_DCC_7 | 710 | 720 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 45 | 53 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 655 | 664 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 793 | 802 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 813 | 819 | PF00069 | 0.220 |
DOC_MAPK_MEF2A_6 | 208 | 215 | PF00069 | 0.252 |
DOC_MAPK_MEF2A_6 | 239 | 248 | PF00069 | 0.285 |
DOC_MAPK_RevD_3 | 575 | 591 | PF00069 | 0.449 |
DOC_MAPK_RevD_3 | 800 | 814 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 850 | 856 | PF00149 | 0.425 |
DOC_PP2B_LxvP_1 | 749 | 752 | PF13499 | 0.516 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.537 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.335 |
DOC_PP4_FxxP_1 | 683 | 686 | PF00568 | 0.414 |
DOC_PP4_FxxP_1 | 855 | 858 | PF00568 | 0.452 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 839 | 843 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 115 | 119 | PF12436 | 0.500 |
DOC_USP7_UBL2_3 | 91 | 95 | PF12436 | 0.427 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 854 | 859 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 247 | 256 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 582 | 588 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 618 | 623 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 813 | 819 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 840 | 844 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 852 | 858 | PF00244 | 0.574 |
LIG_Actin_WH2_2 | 234 | 249 | PF00022 | 0.335 |
LIG_Actin_WH2_2 | 60 | 76 | PF00022 | 0.355 |
LIG_Actin_WH2_2 | 644 | 659 | PF00022 | 0.536 |
LIG_BIR_III_2 | 275 | 279 | PF00653 | 0.211 |
LIG_BIR_III_4 | 453 | 457 | PF00653 | 0.641 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.618 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.441 |
LIG_EH_1 | 20 | 24 | PF12763 | 0.545 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.335 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.335 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.494 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.260 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.636 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.684 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.600 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.517 |
LIG_FHA_1 | 770 | 776 | PF00498 | 0.378 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.635 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.543 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.346 |
LIG_FHA_2 | 619 | 625 | PF00498 | 0.486 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.605 |
LIG_Integrin_isoDGR_2 | 24 | 26 | PF01839 | 0.628 |
LIG_LIR_Apic_2 | 17 | 22 | PF02991 | 0.531 |
LIG_LIR_Apic_2 | 182 | 188 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 402 | 406 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 681 | 686 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 175 | 186 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.211 |
LIG_LIR_Gen_1 | 332 | 340 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 347 | 358 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 384 | 395 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 603 | 612 | PF02991 | 0.411 |
LIG_LIR_LC3C_4 | 798 | 802 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 603 | 607 | PF02991 | 0.423 |
LIG_OCRL_FandH_1 | 166 | 178 | PF00620 | 0.390 |
LIG_PCNA_yPIPBox_3 | 710 | 721 | PF02747 | 0.543 |
LIG_PDZ_Class_1 | 854 | 859 | PF00595 | 0.451 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.534 |
LIG_Pex14_2 | 266 | 270 | PF04695 | 0.321 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.650 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.651 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.625 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.607 |
LIG_SH2_GRB2like | 11 | 14 | PF00017 | 0.393 |
LIG_SH2_NCK_1 | 345 | 349 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 11 | 15 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 757 | 761 | PF00017 | 0.472 |
LIG_SH2_STAT3 | 803 | 806 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 742 | 745 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 788 | 791 | PF00017 | 0.353 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.669 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.561 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.441 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.504 |
LIG_SH3_3 | 723 | 729 | PF00018 | 0.417 |
LIG_SH3_3 | 829 | 835 | PF00018 | 0.374 |
LIG_SUMO_SIM_anti_2 | 290 | 296 | PF11976 | 0.331 |
LIG_SUMO_SIM_anti_2 | 500 | 505 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 631 | 636 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 729 | 734 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 771 | 776 | PF11976 | 0.367 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.358 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.455 |
MOD_CDK_SPxK_1 | 357 | 363 | PF00069 | 0.506 |
MOD_CDK_SPxK_1 | 427 | 433 | PF00069 | 0.535 |
MOD_CDK_SPxxK_3 | 98 | 105 | PF00069 | 0.488 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.458 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.544 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.378 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.488 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.715 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.721 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.718 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.426 |
MOD_CK1_1 | 841 | 847 | PF00069 | 0.533 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.351 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.616 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.518 |
MOD_CK2_1 | 618 | 624 | PF00069 | 0.526 |
MOD_CK2_1 | 812 | 818 | PF00069 | 0.410 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.764 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.676 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.307 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.445 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.401 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.371 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.391 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.515 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.724 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.750 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.629 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.684 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.545 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.345 |
MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.523 |
MOD_GlcNHglycan | 814 | 817 | PF01048 | 0.405 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.713 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.548 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.568 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.544 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.244 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.473 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.432 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.542 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.408 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.577 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.719 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.579 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.483 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.450 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.308 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.402 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.441 |
MOD_LATS_1 | 379 | 385 | PF00433 | 0.304 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.526 |
MOD_N-GLC_1 | 666 | 671 | PF02516 | 0.476 |
MOD_N-GLC_1 | 673 | 678 | PF02516 | 0.427 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.628 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.279 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.335 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.535 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.469 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.481 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.526 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.449 |
MOD_NEK2_1 | 735 | 740 | PF00069 | 0.590 |
MOD_NEK2_1 | 769 | 774 | PF00069 | 0.385 |
MOD_NEK2_1 | 817 | 822 | PF00069 | 0.349 |
MOD_NEK2_2 | 262 | 267 | PF00069 | 0.354 |
MOD_NEK2_2 | 757 | 762 | PF00069 | 0.376 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.612 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.211 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.211 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.572 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.341 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.524 |
MOD_PIKK_1 | 841 | 847 | PF00454 | 0.500 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.395 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.446 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.633 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.685 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.544 |
MOD_PKA_2 | 692 | 698 | PF00069 | 0.650 |
MOD_PKA_2 | 812 | 818 | PF00069 | 0.478 |
MOD_PKA_2 | 839 | 845 | PF00069 | 0.411 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.539 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.329 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.335 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.486 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.481 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.404 |
MOD_Plk_2-3 | 295 | 301 | PF00069 | 0.335 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.596 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.373 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.335 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.321 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.545 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.484 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.427 |
MOD_Plk_4 | 738 | 744 | PF00069 | 0.430 |
MOD_Plk_4 | 769 | 775 | PF00069 | 0.380 |
MOD_Plk_4 | 805 | 811 | PF00069 | 0.522 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.571 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.506 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.488 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.616 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.485 |
MOD_SUMO_rev_2 | 410 | 420 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_3 | 625 | 631 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 463 | 468 | PF01217 | 0.648 |
TRG_DiLeu_BaLyEn_6 | 716 | 721 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.625 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 591 | 594 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 692 | 694 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 812 | 814 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.562 |
TRG_NLS_MonoExtC_3 | 589 | 594 | PF00514 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.304 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 719 | 724 | PF00026 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 795 | 799 | PF00026 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCJ6 | Leptomonas seymouri | 59% | 77% |
A0A1X0NSB2 | Trypanosomatidae | 50% | 100% |
A0A3Q8IGY7 | Leishmania donovani | 80% | 92% |
A0A422NKI2 | Trypanosoma rangeli | 49% | 100% |
A4I3Y5 | Leishmania infantum | 80% | 92% |
D0A956 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9B075 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 92% |
Q383A1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 46% | 100% |
Q4Q810 | Leishmania major | 79% | 100% |
V5BL79 | Trypanosoma cruzi | 50% | 100% |