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:0043596 | nuclear replication fork | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005634 | nucleus | 5 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
Related structures:
AlphaFold database: Q4QAS2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006275 | regulation of DNA replication | 6 | 2 |
GO:0006281 | DNA repair | 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:0008152 | metabolic process | 1 | 11 |
GO:0008156 | negative regulation of DNA replication | 7 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031297 | replication fork processing | 6 | 11 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 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:0045005 | DNA-templated DNA replication maintenance of fidelity | 5 | 11 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0048478 | obsolete replication fork protection | 6 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051052 | regulation of DNA metabolic process | 5 | 2 |
GO:0051053 | negative regulation of DNA metabolic process | 6 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:0090329 | regulation of DNA-templated DNA replication | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:2000104 | negative regulation of DNA-templated DNA replication | 8 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003697 | single-stranded DNA binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004386 | helicase activity | 2 | 10 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 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:0036310 | ATP-dependent DNA/DNA annealing activity | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0051213 | dioxygenase activity | 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:0140658 | ATP-dependent chromatin remodeler activity | 3 | 11 |
GO:0140666 | annealing activity | 4 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:1990814 | DNA/DNA annealing activity | 5 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.737 |
CLV_C14_Caspase3-7 | 678 | 682 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 928 | 932 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 1006 | 1008 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 852 | 854 | PF00675 | 0.589 |
CLV_PCSK_KEX2_1 | 1006 | 1008 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 741 | 743 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 852 | 854 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 913 | 915 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 929 | 931 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.233 |
CLV_PCSK_PC1ET2_1 | 913 | 915 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 929 | 931 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 1007 | 1011 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 853 | 857 | PF00082 | 0.596 |
DEG_APCC_DBOX_1 | 1005 | 1013 | PF00400 | 0.695 |
DEG_APCC_DBOX_1 | 108 | 116 | PF00400 | 0.459 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.503 |
DEG_ODPH_VHL_1 | 33 | 46 | PF01847 | 0.588 |
DEG_ODPH_VHL_1 | 963 | 974 | PF01847 | 0.515 |
DEG_SCF_FBW7_1 | 1001 | 1008 | PF00400 | 0.573 |
DEG_SCF_FBW7_1 | 317 | 324 | PF00400 | 0.420 |
DEG_SCF_FBW7_1 | 650 | 656 | PF00400 | 0.481 |
DEG_SPOP_SBC_1 | 1000 | 1004 | PF00917 | 0.529 |
DEG_SPOP_SBC_1 | 429 | 433 | PF00917 | 0.624 |
DEG_SPOP_SBC_1 | 987 | 991 | PF00917 | 0.627 |
DOC_CKS1_1 | 650 | 655 | PF01111 | 0.604 |
DOC_CYCLIN_RxL_1 | 588 | 598 | PF00134 | 0.329 |
DOC_MAPK_DCC_7 | 126 | 135 | PF00069 | 0.450 |
DOC_MAPK_DCC_7 | 711 | 719 | PF00069 | 0.486 |
DOC_MAPK_FxFP_2 | 111 | 114 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 299 | 307 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 309 | 317 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 395 | 404 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 218 | 226 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 711 | 719 | PF00069 | 0.697 |
DOC_MAPK_MEF2A_6 | 86 | 94 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 898 | 906 | PF00069 | 0.642 |
DOC_MAPK_RevD_3 | 900 | 914 | PF00069 | 0.595 |
DOC_PP1_RVXF_1 | 482 | 489 | PF00149 | 0.420 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.396 |
DOC_PP4_FxxP_1 | 664 | 667 | PF00568 | 0.710 |
DOC_SPAK_OSR1_1 | 358 | 362 | PF12202 | 0.433 |
DOC_USP7_MATH_1 | 1000 | 1004 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 683 | 687 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 691 | 695 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 758 | 762 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 794 | 798 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 799 | 803 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 870 | 874 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 987 | 991 | PF00917 | 0.766 |
DOC_USP7_MATH_2 | 369 | 375 | PF00917 | 0.439 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.474 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.433 |
DOC_WW_Pin1_4 | 1019 | 1024 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 649 | 654 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 759 | 764 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 768 | 773 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 808 | 813 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 828 | 833 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 996 | 1001 | PF00397 | 0.757 |
LIG_14-3-3_CanoR_1 | 1006 | 1010 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 350 | 356 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 692 | 696 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 742 | 751 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 785 | 792 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 852 | 856 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 969 | 973 | PF00244 | 0.588 |
LIG_Actin_WH2_2 | 259 | 277 | PF00022 | 0.514 |
LIG_APCC_ABBA_1 | 716 | 721 | PF00400 | 0.632 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 101 | 111 | PF00928 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 233 | 242 | PF00928 | 0.420 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.465 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.433 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.540 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.493 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.580 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.591 |
LIG_FHA_1 | 836 | 842 | PF00498 | 0.754 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.493 |
LIG_FHA_1 | 897 | 903 | PF00498 | 0.640 |
LIG_FHA_1 | 969 | 975 | PF00498 | 0.746 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.433 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.448 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.485 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.613 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.390 |
LIG_FHA_2 | 890 | 896 | PF00498 | 0.523 |
LIG_FHA_2 | 915 | 921 | PF00498 | 0.620 |
LIG_LIR_Apic_2 | 662 | 667 | PF02991 | 0.708 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 270 | 277 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 39 | 49 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 512 | 521 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 559 | 569 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 512 | 516 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.579 |
LIG_MLH1_MIPbox_1 | 139 | 143 | PF16413 | 0.422 |
LIG_MYND_1 | 338 | 342 | PF01753 | 0.439 |
LIG_MYND_1 | 714 | 718 | PF01753 | 0.627 |
LIG_MYND_2 | 713 | 717 | PF01753 | 0.627 |
LIG_NRBOX | 371 | 377 | PF00104 | 0.433 |
LIG_Pex14_1 | 235 | 239 | PF04695 | 0.476 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.384 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.451 |
LIG_PTB_Apo_2 | 276 | 283 | PF02174 | 0.388 |
LIG_Rb_LxCxE_1 | 270 | 290 | PF01857 | 0.514 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.343 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.378 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.420 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.476 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.439 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.525 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.564 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.578 |
LIG_SH2_PTP2 | 513 | 516 | PF00017 | 0.420 |
LIG_SH2_SRC | 11 | 14 | PF00017 | 0.549 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 156 | 160 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.324 |
LIG_SH3_3 | 1017 | 1023 | PF00018 | 0.647 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.514 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.510 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.419 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.345 |
LIG_SH3_3 | 712 | 718 | PF00018 | 0.671 |
LIG_SH3_3 | 757 | 763 | PF00018 | 0.632 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.624 |
LIG_SH3_3 | 826 | 832 | PF00018 | 0.755 |
LIG_SH3_3 | 884 | 890 | PF00018 | 0.686 |
LIG_SH3_3 | 891 | 897 | PF00018 | 0.726 |
LIG_SH3_3 | 899 | 905 | PF00018 | 0.706 |
LIG_SH3_3 | 962 | 968 | PF00018 | 0.732 |
LIG_SUMO_SIM_anti_2 | 539 | 544 | PF11976 | 0.514 |
LIG_SUMO_SIM_anti_2 | 778 | 785 | PF11976 | 0.693 |
LIG_SUMO_SIM_par_1 | 283 | 290 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 313 | 318 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 537 | 544 | PF11976 | 0.514 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.472 |
LIG_TRAF2_1 | 686 | 689 | PF00917 | 0.595 |
LIG_TRAF2_2 | 153 | 158 | PF00917 | 0.414 |
LIG_TRAF2_2 | 507 | 512 | PF00917 | 0.417 |
LIG_TRFH_1 | 31 | 35 | PF08558 | 0.450 |
LIG_TYR_ITIM | 269 | 274 | PF00017 | 0.420 |
LIG_TYR_ITIM | 399 | 404 | PF00017 | 0.420 |
LIG_TYR_ITIM | 511 | 516 | PF00017 | 0.420 |
LIG_UBA3_1 | 399 | 407 | PF00899 | 0.474 |
LIG_WRC_WIRS_1 | 138 | 143 | PF05994 | 0.419 |
LIG_WW_3 | 966 | 970 | PF00397 | 0.471 |
MOD_CDK_SPK_2 | 1001 | 1006 | PF00069 | 0.576 |
MOD_CDK_SPK_2 | 687 | 692 | PF00069 | 0.694 |
MOD_CDK_SPK_2 | 768 | 773 | PF00069 | 0.524 |
MOD_CDK_SPxK_1 | 1001 | 1007 | PF00069 | 0.575 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.445 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.567 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.620 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.514 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.433 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.622 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.647 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.664 |
MOD_CK1_1 | 735 | 741 | PF00069 | 0.642 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.606 |
MOD_CK1_1 | 761 | 767 | PF00069 | 0.662 |
MOD_CK1_1 | 851 | 857 | PF00069 | 0.647 |
MOD_CK1_1 | 865 | 871 | PF00069 | 0.657 |
MOD_CK1_1 | 873 | 879 | PF00069 | 0.712 |
MOD_CK1_1 | 923 | 929 | PF00069 | 0.621 |
MOD_CK1_1 | 989 | 995 | PF00069 | 0.698 |
MOD_CK1_1 | 996 | 1002 | PF00069 | 0.619 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.420 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.433 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.448 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.474 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.578 |
MOD_CK2_1 | 683 | 689 | PF00069 | 0.608 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.609 |
MOD_CK2_1 | 889 | 895 | PF00069 | 0.525 |
MOD_CK2_1 | 914 | 920 | PF00069 | 0.617 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.528 |
MOD_GlcNHglycan | 1014 | 1017 | PF01048 | 0.687 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.220 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.576 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.422 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.251 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.276 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.204 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.332 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.627 |
MOD_GlcNHglycan | 729 | 732 | PF01048 | 0.633 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.564 |
MOD_GlcNHglycan | 773 | 776 | PF01048 | 0.738 |
MOD_GlcNHglycan | 796 | 799 | PF01048 | 0.647 |
MOD_GlcNHglycan | 820 | 823 | PF01048 | 0.636 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.680 |
MOD_GlcNHglycan | 879 | 882 | PF01048 | 0.725 |
MOD_GlcNHglycan | 922 | 925 | PF01048 | 0.720 |
MOD_GlcNHglycan | 934 | 937 | PF01048 | 0.695 |
MOD_GlcNHglycan | 995 | 998 | PF01048 | 0.709 |
MOD_GSK3_1 | 1014 | 1021 | PF00069 | 0.775 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.320 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.449 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.359 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.439 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.510 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.560 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.489 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.514 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.610 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.617 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.533 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.515 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.551 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.632 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.567 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.627 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.517 |
MOD_GSK3_1 | 771 | 778 | PF00069 | 0.500 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.614 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.599 |
MOD_GSK3_1 | 828 | 835 | PF00069 | 0.711 |
MOD_GSK3_1 | 854 | 861 | PF00069 | 0.752 |
MOD_GSK3_1 | 862 | 869 | PF00069 | 0.710 |
MOD_GSK3_1 | 870 | 877 | PF00069 | 0.637 |
MOD_GSK3_1 | 920 | 927 | PF00069 | 0.715 |
MOD_GSK3_1 | 986 | 993 | PF00069 | 0.719 |
MOD_GSK3_1 | 996 | 1003 | PF00069 | 0.787 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.220 |
MOD_N-GLC_1 | 735 | 740 | PF02516 | 0.713 |
MOD_N-GLC_1 | 775 | 780 | PF02516 | 0.747 |
MOD_N-GLC_1 | 814 | 819 | PF02516 | 0.612 |
MOD_NEK2_1 | 1012 | 1017 | PF00069 | 0.495 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.452 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.433 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.425 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.465 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.497 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.498 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.349 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.411 |
MOD_NEK2_1 | 726 | 731 | PF00069 | 0.755 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.560 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.605 |
MOD_NEK2_1 | 839 | 844 | PF00069 | 0.700 |
MOD_NEK2_1 | 856 | 861 | PF00069 | 0.605 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.610 |
MOD_NEK2_1 | 875 | 880 | PF00069 | 0.550 |
MOD_NEK2_1 | 941 | 946 | PF00069 | 0.576 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.558 |
MOD_NEK2_1 | 986 | 991 | PF00069 | 0.692 |
MOD_NEK2_2 | 1005 | 1010 | PF00069 | 0.640 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.514 |
MOD_NEK2_2 | 691 | 696 | PF00069 | 0.573 |
MOD_NEK2_2 | 801 | 806 | PF00069 | 0.627 |
MOD_PIKK_1 | 653 | 659 | PF00454 | 0.628 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.532 |
MOD_PIKK_1 | 694 | 700 | PF00454 | 0.656 |
MOD_PIKK_1 | 751 | 757 | PF00454 | 0.552 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.422 |
MOD_PIKK_1 | 973 | 979 | PF00454 | 0.641 |
MOD_PKA_2 | 1005 | 1011 | PF00069 | 0.695 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.514 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.433 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.424 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.568 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.681 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.656 |
MOD_PKA_2 | 784 | 790 | PF00069 | 0.686 |
MOD_PKA_2 | 851 | 857 | PF00069 | 0.632 |
MOD_PKA_2 | 968 | 974 | PF00069 | 0.488 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.449 |
MOD_Plk_1 | 775 | 781 | PF00069 | 0.705 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.476 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.382 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.420 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.482 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.446 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.327 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.652 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.422 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.354 |
MOD_Plk_4 | 776 | 782 | PF00069 | 0.580 |
MOD_Plk_4 | 862 | 868 | PF00069 | 0.623 |
MOD_Plk_4 | 975 | 981 | PF00069 | 0.504 |
MOD_ProDKin_1 | 1019 | 1025 | PF00069 | 0.650 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.420 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.539 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.420 |
MOD_ProDKin_1 | 649 | 655 | PF00069 | 0.625 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.664 |
MOD_ProDKin_1 | 759 | 765 | PF00069 | 0.645 |
MOD_ProDKin_1 | 768 | 774 | PF00069 | 0.572 |
MOD_ProDKin_1 | 808 | 814 | PF00069 | 0.505 |
MOD_ProDKin_1 | 828 | 834 | PF00069 | 0.712 |
MOD_ProDKin_1 | 996 | 1002 | PF00069 | 0.757 |
MOD_SUMO_rev_2 | 14 | 19 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 406 | 412 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.420 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 602 | 607 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 712 | 717 | PF01217 | 0.650 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 1005 | 1007 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 741 | 744 | PF00400 | 0.609 |
TRG_NLS_MonoCore_2 | 912 | 917 | PF00514 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Z2 | Leptomonas seymouri | 60% | 88% |
A0A0S4JHP8 | Bodo saltans | 44% | 100% |
A0A1X0NIV9 | Trypanosomatidae | 55% | 100% |
A0A3Q8IC06 | Leishmania donovani | 86% | 93% |
A0A3R7MWL4 | Trypanosoma rangeli | 53% | 100% |
A4HDB9 | Leishmania braziliensis | 73% | 94% |
A4I0P9 | Leishmania infantum | 86% | 93% |
E9AWQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 95% |
Q9UR24 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
V5DSK3 | Trypanosoma cruzi | 53% | 100% |