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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QAA2
Term | Name | Level | Count |
---|---|---|---|
GO:0000018 | regulation of DNA recombination | 6 | 2 |
GO:0000019 | regulation of mitotic recombination | 7 | 2 |
GO:0000717 | nucleotide-excision repair, DNA duplex unwinding | 9 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006351 | DNA-templated transcription | 7 | 2 |
GO:0006366 | transcription by RNA polymerase II | 8 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0032392 | DNA geometric change | 7 | 2 |
GO:0032508 | DNA duplex unwinding | 8 | 2 |
GO:0032774 | RNA biosynthetic process | 5 | 2 |
GO:0033683 | obsolete nucleotide-excision repair, DNA incision | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0045911 | positive regulation of DNA recombination | 7 | 2 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0045951 | positive regulation of mitotic recombination | 8 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051052 | regulation of DNA metabolic process | 5 | 2 |
GO:0051054 | positive regulation of DNA metabolic process | 6 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051276 | chromosome organization | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071103 | DNA conformation change | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:0097659 | nucleic acid-templated transcription | 6 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006289 | nucleotide-excision repair | 6 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 3 | 12 |
GO:0003684 | damaged DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 539 | 543 | PF00656 | 0.455 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 753 | 755 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 803 | 805 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.124 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 691 | 693 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 691 | 693 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 805 | 807 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.266 |
CLV_Separin_Metazoa | 640 | 644 | PF03568 | 0.455 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.506 |
DEG_APCC_KENBOX_2 | 249 | 253 | PF00400 | 0.347 |
DEG_Kelch_actinfilin_1 | 491 | 495 | PF01344 | 0.400 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.365 |
DEG_SCF_FBW7_1 | 471 | 478 | PF00400 | 0.442 |
DOC_CDC14_PxL_1 | 629 | 637 | PF14671 | 0.455 |
DOC_CYCLIN_RxL_1 | 102 | 110 | PF00134 | 0.528 |
DOC_CYCLIN_RxL_1 | 370 | 378 | PF00134 | 0.496 |
DOC_CYCLIN_RxL_1 | 466 | 474 | PF00134 | 0.357 |
DOC_MAPK_DCC_7 | 186 | 194 | PF00069 | 0.541 |
DOC_MAPK_DCC_7 | 487 | 495 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 186 | 194 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 353 | 362 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 408 | 417 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 487 | 495 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 569 | 578 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 610 | 619 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 643 | 651 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 678 | 687 | PF00069 | 0.455 |
DOC_MAPK_HePTP_8 | 184 | 196 | PF00069 | 0.516 |
DOC_MAPK_HePTP_8 | 677 | 689 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 186 | 194 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 34 | 42 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 48 | 57 | PF00069 | 0.260 |
DOC_MAPK_MEF2A_6 | 645 | 653 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 680 | 689 | PF00069 | 0.455 |
DOC_MIT_MIM_1 | 365 | 375 | PF04212 | 0.516 |
DOC_PP1_RVXF_1 | 325 | 332 | PF00149 | 0.466 |
DOC_PP1_RVXF_1 | 467 | 474 | PF00149 | 0.367 |
DOC_PP1_RVXF_1 | 572 | 578 | PF00149 | 0.455 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.541 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.373 |
DOC_PP4_FxxP_1 | 630 | 633 | PF00568 | 0.455 |
DOC_PP4_FxxP_1 | 634 | 637 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.426 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.273 |
LIG_14-3-3_CanoR_1 | 135 | 140 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 338 | 344 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 450 | 455 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 497 | 504 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 667 | 676 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 678 | 687 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 757 | 765 | PF00244 | 0.642 |
LIG_Actin_WH2_2 | 249 | 266 | PF00022 | 0.478 |
LIG_Actin_WH2_2 | 429 | 447 | PF00022 | 0.381 |
LIG_APCC_ABBA_1 | 1 | 6 | PF00400 | 0.415 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.541 |
LIG_Clathr_ClatBox_1 | 575 | 579 | PF01394 | 0.455 |
LIG_EH1_1 | 682 | 690 | PF00400 | 0.455 |
LIG_eIF4E_1 | 387 | 393 | PF01652 | 0.522 |
LIG_eIF4E_1 | 4 | 10 | PF01652 | 0.441 |
LIG_eIF4E_1 | 553 | 559 | PF01652 | 0.466 |
LIG_eIF4E_1 | 683 | 689 | PF01652 | 0.466 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.480 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.463 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.511 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.449 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.350 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.415 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.455 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.455 |
LIG_FHA_1 | 742 | 748 | PF00498 | 0.516 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.445 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.537 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.462 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.455 |
LIG_FHA_2 | 783 | 789 | PF00498 | 0.695 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.455 |
LIG_IRF3_LxIS_1 | 651 | 656 | PF10401 | 0.541 |
LIG_LIR_Apic_2 | 15 | 19 | PF02991 | 0.366 |
LIG_LIR_Apic_2 | 406 | 412 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 274 | 283 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 526 | 537 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 549 | 559 | PF02991 | 0.455 |
LIG_LIR_LC3C_4 | 6 | 11 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 657 | 663 | PF02991 | 0.459 |
LIG_LYPXL_S_1 | 466 | 470 | PF13949 | 0.355 |
LIG_LYPXL_SIV_4 | 181 | 189 | PF13949 | 0.466 |
LIG_LYPXL_yS_3 | 467 | 470 | PF13949 | 0.358 |
LIG_MYND_1 | 633 | 637 | PF01753 | 0.455 |
LIG_NRBOX | 371 | 377 | PF00104 | 0.496 |
LIG_PCNA_PIPBox_1 | 87 | 96 | PF02747 | 0.541 |
LIG_Pex14_2 | 630 | 634 | PF04695 | 0.455 |
LIG_REV1ctd_RIR_1 | 726 | 734 | PF16727 | 0.411 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.533 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.466 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.505 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 409 | 413 | PF00017 | 0.443 |
LIG_SH2_PTP2 | 16 | 19 | PF00017 | 0.355 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.377 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 14 | 18 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 150 | 154 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 529 | 533 | PF00017 | 0.347 |
LIG_SH2_STAT3 | 18 | 21 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.162 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.455 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.484 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.455 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.419 |
LIG_SH3_3 | 630 | 636 | PF00018 | 0.455 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.343 |
LIG_SH3_3 | 777 | 783 | PF00018 | 0.675 |
LIG_SH3_3 | 793 | 799 | PF00018 | 0.520 |
LIG_Sin3_3 | 521 | 528 | PF02671 | 0.508 |
LIG_SUMO_SIM_anti_2 | 219 | 225 | PF11976 | 0.480 |
LIG_SUMO_SIM_anti_2 | 49 | 54 | PF11976 | 0.339 |
LIG_SUMO_SIM_anti_2 | 6 | 12 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 217 | 225 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 48 | 54 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 491 | 496 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 685 | 690 | PF11976 | 0.455 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.537 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.466 |
LIG_TRAF2_1 | 785 | 788 | PF00917 | 0.627 |
LIG_UBA3_1 | 532 | 538 | PF00899 | 0.323 |
LIG_UBA3_1 | 604 | 612 | PF00899 | 0.466 |
LIG_UBA3_1 | 685 | 691 | PF00899 | 0.541 |
LIG_WRC_WIRS_1 | 765 | 770 | PF05994 | 0.612 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.496 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.518 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.487 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.417 |
MOD_CK1_1 | 748 | 754 | PF00069 | 0.481 |
MOD_CK1_1 | 778 | 784 | PF00069 | 0.772 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.556 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.402 |
MOD_CK2_1 | 653 | 659 | PF00069 | 0.516 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.455 |
MOD_CK2_1 | 764 | 770 | PF00069 | 0.668 |
MOD_CK2_1 | 782 | 788 | PF00069 | 0.669 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.455 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.289 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.166 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.390 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.346 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.384 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.266 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.607 |
MOD_GlcNHglycan | 800 | 803 | PF01048 | 0.625 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.481 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.447 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.458 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.363 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.391 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.489 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.489 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.453 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.591 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.758 |
MOD_LATS_1 | 364 | 370 | PF00433 | 0.455 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.425 |
MOD_N-GLC_1 | 678 | 683 | PF02516 | 0.255 |
MOD_N-GLC_1 | 711 | 716 | PF02516 | 0.436 |
MOD_N-GLC_1 | 775 | 780 | PF02516 | 0.625 |
MOD_N-GLC_2 | 114 | 116 | PF02516 | 0.255 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.480 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.480 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.455 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.518 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.452 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.451 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.389 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.425 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.395 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.455 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.445 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.507 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.641 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.466 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.455 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.455 |
MOD_PK_1 | 450 | 456 | PF00069 | 0.379 |
MOD_PKA_1 | 243 | 249 | PF00069 | 0.604 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.459 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.504 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.444 |
MOD_PKA_2 | 756 | 762 | PF00069 | 0.577 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.503 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.480 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.487 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.347 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.467 |
MOD_Plk_1 | 714 | 720 | PF00069 | 0.397 |
MOD_Plk_1 | 775 | 781 | PF00069 | 0.759 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.455 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.475 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.350 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.457 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.494 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.338 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.408 |
MOD_Plk_4 | 742 | 748 | PF00069 | 0.440 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.369 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.268 |
MOD_SUMO_for_1 | 354 | 357 | PF00179 | 0.496 |
MOD_SUMO_for_1 | 783 | 786 | PF00179 | 0.728 |
MOD_SUMO_rev_2 | 166 | 173 | PF00179 | 0.470 |
TRG_AP2beta_CARGO_1 | 657 | 667 | PF09066 | 0.541 |
TRG_DiLeu_BaEn_1 | 235 | 240 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_1 | 274 | 279 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 86 | 91 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_2 | 409 | 415 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 765 | 768 | PF00928 | 0.686 |
TRG_ER_diArg_1 | 593 | 595 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 642 | 645 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 752 | 754 | PF00400 | 0.562 |
TRG_NES_CRM1_1 | 427 | 439 | PF08389 | 0.499 |
TRG_NES_CRM1_1 | 644 | 659 | PF08389 | 0.455 |
TRG_NLS_MonoCore_2 | 803 | 808 | PF00514 | 0.724 |
TRG_NLS_MonoExtC_3 | 803 | 808 | PF00514 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.298 |
TRG_Pf-PMV_PEXEL_1 | 704 | 708 | PF00026 | 0.341 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6K3 | Leptomonas seymouri | 25% | 85% |
A0A0N1PBH5 | Leptomonas seymouri | 89% | 100% |
A0A0P0V4R0 | Oryza sativa subsp. japonica | 23% | 80% |
A0A0S4KNN1 | Bodo saltans | 67% | 100% |
A0A1X0NWG0 | Trypanosomatidae | 74% | 99% |
A0A3R7REL5 | Trypanosoma rangeli | 74% | 100% |
A0A3S7WYU3 | Leishmania donovani | 97% | 100% |
A0A3S7X2X3 | Leishmania donovani | 25% | 85% |
A4HDT9 | Leishmania braziliensis | 94% | 100% |
A4HHR4 | Leishmania braziliensis | 24% | 85% |
A4I136 | Leishmania infantum | 97% | 100% |
A4I4X4 | Leishmania infantum | 25% | 85% |
A4K436 | Bos taurus | 25% | 67% |
A6QLJ0 | Bos taurus | 44% | 100% |
A8MPP1 | Homo sapiens | 21% | 90% |
A8WS58 | Caenorhabditis briggsae | 24% | 82% |
B0W9F4 | Culex quinquefasciatus | 24% | 83% |
B3MSG8 | Drosophila ananassae | 24% | 82% |
B3NSW1 | Drosophila erecta | 25% | 83% |
B4I0K4 | Drosophila sechellia | 24% | 84% |
B4JNS2 | Drosophila grimshawi | 25% | 82% |
B4L1Z2 | Drosophila mojavensis | 25% | 80% |
B4M891 | Drosophila virilis | 25% | 81% |
B4PZB4 | Drosophila yakuba | 25% | 83% |
C9ZW71 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 99% |
E9AEC8 | Leishmania major | 24% | 85% |
E9ALF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 85% |
E9AX74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
F4HQE2 | Arabidopsis thaliana | 23% | 78% |
O08811 | Mus musculus | 44% | 100% |
P06839 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 39% | 100% |
P0C928 | Danio rerio | 24% | 69% |
P18074 | Homo sapiens | 43% | 100% |
P26659 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 100% |
Q16X92 | Aedes aegypti | 24% | 80% |
Q55G81 | Dictyostelium discoideum | 39% | 100% |
Q5SXJ3 | Mus musculus | 24% | 69% |
Q60452 | Cricetulus griseus | 44% | 100% |
Q6AXC6 | Mus musculus | 21% | 90% |
Q6BZD9 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 23% | 99% |
Q7QEI1 | Anopheles gambiae | 24% | 82% |
Q8W4M7 | Arabidopsis thaliana | 41% | 100% |
Q92771 | Homo sapiens | 21% | 86% |
Q93575 | Caenorhabditis elegans | 24% | 82% |
Q96FC9 | Homo sapiens | 21% | 84% |
Q9NZ71 | Homo sapiens | 23% | 67% |
V5B587 | Trypanosoma cruzi | 74% | 100% |