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:0000109 | nucleotide-excision repair complex | 3 | 2 |
GO:0000112 | nucleotide-excision repair factor 3 complex | 4 | 2 |
GO:0005667 | transcription regulator complex | 2 | 2 |
GO:0005675 | transcription factor TFIIH holo complex | 4 | 2 |
GO:0032806 | carboxy-terminal domain protein kinase complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0032993 | protein-DNA complex | 2 | 2 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 2 |
GO:0090575 | RNA polymerase II transcription regulator complex | 3 | 2 |
GO:0097550 | transcription preinitiation complex | 3 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1902554 | serine/threonine protein kinase complex | 6 | 2 |
GO:1902911 | protein kinase complex | 5 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4Q4N0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006352 | DNA-templated transcription initiation | 6 | 6 |
GO:0006367 | transcription initiation at RNA polymerase II promoter | 7 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009058 | biosynthetic process | 2 | 6 |
GO:0009059 | macromolecule biosynthetic process | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016070 | RNA metabolic process | 5 | 6 |
GO:0018130 | heterocycle biosynthetic process | 4 | 6 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 6 |
GO:0032774 | RNA biosynthetic process | 5 | 6 |
GO:0033683 | obsolete nucleotide-excision repair, DNA incision | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 6 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 6 |
GO:1901576 | organic substance biosynthetic process | 3 | 6 |
GO:0006259 | DNA metabolic process | 4 | 4 |
GO:0006281 | DNA repair | 5 | 4 |
GO:0006289 | nucleotide-excision repair | 6 | 4 |
GO:0006950 | response to stress | 2 | 4 |
GO:0006974 | DNA damage response | 4 | 4 |
GO:0033554 | cellular response to stress | 3 | 4 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 4 |
GO:0050896 | response to stimulus | 1 | 4 |
GO:0051716 | cellular response to stimulus | 2 | 4 |
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: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:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
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:0043138 | 3'-5' DNA helicase activity | 4 | 2 |
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 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.419 |
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.383 |
CLV_C14_Caspase3-7 | 701 | 705 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 737 | 739 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.356 |
CLV_PCSK_FUR_1 | 738 | 742 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 739 | 741 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.356 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.219 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 739 | 741 | PF00082 | 0.619 |
CLV_PCSK_PC7_1 | 366 | 372 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.314 |
CLV_Separin_Metazoa | 502 | 506 | PF03568 | 0.358 |
DEG_APCC_DBOX_1 | 112 | 120 | PF00400 | 0.303 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.419 |
DEG_APCC_DBOX_1 | 42 | 50 | PF00400 | 0.384 |
DEG_APCC_KENBOX_2 | 371 | 375 | PF00400 | 0.419 |
DEG_SCF_FBW7_1 | 287 | 293 | PF00400 | 0.219 |
DEG_SPOP_SBC_1 | 353 | 357 | PF00917 | 0.342 |
DEG_SPOP_SBC_1 | 651 | 655 | PF00917 | 0.527 |
DOC_CKS1_1 | 287 | 292 | PF01111 | 0.219 |
DOC_CKS1_1 | 458 | 463 | PF01111 | 0.301 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.219 |
DOC_CYCLIN_yCln2_LP_2 | 379 | 385 | PF00134 | 0.314 |
DOC_CYCLIN_yCln2_LP_2 | 63 | 69 | PF00134 | 0.219 |
DOC_MAPK_gen_1 | 259 | 267 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 36 | 42 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 668 | 678 | PF00069 | 0.717 |
DOC_MAPK_MEF2A_6 | 249 | 256 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 259 | 267 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 479 | 488 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 565 | 573 | PF00069 | 0.299 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.370 |
DOC_PP2B_LxvP_1 | 379 | 382 | PF13499 | 0.419 |
DOC_PP2B_LxvP_1 | 531 | 534 | PF13499 | 0.299 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.445 |
DOC_USP7_UBL2_3 | 372 | 376 | PF12436 | 0.419 |
DOC_USP7_UBL2_3 | 664 | 668 | PF12436 | 0.698 |
DOC_USP7_UBL2_3 | 720 | 724 | PF12436 | 0.307 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.301 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.219 |
LIG_14-3-3_CanoR_1 | 36 | 40 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 43 | 53 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 766 | 772 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 787 | 795 | PF00244 | 0.666 |
LIG_APCC_ABBA_1 | 153 | 158 | PF00400 | 0.522 |
LIG_APCC_ABBA_1 | 546 | 551 | PF00400 | 0.299 |
LIG_APCC_ABBAyCdc20_2 | 545 | 551 | PF00400 | 0.299 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.689 |
LIG_BIR_III_4 | 300 | 304 | PF00653 | 0.260 |
LIG_BIR_III_4 | 407 | 411 | PF00653 | 0.333 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.384 |
LIG_CaM_NSCaTE_8 | 615 | 622 | PF13499 | 0.293 |
LIG_Clathr_ClatBox_1 | 385 | 389 | PF01394 | 0.299 |
LIG_Clathr_ClatBox_1 | 794 | 798 | PF01394 | 0.576 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.521 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.299 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.289 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.416 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.299 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.263 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.337 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.313 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.519 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.389 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.416 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.333 |
LIG_Integrin_isoDGR_2 | 608 | 610 | PF01839 | 0.445 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 283 | 291 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 336 | 344 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 38 | 46 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 427 | 437 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 681 | 692 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 770 | 777 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 526 | 530 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 648 | 652 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 681 | 687 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 770 | 774 | PF02991 | 0.642 |
LIG_Pex14_1 | 729 | 733 | PF04695 | 0.439 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.299 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.314 |
LIG_SH2_CRK | 617 | 621 | PF00017 | 0.299 |
LIG_SH2_CRK | 771 | 775 | PF00017 | 0.646 |
LIG_SH2_GRB2like | 39 | 42 | PF00017 | 0.219 |
LIG_SH2_NCK_1 | 617 | 621 | PF00017 | 0.299 |
LIG_SH2_PTP2 | 27 | 30 | PF00017 | 0.381 |
LIG_SH2_PTP2 | 39 | 42 | PF00017 | 0.333 |
LIG_SH2_SRC | 157 | 160 | PF00017 | 0.503 |
LIG_SH2_SRC | 39 | 42 | PF00017 | 0.260 |
LIG_SH2_SRC | 437 | 440 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 642 | 646 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.316 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.308 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.314 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.299 |
LIG_SH3_3 | 689 | 695 | PF00018 | 0.701 |
LIG_SUMO_SIM_anti_2 | 519 | 526 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 384 | 390 | PF11976 | 0.419 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.503 |
LIG_TRAF2_2 | 306 | 311 | PF00917 | 0.219 |
LIG_TRFH_1 | 62 | 66 | PF08558 | 0.419 |
LIG_TYR_ITIM | 282 | 287 | PF00017 | 0.384 |
LIG_UBA3_1 | 251 | 259 | PF00899 | 0.325 |
LIG_UBA3_1 | 428 | 435 | PF00899 | 0.375 |
LIG_UBA3_1 | 521 | 525 | PF00899 | 0.318 |
LIG_WRC_WIRS_1 | 169 | 174 | PF05994 | 0.487 |
LIG_WW_3 | 289 | 293 | PF00397 | 0.219 |
MOD_CDK_SPxK_1 | 148 | 154 | PF00069 | 0.478 |
MOD_CDK_SPxK_1 | 286 | 292 | PF00069 | 0.219 |
MOD_CDK_SPxxK_3 | 457 | 464 | PF00069 | 0.314 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.463 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.484 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.397 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.318 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.308 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.572 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.576 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.500 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.404 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.333 |
MOD_CK2_1 | 679 | 685 | PF00069 | 0.660 |
MOD_CK2_1 | 724 | 730 | PF00069 | 0.430 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.299 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.716 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.721 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.562 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.728 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.615 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.404 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.514 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.560 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.482 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.536 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.307 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.255 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.314 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.314 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.364 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.299 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.299 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.234 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.404 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.657 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.584 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.396 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.526 |
MOD_N-GLC_1 | 753 | 758 | PF02516 | 0.692 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.702 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.303 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.462 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.455 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.303 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.116 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.376 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.199 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.293 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.376 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.299 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.609 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.384 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.529 |
MOD_NEK2_2 | 395 | 400 | PF00069 | 0.419 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.435 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.445 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.419 |
MOD_PIKK_1 | 537 | 543 | PF00454 | 0.419 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.299 |
MOD_PKA_1 | 740 | 746 | PF00069 | 0.645 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.345 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.384 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.351 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.307 |
MOD_PKA_2 | 740 | 746 | PF00069 | 0.658 |
MOD_PKA_2 | 786 | 792 | PF00069 | 0.655 |
MOD_PKB_1 | 738 | 746 | PF00069 | 0.658 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.419 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.501 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.443 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.372 |
MOD_Plk_1 | 567 | 573 | PF00069 | 0.299 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.419 |
MOD_Plk_2-3 | 158 | 164 | PF00069 | 0.592 |
MOD_Plk_2-3 | 283 | 289 | PF00069 | 0.414 |
MOD_Plk_2-3 | 325 | 331 | PF00069 | 0.299 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.496 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.285 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.285 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.286 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.314 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.326 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.299 |
MOD_Plk_4 | 679 | 685 | PF00069 | 0.666 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.699 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.514 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.568 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.355 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.301 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.314 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.219 |
MOD_SUMO_for_1 | 678 | 681 | PF00179 | 0.562 |
MOD_SUMO_for_1 | 774 | 777 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 402 | 411 | PF00179 | 0.336 |
MOD_SUMO_rev_2 | 421 | 426 | PF00179 | 0.317 |
TRG_DiLeu_BaEn_1 | 526 | 531 | PF01217 | 0.299 |
TRG_DiLeu_BaEn_1 | 98 | 103 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_2 | 12 | 18 | PF01217 | 0.490 |
TRG_DiLeu_BaEn_2 | 80 | 86 | PF01217 | 0.356 |
TRG_DiLeu_BaEn_3 | 133 | 139 | PF01217 | 0.419 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 649 | 652 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 684 | 687 | PF00928 | 0.697 |
TRG_ENDOCYTIC_2 | 771 | 774 | PF00928 | 0.640 |
TRG_ENDOCYTIC_2 | 803 | 806 | PF00928 | 0.577 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 693 | 696 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 738 | 741 | PF00400 | 0.640 |
TRG_NLS_MonoCore_2 | 737 | 742 | PF00514 | 0.638 |
TRG_NLS_MonoExtC_3 | 737 | 742 | PF00514 | 0.612 |
TRG_NLS_MonoExtN_4 | 738 | 743 | PF00514 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 100 | 105 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 501 | 506 | PF00026 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIS9 | Leptomonas seymouri | 76% | 99% |
A0A0S4J760 | Bodo saltans | 46% | 75% |
A0A1X0NS07 | Trypanosomatidae | 57% | 100% |
A0A3R7MM80 | Trypanosoma rangeli | 59% | 100% |
A0A3S7X6B2 | Leishmania donovani | 95% | 100% |
A4HH67 | Leishmania braziliensis | 30% | 73% |
A4HL29 | Leishmania braziliensis | 83% | 100% |
A4I8L0 | Leishmania infantum | 95% | 100% |
A6WE36 | Kineococcus radiotolerans (strain ATCC BAA-149 / DSM 14245 / SRS30216) | 32% | 100% |
A9CRJ7 | Enterocytozoon bieneusi (strain H348) | 34% | 100% |
C4V922 | Nosema ceranae (strain BRL01) | 35% | 100% |
D0AAK6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B3H0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O00835 | Dictyostelium discoideum | 34% | 100% |
O13768 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
O53873 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 29% | 100% |
P19447 | Homo sapiens | 34% | 100% |
P49135 | Mus musculus | 35% | 100% |
Q00578 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 96% |
Q1RMT1 | Bos taurus | 35% | 100% |
Q381F9 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 55% | 100% |
Q38861 | Arabidopsis thaliana | 33% | 100% |
Q4G005 | Rattus norvegicus | 34% | 100% |
Q5RA62 | Pongo abelii | 34% | 100% |
Q5ZKK7 | Gallus gallus | 34% | 100% |
Q60HG1 | Macaca fascicularis | 34% | 100% |
Q6E6J3 | Antonospora locustae | 36% | 100% |
Q7ZVV1 | Danio rerio | 34% | 100% |
Q8SSK1 | Encephalitozoon cuniculi (strain GB-M1) | 36% | 100% |
Q9FUG4 | Arabidopsis thaliana | 34% | 100% |
V5BDD7 | Trypanosoma cruzi | 58% | 100% |