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. | yes | yes: 15 |
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005657 | replication fork | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AVA3
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 13 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006259 | DNA metabolic process | 4 | 13 |
GO:0006281 | DNA repair | 5 | 13 |
GO:0006310 | DNA recombination | 5 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0006950 | response to stress | 2 | 13 |
GO:0006974 | DNA damage response | 4 | 13 |
GO:0006996 | organelle organization | 4 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016043 | cellular component organization | 3 | 13 |
GO:0032200 | telomere organization | 6 | 13 |
GO:0033554 | cellular response to stress | 3 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0050896 | response to stimulus | 1 | 13 |
GO:0051276 | chromosome organization | 5 | 13 |
GO:0051716 | cellular response to stimulus | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
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 | 13 |
GO:0003678 | DNA helicase activity | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0016887 | ATP hydrolysis activity | 7 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
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 | 164 | 168 | PF00656 | 0.715 |
CLV_MEL_PAP_1 | 508 | 514 | PF00089 | 0.557 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 684 | 686 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 769 | 771 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 769 | 771 | PF00082 | 0.790 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 769 | 773 | PF00082 | 0.797 |
DEG_COP1_1 | 614 | 624 | PF00400 | 0.262 |
DEG_SPOP_SBC_1 | 205 | 209 | PF00917 | 0.554 |
DEG_SPOP_SBC_1 | 210 | 214 | PF00917 | 0.602 |
DEG_SPOP_SBC_1 | 407 | 411 | PF00917 | 0.313 |
DOC_CYCLIN_yCln2_LP_2 | 400 | 406 | PF00134 | 0.313 |
DOC_MAPK_gen_1 | 639 | 646 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 683 | 692 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 93 | 100 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 349 | 358 | PF00069 | 0.185 |
DOC_MAPK_MEF2A_6 | 639 | 646 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 654 | 662 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 685 | 694 | PF00069 | 0.249 |
DOC_PP1_RVXF_1 | 248 | 254 | PF00149 | 0.583 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.313 |
DOC_PP2B_LxvP_1 | 404 | 407 | PF13499 | 0.283 |
DOC_PP2B_LxvP_1 | 436 | 439 | PF13499 | 0.301 |
DOC_SPAK_OSR1_1 | 511 | 515 | PF12202 | 0.545 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.822 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.850 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 749 | 753 | PF00917 | 0.787 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.550 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.770 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.820 |
LIG_14-3-3_CanoR_1 | 322 | 331 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 413 | 423 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 544 | 553 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 612 | 620 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 634 | 638 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 763 | 769 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.423 |
LIG_Actin_WH2_2 | 236 | 254 | PF00022 | 0.461 |
LIG_Actin_WH2_2 | 555 | 573 | PF00022 | 0.452 |
LIG_APCC_ABBA_1 | 22 | 27 | PF00400 | 0.467 |
LIG_APCC_ABBAyCdc20_2 | 21 | 27 | PF00400 | 0.475 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.641 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_1 | 538 | 542 | PF00533 | 0.568 |
LIG_CaM_IQ_9 | 113 | 129 | PF13499 | 0.602 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.380 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.461 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.595 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.313 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.396 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.387 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.511 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.581 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.591 |
LIG_FHA_1 | 763 | 769 | PF00498 | 0.578 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.445 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.455 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.434 |
LIG_FHA_2 | 691 | 697 | PF00498 | 0.425 |
LIG_LIR_Gen_1 | 387 | 397 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 434 | 441 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 547 | 558 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 710 | 714 | PF02991 | 0.474 |
LIG_MAD2 | 398 | 406 | PF02301 | 0.360 |
LIG_RPA_C_Fungi | 758 | 770 | PF08784 | 0.468 |
LIG_SH2_CRK | 550 | 554 | PF00017 | 0.503 |
LIG_SH2_NCK_1 | 550 | 554 | PF00017 | 0.534 |
LIG_SH2_PTP2 | 678 | 681 | PF00017 | 0.354 |
LIG_SH2_STAT3 | 529 | 532 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 678 | 681 | PF00017 | 0.354 |
LIG_SH3_2 | 216 | 221 | PF14604 | 0.629 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.696 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.317 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.570 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.469 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.441 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.518 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.451 |
LIG_SUMO_SIM_anti_2 | 375 | 381 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 691 | 696 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 375 | 381 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 575 | 581 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 693 | 698 | PF11976 | 0.435 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.596 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.447 |
MOD_CDK_SPxxK_3 | 490 | 497 | PF00069 | 0.360 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.751 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.717 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.400 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.420 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.525 |
MOD_CK1_1 | 719 | 725 | PF00069 | 0.780 |
MOD_CK1_1 | 752 | 758 | PF00069 | 0.711 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.639 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.756 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.815 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.449 |
MOD_CK2_1 | 667 | 673 | PF00069 | 0.479 |
MOD_Cter_Amidation | 504 | 507 | PF01082 | 0.531 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.700 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.466 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.755 |
MOD_GlcNHglycan | 173 | 177 | PF01048 | 0.674 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.708 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.404 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.355 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.522 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.541 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.829 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.700 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.692 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.627 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.747 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.652 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.465 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.648 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.489 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.702 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.605 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.502 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.637 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.719 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.626 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.360 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.447 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.509 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.502 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.499 |
MOD_NEK2_1 | 759 | 764 | PF00069 | 0.503 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.423 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.301 |
MOD_NEK2_2 | 648 | 653 | PF00069 | 0.362 |
MOD_NEK2_2 | 749 | 754 | PF00069 | 0.536 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.781 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.357 |
MOD_PIKK_1 | 720 | 726 | PF00454 | 0.765 |
MOD_PK_1 | 94 | 100 | PF00069 | 0.556 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.796 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.707 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.325 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.444 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.483 |
MOD_PKA_2 | 611 | 617 | PF00069 | 0.559 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.567 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.732 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.764 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.469 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.361 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.518 |
MOD_Plk_1 | 560 | 566 | PF00069 | 0.453 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.518 |
MOD_Plk_1 | 688 | 694 | PF00069 | 0.420 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.818 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.424 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.495 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.455 |
MOD_Plk_4 | 667 | 673 | PF00069 | 0.526 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.280 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.434 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.451 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.759 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.356 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.771 |
MOD_SUMO_for_1 | 771 | 774 | PF00179 | 0.649 |
TRG_DiLeu_BaEn_1 | 515 | 520 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 678 | 681 | PF00928 | 0.354 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 413 | 416 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.404 |
TRG_NES_CRM1_1 | 656 | 668 | PF08389 | 0.555 |
TRG_NLS_MonoExtC_3 | 768 | 774 | PF00514 | 0.797 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IK87 | Bodo saltans | 30% | 84% |
A0A0S4JCS0 | Bodo saltans | 41% | 100% |
A0A1X0NZA2 | Trypanosomatidae | 38% | 91% |
A0A3Q8IBY0 | Leishmania donovani | 91% | 99% |
A0A3R7MKN4 | Trypanosoma rangeli | 29% | 81% |
A0A422NAK1 | Trypanosoma rangeli | 48% | 99% |
A4HBX5 | Leishmania braziliensis | 79% | 99% |
A4HZ95 | Leishmania infantum | 90% | 99% |
C9ZUJ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 78% |
D0A177 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 97% |
Q38CE9 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 44% | 97% |
Q4QC77 | Leishmania major | 90% | 100% |
Q57YG0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 29% | 78% |
Q9UUA2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 96% |
V5B8C2 | Trypanosoma cruzi | 30% | 80% |
V5BE68 | Trypanosoma cruzi | 47% | 98% |