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:0005634 | nucleus | 5 | 10 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0042555 | MCM complex | 2 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4HKT9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006270 | DNA replication initiation | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 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:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 |
GO:0006268 | DNA unwinding involved in DNA replication | 9 | 1 |
GO:0006271 | DNA strand elongation involved in DNA replication | 6 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022616 | DNA strand elongation | 5 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 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 | 8 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0016887 | ATP hydrolysis activity | 7 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
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:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.391 |
CLV_C14_Caspase3-7 | 661 | 665 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.255 |
CLV_PCSK_FUR_1 | 491 | 495 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 493 | 495 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 573 | 575 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 6 | 8 | PF00082 | 0.693 |
CLV_PCSK_PC7_1 | 24 | 30 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.478 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 451 | 459 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 510 | 518 | PF00400 | 0.559 |
DEG_APCC_DBOX_1 | 607 | 615 | PF00400 | 0.469 |
DEG_MDM2_SWIB_1 | 512 | 519 | PF02201 | 0.455 |
DEG_SPOP_SBC_1 | 659 | 663 | PF00917 | 0.521 |
DOC_ANK_TNKS_1 | 257 | 264 | PF00023 | 0.523 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.712 |
DOC_CYCLIN_RxL_1 | 605 | 612 | PF00134 | 0.471 |
DOC_MAPK_DCC_7 | 53 | 62 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 126 | 132 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 169 | 178 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 223 | 232 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 367 | 376 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 676 | 683 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 702 | 712 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 169 | 178 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 511 | 519 | PF00069 | 0.455 |
DOC_PP1_RVXF_1 | 620 | 626 | PF00149 | 0.469 |
DOC_PP2B_LxvP_1 | 120 | 123 | PF13499 | 0.378 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.455 |
DOC_USP7_UBL2_3 | 292 | 296 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 367 | 376 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 553 | 560 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 595 | 600 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 608 | 614 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 615 | 623 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 624 | 630 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 651 | 660 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 676 | 682 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 7 | 17 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 702 | 708 | PF00244 | 0.425 |
LIG_Actin_WH2_2 | 609 | 626 | PF00022 | 0.469 |
LIG_APCC_ABBA_1 | 575 | 580 | PF00400 | 0.507 |
LIG_APCC_ABBA_1 | 58 | 63 | PF00400 | 0.460 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.455 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.455 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.465 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.455 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.455 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.469 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.323 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.507 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.455 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.554 |
LIG_FHA_2 | 659 | 665 | PF00498 | 0.505 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.435 |
LIG_FHA_2 | 704 | 710 | PF00498 | 0.436 |
LIG_FHA_2 | 716 | 722 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 93 | 97 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 184 | 195 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 442 | 451 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 510 | 519 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 588 | 599 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 666 | 675 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 706 | 715 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 510 | 515 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 666 | 671 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 706 | 710 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.500 |
LIG_PCNA_yPIPBox_3 | 205 | 216 | PF02747 | 0.455 |
LIG_PCNA_yPIPBox_3 | 76 | 85 | PF02747 | 0.535 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.469 |
LIG_Pex14_2 | 512 | 516 | PF04695 | 0.455 |
LIG_Pex14_2 | 560 | 564 | PF04695 | 0.425 |
LIG_PTB_Apo_2 | 483 | 490 | PF02174 | 0.455 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.507 |
LIG_SH2_GRB2like | 20 | 23 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 9 | 13 | PF00017 | 0.665 |
LIG_SH2_PTP2 | 578 | 581 | PF00017 | 0.559 |
LIG_SH2_PTP2 | 94 | 97 | PF00017 | 0.378 |
LIG_SH2_SRC | 307 | 310 | PF00017 | 0.497 |
LIG_SH2_SRC | 578 | 581 | PF00017 | 0.559 |
LIG_SH2_SRC | 94 | 97 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.665 |
LIG_SH2_STAT3 | 43 | 46 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 707 | 710 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.429 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.455 |
LIG_SUMO_SIM_anti_2 | 154 | 159 | PF11976 | 0.455 |
LIG_SUMO_SIM_anti_2 | 609 | 615 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 173 | 180 | PF11976 | 0.455 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.535 |
LIG_TRAF2_1 | 306 | 309 | PF00917 | 0.489 |
LIG_TYR_ITIM | 225 | 230 | PF00017 | 0.465 |
LIG_TYR_ITSM | 291 | 298 | PF00017 | 0.499 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.540 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.465 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.455 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.507 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.464 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.441 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.535 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.455 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.473 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.455 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.455 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.562 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.479 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.491 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.308 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.185 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.251 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.504 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.455 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.475 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.455 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.455 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.455 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.486 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.552 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.567 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.501 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.507 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.255 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.460 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.512 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.455 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.489 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.455 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.455 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.469 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.455 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.455 |
MOD_PIKK_1 | 614 | 620 | PF00454 | 0.469 |
MOD_PK_1 | 595 | 601 | PF00069 | 0.448 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.535 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.529 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.339 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.505 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.385 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.455 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.465 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.655 |
MOD_PKA_2 | 599 | 605 | PF00069 | 0.481 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.434 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.469 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.480 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.431 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.444 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.455 |
MOD_Plk_1 | 450 | 456 | PF00069 | 0.455 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.455 |
MOD_Plk_1 | 663 | 669 | PF00069 | 0.533 |
MOD_Plk_2-3 | 303 | 309 | PF00069 | 0.473 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.465 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.389 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.484 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.455 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.469 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.533 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.513 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.455 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.455 |
MOD_SUMO_rev_2 | 341 | 351 | PF00179 | 0.455 |
TRG_DiLeu_BaEn_1 | 427 | 432 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 636 | 641 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.455 |
TRG_DiLeu_LyEn_5 | 636 | 641 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 591 | 594 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 622 | 625 | PF00400 | 0.469 |
TRG_NES_CRM1_1 | 63 | 75 | PF08389 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.190 |
TRG_Pf-PMV_PEXEL_1 | 628 | 632 | PF00026 | 0.286 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P686 | Leptomonas seymouri | 34% | 84% |
A0A0N0P9H0 | Leptomonas seymouri | 30% | 79% |
A0A0N1I2J6 | Leptomonas seymouri | 34% | 81% |
A0A0N1I371 | Leptomonas seymouri | 90% | 100% |
A0A0N1PC47 | Leptomonas seymouri | 30% | 91% |
A0A0S4IVB8 | Bodo saltans | 33% | 83% |
A0A0S4IW18 | Bodo saltans | 34% | 90% |
A0A0S4IYQ3 | Bodo saltans | 29% | 90% |
A0A0S4J4D4 | Bodo saltans | 30% | 78% |
A0A0S4J5X8 | Bodo saltans | 31% | 96% |
A0A0S4JM41 | Bodo saltans | 37% | 92% |
A0A1X0NQM5 | Trypanosomatidae | 33% | 82% |
A0A1X0NSY3 | Trypanosomatidae | 35% | 85% |
A0A1X0NT66 | Trypanosomatidae | 77% | 99% |
A0A1X0NVE7 | Trypanosomatidae | 30% | 91% |
A0A1X0NZT6 | Trypanosomatidae | 35% | 77% |
A0A1X0P1Q1 | Trypanosomatidae | 31% | 100% |
A0A3Q8IQ79 | Leishmania donovani | 30% | 80% |
A0A3R7K9K0 | Trypanosoma rangeli | 36% | 91% |
A0A3R7MUG3 | Trypanosoma rangeli | 33% | 96% |
A0A3S5H7J9 | Leishmania donovani | 33% | 82% |
A0A3S5H7S8 | Leishmania donovani | 94% | 100% |
A0A3S7WY81 | Leishmania donovani | 29% | 91% |
A0A3S7X726 | Leishmania donovani | 33% | 82% |
A0A422N694 | Trypanosoma rangeli | 32% | 100% |
A0A422NHH5 | Trypanosoma rangeli | 30% | 94% |
A0A422NZW3 | Trypanosoma rangeli | 77% | 99% |
A4FUD9 | Bos taurus | 38% | 90% |
A4HDE7 | Leishmania braziliensis | 30% | 100% |
A4HGC9 | Leishmania braziliensis | 34% | 75% |
A4HGU2 | Leishmania braziliensis | 34% | 82% |
A4HLY1 | Leishmania braziliensis | 34% | 83% |
A4I0T0 | Leishmania infantum | 29% | 91% |
A4I3W9 | Leishmania infantum | 33% | 82% |
A4I8B8 | Leishmania infantum | 94% | 100% |
A4I9B0 | Leishmania infantum | 33% | 82% |
A4IC27 | Leishmania infantum | 30% | 80% |
B8AEH3 | Oryza sativa subsp. indica | 35% | 99% |
B8AZ14 | Oryza sativa subsp. indica | 33% | 92% |
B8AZ99 | Oryza sativa subsp. indica | 33% | 94% |
B8AZX3 | Oryza sativa subsp. indica | 36% | 87% |
B8B406 | Oryza sativa subsp. indica | 33% | 100% |
B8BKI8 | Oryza sativa subsp. indica | 36% | 75% |
B8BMI1 | Oryza sativa subsp. indica | 43% | 100% |
B9FKM7 | Oryza sativa subsp. japonica | 33% | 92% |
C9ZJB6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 89% |
C9ZYH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 94% |
D0A4I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A759 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 94% |
D0A936 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 84% |
D0A999 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 87% |
D0AAI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 77% | 99% |
D3ZVK1 | Rattus norvegicus | 32% | 87% |
E1BPX4 | Bos taurus | 32% | 89% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 91% |
E9B059 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 82% |
E9B377 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B4B0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 83% |
E9B719 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 80% |
F4IFF3 | Arabidopsis thaliana | 33% | 100% |
F4KAB8 | Arabidopsis thaliana | 37% | 87% |
I0IUP3 | Gallus gallus | 34% | 87% |
O75001 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 95% |
O80786 | Arabidopsis thaliana | 35% | 100% |
P25205 | Homo sapiens | 38% | 90% |
P25206 | Mus musculus | 38% | 89% |
P29458 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 78% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 84% |
P29496 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 94% |
P30664 | Xenopus laevis | 38% | 84% |
P30665 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 78% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 82% |
P33991 | Homo sapiens | 38% | 84% |
P33992 | Homo sapiens | 35% | 99% |
P33993 | Homo sapiens | 42% | 100% |
P34647 | Caenorhabditis elegans | 31% | 90% |
P38132 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 86% |
P40377 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 87% |
P41389 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P43299 | Arabidopsis thaliana | 42% | 100% |
P49717 | Mus musculus | 39% | 84% |
P49718 | Mus musculus | 35% | 99% |
P49731 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 81% |
P49735 | Drosophila melanogaster | 35% | 82% |
P49736 | Homo sapiens | 34% | 80% |
P49739 | Xenopus laevis | 39% | 90% |
P55861 | Xenopus laevis | 35% | 82% |
P55862 | Xenopus laevis | 35% | 99% |
P97310 | Mus musculus | 33% | 80% |
P97311 | Mus musculus | 31% | 88% |
Q0DHC4 | Oryza sativa subsp. japonica | 33% | 94% |
Q0V8B7 | Bos taurus | 35% | 99% |
Q0V9Q6 | Xenopus tropicalis | 33% | 86% |
Q0WVF5 | Arabidopsis thaliana | 39% | 86% |
Q14566 | Homo sapiens | 31% | 88% |
Q21902 | Caenorhabditis elegans | 33% | 96% |
Q26454 | Drosophila melanogaster | 34% | 84% |
Q28BS0 | Xenopus tropicalis | 38% | 90% |
Q28CM3 | Xenopus tropicalis | 32% | 88% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 31% | 89% |
Q2KIZ8 | Bos taurus | 31% | 88% |
Q2QNM1 | Oryza sativa subsp. japonica | 43% | 100% |
Q2R482 | Oryza sativa subsp. japonica | 36% | 75% |
Q3ZBH9 | Bos taurus | 42% | 100% |
Q43704 | Zea mays | 37% | 94% |
Q498J7 | Xenopus laevis | 30% | 88% |
Q4Q3R6 | Leishmania major | 34% | 82% |
Q4Q826 | Leishmania major | 33% | 82% |
Q4QAP2 | Leishmania major | 29% | 100% |
Q54CP4 | Dictyostelium discoideum | 33% | 96% |
Q561P5 | Xenopus tropicalis | 34% | 99% |
Q57809 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 30% | 96% |
Q58371 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 29% | 95% |
Q58884 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 27% | 100% |
Q5F310 | Xenopus laevis | 33% | 87% |
Q5FWY4 | Xenopus laevis | 32% | 88% |
Q5JKB0 | Oryza sativa subsp. japonica | 40% | 84% |
Q5R8G6 | Pongo abelii | 38% | 90% |
Q5XK83 | Xenopus laevis | 38% | 84% |
Q5ZMN2 | Gallus gallus | 38% | 89% |
Q61881 | Mus musculus | 42% | 100% |
Q61J08 | Caenorhabditis briggsae | 33% | 90% |
Q69QA6 | Oryza sativa subsp. japonica | 33% | 100% |
Q6DIH3 | Xenopus tropicalis | 35% | 82% |
Q6F353 | Oryza sativa subsp. japonica | 36% | 87% |
Q6GL41 | Xenopus tropicalis | 38% | 84% |
Q6KAJ4 | Oryza sativa subsp. japonica | 32% | 99% |
Q6NX31 | Xenopus tropicalis | 42% | 100% |
Q6P1V8 | Xenopus tropicalis | 30% | 88% |
Q6PCI7 | Xenopus laevis | 35% | 99% |
Q7Q0Q1 | Anopheles gambiae | 31% | 89% |
Q7ZXB1 | Xenopus laevis | 42% | 100% |
Q7ZXZ0 | Xenopus laevis | 38% | 90% |
Q7ZY18 | Xenopus laevis | 31% | 88% |
Q86B14 | Dictyostelium discoideum | 32% | 84% |
Q91876 | Xenopus laevis | 42% | 100% |
Q95XQ8 | Caenorhabditis elegans | 36% | 88% |
Q9CWV1 | Mus musculus | 33% | 87% |
Q9FL33 | Arabidopsis thaliana | 38% | 93% |
Q9LPD9 | Arabidopsis thaliana | 37% | 77% |
Q9SF37 | Arabidopsis thaliana | 31% | 91% |
Q9SX03 | Zea mays | 37% | 94% |
Q9SX04 | Zea mays | 37% | 94% |
Q9U1E0 | Leishmania major | 94% | 100% |
Q9UJA3 | Homo sapiens | 33% | 86% |
Q9UXG1 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 33% | 100% |
Q9V461 | Drosophila melanogaster | 31% | 89% |
Q9VGW6 | Drosophila melanogaster | 35% | 99% |
Q9XYU0 | Drosophila melanogaster | 40% | 100% |
Q9XYU1 | Drosophila melanogaster | 37% | 89% |
V5BAH7 | Trypanosoma cruzi | 36% | 83% |
V5BGQ5 | Trypanosoma cruzi | 32% | 85% |
V5BHZ8 | Trypanosoma cruzi | 79% | 100% |
V5BQA9 | Trypanosoma cruzi | 34% | 93% |
V5BSG2 | Trypanosoma cruzi | 33% | 83% |
V5C0K6 | Trypanosoma cruzi | 30% | 94% |