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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HKL3
Term | Name | Level | Count |
---|---|---|---|
GO:0000463 | maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 2 |
GO:0000470 | maturation of LSU-rRNA | 9 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003676 | nucleic acid binding | 3 | 15 |
GO:0003723 | RNA binding | 4 | 14 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0004386 | helicase activity | 2 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 15 |
GO:0140657 | ATP-dependent activity | 1 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0003724 | RNA helicase activity | 3 | 3 |
GO:0003743 | translation initiation factor activity | 4 | 3 |
GO:0008135 | translation factor activity, RNA binding | 3 | 3 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 3 |
GO:0045182 | translation regulator activity | 1 | 3 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 3 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.457 |
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.160 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 739 | 741 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.569 |
CLV_PCSK_FUR_1 | 168 | 172 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.222 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 724 | 726 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 738 | 740 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 169 | 171 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 724 | 726 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.298 |
DEG_APCC_DBOX_1 | 203 | 211 | PF00400 | 0.386 |
DEG_APCC_DBOX_1 | 360 | 368 | PF00400 | 0.510 |
DEG_APCC_DBOX_1 | 410 | 418 | PF00400 | 0.487 |
DEG_APCC_DBOX_1 | 695 | 703 | PF00400 | 0.257 |
DEG_APCC_DBOX_1 | 737 | 745 | PF00400 | 0.584 |
DOC_ANK_TNKS_1 | 371 | 378 | PF00023 | 0.411 |
DOC_CKS1_1 | 341 | 346 | PF01111 | 0.411 |
DOC_CKS1_1 | 623 | 628 | PF01111 | 0.303 |
DOC_CYCLIN_RxL_1 | 358 | 371 | PF00134 | 0.446 |
DOC_CYCLIN_yClb1_LxF_4 | 618 | 624 | PF00134 | 0.317 |
DOC_MAPK_gen_1 | 404 | 414 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 517 | 524 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 644 | 651 | PF00069 | 0.262 |
DOC_PP1_RVXF_1 | 251 | 258 | PF00149 | 0.449 |
DOC_PP2B_LxvP_1 | 280 | 283 | PF13499 | 0.452 |
DOC_PP2B_LxvP_1 | 584 | 587 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 649 | 652 | PF13499 | 0.290 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.574 |
DOC_PP4_FxxP_1 | 623 | 626 | PF00568 | 0.318 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.534 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 465 | 469 | PF12436 | 0.452 |
DOC_USP7_UBL2_3 | 726 | 730 | PF12436 | 0.484 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.305 |
LIG_14-3-3_CanoR_1 | 128 | 137 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 148 | 153 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 393 | 397 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 411 | 415 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 506 | 512 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 607 | 617 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 732 | 737 | PF00244 | 0.497 |
LIG_14-3-3_CterR_2 | 766 | 770 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 673 | 691 | PF00022 | 0.392 |
LIG_APCC_ABBA_1 | 563 | 568 | PF00400 | 0.452 |
LIG_BIR_III_2 | 486 | 490 | PF00653 | 0.485 |
LIG_BIR_III_4 | 55 | 59 | PF00653 | 0.591 |
LIG_BRCT_BRCA1_1 | 529 | 533 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 619 | 623 | PF00533 | 0.361 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_1 | 702 | 706 | PF00533 | 0.389 |
LIG_Clathr_ClatBox_1 | 207 | 211 | PF01394 | 0.364 |
LIG_Clathr_ClatBox_1 | 364 | 368 | PF01394 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 568 | 575 | PF00928 | 0.422 |
LIG_eIF4E_1 | 131 | 137 | PF01652 | 0.565 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.545 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.467 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.462 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.431 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.543 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.405 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.257 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.370 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.499 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.360 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.566 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.302 |
LIG_FHA_2 | 718 | 724 | PF00498 | 0.558 |
LIG_IRF3_LxIS_1 | 417 | 422 | PF10401 | 0.347 |
LIG_LIR_Apic_2 | 254 | 260 | PF02991 | 0.449 |
LIG_LIR_Apic_2 | 47 | 53 | PF02991 | 0.617 |
LIG_LIR_Apic_2 | 620 | 626 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 239 | 247 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 628 | 634 | PF02991 | 0.339 |
LIG_MLH1_MIPbox_1 | 64 | 68 | PF16413 | 0.629 |
LIG_MYND_1 | 597 | 601 | PF01753 | 0.411 |
LIG_PCNA_yPIPBox_3 | 372 | 386 | PF02747 | 0.516 |
LIG_PCNA_yPIPBox_3 | 650 | 662 | PF02747 | 0.293 |
LIG_Pex14_1 | 591 | 595 | PF04695 | 0.449 |
LIG_Pex14_1 | 756 | 760 | PF04695 | 0.371 |
LIG_REV1ctd_RIR_1 | 65 | 73 | PF16727 | 0.635 |
LIG_RPA_C_Fungi | 190 | 202 | PF08784 | 0.583 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.243 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.354 |
LIG_SH2_CRK | 595 | 599 | PF00017 | 0.243 |
LIG_SH2_NCK_1 | 451 | 455 | PF00017 | 0.484 |
LIG_SH2_PTP2 | 315 | 318 | PF00017 | 0.171 |
LIG_SH2_SRC | 595 | 598 | PF00017 | 0.243 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.171 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.464 |
LIG_SH3_1 | 595 | 601 | PF00018 | 0.243 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.295 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.295 |
LIG_SH3_3 | 711 | 717 | PF00018 | 0.261 |
LIG_SH3_3 | 761 | 767 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 185 | 192 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 148 | 155 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 363 | 369 | PF11976 | 0.423 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.612 |
LIG_TRAF2_1 | 625 | 628 | PF00917 | 0.324 |
LIG_TRAF2_1 | 720 | 723 | PF00917 | 0.495 |
LIG_UBA3_1 | 261 | 266 | PF00899 | 0.313 |
LIG_WRC_WIRS_1 | 508 | 513 | PF05994 | 0.389 |
MOD_CDK_SPxK_1 | 340 | 346 | PF00069 | 0.295 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.718 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.243 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.184 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.293 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.513 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.171 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.309 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.539 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.305 |
MOD_CK2_1 | 717 | 723 | PF00069 | 0.509 |
MOD_Cter_Amidation | 4 | 7 | PF01082 | 0.479 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.590 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.604 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.557 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.249 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.300 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.295 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.389 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.304 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.570 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.688 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.370 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.295 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.295 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.465 |
MOD_N-GLC_1 | 273 | 278 | PF02516 | 0.310 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.339 |
MOD_N-GLC_1 | 749 | 754 | PF02516 | 0.603 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.534 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.304 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.404 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.319 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.295 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.296 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.320 |
MOD_NEK2_2 | 265 | 270 | PF00069 | 0.270 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.243 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.298 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.458 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.534 |
MOD_PKA_2 | 717 | 723 | PF00069 | 0.605 |
MOD_PKB_1 | 329 | 337 | PF00069 | 0.389 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.389 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.195 |
MOD_Plk_2-3 | 29 | 35 | PF00069 | 0.547 |
MOD_Plk_2-3 | 426 | 432 | PF00069 | 0.593 |
MOD_Plk_2-3 | 475 | 481 | PF00069 | 0.705 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.351 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.302 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.295 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.500 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.389 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.335 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.377 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.295 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.476 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.303 |
MOD_SUMO_for_1 | 175 | 178 | PF00179 | 0.498 |
MOD_SUMO_for_1 | 183 | 186 | PF00179 | 0.450 |
TRG_DiLeu_BaEn_1 | 186 | 191 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_2 | 626 | 632 | PF01217 | 0.280 |
TRG_DiLeu_BaEn_2 | 756 | 762 | PF01217 | 0.534 |
TRG_DiLeu_BaEn_4 | 327 | 333 | PF01217 | 0.195 |
TRG_DiLeu_BaEn_4 | 627 | 633 | PF01217 | 0.311 |
TRG_DiLeu_BaLyEn_6 | 203 | 208 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 257 | 262 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.390 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.243 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.171 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.297 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.352 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 557 | 560 | PF00400 | 0.243 |
TRG_ER_diArg_1 | 59 | 62 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 738 | 740 | PF00400 | 0.458 |
TRG_NLS_Bipartite_1 | 86 | 108 | PF00514 | 0.709 |
TRG_NLS_MonoCore_2 | 167 | 172 | PF00514 | 0.498 |
TRG_NLS_MonoExtC_3 | 103 | 108 | PF00514 | 0.662 |
TRG_NLS_MonoExtC_3 | 6 | 11 | PF00514 | 0.530 |
TRG_NLS_MonoExtN_4 | 104 | 109 | PF00514 | 0.685 |
TRG_NLS_MonoExtN_4 | 168 | 173 | PF00514 | 0.617 |
TRG_NLS_MonoExtN_4 | 4 | 11 | PF00514 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 125 | 130 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 363 | 368 | PF00026 | 0.238 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.251 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWK5 | Leptomonas seymouri | 73% | 98% |
A0A0N1I6K5 | Leptomonas seymouri | 35% | 100% |
A0A0S4IWD0 | Bodo saltans | 35% | 100% |
A0A0S4JDX4 | Bodo saltans | 32% | 88% |
A0A0S4KKU4 | Bodo saltans | 64% | 100% |
A0A1X0NVK0 | Trypanosomatidae | 56% | 100% |
A0A1X0P7S4 | Trypanosomatidae | 35% | 100% |
A0A3R7M1K3 | Trypanosoma rangeli | 56% | 100% |
A0A3S5H5X3 | Leishmania donovani | 28% | 100% |
A0A3S5H6T7 | Leishmania donovani | 30% | 100% |
A0A3S7X579 | Leishmania donovani | 27% | 100% |
A0A3S7X5R1 | Leishmania donovani | 83% | 100% |
A0A3S7XAN8 | Leishmania donovani | 36% | 100% |
A0A3S7XAT8 | Leishmania donovani | 30% | 100% |
A1CB55 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 27% | 100% |
A1CL59 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 28% | 100% |
A1D699 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 28% | 100% |
A1DE84 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 27% | 100% |
A1DNF9 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 28% | 95% |
A2RA55 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 27% | 100% |
A2XVF7 | Oryza sativa subsp. indica | 28% | 93% |
A3AVH5 | Oryza sativa subsp. japonica | 28% | 93% |
A3GGE9 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 29% | 100% |
A3LNR6 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 33% | 100% |
A3LWH3 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 27% | 100% |
A3LX02 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 26% | 100% |
A4H481 | Leishmania braziliensis | 27% | 100% |
A4H4Y0 | Leishmania braziliensis | 30% | 100% |
A4HP48 | Leishmania braziliensis | 35% | 100% |
A4HP49 | Leishmania braziliensis | 30% | 100% |
A4HWB0 | Leishmania infantum | 29% | 100% |
A4I7M5 | Leishmania infantum | 27% | 100% |
A4I846 | Leishmania infantum | 83% | 100% |
A4IDF5 | Leishmania infantum | 36% | 100% |
A4IDF6 | Leishmania infantum | 30% | 100% |
A5DAR2 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 27% | 100% |
A5DGM4 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 27% | 100% |
A5DLF4 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 30% | 100% |
A5E2I8 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 27% | 100% |
A6R918 | Ajellomyces capsulatus (strain NAm1 / WU24) | 28% | 100% |
A6RMZ2 | Botryotinia fuckeliana (strain B05.10) | 30% | 100% |
A6RSH5 | Botryotinia fuckeliana (strain B05.10) | 27% | 88% |
A6ZPU3 | Saccharomyces cerevisiae (strain YJM789) | 32% | 100% |
A6ZZY8 | Saccharomyces cerevisiae (strain YJM789) | 27% | 100% |
A7F2S3 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 28% | 100% |
A7F8V8 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 27% | 88% |
A7TJ71 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 30% | 100% |
A7TNT1 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 27% | 100% |
C9ZUC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 76% |
D0A331 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0AAB3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AKE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AM86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AQ10 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ASV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AZV0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 86% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B2I0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B304 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
O49289 | Arabidopsis thaliana | 26% | 91% |
O60173 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
O80792 | Arabidopsis thaliana | 26% | 91% |
P0CQ82 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 31% | 90% |
P0CQ83 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 31% | 90% |
P0CQ84 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 35% | 100% |
P0CQ85 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 35% | 100% |
P15424 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
P20448 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
P36120 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
Q09916 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q0CF43 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 27% | 100% |
Q0D622 | Oryza sativa subsp. japonica | 30% | 100% |
Q0DBS1 | Oryza sativa subsp. japonica | 31% | 100% |
Q0DBU5 | Oryza sativa subsp. japonica | 29% | 100% |
Q0DLB9 | Oryza sativa subsp. japonica | 31% | 100% |
Q0UHM7 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 24% | 93% |
Q0UP45 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 28% | 100% |
Q0UR48 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 33% | 100% |
Q13206 | Homo sapiens | 30% | 88% |
Q1E1R7 | Coccidioides immitis (strain RS) | 28% | 100% |
Q1E9T9 | Coccidioides immitis (strain RS) | 28% | 100% |
Q2GV49 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 25% | 100% |
Q2NL08 | Bos taurus | 31% | 100% |
Q2UBZ5 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 28% | 100% |
Q2UE66 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 28% | 100% |
Q4HVW2 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 28% | 100% |
Q4HZ68 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 28% | 100% |
Q4P0Y5 | Ustilago maydis (strain 521 / FGSC 9021) | 26% | 79% |
Q4P9E5 | Ustilago maydis (strain 521 / FGSC 9021) | 30% | 100% |
Q4Q1N9 | Leishmania major | 30% | 100% |
Q4Q1P0 | Leishmania major | 36% | 100% |
Q4Q552 | Leishmania major | 83% | 99% |
Q4Q5M6 | Leishmania major | 26% | 100% |
Q4QFH1 | Leishmania major | 30% | 100% |
Q4QIQ9 | Leishmania major | 29% | 100% |
Q4QJG6 | Leishmania major | 27% | 100% |
Q4WM60 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 98% |
Q4WV71 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 100% |
Q4WYJ7 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 100% |
Q54EC2 | Dictyostelium discoideum | 26% | 100% |
Q59N29 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 26% | 100% |
Q59S50 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 27% | 100% |
Q5AF95 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 100% |
Q5AK59 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 35% | 100% |
Q5BGX6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 29% | 99% |
Q5ZBH5 | Oryza sativa subsp. japonica | 29% | 100% |
Q5ZJF6 | Gallus gallus | 30% | 88% |
Q5ZLN8 | Gallus gallus | 32% | 100% |
Q6AZV7 | Xenopus laevis | 31% | 100% |
Q6BKH3 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 25% | 96% |
Q6BSM3 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 27% | 100% |
Q6C193 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 26% | 100% |
Q6C835 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 30% | 96% |
Q6CGD1 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 30% | 100% |
Q6CK32 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 100% |
Q6CRF4 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 32% | 100% |
Q6FNA2 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 79% |
Q6FPT7 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 31% | 100% |
Q6K7R9 | Oryza sativa subsp. japonica | 28% | 95% |
Q754J2 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 28% | 100% |
Q75C76 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 32% | 100% |
Q7XJN0 | Arabidopsis thaliana | 31% | 100% |
Q80Y44 | Mus musculus | 30% | 88% |
Q84T03 | Oryza sativa subsp. japonica | 34% | 100% |
Q86B47 | Drosophila melanogaster | 30% | 79% |
Q873H9 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 100% |
Q8JHJ2 | Danio rerio | 30% | 100% |
Q8K363 | Mus musculus | 33% | 100% |
Q8NHQ9 | Homo sapiens | 31% | 100% |
Q8TFL3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 100% |
Q93Y39 | Arabidopsis thaliana | 27% | 93% |
Q9H8H2 | Homo sapiens | 32% | 90% |
Q9SB89 | Arabidopsis thaliana | 35% | 100% |
Q9SW44 | Arabidopsis thaliana | 27% | 100% |
Q9UTP9 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
Q9VHU1 | Drosophila melanogaster | 30% | 100% |
V5DCA1 | Trypanosoma cruzi | 56% | 100% |