Pyrimidine metabolism, Pseudouridylate synthase-like
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 | 1 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I1X8
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006399 | tRNA metabolic process | 7 | 7 |
GO:0006400 | tRNA modification | 6 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008033 | tRNA processing | 8 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009451 | RNA modification | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0031119 | tRNA pseudouridine synthesis | 7 | 5 |
GO:0034470 | ncRNA processing | 7 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0034660 | ncRNA metabolic process | 6 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:1990481 | mRNA pseudouridine synthesis | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004730 | pseudouridylate synthase activity | 5 | 8 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016829 | lyase activity | 2 | 8 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 8 |
GO:0016836 | hydro-lyase activity | 4 | 8 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 681 | 685 | PF00656 | 0.708 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 694 | 696 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.541 |
CLV_PCSK_FUR_1 | 444 | 448 | PF00082 | 0.474 |
CLV_PCSK_FUR_1 | 689 | 693 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 691 | 693 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 694 | 696 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 653 | 655 | PF00082 | 0.438 |
CLV_PCSK_PC7_1 | 442 | 448 | PF00082 | 0.319 |
CLV_PCSK_PC7_1 | 9 | 15 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 441 | 449 | PF00400 | 0.321 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.696 |
DEG_SPOP_SBC_1 | 338 | 342 | PF00917 | 0.565 |
DOC_CKS1_1 | 409 | 414 | PF01111 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 161 | 164 | PF00134 | 0.369 |
DOC_MAPK_DCC_7 | 194 | 204 | PF00069 | 0.428 |
DOC_MAPK_FxFP_2 | 288 | 291 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 149 | 158 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 19 | 29 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.280 |
DOC_MAPK_MEF2A_6 | 280 | 289 | PF00069 | 0.261 |
DOC_MAPK_MEF2A_6 | 96 | 103 | PF00069 | 0.265 |
DOC_PP1_RVXF_1 | 284 | 290 | PF00149 | 0.387 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.322 |
DOC_PP2B_LxvP_1 | 161 | 164 | PF13499 | 0.321 |
DOC_PP4_FxxP_1 | 288 | 291 | PF00568 | 0.291 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.722 |
DOC_WD40_RPTOR_TOS_1 | 251 | 256 | PF00400 | 0.465 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 259 | 269 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 324 | 329 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 407 | 412 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 96 | 102 | PF00244 | 0.249 |
LIG_Actin_WH2_2 | 49 | 64 | PF00022 | 0.282 |
LIG_APCC_ABBA_1 | 304 | 309 | PF00400 | 0.517 |
LIG_APCC_ABBAyCdc20_2 | 666 | 672 | PF00400 | 0.438 |
LIG_BIR_III_4 | 450 | 454 | PF00653 | 0.370 |
LIG_BIR_III_4 | 662 | 666 | PF00653 | 0.482 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.337 |
LIG_EH1_1 | 92 | 100 | PF00400 | 0.265 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.349 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.404 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.404 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.307 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.624 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.341 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.490 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.581 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.482 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.458 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.758 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.634 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.491 |
LIG_FHA_2 | 674 | 680 | PF00498 | 0.771 |
LIG_LIR_Apic_2 | 195 | 200 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 198 | 209 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 531 | 539 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 627 | 637 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 513 | 517 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 531 | 536 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.366 |
LIG_PAM2_1 | 356 | 368 | PF00658 | 0.319 |
LIG_PCNA_yPIPBox_3 | 144 | 155 | PF02747 | 0.288 |
LIG_Pex14_2 | 648 | 652 | PF04695 | 0.499 |
LIG_RPA_C_Fungi | 254 | 266 | PF08784 | 0.527 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.270 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.284 |
LIG_SH2_CRK | 197 | 201 | PF00017 | 0.297 |
LIG_SH2_CRK | 514 | 518 | PF00017 | 0.454 |
LIG_SH2_GRB2like | 248 | 251 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 197 | 201 | PF00017 | 0.273 |
LIG_SH2_PTP2 | 201 | 204 | PF00017 | 0.372 |
LIG_SH2_SRC | 660 | 663 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 429 | 433 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 660 | 664 | PF00017 | 0.367 |
LIG_SH2_STAT3 | 420 | 423 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.314 |
LIG_SH3_2 | 516 | 521 | PF14604 | 0.454 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.532 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.397 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.323 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.383 |
LIG_SUMO_SIM_par_1 | 471 | 476 | PF11976 | 0.320 |
LIG_SxIP_EBH_1 | 135 | 149 | PF03271 | 0.335 |
LIG_SxIP_EBH_1 | 515 | 528 | PF03271 | 0.396 |
LIG_TRAF2_1 | 636 | 639 | PF00917 | 0.408 |
LIG_TRFH_1 | 159 | 163 | PF08558 | 0.389 |
LIG_TYR_ITIM | 199 | 204 | PF00017 | 0.414 |
LIG_UBA3_1 | 376 | 382 | PF00899 | 0.253 |
LIG_UBA3_1 | 57 | 62 | PF00899 | 0.314 |
LIG_WW_3 | 321 | 325 | PF00397 | 0.490 |
MOD_CDC14_SPxK_1 | 404 | 407 | PF00782 | 0.364 |
MOD_CDK_SPxK_1 | 401 | 407 | PF00069 | 0.349 |
MOD_CDK_SPxxK_3 | 401 | 408 | PF00069 | 0.372 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.455 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.399 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.386 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.600 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.487 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.300 |
MOD_CK1_1 | 614 | 620 | PF00069 | 0.673 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.304 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.392 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.539 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.451 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.440 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.422 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.609 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.480 |
MOD_DYRK1A_RPxSP_1 | 408 | 412 | PF00069 | 0.444 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.500 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.473 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.514 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.402 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.486 |
MOD_GlcNHglycan | 615 | 619 | PF01048 | 0.522 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.574 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.572 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.489 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.426 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.494 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.458 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.292 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.405 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.344 |
MOD_N-GLC_1 | 594 | 599 | PF02516 | 0.692 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.428 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.325 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.737 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.263 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.394 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.389 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.343 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.490 |
MOD_PKA_1 | 407 | 413 | PF00069 | 0.344 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.627 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.311 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.347 |
MOD_PKB_1 | 492 | 500 | PF00069 | 0.404 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.333 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.417 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.444 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.300 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.626 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.362 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.464 |
MOD_Plk_2-3 | 673 | 679 | PF00069 | 0.574 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.421 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.476 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.281 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.341 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.313 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.345 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.374 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.487 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.394 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.550 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.548 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.358 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.320 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.559 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.705 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.507 |
MOD_SUMO_rev_2 | 221 | 229 | PF00179 | 0.310 |
MOD_SUMO_rev_2 | 510 | 517 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 586 | 594 | PF00179 | 0.590 |
TRG_DiLeu_BaEn_2 | 370 | 376 | PF01217 | 0.252 |
TRG_DiLeu_BaEn_2 | 528 | 534 | PF01217 | 0.277 |
TRG_DiLeu_BaLyEn_6 | 532 | 537 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.231 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.445 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 654 | 657 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 689 | 692 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 694 | 696 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.350 |
TRG_NLS_MonoExtC_3 | 652 | 657 | PF00514 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 554 | 558 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5J6 | Leptomonas seymouri | 59% | 100% |
A0A0S4JH91 | Bodo saltans | 26% | 100% |
A0A0S4KL20 | Bodo saltans | 36% | 94% |
A0A1X0NSY0 | Trypanosomatidae | 40% | 100% |
A0A3Q8ICM8 | Leishmania donovani | 99% | 100% |
A0A3R7KTM1 | Trypanosoma rangeli | 40% | 100% |
A4HEP8 | Leishmania braziliensis | 79% | 100% |
C9ZS41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AY24 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q9E9 | Leishmania major | 94% | 100% |