Appears to be a secreted chaperone, related to mammalian HYOU1 proteins. Probably ER-localized as in other eukaryotes
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: 20 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 11, no: 3 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034663 | endoplasmic reticulum chaperone complex | 3 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HND7
Term | Name | Level | Count |
---|---|---|---|
GO:0001666 | response to hypoxia | 3 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0009968 | negative regulation of signal transduction | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0010648 | negative regulation of cell communication | 5 | 1 |
GO:0010941 | regulation of cell death | 4 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0023057 | negative regulation of signaling | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0036293 | response to decreased oxygen levels | 4 | 1 |
GO:0036294 | cellular response to decreased oxygen levels | 5 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0042981 | regulation of apoptotic process | 6 | 1 |
GO:0043066 | negative regulation of apoptotic process | 7 | 1 |
GO:0043067 | regulation of programmed cell death | 5 | 1 |
GO:0043069 | negative regulation of programmed cell death | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0048585 | negative regulation of response to stimulus | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0060548 | negative regulation of cell death | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070482 | response to oxygen levels | 3 | 1 |
GO:0070887 | cellular response to chemical stimulus | 3 | 1 |
GO:0071453 | cellular response to oxygen levels | 4 | 1 |
GO:0071456 | cellular response to hypoxia | 4 | 1 |
GO:0080134 | regulation of response to stress | 4 | 1 |
GO:0080135 | regulation of cellular response to stress | 4 | 1 |
GO:1900037 | regulation of cellular response to hypoxia | 5 | 1 |
GO:1900038 | negative regulation of cellular response to hypoxia | 5 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
GO:1902532 | negative regulation of intracellular signal transduction | 6 | 1 |
GO:1903297 | regulation of hypoxia-induced intrinsic apoptotic signaling pathway | 7 | 1 |
GO:1903298 | negative regulation of hypoxia-induced intrinsic apoptotic signaling pathway | 6 | 1 |
GO:2001233 | regulation of apoptotic signaling pathway | 5 | 1 |
GO:2001234 | negative regulation of apoptotic signaling pathway | 6 | 1 |
GO:2001242 | regulation of intrinsic apoptotic signaling pathway | 6 | 1 |
GO:2001243 | negative regulation of intrinsic apoptotic signaling pathway | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 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:0044183 | protein folding chaperone | 1 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140657 | ATP-dependent activity | 1 | 15 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 486 | 490 | PF00656 | 0.347 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 694 | 696 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.479 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.525 |
DEG_APCC_DBOX_1 | 454 | 462 | PF00400 | 0.404 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.623 |
DOC_CYCLIN_RxL_1 | 424 | 434 | PF00134 | 0.479 |
DOC_CYCLIN_RxL_1 | 451 | 463 | PF00134 | 0.407 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.618 |
DOC_MAPK_gen_1 | 278 | 286 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 310 | 317 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 579 | 587 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 99 | 107 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 492 | 499 | PF00069 | 0.396 |
DOC_PP1_RVXF_1 | 216 | 223 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 4 | 10 | PF00149 | 0.527 |
DOC_PP1_RVXF_1 | 436 | 442 | PF00149 | 0.465 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.445 |
DOC_USP7_MATH_2 | 596 | 602 | PF00917 | 0.280 |
DOC_USP7_UBL2_3 | 569 | 573 | PF12436 | 0.457 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.409 |
LIG_14-3-3_CanoR_1 | 242 | 252 | PF00244 | 0.241 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 456 | 462 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 492 | 498 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 508 | 513 | PF00244 | 0.229 |
LIG_14-3-3_CanoR_1 | 57 | 66 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 624 | 631 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 695 | 705 | PF00244 | 0.241 |
LIG_AP2alpha_2 | 134 | 136 | PF02296 | 0.493 |
LIG_APCC_ABBA_1 | 109 | 114 | PF00400 | 0.429 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.424 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 470 | 474 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.383 |
LIG_Clathr_ClatBox_1 | 536 | 540 | PF01394 | 0.392 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.500 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.352 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.472 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.392 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.440 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.348 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.419 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.760 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.374 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.361 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.339 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.459 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.449 |
LIG_GBD_Chelix_1 | 24 | 32 | PF00786 | 0.493 |
LIG_LIR_Apic_2 | 590 | 596 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 139 | 148 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 300 | 308 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 34 | 42 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 348 | 359 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 368 | 377 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 491 | 502 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 300 | 305 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 348 | 354 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 368 | 372 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 638 | 643 | PF02991 | 0.393 |
LIG_MLH1_MIPbox_1 | 105 | 109 | PF16413 | 0.241 |
LIG_OCRL_FandH_1 | 107 | 119 | PF00620 | 0.241 |
LIG_PCNA_TLS_4 | 628 | 635 | PF02747 | 0.409 |
LIG_PDZ_Class_3 | 719 | 724 | PF00595 | 0.798 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.241 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.493 |
LIG_PTB_Apo_2 | 363 | 370 | PF02174 | 0.493 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.459 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 36 | 39 | PF00017 | 0.392 |
LIG_SH2_SRC | 113 | 116 | PF00017 | 0.493 |
LIG_SH2_SRC | 541 | 544 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 541 | 545 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 687 | 691 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.479 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.409 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.409 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.377 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.482 |
LIG_SH3_4 | 569 | 576 | PF00018 | 0.241 |
LIG_Sin3_3 | 542 | 549 | PF02671 | 0.241 |
LIG_SUMO_SIM_par_1 | 124 | 131 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 313 | 319 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 583 | 588 | PF11976 | 0.366 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.364 |
LIG_TRAF2_1 | 368 | 371 | PF00917 | 0.241 |
LIG_TRAF2_1 | 600 | 603 | PF00917 | 0.479 |
LIG_TRAF2_1 | 667 | 670 | PF00917 | 0.469 |
LIG_TYR_ITIM | 3 | 8 | PF00017 | 0.416 |
LIG_TYR_ITSM | 636 | 643 | PF00017 | 0.241 |
LIG_UBA3_1 | 387 | 393 | PF00899 | 0.452 |
LIG_UBA3_1 | 95 | 100 | PF00899 | 0.280 |
LIG_WRC_WIRS_1 | 104 | 109 | PF05994 | 0.454 |
LIG_WRC_WIRS_1 | 372 | 377 | PF05994 | 0.479 |
MOD_CDK_SPK_2 | 381 | 386 | PF00069 | 0.392 |
MOD_CDK_SPxxK_3 | 170 | 177 | PF00069 | 0.479 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.364 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.398 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.298 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.457 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.429 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.370 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.464 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.356 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.362 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.404 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.427 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.401 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.452 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.482 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.465 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.502 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.464 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.423 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.474 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.375 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.315 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.324 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.263 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.359 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.375 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.389 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.364 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.484 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.711 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.295 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.377 |
MOD_N-GLC_1 | 365 | 370 | PF02516 | 0.453 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.343 |
MOD_N-GLC_1 | 519 | 524 | PF02516 | 0.386 |
MOD_N-GLC_1 | 531 | 536 | PF02516 | 0.342 |
MOD_N-GLC_1 | 558 | 563 | PF02516 | 0.378 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.479 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.376 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.438 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.315 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.441 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.456 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.413 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.326 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.393 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.163 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.372 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.452 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.387 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.500 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.500 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.479 |
MOD_PKA_1 | 99 | 105 | PF00069 | 0.479 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.435 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.420 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.449 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.364 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.423 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.377 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.353 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.442 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.395 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.473 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.367 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.365 |
MOD_Plk_1 | 571 | 577 | PF00069 | 0.454 |
MOD_Plk_1 | 663 | 669 | PF00069 | 0.493 |
MOD_Plk_2-3 | 371 | 377 | PF00069 | 0.479 |
MOD_Plk_2-3 | 598 | 604 | PF00069 | 0.435 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.424 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.484 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.449 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.308 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.443 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.259 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.502 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.392 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.392 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.409 |
MOD_SUMO_rev_2 | 128 | 135 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 563 | 571 | PF00179 | 0.480 |
TRG_DiLeu_BaEn_3 | 139 | 145 | PF01217 | 0.409 |
TRG_DiLeu_BaEn_3 | 706 | 712 | PF01217 | 0.762 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 386 | 390 | PF00026 | 0.378 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDD3 | Leptomonas seymouri | 25% | 86% |
A0A0N1PEF0 | Leptomonas seymouri | 68% | 97% |
A0A0S4IUZ2 | Bodo saltans | 34% | 82% |
A0A0S4JJU2 | Bodo saltans | 39% | 95% |
A0A1X0P2S1 | Trypanosomatidae | 29% | 83% |
A0A1X0P4V9 | Trypanosomatidae | 46% | 100% |
A0A3S5H744 | Leishmania donovani | 27% | 88% |
A0A3S5H808 | Leishmania donovani | 82% | 100% |
A0A3S7WZX1 | Leishmania donovani | 23% | 100% |
A0A422NGS3 | Trypanosoma rangeli | 32% | 78% |
A0A422P1B1 | Trypanosoma rangeli | 45% | 100% |
A2Q0Z1 | Equus caballus | 22% | 100% |
A4H9P0 | Leishmania braziliensis | 26% | 100% |
A4I253 | Leishmania infantum | 23% | 100% |
A4IC10 | Leishmania infantum | 82% | 100% |
A5A8V7 | Sus scrofa | 25% | 100% |
C9ZXL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 87% |
C9ZYJ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A590 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 89% |
D0A8Z2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AFU8 | Leishmania major | 81% | 100% |
E9AGQ5 | Leishmania infantum | 27% | 88% |
E9ARS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 88% |
E9AYA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B700 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
F4HQD4 | Arabidopsis thaliana | 26% | 87% |
F4JMJ1 | Arabidopsis thaliana | 26% | 84% |
O59838 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
O74225 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 100% |
O88600 | Rattus norvegicus | 26% | 86% |
O95757 | Homo sapiens | 26% | 86% |
O97125 | Drosophila melanogaster | 24% | 100% |
P08418 | Schistosoma mansoni | 23% | 100% |
P0CB32 | Bos taurus | 25% | 100% |
P0DMV8 | Homo sapiens | 24% | 100% |
P0DMV9 | Homo sapiens | 24% | 100% |
P0DMW0 | Rattus norvegicus | 24% | 100% |
P0DMW1 | Rattus norvegicus | 24% | 100% |
P11142 | Homo sapiens | 22% | 100% |
P16627 | Mus musculus | 25% | 100% |
P17879 | Mus musculus | 24% | 100% |
P19120 | Bos taurus | 22% | 100% |
P19378 | Cricetulus griseus | 23% | 100% |
P20030 | Trypanosoma brucei brucei | 25% | 100% |
P32589 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P32590 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P34930 | Sus scrofa | 24% | 100% |
P34931 | Homo sapiens | 24% | 100% |
P34932 | Homo sapiens | 26% | 86% |
P36415 | Dictyostelium discoideum | 25% | 100% |
P41827 | Anopheles albimanus | 24% | 100% |
P47773 | Ictalurus punctatus | 22% | 100% |
P55063 | Rattus norvegicus | 25% | 100% |
P59769 | Aspergillus awamori | 24% | 100% |
P63017 | Mus musculus | 22% | 100% |
P63018 | Rattus norvegicus | 22% | 100% |
P78695 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 100% |
P83616 | Aspergillus niger | 24% | 100% |
P83617 | Aspergillus kawachii | 24% | 100% |
Q01PM8 | Solibacter usitatus (strain Ellin6076) | 25% | 100% |
Q05036 | Caenorhabditis elegans | 25% | 93% |
Q06068 | Strongylocentrotus purpuratus | 27% | 81% |
Q0VA61 | Xenopus tropicalis | 30% | 100% |
Q24789 | Echinococcus granulosus | 23% | 100% |
Q27965 | Bos taurus | 24% | 100% |
Q27975 | Bos taurus | 24% | 100% |
Q2TFN9 | Canis lupus familiaris | 27% | 86% |
Q4L6T0 | Staphylococcus haemolyticus (strain JCSC1435) | 23% | 100% |
Q4Q970 | Leishmania major | 24% | 100% |
Q4QDQ2 | Leishmania major | 26% | 100% |
Q4R888 | Macaca fascicularis | 24% | 100% |
Q4U0F3 | Bos mutus grunniens | 24% | 100% |
Q54BE0 | Dictyostelium discoideum | 25% | 100% |
Q566I3 | Xenopus laevis | 31% | 100% |
Q5NVM9 | Pongo abelii | 22% | 100% |
Q5R7D3 | Pongo abelii | 24% | 100% |
Q5RDM4 | Pongo abelii | 26% | 86% |
Q5ZLK7 | Gallus gallus | 28% | 72% |
Q60432 | Cricetulus griseus | 30% | 72% |
Q61316 | Mus musculus | 28% | 86% |
Q61696 | Mus musculus | 24% | 100% |
Q63617 | Rattus norvegicus | 30% | 72% |
Q6FJI3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 23% | 100% |
Q6L590 | Oryza sativa subsp. japonica | 23% | 100% |
Q6S4N2 | Sus scrofa | 24% | 100% |
Q6TMK3 | Dictyostelium discoideum | 23% | 94% |
Q71U34 | Saguinus oedipus | 22% | 100% |
Q74ZJ0 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 100% |
Q7YQC6 | Canis lupus familiaris | 24% | 100% |
Q7ZUW2 | Danio rerio | 29% | 74% |
Q875V0 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 25% | 100% |
Q90473 | Danio rerio | 23% | 100% |
Q94738 | Mesocentrotus franciscanus | 27% | 82% |
Q96VB9 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 100% |
Q9GSU7 | Drosophila simulans | 24% | 100% |
Q9JKR6 | Mus musculus | 30% | 72% |
Q9N1U2 | Saguinus oedipus | 24% | 100% |
Q9S7C0 | Arabidopsis thaliana | 26% | 87% |
Q9SAB1 | Arabidopsis thaliana | 24% | 95% |
Q9Y4L1 | Homo sapiens | 31% | 72% |
V5ARL4 | Trypanosoma cruzi | 45% | 100% |
V5DD81 | Trypanosoma cruzi | 31% | 89% |