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:0000407 | phagophore assembly site | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QIU4
Term | Name | Level | Count |
---|---|---|---|
GO:0000045 | autophagosome assembly | 6 | 2 |
GO:0000422 | autophagy of mitochondrion | 4 | 2 |
GO:0006497 | protein lipidation | 5 | 2 |
GO:0006501 | C-terminal protein lipidation | 6 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006914 | autophagy | 3 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006995 | cellular response to nitrogen starvation | 5 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007005 | mitochondrion organization | 5 | 2 |
GO:0007033 | vacuole organization | 5 | 2 |
GO:0007154 | cell communication | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009267 | cellular response to starvation | 4 | 2 |
GO:0009605 | response to external stimulus | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0009991 | response to extracellular stimulus | 3 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016237 | lysosomal microautophagy | 4 | 2 |
GO:0018410 | C-terminal protein amino acid modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0022411 | cellular component disassembly | 4 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0031667 | response to nutrient levels | 4 | 2 |
GO:0031668 | cellular response to extracellular stimulus | 3 | 2 |
GO:0031669 | cellular response to nutrient levels | 4 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034727 | piecemeal microautophagy of the nucleus | 5 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0042594 | response to starvation | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043562 | cellular response to nitrogen levels | 5 | 2 |
GO:0043687 | post-translational protein modification | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044804 | autophagy of nucleus | 4 | 2 |
GO:0044805 | late nucleophagy | 5 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0061726 | mitochondrion disassembly | 6 | 2 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071496 | cellular response to external stimulus | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1903008 | organelle disassembly | 5 | 2 |
GO:1905037 | autophagosome organization | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 11 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 11 |
GO:0019778 | Atg12 activating enzyme activity | 3 | 2 |
GO:0019779 | Atg8 activating enzyme activity | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 152 | 156 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.540 |
CLV_C14_Caspase3-7 | 445 | 449 | PF00656 | 0.418 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.406 |
DEG_APCC_DBOX_1 | 110 | 118 | PF00400 | 0.505 |
DEG_APCC_DBOX_1 | 367 | 375 | PF00400 | 0.401 |
DEG_APCC_DBOX_1 | 635 | 643 | PF00400 | 0.539 |
DEG_COP1_1 | 506 | 517 | PF00400 | 0.373 |
DEG_SIAH_1 | 458 | 466 | PF03145 | 0.451 |
DOC_ANK_TNKS_1 | 539 | 546 | PF00023 | 0.218 |
DOC_CKS1_1 | 562 | 567 | PF01111 | 0.373 |
DOC_CYCLIN_RxL_1 | 25 | 34 | PF00134 | 0.557 |
DOC_CYCLIN_RxL_1 | 388 | 399 | PF00134 | 0.308 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 105 | 114 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 122 | 128 | PF00134 | 0.505 |
DOC_MAPK_DCC_7 | 375 | 384 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 344 | 353 | PF00069 | 0.591 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.307 |
DOC_MAPK_HePTP_8 | 117 | 129 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 120 | 129 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 213 | 221 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 244 | 252 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 295 | 303 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 375 | 384 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 464 | 472 | PF00069 | 0.356 |
DOC_PP1_RVXF_1 | 298 | 304 | PF00149 | 0.534 |
DOC_PP1_RVXF_1 | 326 | 332 | PF00149 | 0.456 |
DOC_PP1_RVXF_1 | 421 | 427 | PF00149 | 0.393 |
DOC_PP2B_PxIxI_1 | 167 | 173 | PF00149 | 0.446 |
DOC_PP2B_PxIxI_1 | 524 | 530 | PF00149 | 0.451 |
DOC_PP4_FxxP_1 | 356 | 359 | PF00568 | 0.486 |
DOC_PP4_FxxP_1 | 57 | 60 | PF00568 | 0.501 |
DOC_PP4_FxxP_1 | 619 | 622 | PF00568 | 0.384 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.307 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.307 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.472 |
LIG_14-3-3_CanoR_1 | 201 | 207 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 267 | 277 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 421 | 427 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 431 | 435 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 49 | 58 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 594 | 604 | PF00244 | 0.379 |
LIG_Actin_WH2_2 | 273 | 291 | PF00022 | 0.535 |
LIG_Actin_WH2_2 | 98 | 113 | PF00022 | 0.501 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.702 |
LIG_BIR_III_4 | 138 | 142 | PF00653 | 0.501 |
LIG_BIR_III_4 | 713 | 717 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 579 | 583 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 690 | 694 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 97 | 101 | PF00533 | 0.501 |
LIG_Clathr_ClatBox_1 | 434 | 438 | PF01394 | 0.418 |
LIG_deltaCOP1_diTrp_1 | 138 | 145 | PF00928 | 0.458 |
LIG_EH_1 | 215 | 219 | PF12763 | 0.453 |
LIG_EH_1 | 662 | 666 | PF12763 | 0.477 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.473 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.501 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.501 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.379 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.411 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.318 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.418 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.480 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.501 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.307 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.411 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.435 |
LIG_GBD_Chelix_1 | 310 | 318 | PF00786 | 0.357 |
LIG_GBD_Chelix_1 | 600 | 608 | PF00786 | 0.379 |
LIG_LIR_Apic_2 | 54 | 60 | PF02991 | 0.501 |
LIG_LIR_Apic_2 | 611 | 616 | PF02991 | 0.418 |
LIG_LIR_Apic_2 | 617 | 622 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 11 | 19 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 226 | 237 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 296 | 306 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 322 | 329 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 425 | 434 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 534 | 544 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 11 | 15 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 158 | 162 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 425 | 429 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.418 |
LIG_PAM2_1 | 334 | 346 | PF00658 | 0.557 |
LIG_Pex14_1 | 331 | 335 | PF04695 | 0.533 |
LIG_Rb_pABgroove_1 | 247 | 255 | PF01858 | 0.501 |
LIG_SH2_GRB2like | 222 | 225 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 130 | 134 | PF00017 | 0.501 |
LIG_SH2_SRC | 153 | 156 | PF00017 | 0.533 |
LIG_SH2_SRC | 613 | 616 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.312 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.550 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.499 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.415 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.401 |
LIG_SH3_3 | 686 | 692 | PF00018 | 0.401 |
LIG_SUMO_SIM_anti_2 | 415 | 420 | PF11976 | 0.314 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.531 |
LIG_TRAF2_1 | 305 | 308 | PF00917 | 0.528 |
LIG_TRAF2_1 | 719 | 722 | PF00917 | 0.624 |
LIG_TRAF2_2 | 359 | 364 | PF00917 | 0.497 |
LIG_UBA3_1 | 114 | 120 | PF00899 | 0.499 |
LIG_UBA3_1 | 150 | 157 | PF00899 | 0.557 |
LIG_WRC_WIRS_1 | 229 | 234 | PF05994 | 0.505 |
LIG_WRC_WIRS_1 | 434 | 439 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 96 | 101 | PF05994 | 0.535 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.617 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.506 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.504 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.330 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.414 |
MOD_CK1_1 | 582 | 588 | PF00069 | 0.356 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.393 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.441 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.543 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.546 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.566 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.517 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.442 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.427 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.652 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.634 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.332 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.307 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.320 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.306 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.368 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.284 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.451 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.322 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.468 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.301 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.545 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.530 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.390 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.548 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.480 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.403 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.121 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.552 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.357 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.363 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.357 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.501 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.321 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.504 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.525 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.401 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.526 |
MOD_NEK2_2 | 430 | 435 | PF00069 | 0.418 |
MOD_NEK2_2 | 558 | 563 | PF00069 | 0.451 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.473 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.558 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.349 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.262 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.455 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.376 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.558 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.467 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.467 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.362 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.386 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.514 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.498 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.519 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.478 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.467 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.372 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.241 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.307 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.307 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.379 |
MOD_Plk_4 | 690 | 696 | PF00069 | 0.434 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.484 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.485 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.418 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.475 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.373 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.470 |
MOD_SUMO_for_1 | 706 | 709 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 438 | 445 | PF00179 | 0.456 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.557 |
TRG_DiLeu_BaEn_2 | 293 | 299 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_4 | 103 | 109 | PF01217 | 0.557 |
TRG_DiLeu_BaEn_4 | 333 | 339 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.307 |
TRG_ER_diArg_1 | 421 | 424 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 489 | 491 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 636 | 639 | PF00400 | 0.560 |
TRG_NLS_MonoCore_2 | 343 | 348 | PF00514 | 0.533 |
TRG_NLS_MonoExtC_3 | 343 | 349 | PF00514 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 484 | 488 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 490 | 494 | PF00026 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 584 | 588 | PF00026 | 0.307 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2V7 | Leptomonas seymouri | 65% | 100% |
A0A1X0P0S1 | Trypanosomatidae | 37% | 88% |
A0A3R7K2D8 | Trypanosoma rangeli | 41% | 95% |
A0A3S5H5V4 | Leishmania donovani | 96% | 100% |
A3LPA1 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 30% | 100% |
A4H4U4 | Leishmania braziliensis | 84% | 100% |
A4HT22 | Leishmania infantum | 96% | 100% |
A5DLC6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 31% | 100% |
A5E0T7 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 31% | 100% |
A6QXC6 | Ajellomyces capsulatus (strain NAm1 / WU24) | 32% | 100% |
A6ZT79 | Saccharomyces cerevisiae (strain YJM789) | 31% | 100% |
A7EI75 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 31% | 100% |
A7KAI6 | Pichia angusta | 30% | 100% |
A7KAL8 | Penicillium rubens (strain ATCC 28089 / DSM 1075 / NRRL 1951 / Wisconsin 54-1255) | 31% | 100% |
A7TEY0 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 30% | 100% |
D0A4R0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 96% |
E9AL10 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
F7W4M2 | Sordaria macrospora (strain ATCC MYA-333 / DSM 997 / K(L3346) / K-hell) | 32% | 100% |
G2XR75 | Botryotinia fuckeliana (strain T4) | 30% | 100% |
I1S0J7 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 34% | 100% |
M7U9B9 | Botryotinia fuckeliana (strain BcDW1) | 30% | 95% |
O43069 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
O93922 | Komagataella pastoris | 30% | 100% |
O95352 | Homo sapiens | 31% | 100% |
P0CM38 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 32% | 100% |
P0CM39 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 32% | 100% |
P38862 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q52CS0 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 30% | 100% |
Q5AWA2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 34% | 100% |
Q5ZKY2 | Gallus gallus | 33% | 100% |
Q641Y5 | Rattus norvegicus | 32% | 100% |
Q6BGV9 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 30% | 100% |
Q6CBC3 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 31% | 100% |
Q6FQY7 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 29% | 100% |
Q86CR9 | Dictyostelium discoideum | 31% | 100% |
Q871U2 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 100% |
Q94CD5 | Arabidopsis thaliana | 32% | 100% |
Q9D906 | Mus musculus | 33% | 100% |
V5B6Z1 | Trypanosoma cruzi | 41% | 95% |