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 |
Related structures:
AlphaFold database: A4HFQ3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009056 | catabolic process | 2 | 11 |
GO:0009057 | macromolecule catabolic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016579 | protein deubiquitination | 6 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044248 | cellular catabolic process | 3 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 11 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 11 |
GO:0070646 | protein modification by small protein removal | 5 | 11 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1901575 | organic substance catabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008234 | cysteine-type peptidase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 11 |
GO:0101005 | deubiquitinase activity | 5 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.324 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.262 |
CLV_C14_Caspase3-7 | 560 | 564 | PF00656 | 0.338 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.566 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.330 |
CLV_PCSK_PC7_1 | 117 | 123 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.462 |
DEG_APCC_DBOX_1 | 340 | 348 | PF00400 | 0.297 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.495 |
DEG_SPOP_SBC_1 | 425 | 429 | PF00917 | 0.260 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.472 |
DOC_CYCLIN_RxL_1 | 338 | 345 | PF00134 | 0.186 |
DOC_CYCLIN_RxL_1 | 460 | 471 | PF00134 | 0.255 |
DOC_CYCLIN_RxL_1 | 60 | 71 | PF00134 | 0.467 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 561 | 570 | PF00134 | 0.328 |
DOC_MAPK_gen_1 | 22 | 28 | PF00069 | 0.345 |
DOC_MAPK_gen_1 | 245 | 251 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 517 | 525 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 97 | 105 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 412 | 420 | PF00069 | 0.272 |
DOC_PP1_RVXF_1 | 168 | 174 | PF00149 | 0.504 |
DOC_PP1_RVXF_1 | 356 | 362 | PF00149 | 0.385 |
DOC_PP1_RVXF_1 | 463 | 470 | PF00149 | 0.307 |
DOC_PP1_RVXF_1 | 61 | 68 | PF00149 | 0.438 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.766 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.289 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.312 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.428 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.286 |
LIG_14-3-3_CanoR_1 | 170 | 179 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 356 | 362 | PF00244 | 0.271 |
LIG_APCC_ABBAyCdc20_2 | 63 | 69 | PF00400 | 0.454 |
LIG_BIR_III_4 | 540 | 544 | PF00653 | 0.385 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.332 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.253 |
LIG_BRCT_BRCA1_1 | 496 | 500 | PF00533 | 0.388 |
LIG_Clathr_ClatBox_1 | 65 | 69 | PF01394 | 0.466 |
LIG_deltaCOP1_diTrp_1 | 545 | 551 | PF00928 | 0.297 |
LIG_eIF4E_1 | 60 | 66 | PF01652 | 0.429 |
LIG_EVH1_1 | 211 | 215 | PF00568 | 0.469 |
LIG_EVH1_2 | 473 | 477 | PF00568 | 0.385 |
LIG_FAT_LD_1 | 164 | 172 | PF03623 | 0.620 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.704 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.719 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.318 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.432 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.525 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.591 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.249 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.305 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.385 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.582 |
LIG_LIR_Apic_2 | 186 | 191 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 450 | 455 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 295 | 303 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 338 | 347 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 392 | 401 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 518 | 526 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 545 | 556 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 9 | 18 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 338 | 342 | PF02991 | 0.210 |
LIG_LIR_Nem_3 | 360 | 364 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 392 | 396 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 9 | 13 | PF02991 | 0.342 |
LIG_LYPXL_SIV_4 | 57 | 65 | PF13949 | 0.423 |
LIG_NRBOX | 339 | 345 | PF00104 | 0.173 |
LIG_Pex14_1 | 379 | 383 | PF04695 | 0.385 |
LIG_PTB_Apo_2 | 250 | 257 | PF02174 | 0.253 |
LIG_PTB_Apo_2 | 53 | 60 | PF02174 | 0.438 |
LIG_PTB_Phospho_1 | 250 | 256 | PF10480 | 0.253 |
LIG_PTB_Phospho_1 | 53 | 59 | PF10480 | 0.438 |
LIG_REV1ctd_RIR_1 | 498 | 507 | PF16727 | 0.385 |
LIG_REV1ctd_RIR_1 | 65 | 73 | PF16727 | 0.509 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.253 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.253 |
LIG_SH2_CRK | 520 | 524 | PF00017 | 0.253 |
LIG_SH2_GRB2like | 256 | 259 | PF00017 | 0.253 |
LIG_SH2_GRB2like | 54 | 57 | PF00017 | 0.437 |
LIG_SH2_GRB2like | 60 | 63 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 470 | 474 | PF00017 | 0.361 |
LIG_SH2_NCK_1 | 520 | 524 | PF00017 | 0.173 |
LIG_SH2_NCK_1 | 54 | 58 | PF00017 | 0.378 |
LIG_SH2_SRC | 54 | 57 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 537 | 541 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.332 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.470 |
LIG_SH2_STAT3 | 378 | 381 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.310 |
LIG_SH3_2 | 212 | 217 | PF14604 | 0.467 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.712 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.634 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.565 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.170 |
LIG_TRAF2_1 | 395 | 398 | PF00917 | 0.272 |
LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.261 |
LIG_TYR_ITSM | 516 | 523 | PF00017 | 0.272 |
LIG_UBA3_1 | 1 | 7 | PF00899 | 0.300 |
LIG_UBA3_1 | 476 | 481 | PF00899 | 0.262 |
LIG_WRC_WIRS_1 | 293 | 298 | PF05994 | 0.299 |
MOD_CAAXbox | 571 | 574 | PF01239 | 0.416 |
MOD_CDC14_SPxK_1 | 315 | 318 | PF00782 | 0.332 |
MOD_CDK_SPxK_1 | 312 | 318 | PF00069 | 0.332 |
MOD_CDK_SPxxK_3 | 210 | 217 | PF00069 | 0.469 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.562 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.672 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.579 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.625 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.377 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.380 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.385 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.375 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.538 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.664 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.743 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.314 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.286 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.419 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.498 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.535 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.469 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.188 |
MOD_GlcNHglycan | 398 | 402 | PF01048 | 0.328 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.170 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.557 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.438 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.339 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.287 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.234 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.452 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.308 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.413 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.572 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.574 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.385 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.288 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.385 |
MOD_N-GLC_1 | 385 | 390 | PF02516 | 0.270 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.328 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.392 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.385 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.364 |
MOD_N-GLC_2 | 253 | 255 | PF02516 | 0.253 |
MOD_N-GLC_2 | 62 | 64 | PF02516 | 0.424 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.399 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.467 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.479 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.270 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.253 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.227 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.398 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.300 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.385 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.253 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.253 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.309 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.289 |
MOD_NEK2_2 | 510 | 515 | PF00069 | 0.170 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.578 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.207 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.297 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.551 |
MOD_PK_1 | 172 | 178 | PF00069 | 0.571 |
MOD_PK_1 | 385 | 391 | PF00069 | 0.332 |
MOD_PK_1 | 503 | 509 | PF00069 | 0.170 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.558 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.281 |
MOD_PKB_1 | 170 | 178 | PF00069 | 0.566 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.170 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.268 |
MOD_Plk_1 | 385 | 391 | PF00069 | 0.294 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.294 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.243 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.376 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.385 |
MOD_Plk_2-3 | 160 | 166 | PF00069 | 0.615 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.285 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.332 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.253 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.272 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.392 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.191 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.774 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.652 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.286 |
MOD_SUMO_for_1 | 45 | 48 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 552 | 557 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 89 | 98 | PF00179 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.385 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.271 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.283 |
TRG_NLS_Bipartite_1 | 464 | 485 | PF00514 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 341 | 345 | PF00026 | 0.237 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1S4 | Leptomonas seymouri | 64% | 97% |
A0A0S4IVV7 | Bodo saltans | 28% | 97% |
A0A1X0NIL8 | Trypanosomatidae | 25% | 75% |
A0A1X0P5M1 | Trypanosomatidae | 44% | 100% |
A0A3Q8IGB5 | Leishmania donovani | 84% | 100% |
A0A422NFS3 | Trypanosoma rangeli | 43% | 100% |
A4I2S8 | Leishmania infantum | 84% | 100% |
B2GUX4 | Rattus norvegicus | 31% | 100% |
D0A5Z2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9ADA6 | Leishmania major | 83% | 100% |
E9AZ31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
O94269 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
P36026 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 80% |
Q2KJ72 | Bos taurus | 30% | 100% |
Q6NTR6 | Xenopus laevis | 26% | 83% |
Q7ZUM8 | Danio rerio | 28% | 83% |
Q91W36 | Mus musculus | 28% | 100% |
Q9H0E7 | Homo sapiens | 26% | 81% |
Q9HFS7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 27% | 72% |
Q9QZL6 | Mus musculus | 30% | 100% |
Q9Y6I4 | Homo sapiens | 28% | 100% |
V5BQL0 | Trypanosoma cruzi | 44% | 100% |