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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HTT8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.375 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.328 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.507 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.269 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.542 |
DOC_PP1_RVXF_1 | 464 | 471 | PF00149 | 0.394 |
DOC_PP2B_LxvP_1 | 215 | 218 | PF13499 | 0.457 |
DOC_PP2B_PxIxI_1 | 14 | 20 | PF00149 | 0.386 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 421 | 424 | PF00568 | 0.392 |
DOC_SPAK_OSR1_1 | 62 | 66 | PF12202 | 0.269 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.274 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.328 |
LIG_14-3-3_CanoR_1 | 155 | 160 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 265 | 273 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 346 | 350 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 466 | 471 | PF00244 | 0.509 |
LIG_Actin_WH2_2 | 480 | 497 | PF00022 | 0.375 |
LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.216 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.328 |
LIG_DLG_GKlike_1 | 466 | 474 | PF00625 | 0.335 |
LIG_eIF4E_1 | 221 | 227 | PF01652 | 0.463 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.573 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.594 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.433 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.300 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.448 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.444 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.381 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.341 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.392 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.383 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.703 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.747 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.477 |
LIG_LIR_Apic_2 | 158 | 164 | PF02991 | 0.644 |
LIG_LIR_Apic_2 | 348 | 352 | PF02991 | 0.319 |
LIG_LIR_Apic_2 | 418 | 424 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 12 | 17 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 52 | 56 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.269 |
LIG_Pex14_2 | 421 | 425 | PF04695 | 0.546 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.569 |
LIG_SH2_CRK | 485 | 489 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.623 |
LIG_SH2_SRC | 161 | 164 | PF00017 | 0.628 |
LIG_SH2_STAT3 | 428 | 431 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.382 |
LIG_SH3_1 | 70 | 76 | PF00018 | 0.386 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.489 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.472 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.427 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.293 |
LIG_SUMO_SIM_par_1 | 434 | 439 | PF11976 | 0.324 |
LIG_TYR_ITIM | 483 | 488 | PF00017 | 0.342 |
LIG_WW_1 | 218 | 221 | PF00397 | 0.560 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.622 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.591 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.674 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.443 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.701 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.634 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.535 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.639 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.575 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.652 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.540 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.625 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.527 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.648 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.328 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.413 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.498 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.763 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.515 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.324 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.539 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.407 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.323 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.520 |
MOD_LATS_1 | 244 | 250 | PF00433 | 0.645 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.590 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.532 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.594 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.363 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.359 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.331 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.488 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.597 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.396 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.646 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.319 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.440 |
MOD_PKA_1 | 466 | 472 | PF00069 | 0.299 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.372 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.322 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.312 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.563 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.637 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.441 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.545 |
MOD_Plk_2-3 | 345 | 351 | PF00069 | 0.399 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.535 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.504 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.375 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.394 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.250 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.358 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.374 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.272 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.602 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.526 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.328 |
MOD_SUMO_for_1 | 352 | 355 | PF00179 | 0.422 |
TRG_DiLeu_BaEn_2 | 11 | 17 | PF01217 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.521 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.510 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.399 |
TRG_NES_CRM1_1 | 24 | 36 | PF08389 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 486 | 490 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5R3 | Leptomonas seymouri | 45% | 100% |
A0A1X0NNG0 | Trypanosomatidae | 33% | 100% |
A0A3R7K8K9 | Trypanosoma rangeli | 32% | 100% |
A0A3S5H6B6 | Leishmania donovani | 100% | 100% |
E9AML9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
Q4QI06 | Leishmania major | 92% | 100% |
V5BMV9 | Trypanosoma cruzi | 31% | 100% |