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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HD34
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.557 |
DEG_APCC_DBOX_1 | 248 | 256 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 297 | 305 | PF00400 | 0.446 |
DOC_ANK_TNKS_1 | 18 | 25 | PF00023 | 0.574 |
DOC_CYCLIN_RxL_1 | 134 | 145 | PF00134 | 0.400 |
DOC_MAPK_DCC_7 | 406 | 415 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 10 | 16 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 136 | 142 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 219 | 228 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 295 | 303 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 219 | 228 | PF00069 | 0.611 |
DOC_MAPK_MEF2A_6 | 406 | 415 | PF00069 | 0.567 |
DOC_MAPK_NFAT4_5 | 223 | 231 | PF00069 | 0.605 |
DOC_MAPK_RevD_3 | 234 | 249 | PF00069 | 0.470 |
DOC_PP2B_LxvP_1 | 418 | 421 | PF13499 | 0.488 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.616 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.611 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 194 | 202 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 31 | 35 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 464 | 470 | PF00244 | 0.718 |
LIG_AP2alpha_1 | 362 | 366 | PF02296 | 0.443 |
LIG_APCC_ABBA_1 | 12 | 17 | PF00400 | 0.546 |
LIG_APCC_ABBAyCdc20_2 | 11 | 17 | PF00400 | 0.560 |
LIG_BIR_III_2 | 100 | 104 | PF00653 | 0.469 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.518 |
LIG_CtBP_PxDLS_1 | 410 | 414 | PF00389 | 0.590 |
LIG_deltaCOP1_diTrp_1 | 346 | 351 | PF00928 | 0.460 |
LIG_EH1_1 | 166 | 174 | PF00400 | 0.371 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.518 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.618 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.450 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.609 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.546 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.616 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.350 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.508 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.574 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.670 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.565 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.527 |
LIG_LIR_Apic_2 | 211 | 216 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.562 |
LIG_NRBOX | 454 | 460 | PF00104 | 0.556 |
LIG_PCNA_PIPBox_1 | 40 | 49 | PF02747 | 0.409 |
LIG_Pex14_2 | 362 | 366 | PF04695 | 0.511 |
LIG_Pex14_2 | 393 | 397 | PF04695 | 0.480 |
LIG_REV1ctd_RIR_1 | 13 | 23 | PF16727 | 0.555 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.455 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.607 |
LIG_SUMO_SIM_anti_2 | 299 | 305 | PF11976 | 0.437 |
LIG_SUMO_SIM_anti_2 | 39 | 45 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 323 | 330 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 39 | 45 | PF11976 | 0.579 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.566 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.591 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.565 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.444 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.626 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.566 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.587 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.675 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.484 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.558 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.519 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.596 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.619 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.574 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.373 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.552 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.659 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.524 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.559 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.589 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.611 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.475 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.496 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.526 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.599 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.681 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.464 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.647 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.566 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.478 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.621 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.559 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.600 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.391 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.691 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.634 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.562 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.572 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.470 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.443 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.499 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.636 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.476 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.642 |
MOD_NEK2_2 | 399 | 404 | PF00069 | 0.535 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.700 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.360 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.561 |
MOD_PK_1 | 118 | 124 | PF00069 | 0.581 |
MOD_PKA_1 | 248 | 254 | PF00069 | 0.498 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.574 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.658 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.529 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.639 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.593 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.398 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.513 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.581 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.539 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.689 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.525 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.639 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.714 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.510 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.650 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.377 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.465 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.495 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.568 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 403 | 406 | PF00400 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 128 | 132 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 222 | 227 | PF00026 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 425 | 429 | PF00026 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G3 | Leptomonas seymouri | 37% | 100% |
A0A3Q8ICP2 | Leishmania donovani | 74% | 100% |
A4I0M1 | Leishmania infantum | 73% | 100% |
E9AWI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QAY8 | Leishmania major | 74% | 100% |
V5ARA2 | Trypanosoma cruzi | 24% | 100% |