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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HGV1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.540 |
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.628 |
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.744 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.626 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.578 |
CLV_PCSK_FUR_1 | 206 | 210 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.562 |
DEG_APCC_DBOX_1 | 317 | 325 | PF00400 | 0.516 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.554 |
DOC_CYCLIN_RxL_1 | 456 | 469 | PF00134 | 0.399 |
DOC_MAPK_gen_1 | 306 | 315 | PF00069 | 0.609 |
DOC_MAPK_gen_1 | 498 | 506 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 52 | 59 | PF00069 | 0.561 |
DOC_PP1_RVXF_1 | 130 | 136 | PF00149 | 0.495 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.525 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.510 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 456 | 465 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 491 | 497 | PF00244 | 0.338 |
LIG_APCC_ABBA_1 | 57 | 62 | PF00400 | 0.573 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.594 |
LIG_CaM_IQ_9 | 476 | 492 | PF13499 | 0.406 |
LIG_deltaCOP1_diTrp_1 | 406 | 413 | PF00928 | 0.586 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.671 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.636 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.520 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.560 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.553 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.578 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.534 |
LIG_FXI_DFP_1 | 410 | 414 | PF00024 | 0.651 |
LIG_HCF-1_HBM_1 | 365 | 368 | PF13415 | 0.531 |
LIG_LIR_Apic_2 | 35 | 40 | PF02991 | 0.524 |
LIG_LIR_Apic_2 | 365 | 371 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 406 | 413 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.594 |
LIG_PDZ_Class_1 | 508 | 513 | PF00595 | 0.570 |
LIG_Rb_LxCxE_1 | 435 | 453 | PF01857 | 0.374 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.528 |
LIG_SH2_CRK | 493 | 497 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 311 | 315 | PF00017 | 0.616 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.608 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.546 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.605 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.664 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.508 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.352 |
LIG_SUMO_SIM_anti_2 | 426 | 432 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 429 | 435 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 501 | 507 | PF11976 | 0.564 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.581 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.552 |
LIG_UBA3_1 | 464 | 470 | PF00899 | 0.313 |
LIG_WW_3 | 49 | 53 | PF00397 | 0.643 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.816 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.665 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.539 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.536 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.599 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.580 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.547 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.603 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.546 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.553 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.500 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.519 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.584 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.609 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.608 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.650 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.690 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.674 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.668 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.579 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.542 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.540 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.633 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.679 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.543 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.339 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.291 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.658 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.526 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.678 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.642 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.717 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.655 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.549 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.528 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.631 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.510 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.599 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.497 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.598 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.627 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.511 |
MOD_Plk_2-3 | 277 | 283 | PF00069 | 0.524 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.675 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.534 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.508 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.603 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.700 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.679 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.563 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.549 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.741 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.500 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.487 |
MOD_SUMO_rev_2 | 322 | 332 | PF00179 | 0.535 |
TRG_DiLeu_BaEn_2 | 452 | 458 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_4 | 406 | 412 | PF01217 | 0.560 |
TRG_DiLeu_BaEn_4 | 420 | 426 | PF01217 | 0.585 |
TRG_DiLeu_BaLyEn_6 | 460 | 465 | PF01217 | 0.383 |
TRG_DiLeu_LyEn_5 | 187 | 192 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 305 | 308 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.645 |
TRG_NLS_Bipartite_1 | 193 | 211 | PF00514 | 0.578 |
TRG_NLS_MonoExtC_3 | 206 | 211 | PF00514 | 0.588 |
TRG_NLS_MonoExtN_4 | 206 | 211 | PF00514 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 318 | 322 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 462 | 466 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA28 | Leptomonas seymouri | 42% | 100% |
A0A3S5H7K0 | Leishmania donovani | 64% | 99% |
A4I3Y1 | Leishmania infantum | 64% | 99% |
E9B071 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4Q814 | Leishmania major | 65% | 98% |