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: A4HGH4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.426 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.441 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.678 |
DEG_SPOP_SBC_1 | 228 | 232 | PF00917 | 0.468 |
DEG_SPOP_SBC_1 | 342 | 346 | PF00917 | 0.532 |
DOC_MAPK_gen_1 | 37 | 46 | PF00069 | 0.315 |
DOC_MAPK_gen_1 | 432 | 442 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.315 |
DOC_MAPK_MEF2A_6 | 435 | 444 | PF00069 | 0.542 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.621 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.601 |
DOC_USP7_MATH_2 | 181 | 187 | PF00917 | 0.524 |
DOC_USP7_MATH_2 | 257 | 263 | PF00917 | 0.478 |
DOC_USP7_UBL2_3 | 10 | 14 | PF12436 | 0.517 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 195 | 200 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 227 | 236 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 406 | 415 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 433 | 442 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 69 | 77 | PF00244 | 0.344 |
LIG_Actin_WH2_2 | 189 | 204 | PF00022 | 0.594 |
LIG_APCC_ABBA_1 | 44 | 49 | PF00400 | 0.315 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.520 |
LIG_Clathr_ClatBox_1 | 249 | 253 | PF01394 | 0.611 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.558 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.666 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.695 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.601 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.590 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.568 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.311 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 443 | 450 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 443 | 447 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.306 |
LIG_LYPXL_SIV_4 | 354 | 362 | PF13949 | 0.509 |
LIG_Rb_pABgroove_1 | 291 | 299 | PF01858 | 0.404 |
LIG_RPA_C_Fungi | 298 | 310 | PF08784 | 0.439 |
LIG_SH2_CRK | 220 | 224 | PF00017 | 0.533 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.495 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.437 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.315 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.315 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 360 | 364 | PF00017 | 0.452 |
LIG_SH2_SRC | 187 | 190 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.520 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.708 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.651 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.465 |
LIG_SUMO_SIM_par_1 | 279 | 288 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 289 | 294 | PF11976 | 0.380 |
LIG_TRAF2_1 | 186 | 189 | PF00917 | 0.495 |
LIG_TYR_ITIM | 353 | 358 | PF00017 | 0.515 |
LIG_WW_1 | 18 | 21 | PF00397 | 0.443 |
MOD_CDK_SPxxK_3 | 231 | 238 | PF00069 | 0.519 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.656 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.628 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.564 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.561 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.553 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.617 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.532 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.591 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.620 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.614 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.522 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.487 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.311 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.305 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.733 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.468 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.562 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.653 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.493 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.320 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.698 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.659 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.725 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.567 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.728 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.787 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.632 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.472 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.457 |
MOD_LATS_1 | 38 | 44 | PF00433 | 0.227 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.552 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.661 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.567 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.233 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.543 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.605 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.443 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.447 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.430 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.583 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.424 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.461 |
MOD_PKA_1 | 40 | 46 | PF00069 | 0.315 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.608 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.497 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.330 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.552 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.523 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.556 |
MOD_Plk_2-3 | 183 | 189 | PF00069 | 0.519 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.487 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.522 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.518 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.551 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.588 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.561 |
TRG_DiLeu_BaEn_1 | 245 | 250 | PF01217 | 0.565 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 386 | 391 | PF01217 | 0.524 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 389 | 394 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILU4 | Leptomonas seymouri | 42% | 96% |
A0A3Q8IEL1 | Leishmania donovani | 71% | 96% |
A4I3K6 | Leishmania infantum | 71% | 96% |
E9AZU6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 94% |
Q4Q8D9 | Leishmania major | 70% | 100% |