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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HQ97
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.693 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.543 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.529 |
DEG_Kelch_Keap1_1 | 232 | 237 | PF01344 | 0.544 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.497 |
DOC_CYCLIN_RxL_1 | 264 | 271 | PF00134 | 0.467 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.472 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.515 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.602 |
DOC_USP7_MATH_2 | 133 | 139 | PF00917 | 0.471 |
DOC_USP7_UBL2_3 | 386 | 390 | PF12436 | 0.667 |
DOC_USP7_UBL2_3 | 432 | 436 | PF12436 | 0.355 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.540 |
LIG_14-3-3_CterR_2 | 445 | 447 | PF00244 | 0.433 |
LIG_BIR_III_4 | 222 | 226 | PF00653 | 0.513 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.567 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.691 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.490 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.555 |
LIG_LIR_Gen_1 | 299 | 308 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 317 | 325 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 66 | 75 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.501 |
LIG_LYPXL_SIV_4 | 300 | 308 | PF13949 | 0.473 |
LIG_NRBOX | 265 | 271 | PF00104 | 0.531 |
LIG_NRBOX | 340 | 346 | PF00104 | 0.518 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.308 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.336 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.588 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.648 |
LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 2 | 8 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 405 | 412 | PF11976 | 0.371 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.555 |
LIG_TYR_ITIM | 15 | 20 | PF00017 | 0.569 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.694 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.576 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.573 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.642 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.436 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.482 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.614 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.432 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.555 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.648 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.561 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.451 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.498 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.611 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.532 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.719 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.444 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.461 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.557 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.268 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.383 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.648 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.573 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.668 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.650 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.576 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.643 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.411 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.672 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.734 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.509 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.436 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.540 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.522 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.503 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.558 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.510 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.680 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.372 |
MOD_PKA_1 | 170 | 176 | PF00069 | 0.564 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.428 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.543 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.659 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.532 |
MOD_Plk_2-3 | 228 | 234 | PF00069 | 0.718 |
MOD_Plk_2-3 | 412 | 418 | PF00069 | 0.354 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.503 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.447 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.597 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.516 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.550 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.650 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.472 |
TRG_DiLeu_BaEn_1 | 419 | 424 | PF01217 | 0.599 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.584 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.468 |
TRG_NLS_MonoCore_2 | 384 | 389 | PF00514 | 0.554 |
TRG_NLS_MonoExtC_3 | 384 | 389 | PF00514 | 0.554 |
TRG_NLS_MonoExtN_4 | 385 | 391 | PF00514 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 251 | 256 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEF3 | Leptomonas seymouri | 44% | 84% |
A0A1X0NLI7 | Trypanosomatidae | 26% | 100% |
A0A3Q8IPS4 | Leishmania donovani | 70% | 100% |
A0A3R7NLX1 | Trypanosoma rangeli | 28% | 100% |
D0A414 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AHY4 | Leishmania infantum | 71% | 100% |
E9AU15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q0I0 | Leishmania major | 69% | 100% |