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: A4H6T2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.501 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.448 |
CLV_PCSK_FUR_1 | 16 | 20 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.385 |
DEG_COP1_1 | 186 | 195 | PF00400 | 0.520 |
DEG_SPOP_SBC_1 | 60 | 64 | PF00917 | 0.552 |
DOC_CDC14_PxL_1 | 149 | 157 | PF14671 | 0.468 |
DOC_CYCLIN_RxL_1 | 128 | 140 | PF00134 | 0.536 |
DOC_CYCLIN_RxL_1 | 94 | 106 | PF00134 | 0.434 |
DOC_CYCLIN_yClb1_LxF_4 | 49 | 55 | PF00134 | 0.484 |
DOC_MAPK_DCC_7 | 128 | 137 | PF00069 | 0.433 |
DOC_MAPK_DCC_7 | 208 | 217 | PF00069 | 0.627 |
DOC_MAPK_JIP1_4 | 133 | 139 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 133 | 141 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 208 | 217 | PF00069 | 0.656 |
DOC_MAPK_MEF2A_6 | 26 | 33 | PF00069 | 0.392 |
DOC_MAPK_NFAT4_5 | 26 | 34 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 98 | 105 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 37 | 40 | PF13499 | 0.449 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.518 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.416 |
LIG_14-3-3_CanoR_1 | 115 | 124 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 133 | 138 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 326 | 332 | PF00244 | 0.514 |
LIG_APCC_ABBAyCdc20_2 | 100 | 106 | PF00400 | 0.411 |
LIG_BIR_III_2 | 336 | 340 | PF00653 | 0.503 |
LIG_BRCT_BRCA1_1 | 301 | 305 | PF00533 | 0.527 |
LIG_CaM_IQ_9 | 8 | 24 | PF13499 | 0.454 |
LIG_CtBP_PxDLS_1 | 134 | 138 | PF00389 | 0.423 |
LIG_eIF4E_1 | 23 | 29 | PF01652 | 0.407 |
LIG_eIF4E_1 | 98 | 104 | PF01652 | 0.498 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.433 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.537 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.479 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.394 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.404 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.531 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.380 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.741 |
LIG_LIR_Gen_1 | 76 | 87 | PF02991 | 0.536 |
LIG_LIR_LC3C_4 | 311 | 316 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.738 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.542 |
LIG_MYND_1 | 130 | 134 | PF01753 | 0.440 |
LIG_MYND_1 | 339 | 343 | PF01753 | 0.511 |
LIG_Pex14_1 | 233 | 237 | PF04695 | 0.592 |
LIG_SH2_GRB2like | 375 | 378 | PF00017 | 0.467 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 98 | 101 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.534 |
LIG_SH3_1 | 208 | 214 | PF00018 | 0.674 |
LIG_SH3_2 | 211 | 216 | PF14604 | 0.557 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.654 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.588 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 138 | 143 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 308 | 316 | PF11976 | 0.669 |
LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 344 | 349 | PF11976 | 0.531 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.592 |
LIG_UBA3_1 | 27 | 35 | PF00899 | 0.406 |
LIG_WW_2 | 211 | 214 | PF00397 | 0.580 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.583 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.634 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.458 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.538 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.513 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.588 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.669 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.564 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.515 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.372 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.510 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.668 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.550 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.546 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.418 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.610 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.489 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.498 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.713 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.463 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.596 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.705 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.430 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.419 |
MOD_NEK2_2 | 117 | 122 | PF00069 | 0.387 |
MOD_NEK2_2 | 294 | 299 | PF00069 | 0.534 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.485 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.597 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.621 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.534 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.401 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.423 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.623 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.572 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.695 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.490 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.586 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.482 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.605 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.593 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.507 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.398 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.348 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.499 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.552 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.549 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.421 |
TRG_DiLeu_BaEn_1 | 266 | 271 | PF01217 | 0.476 |
TRG_DiLeu_BaLyEn_6 | 23 | 28 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.777 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 100 | 105 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD33 | Leptomonas seymouri | 30% | 91% |
A0A3S7WRT8 | Leishmania donovani | 62% | 100% |
E9AGA6 | Leishmania infantum | 62% | 100% |
E9ANU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
Q4QGS6 | Leishmania major | 63% | 100% |