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: A0A3Q8IFN6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.397 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.643 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.767 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.661 |
DOC_CKS1_1 | 226 | 231 | PF01111 | 0.360 |
DOC_CKS1_1 | 66 | 71 | PF01111 | 0.590 |
DOC_CYCLIN_RxL_1 | 175 | 184 | PF00134 | 0.354 |
DOC_MAPK_gen_1 | 253 | 262 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 162 | 170 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.361 |
DOC_PP1_RVXF_1 | 365 | 371 | PF00149 | 0.325 |
DOC_PP2B_LxvP_1 | 171 | 174 | PF13499 | 0.351 |
DOC_PP2B_LxvP_1 | 260 | 263 | PF13499 | 0.371 |
DOC_PP4_FxxP_1 | 62 | 65 | PF00568 | 0.576 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.317 |
DOC_USP7_UBL2_3 | 251 | 255 | PF12436 | 0.438 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 120 | 129 | PF00244 | 0.773 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 44 | 49 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.567 |
LIG_APCC_ABBA_1 | 397 | 402 | PF00400 | 0.365 |
LIG_BIR_III_2 | 330 | 334 | PF00653 | 0.421 |
LIG_BRCT_BRCA1_1 | 151 | 155 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.574 |
LIG_deltaCOP1_diTrp_1 | 290 | 300 | PF00928 | 0.394 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.540 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.396 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.443 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.372 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.371 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.517 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.401 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.402 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.662 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 222 | 229 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 332 | 340 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.599 |
LIG_Pex14_1 | 294 | 298 | PF04695 | 0.455 |
LIG_Pex14_1 | 300 | 304 | PF04695 | 0.405 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.580 |
LIG_RPA_C_Fungi | 80 | 92 | PF08784 | 0.518 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.566 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.519 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.598 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.487 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.626 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.737 |
LIG_SUMO_SIM_par_1 | 141 | 148 | PF11976 | 0.531 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.665 |
LIG_WRC_WIRS_1 | 295 | 300 | PF05994 | 0.385 |
LIG_WW_1 | 64 | 67 | PF00397 | 0.568 |
MOD_CDK_SPK_2 | 136 | 141 | PF00069 | 0.660 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.584 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.754 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.476 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.556 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.414 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.601 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.726 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.763 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.598 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.419 |
MOD_DYRK1A_RPxSP_1 | 106 | 110 | PF00069 | 0.603 |
MOD_DYRK1A_RPxSP_1 | 56 | 60 | PF00069 | 0.525 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.688 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.602 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.549 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.608 |
MOD_GlcNHglycan | 34 | 38 | PF01048 | 0.616 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.460 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.766 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.639 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.499 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.502 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.543 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.419 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.568 |
MOD_LATS_1 | 118 | 124 | PF00433 | 0.693 |
MOD_LATS_1 | 217 | 223 | PF00433 | 0.434 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.475 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.349 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.645 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.360 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.525 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.365 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.549 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.349 |
MOD_PK_1 | 141 | 147 | PF00069 | 0.612 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.609 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.594 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.614 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.559 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.483 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.580 |
MOD_Plk_2-3 | 15 | 21 | PF00069 | 0.558 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.356 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.414 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.384 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.505 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.307 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.350 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.502 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.655 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.595 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.365 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.396 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.426 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.636 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.651 |
TRG_DiLeu_BaEn_1 | 375 | 380 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5M5 | Leptomonas seymouri | 58% | 100% |
A4HNH9 | Leishmania braziliensis | 78% | 100% |
A4IC35 | Leishmania infantum | 100% | 100% |
E9AFZ0 | Leishmania major | 94% | 100% |
E9B743 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |