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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4Q903
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.423 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 33 | 39 | PF00134 | 0.528 |
DOC_PP1_RVXF_1 | 51 | 57 | PF00149 | 0.403 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.434 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.555 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.424 |
LIG_14-3-3_CanoR_1 | 152 | 157 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.567 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.546 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.321 |
LIG_BRCT_BRCA1_1 | 292 | 296 | PF00533 | 0.426 |
LIG_deltaCOP1_diTrp_1 | 270 | 273 | PF00928 | 0.659 |
LIG_EH_1 | 196 | 200 | PF12763 | 0.431 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.493 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.436 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.372 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.660 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.505 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.377 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.402 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.588 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 25 | 29 | PF02991 | 0.380 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.657 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.394 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.413 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 188 | 192 | PF00017 | 0.348 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.457 |
LIG_SH2_STAT3 | 241 | 244 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.267 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.528 |
LIG_SUMO_SIM_par_1 | 12 | 17 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 165 | 170 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.527 |
LIG_WRC_WIRS_1 | 304 | 309 | PF05994 | 0.513 |
MOD_CAAXbox | 314 | 317 | PF01239 | 0.595 |
MOD_CDK_SPK_2 | 25 | 30 | PF00069 | 0.393 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.621 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.614 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.415 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.473 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.604 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.545 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.614 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.469 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.741 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.540 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.360 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.409 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.651 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.502 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.605 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.662 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.369 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.603 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.544 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.563 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.668 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.584 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.763 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.499 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.419 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.439 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.449 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.626 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.433 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.465 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.498 |
MOD_NEK2_2 | 48 | 53 | PF00069 | 0.349 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.727 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.525 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.446 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.485 |
MOD_PK_1 | 260 | 266 | PF00069 | 0.545 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.565 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.391 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.656 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.340 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.626 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.546 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.468 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.701 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.546 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.611 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.374 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.444 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.401 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.422 |
TRG_DiLeu_BaEn_1 | 108 | 113 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.600 |
TRG_DiLeu_LyEn_5 | 17 | 22 | PF01217 | 0.466 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 185 | 189 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7P7 | Leptomonas seymouri | 58% | 94% |
A0A1X0P7Q6 | Trypanosomatidae | 35% | 100% |
A0A3Q8ICA3 | Leishmania donovani | 91% | 100% |
A4HF34 | Leishmania braziliensis | 75% | 99% |
A4I2B8 | Leishmania infantum | 91% | 100% |
E9AYG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5AV59 | Trypanosoma cruzi | 35% | 100% |