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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8IGM7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.517 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.516 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.533 |
DOC_MAPK_FxFP_2 | 3 | 6 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 253 | 262 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 30 | 40 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 230 | 237 | PF00069 | 0.491 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.395 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 226 | 230 | PF12436 | 0.561 |
LIG_14-3-3_CanoR_1 | 171 | 180 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 210 | 217 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 253 | 262 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 34 | 38 | PF00244 | 0.408 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.488 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.317 |
LIG_Clathr_ClatBox_1 | 18 | 22 | PF01394 | 0.432 |
LIG_Clathr_ClatBox_1 | 244 | 248 | PF01394 | 0.496 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.488 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.510 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.423 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.479 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.480 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.314 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.523 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.528 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.447 |
LIG_GBD_Chelix_1 | 99 | 107 | PF00786 | 0.516 |
LIG_LIR_Gen_1 | 10 | 19 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 216 | 224 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 49 | 56 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 10 | 14 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 216 | 220 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.459 |
LIG_NRBOX | 190 | 196 | PF00104 | 0.520 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.350 |
LIG_Pex14_2 | 89 | 93 | PF04695 | 0.317 |
LIG_SH2_CRK | 217 | 221 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 143 | 147 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 50 | 54 | PF00017 | 0.487 |
LIG_SH2_STAT3 | 17 | 20 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.440 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.460 |
LIG_SUMO_SIM_par_1 | 93 | 98 | PF11976 | 0.451 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.465 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.533 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.535 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.444 |
MOD_Cter_Amidation | 32 | 35 | PF01082 | 0.528 |
MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.479 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.453 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.439 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.551 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.435 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.472 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.419 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.428 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.484 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.425 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.404 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.415 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.391 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.449 |
MOD_PKA_1 | 171 | 177 | PF00069 | 0.540 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.566 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.480 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.337 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.515 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.423 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.422 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.436 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.438 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.456 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.475 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7K0 | Leptomonas seymouri | 61% | 100% |
A0A1X0P1S9 | Trypanosomatidae | 29% | 100% |
A0A3R7MBB6 | Trypanosoma rangeli | 30% | 98% |
A4HLM6 | Leishmania braziliensis | 85% | 100% |
A4I937 | Leishmania infantum | 100% | 100% |
C9ZIV4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 98% |
E9B402 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4Q422 | Leishmania major | 96% | 100% |
V5AXA5 | Trypanosoma cruzi | 29% | 98% |