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: A4HBJ8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.281 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.502 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.435 |
CLV_PCSK_PC7_1 | 5 | 11 | PF00082 | 0.432 |
CLV_PCSK_PC7_1 | 75 | 81 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.493 |
DEG_APCC_DBOX_1 | 112 | 120 | PF00400 | 0.386 |
DEG_APCC_DBOX_1 | 164 | 172 | PF00400 | 0.348 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.412 |
DOC_MAPK_gen_1 | 235 | 244 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 75 | 85 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 100 | 108 | PF00069 | 0.460 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.516 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.278 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 5 | 9 | PF00244 | 0.568 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.494 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.353 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.322 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.364 |
LIG_BRCT_BRCA1_2 | 63 | 69 | PF00533 | 0.350 |
LIG_CtBP_PxDLS_1 | 134 | 140 | PF00389 | 0.339 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.522 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.243 |
LIG_LIR_Apic_2 | 143 | 147 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.326 |
LIG_MYND_3 | 249 | 253 | PF01753 | 0.456 |
LIG_PCNA_yPIPBox_3 | 28 | 40 | PF02747 | 0.299 |
LIG_PDZ_Class_3 | 250 | 255 | PF00595 | 0.407 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.380 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.360 |
LIG_UBA3_1 | 248 | 254 | PF00899 | 0.344 |
MOD_CDK_SPxxK_3 | 62 | 69 | PF00069 | 0.540 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.283 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.486 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.662 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.494 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.240 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.340 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.359 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.338 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.469 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.455 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.390 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.352 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.352 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.420 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.293 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.471 |
MOD_N-GLC_2 | 97 | 99 | PF02516 | 0.403 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.379 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.526 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.445 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.344 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.632 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.231 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.468 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.564 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.327 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.486 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.721 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.424 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.486 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.464 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.284 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.475 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.443 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.574 |
MOD_SUMO_for_1 | 201 | 204 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 224 | 230 | PF00179 | 0.380 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.434 |
TRG_NES_CRM1_1 | 207 | 220 | PF08389 | 0.333 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IYT2 | Bodo saltans | 29% | 79% |
A0A1X0NXA5 | Trypanosomatidae | 30% | 94% |
A0A3Q8IB00 | Leishmania donovani | 63% | 100% |
A0A3R7N8W3 | Trypanosoma rangeli | 30% | 97% |
D0A1J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 85% |
E9AGU4 | Leishmania infantum | 63% | 100% |
E9AUW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
Q4QCL5 | Leishmania major | 65% | 100% |