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: 5 |
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: Q4QHA8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 228 | 230 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.550 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.518 |
DOC_MAPK_gen_1 | 195 | 204 | PF00069 | 0.490 |
DOC_MAPK_RevD_3 | 215 | 229 | PF00069 | 0.441 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.619 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.572 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 229 | 235 | PF00244 | 0.530 |
LIG_Actin_WH2_2 | 215 | 230 | PF00022 | 0.502 |
LIG_Clathr_ClatBox_1 | 311 | 315 | PF01394 | 0.433 |
LIG_EH1_1 | 311 | 319 | PF00400 | 0.543 |
LIG_EVH1_1 | 21 | 25 | PF00568 | 0.518 |
LIG_EVH1_2 | 160 | 164 | PF00568 | 0.507 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.592 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.548 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.616 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.560 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.558 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.670 |
LIG_LIR_Apic_2 | 18 | 24 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 174 | 182 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.373 |
LIG_Pex14_2 | 134 | 138 | PF04695 | 0.387 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.567 |
LIG_PTB_Apo_2 | 132 | 139 | PF02174 | 0.472 |
LIG_SH2_GRB2like | 133 | 136 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.407 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.515 |
LIG_SUMO_SIM_par_1 | 50 | 56 | PF11976 | 0.533 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.584 |
LIG_WRC_WIRS_1 | 172 | 177 | PF05994 | 0.371 |
LIG_WW_1 | 160 | 163 | PF00397 | 0.516 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.484 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.629 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.534 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.721 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.431 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.437 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.492 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.469 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.596 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.601 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.579 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.508 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.679 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.643 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.371 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.676 |
MOD_GlcNHglycan | 9 | 13 | PF01048 | 0.642 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.486 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.381 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.469 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.482 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.439 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.552 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.392 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.583 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.483 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.378 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.531 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.553 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.621 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.475 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.400 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.668 |
MOD_Plk_2-3 | 171 | 177 | PF00069 | 0.414 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.623 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.476 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.653 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.566 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5X0 | Leptomonas seymouri | 49% | 95% |
A0A1X0NS26 | Trypanosomatidae | 31% | 100% |
A0A3S7WRA2 | Leishmania donovani | 91% | 100% |
A0A422NGN0 | Trypanosoma rangeli | 32% | 100% |
A4H694 | Leishmania braziliensis | 85% | 100% |
A4HUL7 | Leishmania infantum | 91% | 100% |
C9ZVP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ANB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5DKP6 | Trypanosoma cruzi | 35% | 100% |