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: 1, no: 12 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: A4H5N9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 44 | 48 | PF00656 | 0.547 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.334 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.468 |
DEG_APCC_DBOX_1 | 203 | 211 | PF00400 | 0.503 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 117 | 125 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 29 | 37 | PF00069 | 0.367 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.484 |
DOC_SPAK_OSR1_1 | 235 | 239 | PF12202 | 0.532 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.312 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.359 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.388 |
LIG_deltaCOP1_diTrp_1 | 174 | 179 | PF00928 | 0.444 |
LIG_Dynein_DLC8_1 | 179 | 185 | PF01221 | 0.368 |
LIG_eIF4E_1 | 216 | 222 | PF01652 | 0.377 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.490 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.421 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.455 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.433 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.502 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.466 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.495 |
LIG_MLH1_MIPbox_1 | 185 | 189 | PF16413 | 0.388 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 188 | 191 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.459 |
LIG_SH3_1 | 134 | 140 | PF00018 | 0.419 |
LIG_SH3_2 | 304 | 309 | PF14604 | 0.515 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.332 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.523 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.460 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.378 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.536 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.391 |
LIG_SUMO_SIM_anti_2 | 129 | 135 | PF11976 | 0.344 |
LIG_WRC_WIRS_1 | 28 | 33 | PF05994 | 0.316 |
LIG_WW_3 | 273 | 277 | PF00397 | 0.437 |
LIG_WW_3 | 310 | 314 | PF00397 | 0.543 |
MOD_CDK_SPK_2 | 300 | 305 | PF00069 | 0.469 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.527 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.542 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.653 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.537 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.447 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.422 |
MOD_NEK2_2 | 261 | 266 | PF00069 | 0.314 |
MOD_NEK2_2 | 27 | 32 | PF00069 | 0.355 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.513 |
MOD_PK_1 | 225 | 231 | PF00069 | 0.522 |
MOD_PK_1 | 234 | 240 | PF00069 | 0.378 |
MOD_PKA_1 | 180 | 186 | PF00069 | 0.334 |
MOD_PKA_1 | 234 | 240 | PF00069 | 0.500 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.368 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.500 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.415 |
MOD_Plk_2-3 | 190 | 196 | PF00069 | 0.334 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.569 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.575 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.516 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.363 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.399 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.473 |
MOD_SUMO_rev_2 | 228 | 236 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_1 | 104 | 109 | PF01217 | 0.349 |
TRG_DiLeu_BaEn_1 | 202 | 207 | PF01217 | 0.317 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.347 |
TRG_Pf-PMV_PEXEL_1 | 204 | 209 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P758 | Leptomonas seymouri | 65% | 97% |
A0A0S4J3K3 | Bodo saltans | 35% | 80% |
A0A0S4J3X3 | Bodo saltans | 35% | 84% |
A0A1X0NMM8 | Trypanosomatidae | 52% | 91% |
A0A3R7NP68 | Trypanosoma rangeli | 51% | 94% |
A0A3S7WQN6 | Leishmania donovani | 86% | 100% |
A4H5Q0 | Leishmania braziliensis | 99% | 100% |
A4HTZ0 | Leishmania infantum | 86% | 100% |
D0A8W8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 94% |
E9AMS0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QHV5 | Leishmania major | 86% | 100% |
V5BSP2 | Trypanosoma cruzi | 47% | 82% |