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: 20 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 2, no: 14 |
NetGPI | no | yes: 0, no: 16 |
Related structures:
AlphaFold database: A4H5A1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.356 |
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.577 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.385 |
DEG_COP1_1 | 130 | 137 | PF00400 | 0.271 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.519 |
DEG_SPOP_SBC_1 | 29 | 33 | PF00917 | 0.463 |
DOC_MAPK_gen_1 | 226 | 234 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.411 |
DOC_PP2B_PxIxI_1 | 229 | 235 | PF00149 | 0.361 |
DOC_PP4_FxxP_1 | 227 | 230 | PF00568 | 0.416 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.481 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 37 | 44 | PF00244 | 0.534 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.462 |
LIG_deltaCOP1_diTrp_1 | 94 | 98 | PF00928 | 0.266 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.383 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.540 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.503 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.454 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.629 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.354 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.577 |
LIG_LIR_Apic_2 | 224 | 230 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 43 | 51 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 94 | 103 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 43 | 47 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.379 |
LIG_MYND_1 | 22 | 26 | PF01753 | 0.492 |
LIG_Pex14_2 | 238 | 242 | PF04695 | 0.383 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.311 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.407 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.326 |
LIG_SH2_STAT3 | 104 | 107 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.495 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.426 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.578 |
LIG_SH3_4 | 229 | 236 | PF00018 | 0.464 |
LIG_UBA3_1 | 231 | 236 | PF00899 | 0.425 |
LIG_WRC_WIRS_1 | 235 | 240 | PF05994 | 0.291 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.481 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.527 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.503 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.490 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.469 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.599 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.568 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.389 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.536 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.561 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.492 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.561 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.486 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.552 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.555 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.519 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.365 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.481 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.536 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.602 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.508 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.431 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.313 |
MOD_NEK2_2 | 93 | 98 | PF00069 | 0.335 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.433 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.505 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.420 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.543 |
MOD_PKA_1 | 288 | 294 | PF00069 | 0.496 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.482 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.496 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.432 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.402 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.362 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.441 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.460 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.291 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.491 |
TRG_DiLeu_BaEn_1 | 43 | 48 | PF01217 | 0.351 |
TRG_DiLeu_BaEn_2 | 93 | 99 | PF01217 | 0.344 |
TRG_DiLeu_LyEn_5 | 43 | 48 | PF01217 | 0.351 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.349 |
TRG_NES_CRM1_1 | 172 | 185 | PF08389 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I400 | Leptomonas seymouri | 59% | 100% |
A0A3S5H641 | Leishmania donovani | 37% | 100% |
A0A3S5H642 | Leishmania donovani | 47% | 100% |
A0A3S7WQ71 | Leishmania donovani | 67% | 96% |
A4H5A0 | Leishmania braziliensis | 39% | 100% |
A4H5A2 | Leishmania braziliensis | 49% | 100% |
A4HTI1 | Leishmania infantum | 37% | 100% |
A4HTI2 | Leishmania infantum | 67% | 96% |
A4HTI3 | Leishmania infantum | 47% | 100% |
E9AMA9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AMB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
E9AMB1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
Q4QID7 | Leishmania major | 46% | 100% |
Q4QID8 | Leishmania major | 67% | 100% |
Q4QID9 | Leishmania major | 39% | 100% |