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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 8 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HD71
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.421 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 359 | 361 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.535 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.637 |
DOC_MAPK_gen_1 | 188 | 195 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 295 | 304 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 350 | 358 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 86 | 95 | PF00069 | 0.410 |
DOC_MAPK_HePTP_8 | 85 | 97 | PF00069 | 0.255 |
DOC_MAPK_MEF2A_6 | 298 | 306 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 88 | 97 | PF00069 | 0.377 |
DOC_PP4_FxxP_1 | 166 | 169 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.570 |
DOC_USP7_UBL2_3 | 261 | 265 | PF12436 | 0.497 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.363 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 350 | 358 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 6 | 14 | PF00244 | 0.526 |
LIG_APCC_ABBA_1 | 302 | 307 | PF00400 | 0.434 |
LIG_CtBP_PxDLS_1 | 247 | 251 | PF00389 | 0.474 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.389 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.401 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.406 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.412 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.422 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.325 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.374 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.486 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.533 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.255 |
LIG_LIR_Apic_2 | 165 | 169 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 179 | 190 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.574 |
LIG_Pex14_1 | 344 | 348 | PF04695 | 0.420 |
LIG_Pex14_2 | 182 | 186 | PF04695 | 0.404 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.504 |
LIG_SH2_GRB2like | 314 | 317 | PF00017 | 0.419 |
LIG_SH2_GRB2like | 321 | 324 | PF00017 | 0.387 |
LIG_SH2_NCK_1 | 327 | 331 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.517 |
LIG_SH2_STAT3 | 321 | 324 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.382 |
LIG_SH3_1 | 339 | 345 | PF00018 | 0.326 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.481 |
LIG_UBA3_1 | 128 | 135 | PF00899 | 0.474 |
LIG_UBA3_1 | 181 | 189 | PF00899 | 0.433 |
LIG_UBA3_1 | 59 | 67 | PF00899 | 0.293 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.448 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.333 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.369 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.255 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.455 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.413 |
MOD_GlcNHglycan | 236 | 240 | PF01048 | 0.397 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.294 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.468 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.546 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.396 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.567 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.585 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.384 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.604 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.397 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.406 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.556 |
MOD_PKA_1 | 359 | 365 | PF00069 | 0.565 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.345 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.549 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.521 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.460 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.436 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.417 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.363 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.363 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.363 |
MOD_SUMO_for_1 | 384 | 387 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 238 | 247 | PF00179 | 0.512 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.474 |
TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.363 |
TRG_DiLeu_BaLyEn_6 | 77 | 82 | PF01217 | 0.263 |
TRG_DiLeu_LyEn_5 | 225 | 230 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 28 | 32 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I340 | Leptomonas seymouri | 82% | 100% |
A0A0S4J2H9 | Bodo saltans | 26% | 69% |
A0A1X0NIN0 | Trypanosomatidae | 65% | 100% |
A0A3Q8ICQ2 | Leishmania donovani | 87% | 100% |
A0A3R7N419 | Trypanosoma rangeli | 63% | 100% |
A6NHY2 | Homo sapiens | 23% | 75% |
C9ZRD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 95% |
D0A6Y4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
D3J162 | Medicago truncatula | 27% | 73% |
E5RJM6 | Homo sapiens | 29% | 99% |
E9AH25 | Leishmania infantum | 87% | 100% |
E9AWK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q337A0 | Oryza sativa subsp. japonica | 32% | 76% |
Q3V096 | Mus musculus | 27% | 75% |
Q495B1 | Homo sapiens | 27% | 75% |
Q4FE45 | Arabidopsis thaliana | 28% | 77% |
Q4QAW7 | Leishmania major | 86% | 100% |
Q5UPG5 | Acanthamoeba polyphaga mimivirus | 28% | 94% |
Q6AWW5 | Arabidopsis thaliana | 28% | 75% |
Q6KAE5 | Oryza sativa subsp. japonica | 32% | 79% |
Q7EZ44 | Oryza sativa subsp. japonica | 30% | 80% |
Q8N9B4 | Homo sapiens | 27% | 100% |
Q8Q0U0 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 29% | 100% |
Q9H560 | Homo sapiens | 24% | 100% |
Q9J4Z5 | Fowlpox virus (strain NVSL) | 28% | 90% |
Q9J516 | Fowlpox virus (strain NVSL) | 26% | 91% |
Q9J5A7 | Fowlpox virus (strain NVSL) | 26% | 73% |
Q9J5G9 | Fowlpox virus (strain NVSL) | 23% | 95% |
Q9J5H9 | Fowlpox virus (strain NVSL) | 25% | 68% |
Q9SAR5 | Arabidopsis thaliana | 28% | 100% |
V5BW01 | Trypanosoma cruzi | 65% | 100% |