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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HID1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 275 | 281 | PF00089 | 0.514 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.486 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.321 |
DEG_COP1_1 | 312 | 322 | PF00400 | 0.514 |
DEG_SPOP_SBC_1 | 147 | 151 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.573 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 238 | 247 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 277 | 287 | PF00244 | 0.534 |
LIG_APCC_ABBA_1 | 190 | 195 | PF00400 | 0.399 |
LIG_APCC_ABBAyCdc20_2 | 220 | 226 | PF00400 | 0.503 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.521 |
LIG_eIF4E_1 | 227 | 233 | PF01652 | 0.388 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.508 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.298 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.603 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.482 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.473 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.562 |
LIG_LIR_Gen_1 | 168 | 179 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 22 | 28 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 225 | 235 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 293 | 300 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 304 | 314 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.457 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.461 |
LIG_NRP_CendR_1 | 335 | 337 | PF00754 | 0.459 |
LIG_PCNA_PIPBox_1 | 36 | 45 | PF02747 | 0.461 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.429 |
LIG_SH2_GRB2like | 109 | 112 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 258 | 262 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.486 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.469 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.515 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.503 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.732 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.439 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.581 |
MOD_CDK_SPxK_1 | 329 | 335 | PF00069 | 0.416 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.550 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.669 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.729 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.604 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.544 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.475 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.468 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.604 |
MOD_GlcNHglycan | 195 | 199 | PF01048 | 0.328 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.583 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.220 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.476 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.536 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.631 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.547 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.481 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.477 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.684 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.503 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.433 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.544 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.434 |
MOD_PKA_1 | 277 | 283 | PF00069 | 0.490 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.503 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.541 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.363 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.658 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.414 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.602 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.427 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.500 |
TRG_DiLeu_BaEn_1 | 139 | 144 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_3 | 22 | 28 | PF01217 | 0.320 |
TRG_DiLeu_BaLyEn_6 | 59 | 64 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 135 | 139 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 154 | 159 | PF00026 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8N5 | Leptomonas seymouri | 56% | 100% |
A0A0S4JM68 | Bodo saltans | 29% | 100% |
A0A3Q8IJF7 | Leishmania donovani | 78% | 99% |
A0A422P3H1 | Trypanosoma rangeli | 37% | 100% |
A4I5M4 | Leishmania infantum | 78% | 99% |
C9ZQZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9B0W9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
Q4Q797 | Leishmania major | 78% | 100% |
Q9W1V7 | Drosophila melanogaster | 24% | 75% |
V5BYU5 | Trypanosoma cruzi | 40% | 100% |