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 | yes | yes: 7, no: 2 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4IDV9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.621 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.578 |
CLV_PCSK_FUR_1 | 137 | 141 | PF00082 | 0.539 |
CLV_PCSK_FUR_1 | 175 | 179 | PF00082 | 0.451 |
CLV_PCSK_FUR_1 | 237 | 241 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 380 | 382 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.644 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.569 |
DOC_CYCLIN_RxL_1 | 235 | 246 | PF00134 | 0.500 |
DOC_CYCLIN_yClb1_LxF_4 | 262 | 268 | PF00134 | 0.401 |
DOC_CYCLIN_yCln2_LP_2 | 241 | 247 | PF00134 | 0.416 |
DOC_MAPK_MEF2A_6 | 13 | 20 | PF00069 | 0.489 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.415 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.569 |
DOC_PP4_FxxP_1 | 367 | 370 | PF00568 | 0.472 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.560 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 103 | 110 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 184 | 194 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.489 |
LIG_BRCT_BRCA1_1 | 287 | 291 | PF00533 | 0.463 |
LIG_deltaCOP1_diTrp_1 | 129 | 133 | PF00928 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 358 | 367 | PF00928 | 0.377 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.569 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.539 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.387 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.506 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.701 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.446 |
LIG_LIR_Apic_2 | 54 | 60 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 288 | 297 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 325 | 334 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.511 |
LIG_NRBOX | 237 | 243 | PF00104 | 0.514 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.406 |
LIG_Pex14_1 | 313 | 317 | PF04695 | 0.291 |
LIG_PTB_Apo_2 | 281 | 288 | PF02174 | 0.507 |
LIG_PTB_Apo_2 | 304 | 311 | PF02174 | 0.375 |
LIG_PTB_Phospho_1 | 281 | 287 | PF10480 | 0.505 |
LIG_PTB_Phospho_1 | 304 | 310 | PF10480 | 0.373 |
LIG_RPA_C_Fungi | 173 | 185 | PF08784 | 0.533 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.479 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.580 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.498 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.516 |
LIG_SH2_NCK_1 | 57 | 61 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.509 |
LIG_SH3_2 | 244 | 249 | PF14604 | 0.542 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.522 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.477 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.681 |
LIG_Sin3_3 | 15 | 22 | PF02671 | 0.437 |
LIG_SUMO_SIM_anti_2 | 39 | 44 | PF11976 | 0.364 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.581 |
LIG_TRFH_1 | 222 | 226 | PF08558 | 0.382 |
LIG_WRC_WIRS_1 | 411 | 416 | PF05994 | 0.498 |
MOD_CDC14_SPxK_1 | 246 | 249 | PF00782 | 0.582 |
MOD_CDK_SPxK_1 | 243 | 249 | PF00069 | 0.552 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.609 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.407 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.587 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.415 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.654 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.544 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.663 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.387 |
MOD_CMANNOS | 130 | 133 | PF00535 | 0.517 |
MOD_CMANNOS | 313 | 316 | PF00535 | 0.404 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.464 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.497 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.489 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.563 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.590 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.573 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.566 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.703 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.537 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.642 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.751 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.377 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.411 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.656 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.482 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.692 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.601 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.559 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.465 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.664 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.502 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.707 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.627 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.402 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.517 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.718 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.509 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.368 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.728 |
MOD_PKB_1 | 366 | 374 | PF00069 | 0.527 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.617 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.440 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.547 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.527 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.339 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.469 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.576 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.586 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.564 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.615 |
TRG_DiLeu_BaEn_1 | 154 | 159 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_4 | 154 | 160 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.406 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 205 | 210 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 390 | 394 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P921 | Leptomonas seymouri | 58% | 100% |
A0A1X0P090 | Trypanosomatidae | 29% | 100% |
A0A3Q8IRP6 | Leishmania donovani | 100% | 100% |
A0A422NKF7 | Trypanosoma rangeli | 32% | 100% |
A4HQ60 | Leishmania braziliensis | 79% | 100% |
D0A457 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ATY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q0L6 | Leishmania major | 92% | 100% |