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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HE19
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.420 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.626 |
CLV_PCSK_PC7_1 | 221 | 227 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.443 |
DEG_APCC_DBOX_1 | 379 | 387 | PF00400 | 0.536 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.479 |
DOC_CYCLIN_RxL_1 | 247 | 259 | PF00134 | 0.583 |
DOC_CYCLIN_yCln2_LP_2 | 17 | 23 | PF00134 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 203 | 209 | PF00134 | 0.466 |
DOC_MAPK_gen_1 | 167 | 173 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 78 | 86 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 88 | 96 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 183 | 192 | PF00069 | 0.494 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.742 |
DOC_USP7_UBL2_3 | 398 | 402 | PF12436 | 0.695 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 220 | 228 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 263 | 273 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.502 |
LIG_APCC_ABBA_1 | 304 | 309 | PF00400 | 0.444 |
LIG_BIR_III_2 | 7 | 11 | PF00653 | 0.492 |
LIG_deltaCOP1_diTrp_1 | 227 | 235 | PF00928 | 0.462 |
LIG_eIF4E_1 | 165 | 171 | PF01652 | 0.495 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.542 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.623 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.385 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.572 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.537 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.452 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.504 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.434 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.458 |
LIG_LIR_Apic_2 | 227 | 231 | PF02991 | 0.677 |
LIG_LIR_Apic_2 | 234 | 239 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 166 | 173 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.637 |
LIG_LIR_Gen_1 | 82 | 87 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 117 | 121 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.512 |
LIG_Pex14_1 | 44 | 48 | PF04695 | 0.511 |
LIG_Pex14_2 | 158 | 162 | PF04695 | 0.365 |
LIG_PTB_Apo_2 | 229 | 236 | PF02174 | 0.462 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.380 |
LIG_SH2_SRC | 236 | 239 | PF00017 | 0.610 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 317 | 320 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.265 |
LIG_SH3_2 | 111 | 116 | PF14604 | 0.607 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.499 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.438 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.408 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.433 |
LIG_TRFH_1 | 235 | 239 | PF08558 | 0.480 |
LIG_WRC_WIRS_1 | 83 | 88 | PF05994 | 0.338 |
MOD_CDC14_SPxK_1 | 417 | 420 | PF00782 | 0.524 |
MOD_CDK_SPxK_1 | 414 | 420 | PF00069 | 0.549 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.641 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.539 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.518 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.516 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.573 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.410 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.423 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.508 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.498 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.351 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.674 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.700 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.619 |
MOD_GlcNHglycan | 103 | 108 | PF01048 | 0.583 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.455 |
MOD_GlcNHglycan | 194 | 198 | PF01048 | 0.507 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.592 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.605 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.819 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.722 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.821 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.582 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.686 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.519 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.572 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.609 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.490 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.754 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.485 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.539 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.623 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.566 |
MOD_N-GLC_2 | 151 | 153 | PF02516 | 0.545 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.476 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.448 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.711 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.421 |
MOD_NEK2_2 | 231 | 236 | PF00069 | 0.459 |
MOD_NEK2_2 | 302 | 307 | PF00069 | 0.439 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.470 |
MOD_PKA_1 | 220 | 226 | PF00069 | 0.647 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.487 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.498 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.647 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.750 |
MOD_PKB_1 | 262 | 270 | PF00069 | 0.511 |
MOD_PKB_1 | 324 | 332 | PF00069 | 0.503 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.607 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.459 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.534 |
MOD_Plk_2-3 | 124 | 130 | PF00069 | 0.527 |
MOD_Plk_2-3 | 240 | 246 | PF00069 | 0.497 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.534 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.431 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.543 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.568 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.550 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.497 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.515 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.705 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.547 |
MOD_SUMO_rev_2 | 327 | 334 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_1 | 124 | 129 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.761 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.569 |
TRG_NLS_MonoExtC_3 | 87 | 93 | PF00514 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILI8 | Leptomonas seymouri | 50% | 100% |
A0A1X0P4C2 | Trypanosomatidae | 31% | 100% |
A0A3S7WYY8 | Leishmania donovani | 68% | 100% |
A0A422MPP3 | Trypanosoma rangeli | 36% | 100% |
A4I1C6 | Leishmania infantum | 68% | 100% |
E9AXG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
Q4QA10 | Leishmania major | 64% | 100% |
V5BXG5 | Trypanosoma cruzi | 33% | 100% |